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EUROPEAN Device Guide Search Results for “”
Aortic (AAA) / Main Body Grafts
View Chart| Company Name | Product Name | Main Body Diameter (mm) | Main Body Length (cm) | Main Body Delivery System Profile: Device OD (F) | Sheath Required for Delivery | Delivery Sheath OD (F) | Fixation Location | Stent Expansion | Stent Material | Graft Material | Comments |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Artivion, Inc. | E-tegra Stent Graft System | 23, 26, 29, 32, 36 | 10, 12.5, 13.5, 15.5, 16 | 18 (23–29 mm), 20 (32, 36 mm) | No | – | Suprarenal | Self expanding | Nitinol | Woven polyester | – |
| Cook Medical | Zenith Alpha Abdominal | 22, 24, 26, 28, 30, 32, 36 | 7, 8.4, 9.8, 10.8, 11.8, 12.8 | 18 (22–32-mm grafts), 19 (36-mm grafts) | No | 18 (22–32-mm grafts), 19 (36-mm grafts) | Suprarenal | Self expanding | Nitinol | Woven polyester | – |
| Cook Medical | Zenith Fenestrated AAA Endovascular Graft (Distal Bifurcated Body) | 24 | 7.6, 9.4, 10.9, 12.4 | 23 | No | – | – | Self expanding | Stainless steel | Woven polyester | – |
| Cook Medical | Zenith Fenestrated AAA Endovascular Graft (One Proximal Seal Stent) | 24, 26, 28, 30, 32, 34, 36 | 7.6, 9.1, 10.6, 12.1 (24–32-mm grafts); 8.4, 9.9, 11.4, 12.9 (34–36-mm grafts) | 23 (24–34-mm grafts), 26 (36-mm graft) | No | – | Suprarenal | Self expanding | Stainless steel | Woven polyester | – |
| Cook Medical | Zenith Fenestrated AAA Endovascular Graft (Two Proximal Seal Stents) | 24, 26, 28, 30, 32, 34, 36 | 9.4, 10.9, 12.4 (24–32-mm grafts); 10.7, 12.2, 13.7 (34–36-mm grafts) | 23 (24–34-mm grafts), 26 (36-mm graft) | No | – | Suprarenal | Self expanding | Stainless steel and nitinol | Woven polyester | – |
| Cook Medical | Zenith Flex With Z-Trak | 22, 24, 26, 28 30, 32, 36 | 8.2, 9.6, 11.1, 12.5, 14 (22–32-mm grafts), 9.5, 11.3, 13.1, 14.9 (36-mm grafts) | 21 (22–26-mm grafts), 23 (28–32-mm grafts), 26 (36-mm grafts) | No | – | Suprarenal | Self expanding | Stainless steel and nitinol | Woven polyester | – |
| Cordis | Incraft AAA Stent Graft System | 22, 26, 30, 34 | 8.6 (contralateral side), 9.4 (ipsilateral side) | 14, 16 (for 34 main body) | No (integrated sheath included in OD) | 14 (16 for 34 main body) | Suprarenal | Self expanding | Nitinol | Woven polyester | – |
| Endologix | AFX Endovascular AAA System – AFX2 Bifurcated Endograft System | 22, 25, 28 | 6, 7, 8, 9, 10, 11, 12 | 17 | Yes, AFX introducer system 7 F (contralateral), 17 F (ipsilateral) | 9 (contralateral), 19 (ipsilateral) | Fixation at bifurcation, infrarenal, or suprarenal configurations for seal | Self expanding | Cobalt chromium alloy | Duraply multilayer ePTFE | – |
| Endologix | Alto Abdominal Stent Graft System | 20, 23, 26, 29, 34 | 8 | 15 | No, integrated sheath | Integrated 15-F OD sheath | Suprarenal | Nonexpansive polymer-filled ring* | Nitinol | PTFE | *With a 7-mm neck indication, the aortic main body seals using an adaptive, patient-specific, polymer technology rather than self-expanding stents |
| Endologix | Ovation iX Abdominal Stent Graft System | 20, 23, 26, 29, 34 | 8 | 14, 15 | No; integrated 12–13-F sheath | – | Suprarenal | Nonexpansive polymer-filled ring* | Nitinol | PTFE | *The Ovation main body seals using CustomSeal polymer rather than self-expanding stents; only the limbs include self-expanding stents |
| Gore & Associates | Gore Excluder AAA Endoprosthesis featuring C3 Delivery System | 23,* 26,* 28.5,* 31,† 35‡ | 12, 13, 14, 15, 16, 17, 18 | 16, 18 | Yes | 18.3, 20.1 | Infrarenal | Self expanding | Nitinol | ePTFE | *23, 26, and 28.5-mm graft lengths: 12, 14, 16, 18 cm; †31-mm graft lengths: 13, 15, 17 cm; ‡35-mm graft lengths: 14, 16, 18 cm |
| Gore & Associates | Gore Excluder Conformable AAA Endoprosthesis with Active Control System | 20,* 23,* 26,* 28.5,* 32,† 36† | 12,* 14† | 16, 18 | Yes | 18.3, 20.1 | Infrarenal | Self expanding | Nitinol | ePTFE | *20, 23, 26, 28.5-mm graft lengths: 12 cm; †32- and 36-mm graft lengths: 14 cm |
| Medtronic | Endurant II AAA Stent Graft System | 23, 25, 28, 32, 36 | 12.4, 14.5, 16.6 | 18, 20 | No | – | Suprarenal | Self expanding | Nitinol | Woven polyester | CE Mark approved for ChEVAR with ≥ 2-mm neck combined with balloon-expandable covered renal stents; CE Mark approved short neck indication: Endurant + Heli-FX with 10 mm down to ≥ 4 mm |
| Medtronic | Endurant II AUI Stent Graft System | 23, 25, 28, 32, 36 | 10.2 | 18, 20 | No | – | Suprarenal | Self expanding | Nitinol | Woven polyester | CE Mark approved for ChEVAR with ≥ 2-mm neck combined with balloon-expandable covered renal stents |
| Medtronic | Endurant IIs AAA Stent Graft System | 23, 25, 28, 32, 36 | 10.3 | 18, 20 | No | – | Suprarenal | Self expanding | Nitinol | Woven polyester | CE Mark approved for ChEVAR with ≥ 2-mm neck combined with balloon-expandable covered renal stents; CE Mark approved short neck indication: Endurant + Heli-FX with 10 mm down to ≥ 4 mm |
| Terumo Aortic | Anaconda | 21.5, 23.5, 25.5, 28, 30.5, 32, 34 | 7.7 (4 cm from peak to bifurcation) | 20 (21.5- and 23.5-mm grafts); 23 (25.5-, 28-, 30.5-, 32-, and 34-mm grafts) | No | – | Infrarenal | Self expanding | Nitinol | Woven polyester | – |
| Terumo Aortic | Anaconda (Custom-made) | – | Fully customized fenestrated stent graft | 20, 22 | No | – | Suprarenal | Self expanding | Nitinol | Woven polyester | – |
| Terumo Aortic | Anaconda LoPro90 | 21.5, 23.5, 25.5, 28, 30.5, 32, 34 | 7.7 (4 cm from peak to bifurcation) | 20 (21.5-, 23.5-, 25.5-, 28-, and 30.5-mm grafts); 22 (32- and 34-mm grafts) | No | – | Infrarenal | Self expanding | Nitinol | Woven polyester | – |
| Terumo Aortic | Treo | 20, 22, 24, 26, 28, 30, 33, 36 | 8, 10, 12 | 18, 19 (for 30, 33, 36 main bodies) | No | 18, 19 (for 30, 33, 36 main bodies) | Suprarenal, infrarenal | Self expanding | Nitinol | Tightly woven polyester | – |
| Lombard Medical Limited | Altura Aortic Stent-Graft System | 24, 27, 30 | 9 | 14 | No | – | Suprarenal | Self expanding | Nitinol | Woven polyester | – |
| Lombard Medical Limited (manufactured by MicroPort Endovastec) | Minos Abdominal Aortic Stent-Graft System | 22, 24, 26, 28, 30,32, 34 | 10 | 14 (22-26-mm grafts), 16 (28 34-mm grafts) | No | – | Suprarenal | Self expanding | Nitinol | Woven polyester | – |
| Lombard Medical Limited | Aorfix Abdominal Aortic Stent-Graft System | 24, 27, 31 | 8.1, 9.6, 11.1, 12.6 | 16, 18 (ID) | No | – | Infrarenal | Self expanding | Nitinol | Woven polyester | 12 (distal ipsilateral leg diameter), 63 (ipsilateral leg length) |
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Aortic (AAA) / Iliac Limbs
View Chart| Company Name | Product Name | Iliac Limb Diameter (mm) | Iliac Limb Length (cm) | Comments |
|---|---|---|---|---|
| Artivion, Inc. | E-tegra Stent Graft System | 10, 13, 16, 19, 22, 25 | 3, 5, 6.5, 7, 9, 10.5 (working length) | Overall length is the working length +3 cm |
| Cook Medical | Zenith Alpha Abdominal | 9, 11, 13, 16, 20, 24 | 4.2, 5.9, 7.7, 9.3, 11,* 12.5* | *Only available in 9-, 11-, and 13-mm diameter |
| Cook Medical | Zenith Fenestrated AAA Endovascular Graft (Distal Bifurcated Body) | 12, 16, 20, 24* | 2.8, 4.5, 6.2 | *Not available in 2.8-cm length |
| Cook Medical | Zenith Spiral-Z Iliac Leg Graft | 9, 11, 13, 16, 20, 24 | 3.9, 5.6, 7.4, 9, 10.7,* 12.2* | *Only available in 9-, 11-, and 13-mm diameter |
| Cordis | Incraft AAA Stent Graft System | 10, 13, 16, 20, 24 | 8, 10, 12, 14 | – |
| Endologix | AFX Endovascular AAA System – AFX2 Bifurcated Endograft System | 13,* 16, 20 | 3,† 4, 5.5 | *Diameter available with 6- or 8-cm main body only; †length available with 7- and 9-cm main body length |
| Endologix | Ovation iX Abdominal Stent Graft System | 10, 12, 14, 16, 18, 22, 28 | 8, 10, 12, 14, 16 | *The main body seals using CustomSeal polymer rather than self-expanding stents; only the limbs include self-expanding stents |
| Gore & Associates | Gore Excluder AAA Endoprosthesis | 12, 14.5, 16, 18, 20, 23, 27 | 9.5,* 10, 11.5,* 12, 13.5,* 14 | *Lengths for 16-, 18-, and 20-mm diameter grafts only |
| Medtronic | Endurant II AAA Stent Graft System | 10, 13, 16, 20, 24, 28 | 8.2, 9.3, 12.4, 15.6, 19.9* | *Reflects total limb length |
| Medtronic | Endurant II AUI Stent Graft System | 10, 13, 16, 20, 24, 28 | 8.2, 9.3, 12.4, 15.6, 19.9* | *Reflects total limb length |
| Medtronic | Endurant IIs AAA Stent Graft System | 10, 13, 16, 20, 24, 28 | 8.2, 9.3, 12.4, 15.6, 19.9* | *Reflects total limb length |
| Terumo Aortic | Anaconda | 9–23 mm (distal flared/tapered options are available) | 6, 8, 8.5, 10, 11, 12, 13, 14, 15, 16, 17, 18 | 9–23-mm diameter available; only legs with a 12-mm diameter docking zone at the proximal end of the grafts are compatible with Anaconda Body Systems |
| Terumo Aortic | Anaconda (Custom-made) | 10–23 mm (distal flared/tapered options are available) | 6, 8, 8.5, 10, 11, 12, 13, 14, 15, 16, 17, 18 | 10–23-mm diameter available; only legs with a 12-mm diameter docking zone at the proximal end of the grafts are compatible with Anaconda Body Systems |
| Terumo Aortic | Anaconda LoPro90 | 10–23 mm (distal flared/tapered options are available) | 6, 8, 8.5, 10, 11, 12, 13, 14, 15, 16, 17, 18 | 10–23 mm diameter available; only legs with a 12-mm diameter docking zone at the proximal end of the grafts are compatible with Anaconda Body Systems |
| Terumo Aortic | Treo | 9, 11, 13, 15, 17, 20, 24 | 8, 10, 12, 14, 16 | 13 F: 9, 11, 13, 15 mm; 14 F: 17, 20, 24 mm |
| Lombard Medical Limited | Altura Aortic Stent-Graft System | 13, 17, 21 | 6.5 | – |
| Lombard Medical Limited (manufactured by MicroPort Endovastec) | Minos Abdominal Aortic Stent-Graft System | 10, 13, 16, 18, 20, 24 | 8, 10, 12, 14 | 12F OD |
| Lombard Medical Limited | Aorfix Abdominal Aortic Stent-Graft System | 10, 12, 14, 16, 18, 20 | 5.6, 7.3, 9.0, 10.6 (L3 > 8.1) (working length) | – |
Aortic (AAA) / Iliac Branch
View Chart| Company Name | Product Name | Common Iliac Artery Length (cm) | External Artery Length (cm) | Distal Device Diameter (mm) | Proximal Device Diameter (mm) | Branch Diameter (mm) | Delivery System Profile: Device OD (mm) | Sheath Required for Delivery | Delivery Sheath OD (F) | Fixation Location | Stent Expansion | Stent Material | Graft Material |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Artivion, Inc. | E-liac Stent Graft System | 5.3, 6.5 | 4.4, 5.6 | 10, 12, 14 | 14, 16, 18 | 8 | 6.25 | No | 18 | Aorto-iliac or isolated iliac aneurysms | Self expanding | Nitinol | Woven polyester |
| Cook Medical | Zenith Branch Endovascular Graft - Iliac Bifurcation | 4.5, 6.1 | 4.1, 5.8 | 10, 12 | 12 | 8 | 7.7 | No | 23 | Internal and external iliac artery | Self expanding | Nitinol/stainless steel | Woven polyester |
| Gore & Associates | Gore Excluder Iliac Branch Component | 5.5 (can be deployed above aortic bifurcation) | 4.5 | 10, 12, 14.5 | 23 | 13 | 6.2 | Yes | 18.3 | Internal and external iliac artery | Self expanding | Nitinol | ePTFE |
| Gore & Associates | Gore Excluder Internal Iliac Component | – | 4.5 (internal artery length) | 10, 12, 14.5 | 16 | – | 5 | Yes | 14.1 | Internal iliac artery | Self expanding | Nitinol | ePTFE |
Aortic (AAA) / Ancillary Components
View Chart| Company Name | Product Name | Main Body Extensions Diameter (mm) | Main Body Extensions Length (cm) | Iliac Leg Extensions Diameter (mm) | Iliac Leg Extensions Length (cm) | Aorto-Uni-Iliac/Converter Proximal Diameter (mm) | Aorto-Uni-Iliac/Converter Length (cm) | Occluders Diameter (mm) | Comments |
|---|---|---|---|---|---|---|---|---|---|
| AndraTec GmbH Germany | Optimus-CVS PTFE Covered Stent | 8–28 | 1.8–5.7 | 5–100 | 8–100 mm | 18–100 | 5–57 mm | 28 | BX stent adaptable |
| AndraTec GmbH Germany | Optimus-XL Stent | 18–57 | 8–28 mm | 5–10 | 1.8–5.7 | BX adaptable | BX adaptable | 25 | BX CoCr stent |
| Artivion, Inc. | E-tegra Stent Graft System | 23, 26, 29, 32, 36, 38 | 5 | 13, 19, 22, 27 | 5 | 23, 26, 29, 32, 36 | 105 | – | – |
| Cook Medical | Zenith Ancillary Components | 22, 24, 26, 28, 30, 32, 36 | 3.9, 4.5,* 5, 5.8,* 7.3† | – | – | 24, 28, 32, 36 | 6.6,* 8, 8.2† | – | *Zenith Alpha AAA; †lengths for 36-mm diameter grafts only |
| Cordis | Incraft Aortic Extension | 22, 26, 30, 34 | 4.2 | – | – | – | – | – | – |
| Endologix | AFX Endovascular AAA System – Limb Extensions | – | – | 16, 20 (straight); 20–25 (stepped); 13–20 (taper) | 5.5, 8.8 (straight); 5.5, 6.5 (stepped); 7, 8.8 (taper) | – | – | – | – |
| Endologix | AFX Endovascular AAA System – Vela Proximal Endograft System | 25, 28, 34 (infrarenal/suprarenal) | 5.5, 7.5, 8, 9.5, 10 (infrarenal); 7.5, 8, 9.5, 10 (suprarenal) | – | – | – | – | – | – |
| Endologix | Ovation iX Abdominal Stent Graft System | – | – | 10, 12, 14, 16, 18, 22, 28 | 4.5 | – | – | – | – |
| Gore & Associates | Gore Excluder AAA Endoprosthesis | 20, 23, 26, 28.5, 32, 36 | 3.3, 4.5 | 10, 12, 14.5, 16, 18, 20, 23, 27 | 7,* 9.5,† 10, 11.5,† 12, 13.5,† 14 | – | – | – | *Length is for 10-, 12-, and 14.5-mm diameter only; 10-mm diameter only comes with a 7-cm length; †lengths are for 16-, 18-, and 20-mm diameter grafts only |
| Medtronic | Endurant II AAA Stent Graft System | 23, 25, 28, 32, 36 | 4.9, 7 | 10, 13, 20, 24, 28 | 8.2 | 23, 25, 28, 32, 36 | 10.2 | – | – |
| Terumo Aortic | Anaconda (Custom-made) Cuff | 21–36 | Up to 12 | – | – | – | – | – | – |
| Terumo Aortic | Anaconda Aortic Extension Cuff | 19.5, 21.5, 23.5, 25.5, 28, 30.5, 32, 34 | 3.2 | – | – | – | – | – | – |
| Terumo Aortic | Treo Aorto-Uni-Iliac Body | 20, 22, 24, 26, 28, 30, 33, 36 | 10 | – | – | 20, 22, 24, 26, 28, 30, 33, 36 | 10 | 8, 10, 12, 14, 17, 20, 24 | 18 F (20-28 mm); 19 F (30-36 mm) |
| Terumo Aortic | Treo Occluder | 8, 10, 12, 14, 17, 20, 24 | – | – | 3.1, 3.3, 3.5 | – | – | – | 14-F delivery system |
| Terumo Aortic | Treo Proximal Aortic Cuff | 20, 22, 24, 26, 28, 30, 33, 36 | 4, 5.5, 7 | – | – | – | – | – | 18 F (20–28 mm); 19 F (30–36 mm) |
| Lombard Medical Limited | Aorfix Abdominal Aortic Stent-Graft System - Proximal Extender | 24, 27, 31 | 3.8 | – | – | – | – | – | – |
| Lombard Medical Limited (manufactured by MicroPort Endovastec) | Minos Abdominal Aortic Stent-Graft System | 22, 24, 26, 28, 30, 32, 34 | 4 | – | – | – | – | – | 16 F (OD) |
| Lombard Medical Limited | Aorfix Abdominal Aortic Stent-Graft System - Distal Extender | – | – | 10, 12, 14, 16, 18, 20 | 5.1, 8.2 | – | – | – | Length 5.1 cm; for 12-mm extension, 8.2 cm length available |
Aortic (AAA) / Diagnostic Catheters
View Chart| Company Name | Product Name | Catheter Type | Size (F) | Recommended Introducer Size (F) | Guidewire Compatibility (inch) | Catheter Length (cm) |
|---|---|---|---|---|---|---|
| AngioDynamics | Accu-Vu Sizing Catheter | Sizing catheter, flush (2RO, 21RO, 10RO) (nonbraided) | 4, 5 | 4, 5 | 0.035, 0.038 | 70, 90, 100 |
| AngioDynamics | Mariner Hydrophilic Angiographic Catheter | Hydrophilic diagnostic catheter, flush and selective (nonbraided and braided) | 4, 5 | 4, 5 | 0.035, 0.038 | 40–150 |
| AngioDynamics | Soft-Vu Angiographic Catheter | Diagnostic catheter, flush and selective (nonbraided and braided) | 4, 5, 6 | 4, 5, 6 | 0.035, 0.038 | 25–150 |
| Cook Medical | Aurous Centimeter Sizing Catheters | Sizing | 5 | 5 | 0.035 | 100 |
| Cook Medical | CXI Support Catheter | Support (DAV) | 4 | – | 0.035 | 90, 135, 150 |
| Cook Medical | Royal Flush Plus Flush Catheter | Angiographic flush | 5 | 5 | 0.035, 0.038 | 70, 100 |
| Cook Medical | Torcon NB Advantage Angiographic Catheter | Angiography (KMP, H1, DAV, MPA, VERT) | 5 | 5 | 0.038 | 40, 65, 100 |
| Merit Medical Systems, Inc. | Performa Vessel Sizing Catheters | Vessel sizing | 4, 5 | 4, 5 | 0.035 | 65, 80, 100 |
Aortic (AAA) / Dilators
View Chart| Company Name | Product Name | Size (F) | Dilator Length (cm) | Guidewire Compatibility (inch) |
|---|---|---|---|---|
| Cook Medical | Endovascular Dilator and Sets | 14, 16/18, 20/22, 24/26 | 45 | 0.035 |
Aortic (AAA) / Endograft Fixation Systems
View Chart| Company Name | Product Name | Components | Sizes | Comments | CE Mark Indications |
|---|---|---|---|---|---|
| Medtronic | Heli-FX EndoAnchor System | Heli-FX Guide | Deflecting tip length: 22, 28 mm; 16-F OD; 62-cm working length; 0.035-inch wire compatible | Deflecting guide catheter used to position Heli-FX Applier to EndoAnchor implants | Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic AneuRx, Medtronic Endurant, Medtronic Talent AAA, Medtronic Talent TAA, Medtronic Valiant Xcelerant, Medtronic Valiant Captivia, and Medtronic Valiant Navion endografts; use with other endografts has not been evaluated |
| Medtronic | Heli-FX EndoAnchor System | Heli-FX Applier with EndoAnchor Cassette (contains 10 EndoAnchors) | 12-F OD; 86-cm working length | Battery-operated delivery system with two-stage EndoAnchor deployment with repositioning capability; packaged with an EndoAnchor cassette (includes 10 EndoAnchor implants); EndoAnchor implants are 3-mm diameter X 4.5-mm length helix shape, with 0.5-mm wire thickness | Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic AneuRx, Medtronic Endurant, Medtronic Talent AAA, Medtronic Talent TAA, Medtronic Valiant Xcelerant, Medtronic Valiant Captivia, and Medtronic Valiant Navion endografts; use with other endografts has not been evaluated |
| Medtronic | Heli-FX EndoAnchor System | Ancillary EndoAnchor Cassette (contains five EndoAnchors) | EndoAnchor implants are 3-mm diameter X 4.5-mm length helix shape, with 0.5-mm wire thickness | Provides additional EndoAnchor implants to supplement independent transmural sealing and fixation of an endograft to the aortic wall | Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic AneuRx, Medtronic Endurant, Medtronic Talent AAA, Medtronic Talent TAA, Medtronic Valiant Xcelerant, Medtronic Valiant Captivia, and Medtronic Valiant Navion endografts; use with other endografts has not been evaluated |
Aortic (AAA) / Endovascular Aneurysm Sealing Systems
View Chart| Company Name | Product Name | Length (cm) | Diameter (mm) | Delivery System Profile: Device Outer Diameter (F) | Sheath Required for Delivery | Polymer | Polymer Cartridge Size (mL) | Stent Material | Stent Expansion | Comments |
|---|---|---|---|---|---|---|---|---|---|---|
| Endologix | Nellix EndoVascular Sealing System | 10–20 | 2 X 10* | 17 | No | Polyethylene glycol-based | 40, 70 | ePTFE-covered CoCr | Balloon expandable | *Single stent flow lumen diameter |
Aortic (AAA) / Guidewires
View Chart| Company Name | Product Name | Diameter (inch) | Length (cm) | Flexible Tip Length (cm) |
|---|---|---|---|---|
| Abbott | Supracore | 0.035 | 145, 190, 300 | 10 |
| AndraTec GmbH Germany | Lokum Amplatz Stiff Type | 0.035 | 180, 260, 320, 360 | 5 |
| AndraTec GmbH Germany | Lokum L-Quest Extra Stiff Type Guide Wire | 0.035 | 90, 150, 180, 260 | 5, 10, 15 |
| Artivion, Inc. | E-wire Guidewire: E-xtra Stiff | 0.035 | 190, 300 | 6 |
| Boston Scientific Corporation | Amplatz Super Stiff Guidewire | 0.038 (0.97 mm) | 75, 145, 180, 260 | 6 |
| Boston Scientific Corporation | Amplatz Super Stiff Guidewire | 0.035 (0.89 mm) | 75, 145, 180, 260 | 7 |
| Boston Scientific Corporation | Amplatz Super Stiff J Guidewire | 0.035 (0.89 mm) | 145, 180, 260 | 6 |
| Boston Scientific Corporation | Amplatz Super Stiff J Guidewire | 0.038 (0.97 mm) | 145, 180 | 6 |
| Boston Scientific Corporation | Amplatz Super Stiff ST Guidewire | 0.035 (0.89 mm), 0.038 (0.97 mm) | 260 | 1 |
| Boston Scientific Corporation | Amplatz Super Stiff ST Guidewire | 0.035 (0.89 mm), 0.038 (0.97 mm) | 145 | 4 |
| Boston Scientific Corporation | Meier C Curve | 0.035 (0.89 mm) | 300 | 11 |
| Boston Scientific Corporation | Meier J Curve | 0.035 (0.89 mm) | 185 | 16 |
| Cook Medical | Amplatz Extra-Stiff Straight | 0.035 | 180, 260, 300 | 1 |
| Cook Medical | Amplatz Ultra-Stiff Curved | 0.035 | 260 | 7 |
| Cook Medical | Amplatz Ultra-Stiff Straight | 0.035 | 260 | 7 |
| Cook Medical | Classic Bentson Wire Guides | 0.035 | 180, 260 | 20 |
| Cook Medical | Classic Rosen Curved Wire Guides | 0.035 | 145, 180, 260 | 6 |
| Cook Medical | Lunderquist Double Curved Exchange | 0.035 | 260, 300 | 4 |
| Cook Medical | Lunderquist Extended Double Curved Exchange | 0.035 | 260, 300 | 4 |
| Cook Medical | Lunderquist Extra Stiff Wire Guides | 0.035 | 260, 300 | 4 |
| Merit Medical Systems, Inc. | InQwire Amplatz Guide Wires | 0.035, 0.038 | 75, 145, 180, 260 | 1, 3.5, 4, 6, 7; 3-mm J-shaped tip |
| Merit Medical Systems, Inc. | InQwire Guide Wires | 0.014, 0.018, 0.025, 0.035, 0.038 | 80, 150, 180, 260 | Bentson: 10, 15, and 23; Newton: 15, 18, and 23; J: 1.5, 3, 6, and 15 |
Aortic (AAA) / Introducers
View Chart| Company Name | Product Name | Size (F) | Length (cm) | Guidewire Compatibility (inch) | Curved/Straight | Radiopaque Tip (Yes/No) | Hydrophilic Coating (Yes/No) |
|---|---|---|---|---|---|---|---|
| AngioDynamics | Mini Stick MAX Coaxial Microintroducer Kits | 4, 5 (microintroducer; standard or stiff) | 10 | 0.018- X 45-cm (stainless/stainless, nitinol/tungsten, stainless/tungsten) | Straight | Available | No |
| Cook Medical | Extra Large Check-Flo Introducers | 20, 22, 24 | 25, 40 | 0.035 | Straight | No | No |
| Cook Medical | Flexor: Ansel With High Flex Dilator | 7, 8 | 55 | 0.035 | Straight/curved | Yes | Yes |
| Cook Medical | Flexor: Ansel With High Flex Dilator | 10, 12 | 45 | 0.035 | Straight/curved | Yes | Yes |
| Cook Medical | Large Check-Flo Performer Introducers | 16, 18 | 30 | 0.038 | Straight | Yes | No |
| Cook Medical | Performer Introducer | 14 | 30 | 0.038 | Straight | Yes | No |
| Cook Medical | Performer Introducer | 5, 6, 7 | 13 | 0.035 | Straight | Yes | No |
Aortic (AAA) / Occlusion/Molding Balloons
View Chart| Company Name | Product Name | Size (F) | Recommended Introducer Size (F) | Guidewire Compatibility (inch) | Catheter Length (cm) | Maximum Inflated Balloon Diameter (mm) |
|---|---|---|---|---|---|---|
| AndraTec GmbH Germany | AltoSa-SFT | 10.5 | 12 | 0.035 | 65, 100, 130 | 46 |
| Artivion, Inc. | E-xpand Stent Graft Balloon Catheter | 12 | 12 | 0.035 or smaller | 100 | 50 |
| Boston Scientific Corporation | Equalizer Balloon Catheter | 7 (2.3 mm) | 14, 16 (4.7–5.3 mm) | 0.038 (0.97 mm) | 65, 100 | 20, 27, 33, 40 |
| Cook Medical | Coda Balloon Catheter | 10 | 14 | 0.035 | 140 | 46 |
| Cook Medical | Coda LP Balloon Catheter | 9 | 12 | 0.035 | 120 | 32 |
| Gore & Associates | Gore Molding & Occlusion Balloon | 10 | 10 | 0.035 | 90 | 37 |
| Medtronic | Reliant Stent Graft Balloon Catheter | 8 | 12 | 0.038 or smaller | 100 | 46 |
| Merit Medical Systems, Inc. | Q50X Stent Graft Balloon Catheter | 8 | 10 | 0.038 or smaller | 65, 100 | 50 |
| Prytime Medical Devices, Inc. | ER-REBOA PLUS Catheter | 6 | 7 | Guidewire free | 72 | 32 |
| Front Line Medical Technologies Inc. | COBRA-OS | 4 | 4 | Guidewire free | 55 working length | 25 |
Aortic (AAA) / Other Accessories
View Chart| Company Name | Product Name | Size (F) | Guidewire Compatibility (inch) | Comments |
|---|---|---|---|---|
| Cook Medical | Nester Platinum Embolization Coils | – | 0.035 | Occludes a wider range of vessel sizes with Nester coils |
| Cook Medical | Tornado Platinum Embolization Coils | – | 0.035 | Tornado embolization coil for vessel applications |
| Cook Medical | Vascular Retrieval Forceps | 3 | – | Vascular retrieval forceps |
| Gore & Associates | Gore DrySeal Flex Introducer Sheath | 10, 12, 14, 15, 16, 18, 20, 22, 24, 26 | 0.035 | A new standard of flexibility to treat more challenging anatomies |
| Gore & Associates | Gore Tri-Lobe Balloon Catheter | 18 | 0.035 | Unique Tri-Lobe design allows for continuous blood flow |
| Medtronic | Sentrant Introducer Sheath With Hydrophilic Coating | 12–26 | 0.035 | Hemostatic and kink-resistant introducer sheath |
| Medtronic | TourGuide Steerable Sheath With Hydrophobic Coating | 6.5, 7, 8.5 | 0.035, 0.038 | Steerable hydrophobic coating, self-locking rotating knob, and wide variety of applications within the human vasculature, from the periphery to the intracardiac |
Aortic (AAA) / Snares
View Chart| Company Name | Product Name | Catheter Size/Length (F/cm) | Working Diameter (mm) | Snare Type |
|---|---|---|---|---|
| AndraTec GmbH Germany | Exeter Snare | 4/65, 4/125, 4/150, 5/65, 5/125, 5/150 | 5–35 | Open loop snare for 3D retrieval |
| Cook Medical | Indy OTW Vascular Retriever | 8/55, 8/100 | 40 | Four-loop 40-mm radiopaque metal OTW vascular retriever snare with Flexor sheath and Tuohy-Borst hemostatic valve (55 and 100 cm); compatible with 0.035-inch guidewires |
Aortic (TAA) / Thoracic Stent Grafts
View Chart| Company Name | Product Name | Stent Material | Graft Material | Stent Expansion | Length (cm) | Diameter (mm) | Sheath Required for Delivery | Sheath Compatibility (F) |
|---|---|---|---|---|---|---|---|---|
| Cook Medical | Zenith Alpha Thoracic Endovascular Graft: Distal Component | Nitinol | Polyester | Self expanding | 142–211 mm | 28–46 | No | 16–20 (ID) |
| Cook Medical | Zenith Alpha Thoracic Endovascular Graft: Distal Extension | Nitinol | Polyester | Self expanding | 91–112 mm | 26–46 | No | 16–20 (ID) |
| Cook Medical | Zenith Alpha Thoracic Endovascular Graft: Proximal Component | Nitinol | Polyester | Self expanding | 105–233 mm | 24–46 | No | 16–20 (ID) |
| Cook Medical | Zenith Alpha Thoracic Endovascular Graft: Proximal Tapered Component | Nitinol | Polyester | Self expanding | 108–233 mm | 30–46 | No | 16–20 (ID) |
| Cook Medical | Zenith Dissection Endovascular Stent | Nitinol | – | Self expanding | 80–185 mm | 36–46 | No | 16 (ID) |
| Cook Medical | Zenith TX2 Dissection Endovascular Graft With Pro-Form: Double Tapered Components 8 mm | Stainless steel | Polyester | Self expanding | 156–210 mm | 32–42 | No | 20–22 (ID) |
| Cook Medical | Zenith TX2 Dissection Endovascular Graft With Pro-Form: Straight Components | Stainless steel | Polyester | Self expanding | 79–218 mm | 22–42 | No | 20–22 (ID) |
| Cook Medical | Zenith TX2 Dissection Endovascular Graft With Pro-Form: Tapered Component 4 mm | Stainless steel | Polyester | Self expanding | 154–210 mm | 32–42 | No | 20–22 (ID) |
| Cook Medical | Zenith TX2 TAA Endovascular Graft With Pro-Form: Proximal Double Tapered Components 10 mm | Stainless steel | Polyester | Self expanding | 159–205 mm | 38–42 | No | 20–22 (ID) |
| Gore & Associates | Gore TAG Conformable Thoracic Stent Graft With Active Control System | Nitinol | ePTFE | Self expanding | 10, 15, 20 | 21, 26, 28, 31, 34, 37, 40, 45; tapered: 26 X 21, 31 X 26 | Yes | 18, 20, 22, 24 (ID) |
| Kawasumi Laboratories, Inc | Najuta Thoracic Stent Graft System | Stainless steel | PTFE | Self expanding | 102–178 mm | 24, 26, 28, 30, 32, 34, 36, 38, 40, 42; tapered: 28, 30, 32, 34, 36, 38, 40, 42 | No | 21–23 (OD) |
| Medtronic | Valiant Thoracic Stent Graft on Captivia Delivery System | Nitinol | Woven polyester | Self expanding | 10, 15, 20 | 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46; tapered: 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46 | No | 22, 24, 25 (OD) |
| Terumo Aortic | RelayPlus | Nitinol | Woven polyester | Self expanding | 10, 15, 20, 25 | 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46; tapered: 28, 30, 32, 34, 36, 38, 40, 42, 44, 46 | No | 22–26 (OD) |
| Terumo Aortic | RelayPRO | Nitinol | Woven polyester | Self expanding | 10, 15, 20, 25; tapered: 15, 20, 25 | 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44, 46; tapered: 28, 30, 32, 34, 36, 38, 40, 42, 44, 46 | No | 19–22, 23 (NBS only) |
| Gore & Associates | Gore TAG Thoracic Branch Endoprosthesis - Aortic Component | Nitinol | ePTFE | Self-expandable | 10, 15 | 21, 26, 28, 31, 34, 37, 40, 45 with 8-mm or 12-mm internal portals for Gore TAG Thoracic Branch Endoprosthesis Side Branch components | Yes | 20, 22, 24, 26 (ID) |
| Gore & Associates | Gore TAG Thoracic Branch Endoprosthesis - Aortic Extender | Nitinol | ePTFE | Self expandable | 3.6–4.6 depending on device diameter | 21, 26, 28, 31, 34, 37, 40, 45 | Yes (to be delivered through the same sheath used for Gore TAG Thoracic Branch Endoprosthesis Aortic component) | 20, 22, 24, 26 (ID) |
| Gore & Associates | Gore TAG Thoracic Branch Endoprosthesis - Side Branch Component | Nitinol | ePTFE | Self-expandable | 6 | 8, 10, 12, 15, 17 for 8-mm portal Gore TAG Thoracic Branch Endoprosthesis Aortic components; 15, 17, 20 for 12-mm portal Aortic components | Yes (to be delivered through the same sheath used for Gore TAG Thoracic Branch Endoprosthesis Aortic component) | 14 (ID) |
| Lombard Medical Limited (manufactured by MicroPort Endovastec) | Hercules | Nitinol | Woven polyester | Self expanding | 10 | 20, 22, 24, 26, 28, 30, 32, 34, 36, 38, 40, 42, 44 | No | 18, 20 (OD) |
| Lombard Medical Limited (manufactured by MicroPort Endovastec) | Hercules | Nitinol | Woven polyester | Self expanding | 16, 20 | 26, 28, 30, 32, 34, 36, 38, 40 (4 mm tapering) | No | 18, 20 (OD) |
| Lombard Medical Limited (manufactured by MicroPort Endovastec) | Hercules | Nitinol | Woven polyester | Self expanding | 20 | 28, 30, 32, 34, 36, 38, 40 (8 mm tapering) | No | 18, 20 (OD) |
| Lombard Medical Limited (manufactured by MicroPort Endovastec) | Castor (Custom Made Device) | Nitinol | Woven polyester | Self expanding | 10, 12, 15, 17, 18, 20, 21 | 26, 28, 30, 32, 34, 36, 38, 40, 42, 44 | No | 24 (OD) |
| Lombard Medical Limited (manufactured by MicroPort Endovastec) | Cratos (Custom Made Device) | Nitinol | Woven polyester | Self expanding | 10, 12, 15, 17, 18, 20, 21 | 26, 28, 30, 32, 34, 36, 38, 40, 42, 44 | No | 22, 24 (OD) |
Aortic (TAA) / Hybrid Grafts
View Chart| Company Name | Product Name | Stent Material | Graft Material | Stent Expansion | Length (cm) | Diameter (mm) | Cuff Length (cm) | Cuff Diameter (mm) | Branched Design | Sheath Required for Delivery | CE Mark Indications |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Artivion, Inc. | E-vita Open Neo | Nitinol | Woven polyester | Self expanding | 12, 13, 17.5, 18 | 20–40 | 10 minimum | 26, 28, 30 | Perfusion only: 4 individual branches (perfusion and SATs), 4 combined (perfusion and trifurcated) | No | Surgical treatment of patients with aortic dissections or aneurysms having the following characteristics: acute or chronic aortic dissection, DeBakey type I; acute or chronic aortic dissection, DeBakey type III, with retrograde progression in the aortic arch, with or without involvement of the ascending aorta; thoracic aortic aneurysm involving the descending thoracic aorta and the aortic arch; with or without involvement of the ascending aorta |
| Artivion, Inc. (manufactured by Ascyrus Medical GmbH) | AMDS Hybrid Prosthesis | Nitinol | PTFE | Self expanding | 15.5–22.5 (adjusts to the true lumen diameter) | 40–55 | 1 | 24–32 | – | No | Acute DeBakey type I dissection within 14 days from onset |
| Terumo Aortic | Thoraflex Hybrid (Ante-Flo and Plexus designs) | Nitinol | Gelatin-sealed woven polyester | Self expanding | 10, 15 | 24–40 | 12 | 22–32 | Yes; single and four branched | No | Indicated for single stage open surgical repair or replacement of damaged or diseased vessels of the aortic arch and descending aorta with or without involvement of the ascending aorta in cases of aneurysm and/or dissection |
Aortic (TAA) / TAAA Grafts
View Chart| Company Name | Product Name | Stent Material | Graft Material | Stent Expansion | Length (mm) | Diameter (mm) | Sheath Required for Delivery | Sheath Compatibility (F) |
|---|---|---|---|---|---|---|---|---|
| Artivion, Inc. | E-nside TAAA Multibranch Stent Graft System | Nitinol | Polyester | Self expanding | 222 | Proximal: 33, 38; distal: 26, 30 | No | 24 |
| Cook Medical | Zenith t-Branch Thoracoabdominal Endovascular Graft | Stainless steel | Polyester | Self expanding | 202 | 34/18 | No | 22 (ID) |
Aortic (TAA) / Access Needles
View Chart| Company Name | Product Name | Gauge | Length (cm) |
|---|---|---|---|
| Cook Medical | Percutaneous Entry Thinwall Needle | 19 UTW | 7 |
| Merit Medical Systems, Inc. | Merit Advance Angiographic Needles | 18, 19, 20, 21 (smooth and echo-enhanced) | 2.5, 4, 7, 9 |
| Merit Medical Systems, Inc. | Merit Advance Angiographic Safety Needles | 18, 21 | 7 |
| Galt | Percutaneous Entry Thin Wall Needles | 21 | 12 |
Aortic (TAA) / Diagnostic Catheters
View Chart| Company Name | Product Name | Catheter Type | Size (F) | Recommended Introducer Size (F) | Guidewire Compatibility (inch) | Catheter Length (cm) |
|---|---|---|---|---|---|---|
| AngioDynamics | Accu-Vu Sizing Catheter | Sizing catheter, flush (2RO, 21RO, 10RO) (nonbraided) | 4, 5 | 4, 5 | 0.035, 0.038 | 70, 90, 100 |
| AngioDynamics | Mariner Hydrophilic Angiographic Catheter | Hydrophilic diagnostic catheter, flush and selective (nonbraided, braided) | 4, 5 | 4, 5 | 0.035, 0.038 | 40–150 |
| AngioDynamics | Soft-Vu Angiographic Catheter | Diagnostic catheter, flush and selective (nonbraided and braided) | 4, 5, 6 | 4, 5, 6 | 0.035, 0.038 | 25–150 |
| Cook Medical | Aurous Centimeter Sizing Catheter | Sizing | 5 | 5 | 0.035 | 100 |
| Cook Medical | Royal Flush Plus Flush Catheter | Angiographic flush | 5 | 5 | 0.035 | 100 |
| Merit Medical Systems, Inc. | Impress Diagnostic Catheters | Peripheral diagnostic, braided and nonbraided, selective and flush | 4, 5 | 4, 5 | 0.035, 0.038 | 30, 40, 65, 80, 90, 100, 110, 125 |
| Merit Medical Systems, Inc. | Impress Hydrophilic Diagnostic Catheters Coated (Legato) | Hydrophilic, braided and nonbraided, peripheral diagnostic, selective and flush catheters | 4, 5 | 4, 5 | 0.038 | 40, 65, 80, 100, 125 |
| Merit Medical Systems, Inc. | Performa Diagnostic Catheters | Peripheral diagnostic, braided and nonbraided, selective and flush | 4, 5, 6 | 4, 5, 6 | 0.035, 0.038 | 40, 65, 80, 90, 100, 110, 120, 125 |
| Merit Medical Systems, Inc. | Performa Vessel Sizing Catheters | Vessel sizing | 4, 5 | 4, 5 | 0.035 | 65, 80, 100 |
Aortic (TAA) / Endograft Fixation Systems
View Chart| Company Name | Product Name | Components | Sizes | Comments | CE Mark Indications |
|---|---|---|---|---|---|
| Medtronic | Heli-FX Thoracic EndoAnchor System | Heli-FX Applier with EndoAnchor cassette (contains 10 EndoAnchors) | 12-F OD; 114-cm working length | Battery-operated delivery system with two-stage EndoAnchor deployment with repositioning capability; packaged with an EndoAnchor cassette (includes 10 EndoAnchor implants); EndoAnchor implants are 3-mm diameter X 4.5-mm length helix shape, with 0.5-mm wire thickness | Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic Endurant, Medtronic AneuRx, Medtronic Talent, Medtronic Valiant, Medtronic Valiant Navion, and Jotec E-vita thoracic endografts; use with other thoracic endografts has not been evaluated |
| Medtronic | Heli-FX Thoracic EndoAnchor System | Heli-FX Guide | Deflecting tip lengths: 22, 32, 42 mm; 18-F OD; 90-cm working length; 0.035-inch wire compatible | Deflecting guide catheter used to position Heli-FX Applier to implant EndoAnchor implants | Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic Endurant, Medtronic AneuRx, Medtronic Talent, Medtronic Valiant, Medtronic Valiant Navion, and Jotec E-vita thoracic endografts; use with other thoracic endografts has not been evaluated |
| Medtronic | Heli-FX Thoracic EndoAnchor System | Ancillary EndoAnchor cassette (contains five EndoAnchors) | EndoAnchor implants are 3-mm diameter X 4.5-mm length helix shape, with 0.5-mm wire thickness | Provides additional EndoAnchor implants to supplement independent transmural sealing and fixation of an endograft to the aortic wall | Indicated for use in patients whose endografts have exhibited migration or endoleak, or are at risk of such complications, in whom augmented fixation and/or sealing is required to regain or maintain adequate aneurysm exclusion; evaluated via in vitro testing and determined to be compatible with the Cook Zenith, Cook Zenith TX2, Gore Excluder, Gore TAG, Medtronic Endurant, Medtronic AneuRx, Medtronic Talent, Medtronic Valiant, Medtronic Valiant Navion, and Jotec E-vita thoracic endografts; use with other thoracic endografts has not been evaluated |
Aortic (TAA) / Guidewires
View Chart| Company Name | Product Name | Diameter (inch) | Length (cm) | Flexible Tip Length (cm) |
|---|---|---|---|---|
| AndraTec GmbH Germany | Lokum Amplatz Stiff Type | 0.035 | 180, 260, 320, 360 | 5 |
| AndraTec GmbH Germany | Lokum L-Quest Extra Stiff Type Guide Wire | 0.035 | 90, 150, 180–260 | 5, 10, 15 |
| Artivion, Inc. | E-wire Guidewire: E-xtra Stiff | 0.035 | 190, 300 | 6 |
| Boston Scientific Corporation | Amplatz Super Stiff Guidewire | 0.035 (0.89 mm) | 75, 145, 180, 260 | 7 |
| Boston Scientific Corporation | Amplatz Super Stiff Guidewire | 0.038 (0.97 mm) | 75, 145, 180, 260 | 6 |
| Boston Scientific Corporation | Amplatz Super Stiff J Guidewire | 0.035 (0.89 mm), 0.038 (0.97 mm) | 145, 180, 260 (0.038 only) | 6 |
| Boston Scientific Corporation | Amplatz Super Stiff ST Guidewire | 0.035 (0.89 mm), 0.038 (0.97 mm) | 260 | 1 |
| Boston Scientific Corporation | Amplatz Super Stiff ST Guidewire | 0.035 (0.89 mm), 0.038 (0.97 mm) | 145 | 4 |
| Boston Scientific Corporation | Meier C Curve | 0.035 (0.89 mm) | 300 | 11 |
| Boston Scientific Corporation | Meier J Curve | 0.035 (0.89 mm) | 185 | 16 |
| Cook Medical | Amplatz Ultra-Stiff | 0.035 | 300 | 7 |
| Cook Medical | Lunderquist Extra-Stiff: Double Curve | 0.035 | 260, 300 | 4 |
| Cook Medical | Lunderquist Extra-Stiff: Extended Curve | 0.035 | 260, 300 | 4 |
| Cook Medical | Lunderquist Extra-Stiff: Single Curve | 0.035 | 260, 300 | 4 |
| Cook Medical | Lunderquist Extra-Stiff: Straight | 0.035 | 260, 300 | 4 |
| Cook Medical | Roadrunner Extra-Support Wire Guides | 0.018 | 300 | 5 |
| Merit Medical Systems, Inc. | InQwire Amplatz Guide Wires | 0.035, 0.038 | 75, 145, 180, 260 | 1, 3.5, 4, 6, 7; 3-mm J-shaped |
| Merit Medical Systems, Inc. | InQwire Guide Wires | 0.014, 0.018, 0.025, 0.035, 0.038 | 80, 100, 150, 180, 260 | Bentson: 10, 15, 23; Newton: 15, 18, 23; J: 1.5, 3, 6, and 15 |
Aortic (TAA) / Occlusion/Molding Balloons
View Chart| Company Name | Product Name | Size (F) | Recommended Introducer Size (F) | Guidewire Compatibility (inch) | Catheter Length (cm) | Maximum Inflated Balloon Diameter (mm) |
|---|---|---|---|---|---|---|
| AndraTec GmbH Germany | AltoSa SFT | 10.5 | 12 | 0.035 | 65, 100, 130 | 46 |
| Artivion, Inc. | E-xpand Stent Graft Balloon Catheter | 12 | 12 | 0.035 or smaller | 100 | 50 |
| Boston Scientific Corporation | Equalizer Balloon Catheter | 7 (2.3 mm) | 14 (20, 27 mm), 16 (33 mm) (40-mm Equalizer should be inserted via cutdown only) | 0.038 (0.97 mm) | 65, 100 | 20, 27, 33, 40 |
| Cook Medical | Coda Balloon Catheter | 10 | 14 | 0.035 | 140 | 46 |
| Gore & Associates | Gore Tri-Lobe Balloon Catheter | 18 | 18 | 0.035 | 100 | 32, 42 |
| Medtronic | Reliant Stent Graft Balloon Catheter | 8 | 12 | 0.038 or smaller | 100 | 46 |
| Merit Medical Systems, Inc. | Q50X Stent Graft Balloon Catheter | 8 | 10 | 0.038 or smaller | 65, 100 | 50 |
| Prytime Medical Devices, Inc. | ER-REBOA PLUS Catheter | 6 | 7 | Guidewire free | 72 | 32 |
| Front Line Medical Technologies Inc. | COBRA-OS | 4 | 4 | Guidewire free | 55 working length | 25 |
Aortic (TAA) / Other Accessories
View Chart| Company Name | Product Name | Sizing (F) | Guidewire Compatibility (inch) | Comments |
|---|---|---|---|---|
| Artivion, Inc. | E-xpand Stent Graft Balloon Catheter | 12 (minimum sheaths) | 0.035 | Designed to assist in stent graft procedures; compliant balloon; radiopaque markers for exact placement; short inflation and deflation times |
| Gore & Associates | Gore DrySeal Flex Introducer Sheath | 10, 12, 14, 15, 16, 18, 20, 22, 24, 26 | 0.035 | A new standard of flexibility to treat more challenging anatomies |
| Gore & Associates | Gore Tri-Lobe Balloon Catheter | 18 | 0.035 | – |
| Medtronic | Sentrant Introducer Sheath With Hydrophilic Coating | 12–26 (sheaths) | 0.035 | Hemostatic and kink-resistant introducer sheath |
Aortic (TAA) / Thoracic Introducers
View Chart| Company Name | Product Name | Size (F) | Length (cm) | Guidewire Compatibility (inch) | Curved/Straight | Radiopaque Tip (Yes/No) | Hydrophilic Coating (Yes/No) |
|---|---|---|---|---|---|---|---|
| Cook Medical | Check-Flo Performer | 5, 6, 7 | 13 | 0.035 | Straight | No | No |
Aortic (TAA) / Thoracic Snares
View Chart| Company Name | Product Name | Catheter Size/Length (F/cm) | Working Diameter (mm) | Snare Type |
|---|---|---|---|---|
| AndraTec GmbH Germany | Exeter Snare | 4/125, 4/150, 5/125, 5/150 | 5–35 | Exeter open-loop snare |
| Cook Medical | Indy OTW Vascular Retriever | 8/55, 8/100 | 40-mm basket | Four-loop 40-mm radiopaque metal OTW vascular retriever snare with Flexor sheath and Tuohy-Borst hemostatic valve (55 and 100 cm); compatible with 0.035-inch guidewires |
Balloons / Drug-Coated Balloons
View Chart| Company Name | Product Name | Drug Type | Drug Concentration (µg/mm2) | Excipient Type | Guidewire Compatibility (inch) | Shaft Length (cm) | Sheath Compatibility (F) | Balloon Diameters (mm) | Balloon Lengths (cm) |
|---|---|---|---|---|---|---|---|---|---|
| Aachen Resonance GmbH | Elutax SV Fistula | Paclitaxel | 2.2 | No excipient + topcoating | 0.018 | 50 | 5 | 5, 6 | 2, 4, 6 |
| Aachen Resonance GmbH | Elutax SV Neuro | Paclitaxel | 2.2 | No excipient + topcoating | 0.014 | 135 | 4 | 1.5, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4 | 1, 1.3, 1.5, 2, 2.5, 3 |
| Aachen Resonance GmbH | Elutax SV OTW | Paclitaxel | 2.2 | No excipient + topcoating | 0.018 | 135 | 4 | 1.5, 2, 2.25, 2.5, 2.75, 3, 3.5, 4, 5, 6 | 1, 1.3, 1.5, 2, 2.5, 3, 4, 6, 8, 10, 15, 20, 25 |
| Aachen Resonance GmbH | Elutax SV Rx | Paclitaxel | 2.2 | No excipient + topcoating | 0.014 | 135 | 4 | 1.5, 2, 2.25, 2.5, 2.75, 3, 3.5, 4, 5, 6 | 1, 1.3, 1.5, 2, 2.5, 3, 4, 6, 8, 10, 15, 20, 25 |
| B. Braun Melsungen AG | SeQuent Please OTW 14 | Paclitaxel | 3 | Resveratrol | 0.014 | 130, 150 | 4 | 1.5, 2, 2.5, 3 | 4, 8, 12, 15 |
| B. Braun Melsungen AG | SeQuent Please OTW 18 | Paclitaxel | 3 | Resveratrol | 0.018 | 75, 130 | 4, 5, 6 | 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8 | 4, 6, 8, 12, 15 |
| B. Braun Melsungen AG | SeQuent Please OTW 35 | Paclitaxel | 3 | Resveratrol | 0.035 | 75, 130 | 5, 6 | 4, 5, 6, 7, 8 | 4, 6, 8, 12, 15 |
| Balton | PAK (OTW) | Paclitaxel | 3 | Poligrade | 0.025, 0.035 | 80, 110 | 5–7 | 3–8 | 2–25 |
| BD Interventional | Lutonix 018 Drug Coated Balloon PTA Catheter | Paclitaxel | 2 | Polysorbate and sorbitol | 0.018 | 100, 130 | 4, 5 | 4, 5, 6, 7 | 4, 6, 8, 10, 12, 15, 22 |
| BD Interventional | Lutonix 035 Drug Coated Balloon PTA Catheter | Paclitaxel | 2 | Polysorbate and sorbitol | 0.035 | 75, 100, 130 | 5, 7, 8, 10 | 4, 5, 6, 7, 8, 9, 10, 12 | 4, 6, 8, 10, 12, 15 |
| BD Interventional | Lutonix 014 Drug Coated Balloon PTA Catheter | Paclitaxel | 2 | Polysorbate and sorbitol | 0.014 | 150 | 4 | 2, 2.5, 3, 3.5, 4 | 4, 8, 12, 15 |
| Biosensors International | BioPath 014 OTW PTA Balloon Catheter | Paclitaxel | 3 | Shellac | 0.014 | 120, 150 | 5 | 2, 2.5, 3, 3.5, 4 | 4, 8, 12, 15 |
| Biosensors International | BioPath 035 OTW PTA Balloon Catheter | Paclitaxel | 3 | Shellac | 0.035 | 80, 135 | 5, 6 | 4, 5, 6, 7, 8 | 2, 4, 6, 8, 10, 12, 15 |
| Teleflex | Passeo-18 Lux | Paclitaxel | 3 | Butyryl-tri-hexyl citrate | 0.018 | 90, 130; 150 (2-mm diameter only) | 4 (2–4 mm), 5 (5–7 mm) | 2, 2.5, 3, 4, 5, 6, 7 | 4, 8, 12 |
| Boston Scientific Corporation | Ranger Over-the-Wire Paclitaxel-Coated PTA Balloon Catheter | Paclitaxel | 2 | Transpax technology | 0.018 | 80, 135 | 4, 5, 6 | 4, 5, 6, 7, 8 | 3, 4, 6, 8, 10 |
| Boston Scientific Corporation | Ranger SL Over-the-Wire Paclitaxel-Coated PTA Balloon Catheter | Paclitaxel | 2 | Transpax technology | 0.018 | 90, 150 | 4, 5, 6 | 2, 2.5, 3, 3.5, 4, 5, 6, 7 | 8, 10, 12, 15, 20 |
| Cardionovum GmbH | Aperto | Paclitaxel | 3 | Ammonium shelloic salt | 0.035 | 40, 80 | 6, 7, 8 | 4–12 | 2, 4, 6 |
| Cardionovum GmbH | Legflow 0.018 | Paclitaxel | 3 | Ammonium shelloic salt | 0.018 | 150 | 4, 5 | 2–7 | 4, 6, 8, 10, 12, 15 |
| Cardionovum GmbH | Legflow OTW 0.014 | Paclitaxel | 3 | Ammonium shelloic salt | 0.014 | 150 | 4 | 2– 3.5 (available in 0.5-mm increments) | 4, 8, 12, 15 |
| Cardionovum GmbH | Legflow OTW 0.035 | Paclitaxel | 3 | Ammonium shelloic salt | 0.035 | 80, 135 | 6, 7 | 4–10 | 2, 4, 6, 8, 10, 12, 15 |
| Cardionovum GmbH | Legflow RX | Paclitaxel | 3 | Ammonium shelloic salt | 0.014 | 140 | 5 | 2–4 (available in 0.5-mm increments) | 2, 4, 6, 8, 10, 12, 15, 20 |
| Concept Medical | MagicTouch AVF | Sirolimus | 1.27 | Phospholipid | 0.035 OTW | 45, 90 | 6–8 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 10, 12, 15, 20 |
| Concept Medical | MagicTouch ED | Sirolimus | 1.27 | Phospholipid | 0.014 maximum recommended | 140 | 6 | 1.5, 2, 2.25, 2.5, 2.75, 3, 3.5, 4 | 1, 1.5, 2, 2.5, 3, 3.5, 4 |
| Concept Medical | MagicTouch PTA 0.014 | Sirolimus | 1.27 | Phospholipid | 0.014 OTW | 90, 120, 150 | 5–8 | 2, 2.5, 3, 3.5, 4 | 4, 6, 8, 10, 12, 15, 20 |
| Concept Medical | MagicTouch PTA 0.018 | Sirolimus | 1.27 | Phospholipid | 0.018 OTW | 90, 120, 150 | 5–8 | 2, 2.5, 3, 3.5, 4, 5, 5.5, 6, 7 | 4, 6, 8, 10, 12, 15, 20 |
| Concept Medical | MagicTouch PTA 0.035 | Sirolimus | 1.27 | Phospholipid | 0.035 OTW | 130, 150 | 5–8 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 10, 12, 15, 20 |
| Concept Medical | MagicTouch SCB | Sirolimus | 1.27 | Phospholipid | 0.014 maximum recommended | 140 | 6 | 1.5, 2, 2.25, 2.5, 2.75, 3, 3.5, 4 | 1, 1.5, 2, 2.5, 3, 3.5, 4 |
| Cordis | Selution SLR PTA Drug-Eluting Balloon | Sirolimus | 1 | Cell adherent technology (CAT) coating and microreservoirs | 0.018 | 135 | 5–7 | 2–7 | 4–15 |
| Eurocor GmbH | Freeway 014 Paclitaxel releasing OTW PTA Balloon Catheter | Paclitaxel | 3 | Shellac | 0.014 | 120, 150 | 4 | 2, 2.5, 3, 3.5, 4 | 4, 8, 12, 15 |
| Eurocor GmbH | Freeway 035 Paclitaxel releasing OTW PTA Balloon Catheter | Paclitaxel | 3 | Shellac | 0.035 | 80, 135 | 5, 6 | 4, 5, 6, 7, 8 | 2, 4, 6, 8, 10, 12, 15 |
| Invamed | Extender | Paclitaxel | 3 | No excipient | 0.014, 0.018, 0.035 | 80, 90, 120, 135, 150 | 5, 6, 7 | 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 8, 9, 10 | 1.5, 2, 4, 6, 8, 9, 10, 12, 15, 22 |
| iVascular | Luminor 14 | Paclitaxel | 3 | Water-reduced ester | 0.014 | 100, 150 | 4 | 1.5, 2, 2.5, 3, 3.5, 4 | 4, 6, 8, 12, 15, 20 |
| iVascular | Luminor 18 | Paclitaxel | 3 | Water-reduced ester | 0.018 | 100, 140, 150 | 4 (diameter, 2–4 mm); 5 (diameter, 5–8 mm) | 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8 | 2, 4, 6, 8, 12, 15, 20 |
| iVascular | Luminor 35 | Paclitaxel | 3 | Water-reduced ester | 0.035 | 80, 140 | 5 (diameter, 5 mm); 6 (diameter, 6–7 mm) | 5, 6, 7 | 2, 4, 6, 8, 12, 15 |
| Medtronic | In.Pact Admiral | Paclitaxel | 3.5 | Urea | 0.035 | 40, 80, 130 | 5–7 | 4–12 (available in 1-mm increments up to 10) | 4, 6, 8, 12, 15, 20, 25 |
| Philips | Stellarex Drug-Coated Angioplasty Balloon | Paclitaxel, polyethylene glycol (PEG) | 2 | Polyethylene glycol | 0.014 | 90, 150 | 4 | 2, 2.5, 3, 3.5, 4 | 4, 8, 15 |
| Philips | Stellarex Drug-Coated Angioplasty Balloon | Paclitaxel, polyethylene glycol (PEG) | 2 | Polyethylene glycol | 0.035 | 80, 135 | 6 | 4, 5, 6 | 4, 6, 8, 10, 12, 15, 20 |
| Medtronic | In.Pact 018 | Paclitaxel | 3.5 | Urea | 0.018 | 80, 130 | 5 (4-6 mm), 6 (7 mm) | 4, 5, 6, 7 | 4, 6, 8, 10, 12, 15 |
Balloons / Embolectomy Balloon Catheters
View Chart| Company Name | Product Name | Size (F) | Sheath Compatibility (F) | Shaft Length (cm) | Diameters (mm) | Lengths (cm) |
|---|---|---|---|---|---|---|
| Balton | Embolectomy Catheter | 2–10 | – | 40, 60, 80 | 5–20 | 1.5–2 |
| Edwards Lifesciences | Latex Free Embolectomy Catheter | 2 | – | 40, 60 | 4 | – |
| Edwards Lifesciences | Latex Free Embolectomy Catheter | 3 | – | 40, 80 | 5 | – |
| Edwards Lifesciences | Latex Free Embolectomy Catheter | 4 | – | 40, 80, 100 | 9 | – |
| Edwards Lifesciences | Latex Free Embolectomy Catheter | 5 | – | 40, 80 | 11 | – |
| Edwards Lifesciences | Latex Free Embolectomy Catheter | 6 | – | 40, 80 | 13 | – |
| Edwards Lifesciences | Latex Free Embolectomy Catheter | 7 | – | 40, 80 | 14 | – |
| LeMaitre Vascular, Inc. | LeMaitre Over-the-Wire Embolectomy Catheter | 3 | 4.5 | 40, 80 | 6 | 1.4 |
| LeMaitre Vascular, Inc. | LeMaitre Over-the-Wire Embolectomy Catheter | 4 | 5 | 40, 80 | 10 | 1.7 |
| LeMaitre Vascular, Inc. | LeMaitre Over-the-Wire Embolectomy Catheter | 5 | 6 | 40, 80 | 12 | 2 |
| LeMaitre Vascular, Inc. | LeMaitre Over-the-Wire Embolectomy Catheter | 5+ | 6 | 40, 80 | 12 | 2 |
| LeMaitre Vascular, Inc. | LeMaitre Over-the-Wire Embolectomy Catheter | 6 | 7 | 40, 80 | 13 | 2.5 |
| LeMaitre Vascular, Inc. | LeMaitre Over-the-Wire Embolectomy Catheter | 7 | 8 | 40, 80 | 14 | 2.4 |
| LeMaitre Vascular, Inc. | LeMaitre Single Lumen Embolectomy Catheter | 2 | – | 40, 60 | 4.5 | 1.1 |
| LeMaitre Vascular, Inc. | LeMaitre Single Lumen Embolectomy Catheter | 3 | – | 40, 80 | 8 | 1.4 |
| LeMaitre Vascular, Inc. | LeMaitre Single Lumen Embolectomy Catheter | 4 | – | 40, 80 | 10.5 | 1.7 |
| LeMaitre Vascular, Inc. | LeMaitre Single Lumen Embolectomy Catheter | 5 | – | 40, 80 | 13 | 2 |
| LeMaitre Vascular, Inc. | LeMaitre Single Lumen Embolectomy Catheter | 6 | – | 40, 80 | 13.5 | 2.25 |
| LeMaitre Vascular, Inc. | LeMaitre Single Lumen Embolectomy Catheter | 7 | – | 40, 80 | 14 | 2.4 |
| LeMaitre Vascular, Inc. | NovaSil Latex Free Single Lumen Embolectomy Catheter | 3 | – | 40, 80 | 6 | 1.4 |
| LeMaitre Vascular, Inc. | NovaSil Latex Free Single Lumen Embolectomy Catheter | 4 | – | 40, 80 | 9 | 1.7 |
| LeMaitre Vascular, Inc. | NovaSil Latex Free Single Lumen Embolectomy Catheter | 2 | – | 40, 60 | 4 | 1.1 |
| LeMaitre Vascular, Inc. | NovaSil Latex Free Single Lumen Embolectomy Catheter | 5 | – | 40, 80 | 11 | 2 |
| LeMaitre Vascular, Inc. | NovaSil Latex Free Single Lumen Embolectomy Catheter | 6 | – | 40, 80 | 13 | 2.25 |
| LeMaitre Vascular, Inc. | NovaSil Latex Free Single Lumen Embolectomy Catheter | 7 | – | 40, 80 | 14 | 2.4 |
Balloons / PTA Balloons
View Chart| Company Name | Product Name | Nominal Pressure (atm) | Rated Burst Pressure (atm) | Guidewire Compatibility (inch) | Shaft Length (cm) | Sheath Compatibility (F) | Balloon Diameters (mm) | Balloon Lengths (cm) |
|---|---|---|---|---|---|---|---|---|
| Abbott | Armada 14 PTA Catheter | 8 | 14 | 0.014 | 90, 150 | 4 | 1.5, 2, 2.5, 3, 4 | 2, 4, 6, 8, 12, 20 |
| Abbott | Armada 14 XT PTA Catheter | 8 | 14 | 0.014 | Catheter length: 145 | 4 | 1.2, 1.5, 2 | 1.2, 2 |
| Abbott | Armada 18 PTA Catheter | 8 | 14 | 0.018 | 90, 150 | 4, 5 | 2, 2.5, 3, 4, 5, 5.5, 6 | 2, 4, 6, 8, 10, 12, 15, 18, 20 |
| Abbott | Armada 35 LL PTA Catheter | 6–8 (depending on size) | 12–20 (depending on size) | 0.035 | 80, 135 | 5, 6 | 4, 5, 6, 7 | 15, 20, 25 |
| Abbott | Armada 35 PTA Catheter | 4–8 (depending on size) | 7–28 (depending on size) | 0.035 | 80, 135 | 5, 6, 7 (14-mm diameter) | 3, 4, 5, 6, 7, 8, 9, 10, 12, 14 | 2, 4, 6, 8, 10, 12 |
| Abbott | RX Viatrac 14 Plus Peripheral Dilatation Catheter | 8 | 14 | 0.014 | 80, 135 | 4, 5 | 4, 4.5, 5, 5.5, 6, 6.5, 7 | 1.5, 2, 3, 4 |
| amg International GmbH | Allunga 014 PTA Balloon Catheter | 9 | 18 | 0.014 | 120, 150, 160 | 4 (1.25–4.5 mm), 5 (5 mm) | 1.25, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5 | 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 14, 15, 17, 20, 22, 25, 28 |
| amg International GmbH | Allunga 018 PTA Balloon Catheter | 9 | 18 | 0.018 | 80, 135 | 4 (2–4.5 mm), 5 (5–6 mm), 6 (6.5–7 mm) | 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7 | 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 20, 22, 28 |
| amg International GmbH | Allunga 018D PTA Balloon Catheter: Dialysis Fistulae | 9 | 18 (6, 7 X 40 mm), 20 (6, 7 X 20 mm), 22 (4–5 mm) | 0.018 | 45, 80 | 4 (4 mm), 5 (5–6 mm), 6 (7 mm) | 4, 5, 6, 7 | 2, 4 |
| amg International GmbH | Allunga 035 PTA Balloon Catheter | 7 | 10 (3.5–12 mm), 13 (3 mm) | 0.035 | 45, 80, 120, 150 | 5 (3–5 mm), 6 (5.5–10 mm), 9 (12 mm) | 3, 3.5, 4, 4.5, 5.5, 6, 7, 8, 9, 10, 12 | 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 20, 22, 28 |
| amg International GmbH | Allunga-e PTA Balloon Catheter | 7 | 10 | 0.035 | 80, 135 | 6 (6–10 mm), 9 (12 mm) | 6–10, 12 | 6, 8, 10 |
| Andramed GmbH | Andra2Balloon - Double Balloon System | 3 | 5 | 0.035 | 100 | 10, 11, 12, 13, 14 | 24, 26, 28, 30, 32 | 4 |
| Andramed GmbH | AndraBalloon | 3 | 5 | 0.035 | 80, 120 | 10, 11, 12, 13 | 14, 16, 18, 20, 22, 24, 26, 28, 30, 32 | 4, 6 |
| AndraTec GmbH Germany | AltoSa-Premier | 8 | 18 | 0.035 | 75 | 7, 8 | 12, 14, 16 | 4 |
| AndraTec GmbH Germany | AltoSa-SFT | 1 | 4 | 0.035 | 65, 100, 130 | 12 | 46 | 4 |
| AndraTec GmbH Germany | AltoSa-XL PTA Balloon | 3 | 12 | 0.035 | 110 | 7–11 | 14–30 | 2, 3, 4, 6 |
| AndraTec GmbH Germany | AltoSa-XL-Gemini Dual PTA Balloon | 3 | 10 | 0.035 | 110 | 8–16 | 14–30 | 3, 4, 5, 6, 10 |
| Arthesys | Lynx RX 14 | 6 | 14 or 16 (depending on size) | 0.014 | 80, 140 | 5, 6, 7 | 2, 2.25, 2.5, 2.75, 3, 3.5, 4, 4.5, 5, 6, 7 | 0.8, 1, 2, 3, 4, 6, 8, 12, 15, 20 |
| Balton | Lovix (OTW) | 6 | 10 | 0.025, 0.035 | 80–170 | 5–8 | 3–16 | 2–20 |
| Balton | Lovix (RX) | 10 | 16 | 0.014 | 140 | 5–6 | 1.25–7 | 1–20 |
| BD Interventional | Dorado 40 PTA Dilatation Catheter | 8 | 20–24 | 0.035 | 40, 80, 120, 135 | 5, 6, 7 | 3, 4, 5, 6, 7, 8, 9, 10 | 2, 4, 6, 8, 10, 12, 15, 17, 20 |
| BD Interventional | Atlas Gold PTA Dilatation Catheter | 4–6 | 12–18 | 0.035 | 80, 120 | 7, 8, 9, 10, 12 | 12, 14, 16, 18, 20, 22, 24, 26 | 2, 4, 6 |
| BD Interventional | Conquest 40 PTA Dilatation Catheter | 8 | 30–40 | 0.035 | 50, 75 | 6, 7, 8 | 4, 5, 6, 7, 8, 9, 10, 12 | 2, 3, 4, 6, 8, 10 |
| BD Interventional | Conquest PTA Dilatation Catheter | 8 | 20–30 | 0.035 | 50, 75, 120 | 6, 7, 8 | 5, 6, 7, 8, 9, 10, 12 | 2, 3, 4, 6, 8 |
| BD Interventional | LitePAC Rapid Exchange PTA Balloon Catheter | 6 | 12–16 | 0.014 | 150, 155 | 4, 5 | 2, 2.5, 3, 3.5, 4, 5, 5.5, 6, 7 | 1.5, 2, 3, 4, 5, 6, 8, 10, 12, 15, 18, 20, 22 |
| BD Interventional | Ultraverse 014 PTA Dilatation Catheter | 6 | 13–16 | 0.014 | 150 | 4, 5 | 1.5, 2, 3, 3.5, 4, 5 | 2, 4, 8, 10, 12, 15, 22, 30 |
| BD Interventional | Ultraverse 018 PTA Dilatation Catheter | 6 | 11–16 | 0.018 | 75, 130, 200 | 4, 5, 6 | 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8, 9 | 2, 4, 6, 8, 10, 12, 15, 20, 22, 30 |
| BD Interventional | Ultraverse 035 PTA Balloon Dilatation Catheter | 6–8 | 9–21 (depending on size) | 0.035 | 75, 130 | 5, 6, 7 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 10 , 12, 15, 20, 25, 30 |
| BD Interventional | Ultraverse RX PTA Dilatation Catheter | 6 | 12–16 | 0.014 | 150, 200 | 4, 5 | 1.25, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 7 | 1.5, 2, 4, 8, 10, 12, 15,20, 30 |
| Teleflex | Oscar Peripheral Multifunctional Catheter | 8 | 14 (ø 3.5 mm), 16 (ø 2, 2.5, 3 mm) | 0.014 | 127 | 4 (only to be used with the matching Oscar Peripheral Multifunctional Support Catheter system) | 2, 2.5, 3, 3.5 | Variable from 2–18 |
| Teleflex | Oscar Peripheral Multifunctional Catheter | 6 | 12 (ø 7 mm), 14 (ø 4, 5, 6 mm) | 0.018 | 72 (ø 7 mm), 80, 128 | 6 (only to be used with the matching Oscar Peripheral Multifunctional Support Catheter system) | 4, 5, 6, 7 | Variable from 2–10 (ø 7 mm), 2–18 |
| Teleflex | Passeo-14 | 7 | 14 | 0.014 | 90, 120, 150 | 4 | 1.5, 2, 2.5, 3, 3.5, 4 | 2, 4, 7, 10, 14, 18, 22 |
| Teleflex | Passeo-18 | 6 | 12–15 | 0.018 | 90, 130, 150 | 4–5 | 2, 2.5, 3, 3.5, 4, 5, 6, 7 | 2, 4, 6, 8, 12, 15, 17, 20 |
| Teleflex | Passeo-35 | 7 | 12–20 | 0.035 | 80, 130 | 5–6 | 3, 4, 5, 6, 7, 8, 9, 10 | 2, 4, 6, 8, 10, 12, 15, 17, 20 |
| Teleflex | Passeo-35 HP | 12, 14 | 18–27 | 0.035 | 40, 75 | 6, 7, 8 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 10 |
| Teleflex | Passeo-35 Xeo | 8, 9 | 10–21 | 0.035 | 90, 130, 170 | 5–7 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 10, 12, 15, 17, 20, 25 |
| Boston Scientific Corporation | Charger Balloon Dilatation Catheter | 8 (9–10 mm), 10 (3–8, 12 mm) | Up to 20 (2,027 KPa) | 0.035 (0.89 mm) | 75, 135 | 5/1.7 mm (3–6 mm), 6/2 mm (6–10 mm), 7/2.3 mm (12 mm) | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 10, 12, 15, 20 |
| Boston Scientific Corporation | Coyote & Coyote ES Monorail Balloon Dilatation Catheter | 8 (810.6 KPa) | 12 (1,216 KPa), 14 (1,418 KPa) | 0.014 (0.36 mm) | 90, 143, 144, 145, 146, 150 | 4 (1.33 mm) | 1.5, 2, 2.5, 3, 3.5, 4 | 2, 3, 4, 6, 8, 10, 12, 15, 22 |
| Boston Scientific Corporation | Coyote & Coyote ES Over-the-Wire Balloon Dilatation Catheter | 6 (607.9 KPa), 8 (810.6 KPa) | 12 (1,216 KPa), 14 (1,418 KPa) | 0.014 (0.36 mm) | 90, 142, 143, 144, 145, 150 | 4 (1.33 mm) | 1.5, 2, 2.5, 3, 3.5, 4 | 2, 3, 4, 6, 8, 10, 12, 15, 22 |
| Boston Scientific Corporation | Mustang Balloon Dilatation Catheter | 8 (9–10 mm), 10 (3–8 mm, 12 mm) | Up to 24 (2,431 KPa) | 0.035 (0.89 mm) | 40, 75, 135 | 5/1.7 mm (3–7 mm), 6/2 mm (8–10 mm), 7/2.3 mm (12 mm) | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 3, 4, 6, 8, 10, 12, 15, 18, 20 |
| Boston Scientific Corporation | Peripheral Cutting Balloon Monorail System Flextome Microsurgical Dilatation Device | 6 (607.9 KPa) | 12 (1,216 KPa) | 0.014 (0.36 mm) | 140 | 6 (2 mm) | 2, 2.5, 3, 3.5, 4 | 1.5 |
| Boston Scientific Corporation | Peripheral Cutting Balloon Over-the-Wire Microsurgical Dilatation Device | 6 (607.9 KPa) | 10 (1,013 KPa) | 0.018 (0.46 mm) | 50, 90, 135 | 7 (2.33 mm) | 5, 6, 7, 8 | 2 |
| Boston Scientific Corporation | Sterling & Sterling SL Monorail Balloon Dilatation Catheter | 6 (607.9 KPa) | 12/1,216 KPa (8 mm), 14/1,418 KPa (2–7 mm) | 0.018 (0.46 mm) | 80, 90, 135, 150 | 4/1.33 mm (up to 8 X 3), 5/1.7 mm (up to 8 X 6) | 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 8 | 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 22 |
| Boston Scientific Corporation | Sterling & Sterling SL Over-the-Wire Balloon Dilatation Catheter | 6 (607.9 KPa) | 10/1,013 KPa (9–10 mm), 12/1,216 KPa (8 mm), 14/1,418 KPa (2–7 mm) | 0.018 (0.46 mm) | 40, 80, 90, 135, 150 | 4/1.33 mm (up to 8 X 4), 5/1.7 mm (up to 10 X 6), 6/2 mm (up to 10 X 8) | 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8, 9, 10 | 2, 3, 4, 6, 8, 10, 12, 15, 20, 22 |
| Boston Scientific Corporation | Ultra-Soft SV Monorail Balloon Dilatation Catheter | – | 12/1,216 KPa (1.5, 2, 3.5, 4 mm), 14/1,419 KPa (2.5, 3, 4–7 mm) | 0.014 (0.36 mm), 0.018 (0.46 mm) | 90, 140, 150 | 4/1.33 mm (1.5–5 mm), 5/1.7 mm (5–7 mm) | 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7 | 1.5, 2, 3 |
| Boston Scientific Corporation | XXL Balloon Dilatation Catheter | – | 5/507 KPa (16, 18 mm), 8/810 KPa (12, 14 mm) | 0.035 (0.89 mm) | 75, 120 | 7/2.33 mm (12, 14 mm), 8/2.67 mm (16, 18 mm) | 12, 14, 16, 18 | 2, 4, 6 |
| BrosMed Medical | Achilles NC OTW PTA Balloon Dilatation Catheter | 12 | 18 (ø, 7–8 mm), 20 (ø, 4.5–6 mm), 22 (ø, 2–4 mm) | 0.018 | 40, 70, 90, 150 | 4 (ø, 2–4 mm), 5 (ø, 4.5-5.5 mm), 6 (ø, 6–8 mm) | 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 7, 8 | 1, 1.5, 2, 3, 4, 6, 8, 10, 15 |
| BrosMed Medical | Atropos SC OTW PTA Balloon Dilatation Catheter | 6 | 14 | 0.035 | 40, 70, 90, 150 | 5 (ø, 3–5 mm), 6 (ø, 6–8 mm), 7 (ø, 9–10 mm) | 3, 4, 5, 6, 7, 8, 9, 10 | 2, 3, 4, 6, 8, 10, 12, 15, 20 |
| BrosMed Medical | Castor NC OTW PTA Balloon Dilatation Catheter | 12 | 18 (ø, 7–8 mm), 20 (ø, 4.5–6 mm), 22 (ø, 2–4 mm) | 0.014 | 70, 90, 150 | 4 (ø, 2–4 mm), 5 (ø, 4.5–6 mm), 6 (ø, 7–8 mm) | 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 7, 8 | 1, 1.5, 2, 3, 4, 6, 8, 10, 15 |
| BrosMed Medical | Hermes NC OTW PTA Balloon Dilatation Catheter | 12 | 18 (ø, 7–10 mm), 20 (ø, 5–6 mm), 22 (ø, 3–4 mm) | 0.035 | 40, 70, 90, 150 | 5 (ø, 3–5 mm), 6 (ø, 6–8 mm), 7 (ø, 9–10 mm) | 3, 4, 5, 6, 7, 8, 9, 10 | 2, 3, 4, 6, 8, 10, 15 |
| BrosMed Medical | Minerva SC OTW PTA Balloon Dilatation Catheter | 6 | 14 | 0.018 | 40, 70, 90, 150 | 4 (ø, 1.5–4 mm), 5 (ø, 4.5–6 mm), 6 (ø, 7–9 mm), 7 (ø, 10 mm) | 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 7, 8, 9, 10 | 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 20 |
| BrosMed Medical | Polux SC OTW PTA Balloon Dilatation Catheter | 6 | 14 | 0.014 | 70, 90, 150 | 4 (ø, 1.5–4 mm), 5 (ø, 4.5–6 mm) | 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6 | 0.5, 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 20 |
| BrosMed Medical | Tiche High Pressure PTA Balloon Dilatation Catheter | 10 (ø 10–12 mm), 12 (ø 3–9 mm) | 14 (ø 10–12 X 20–80 mm), 18 (ø 7–8 X 120–200 mm, ø 9 X 20–80 mm), 20 (ø 7–8 X 20–100 mm), 22 (ø 6 X 120–200 mm), 24 (ø 3–5 X 20–200 mm, ø 6 X 20–100 mm) | 0.035 | 40, 75, 120, 135 | 5 (ø 3–7 mm), 6 (ø 8–10.0), 7 (ø 12 mm) | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 3, 4, 6, 8, 10, 12, 15 ,18, 20 |
| Concept Medical | MagicTouch PTA 0.014 OTW | 5 | 16 | 0.014 | 90, 120, 150 | 5–8 | 2, 2.50, 3, 3.50, 4 | 4, 6, 8, 10, 12, 15, 20 |
| Concept Medical | MagicTouch PTA 0.018 OTW | 5 | 16 | 0.018 | 90, 120, 150 | 5–8 | 2, 2.50, 3, 3.50, 4, 5, 5.50, 6, 7 | 4, 6, 8, 10, 12, 15, 20 |
| Concept Medical | MagicTouch PTA 0.035 OTW | 5 | 16 | 0.035 | 130, 150 | 5–8 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 10, 12, 15, 20 |
| Cook Medical | Advance 14LP Low Profile PTA Balloon Catheter | 8 | 16 | 0.014 | 170 | 4 | 2, 2.5, 3, 4 | 2, 4, 6, 8, 12, 16, 20 |
| Cook Medical | Advance 18LP Low Profile PTA Balloon Catheter | 8 | Up to 14 | 0.018 | 80, 135, 150 | 4 (up to 7 X 100 mm), 5 (from 6 X 120 mm), 6 (from 8 X 120 mm), 7 (10 X 80, 100 mm) | 2, 3, 4, 5, 6, 7, 8, 9, 10 | 2, 4, 6, 8, 10, 12, 15, 17, 20 |
| Cook Medical | Advance 35LP Low Profile PTA Balloon Catheter | 5–10 | Up to 15 | 0.035 | 80, 135 | 5 (up to 8 X 8 mm), 6 (from 7 X 100 mm), 7 (from 10 X 100 mm) | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 3, 4, 6, 8, 10, 12, 14, 17, 20 |
| Cook Medical | Advance Micro 14 Ultra Low-Profile PTA Balloon Dilatation Catheter | 8 | 16 | 0.014 | 50, 90, 150 | 3 (can also be used through the Micropuncture Pedal Access set from Cook Medical) | 1.5, 2, 2.5, 3 | 2, 3, 4, 6, 8, 10, 12 |
| Cook Medical | Advance Serenity 14 Hydrophilic PTA Balloon Dilatation Catheter | 6 | 16 | 0.014 | 120, 150 | 4 | 2, 2.5, 3, 3.5, 4 | 2, 4, 6, 8, 10, 15, 22 |
| Cook Medical | Advance Serenity 18 Hydrophilic PTA Balloon Dilatation Catheter | 8 | Up to 16 | 0.018 | 90, 120, 135, 150 | 4 (up to 8 X 40 mm), 5 (from 7 X 80 mm) | 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8, 9, 10 | 2, 4, 6, 8, 10, 15, 22 |
| Cordis | Aviator Plus | – | Up to 14 | 0.014 | 142 | 4 | 4–7 | 1.5, 2, 3, 4 |
| Cordis | Powerflex Pro | – | 8–18 | 0.035 | 80, 135 | 5, 6, 7 | 3–12 | 2, 3, 4, 6, 8, 10, 12, 15, 22 |
| Cordis | Saber .035 PTA Dilatation Catheter | 8 (9–12 mm), 10 (3–8 mm) | Up to 24 | 0.035 | 40, 80, 135 | 5, 6, 7 | 3–12 | 2–30 |
| Cordis | Saber PTA Dilatation Catheter | 6 (7–10 mm), 8 (2–6 mm) | Up to 18 | 0.018 | 90, 150 | 4 (4 X 300, 5 X 100, 6 X 60, 7/8 X 40), 5, 6 | 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8, 9, 10 | 2, 3, 4, 6, 8, 10, 15, 20, 25, 30 |
| eucatech AG | Euca Deep | 8 | Up to 19 | 0.014 | 138 | – | 1.5, 2, 2.25, 2.5, 2.75, 3, 3.5, 4 | 1, 1.5, 2, 3, 4 |
| eucatech AG | Euca PW | 8 | Up to 14 | 0.035 | 85, 135 | 5–8 | 4, 5, 6, 7, 8, 9, 10, 12 | 2, 3, 4, 6, 8, 10, 12, 15, 17, 20 |
| eucatech AG | Euca PWSV | 8 | Up to 19 | 0.018 | 85, 135, 150 | 4 | 2, 2.5, 3, 4, 5 | 2, 4, 6, 8, 12, 15 |
| Eurocor GmbH | Joker 014 | 6 | 16 (diameter, 2–2.5 mm); 14 (diameter, 3–4 mm) | 0.014 | 120, 150 | 4 | 2, 2.5, 3, 3.5, 4 | 4, 8, 12, 15 |
| Eurocor GmbH | Joker 035 | 6 | 16 (2/4/6 cm; diameter, 4–6 mm), (8/10/12/15 cm; diameter, 4 mm); 14 (2/4/6 cm; diameter, 7–8 mm) (8/10/12/15 cm; diameter, 5–6 mm); 12 (8/10/12/15 cm, diameter 7–8 mm) | 0.035 | 80, 135 | 5, 6 | 4, 5, 6, 7, 8 | 2, 4, 6, 8, 10, 12, 15 |
| iVascular | Oceanus 14 pro | 7 | 16 | 0.014 | 100, 150 | 4 | 1.25, 1.5, 2, 2.5, 3, 3.5, 4 | 1, 1.5, 2, 4, 6, 8, 12, 15, 20 |
| iVascular | Oceanus 18 | 7 | 16 (8 mm diameter: 14) | 0.018 (0.014 compatible) | 100, 140, 150 | 4, 5 | 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8 | 2, 4, 6, 8, 12, 15, 20 |
| iVascular | Oceanus 35 | 6, 7 | 13–16 | 0.035 | 80, 140, 200 | 5 (diameter 3–7 mm), 6 (diameter 7–12 mm) | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 12, 15, 20 |
| Medtronic | Admiral Xtreme OTW PTA Balloon Catheter | 6, 8 | Up to 18 | 0.035 | 80, 130 | 5–7 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 12, 15, 20, 25, 30 |
| Medtronic | Amphirion Deep OTW PTA Balloon Catheter | 7 | 14 | 0.014 | 120, 150 | 4 | 1.5, 2, 2.5, 3, 3.5, 4 | 2, 4, 8, 12, 15, 21 |
| Medtronic | Chameleon High-Pressure PTA Balloon | 12, 14 | 14, 18, 22, 25 | 0.035 | 75 | 6, 7, 8 | 5, 6, 7, 8, 9, 10, 12 | 4 |
| Medtronic | Chocolate PTA | 6 (5–6), 9 (2.5–4) | 12 (5–6), 14 (2.5–4) | 0.014 (2.5–4), 0.018 (5–6) | 120 (5–6), 135 (3.5–4), 150 (2.5, 3) | 5 (2.5–4), 6 (5–6) | 2.5, 3, 3.5, 4, 5, 5.5, 6 | 4, 8, 12 |
| Medtronic | EverCross 0.035 PTA Balloon | 7, 8, 10 | 10, 11, 12, 14, 16, 18, 20 | 0.035 | 40, 80, 135 | 5, 6, 7 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 3, 4, 6, 8, 10, 12, 15, 20 |
| Medtronic | NanoCross Elite 0.014 PTA Balloon | 7, 8, 10 | 14 | 0.014 | 90, 150 | 4 | 1.5, 2, 2.5, 3, 3.5, 4 | 2, 4, 6, 8, 10, 12, 15, 21 |
| Medtronic | Pacific Plus OTW PTA Catheter | 8 | 12, 14, 16, 22 | Up to 0.018 | 90, 130, 180 | 4, 5 | 2, 2.5, 3, 3.5, 4, 5, 6, 7 | 2, 4, 6, 8, 12, 15 |
| Medtronic | Pacific Xtreme PTA Balloon Catheter | 6, 7, 9 | 12, 14, 16, 20, 25 | 0.018 | 90, 130 | 4, 5 | 4, 5, 6, 7 | 15, 20, 25, 30 |
| Medtronic | RapidCross 0.014 Rapid Exchange PTA Balloon Dilatation Catheter | 8 | 14 | 0.014 | 90, 170 | 4 | 2, 2.5, 3, 3.5, 4 | 2, 4, 6, 8, 10, 12, 15, 21 |
| Meril Life Sciences Pvt. Ltd. | Mozec PTA Balloon Dilatation Catheter | 6, 7 (depending on balloon length and diameter) | 11–14 (depending on balloon length and diameter) | 0.035 | 80 ± 2, 135 ± 2 | 5–7 (depending on balloon length and diameter) | 3, 4, 5, 6, 7, 8, 9, 10 | 2, 3, 4, 5, 6, 8, 12 |
| Natec Medical Ltd | Ebony 0.014 OTW | 8 | 12 (8 mm), 13 (7 mm), 14 (2–6 mm) | 0.014 | 120, 150 | 4–5 | 1.5, 2, 2.5, 3, 3.5, 4 | 2, 4, 6, 8, 10, 12, 15, 20 |
| Natec Medical Ltd | Ebony 0.014 RX | 8 | 12 (8 mm), 13 (7 mm), 14 (2–6 mm) | 0.014 | 150 | 4 (2–4.5 mm), 5 (5–8 mm): for lengths up to 60 mm; 4 (2–4.5 mm), 5 (5–7 mm): for lengths 100–120 mm; 4 (2–4 mm), 5 (4.5–6 mm): for lengths 150–200 mm | 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 7, 8 | 1, 2, 3, 4, 6, 8, 10, 12, 15, 20 |
| Natec Medical Ltd | Ebony 0.018 OTW | 8 | 12 (8 mm), 13 (7 mm), 14 (2–6 mm) | 0.018 | 120, 150 | 5–7 | 2, 2.5, 3, 3.5, 4, 5, 5.5, 6, 7 | 4, 6, 8, 10, 12, 15, 20 |
| Natec Medical Ltd | Ebony 0.035 OTW | 6 (10–12 mm), 8 (3–9 mm) | 10 (10–12 mm), 12 (8–9 mm), 13 (7 mm), 14 (5–6 mm) | 0.035 | 80, 130, 150 | 5–7 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 10, 12, 15, 20 |
| optimed Medizinische Instrumente GmbH | NyloTrack + 18 PTA Balloon Catheter | 6–8 | 12–14 | 0.018 | 120, 150 | 4, 5 | 2, 2.5, 3, 3.5, 4, 5, 6, 7 | 2, 4, 6, 8, 10, 12, 15, 20 |
| optimed Medizinische Instrumente GmbH | NyloTrack + 35 PTA Balloon Catheter | 5–8 | 10–14 | 0.035 | 80, 130, 150 | 5, 6, 7 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 10, 12, 15, 20 |
| phenox GmbH | pITA Rapid Exchange Neurovascular PTA Balloon Catheter | 6, 10 | 14, 18 | 0.016 | 160 | > 4.2 | 1.25, 1.5, 2, 2.25, 2.5, 2.75, 3, 3.5, 4 | 1, 1.5, 2, 2.5, 3, 3.5, 4 |
| Philips | AngioSculpt PTA scoring balloon catheter | 6–8 (depending on size) | 12–20 (depending on size) | 0.014, 0.018 (depending on size) | 50, 90, 137, 155 (depending on size) | 5, 6 (depending on size) | 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8 | 2, 4, 10, 20 |
| Q3 Medical Group | 014 PTA Balloon Catheter (PVQ) | 9 | 18 | 0.014 | 120, 150, 160 | 4 (1.2–4.5 mm), 5 (5 mm) | 1.25, 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5 | 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 14, 15, 17, 20, 22, 25, 28 |
| Q3 Medical Group | 018 PTA Balloon Catheter (PVQ) | 9 | 18 | 0.018 | 80, 135 | 4 (2–4.5 mm), 5 (5–6 mm), 6 (6.5–7 mm) | 2, 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7 | 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 20, 22, 28 |
| Q3 Medical Group | 018D PTA Balloon Catheter (PVQ): Dialysis Fistulae Catheter | 9 | 18 (6, 7 X 40 mm), 20 (6, 7 X 20 mm), 22 (4–5 mm) | 0.018 | 45, 80 | 4 (2–4.5 mm), 5 (5–6 mm), 6 (6.5–7 mm) | 4, 5, 6, 7 | 2, 4 |
| Q3 Medical Group | 035 PTA Balloon Catheter (PVQ) | 7 | 10 (3.5–12 mm), 13 (3 mm) | 0.035 | 45, 80, 120, 150 | 5 (3–5 mm), 6 (5.5, 10 mm), 9 (12 mm) | 3, 3.5, 4, 4.5, 5.5, 6, 7, 8, 9, 10, 12 | 1, 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 20, 22, 28 |
| Q3 Medical Group | EVAR PTA Balloon Catheter (PVQ) | 7 | 10 | 0.035 | 80, 135 | 6 (6–10 mm), 9 (12 mm) | 6–10, 12 | 6, 8, 10 |
| Rontis AG | Cronus Advanced OTW | 6 | 12–16 | 0.035 | 80, 120 | 5 (4–6 mm), 6 (7–9 mm), 7 (10 mm) | 4, 5, 6, 7, 8, 9, 10 | 2, 3, 4, 6, 8, 10, 12 |
| Rontis AG | Cronus HP-OTW | 10 | 26 (all range) | 0.035 | 45, 80 | 6–8 | 4, 5, 6, 7, 8, 9, 10 | 2, 3, 4, 6 |
| Rontis AG | Cronus NV-OTW | 6 | 12–16 | 0.035 | 45 | 5 (4–6 mm), 6 (7–9 mm), 7 (10 mm) | 4, 5, 6, 7, 8, 9, 10 | 2, 3, 4, 6, 8 |
| Rontis AG | Triton BTK Rx-OTW | 8 | 16 | 0.014 | 155 | 5 | 2, 2.5, 3, 3.5, 4, 4.5, 5 | 9, 12, 15, 18, 21 |
| Rontis AG | Triton Plus-Rx | 6 | 15–18 | 0.018 | 80, 135 | 4 (3–4.5 mm), 5 (5–6.5 mm), 6 (7–8 mm) | 3, 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 7.5, 8 | 1, 2, 3, 4, 6 |
| Simeks Medical | Simpass Endo14 RX PTA Balloon Catheter | 8 | 16 | 0.014 | 90, 145 | 4, 5 (depending on size) | 1.5, 2, 2.5, 3, 3.5, 4, 4.5, 5, 6, 7 | 1.5, 2, 3, 4, 6, 8, 10, 12, 15, 22 |
| Simeks Medical | Simpass Endo18 OTW PTA Balloon Catheter | 8 | 16 | 0.018 | 80, 130, 150 | 4, 5, 6, 7 (depending on size) | 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8 | 1, 2, 2.5, 3, 4, 6, 8, 10, 12, 15, 22 |
| Simeks Medical | Simpass Endo35 OTW PTA Balloon Catheter | 8 | 14, 16 (depending on size) | 0.035 | 50, 80, 130 | 5, 6, 7 (depending on size) | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 3, 4, 5, 6, 8, 10, 12, 15, 20, 22 |
| Stryker | Gateway PTA Balloon Catheter | 6 | 12, 14 (for 2.25–3.25 mm only) | – | 136 | 6 | 1.5, 2, 2.25, 2.5, 2.75, 3, 3.25, 3.5, 3.75, 4 | 9, 15, 20 |
| Terumo Europe | Crosperio RX 0.014" PTA Balloon Dilatation Catheter | 8 | 14 | 0.014 | 150 | 4 | 1.5, 2, 2.5, 3, 3.5, 4 | 2, 4, 8, 12, 15, 20 |
| Terumo Europe | Crosstella OTW 0.018" PTA Balloon Dilatation Catheter | 8 | 14 | 0.018 | 90, 150 | 4–5 | 2, 2.5, 3, 4, 5, 6 | 2, 4, 6, 8, 10, 12, 15, 20 |
| Terumo Europe | Metacross OTW 0.035" PTA Balloon Dilatation Catheter | 8 (6–12 mm), 10 (3–5 mm) | 12 (9–12 mm), 14 (6–8 mm), 18 (5 mm), 20 (3–4 mm) | 0.035 | 90, 135 | 5–7 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 10, 12, 15, 20 |
| Terumo Europe | Metacross RX 0.035" PTA Balloon Dilatation Catheter | 8 (6–12 mm), 10 (3–5 mm) | 12 (9–12 mm), 14 (6–8 mm), 18 (5 mm), 20 (3–4 mm) | 0.035 | 135 | 6–7 | 3, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 6, 8, 10, 12, 15, 20 |
| Terumo Europe | Senri 0.018" PTA Balloon Dilatation Catheter | 8 | 12–14 | 0.018 | 150 | 4–6 | 2, 3, 4, 5, 6, 7, 8 | 4, 6, 8, 10, 12, 15 |
| Terumo Europe | Tercross 0.014" OTW PTA Balloon Dilatation Catheter | 6 (1.25–1.5 mm), 8 (2–4 mm) | 14 (1.25–1.5 mm), 18 (3.5–4 mm), 20 (2–3 mm) | 0.014 | 100, 148 | 4 | 1.25, 1.5, 2, 2.5, 3, 3.5, 4 | 2, 4, 8, 12, 15, 20 |
| TriReme Medical LLC | GliderfleX PTA | 8 (5–6), 9 (2–4) | 12 (5–6), 14 (2–4) | 0.014 (2.5–4), 0.018 (4.5–6) | 120 (5–6), 135 (2–4) | 5–6 | 2, 2.5, 3, 3.5, 4, 5, 6 | 2, 4, 6, 8, 10, 12, 15, 20 |
| BrosMed Medical | Atropos Pro SC PTA Balloon Dilatation Catheter | 6 | 16, 14, 12 | 0.035 | 40, 70, 90, 120, 150, 200 | 5, 6, 7 | 3–12 | 20–300 |
| BrosMed Medical | Minerva Pro SC PTA Balloon Dilatation Catheter | 6 | 12, 14, 16 | 0.018 | 40, 70, 90, 120, 150, 200 | 4, 5, 6 | 1.5–10 | 10–300 |
| BrosMed Medical | Polux Pro SC PTA Balloon Dilatation Catheter | 6 | 14, 16 | 0.014 | 70, 90, 120, 150, 200 | 4, 5 | 1–7 | 15–300 |
| optimed Medizinische Instrumente GmbH | NyloTrack + 14 PTA Balloon Catheter | 6–8 | 12–16 | 0.014 | 120, 150 | 4 | 1.5, 2, 2.5 3, 3.5, 4 | 2, 4, 6, 8, 10, 12, 15, 20 |
| Cordis | SaberX Radianz | up to 8 | up to 18 | 0.018 | 190 | 4, 5, 6 | 4, 5, 6, 7, 8, 9, 10 | 20, 30, 40, 60, 80, 100, 150, 200, 250, 300 |
Balloons / Specialty Balloons
View Chart| Company Name | Product Name | Nominal Pressure (atm) | Rated Burst Pressure (atm) | Guidewire Compatibility (inch) | Size (F) | Sheath Compatibility (F) | Shaft Length (cm) | Balloon Diameters (mm) | Balloon Lengths (cm) |
|---|---|---|---|---|---|---|---|---|---|
| AndraTec GmbH Germany | AltoSa-Premier | 10 | 18 | 0.035 | 6, 7 | 7, 8 | 75 | 12–16 | 4 |
| AndraTec GmbH Germany | AltoSa-SFT | 1 | 4 | 0.035 | 10.5 | 12 | 65, 100 | 46 | 4 |
| AndraTec GmbH Germany | AltoSa-XL PTA Balloon | 3–8 | 4–10 | 0.035 | 6.5–8 shaft | 7–11 | 110 | 12–30 | 2, 3, 4, 5, 6 |
| AndraTec GmbH Germany | Altosa-XL-Gemini Dual PTA Balloon | 4 | 10 | 0.035 | 8 | 8–16 | 110 | 14–30 | 3, 4, 5, 6, 10 |
| B. Braun Melsungen AG | Aperta NSE PTA, PTA Scoring Balloon Catheter | 10 | 14 (diameter 7 and 8); 20 (diameter 4 to 6) | 0.018 | 4.9 | 5, 6 | 50, 90, 145 | 4, 5, 6, 7, 8 | 4 |
| BD Interventional | True Dilatation Balloon Valvuloplasty Catheter | 3 | 6 | 0.035 | – | 11–14 | 110 | 18–28 | 4.5 |
| BD Interventional | True Flow Valvuloplasty Perfusion Catheter | 3 | 6 | 0.035 | – | 11, 12, 14, 16 | 110 | 18, 20, 22, 24, 26 | 3.5 |
| BD Interventional | UltraScore Focused Force PTA Balloon | 6–8 | Up to 14 | 0.014 (2–7 mm), 0.035 (4–8 mm) | – | 4, 5, 6 | 130, 150 | 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8, 9, 10, 12 | 2, 4, 8, 10, 12, 15, 20, 30 |
| Teleflex | Oscar Peripheral Multifunctional Catheter | 6 (4–7 mm); 8 (2–3.5 mm) | 12 (7 mm); 14 (3.5–6 mm); 16 (2–4 mm) | 0.014 (2–3.5 mm); 0.018 (4–7 mm) | 4 (2–3.5 mm); 6 (4–7 mm) | 4 (2–3.5 mm); 6 (4–7 mm) | 80, 128 | 2, 2.5, 3, 3.5, 4, 5, 6, 7 | 2–18 (length-adjustable) |
| Boston Scientific Corporation | Peripheral Cutting Balloon Monorail System Flextome Microsurgical Dilatation Device | 6 (607.9 KPa) | 12 (1,216 KPa) | 0.014 (0.36 mm) | 6 (2 mm) | 6 (2 mm) | 140 | 2, 2.5, 3, 3.5, 4 | 1.5 |
| Boston Scientific Corporation | Peripheral Cutting Balloon Over-the-Wire Microsurgical Dilatation Device | 6 (607.9 KPa) | 10 (1,013 KPa) | 0.018 (0.46 mm) | 7 (2.33 mm) | 7 (2.33 mm) | 50, 90, 135 | 5, 6, 7, 8 | 2 |
| BrosMed Medical | Tri-Wedge PTA Scoring Balloon Dilatation Catheter | 12 | 16 (ø, 7–8 mm), 20 (ø, 3–6 mm) | 0.018, 0.035 | 0.018 (proximal shaft OD 4 F, distal shaft OD 5 F), 0.035 (proximal shaft OD 5 F, distal shaft OD 6 F) | 5 (0.018; ø, 3–6 mm), 6 (0.018; ø, 7–8 mm, 0.035; ø, 3–6 mm), 7 (0.035; ø, 7–8 mm) | 0.018 (50, 90), 0.035 (50, 75) | 3, 4, 5, 6, 7, 8 | 2, 3, 4, 6 |
| Cagent Vascular | Serranator PTA Serration Balloon Catheter | 6 | 12 | 0.014, 0.018 | 6 | 6, 7 | 110, 150 | 2.5, 3, 3.5, 4, 5, 6, 7, 8 | 4, 8, 12 |
| Cerenovus | Ascent Occlusion Balloon Catheter | – | – | 0.017 | 2.9 | 5 | 150 | 4, 6 | 7, 9, 10, 15 mm |
| Concept Medical | MagicTouch ED | 8 bar | 14 bar | 0.014 | 6 | – | – | 1.50, 2, 2.25, 2.50, 2.75, 3, 3.50, 4 | 1, 1.5, 2, 2.5, 3, 3.5, 4 |
| Cook Medical | Advance Enforcer 35 | 6–10 | 10–16 | 0.035 | – | 6–8 | 50, 80, 135 | 6, 8, 10, 12 | 4 |
| Medtronic (manufactured by TriReme Medical) | Chocolate PTA | 6 (5–6), 8 (4.5), 9 (2.5–4) | 12 (4.5–6), 14 (2.5–4) | 0.014 (2.5–4), 0.018 (4.5–6) | – | 5 (2.5–4), 6 (4.5–6) | 120 (4.5–6), 135 (3.5–4), 150 (2.5, 3) | 2.5, 3, 3.5, 4, 4.5, 5, 5.5, 6 | 4, 8, 12 |
| Terumo Neuro | Scepter C Occlusion Balloon | – | 20.4 | 0.0165 | 2.8 | 4 | 150 | 4 | 1.5, 2 |
| Terumo Neuro | Scepter Mini | – | 47.6 | 0.008 | 2.8 | 4 | 165 | 2.2 | 0.9 |
| Terumo Neuro | Scepter XC Occlusion Balloon | – | 20.4 | 0.0165 | 2.8 | 4 | 150 | 4 | 1.1 |
| Philips | AngioSculpt PTA Scoring Balloon Catheter | 6–8 (depending on size) | 12–20 (depending on size) | 0.014, 0.018 (depending on size) | – | 5, 6 (depending on size) | 50, 90, 137, 155 (depending on size) | 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8 | 2, 4, 10, 20 |
| Stryker | TransForm Occlusion Balloon Catheter – Compliant | – | – | 0.014 | 2.8 | 5 | 150 | 3 | 1, 1.5 |
| Stryker | TransForm Occlusion Balloon Catheter – Compliant | – | – | 0.014 | 2.8 | 5 | 150 | 4, 5 | 1, 1.5, 2 |
| Stryker | TransForm Occlusion Balloon Catheter – Super Compliant | – | – | 0.014 | 2.8 | 5 | 150 | 3 | 0.5 |
| Stryker | TransForm Occlusion Balloon Catheter – Super Compliant | – | – | 0.014 | 2.8 | 5 | 150 | 4 | 0.7, 1 |
| Stryker | TransForm Occlusion Balloon Catheter – Super Compliant | – | – | 0.014 | 2.8 | 5 | 150 | 7 | 0.7, 1, 1.5 |
| ThermopeutiX, Inc. | TAPAS Targeted Drug Delivery System | – | – | 0.014 | 1.8 mm (minimum vessel) | 7 | 175 | 2.5–10 | 1 |
Catheters / Angiographic Catheters: Flush
View Chart| Company Name | Product Name | Type | Size (F) | Length (cm) | Guidewire Compatibility (inch) | Radiopaque Tip (Yes/No) | Variety of Selective Shapes |
|---|---|---|---|---|---|---|---|
| AngioDynamics | Accu-Vu Sizing Catheter | Sizing catheter (2RO, 21RO, 10RO), flush (nonbraided) | 4, 5 | 70, 90, 100 | 0.035, 0.038 | Yes | Omni Flush, pigtail, straight |
| AngioDynamics | Mariner Hydrophilic Angiographic Catheter | Hydrophilic diagnostic catheter, flush (nonbraided) | 4, 5 | 65–110 | 0.035, 0.038 | Yes | Omni Flush, pigtail, straight, Racket; full line of selective shapes |
| AngioDynamics | Soft-Vu Angiographic Catheter | Diagnostic catheter, flush (nonbraided) | 4, 5, 6 | 65–130 | 0.035, 0.038 | Yes | Omni Flush, pigtail, 90° pigtail, straight, Racket; full line of selective shapes |
| Boston Scientific Corporation | Imager II Angiographic Catheter | Braided | 4 (1.38 mm), 5 (1.7 mm) | 65, 90, 100 | 0.035 (0.89 mm), 0.038 (0.97 mm) | Yes | Contralateral, pigtail, straight, tennis racquet; full line of selective shapes |
| Cook Medical | Royal Flush Plus High-Flow | Nonbraided | 4, 5, 6 | 70, 100 | 0.035, 0.038 | No | Pediatric pigtail, pigtail, Centra-Flo pigtail, straight |
| Cordis | Super Torque | Braided polyurethane body | 4, 5, 6 | 65, 90, 100, 110 | 0.035, 0.038 | No | Wide variety |
| Cordis | Tempo | Braided nylon body | 4, 5 | 65, 90, 100, 110 | 0.035, 0.038 | Yes | Wide variety |
| Merit Medical Systems, Inc. | Performa/Impress | Both | 4, 5, 6 | 30, 40, 65, 80, 90, 110, 125 | 0.035, 0.038 | Yes | Pigtail, straight, contralateral (modified hook), ultra bolus (racquet) pediatric |
Catheters / Angiographic Catheters: Flush, Radiopaque Bands
View Chart| Company Name | Product Name | Measuring Increments | Size (F) | Length (cm) | Guidewire Compatibility (inch) | Radiopaque Tip (Yes/No) | Variety of Selective Shapes |
|---|---|---|---|---|---|---|---|
| AngioDynamics | Accu-Vu Sizing Catheter | 2, 20, 25 (cm), 28 (mm) | 4, 5 | 70, 90, 100 | 0.035, 0.038 | Yes | Omni Flush, pigtail, straight |
| Cordis | SuperTorque MB | 2, 10, 20 bands | 5 | 65, 70, 110 | 0.035 | Yes | Pigtail |
| Merit Medical Systems, Inc. | Pediatric | 1 cm | 3 | 65, 80 | 0.035 | Yes | Pigtail |
| Merit Medical Systems, Inc. | Performa | 1, 2 cm | 4, 5 | 65, 80, 90, 100 | 0.035 | Yes | Pigtail, straight, ultra bolus, modified hook |
Catheters / Angiographic Catheters: Selective, Hydrophilic Coated
View Chart| Company Name | Product Name | Type | Size (F) | Length (cm) | Guidewire Compatibility (inch) | Radiopaque Tip (Yes/No) | Variety of Selective Shapes |
|---|---|---|---|---|---|---|---|
| AngioDynamics | Mariner | Braided and nonbraided | 4, 5 | 40, 65, 80, 90, 100, 110, 130, 150 | 0.035, 0.038 | Yes | Wide variety of flush, cerebral, visceral, and multipurpose |
| Cordis | Tempo | Braided nylon body | 4, 5 | 40, 65, 80, 100, 110 | 0.035 and 0.038 | Yes | Select offering |
| Cordis | Tempo Aqua | Braided nylon body | 4, 5 | 65, 80, 90, 100, 125 | 0.038 | Yes | Select offering |
| Merit Medical Systems, Inc. | Impress Hydrophilic Catheters Coated (Legato) | Braided, selective, and flush | 4–5 | 40, 65, 80, 100, 125 | 0.038 | Yes | Wide variety of cerebral, visceral, and multipurpose available |
| Pediavascular | Mongoose | Pediatric angiography | 3, 4 | 40, 60, 80 | 0.030, 0.035, 0.038 | No | Cobra, JB1, JL1, JL 1.5, JR1, JR2, MP, Pig |
| Reflow Medical, Inc | Spex35 Shapeable Support Microcatheter | Shapeable tip, braid reinforced | 4.6 | 50, 90, 135, 150 | 0.035 | Yes | User's choice |
| Terumo Europe | Radifocus Glidecath | Hydrophilic angiographic catheter | 4, 5 | 40, 65, 70, 80, 90, 100, 110, 120, 150 | 0.038 | No | Wide variety of straight, angled, visceral, and cerebral shapes available |
| Reflow Medical, Inc | SpexLP 14 Shapeable Support Microcatheter | Low profile, shapeable tip, braid reinforced | 2.2 | 90, 135, 150 | 0.014 | Yes | User's choice |
| Reflow Medical, Inc | SpexLP 18 Shapeable Support Microcatheter | Low profile, shapeable tip, braid reinforced | 2.5 | 90, 135, 150 | 0.018 | Yes | User's choice |
| Reflow Medical, Inc | SpexLP 35 Shapeable Support Microcatheter | Low profile, shapeable tip, braid reinforced | 3.8 | 90, 135, 150 | 0.035 | Yes | User's choice |
Catheters / Angiographic Catheters: Selective, Nonhydrophilic Coated
View Chart| Company Name | Product Name | Type | Size (F) | Length (cm) | Guidewire Compatibility (inch) | Radiopaque Tip | Variety of Selective Shapes |
|---|---|---|---|---|---|---|---|
| AngioDynamics | Soft-Vu | Braided and nonbraided | 4, 5, 6 | 25, 40, 50, 65, 80, 90, 100, 110, 130, 140 | 0.035, 0.038, 0.046, 0.054 | Yes | Wide variety of cerebral, visceral, and multipurpose available |
| Boston Scientific Corporation | Imager II Angiographic Catheter | Braided | 4 (1.38 mm), 5 (1.7 mm) | 40, 65, 100 | 0.035 (0.89 mm), 0.038 (0.97 mm) | Yes | Wide variety of cerebral, visceral, and multipurpose shapes available |
| Cook Medical | Beacon Tip Torcon NB Advantage | Braided | 5 | 40, 60, 65, 80, 100, 125 | 0.038, 0.035 | Yes | Cerebral, angled, multipurpose, visceral |
| Cook Medical | Torcon NB Advantage | Braided | 4.1, 5, 6, 7 | 40, 65, 80, 100, 110, 125 | 0.035, 0.038 | No | Cerebral, angled, multipurpose, visceral |
| Cordis | Supertorque (Cerebral) | Braided polyurethane body | 4, 5, 6 | 65, 80, 100, 110 | 0.035, 0.038 | Yes | Wide variety |
| Cordis | Supertorque (Multipurpose) | Braided polyurethane body | 4, 5, 6 | 65, 80, 100, 110 | 0.035, 0.038 | Yes | Wide variety |
| Cordis | Supertorque (Visceral) | Braided polyurethane body | 4, 5, 6 | 65, 80, 100, 110 | 0.035, 0.038 | Yes | Wide variety |
| Cordis | Tempo | Braided nylon body | 4, 5 | 40, 65, 80, 90, 100, 110 | 0.035, 0.039 | Yes | Wide variety |
| Cordis | Tempo Aqua | Braided nylon body | 4, 5 | 65, 80 90, 100, 125 | 0.035, 0.040 | Yes | Wide variety |
| Medtronic | Pro-Flo | Single-wire braid | 6, 7 | 80, 100, 110, 125 | 0.050 (6 F), 0.061 (7 F) | Yes | Wide variety |
| Medtronic | SiteSeer | Double-wire braid | 4, 5, 6 | 80, 100, 110, 125 | 0.042 (4 F), 0.045 (5 F), 0.055 (6 F) | Yes | Wide variety |
| Merit Medical Systems, Inc. | Impress Diagnostic Catheters | Peripheral diagnostic, braided and nonbraided, selective | 4, 5 | 30, 40, 65, 80, 90, 100, 110, 120, 125 | 0.035, 0.038 | Yes | Wide variety of cerebral, visceral, and peripheral shapes |
| Merit Medical Systems, Inc. | Performa Diagnostic Catheters | Peripheral, braided and nonbraided, selective and flush | 4, 5, 6 | 40, 65, 80, 90, 110, 125 | 0.035, 0.038 | Yes | Wide variety |
| Terumo Europe | Outlook | Angiographic catheter | 4 | 20, 30, 40, 65, 80, 90, 100, 110 | 0.038 | No | Amplatz left, bypass Judkins left and right, Cobra middle, internal mammary, Judkins left, Judkins right, mini cath-standard, multipurpose, right, radial right, radial left, IMA, straight, angled pigtail, vertebral |
| Terumo Europe | Radifocus | Angiographic catheter | 5 | 65, 80, 100, 110 | 0.038 | No | Wide variety of straight, pigtail, visceral, and cerebral shapes available |
| Terumo Europe | Radifocus Optitorque | Angiographic catheter | 4, 5, 6 | 20, 65, 80 , 90, 100, 110, 125 | 0.038 | No | Wide variety of angled, pigtail, visceral, and cerebral shapes |
Catheters / Drainage Catheters
View Chart| Company Name | Product Name | Type | Tip | Size (F) | Length (cm) | Durometer | Radiopaque Tip (Yes/No) |
|---|---|---|---|---|---|---|---|
| Argon Medical Devices, Inc. | Skater All-Purpose and Nephrostomy Drainage Catheters | Multipurpose and nephrostomy percutaneous drainage | Locking pigtail | 6, 7, 8, 10, 12, 14, 16 | 15, 20, 25, 30, 35, 45, 60 | Polyurethane | No |
| Argon Medical Devices, Inc. | Skater All-Purpose and Nephrostomy Drainage Catheters | Multipurpose and nephrostomy percutaneous drainage | Nonlocking pigtail | 6, 7, 8, 10, 12, 14, 16 | 15, 20, 25, 30 | Polyurethane | No |
| Argon Medical Devices, Inc. | Skater Biliary Drainage Catheters | Percutaneous biliary drainage | Locking pigtail | 8, 10, 12 | 40 | Polyurethane | Yes |
| Argon Medical Devices, Inc. | Skater Centesis Catheters | Centesis drainage | Straight | 4, 5 | 7, 10, 15, 20 | Polyurethane | No |
| Argon Medical Devices, Inc. | Skater Mini-Loop Drainage Catheters | Multipurpose and nephrostomy percutaneous drainage | Locking pigtail | 6, 7, 8, 10, 12, 14 | 15, 20, 25 | Polyurethane | No |
| Argon Medical Devices, Inc. | Skater Safety Centesis Catheters | Centesis drainage | Nonlocking pigtail | 6, 8 | 13 | Polyurethane | No |
| Argon Medical Devices, Inc. | Skater Safety Centesis Catheters | Centesis drainage | Straight | 5, 8 | 10, 12 | Polyurethane | No |
| Cook Medical | Amplatz Ureteral Stent Set | Ureteral stent | Double J | 8.5 | 12, 20, 22, 24, 26, 28 | Ultrathane | Yes |
| Cook Medical | Biliary Drainage Catheter | Biliary drainage catheter | Biliary locking pigtail | 8.5, 10.2, 12, 14 | 40 | Ultrathane | Yes |
| Cook Medical | Cope Nephroureterostomy Set | Nephroureteral stent | Double locking pigtail | 8.5 | 22, 24, 26, 28 | Ultrathane | Yes |
| Cook Medical | Dawson-Mueller Drainage Catheter | Multipurpose drainage catheter | Locking pigtail | 5, 6.3, 7, 8.5, 10.2, 12, 14 | 15, 25 | Ultrathane | Yes |
| Cook Medical | Gordon Large-Bore Drainage Catheter | Multipurpose drainage catheter | Curved | 16, 18, 20, 22 | 40 | Ultrathane | No |
| Cook Medical | Multipurpose Drainage Catheter | Multipurpose drainage catheter | (Non)locking pigtail | 8.5, 10.2, 12, 14 | 25 | Ultrathane | No |
| Cook Medical | Multipurpose Drainage Catheter Set | Multipurpose pigtail drainage catheter with micropuncture access set | Locking pigtail | 8.5, 10.2, 12 | 25 | Ultrathane | Yes |
| Cook Medical | Ring-McLean Sump Drainage Catheter | Abscess drainage catheter with sump lumen | Straight, curved, pigtail | 12, 14, 16 | 18, 30 | Ultrathane | No |
| Cook Medical | Straight Drainage Catheter | Multipurpose drainage catheter | Straight | 8.5, 10.2 | 40 | Ultrathane | No |
| Cook Medical | Thal-Quick Abscess Drainage Catheter | Abscess drainage catheter | J–tip | 12, 14, 16, 18, 20, 24, 28 | 33, 41 | PVC | Radiopaque stripe from tip to hub |
| Cook Medical | Universal Curved Drainage Catheter | Multipurpose drainage catheter | Curved | 6, 7, 8.5, 10.2 | 25 | Ultrathane | No |
| Cook Medical | Yueh Centesis Catheter Needle | Centisis catheter needle | Straight | 5 | 10, 15 | Radiopaque nylon | No |
| Galt | Centeze Centesis Catheter | Centesis drainage | Straight | 4, 5, 6 | 7, 10, 15 | Standard | Echogenic needle |
| Merit Medical Systems, Inc. | Aspira Tunneled Pleural and Peritoneal Catheter | Tunneled pleural and peritoneal | Straight | 15.5 | 72 | Silicone | Yes |
| Merit Medical Systems, Inc. | One-Step | Centesis | Pigtail | 4, 5, 6, 8 | 7, 10, 12, 15, 17 | FEP, polyurethane | No |
| Merit Medical Systems, Inc. | ReSolve Biliary | Biliary | Pigtail | 8, 10, 12, 14 | 40 | Polyurethane | Yes |
| Merit Medical Systems, Inc. | ReSolve Locking | General | Pigtail | 6.5, 7.5, 8.5, 10, 12, 14 | 15, 25, 40 | Polyurethane | Yes |
| Merit Medical Systems, Inc. | ReSolve Mini | General | Mini pigtail | 6.5, 7.5, 8.5, 10, 12, 14 | 17, 27, 42 | Polyurethane | Yes |
| Merit Medical Systems, Inc. | ReSolve Non-Locking | General | J | 6.5, 7.5, 8.5, 10, 12 | 20, 25 | Polyurethane | Yes |
Catheters / Guiding Catheters
View Chart| Company Name | Product Name | Type | Size (F) | Length (cm) | Internal Diameter (inch) | Radiopaque Tip (Yes/No) | Hydrophilic Coated |
|---|---|---|---|---|---|---|---|
| ArtVentive Medical Group, Inc. | EOS Guiding Catheter (including dilator) | Endoluminal occlusion system | 6 | 89 (dilator length, 96) | 0.067 | Yes | Yes |
| ArtVentive Medical Group, Inc. | EOS Guiding Catheter (including dilator) | Endoluminal occlusion system | 7.5 | 89 (dilator length, 96) | 0.082 | Yes | Yes |
| Asahi Intecc Co Ltd. | Asahi Fubuki 043 | Braided | 4.2 | 120, 125, 130 | 0.043 (1.10 mm) | Yes | Yes |
| Asahi Intecc Co Ltd. | Asahi Fubuki 6Fr | Braided | 6 | 80, 90, 100, 110 | 0.071 (1.80 mm) | Yes | Yes |
| Asahi Intecc Co Ltd. | Asahi Fubuki 7Fr | Braided | 7 | 80, 90, 100, 110 | 0.081 (2.05 mm) | Yes | Yes |
| Asahi Intecc Co Ltd. | Asahi Fubuki 8Fr | Braided | 8 | 80, 90, 100, 110 | 0.090 (2.28 mm) | Yes | Yes |
| Asahi Intecc Co Ltd. | Asahi SheathLess PV | Sheathless braided guiding catheter; hydrophilic coated | 8.5 | 55, 90, 120 | 0.090 (2.29 mm) | Yes | Yes |
| BioCardia, Inc. | Morph Deflectable Tip Guide Catheter | Braided | 8 | 110 | 0.068 | Yes | Nonhydrophilic coated |
| Boston Scientific Corporation | Mach1 Peripheral Guide Catheter | Braided | 8 (2.7 mm) | 55, 90 | 0.091 (2.3 mm) | Yes | Nonhydrophilic coated |
| Boston Scientific Corporation | Mach1 Peripheral Guide Catheter | Braided | 6 (2.1 mm) | 55, 90 | 0.070 (1.7 mm) | Yes | Nonhydrophilic coated |
| Boston Scientific Corporation | Mach1 Peripheral Guide Catheter | Braided | 7 (2.4 mm) | 55, 90 | 0.081 (2 mm) | Yes | Nonhydrophilic coated |
| Cerenovus | Envoy DA (Distal Access) Guiding Catheter | Stainless steel braid | 6 | 95, 105 | 0.071 | Yes, brite tip and additional marker | Yes |
| Cerenovus | Envoy DA XB (Distal Access, Extra Back Up) Guiding Catheter | Stainless steel braid | 6 | 95, 105 | 0.071 | Yes, brite tip and additional marker | Yes |
| Cerenovus | Envoy Guiding Catheter | Stainless steel braid | 5 | 90, 100 | 0.056 | Yes, brite tip | Yes |
| Cerenovus | Envoy Guiding Catheter | Stainless steel braid | 6 | 90, 100 | 0.070 | Yes, brite tip | Yes |
| Cerenovus | Envoy Guiding Catheter | Stainless steel braid | 7 | 90, 100 | 0.078 | Yes, brite tip | Yes |
| Cerenovus | Envoy XB (Extra Back Up) Guiding Catheter | Stainless steel braid | 6 | 90, 100 | 0.070 | Yes, brite tip | Yes |
| Cerenovus | Revive IC Intermediate Catheter | Coil reinforced | 4 | 115, 130 | 0.044 | Yes, brite tip | Yes |
| Cerenovus | Revive IC Intermediate Catheter | Coil reinforced | 5 | 115, 125 | 0.056 | Yes, brite tip | Yes |
| Cordis | Vista Brite Tip | Braided shaft | 6, 7, 8, 9 | 55, 90, 95 | 0.070 (6 F), 0.078 (7 F), 0.088 (8 F), 0.098 (9 F) | Yes | Nonhydrophilic coated |
| Cordis | Vista Brite Tip IG | Braided shaft | 7, 8, 9 | 55, 95 | 0.070 (6 F), 0.078 (7 F), 0.088 (8 F), 0.098 (9 F) | Yes | Nonhydrophilic coated |
| Medtronic | Launcher | Braided | 6 | 47, 55, 100 | 0.071 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Launcher | Braided | 7 | 47, 55, 100 | 0.081 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Launcher | Braided | 8 | 47, 55, 100 | 0.090 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Piton GC | Braided | 8 | 85 | 5 F | Yes | Yes |
| Medtronic | Sherpa NX Active | Braided | 5 | 47, 55, 100 | 0.058 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Sherpa NX Balanced | Braided | 6 | 47, 55, 100 | 0.070 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Sherpa NX Balanced | Braided | 7 | 47, 55, 100 | 0.080 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Sherpa NX Balanced | Braided | 8 | 47, 55, 100 | 0.088 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Z2 | Braided | 6 | 47, 55, 100 | 0.070 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Z2 | Braided | 7 | 47, 55, 100 | 0.081 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Z2 | Braided | 8 | 47, 55, 100 | 0.091 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Zuma | Braided | 6 | 100 | 0.068 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Zuma | Braided | 7 | 47, 55, 100 | 0.081 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Medtronic | Zuma | Braided | 9 | 47, 55, 100 | 0.103 | No (radiopaque markerband 3 mm from the tip) | Yes |
| Terumo Neuro | Chaperon Guiding Catheter Single | PTFE layer with flat wire braid guiding catheter STR or MP2 tip shape | 5 | 95 | 0.059 | Yes | Yes |
| Terumo Neuro | Chaperon Guiding Catheter Single | PTFE layer with flat wire braid guiding catheter STR or MP2 tip shape | 6 | 95 | 0.071 | Yes | Yes |
| Terumo Neuro | Chaperon Guiding Catheter System | Guiding catheter with inner catheter system: STR/JB2, STR/VTR, STR/SIM, MP2/JB2, MP2/VTR, MP2/SIM tip shapes | 4, 5 | 95, 117 | 0.041, 0.059 | Yes | Yes |
| Terumo Neuro | Chaperon Guiding Catheter System | Guiding catheter with inner catheter system: STR/JB2, STR/VTR, STR/SIM, MP2/JB2, MP2/VTR, MP2/SIM, BUR/JB2, BUR/VTR tip shapes | 5, 6 | 95, 117 | 0.048, 0.071 | Yes | Yes |
| Penumbra, Inc. (Neuro) | 5F Select Catheter | Braid reinforced | Distal: 5; proximal: 5.5 | 120, 130 | 0.040 | Yes, radiopaque distal shaft | No |
| Penumbra, Inc. (Neuro) | 6F Select Catheter | Braid reinforced | Distal: 5; proximal: 5.6 | 105, 125 | 0.040 | Yes, radiopaque distal shaft | No |
| Penumbra, Inc. (Neuro) | Benchmark 071 Intracranial Access Kit | Coil reinforced | 6 | 95, 105, 115 | 0.071 | Yes, distal shaft plus markerband | Yes |
| Penumbra, Inc. (Neuro) | Neuron MAX 088 Delivery Catheter | Braid/coil reinforced | 8 | 80, 90, 100 | 0.088 | Yes, distal shaft plus markerband | Yes |
| Stryker | AXS Catalyst 5 Distal Access Catheter | Device delivery and thrombus aspiration catheter | 5.3 distal, 5.6 proximal | 115, 132 | 0.058 | Yes | Yes |
| Stryker | AXS Catalyst 6 Distal Access Catheter | Device delivery and thrombus aspiration catheter | 5.4 distal, 6 proximal | 132 | 0.060 | Yes | Yes |
| Stryker | AXS Catalyst 7 Distal Access Catheter | Device delivery and thrombus aspiration catheter | 6.2 distal, 6.3 proximal | 115, 125, 132 | 0.068 | Yes | Yes |
| Stryker | AXS Infinity LS | Braided | 8 | 70, 80, 90 | 0.088 | Yes | Yes |
| Stryker | AXS Infinity LS Plus | Cross-coil reinforcement | 8 | 70, 80, 90 | 0.091 | Yes | Yes |
| Stryker | AXS Vecta 71 Aspiration Catheter | Device delivery and thrombus aspiration catheter | 6.3 (distal), 6.5 (proximal) | 115, 125, 132 | 0.071 | Yes | Yes |
| Stryker | AXS Vecta 74 Aspiration Catheter | Device delivery and thrombus aspiration catheter | 6.3 (distal), 6.6 (proximal) | 115, 125, 132 | 0.074 | Yes | Yes |
| Stryker | DAC 038 | Braided | 3.9 OD | 125, 136 | 0.038 | Yes | Yes |
| Stryker | DAC 044 | Braided | 4.3 OD | 115, 130, 136 | 0.044 | Yes | Yes |
| Stryker | DAC 057 | Braided | 5.2 OD | 115, 125 | 0.057 | Yes | Yes |
| Stryker | DAC 070 | Braided | 6.3 OD | 105, 120 | 0.070 | Yes | Yes |
| Stryker | FlowGate2 Balloon Guide Catheter | Braided | 8 | 85, 95 | 0.084 | Yes | No |
| Stryker | Guider Softip XF Guide Catheter | Braided | 5, 6, 7, 8 | 90, 100 | 0.053, 0.064, 0.073, 0.086 | Yes; straight, 40, MP shapes | Yes |
| Stryker | Merci Balloon Guide Catheter | Braided | 8 | 80, 95 | 0.078 | Yes | Nonhydrophilic coated |
| Stryker | Merci Balloon Guide Catheter | Braided | 9 | 80, 95 | 0.085 | Yes | Nonhydrophilic coated |
| TriSalus Life Sciences | Flexion Guiding Catheter: Axis, SIM1 | Braided stainless steel, PTFE, multiple durometer Pebax, nitinol tip | 5 | 80 | 0.054 | Yes | No |
| TriSalus Life Sciences | Surefire Guiding Catheter Cobra1, SIM1, Axis | Braided stainless steel, PTFE, multiple durometer Pebax | 5 | 65 | 0.056 | Yes | No |
| Penumbra, Inc. (Neuro) | BMX81 Access System | Laser-cut stainless steel hypotube | 7 | 95, 105, 115 | 0.081 | Yes, full shaft plus markerband | Yes, 18 cm |
| Penumbra, Inc. (Neuro) | BMX96 Access System | Laser-cut stainless steel hypotube | 8 | 80, 90, 100 | 0.096 | Yes, distal shaft plus markerband | Yes, 9 cm |
Catheters / Microcatheters
View Chart| Company Name | Product Name | Type of Catheter Construction | Proximal Size (F) | Middle Size (F) | Distal Size (F) | Catheter Working Length (cm) | Catheter Endhole Diameter ID (inch) | Recommended Guidewire Size (inch) | Radiopaque Tip (Yes/No) | Hydrophilic Coating (Yes/No) |
|---|---|---|---|---|---|---|---|---|---|---|
| Acandis GmbH & Co. KG | NeuroSlider 17 | Stainless steel braiding with inner PTFE liner | 2.1 | – | 1.9 | 155 | 0.0165 | 0.014 (maximum) | Yes, two markers | Yes |
| Acandis GmbH & Co. KG | NeuroSlider 21 | Stainless steel braiding with inner PTFE liner | 2.5 | – | 2.4 | 155 | 0.021 | 0.018 (maximum) | Yes, two markers | Yes |
| Acandis GmbH & Co. KG | NeuroSlider 27 | Stainless steel braiding with inner PTFE liner | 3.6 | – | 3 | 155 | 0.027 | 0.021 (maximum) | Yes, one marker | Yes |
| Asahi Intecc Co Ltd. | Asahi Tellus | SUS braiding | 2.8 | – | 1.9 | 105, 125, 150 | 0.019 | 0.016 | Yes | Yes |
| Asahi Intecc Co Ltd. | Asahi Veloute | Braiding | 2.8 | – | 1.7 | 105, 125, 150 | 0.017 | 0.016 | Yes | Yes |
| Asahi Intecc Co Ltd. | Masters Parkway HF | Tungsten, PTFE | 2.8 | – | 2.6 | 105, 125, 150 | 0.027 | 0.021 | Yes | Yes |
| Asahi Intecc Co Ltd. | Masters Parkway Soft | Tungsten, PTFE | 2.8 | – | 1.9 | 105, 125, 150 | 0.022 | 0.018 (maximum) | Yes | Yes |
| Boston Scientific Corporation | Direxion | Preshaped or shapeable steerable nitinol microcatheter | 2.4 | 2.4 | 2.4 | 105, 130, 155 | 0.021 | Up to 0.018 | Yes (1 or 2 RO) | Yes |
| Boston Scientific Corporation | Direxion Hi-Flo | Preshaped or shapeable steerable nitinol microcatheter | 2.8 | 2.8 | 2.8 | 105, 130, 155 | 0.027 | Up to 0.021 | Yes | Yes |
| Boston Scientific Corporation | Direxion Hi-Flo System | Preshaped or shapeable steerable nitinol preloaded microcatheter | 2.8 | 2.8 | 2.8 | 105, 130, 155 | 0.027 | Preloaded with Transend 18 or Fathom 16 | Yes | Yes |
| Boston Scientific Corporation | Direxion System | Preshaped or shapeable steerable nitinol preloaded microcatheter | 2.4 | 2.4 | 2.4 | 105, 130, 155 | 0.021 | Preloaded with Transend 14 or Fathom 16 | Yes (1 or 2 RO) | Yes |
| Boston Scientific Corporation | Renegade Hi-Flo Fathom Kit | Vortec plus braiding: fiber and platinum braid | 3 (1 mm) | – | 2.8 (0.93 mm) | 105, 115, 135, 150 | 0.027 (0.69 mm) | Includes Fathom-16 guidewire | Yes | Yes |
| Boston Scientific Corporation | Renegade Hi-Flo Fathom Preloaded System | Vortec plus braiding: fiber and platinum braid | 3 (1 mm) | – | 2.8 (0.93 mm) | 105, 115, 135, 150 | 0.027 (0.69 mm) | Includes preloaded Fathom-16 guidewire | Yes | Yes |
| Boston Scientific Corporation | Renegade Hi-Flo Microcatheter | Vortec plus braiding: fiber and platinum braid | 3 (1 mm) | – | 2.8 (0.93 mm) | 105, 115, 135, 150 | 0.027 (0.69 mm) | 0.018 (0.46 mm) (maximum) | Yes | Yes |
| Boston Scientific Corporation | Renegade Hi-Flo Transend Kit | Vortec plus braiding: fiber and platinum braid | 3 (1 mm) | – | 2.8 (0.93 mm) | 105, 115, 135 | 0.027 (0.69 mm) | Includes Transend-18 guidewire | Yes | Yes |
| Boston Scientific Corporation | Renegade Microcatheter | Vortec fiber braiding | 3 (1 mm) | – | 2.5 (0.83 mm) | 130, 150 | 0.021 (0.53 mm) | 0.018 (0.46 mm) (maximum) | Yes | Yes |
| Boston Scientific Corporation | Renegade STC 18 Microcatheter | Vortec fiber and stainless steel braid | 3 (1 mm) | – | 2.4 (0.8 mm) | 105, 130, 150 | 0.021 (0.53 mm) | 0.018 (0.46 mm) (maximum) | Yes | Yes |
| Cerenovus | Prowler 10 | Braid/coil design | 2.3 | – | 1.7 | 150 | 0.015 | 0.012 (maximum) | Yes | Yes |
| Cerenovus | Prowler 14 | Braid/coil design | 2.8 | – | 1.9 | 150, 170 | 0.0165 | 0.014 (maximum) | Yes | Yes |
| Cerenovus | Prowler 27 | Braid/coil design | 3 | – | 2.6 | 150 | 0.027 | 0.018 (maximum) | Yes | Yes |
| Cerenovus | Prowler Plus | Braid/coil design | 2.8 | – | 2.3 | 110, 135, 150 | 0.021 | 0.018 (maximum) | Yes | Yes |
| Cerenovus | Prowler Select LP-ES | Braid/coil design | 2.8 | – | 1.9 | 150 | 0.0165 | 0.014 (maximum) | Yes | Yes |
| Cerenovus | Prowler Select Plus | Braid/coil design | 2.3 | – | 2.3 | 150 | 0.021 | 0.018 (maximum) | Yes | Yes |
| Cerenovus | Rapidtransit Microcatheters | Braid/coil design | 2.3 | – | 2.3 | 75, 155, 175 (proximal, middle, and distal lengths); 100, 135 (proximal lengths) | 0.021 | 0.018 (maximum) | Yes | Yes |
| Cerenovus | Transit Microcatheters | Braid/coil design | 2.8 | – | 2.5 | 135, 150 | 0.021 | 0.018 (maximum) | Yes | Yes |
| Cook Medical | Cantata 2.5 | Braided stainless steel, PTFE, Pebax | 2.5 | 2.5 | 2.5 | 110, 135, 150 | 0.021 | 0.018 (maximum) | Yes (1 or 2 RB) | Yes |
| Cook Medical | Cantata 2.8 | Braided stainless steel, PTFE, Pebax | 2.8 | 2.8 | 2.8 | 110, 135, 150 | 0.025 | 0.021 (maximum) | Yes (1 or 2 RB) | Yes |
| Cook Medical | Cantata 2.9 | Braided stainless steel, PTFE, Pebax | 2.9 | 2.9 | 2.9 | 110, 135, 150 | 0.027 (0.69 mm) | 0.025 (maximum) | Yes | Yes |
| Argon Medical Devices, Inc. | Drakon | Tungsten steel-braided shaft, PTFE inner lumen | 3 | – | 2.8 | 105, 130, 150 | 0.027 | 0.021 (maximum) | Yes | Yes |
| Argon Medical Devices, Inc. | Drakon | Tungsten steel-braided shaft, PTFE inner lumen | 2.9 | – | 2.4 | 105, 130, 150 | 0.022 | 0.018 (maximum) | Yes | Yes |
| Argon Medical Devices, Inc. | Drakon | Tungsten steel-braided shaft, PTFE inner lumen | 2.9 | – | 2.7 | 105, 130, 150 | 0.025 | 0.021 (maximum) | Yes | Yes |
| Argon Medical Devices, Inc. | SeQure | Tungsten steel-braided shaft, PTFE inner lumen | 2.9 | – | 2.4 | 105, 130, 150 | 0.022 | 0.018 (maximum) | Yes, two markerbands | Yes |
| Argon Medical Devices, Inc. | SeQure | Tungsten steel-braided shaft, PTFE inner lumen | 3 | – | 2.8 | 105, 130, 150 | 0.027 | 0.021 (maximum) | Yes, two markerbands | Yes |
| Argon Medical Devices, Inc. | SeQure | Tungsten steel-braided shaft, PTFE inner lumen | 2.9 | – | 2.7 | 105, 130, 150 | 0.025 | 0.021 (maximum) | Yes, two markerbands | Yes |
| Medtronic | Apollo Detachable Tip Microcatheter | Distal nitinol braiding with detachable tip 1.5, 3, and 5 cm | 2.7 | – | 1.5 | 165 | 0.010 | 0.010 (maximum) | Yes | Yes |
| Medtronic | Echelon-10 | Four performance zones with smooth transitions and nitinol braiding with progressive PPI for optimal proximal pushability and support and enhanced torque response; tip configuration straight, 40°, and 90° bends | 2.1 | – | 1.7 | 155 | 0.017 | 0.014 (maximum) | Yes | Yes |
| Medtronic | Echelon-14 | Four performance zones with smooth transitions and nitinol braiding with progressive PPI for optimal proximal pushability and support and enhanced torque response; tip configuration straight, 40°, and 90° bends | 2.4 | – | 1.9 | 155 | 0.017 | 0.014 (maximum) | Yes | Yes |
| Medtronic | Rebar-10 | Stainless steel reinforced microcatheter | 2.3 | – | 1.7 | 153 | 0.012 | 0.012 (maximum) | Yes | Yes |
| Medtronic | Rebar-14 | Stainless steel reinforced microcatheter | 2.4 | – | 1.9 | 153 | 0.014 | 0.014 (maximum) | Yes | Yes |
| Medtronic | Rebar-18 | Stainless steel reinforced microcatheter | 2.8 | – | 2.3 | 130, 153 | 0.018 | 0.018 (maximum) | Yes | Yes |
| Medtronic | Rebar-27 | Stainless steel reinforced microcatheter | 2.8 | – | 2.8 | 130, 145 | 0.027 | 0.027 (maximum) | Yes | Yes |
| Merit Medical Systems, Inc. | Maestro | Nylon ribbon braiding | 2.8, 2.9 | 2.8, 2.9 | 2.1, 2.4, 2.8, 2.9 | 110, 130, 150 | 0.018, 0.020, 0.024, 0.027 | 0.016, 0.018, 0.021 | Yes, one markerband | Yes |
| Merit Medical Systems, Inc. | Pursue Microcatheter | Metal braided | 2.8, 2.9 | 2.8, 2.9 | 1.7, 2 | 110, 130, 150 | 0.016, 0.020 | 0.014, 0.018 | Yes, one markerband | Yes |
| Merit Medical Systems, Inc. | SwiftNinja Steerable Microcatheter | Tungsten-braided shaft | 2.9 (0.97 mm) | 2.9 (0.97 mm) | 2.4 (0.80 mm) | 125 | 0.021 | ≤ 0.018 | Yes, two markerbands | Yes |
| Terumo Neuro | Headway 17 Advanced | Tapered PTFE liner with coil reinforcement | 2.4 | – | 1.7 | 150 | 0.017 | 0.017 | Yes | Yes |
| Terumo Neuro | Headway 17 Advanced Soft | Tapered PTFE liner with coil reinforcement | 2.4 | – | 1.7 | 150 | 0.017 | 0.017 | Yes | Yes |
| Terumo Neuro | Headway 21 | PTFE liner with coil reinforcement | 2.5 | – | 2 | 150 | 0.021 | 0.021 | Yes | Yes |
| Terumo Neuro | Headway 27 | PTFE liner with coil reinforcement | 3.1 | – | 2.6 | 150 | 0.027 | 0.027 | Yes | Yes |
| Terumo Neuro | Headway Duo | Hybrid braid/coil design | 2.1 | – | 1.6 | 167 | 0.0165 | 0.0165 | Yes | Yes |
| Terumo Neuro | Headway Duo | Hybrid braid/coil design | 2.1 | – | 1.6 | 156 | 0.0165 | 0.0165 | Yes | Yes |
| Terumo Neuro | Wedge | Coil reinforcement and distal bulb | 2.5 | – | 2 | 1.5 (distal length) | 0.021 | 0.014 | Yes | Yes |
| Penumbra, Inc. (Neuro) | PX Slim Delivery Microcatheter | Nitinol coil reinforced; eight extrusion zones | 2.95 | – | 2.6 | 150 | 0.025 | ≤ 0.020 | Yes, two markerbands | Yes |
| Penumbra, Inc. (Neuro) | Velocity Delivery Microcatheter | Nitinol coil reinforced; eight extrusion zones | 2.95 | – | 2.6 | 160 | 0.025 | ≤ 0.020 | Yes, one markerband | Yes |
| Penumbra, Inc. (Peripheral Vascular) | Lantern Delivery Microcatheter | Nitinol coil reinforced; eight extrusion zones; three tip shapes: straight, 45°, and 90° | 2.95 | – | 2.6 | 115, 135, 150 | 0.025 | ≤ 0.023 | Yes; two markerbands, radiopaque 3 cm | Yes |
| Reflow Medical, Inc | Wingman14 CTO Crossing Catheter | Braided with extendable beveled tip | 2.7 | 2.7 | 2.7 | 65, 135, 150 | 0.022 | 0.014 | Yes | No |
| Reflow Medical, Inc | Wingman18 CTO Crossing Catheter | Braided with extendable beveled tip | 3.8 | 3.8 | 3.8 | 90, 135, 150 | 0.032 | 0.018 | Yes | Yes |
| Stryker | Excelsior 1018 | Braided, hydrophilic | 2.6 | – | 2 | 150 | 0.019 | 0.016 (maximum) | Yes | Yes |
| Stryker | Excelsior SL-10 | Braided, hydrophilic | 2.4 | – | 1.7 | 150 | 0.0165 | 0.014 (maximum) | Yes | Yes |
| Stryker | Excelsior XT-17 | Braided | 2.4 | – | 1.7 | 150 | 0.017 | 0.014 (maximum) | Yes | Yes |
| Stryker | Excelsior XT-27 | Braided, hydrophilic | 2.9 | – | 2.7 | 135, 150 | 0.027 | 0.018 (maximum) | Yes | Yes |
| Stryker | Neuro Renegade Hi-Flo | Braided, hydrophilic | 3 | – | 2.8 | 135, 150 | 0.027 | 0.018 (maximum) | Yes | Yes |
| Stryker | Renegade 18 | Braided, hydrophilic | 3 | – | 2.5 | 150 | 0.021 | 0.018 (maximum) | Yes | Yes |
| Stryker | Trevo Pro 14 | Braided | 2.4 | – | 2.0 | 157 | 0.017 | 0.014 (maximum) | Yes | Yes |
| Stryker | Trevo Pro 18 | Braided | 2.7 | – | 2.4 | 150 | 0.021 | 0.018 (maximum) | Yes | Yes |
| Stryker | Trevo Trak 21 | Braided | 2.7 | – | 2.4 | 162 | 0.021 | 0.018 (maximum) | Yes | Yes |
| Teleflex | SuperCross Microcatheter OTW - 0.014 Angled Tips: 45°, 90°, 120°, and 90° Extended Tip | Dual coil design; platinum/tungsten coil tip | 3.2 | – | 2.4 | 130, 150 | 0.017 | 0.014 | Yes, platinum/tungsten coil tip | Yes |
| Teleflex | SuperCross Microcatheter OTW - 0.014 Straight and Flexible Tip | Braided | 2.5 | – | 1.8 | 130, 150 | 0.017 | 0.014 | Yes, single markerband | Yes |
| Teleflex | Turnpike Catheter | Hybrid multilayer: dual bidirectional coils with inner braid | 2.9 | 2.6 | 1.6 | 135, 150 | 0.0165 | 0.014 | Yes, tungsten-loaded tip | Yes |
| Teleflex | Turnpike Gold Catheter | Hybrid multilayer: dual bidirectional coils with inner braid and external nylon spiral coil | 2.9 | 2.9 | 2.1 | 135 | 0.0165 | 0.014 | Yes, gold-plated tip | Yes |
| Teleflex | Turnpike LP Catheter | Hybrid multilayer: dual bidirectional coils with inner braid | 2.9 | 2.2 | 1.6 | 135, 150 | 0.0165 | 0.014 | Yes, tungsten-loaded tip | Yes |
| Teleflex | Turnpike Spiral Catheter | Hybrid multilayer: dual bidirectional coils with inner braid and external nylon spiral coil | 2.9 | 2.9 | 1.6 | 135, 150 | 0.0165 | 0.014 | Yes, tungsten-loaded tip | Yes |
| Terumo Europe | Progreat | Hyperselective hydrophilic braided radiopaque microcatheters | 2.4 | 2.7 | 2.8 | 110 (proximal), 130 (middle), 150 (distal) | 0.022, 0.025, 0.027 | < 0.021 | 3-cm gold marker | Yes |
| Tokai Medical Products, Inc | Carnelian 1.7 | Tungsten-braided super-selective microcatheter; tip configuration, straight; 45° and W-angled | 2.8 | – | 1.7 | 110, 135 | 0.017 | 0.016 | Yes | Yes |
| Tokai Medical Products, Inc | Carnelian 1.8 | Tungsten-braided super-selective microcatheter; tip configuration straight; 45° and cobra angled | 2.7 | – | 1.8 | 110, 135, 150 | 0.017 | 0.016 (maximum) | Yes | Yes |
| Tokai Medical Products, Inc | Carnelian 1.9 | Tungsten-braided super-selective microcatheter; tip configuration, straight; 45° and W-angled | 2.8 | – | 1.9 | 110, 135 | 0.019 | 0.018 | Yes | Yes |
| Tokai Medical Products, Inc | Carnelian 2.2 | Tungsten-braided selective microcatheter; tip configuration straight; 45° and cobra angled | 2.9 | – | 2.2 | 70, 110, 130, 135, 150 | 0.021 | 0.018 (maximum) | Yes | Yes |
| Tokai Medical Products, Inc | Carnelian 2.7 | Tungsten-braided high flow microcatheter; tip configuration straight | 2.9 | – | 2.7 | 105, 125 | 0.027 | 0.025 (maximum) | Yes | Yes |
| Tokai Medical Products, Inc | Carnelian SI - Straight Inner | Tungsten-braided super-selective microcatheter with straight inner; tip configuration straight; 45° and W angled | 2.8 | – | 1.9 | 110, 135 | 0.021 | 0.018 | Yes | Yes |
| TriSalus Life Sciences | Surefire Infusion System (SIS) 021 | Braided stainless steel, PTFE, multiple polymers, microvalve tip | 3.2 | 3.2 | 2.8 | 120, 150 | 0.021 | 0.018 (maximum) | Yes | Yes |
| TriSalus Life Sciences | Surefire Infusion System (SIS) 025 | Braided stainless steel, PTFE, multiple polymers, microvalve tip | 3.7 | 3.7 | 3.4 | 120, 150 | 0.025 | 0.018 (maximum) | Yes | Yes |
| Reflow Medical, Inc | Spex35 Shapeable Support Microcatheter | Shapeable tip, braid reinforced | 4.6 | 4.6 | 4.6 | 50, 90, 135, 150 | 0.038 | 0.035 | Yes | Yes |
| Reflow Medical, Inc | SpexLP 14 Shapeable Support Microcatheter | Low profile, shapeable tip, braid reinforced | 2.2 | 2.2 | 1.4 | 90, 135, 150 | 0.018 | 0.014 | Yes | Yes |
| Reflow Medical, Inc | SpexLP 18 Shapeable Support Microcatheter | Low profile, shapeable tip, braid reinforced | 2.5 | 2.5 | 1.6 | 90, 135, 150 | 0.021 | 0.018 | Yes | Yes |
| Reflow Medical, Inc | SpexLP 35 Shapeable Support Microcatheter | Low profile, shapeable tip, braid reinforced | 3.8 | 3.8 | 2.9 | 90, 135, 150 | 0.038 | 0.035 | Yes | Yes |
| Reflow Medical, Inc | Wingman 14C CTO Crossing Catheter | Braided with extendable beveled tip | 2.7 | 2.7 | 2.7 | 90, 135, 150 | 0.024 | 0.014 | Yes | Yes |
| Reflow Medical, Inc | Wingman 35 CTO Crossing Catheter | Braided with extendable beveled tip | 4.6 | 4.6 | 4.6 | 90, 135, 150 | 0.032 | 0.035 | Yes | Yes |
| Tokai Medical Products, Inc | Carnelian NT | Tungsten-braided super-selective microcatheter, specially for triaxial system | 1.8, 1.9 | – | 1.6, 1.9 | 135, 155 | 0.015, 0.017 | 0.014 | Yes | Yes |
Catheters / Specialty Catheters
View Chart| Company Name | Product Name | Catheter Size (F) | Working Length (cm) | Minimum Guiding Catheter ID (inch) | Comments |
|---|---|---|---|---|---|
| BD Interventional | Seeker Crossing Support Catheters | 4 (0.014-inch wire, 0.018-inch wire), 5 (0.035-inch wire) | 65, 90, 135, 150 | 4, 5 F | Hydrophilic-coated support catheter with a 30-cm radiopaque marking system (1 cm in length, positioned 1 cm apart), sized to support standard 0.014-, 0.018-, and 0.035-inch guidewires |
| Bentley InnoMed GmbH | BeBack crossing catheter | 2.9, 4 | 80, 120 | 2.9 F (crossover 5 F); 4 F (crossover 6 F) | A low-profile support catheter that has a crossing and targeted re-entry capability due to the steerable nitinol needle at the tip; a radiopaque marker indicates the direction in which the curved needle will protrude from the catheter’s tip; antegrade, retrograde, and crossover are possible for intraluminal and subintimal approach on 0.014- and 0.018-inch wire platform |
| Boston Scientific Corporation | Rubicon Support Catheter | 4 (1.33 mm), 5 (1.7 mm) | 65, 90, 135, 150 | 0.018 (0.46 mm), 0.022 (0.56 mm), 0.037 (0.95 mm) | Designed to facilitate crossing of tight occlusions; with an ultra-low lesion entry profile, a strong next-generation distal tip for superior push, and three radiopaque markers; engineered for excellent cross when tackling challenging lesions |
| Cook Medical | CrossCath Support Catheter | 1.5, 1.8, 3.1 (distal tip) | 90, 135, 150 | 0.041, 0.046, 0.065 | Tapered, hydrophilic-coated support catheter; single lumen; radiopaque markers |
| Cook Medical | CXI Support Catheter | 2.3 (0.014-inch wire) | 65, 90, 135, 150 | 0.015 | Flexible, braided catheter shaft with hydrophilic coating tracks through complex anatomy and provides support for crossing difficult lesions; radiopaque markerbands assist with placement and sizing |
| Cook Medical | CXI Support Catheter | 2.6 (0.018-inch wire) | 65, 90, 135, 150 | 0.032 | Flexible, braided catheter shaft with hydrophilic coating tracks through complex anatomy and provides support for crossing difficult lesions; radiopaque markers and tip assist with placement and sizing |
| Cook Medical | CXI Support Catheter | 4 (0.035-inch wire) | 90, 135, 150 | 0.052 | Flexible, braided catheter shaft with hydrophilic coating tracks through complex anatomy and provides support for crossing difficult lesions; radiopaque markers and tip assist with placement and sizing |
| Cook Medical | TriForce Peripheral Crossing Set | Inner catheter: 4, outer sheath: 5, tapering to 4 (0.035-inch wire) | 65, 100 | 0.052 | Coaxial peripheral crossing set; both inner catheter and outer sheath are hydrophilically coated; inner catheter is braided with radiopaque tip; outer sheath is coil reinforced to provide exceptional tracking through tortuous anatomy; a tungsten-loaded tip on the outer sheath aids pushability and radiopacity; outer sheath is tapered down to inner catheter to provide additional support, strength, and pushability across challenging lesions |
| Cordis | Super Torque Markerbands Calibration Catheter | 5 | 65, 70, 110 | – | – |
| iVascular | Sergeant Support Catheter | 4 F for all guidewire compatibilities | 65, 90, 130, 150 | 0.032 (0.014-inch guidewire), 0.037 (0.018-inch guidewire), 0.052 (0.035-inch guidewire) | Unique braided design for an exceptional pushability and torque capacity; good navigability (Hydrax Plus proprietary coating) and small profiles 4 F. 0.014-, 0.018-, 0.035-inch guidewire compatibility; straight or 30° angled |
| Medtronic | TrailBlazer Angled Support Catheter 0.014 | 2.3 | 90, 135, 150 | 0.064 | An OTW, single-lumen, braided catheter with a tapered, angled tip |
| Medtronic | TrailBlazer Angled Support Catheter 0.018 | 2.6 | 90, 135, 150 | 0.064 | An OTW, single-lumen, braided catheter with a tapered, angled tip |
| Medtronic | TrailBlazer Angled Support Catheter 0.035 | 3.2 | 65, 90, 135, 150 | 0.064 | An OTW, single-lumen, braided catheter with a tapered, angled tip |
| Medtronic | TrailBlazer Support Catheter 0.014 | 3 | 135, 150 | 0.064 | An OTW, single-lumen catheter with an atraumatic tapered tip |
| Medtronic | TrailBlazer Support Catheter 0.018 | 3.4 | 90, 135, 150 | 0.064 | An OTW, single-lumen catheter with an atraumatic tapered tip |
| Medtronic | TrailBlazer Support Catheter 0.035 | 4.8 | 65, 90, 135, 150 | 0.077 | An OTW, single-lumen catheter with an atraumatic tapered tip |
| Merit Medical Systems, Inc. | SureCross Support Catheter - 0.014 inch | 1.5 distal tip (0.014-inch wire) | 65, 90, 135, 150 | 0.066 (5 F) | Low-profile, hydrophilic-coated, tapered-tip catheter provides seamless catheter-to-guidewire transition to facilitate crossing of challenging lesions and tracking through tortuous anatomy |
| Merit Medical Systems, Inc. | SureCross Support Catheter - 0.018 inch | 1.7 distal tip (0.018-inch wire) | 65, 90, 135, 150 | 0.066 (5 F) | Low-profile, hydrophilic-coated, tapered-tip catheter provides seamless catheter-to-guidewire transition to facilitate crossing of challenging lesions and tracking through tortuous anatomy |
| Merit Medical Systems, Inc. | SureCross Support Catheter - 0.035 inch | 3.1 distal tip (0.035-inch wire) | 65, 90, 135, 150 | 0.079 (6 F) | Low-profile, hydrophilic-coated, tapered-tip catheter provides seamless catheter-to-guidewire transition to facilitate crossing of challenging lesions and tracking through tortuous anatomy |
| Philips | Quick-Cross Extreme Support Catheter | 4 | 90, 135, 150 | 5 F (guide)/4 F (sheath) | Low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, and pushability to track through complex anatomy |
| Philips | Quick-Cross Extreme Support Catheter | 4 | 135, 150 | 5 F (guide)/4 F (sheath) | Low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, and pushability to track through complex anatomy |
| Philips | Quick-Cross Extreme Support Catheter | 5 | 65, 90, 135, 150 | 5 F (sheath) | Low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, and pushability to track through complex anatomy |
| Philips | Quick-Cross Select Support Catheter | 4 | 90, 135, 150 | 5 F (guide)/4 F (sheath) | Angled and low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, and pushability and allows the ability to navigate through complex anatomy |
| Philips | Quick-Cross Select Support Catheter | 5 | 65, 90, 135, 150 | 5 F (sheath) | Angled and low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, and pushability and allows the ability to navigate through complex anatomy |
| Philips | Quick-Cross Select Support Catheter | 4 | 135, 150 | 5 F (guide)/4 F (sheath) | Angled and low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, and pushability and allows the ability to navigate through complex anatomy |
| Philips | Quick-Cross Support Catheter | 4 | 135, 150 | 5 F (guide)/4 F (sheath) | Low-profile, hydrophilic-coated, tapered-tip catheter provides seamless catheter-to-guidewire transition to facilitate crossing of challenging lesions and tracking through tortuous anatomy |
| Philips | Quick-Cross Support Catheter | 5 | 65, 90, 135, 150 | 6 F (guide)/5 F (sheath) | Low-profile, hydrophilic-coated, tapered-tip catheter provides seamless catheter-to-guidewire transition to facilitate crossing of challenging lesions and tracking through tortuous anatomy |
| Philips | Quick-Cross Support Catheter | 4 | 90, 135, 150 | 5 F (guide)/4 F (sheath) | Low-profile, hydrophilic-coated, tapered-tip catheter provides seamless catheter-to-guidewire transition to facilitate crossing of challenging lesions and tracking through tortuous anatomy |
| Prytime Medical Devices, Inc. | ER-REBOA PLUS Catheter | 7 | 72 | – | A large vessel occlusion catheter consisting of an atraumatic distal tip (P-tip), a compliant occlusion balloon, and catheter shaft with a built-in central lumen for blood pressure monitoring |
| Reflow Medical, Inc | Spex35 Shapeable Support Microcatheter | 4.6 | 50, 90, 135, 150 | 0.066 | Single lumen, shapeable tip microcatheters designed to access the peripheral vasculature; allows for exchange of guidewires and other interventional devices and provides a conduit for delivery of saline solutions or diagnostic contrast; available in a variety of lengths; braided support matrix and hydrophilic coating (distal segment); the distal tip of the Spex has one radiopaque marker |
| Reflow Medical, Inc | Wingman14 CTO Crossing Catheter | 2.7 | 65, 135, 150 | 0.039 | A beveled (needle) tip recanalization device intended to provide additional support to a steerable guidewire when accessing discrete regions of the peripheral vasculature; the Wingman CTO Crossing Catheter consists of a support catheter, with a user controlled radiopaque guide tip (5-mm extendable needle tip) and activating handle |
| Reflow Medical, Inc | Wingman18 CTO Crossing Catheter | 3.8 | 90, 135, 150 | 0.052 | A beveled (needle) tip recanalization device intended to provide additional support to a steerable guidewire when accessing discrete regions of the peripheral vasculature; the Wingman CTO Crossing Catheter consists of a support catheter, with a user controlled radiopaque guide tip (5-mm extendable needle tip) and activating handle |
| Reflow Medical, Inc | Wingman35 CTO Crossing Catheter | 4.6 | 65, 90, 135 | 0.066 | A beveled (needle) tip recanalization device intended to provide additional support to a steerable guidewire when accessing discrete regions of the peripheral vasculature; the Wingman CTO Crossing Catheter consists of a support catheter, with a user controlled radiopaque guide tip (5-mm extendable needle tip) and activating handle |
| Teleflex | GuideLiner Navigation Catheter | – | 163 | 5.5 F (model 5570), 6 F (model 5571), 7 F (model 5572), 8 F (model 5573) | Helps to protect the arterial wall during deep-seating of the GuideLiner; its construction combines the advantages of atraumatic vessel navigation with support for GuideLiner advancement in tortuous anatomy |
| Teleflex | GuideLiner V3 Catheter | 5, 5.5, 6, 7, 8 | 150 | ≥ 0.056 (5 F), ≥ 0.066, ≥ 0.070 (6 F), ≥ 0.078 (7 F), ≥ 0.088 (8 F) | Features a half-pipe design for seamless collar transition; this rapid-exchange, coaxial mother-and-child guide extension is delivered through standard guide catheters, resulting in an ID approximately one F size smaller than the guide catheter; used to access discrete regions of the coronary and/or peripheral vasculature and to facilitate placement of interventional devices |
| Teleflex | SuperCross Microcatheter OTW - 0.014 Angled Tips: 45°, 90°, 120°, and 90° Extended Tip | Distal: 2.4; proximal: 3.2 | 130, 150 | 0.014 | Low-profile, hydrophilic-coated, OTW microcatheter is available in multiple tip angle options (45°, 90°, 120°, and 90° extended tip) with a dual coil design for good torque response and delivery into branched anatomy |
| Teleflex | SuperCross Microcatheter OTW - 0.014 Straight and Flexible Tip | Distal: 1.8; proximal: 2.5 | 130, 150 | 0.014 | Low-profile, hydrophilic-coated, braided OTW microcatheter with straight tip and flexible tip options provides support when navigating tortuous anatomy and bifurcated vessels |
| Terumo Europe | NaviCross Support Catheter | 4 (NaviCross 0.035); 2.6 (NaviCross 0.018) | 65, 90, 135, 150 | 0.056 (NaviCross 0.035); 0.034 (NaviCross 0.018) | Double-braided stainless steel catheter with tapered tip, three radiopaque markers, and hydrophilic M coat |
| Terumo Europe | Occlusafe | 2.7, 2.8 | 110, 130, 150 | 0.014 | Balloon catheter allowing blood flow redistribution to increase treatment uptake in liver tumor lesions |
| ThermopeutiX, Inc. | TAPAS Targeted Drug Delivery System | Minimum vessel size: 1.8 mm | 175 | 7 F (sheath) | Targeted delivery of physician-specified drugs; adjustable treatment zone up to 300 mm; able to aspirate out drug after use; multiple use in a single patient |
| Tokai Medical Products, Inc | Carnelian Support 14 | 2.6/1.8 (0.014-inch wire) | 90, 135, 150 | 0.035 | Tungsten braided, low profile, flexible, and hydrophilic coated; designed to facilitate crossing of challenging lesions and tracking through tortuous anatomy in lower limbs |
| Tokai Medical Products, Inc | Carnelian Support 18 | 2.6/1.8 (0.018-inch wire) | 70, 90, 135, 150 | 0.035 | Tungsten braided, low profile, flexible, and hydrophilic coated; designed to facilitate crossing of challenging lesions and tracking through tortuous anatomy in lower limbs; 0.018-inch wire compatible |
| Tokai Medical Products, Inc | Carnelian Support BTA | 2.6/1.6 (0.014-inch wire) | 150 | 0.035 | Tungsten braided, low profile, flexible, and hydrophilic coated; designed to facilitate crossing of challenging lesions and tracking through tortuous anatomy in lower limbs, especially below the ankle |
| Tokai Medical Products, Inc | Carnelian Support DP | 2.6/1.8 (0.014-inch wire) | 60 | 0.035 | Tungsten braided, low profile, flexible, and hydrophilic coated; designed to facilitate crossing of challenging lesions and tracking through tortuous anatomy in lower limbs by distal puncture |
| Tokai Medical Products, Inc | Carnelian Support HD | 2.6/1.8 (0.014-inch wire) | 90, 135, 150 | 0.035 | Tungsten braided, low profile, flexible, and hydrophilic coated; designed to facilitate crossing of challenging lesions and tracking through tortuous anatomy in lower limbs |
| VentureMed Group, Inc. | Flex Vessel Prep System | 6 | 120 | 0.092 | Flex creates precise, controlled-depth microincisions along the entire length of the lesion/stenoses, releasing the circumferential tension to improve compliance and luminal gain at lower balloon pressures for less vessel trauma and complications; intended for use with PTA catheters to facilitate dilation of stenoses in the femoral and popliteal arteries and treatment of obstructive lesions of native or synthetic AV dialysis fistulas; also indicated for ISR |
| VentureMed Group, Inc. | Flex Vessel Prep System | 6 | 40 | 0.092 | Flex creates precise, controlled-depth microincisions along the entire length of the lesion/stenoses, releasing the circumferential tension to improve compliance and luminal gain at lower balloon pressures for less vessel trauma and complications; intended for use with PTA catheters to facilitate dilation of stenoses in the femoral and popliteal arteries and treatment of obstructive lesions of native or synthetic AV dialysis fistulas; also indicated for ISR |
| Reflow Medical, Inc | SpexLP 14 Shapeable Support Microcatheter | 2.2 | 90, 135, 150 | 0.052 | Single lumen, shapeable tip microcatheters designed to access the peripheral vasculature; allows for exchange of guidewires and other interventional devices and provides a conduit for delivery of saline solutions or diagnostic contrast; available in a variety of lengths and diameters; braided support matrix and hydrophilic coating (distal segment); Spex LP has 3 radiopaque markers spaced equally along the distal shaft at 50-mm increments, to aid in estimating geometry within the vascular system |
| Reflow Medical, Inc | SpexLP 18 Shapeable Support Microcatheter | 2.5 | 90, 135, 150 | 0.021 | Single lumen, shapeable tip microcatheters designed to access the peripheral vasculature; allows for exchange of guidewires and other interventional devices and provides a conduit for delivery of saline solutions or diagnostic contrast; available in a variety of lengths and diameters; braided support matrix and hydrophilic coating (distal segment); Spex LP has 3 radiopaque markers spaced equally along the distal shaft at 50-mm increments, to aid in estimating geometry within the vascular system |
| Reflow Medical, Inc | SpexLP 35 Shapeable Support Microcatheter | 3.8 | 90, 135, 150 | 0.052 | Single lumen, shapeable tip microcatheters designed to access the peripheral vasculature; allows for exchange of guidewires and other interventional devices and provides a conduit for delivery of saline solutions or diagnostic contrast; available in a variety of lengths and diameters; braided support matrix and hydrophilic coating (distal segment); Spex LP has 3 radiopaque markers spaced equally along the distal shaft at 50-mm increments, to aid in estimating geometry within the vascular system |
| Reflow Medical, Inc | Wingman 14C CTO Crossing Catheter | 2.7 | 90, 135, 150 | 0.039 | A beveled (needle) tip recanalization device intended to provide additional support to a steerable guidewire when accessing discrete regions of the peripheral vasculature; the Wingman CTO Crossing Catheter consists of a support catheter, with a user controlled radiopaque guide tip (5-mm extendable needle tip) and activating handle |
| Cordis | EliteCross Support Catheter - Angled Extra Support | 5 | 82, 132 | – | – |
Embolization / Cerebral Coils
View Chart| Company Name | Product Name | Materials Used | Coil Type | Method of Detachment | CE Mark Indications | Comments |
|---|---|---|---|---|---|---|
| Balt | Optima Coiling System | Bare platinum | Complex and helical | Thermal | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as AVMs and AVFs; also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Seven configurations with standard, soft, and super soft profiles in both complex and helical shapes |
| Blockade Medical, a Balt Company | Barricade Coil System | Bare platinum | Complex framing, helical filling, complex finishing, helical finishing | Electrolytic | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as AVMs and AVFs; also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Optimized coil design offering a smooth delivery with excellent conformability and performance |
| Cerenovus | Micrus Endovascular Microcoil System | Stretch-resistant bare-platinum and cerecyte-PGA coils | Micrusphere, Presidio, and Cashmere 3D framing coils; Delta Wind filling and finishing coils; Ultipaq and Helipaq 2D filling coils | Mechanical detachment using resistive heating | Intracranial aneurysms, AVMs, and AVFs; embolization of peripheral vasculature | Complete range of coil designs and shapes needed to effectively treat a broad range of aneurysm types |
| Cerenovus | Orbit Galaxy Detachable Coil System | Bare platinum, polypropylene stretch-resistant suture | Complex framing, filling, and finishing coils | Hydraulic detachment | Frame, fill, and Xtrasoft are indicated for embolizing intracranial aneurysms; frame and fill coils are indicated for embolizing intracranial aneurysms, AVMs, AVFs, and embolization of peripheral vasculature | Coil has a unique ability to seek out and fill the open spaces in an aneurysm, enabling greater packing density |
| Cerenovus | Orbit Galaxy G2 Detachable Coil System | Bare platinum, polypropylene stretch-resistant suture | Complex framing, filling, and finishing coils | Mechanical detachment using resistive heating | Frame, fill, and Xtrasoft are indicated for embolizing intracranial aneurysms; frame and fill coils are indicated for embolizing intracranial aneurysms, AVMs, AVFs, and embolization of peripheral vasculature | Coil has a unique ability to seek out and fill the open spaces in an aneurysm, enabling greater packing density |
| Cerenovus | Spectra Family of Coils | Stretch-resistant bare-platinum coils | Micrusframe C and Micrusframe S 3D framing coils; Deltafill fill coils and Deltaxsft finishing coils; Galaxy G3 fill and Galaxy G3 Xsft finishing coils | Mechanical detachment using resistive heating | Micrusframe, Deltafill, Deltaxsft, and Galaxy G3 are indicated for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as AVMs and AVFs; it is also indicated for arterial and venous embolizations in peripheral vasculature; Galaxy G3 Xsft is indicated for endovascular embolization of intracranial aneurysms | Complete range of coil designs and shapes needed to effectively treat a broad range of aneurysms from start to finish |
| Cerenovus | Trufill DCS Orbit Detachable Coil System | Bare platinum | Complex fill, complex standard, mini complex fill, helical fill, tight distal loop technology | Hydraulic detachment | Intracranial aneurysms, AVMs, and AVFs; embolization of peripheral vasculature | Excellent conformability and concentric filling for greater packing density |
| Medtronic | Axium, Axium Prime, and Axium MicroFX Detachable Coils | Bare platinum, with PGLA or nylon microfilament for Axium MicroFX | Framing, filling, finishing; 3D (diameter: 25–2 mm; length: 20–2 cm); Helix (diameter: 20–1.5 mm; length: 50–1 cm) | Mechanical detachment | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities, such as AVMs and AVFs | Stretch-resistance, optimal balance of softness, stability, and volume for increased packing volume, instant detachment |
| Terumo Neuro | Compass Coils | Bare-platinum coils | MicroPlex coil system, complex shape, for framing and filling | V-Grip detachment controller, self-contained integrated power supply, rapid coil detachment: 0.75 seconds | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Platinum coils provide versatile framework, stability, and conformability |
| Terumo Neuro | Complex Coils | Bare-platinum coils | MicroPlex coil system, complex shape, for framing and filling | V-Grip detachment controller, self-contained integrated power supply, rapid coil detachment: 0.75 seconds | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Platinum coils provide versatile framework, stability, and conformability |
| Terumo Neuro | Cosmos Coils | Bare-platinum coils | MicroPlex coil system, complex shape, for framing and filling | V-Grip detachment controller, self-contained integrated power supply, rapid coil detachment: 0.75 seconds | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Platinum coils provide versatile framework, stability, and conformability |
| Terumo Neuro | Helical Coils | Bare-platinum coils | MicroPlex coil system, helical shape, for filling and finishing | V-Grip detachment controller, self-contained integrated power supply, rapid coil detachment: 0.75 seconds | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Platinum coils provide versatile framework, stability, and conformability |
| Terumo Neuro | HydroFill Coils | Hydrogel thread placed inside of platinum coil | HydroCoil Embolic System, helical shape, for filling | V-Grip detachment controller, self-contained integrated power supply, rapid coil detachment: 0.75 seconds | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Hydrogel core of HydroFill coil line expands diameter of coil by 20% for efficient filling |
| Terumo Neuro | HydroFrame Coils | Hydrogel thread placed inside of platinum coil | HydroCoil Embolic System, complex shape, for framing and filling | V-Grip detachment controller, self-contained integrated power supply, rapid coil detachment: 0.75 seconds | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Hydrogel technology provides a scaffold for endothelialization at the aneurysm neck |
| Terumo Neuro | HydroSoft 3D Coils | Hydrogel thread placed inside of platinum coil | HydroCoil embolic system, complex shape, for filling and finishing | V-Grip detachment controller, self-contained integrated power supply, rapid coil detachment: 0.75 seconds | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Hydrogel technology provides a scaffold for endothelialization at the aneurysm neck |
| Terumo Neuro | HydroSoft Helical Coils | Hydrogel thread placed inside of platinum coil | HydroCoil embolic system, helical shape, for filling and finishing | V-Grip detachment controller, self-contained integrated power supply, rapid coil detachment: 0.75 seconds | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Hydrogel technology provides a scaffold for endothelialization at the aneurysm neck |
| Terumo Neuro | HyperSoft 3D Coils | Bare-platinum coils | MicroPlex coil system, complex shape, for filling and finishing | V-Grip detachment controller, self-contained integrated power supply, rapid coil detachment: 0.75 seconds | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Platinum coils provide versatile framework, stability, and conformability |
| Terumo Neuro | HyperSoft Helical Coils | Bare-platinum coils | MicroPlex coil system, helical shape, for filling and finishing | V-Grip detachment controller, self-contained integrated power supply, rapid coil detachment: 0.75 seconds | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | Platinum coils provide versatile framework, stability, and conformability |
| Terumo Neuro | VFC Coils | Bare-platinum coils | MicroPlex coil system, complex shape, for filling | V-Grip detachment controller, self-contained integrated power supply, rapid coil detachment: 0.75 seconds | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature | This coils unique loop/wave shape and long length sizes seek out and fill available space efficiently |
| Penumbra, Inc. (Neuro) | PAC400 | Stretch-resistant bare platinum | Platinum | Instant, physician-controlled mechanical detachment | Indicated for the embolization of intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, arterial and venous embolizations in the peripheral vasculature | Recommended delivery catheter sizes (ID) (inch): 0.025–0.027 high-flow microcatheter (PX SLIM) |
| Penumbra, Inc. (Neuro) | Penumbra Coil 400 | Stretch-resistant bare platinum | Complex standard, complex soft, J-soft, curve extra soft, complex extra soft | Instant, physician-controlled mechanical detachment | Indicated for the endovascular embolization of intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature | Unique larger diameter (0.02 inch) coils with multilayer metal structure |
| Penumbra, Inc. (Neuro) | POD400 | Stretch-resistant bare platinum | Platinum | Instant, physician-controlled mechanical detachment | Indicated for the embolization of intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, arterial and venous embolizations in the peripheral vasculature | Coil length (cm): 20-60; recommended delivery catheter sizes (ID) (inch): 0.025–0.027 high-flow microcatheters (PX SLIM) |
| Penumbra, Inc. (Neuro) | Smart Coil | Stretch-resistant bare platinum | Plus, standard, soft, complex extra soft, wave extra soft | Instant, physician-controlled mechanical detachment | Indicated for the embolization of intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature | Cerebral coil with complex and wave shapes, engineered with varying levels of softness |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Proprietary porous shape memory polyurethane, nitinol, platinum alloy | Shape memory polymer over a coil | TrelliX Detachment Controller (electrolytic detachment mechanism) | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature | The device comprises shape memory polymer over a coil; the porous embolic scaffold of the shape memory polymer supports the rapid formation of small interconnected clots throughout its structure; the biocompatible and noninflammatory polymer promotes rapid conversion to organized thrombus, followed by collagen deposition without chronic active inflammation, which leads to a stable occlusion |
| Stryker | Target Detachable Coils | Bare platinum | 360 XL Standard, 360 XL Soft, 360 Standard, 360 Soft, 360 Ultra, 360 Nano, 3D Standard, Helical XL Soft, Helical Ultra, Helical Nano | Electrolytic, InZone detachment system | Intended to endovascularly obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indicated for endovascular embolization of intracranial aneurysms, other neurovascular abnormalities such as AVMs, AVFs, and arterial and venous embolizations in the peripheral vasculature | Smooth and stable, comprehensive coiling solution |
Embolization / Embolic Particles/Beads
View Chart| Company Name | Product Name | Composition | Type | Sizes (µm) | Color Coded | CE Mark Indications |
|---|---|---|---|---|---|---|
| Balton | Embocure | PVA-based particles | Calibrated sphere | 50–90; 90–125; 125–250; 250–500; 500–710; 710–900; 900–1,400 | Labels are color-coded by microsphere size | Indicated for embolization of hyper vascular tumors, including uterine fibroids and hepatic tumors |
| Balton | Embocure Plus | PVA-based particles | Calibrated microspheres lodable with doxorubicin and irinotecan | 50–90; 90–125; 125–250; 250–500; 500–710; 710–900; 900–1,400 | Labels are color-coded by microsphere size | Indicated for chemoembolization of tumors and pathological lesions in the liver |
| Boston Scientific Corporation | Contour Embolization Particles | PVA particles | Irregularly shaped flakes | 45–150; 150–250; 250–355; 355–500; 500–710; 710–1,000; 1,000–1,180 | Labels are color-coded by particle size | Embolization of peripheral hepatic vascular tumors, including leiomyoma uteri and peripheral AVMs |
| Invamed | Microsphere Drug Loadable Beads | NBCA particles | Irregularly shaped beads | 150–200 | One size; no coding | Embolization of hypervascular tumors, hepatic vascular tumors, including leiomyoma, uteri, and peripheral AVMs |
| Merit Medical Systems, Inc. | Bearing nsPVA Embolization Particles | PVA particles | Irregularly shaped particles | 45–150; 150–250; 250–355; 355–500; 500–710; 710–1,000; 1,000–1,180 | Labels are color-coded by particle size | Indicated for the embolization of AVMs and hypervascular tumors, including symptomatic uterine fibroids |
| Merit Medical Systems, Inc. | EmboGold Microspheres | Trisacryl with gelatin | Colored spherical embolic microspheres | 40–120; 100–300; 300–500; 500–700; 700–900; 900–1,200 | Labels are color-coded by microsphere size | Indicated for the embolization of AVMs, hypervascular tumors, including uterine fibroids, meningiomas, etc., and hemostatic embolization |
| Merit Medical Systems, Inc. | Embosphere Microspheres | Trisacryl with gelatin | Spherical embolic microspheres | 50–100; 40–120; 100–300; 300–500; 500–700; 700–900; 900–1,200 | Labels are color-coded by microsphere size | Indicated for the embolization of AVMs, prostate arteries for relief of symptoms related to benign prostatic hyperplasia, hypervascular tumors, including uterine fibroids, meningiomas, etc., and hemostatic embolization |
| Merit Medical Systems, Inc. | HepaSphere Microspheres | Sodium acrylate alcohol copolymer | Spherical drug-eluting microspheres; doxorubicin and irinotecan | 30–60 (120–240 reconstituted), 50–100 (200–400 reconstituted), 100–150 (400–600 reconstituted), 150–200 (600–800 reconstituted) | Labels are color-coded by microsphere size | Indicated for the embolization of blood vessels with or without delivery of doxorubicin or irinotecan for therapeutic or preoperative purposes in the following procedures: embolization of hepatocellular carcinoma and embolization of metastases to the liver |
| Terumo Europe | HydroPearl | PEG | Bland microspheres | 75; 200; 400; 600; 800; 1,100 | Yes | Benign prostatic hyperplasia, uterine fibroids, hypervascularized tumors, peripheral arteriovenous malformations, hepatocellular carcinoma, bleeding, and preoperative reduction of bleeding |
| Terumo Europe | LifePearl | PEG | Drug-eluting microspheres, loadable with doxorubicin, idarubicin, epirubicin and irinotecan | 100, 200, 400 | Yes | Embolization of blood vessels supplying hypervascular tumors or metastases in the liver |
| Terumo Europe | QuiremSpheres | Ho-166/PLLA | Radioembolization/SIRT procedures | 30 | – | For treatment of advanced unresectable liver tumors |
| Varian Medical Systems | Embozene Microspheres | HydroGel core with Polyzene-F coating | Calibrated sphere | 40; 75; 100; 250; 400; 500; 700; 900; 1,100; 1,300 | Microspheres are color-coded by size for definitive visualization and increased procedural safety, with corresponding color-coded labels and boxes | Embolization for the following conditions: hyper vascular tumors, AVMs, uterine fibroids, tumors of the head, neck, torso and skeletal system, neurovascular and peripheral, hepatocellular carcinoma, bleeding and trauma, and preoperative reduction of bleeding (except for the central nervous system) |
| Varian Medical Systems | Embozene Tandem Drug-Elutable Microspheres | HydroGel core with Polyzene-F coating | Calibrated sphere capable of loading doxorubicin, irinotecan, and idarubicin | 40, 75, 100 | Syringe labels are color-coded by particle size | Embolization of hyper vascular tumors, including hepatocellular carcinoma |
| NextBioMedical Co., Ltd. | UIGB 100 | 300 mg/vial | Gelatin embolic microsphere | 100–300 | Yellow | Liver cancer, uterine fibroid, prostate hyperplasia, bleeding |
| NextBioMedical Co., Ltd. | UIGB 300 | 300 mg/vial | Gelatin embolic microsphere | 300–500 | Blue | Liver cancer, uterine fibroid, prostate hyperplasia, bleeding |
| NextBioMedical Co., Ltd. | UIGB 500 | 300 mg/vial | Gelatin embolic microsphere | 500–700 | Red | Liver cancer, uterine fibroid, prostate hyperplasia, bleeding |
| NextBioMedical Co., Ltd. | UIGB 700 | 300 mg/vial | Gelatin embolic Microsphere | 700–900 | Green | Liver cancer, uterine fibroid, prostate hyperplasia, bleeding |
| NextBioMedical Co., Ltd. | Nexsphere-H | 250 mg/vial | Gelatin embolic Microsphere | 100–300 | Orange | Liver cancer, uterine fibroid, prostate hyperplasia, bleeding |
| NextBioMedical Co., Ltd. | Nexsphere-F | 200 mg/vial | Gelatin embolic microsphere | 100–300 | Brown | Arthritis |
Embolization / Embolization Coils
View Chart| Company Name | Product Name | Type (Detachable, Pushable) | Material | Coil Diameter (mm) | Coil Length (cm) | Recommended Delivery Catheter Sizes (ID) (inch) | CE Mark Indications |
|---|---|---|---|---|---|---|---|
| Balt | Flow Coils (free spirals for injection) | Pushable | Platinum | 2.5 | 5, 10, 20 | 0.010 | Intended for the embolization of vascular malformations of the vasculature |
| Balt | Optima Coil System | Detachable | Bare platinum | 1–24 | 1–65 | 0.0165 | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature |
| Balt | SPI .018 | Pushable | Platinum | 2 | 15 | 0.021 | Intravascular treatment of arteriovascular malformations, fistula arteriovenous malformations, varicoceles, aneurysms |
| Balt | SPI .037 | Pushable | Platinum | 5 to 16 | 3 to 45 | 0.039 | Intravascular treatment of arteriovascular malformations, fistula arteriovenous malformations, varicoceles, aneurysms |
| Blockade Medical, a Balt Company | Barricade Coil System | Detachable | Bare platinum | 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 | 1–50 | 0.017–0.021 | Intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as AVMs and AVFs; it is also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolizations in the peripheral vasculature |
| Boston Scientific Corporation | 2D Helical-35 Fibered Platinum Coils | Pushable | Platinum | 3, 4, 5, 6, 7, 9 | 2, 3, 4, 5, 6 | 0.035 (0.89 mm) | For arterial and venous embolization in the peripheral vasculature |
| Boston Scientific Corporation | Complex Helical-18 Fibered Platinum Coils | Pushable | Platinum | 4, 6, 7, 8, 10, 11 | 2, 3, 4, 5, 6, 7 | 0.021 (0.53 mm) | 0.018-inch (0.46-mm) fibered platinum coils are intended for arterial and venous embolizations in the peripheral vasculature |
| Boston Scientific Corporation | Figure 8-18 Fibered Platinum Coils | Pushable | Platinum | 2 | 5 | 0.021 (0.53 mm) | 0.018-inch (0.46-mm) fibered platinum coils are intended for arterial and venous embolizations in the peripheral vasculature |
| Boston Scientific Corporation | Interlock-18 Fibered IDC Occlusion System | Detachable | Platinum tungsten alloy | 2, 3, 4, 5, 6, 8, 10, 12, 14, 18, 20, 22 | 2.3, 4, 4.1, 5.8, 6, 8, 10, 12, 15, 20, 30, 50, 60 | 0.021 (0.53 mm) | Indicated to obstruct or reduce blood flow in the peripheral vasculature; the device is not intended for neurovascular use |
| Boston Scientific Corporation | Interlock-35 Fibered IDC Occlusion System | Detachable | Platinum tungsten alloy | 3, 4, 6, 8, 10, 12, 15, 18, 20 | 4, 4.5, 6, 9, 10, 14, 20, 25, 30, 40 | 5-F Imager II diagnostic catheter (0.035 [0.89 mm] or 0.097) | Indicated to obstruct or reduce blood flow in the peripheral vasculature; the device is not intended for neurovascular use |
| Boston Scientific Corporation | Multi-Loop-18 Fibered Platinum Coils | Pushable | Platinum | 4 | 3 | 0.021 (0.53 mm) | 0.018-inch (0.46-mm) fibered platinum coils are intended for arterial and venous embolizations in the peripheral vasculature |
| Boston Scientific Corporation | Straight-18 Fibered Platinum Coils | Pushable | Platinum | Straight | 2, 5 | 0.021 (0.53 mm) | 0.018-inch (0.46-mm) fibered platinum coils are intended for arterial and venous embolizations in the peripheral vasculature |
| Boston Scientific Corporation | VortX Diamond-18 Fibered Platinum Coils | Pushable | Platinum | 3, 4, 5, 6 | 2.3, 4.1, 5.8, 8 | 0.021 (0.53 mm) | 0.018-inch (0.46-mm) fibered platinum coils are intended for arterial and venous embolizations in the peripheral vasculature |
| Boston Scientific Corporation | VortX-18 Fibered Platinum Coils | Pushable | Platinum | 3, 4, 5, 6 | 2.2, 4.2, 6, 8.5 | 0.021 (0.53 mm) | 0.018-inch (0.46-mm) fibered platinum coils are intended for arterial and venous embolizations in the peripheral vasculature |
| Boston Scientific Corporation | VortX-35 Fibered Platinum Coils | Pushable | Platinum | 4, 5, 6, 7 | 3, 3.5, 5.3, 6.7 | 0.035 (0.89 mm) | For arterial and venous embolization in the peripheral vasculature |
| Cerenovus | Trufill Pushable Coils | Pushable | Platinum with nylon fibers | 3, 4, 5, 6, 7, 10 | 2–10 | 0.021 | To reduce or block the rate of blood flow in vessels of the peripheral and neuro vasculature; intended for use in the interventional radiologic management of AVMs, AVFs, and other vascular lesions of the brain, spinal cord, and spine |
| Cook Medical | MReye Embolization Coil | Pushable | Inconel with nylon fiber | 3, 4, 5, 6, 7, 8, 10, 12, 15, 20, 30, 45 | 2, 3, 4, 5, 8, 10, 15, 16, 20 | 0.035, 0.038 | Arterial and venous embolization in the peripheral vasculature |
| Cook Medical | Nester Embolization Coil | Pushable | Platinum with nylon fiber | 3, 4, 5, 6, 8, 10, 12, 14, 16, 18, 20 | 7, 14, 20 | 0.035 | Arterial and venous embolization |
| Cook Medical | Nester Embolization Microcoil | Pushable | Platinum with nylon fiber | 2, 3, 4, 5, 6, 8, 10 | 3, 5, 7, 14 | 0.018 | Arterial and venous embolization |
| Cook Medical | Retracta Detachable Embolization Coil | Detachable | Platinum with nylon fiber | 4, 6, 8, 10, 12, 14, 16, 18, 20 | 7, 14 | 0.035 | Arterial and venous embolization in the peripheral vasculature |
| Cook Medical | Tornado Embolization Coil | Pushable | Platinum with nylon fiber | 3–4, 3–5, 3–6, 3–7, 3–10, 4–8, 4–10, 5–8, 5–10 | 2.6–12.5 | 0.035 | Embolization of selective vessel supply to AVMs, trauma, bleeding, and other vascular lesions |
| Cook Medical | Tornado Embolization Microcoil | Pushable | Platinum with nylon fiber | 2–3, 2–4, 2–5, 2–6, 3–4, 3–7, 4–8, 4–10, 5–8, 5–10 | 2–14.2 | 0.018 | Embolization of selective vessel supply to AVMs, trauma, bleeding, and other vascular lesions |
| Medtronic | Concerto Nylon Helical | Detachable | Platinum | 5, 6, 7, 8, 9, 10 | 15, 20, 30 | 0.021 | Indicated for GI bleedings, tumor, portal vein embolization, varicocele, and SIRT/TACE; complements Onyx liquid embolization for indications where coils are either the better clinical solution, the more cost-effective solution, or the gold standard; with a unique instant detachment system, they are easy to use; their softness allows for dense packing and rapid occlusion |
| Medtronic | Concerto Nylon Helical | Detachable | Platinum | 2, 3, 4 | 4, 6, 8 | 0.0165 | Indicated for GI bleedings, tumor, portal vein embolization, varicocele, and SIRT/TACE; complements Onyx liquid embolization for indications where coils are either the better clinical solution, the more cost-effective solution, or the gold standard; with a unique instant detachment system, they are easy to use; their softness allows for dense packing and rapid occlusion |
| Medtronic | Concerto PGLA Helical | Detachable | Platinum | 12, 14, 16, 18, 20 | 30, 40, 50 | 0.021 | Indicated for GI bleedings, tumor, portal vein embolization, varicocele, and SIRT/TACE; complements Onyx liquid embolization for indications where coils are either the better clinical solution, the more cost-effective solution, or the gold standard; with a unique instant detachment system, they are easy to use; their softness allows for dense packing and rapid occlusion |
| Penumbra, Inc. (Peripheral Vascular) | Packing Coil | Detachable | Platinum | Shapeless | 5, 15, 30, 45, 60 | 0.025–0.027 high-flow microcatheters (Lantern) | Indicated for arterial and venous embolizations in the peripheral vasculature |
| Penumbra, Inc. (Peripheral Vascular) | POD | Detachable with dedicated anchor segment for high flow vessel sacrifice | Platinum | 3–14 mm | 20–60 | 0.025–0.027 high-flow microcatheters (Lantern) | Indicated for arterial and venous embolizations in the peripheral vasculature |
| Penumbra, Inc. (Peripheral Vascular) | Ruby Coil | Detachable | Platinum | 2–40 mm (3D complex shape, multiple softness levels) | 1–60 | 0.025–0.027 high-flow microcatheters (Lantern) | Indicated for arterial and venous vessel embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 9 | 15, 20 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 4 | 6, 8, 10, 12 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 5 | 6, 8, 10, 15 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 10 | 15, 20 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 12 | 20 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 11 | 20 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 14 | 20 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 8 | 15, 20 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 16 | 20 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 3 | 2, 4, 6, 8, 10 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 7 | 12, 15, 20 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Shape Memory Medical Inc. | TrelliX Embolic Coil | Detachable | Stretch-resistant platinum-tungsten alloy coil augmented with a self-expanding porous Shape Memory Polymer | 6 | 8, 10, 15 | 0.021 | Intended to obstruct or occlude blood flow in vascular abnormalities of the neurovascular and peripheral vessels; indications include intracranial aneurysms, other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae, and arterial and venous embolizations in the peripheral vasculature |
| Terumo Europe | Azur CX 18 | Detachable | Platinum plus hydrogel | 4 | 13 | 0.021 | Vascular embolization |
| Terumo Europe | Azur Peripheral HydroCoil 18 | Detachable | Platinum coil with expandable hydrogel polymer | 3–20 | 5–30 | 0.021 | – |
| Terumo Europe | Azur Peripheral HydroCoil 18 | Pushable | Platinum coil with expandable hydrogel polymer | 2–10 | 2–14 | 0.021–0.022 | – |
| Terumo Europe | Azur Peripheral HydroCoil 35 | Pushable | Platinum coil with expandable hydrogel polymer | 4–15 | 4–14 | 0.041–0.047 | – |
| Terumo Europe | Azur Peripheral HydroCoil 35 | Detachable | Platinum coil with expandable hydrogel polymer | 4–20 | 5–30 | 0.038 | – |
| Terumo Europe | Azur-Framing Coil 18 | Detachable | Platinum coil | 8–20 | 20–50 | 0.021 | – |
| Wallaby Medical, Inc. | Avenir Embolic Coil System | Detachable | Platinum | (1-25) 1, 1.5, 2, 2.5, 3, 3.5, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 18, 20, 22, 25 | (1-60) 1, 2, 3, 4, 5, 6, 8, 10, 11, 13, 15, 16, 17, 19, 20, 23, 24, 27, 30, 34, 37, 40, 43, 47, 50, 60 | 0.017 | Intended for endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistula; also intended for arterial and venous embolization in the peripheral vasculature |
Embolization / Liquid Embolics
View Chart| Company Name | Product Name | Viscosity | Vial Size (mL) | CE Mark Indications | Comments |
|---|---|---|---|---|---|
| Balt | Squid Peri | 12 | 1.5 | Embolization of lesions in the peripheral vasculature, including arteriovenous malformations and hypervascular tumors | EVOH, DMSO, micronized tantalum |
| Balt | Squid Peri | 12LD (low density) | 1.5 | Embolization of lesions in the peripheral vasculature, including arteriovenous malformations and hypervascular tumors | EVOH, DMSO, micronized tantalum |
| Balt | Squid Peri | 18 | 1.5 | Embolization of lesions in the peripheral vasculature, including arteriovenous malformations and hypervascular tumors | EVOH, DMSO, micronized tantalum |
| Balt | Squid Peri | 18LD (low density) | 1.5 | Embolization of lesions in the peripheral vasculature, including arteriovenous malformations and hypervascular tumors | EVOH, DMSO, micronized tantalum |
| Balt | Squid Peri | 34 | 1.5 | Embolization of lesions in the peripheral vasculature, including arteriovenous malformations and hypervascular tumors | EVOH, DMSO, micronized tantalum |
| Balt | Squid Peri | 34LD (low density) | 1.5 | Embolization of lesions in the peripheral vasculature, including arteriovenous malformations and hypervascular tumors | EVOH, DMSO, micronized tantalum |
| Medtronic | Onyx 34L Liquid Embolic System | 34 | 1.5, 6 | Embolization of lesions in the peripheral vasculature, including endoleaks, arteriovenous malformations, portal veins, bleeding, and tumors | Ethylene vinyl alcohol copolymer designed to provide complete filling and distal penetration of vascular lesions; has a reduced amount of tantalum to reduce the amount of artifacts on CT follow-up compared to the current formulation |
| Medtronic | Onyx Liquid Embolic System | 18, 34 | 1.5 | Embolization of lesions in the peripheral and neurovasculature, including arteriovenous malformations, and hypervascular tumors | Ethylene vinyl alcohol copolymer designed to provide complete filling and distal penetration of vascular lesions |
| Terumo Neuro | Phil Liquid Embolic System | 12, 16, 36, 72 (cSt) | 1 | The Phil device is intended for use in the embolization of lesions in the peripheral and neurovasculature, including arteriovenous malformations and hypervascular tumors | Nonadhesive liquid embolic made of copolymer covalently bonded with iodine and dissolved in DMSO |
Embolization / Vascular Plugs
View Chart| Company Name | Product Name | Material | Sizes (mm) | Delivery Cable Length (cm) | Recommended Catheter Sizes (ID) (inch) | CE Mark Indications |
|---|---|---|---|---|---|---|
| Abbott | Amplatzer Vascular Plug (AVP) | Nitinol | 4–8 | 135 | Guide catheter: 0.056 | Arterial and venous embolization in the peripheral vasculature |
| Abbott | Amplatzer Vascular Plug (AVP) | Nitinol | 10–12 | 135 | Guide catheter: 0.067 | Arterial and venous embolization in the peripheral vasculature |
| Abbott | Amplatzer Vascular Plug (AVP) | Nitinol | 14–16 | 135 | Guide catheter: 0.088 | Arterial and venous embolization in the peripheral vasculature |
| Abbott | Amplatzer Vascular Plug 4 (AVP 4) | Nitinol | 4–8 | 155 | Diagnostic catheter: 0.038 guidewire compatible | Arterial and venous embolization in the peripheral vasculature |
| Abbott | Amplatzer Vascular Plug II (AVP II) | Nitinol | 10–12 | 135 | Guide catheter: 0.070 | Arterial and venous embolization in the peripheral vasculature |
| Abbott | Amplatzer Vascular Plug II (AVP II) | Nitinol | 14–16 | 135 | Guide catheter: 0.086 | Arterial and venous embolization in the peripheral vasculature |
| Abbott | Amplatzer Vascular Plug II (AVP II) | Nitinol | 18–22 | 135 | Guide catheter: 0.098 | Arterial and venous embolization in the peripheral vasculature |
| Abbott | Amplatzer Vascular Plug II (AVP II) | Nitinol | 3–8 | 135 | Guide catheter: 0.056 | Arterial and venous embolization in the peripheral vasculature |
| ArtVentive Medical Group, Inc. | Endoluminal Occlusion System (EOS) | Nitinol coil with PTFE plug | 5, 8, 11 | 105 | 0.067, 0.082 | Immediate arterial and venous embolization in the peripheral vasculature |
| Invamed | Embolization Plug | Hard gel | 1 mL | 135 | Microcatheter: 0.027 | To obstruct or reduce the rate of blood flow in the vasculature |
| Medtronic | MVP-3 Micro Vascular Plug System | Nitinol and PTFE | 1.5–3 | 180 | Microcatheter: 0.021 | To obstruct or reduce the rate of blood flow in the peripheral vasculature |
| Medtronic | MVP-5 Micro Vascular Plug System | Nitinol and PTFE | 3–5 | 180 | Microcatheter: 0.027 | To obstruct or reduce the rate of blood flow in the peripheral vasculature |
| Medtronic | MVP-7 Micro Vascular Plug System | Nitinol and PTFE | 5–7 | 165 | 4 F | To obstruct or reduce the rate of blood flow in the peripheral vasculature |
| Medtronic | MVP-9 Micro Vascular Plug System | Nitinol and PTFE | 7–9 | 165 | 5 F | To obstruct or reduce the rate of blood flow in the peripheral vasculature |
| Shape Memory Medical Inc. | IMP-05, Impede Embolization Plug | Proprietary porous shape memory polyurethane, nitinol, platinum alloy | Vessel diameter, 2–5 | – | 0.038–0.057 | To obstruct or reduce the rate of blood flow in the peripheral vasculature |
| Shape Memory Medical Inc. | IMP-07, Impede Embolization Plug | Proprietary porous shape memory polyurethane, nitinol, platinum alloy | Vessel diameter, 4–7 | – | 0.055–0.071 | To obstruct or reduce the rate of blood flow in the peripheral vasculature |
| Shape Memory Medical Inc. | IMP-10, Impede Embolization Plug | Proprietary porous shape memory polyurethane, nitinol, platinum alloy | Vessel diameter, 6–10 | – | 0.070–0.090 | To obstruct or reduce the rate of blood flow in the peripheral vasculature |
| Shape Memory Medical Inc. | IMP-FX-06, Impede FX Embolization Plug | Proprietary porous shape memory polyurethane, platinum alloy | 6 (expanded diameter) X 10 (length) | – | 0.038–0.057 | To obstruct or reduce the rate of blood flow in the peripheral vasculature |
| Shape Memory Medical Inc. | IMP-FX-08, Impede FX Embolization Plug | Proprietary porous shape memory polyurethane, platinum alloy | 8 (expanded diameter) X 10 (length) | – | 0.055–0.071 | To obstruct or reduce the rate of blood flow in the peripheral vasculature |
| Shape Memory Medical Inc. | IMP-FX-12, Impede FX Embolization Plug | Proprietary porous shape memory polyurethane, platinum alloy | 12 (expanded diameter) X 15 (length) | – | 0.070–0.090 | To obstruct or reduce the rate of blood flow in the peripheral vasculature |
| Shape Memory Medical Inc. | IMP-FX-12x5, Impede FX Rapid Fill Embolization Plug | Proprietary porous shape memory polyurethane, platinum alloy | 12 (expanded diameter) X 15 (length) | – | 0.070–0.090 | To obstruct or reduce the rate of blood flow in the peripheral vasculature |
Sheaths / Reinforced Sheaths
View Chart| Company Name | Product Name | Size (F) | Length (cm) | Guidewire Compatibility (inch) | Curved or Straight | Radiopaque Tip | Hydrophilic Coating |
|---|---|---|---|---|---|---|---|
| Asahi Intecc Co Ltd. | Asahi Fubuki (Dilator Kit) | 4, 5 | 80, 90, 100, 110 | 0.035 | Angled, straight | Yes | Yes |
| Asahi Intecc Co Ltd. | Asahi Fubuki (Dilator Kit) | 6 | 80, 90, 100, 110 | 0.035 | Straight | Yes | Yes |
| Asahi Intecc Co Ltd. | Sheathless PV | 6 | 55, 90, 120 | 0.035 | Straight, RDC, angled 45° | Yes | Yes |
| Balton | Braided Introducer (Coil Type) | 5–9 | 45–100 | 0.035 | Straight | Yes | Yes |
| BD Interventional | Halo One Thin-Walled Guiding Sheath | 4, 5, 6 | 10, 25, 45, 70, 90 | 0.018, 0.035 | Straight | Yes | Yes |
| Teleflex | Fortress | 4, 5, 6, 7, 8 | 45, 65, 90, 100 | 0.035 | Curved, straight | Radiopaque markerband | 5–8 hydrophobic |
| Cook Medical | Flexor: Ansel | 4–9 | 45, 55, 90, 110 | 0.018, 0.035, 0.038 | Curved, straight | Yes | Yes |
| Cook Medical | Flexor: Balkin | 5.5–8, 10, 12 | 40 | 0.038 | Curved | Yes | With or without |
| Cook Medical | Flexor: High-Flex Ansel | 4–8, 10, 12 | 45, 55, 70, 110 | 0.035 | Curved, straight | Yes | Yes |
| Cook Medical | Flexor: Raabe | 4–9 | 55, 70, 90 | 0.035, 0.038 | Straight | Yes | No |
| Cook Medical | Flexor: Shuttle/Shuttle Select | 4–8 | 80, 90, 110 | 0.018, 0.035, 0.038 | Straight | Yes | Yes |
| Cook Medical | Flexor: Standard | 5–8, 10, 12 | 13, 30, 40, 45, 80, 90 | 0.035, 0.038 | Straight | Yes | No |
| Endologix | Destino Twist Deflectable Steerable Guiding Sheath With 7 mm Curve Bend | 6.5 | 55 | 0.038 | Straight/curved | Yes | No |
| optimed Medizinische Instrumente GmbH | Epsylar | 5, 6, 7, 8 | 45, 65, 90, 120 | 0.035 | Freely configurable | Yes | No |
| Oscor Inc. | Adelante Breezeway Delivery Sheath With Hemostatic Valve | 6, 7, 8, 9, 10, 11, 12, 14 | 61, 79, 110 | 0.035, 0.038 | Straight/curved | Yes | – |
| Oscor Inc. | Adelante Magnum Introducer With Hemostatic SureSeal Valve Technology and Sideport for Delivery of Large Medical Devices | 16, 18 | 20, 30, 35 | 0.038 | Straight | Yes | Yes |
| Oscor Inc. | Destino Bi-Directional Steerable Introducer With Hemostatic Valve: Small, Medium, and Large Curves | 8.5, 10, 12 | 61, 67, 71 | 0.038 | Straight/curved | Yes | – |
| Oscor Inc. | Destino Reach Bi-Directional Steerable Introducer With Hemostatic Valve: Small, Medium, and Large Curves | 8.5, 10, 12 | 67, 71, 73, 75, 77 | 0.038 | Straight, curved | Yes | – |
| Oscor Inc. | Destino Twist Uni-Directional Steerable Introducer Sheath With Hemostatic Valve | 6.5, 7, 8.5, 12, 13.8 | 45, 55, 65, 71, 90 | 0.038 | Straight, TD curve | Radiopaque markerband | – |
| Stryker | AXS Infinity LS | 8 | 70, 80, 90 | 0.035, 0.038 | Straight | Yes | Yes |
| Stryker | AXS Infinity LS Plus | 8 | 70, 80, 90 | 0.035, 0.038 | Straight | Yes | Yes |
| Teleflex | Super Arrow-Flex Introducer Sets (Adult) | 5–11 | 11–100 | 0.035 | Straight | Yes | Yes |
| Teleflex | Super Arrow-Flex Sheath Introducer Sets (Pediatric) | 5–6 | 7.5 | 0.021 | Straight | Yes | Yes |
| Terumo Europe | Destination | 5–8 | 45, 65, 90 | 0.038 | Straight, hockey stick, LIMA, multipurpose, RDC, straight | Yes | Yes |
Sheaths / Special Access Sheaths
View Chart| Company Name | Product Name | Size (F) | Length (cm) | Guidewire Compatibility (inch) | Curved or Straight | Radiopaque Tip | Type of Special Access |
|---|---|---|---|---|---|---|---|
| Abbott | Fast-Cath | 4–14 | 5, 8.5, 12, 23, 30, 40, 45, 70, 75, 85, 90, 98, 110 | 0.021, 0.025, 0.032, 0.038 | Straight, 30, 40, 48, 60, 5-, 7-cm J, GSPC | No | Small-vessel catheterizations, brachial artery introduction; introduction of thermal dilution and temporary pacing catheters; atherectomy, laser, valvuloplasty, and other large-diameter catheters; introduction and general management of electrophysiology catheters; biopsy procedures; other procedures in which longer sheath and curve aid physician technique |
| Abbott | Ultimum | 4–8, 12, 14, 16, 18, 20, 22 | 5, 8.5, 25, 30, 35 | 0.035, 0.038 | Straight | Yes, EV line | Small-vessel and large-bore diameter catheters |
| AngioDynamics | Mini Stick MAX Coaxial Microintroducer Kit | 4, 5 | 10, 15 | 0.018 X 40 cm (stainless steel/palladium), 0.018 X 45 cm (nitinol/tungsten, stainless steel) | Straight | Yes, guidewire | For percutaneous introduction of a guidewire into the vascular system |
| Argon Medical Devices, Inc. | OneStic Micro-Access Introducer | 4–8 | 5.75, 11 | 0.018 X 45 cm (nitinol or stainless steel) | Straight | No | A hybrid introducer sheath and micropuncture set to expedite standard sheath access |
| Argon Medical Devices, Inc. | V-Stick Vascular Access Set With Ultrasharp Needle, Standard and Stiff | 4, 5 (with 3-F dilator) | 10 | 0.018 X 40 cm (nitinol or stainless steel) | Straight | No | Used for placement of 0.035- or 0.038-inch diameter guidewires into the vascular system when a small 21-gauge needle stick is desired |
| B. Braun Melsungen AG | Intradyn Arterial Introducer Sheath and Kits | 5–8 | 16 | 0.035 X 40 cm | Straight | No | Designed for the introduction of catheters into the arterial vasculature using the Seldinger technique; full kits or separate sterile sheaths are available |
| B. Braun Melsungen AG | Intradyn Special Introducer Sheath and Kits | 6–9 | 20.5 | 0.035 X 70 cm | Straight | No | Designed for the introduction of catheters into the venous vasculature using the Seldinger technique; full kits or separate sterile sheaths are available |
| B. Braun Melsungen AG | Intradyn Tear-Away Introducer Sheaths and Kits | 6–11 | 16 | 0.035 X 40 cm | Straight | No | Designed for the introduction of catheters into the arterial vasculature using the Seldinger technique; full kits or separate sterile sheaths are available |
| BioCardia, Inc. | Morph AccessPro Steerable Introducer System | 6 | 45, 90 (working lengths) | Accepts 0.014–0.038 (guidewire not provided) | Deflectable | Yes | Allows medical instruments as large as 6 F to be introduced into the peripheral vasculature |
| Boston Scientific Corporation | Vessix Guide Sheath | 7 (2.5 mm) | 45 | 0.014 (0.36 mm), 0.018 (0.46 mm) | RDC, LIMA | No | Designed for Vessix Reduce Catheter: shapes and atraumatic tip designed to facilitate smooth renal artery access |
| Cook Medical | Cope Catheter Introduction System | 6.3 | 22 | 0.035 | Curved | No | Used for nonvascular micropuncture percutaneous access to facilitate placement of a 0.035-inch diameter working wire guide for interventional radiology procedures |
| Cook Medical | Extra Large Check-Flo Sheaths | 20, 22, 24 | 25 | 0.035 | Straight | No | Femoral access for fenestrated cases |
| Cook Medical | Gould Catheter Introduction Set | 5 | 27 | 0.038 | Straight | No | Used for micropuncture percutaneous access to facilitate placement of a 0.038-inch diameter working wire guide for interventional radiology procedures |
| Cook Medical | Kellett Drainage Access Catheter Needle | 5 | 15, 20 | 0.038 | Straight | No | Used for percutaneous access in drainage procedures |
| Cook Medical | Micropuncture Introducer Sets: Stiffened and Nonstiffened | 4–5 | 10 | 0.018 | Straight | No | Used for placement of 0.035- or 0.038-inch diameter guidewires into the vascular system when a small 21-gauge needle stick is desired |
| Cook Medical | Micropuncture Pedal Access Set | 2.9 | 7 | 0.018 | Straight | No | Pedal access |
| Cook Medical | Neff Percutaneous Access Set | 6, 7 | 18 | 0.038 | Straight | Yes | Used for nonvascular micropuncture percutaneous access to facilitate placement of a 0.038-inch diameter working wire guide for interventional radiology procedures |
| Cook Medical | Performer: Hausdorf-Lock | 10–12 | 75 | 0.038 | Curved | Yes | Transseptal access |
| Cook Medical | Performer: Micropuncture | 4, 5, 6 | 13 | 0.018 | Straight | No | A hybrid introducer sheath and micropuncture set to expedite standard sheath access |
| Cook Medical | Performer: Mullins | 6–14 | 63, 75, 85 | 0.038 | Curved | Yes | Transseptal access |
| Cook Medical | Ring Transjugular Intrahepatic Access Set | 9 or 10 Flexor sheath (16-gauge needle) | 38.5-cm sheath length (50.5-cm needle length) | 0.035 (Newton J and Amplatz wires) | Flexor sheath (curved 30°); Torcon catheter (MPB curve); 9-, 10-F Teflon catheter (straight) | On the Flexor sheath | Transjugular liver access; includes an assembled Colapinto needle and catheter, a 9- or 10-F Flexor Check-Flo introducer, an 11-F, 20-cm long dilator, a Torcon NB Advantage catheter (5-F, 0.035-inch diameter end hole, 80-cm long, with MPB curve), a Van Andel dilatation catheter (5-F, 0.035-inch diameter endhole, 80-cm long), a Newton wire guide (0.035-inch diameter, 190-cm long, with 15-mm J-configuration tip), and an Amplatz extra stiff support wire guide (0.035-inch diameter, 190-cm long) |
| Cook Medical | Rösch-Uchida Transjugular Liver Access Set | 10 Flexor sheath (14-gauge stiffening cannula with 10-F Teflon catheter) | 40-cm sheath length (62.5-cm trocar stylet length) | 0.038 | Flexor sheath (straight); stiffening cannula in Teflon catheter (curved) | On the Flexor sheath | Transjugular liver access; includes a 10-F Flexor Check-Flo Introducer, 0.038-inch diameter trocar stylet, 5-F catheter, 10-F Teflon catheter, 14-gauge stiffening cannula, and 12-F dilator |
| Cook Medical | Transjugular Liver Access and Biopsy Needle | 9 | 45 (catheter); 51 (needle length) | – | Curved needle 15 or 16 gauge | – | Transjugular liver access and biopsy needle available in 15 and 16 gauge sizes with precurved catheter and cannula are ideal for hepatic vein access |
| Cook Medical | Transjugular Liver Access and Biopsy Set | 7 sheath (18- or 19-gauge needle) | 50.5 sheath length (60-cm needle length) | – | Stiffening cannula (curved); Torcon catheter (MPB curve); 5-F Teflon catheter (straight) | – | Transjugular liver access; includes a Quick-Core biopsy needle (18 or 19 gauge, 60-cm long, with 20-mm throw length, and 20-mm specimen notch), a Check-Flo Performer Assembly (7 F, 50.5-cm long, with 14 extra thin wall gauge stiffening cannula), a straight catheter (5 F, 0.035-inch diameter, 62-cm long), and a Torcon NB Advantage catheter (5 F, 0.035-inch diameter end hole, 80-cm long, with MPB curve) |
| Cook Medical | Transjugular Renal Access and Biopsy Needle | 9 | 59 (catheter); 64 (needle length) | – | Curved needle, 15 gauge | – | Transjugular renal access and biopsy needle available in 15 gauge size with precurved catheter and cannula are ideal for renal vein access |
| Cook Medical | Transjugular Renal Access and Biopsy Set | 7 (sheath; 19-gauge needle) | 60.5 (sheath); 70 (needle length) | – | Stiffening cannula (curved); Torcon catheter (MPB curve); 5-F Teflon catheter (straight) | – | Transjugular renal access; includes a Quick-Core biopsy needle (19 gauge, 70-cm long, with 20-mm throw length, and 20-mm specimen notch), a Check-Flo Performer Assembly (7 F, 60.5-cm long, with 14 extra-thin wall gauge stiffening cannula), a straight catheter (5 F, 0.035-inch diameter, 72-cm long), and a Torcon NB Advantage catheter (5 F, 0.035-inch diameter end hole, 90-cm long, with MPB curve) |
| Cook Medical | Transluminal Biliary Biopsy Forceps Set | 7 (5.2 forceps size) | 30 (60-cm forceps length) | 0.035 | Straight | Yes | The set is specifically indicated for percutaneous transluminal biliary biopsy and can be used to access and obtain an accurate histologic sample of tissue within the biliary ductal system during the PTC procedure |
| Cordis | Rain Sheath Transradial Hydrophilic Thin-Walled Introducer | 4–7 | 10–16 | 0.021 | Angled and straight | – | Radial |
| Endologix | AFX Introducer System | 17 | 45 | 0.035 | Straight | Yes | Hydrophilic-coated sheath and dilator for AFX AAA graft |
| Endologix | Destino Twist Deflectable Steerable Guiding Sheath With 7 mm Curve Bend | 6.5 | 55 | 0.038 | Straight/curved | Yes | Unidirectional steerable guiding sheath designed to access difficult to reach targets throughout the vasculature |
| Galt | Elite HV F Hemostasis Valve Introducer | 4–9 | 12 | 0.018, 0.035, 0.038 | Straight | With and without | Standard valved introducer sheath or microintroducer/hemostasis valve sheaths |
| Galt | Elite HV Hemostasis Valve Introducer | 4–7 | 5.5, 12 | 0.018 | Straight | With and without | Microintroducer/hemostasis valve sheath together in one device to save a step |
| Galt | Elite HV R Transitionless Radial Access Introducer | 4–7 | 7, 11 | 0.018 | Straight | No | Radial access |
| Galt | Elite HV T Transitionless Hemostasis Valve Introducer | 4–7 | 7, 11 | 0.018 | Straight | No | Microintroducer/hemostasis valve sheath together in one device to save a step |
| Galt | GaltStick Coaxial Sheath With Stiffening Stylet | 6 | 20 | 0.018 X 60 cm (stainless or nitinol core with gold tip), 0.038 x 145 cm (PTFE) | Straight, J-straight | Yes | Allows for the introduction of a 0.018 inch safety and 0.038 inch working guidewire in nonvascular procedures; available with hydrophilic coating |
| Galt | GaltVTI Valved Tearaway Sheath | 5–16 | 13 | 0.018 | Straight | No | Valved tearaway introducer sheath |
| Galt | Micro-Introducer Kit: Bariatric | 4 | 15 | 0.018 X 60 cm (nitinol with gold tip) | Straight | No | Developed to assist in the access of larger patients, includes 12-cm access needle |
| Galt | Micro-Introducer Kits: Regular and Stiffen | 4, 5 | 5, 10 (regular), 10 (stiffen) | 0.018 X 40 or 60 cm (stainless with stainless or gold tip; nitinol with stainless or gold tip) | Straight | No | Microaccess |
| Galt | Micro-Introducer With Side Holes | 4 | 10 | 0.018 | Straight | No | Microaccess |
| Galt | MicroSlide Pediatric Tearaway Sheath | 2, 3 | 3, 7 | 0.008 (2 F), 0.014 (2 F); 0.010 (3 F), 0.018 (3 F) | Straight | No | Pediatric |
| Galt | Tear Away Introducer Sheath | 3–16 (some half sizes) | 3, 5, 7, 10, 14, 30, 44, 50 | 0.018, 0.035, 0.038 | Straight | No | Designed for the introduction of catheters into the vasculature, full kits or separate sterile sheaths available |
| Galt | Transitionless Micro-Introducer Kits: Regular and Stiffen | 4, 5 | 10 | 0.018 X 40 or 60 cm (stainless with stainless or gold tip, nitinol with stainless or gold tip); X-sharp needle included | Straight | No | Microaccess |
| Gore & Associates | Gore DrySeal Flex Introducer Sheath | 10, 12, 14, 15, 16, 18, 20, 22, 24, 26 | 33, 45, 65 | 0.035 | Flexible | Yes | Percutaneous |
| LeMaitre Vascular, Inc. | TT Tortuous Tracker Delivery System | 18–24 | 65, 85 | 0.035, 0.038 | Straight | Yes | Used to introduce balloon catheters, closed-end catheters, and other vascular devices |
| Medcomp | Regular Micro-Stick | 4, 5 | 9 | 0.018 | Straight | Yes | Micro-stick |
| Medcomp | Stiff Micro-Stick | 4, 5 | 9 | 0.018 | Straight | Yes | Micro-stick |
| Medtronic | TourGuide Steerable Sheath | 6.5, 7, 8.5 | 45, 55, 90 (working lengths) | Accepts up to 0.038 (guidewire not included) | Deflectable to 180° | Yes | Steerable sheath that allows for quick access of challenging anatomy and delivery of peripheral vascular products |
| Merit Medical Systems, Inc. | MAK-NV Introducer System | 6 | 20 | 0.018 X 60 cm (nitinol with platinum tip; stainless with platinum tip), 0.038 X 150 cm (double-ended heavy duty) | Straight | Yes | Microaccess for nonvascular procedures; all components are available sterile, standalone |
| Merit Medical Systems, Inc. | Merit MAK, SMAK and PAK: Mini Access Kits Regular and Stiffened, Pedal Access Kits | 4, 5 (available with 21-gauge X 7-cm smooth and echo-enhanced needles and 21-gauge X 4-cm echo-enhanced needles; 4, 5 stiffened dilator kits are available) | 10, 15 | 0.018 X 40, 60 cm (stainless steel mandrel with stainless, platinum coiled tips; nitinol mandrel with platinum or palladium coiled tips) | Straight | No | Microaccess (wire also available as standalone and two additional configurations: 0.018-inch X 60-cm stainless wire with platinum tip and 0.018-inch X 80-cm nitinol wire with platinum tip); 21-gauge X 9-cm smooth and echo-enhanced needles available; all components are available sterile, standalone |
| Merit Medical Systems, Inc. | Prelude Ideal Hydrophilic Sheath Introducer | 4, 5, 6, 7 | 7, 11, 16, 23 | 0.018, 0.021, 0.025 (nitinol mandrel with platinum tips; stainless steel; straight; single-ended floppy; double ended [3-mm J; floppy]; angled plastic jacketed wire) | Straight | No | Hydrophilic coated, radial access |
| Merit Medical Systems, Inc. | Prelude Sheath Introducers | 4–7 | 7, 11, 23 | 0.018, 0.025 (mandrel or stainless steel wires; straight, angled or doubled ended [3-mm J and floppy]) | Straight | With or without | Radial access: combines mini access approach and sheath placement |
| Merit Medical Systems, Inc. | Prelude Short Sheaths | 5–8 | 4 | 0.018, 0.035, 0.038 (mandrel or stainless steel coil wires; straight or double ended [3-mm J and floppy]) | Straight | Yes | Dialysis access management |
| Merit Medical Systems, Inc. | PreludeEase Hydrophilic Sheath Introducers | 4–7 | 7, 11, 16, 23 | 0.018, 0.021, 0.025, 0.035 (nitinol mandrel with platinum tips; stainless steel; straight; single-ended floppy; double ended [3-mm J; floppy]; angled plastic jacketed wire) | Straight | No | Hydrophilic coated; radial access |
| optimed Medizinische Instrumente GmbH | Epsylar | 5 | 120 | 0.035 | Freely configurable | Yes | Extra long sheath designed to facilitate transradial or transbrachial access |
| Oscor Inc. | Adelante Breezeway Delivery Sheath With Hemostatic Valve | 6, 7, 8, 9, 10, 11, 12, 14 | 61, 79, 110 | 0.035, 0.038 | Straight/curved | Yes | Guiding sheath with a fixed curve |
| Oscor Inc. | Adelante Magnum Introducer With Hemostatic SureSeal Valve Technology and Sideport for Delivery of Large Medical Devices | 16, 18 | 20, 30, 35 | 0.038 | Straight | Yes | Designed for the delivery of endovascular catheters, aortic valves, stent graft systems, and the TAVI/TAVR procedure |
| Oscor Inc. | Adelante Radial With Hemostatic Valve and Sideport for Optimal Radial Access | 4, 5, 6 | 7, 10, 25 | 0.018, 0.021 | Straight | No | Radial artery access sheath with hydrophilic coating, sideport, and high kink resistance |
| Oscor Inc. | Destino Bi-Directional Steerable Introducer With Hemostatic Valve: Small, Medium, and Large Curves | 8.5, 10, 12 | 61, 67, 71 | 0.038 | Straight/curved | Yes | Bidirectional steerable guiding sheath designed for introduction and placement of diagnostic and therapeutic devices |
| Oscor Inc. | Destino Reach Bi-Directional Steerable Introducer With Hemostatic Valve: Small, Medium, and Large Curves | 8.5, 10, 12 | 67, 71, 73, 75, 77 | 0.038 | Straight/curved | Yes | Transseptal and peripheral access |
| Oscor Inc. | Destino Twist Uni-Directional Steerable Introducer Sheath With Hemostatic Valve | 6.5, 7, 8.5, 12, 13.8 | 45, 55, 65, 71, 90 | 0.038 (maximum) | Straight, TD | Radiopaque markerband | Deflectable guiding sheath |
| Teleflex | Arrow Radial Access Sheaths | 4, 5, 6 | 7, 11, 24 | 0.018 | Straight | Yes | Radial |
| Teleflex | Super Arrow-Flex Carotid Access Sheath Introducer Set | 7 | 90 | – | Straight | Yes | Carotid |
| Teleflex | Super Arrow-Flex Renal Access Sheath Introducer Sets | 6, 7 | 45 | 0.035–0.038 | Curved, 90° | Yes | Renal |
| Terumo Europe | Glidesheath Slender Transradial Introducer Kit | 5, 6, 7 | 10, 16 | 0.018, 0.021, 0.025 | Straight | No | Radial access, one F size reduction in OD while keeping the larger ID equivalent |
| Terumo Europe | SoloPath Re-collapsible - Balloon Expandable Transfemoral Access System | 19, 22, 24 | 25, 35 | 0.038 or smaller | Straight | Radiopaque tip markerband | Large-bore applications such as percutaneous aortic valve placement, mitral valve placement, and abdominal aortic and thoracic aortic aneurysm graft placement; insertion profile OD 13.5 F (19 F), 15 F (all other sizes) after placement expansion to final diameter; at the end of the procedure recollapsing of the sheath diameter to approximately 30% of the final diameter |
| Terumo Europe | Terumo SoloPath Balloon-Expandable Transfemoral Introducer | 14, 16, 18, 19, 21 | 25, 35 | 0.038 or smaller | Straight | Radiopaque tip markerband | Large-bore applications such as percutaneous aortic valve placement, mitral valve placement, and abdominal aortic and thoracic aortic aneurysm graft placement; insertion profile OD 11.5 F (14 F), 15 F (all other sizes) after placement expansion to final diameter |
| Cordis | Brite Tip Radianz | 6 | 115, 135 | 0.035 | Straight | Yes | Radial access long sheath with detachable valve |
Sheaths / Standard Sheaths
View Chart| Company Name | Product Name | Size (F) | Length (cm) | Guidewire Compatibility (inch) | Curved or Straight | Radiopaque Tip |
|---|---|---|---|---|---|---|
| Abbott | Engage | 4–9 | 12, 25 | 0.035, 0.038 | Straight | No |
| Abbott | Ultimum | 4–12, 14, 16, 18, 20, 22 | 5, 8.5, 12, 23, 25, 30, 35 | 0.035, 0.038 | Straight | Yes, EV line |
| Argon Medical Devices, Inc. | Axcess Percutaneous Introducer | 4–9 | 5.75, 11, 23 | 0.021, 0.025, 0.032 (40 cm), 0.035, 0.038 (45 cm) | Straight | No |
| Argon Medical Devices, Inc. | Introducer Kits With Multi-Purpose Curve | 5–8 | 45, 98 | Accepts 0.035–0.038 | Curved | No |
| Argon Medical Devices, Inc. | Introducer With Detachable Hemostasis Valve (PCI Kit/2) | 4–9 | 5.75, 11 | Accepts 0.021, 0.028, 0.038 | Straight | No |
| Argon Medical Devices, Inc. | Introducer Without Hemostasis Valve (PCI Kit/3) | 4–6 | 11 | 0.021, 0.028, 0.035 | Straight | No |
| Argon Medical Devices, Inc. | One Piece Introducer With Integral Hemostasis Valve | 4–9 | 11 | 0.025, 0.035 | Straight | No |
| Argon Medical Devices, Inc. | Tuohy-Borst Introducer Tray With Integral Hemostasis Valve | 6–9 | 11 | 0.035 | Straight | No |
| Balton | Introducer | 3–18 | 6–90 | 0.018, 0.021, 0.035 | Straight | With or without |
| Boston Scientific Corporation | Super Sheath Introducers | 4 (1.3 mm), 5 (1.7 mm), 6 (2 mm), 7 (2.3 mm), 8 (2.7 mm), 9 (3 mm) | 7, 11, 25 | With wire: 0.035 (0.89 mm); without wire: 0.038 (0.97 mm) compatible | Straight | With or without |
| Boston Scientific Corporation | Super Sheath XL Introducers | 10 (3.3 mm), 11 (3.7 mm), 12 (4 mm), 14 (4.7 mm) | 11, 25 | With wire: 0.035 (0.89 mm); without wire: 0.038 (0.97 mm) compatible | Straight | With or without |
| Cook Medical | Performer: Large Valve | 9, 10, 12, 14, 16, 18 | 13, 30, 45, 70, 80, 85 | 0.038 | Straight | With or without |
| Cook Medical | Performer: Radial | 4–6 | 5.5, 7, 13, 23 | 0.018 | Straight | No |
| Cook Medical | Performer: Small Valve | 4–8 | 13, 30 | 0.035, 0.038 | Straight | With or without |
| Cordis | Avanti + Sheath Introducer | 4, 5, 5.5, 6, 6.5, 7, 8, 9, 10, 11 | 5.5, 11, 23 | 0.035 | Straight | No |
| Cordis | Brite Tip Sheath Introducer | 4–11 | 5.5, 11, 23, 35, 45, 55, 90 | 0.035 | Straight | Yes |
| Endologix | Destino Twist Deflectable Steerable Guiding Sheath With 7 mm Curve Bend | 6.5 | 55 | 0.038 | Straight/curved | Yes |
| Galt | Elite HV F Hemostasis Valve Introducer | 4–9 | 12 | 0.018, 0.035, 0.038 | Straight | With or without |
| Galt | Elite HV Hemostasis Valve Introducer | 4–7 | 5.5, 12 | 0.018 | Straight | With or without |
| Galt | Elite HV T Transitionless Hemostasis Valve Introducer | 4–7 | 7, 11 | 0.018 | Straight | No |
| Galt | Tearaway Introducer Sheaths | 3-16 (some half sizes) | 3, 5, 7, 10, 14, 30, 44, 50 | 0.018, 0.028, 0.038 | Straight | No |
| Gore & Associates | Gore DrySeal Flex Introducer Sheath | 10, 12, 14, 15, 16, 18, 20, 22, 24, 26 | 33, 45, 65 | 0.035 | Flexible | Yes |
| Medcomp | Super Sheath Introducer | 4.5, 5.5, 6 | 7 | – | Straight | – |
| Medcomp | Super Sheath Introducer | 3.5, 4.5, 5, 5.5, 6, 6.5 | 5 | – | Straight | – |
| Medcomp | Super Sheath Introducer | 3, 3.5, 4.5, 5.5, 6, 6.5, 7 | 10 | – | Straight | – |
| Medcomp | Valved Peelable Introducer | 7, 8, 9, 10, 11, 12, 13 | 12 | – | Straight | – |
| Medcomp | Valved Peelable Introducer | 14, 15, 16, 17 | 14 | – | Straight | – |
| Medcomp | Valved Peelable Introducer | 7, 9, 10 | 15 | – | Straight | – |
| Medcomp | Valved Peelable Introducer | 7, 9 | 15 | 0.018 | Straight | – |
| Medtronic | Input PS | 5–9 | 11, 23 | 0.038 | Straight | Yes |
| Medtronic | Input TS | 5–11 | 7, 11, 23 | 0.038 | Straight | Yes |
| Medtronic | Sentrant Introducer Sheath With Hydrophilic Coating | 12, 14, 16, 18, 20, 22, 24, 26 | 28 | 0.035 | Straight | Yes |
| Merit Medical Systems, Inc. | Prelude ACT Sheath Introducers | 4.5, 5.5, 6.5, 7.5, 8.5 | 11 | 0.035, 0.038 (stainless steel wire double ended [3-mm J, floppy]) | Straight | No |
| Merit Medical Systems, Inc. | Prelude Sheath Introducers | 4–8 | 11, 23 | 0.018, 0.025, 0.035, 0.038 (mandrel or stainless steel coils; tips are straight, angled, or double ended [3-mm J, floppy]) | Straight | With or without |
| Oscor Inc. | Adelante Breezeway Delivery Sheath With Hemostatic Valve | 6, 7, 8, 9, 10, 11, 12, 14 | 61, 79, 110 | 0.035, 0.038 | Straight/curved | Yes |
| Oscor Inc. | Adelante Magnum Introducer With Hemostatic SureSeal Valve Technology and Sideport for Delivery of Large Medical Devices | 16, 18 | 20, 30, 35 | 0.038 | Straight | Yes |
| Oscor Inc. | Adelante Peel Away Introducer | 6, 7, 7.5, 8, 8.5, 9, 9.5, 10, 10.5, 11, 12, 12.5 | 16, 23, 30, 45 | 0.038 | Straight | No |
| Oscor Inc. | Adelante Radial With Hemostatic Valve and Sideport for Optimal Radial Access | 4, 5, 6 | 7, 10, 25 | 0.018, 0.021 | Straight | No |
| Oscor Inc. | Adelante SafeSheath II Next Generation Peel Away Introducer With Hemostatic Valve | 6, 7, 8, 8.5, 9, 10, 10.5, 11, 12, 12.5 | 13, 23 | 0.038 | Straight | No |
| Oscor Inc. | Adelante Sigma Introducer With Hemostatic Valve | 4–12 | 10, 23 | 0.038 | Straight | No |
| Oscor Inc. | Destino Bi-Directional Steerable Introducer With Hemostatic Valve: Small, Medium, and Large Curves | 8.5, 10, 12 | 61, 67, 71 | 0.038 | Straight/curved | Yes |
| Oscor Inc. | Destino Reach Bi-Directional Steerable Introducer With Hemostatic Valve: Small, Medium, and Large Curves | 8.5, 10, 12 | 67, 71, 73, 75, 77 | 0.038 | Straight/curved | Yes |
| Oscor Inc. | Destino Twist Uni-Directional Steerable Introducer Sheath With Hemostatic Valve | 6.5, 7, 8.5, 12, 13.8 | 45, 55, 65, 71, 90 | 0.038 (maximum) | Straight, TD curve | Radiopaque markerband |
| Oscor Inc. | SafeSheath Ultra Lite Peel Away Introducer With Hemostatic Valve | 5, 6, 7, 8, 8.5, 9, 10, 11, 13, 15, 16, 16.5 | 13 | 0.038 | Straight | No |
| Pediavascular | Super Sheath | 3 | 5, 7 | 0.018 | Straight | No |
| Teleflex | Arrow Percutaneous Sheath Introducer Kits (Adult) | 4–9 | 11 | 0.035 | Straight | Yes |
| Teleflex | Arrow Percutaneous Sheath Introducer Kits (Pediatric) | 4–6 | 5, 7.5 | 0.021 | Straight | Yes |
| Terumo Europe | Radifocus Introducer II - M Coat | 5, 6 | 10, 16, 25 | 0.021, 0.025 | Straight | No |
| Terumo Europe | Radifocus Introducer II - Pediatric Kit | 4, 5, 6 | 5, 7 | 0.025 | Straight | No |
| Terumo Europe | Radifocus Introducer II - Radiopaque Marker Kit | 4, 5, 6, 7, 8, 9 | 6, 10, 25 | 0.035, 0.038 | Straight | Yes |
| Terumo Europe | Radifocus Introducer II - Standard Kit | 4, 5, 6, 7, 8, 9, 10, 11 | 10, 25 | 0.025, 0.035, 0.038 | Straight | No |
| Terumo Europe | Radifocus Introducer II - Transradial kit | 4, 5, 6, 7 | 7, 10, 16, 25 | 0.018, 0.021, 0.025 | Straight | No |
Stents / Balloon-Expandable Covered Stents
View Chart| Company Name | Product Name | Material Used | Maximum Guidewire Size (inch) | Introducer Size (F) | Stent Diameter (mm) | Stent Length (mm) | Delivery System Length (cm) | CE Mark Indications |
|---|---|---|---|---|---|---|---|---|
| AndraTec GmbH Germany | Optimus-CVS XL | Cobalt chromium-PTFE | 0.035 | 8, 10, 12, 16, 18 | 8–28 | 18–57 extra lengths 8 and 10 cm | 110 | Peripheral |
| Artivion, Inc. | E-ventus BX | Cobalt chromium ePTFE covered stent | 0.035 | 6 (5–6-mm diameter), 7 (7–10-mm diameter) | 5–10 | 18, 22, 23, 27, 28, 37, 38, 57, 58 | 120 | Indicated for intraluminal chronic placement in iliac and renal arteries for restoring and improving vessel patency and treatment of aneurysms, acute perforations, acute ruptures, and fistulas |
| BD Interventional | LifeStream Balloon-Expandable Vascular Covered Stent | 316L stainless steel and ePTFE | 0.035 | 6, 7, 8 | 5, 6, 7, 8, 9, 10, 12 | 16, 26, 37, 38, 58 | 80, 135 | Indicated for the treatment of atherosclerotic lesions in common and external iliac arteries |
| Bentley InnoMed GmbH | BeGraft | Cobalt chromium (L605), ePTFE | 0.035 | 6 (diameter: 5–8 mm), 7 (diameter: 9–10 mm) | 5, 6, 7, 8, 9, 10 | 18, ~23, ~28, ~38, ~58 | 75, 120 | Intraluminal chronic placement in iliac and renal arteries for restoring and improving the patency and to treat aneurysms, acute perforations, ruptures and fistulas |
| Bentley InnoMed GmbH | BeGraft aortic | Cobalt chromium (L605), ePTFE | 0.035 | 9 (diameter: 12 mm); 11 (diameter: 14, 16 mm); 14 (diameter: 18–24 mm) | 12, 14, 16, 18, 20, 22, 24 | 19, 29, ~38, ~48, ~58 | 75, 120 | Implantation in the native and/or recurrent coarctation of the aorta on adolescent or adult patients; restores and improves the patency of the iliac arteries |
| Bentley InnoMed GmbH | BeGraft coronary | Cobalt chromium (L605); ePTFE | 0.014 | 5 (guide catheter) | 2.5, 2.75, 3, 3.5, 4, 4.5, 5 | 8, 12, 16, 18, 21, 24 | 144, 154 | Transluminal implantation in coronary arteries or aortocoronary bypass grafts for the treatment of (1) acute perforation or rupture of coronary arteries; and (2) aneurysm of coronary arteries or coronary bypass-vein graft |
| Bentley InnoMed GmbH | BeGraft peripheral Plus | Double cobalt chromium (L605), double ePTFE (in sandwich design) | 0.035 | 7 (diameter: 5–8 mm); 8 (diameter: 9–10 mm) | 5, 6, 7, 8, 9, 10 | ~27, ~37, ~57 | 120 | Intraluminal chronic placement in iliac and renal arteries for restoring and improving the patency and to treat aneurysms, acute perforations, ruptures, and fistulas |
| Getinge | Advanta V12 Balloon-Expandable Covered Stent | 316 L stainless steel PTFE covered stent | 0.035 | 6, 7 | 5–10 | 16, 22, 32, 38, 59 | 80, 120 | Restoring and improving the patency of the iliac and renal arteries; renal approval includes 5-mm, 6-mm, and 7-mm diameters |
| Getinge | Advanta V12 Balloon-Expandable Covered Stent | 316 L stainless steel, PTFE encapsulated | 0.035 | 9 | 12 | 29, 41, 61 | 80, 120 | Restoring and improving the patency of the iliac arteries |
| Gore & Associates | Gore Viabahn VBX Balloon-Expandable Endoprosthesis | Stainless steel stent/fluoropolymer graft | 0.035 | 7, 8 | 5, 6, 7, 8, 8L, 9, 10, 11 | 15, 19, 29, 39, 59, 79 | 135 | De novo or restenotic lesions in the iliac arteries, including lesions at the aortic bifurcation; de novo or restenotic lesions in the visceral arteries; isolated visceral, iliac, and subclavian artery aneurysms; or traumatic or iatrogenic vessel injuries in arteries that are located in the chest cavity, abdominal cavity, or pelvis (except for aorta, coronary, innominate, carotid, vertebral, and pulmonary arteries) |
| iVascular | iCover | CoCr L605 and ePTFE | 0.035 | 6 (up to 8 mm diameter and 17 mm length), 7 | 5, 6, 7, 8, 9, 10 | 17, 27, 37, 57 | 80, 140 | Indicated for restoring atherosclerotic lesions of the common and external iliac arteries and the renal arteries; treatment of aneurysms and perforations, ruptures and acute fistulas |
| Medtronic | Radiant Balloon-Expandable Covered Stent | 316L stainless steel | 0.035 | 6, 7 | 6, 7 | 22, 32, 38, 59 | 120 | Maintenance of perfusion to the renal arteries when used in conjunction with the Endurant II/IIs stent graft system in the ChEVAR technique |
| Bentley InnoMed GmbH | BeFlared FEVAR | CoCr (L-605), ePTFE covering folded inside and clamped on both ends | 0.035 | 6, 7 | 5/8, 6/8, 7/10, 8/10, 9/11 | 22–37 | 120 | Indicated for use as a bridging stent graft in patients requiring endovascular abdominal aortic aneurysm repair with a fenestrated aortic endovascular graft to keep the visceral artieries perfused |
| Bentley InnoMed GmbH | BeFlow iliac | CoCr (L-605)m ePTFE covering folded inside and clamped on both ends | 0.035 | 6, 7 | 7, 8, 9, 10 | 37, 57 | 75 | Permanent intraluminal placement in iliac arteries for restoring and improving the patency impaired by arteriosclerosis or other stenoses that may be treated by stenting |
| Bentley InnoMed GmbH | BeGraft Plus | CoCr (L-605) | 0.035 | 7/8 F 5 for Ø 5 - 7 mm (depending on indication and access site) 8 F for Ø 8 mm 8/9/10 F 5 for Ø 9 and 10 mm (depending on indication and access site) | Ø 5 and 6 mm (SV = small vessel design) Ø 7 and 8 mm (MV = medium vessel design) Ø 9 and 10 mm (LV = large vessel design) | 28, 38, 58, 78 (SV = small vessel design) 27, 37, 57, 77 (MV = medium vessel design, LV = large vessel design) | 120 | Indicated for permanent intraluminal placement in iliac and renal arteries for restoring and improving the patency impaired by arteriosclerosis or other stenoses that may be treated by stenting; sealing aneurysms, acute perforations, acute ruptures, and fistulas; as bridging stent graft in patients requiring endovascular abdominal aortic aneurysm repair with a branched aortic endovascular graft to keep the visceral arteries perfused Sizes approved when used for permanent intraluminal placement in iliac and renal arteries: Ø 5 mm and 6 mm in lengths of 28 mm, 38 mm, and 58 mm, Ø 7 mm - 10 mm in lengths of 27 mm, 37 mm, and 57 mm Sizes approved when used as a bridging stent graft for BEVAR: Ø 5 mm and 6 mm in lengths of 38 mm, 58 mm, and 78 mm, Ø 7 mm - 10 mm in lengths of 37 mm, 57 mm and 77 mm |
Stents / Balloon-Expandable Stents
View Chart| Company Name | Product Name | Material Used | Maximum Guidewire Size (inch) | Introducer Size (F) | Stent Diameter (mm) | Stent Length (mm) | Delivery System Length (cm) | CE Mark Indications |
|---|---|---|---|---|---|---|---|---|
| Abbott | Omnilink Elite Peripheral Balloon Expandable Stent System | Cobalt chromium | 0.035 | 6 | 4–10 | 12, 16, 19, 29, 39, 59 | 80, 135 | For the treatment of de novo or restenotic atherosclerotic lesions in protected peripheral arteries and palliation of malignant strictures in the biliary tree |
| Abbott | RX Herculink Elite Peripheral Stent System | Cobalt chromium | 0.014 | 5 | 4, 4.5, 5, 5.5, 6, 6.5, 7 | 12, 15, 18 | 80, 135 | To open lumen restrictions in the biliary tree, renal arteries, and protected peripheral arteries |
| Alvimedica | Inperia Advance | Cobalt chromium | 0.014 | 4 | 2.25–4.5 | 7–31 | 142 | BTK |
| Alvimedica | Isthmus Logic | Cobalt chromium | 0.035 | 6 | 6–10 | 19–59 | 75, 135 | Iliac |
| Alvimedica | Radix2 | Stainless steel | 0.018 | 5 | 5–7 | 12, 17 | 75, 150 | Renal |
| amg International GmbH | Facile Inert Peripheral Stent Implantation System | Carbon-ion inert stainless steel | 0.035 | 6 (5–6-mm diameter), 7 (7–8-mm diameter), 8 (9–12-mm diameter) | 5, 6, 7, 8, 9, 10, 12 | 18, 28, 38, 48, 58 | 75, 115, 150 | Peripheral arteries |
| amg International GmbH | Thalis Flex Peripheral Stent Implantation System | Cobalt chromium | 0.018, 0.035 | 5, 7 | 5–10 | 17, 26, 36, 57 | 80, 120 (7 F); 80, 135 (5 F) | Peripheral arteries |
| Andramed GmbH | AndraStent L | Cobalt chromium | Depending on the balloon catheter | 7 (+1) | 8, 12, 15, 18 | 13, 17, 21, 26 | – | Peripheral vascular indications |
| Andramed GmbH | AndraStent XL | Cobalt chromium | Depending on the balloon catheter | 9 (+1) | 15, 18, 20, 22, 25 | 13, 17, 21, 26, 30, 35, 39, 43, 48, 57 | – | Peripheral vascular indications |
| Andramed GmbH | AndraStent XXL | Cobalt chromium | Depending on the balloon catheter | 11 (+1) | 20, 22, 25, 28, 32 | 17, 21, 26, 30, 35, 39, 43, 48, 57 | – | Peripheral vascular indications |
| AndraTec GmbH Germany | Optimus CVS PTFE Covered Stent | Cobalt chromium | 0.035 | 8–12 | 8–28 | 13–100 | Bare BX PTFE covered stent | Peripheral |
| AndraTec GmbH Germany | Optimus XL | Cobalt chromium | 0.035 | 8, 10, 12 | 8–28 | 13–57 | 110 | Peripheral |
| Balton | Nefro C | Cobalt chromium | 0.014 | 6 | 5, 6, 7 | 8–25 | 140 | Renal |
| Balton | Neptun C (OTW) | Cobalt chromium | 0.035 | 6 | 4–9 | 20–100 | 110 | Peripheral |
| Balton | Neptun C (RX) | Cobalt chromium | 0.014 | 5–6 | 2–7 | 8–40 | 140 | Peripheral |
| Bentley InnoMed GmbH | BeSmooth peripheral | Cobalt chromium (L605) | 0.035 | 6 | 5, 6, 7, 8, 9, 10 | 18, 23, ~27, 38, ~57 | 75, 120 | Treatment of de novo or restenotic atherosclerotic lesions in protected peripheral arteries |
| Teleflex | Dynamic | Stainless steel | 0.035 | 6 (5–9 diameter), 7 (10 diameter) | 5, 6, 7, 8, 9, 10 | 15, 25, 38, 56 | 80, 130 | Iliac arteries |
| Teleflex | Dynamic Renal | Cobalt chromium | 0.014 | 4 (4.5–5 diameter), 5 (6–7 diameter) | 4.5, 5, 6, 7 | 12, 15, 19 | 140 | Renal arteries |
| Teleflex | Dynetic-35 | Cobalt chromium | 0.035 | 6 (for all sizes) | 5–10 | 18, 28, 38, 58, 78 | 90, 130, 170 | Iliac arteries |
| Teleflex | Pro-Kinetic Energy Explorer | Cobalt chromium | 0.014 | 4 | 2, 2.5, 3, 3.5, 4, 4.5, 5 | 9, 15, 20, 30, 40 | 140 | Infrapopliteal arteries |
| Boston Scientific Corporation | Express LD Iliac/Biliary Premounted Stent System | 316 L stainless steel | 0.035 (0.89 mm) | 6 (2 mm): up to 8 X 37 mm; 7 (2.51 mm): up to 10 X 57 mm | 5 (biliary indication only), 6–10 | 17, 25, 27, 37, 57 | 75, 135 | Iliac, biliary |
| Boston Scientific Corporation | Express SD Renal Monorail Premounted Stent System | 316 L stainless steel | 0.018 (0.46 mm) | 5 (1.67 mm): up to 6 X 18 mm; 6 (2 mm): up to 7 X 19 mm | 4–7 | 14, 15, 18, 19 | 90, 150 | Renal, biliary |
| Boston Scientific Corporation | Flexive Cobalt Chromium Endovascular Stent System | Cobalt chromium | 0.035 (0.89 mm) | 6 | 5–9 | 20, 30, 40, 50, 60, 80 | 80, 120 | Iliac, renal |
| Cook Medical | Formula 418 Vascular Balloon-Expandable Stent | Stainless steel | 0.018 | 5 (3–6-mm diameter), 6 (7–8-mm diameter) | 3–8 | 3 mm: 12, 16, 20, 24, 30; 4 mm: 12, 16, 20, 30; 5–8 mm: 12, 16, 20, 24, 30 | 80, 135 | Peripheral vascular indication |
| Cook Medical | Formula 535 Vascular Balloon-Expandable Stent | Stainless steel | 0.035 | 5 (4-mm diameter), 6 (5–8-mm diameter), 7 (9–10-mm diameter) | 4–10 | 4 mm: 12, 20 mm; 5 mm: 12, 20, 40, 60 mm; 6 mm: 12, 20, 30, 40, 60 mm; 7 mm: 20, 30, 40, 60 mm; 8 mm: 12, 20, 30, 40, 60 mm; 9–10 mm: 20, 30, 40, 60 mm | 80, 135 | Peripheral vascular indication |
| Cordis | Palmaz Blue | Cobalt chromium | 0.014, 0.018 | 4, 5 (sheath compatibility) | 4–7 | Up to 24 | 80, 135, 142 | Peripheral arteries |
| Cordis | Palmaz Genesis | Stainless steel | 0.035 | 6–7 | 4–10 | Up to 79 | 80, 135 | Peripheral arteries |
| eucatech AG | Euca PWS | Alloy 316 LVM stainless steel | 0.035 | 6, 7, 8, 9 | 4, 5, 6, 7, 8, 9, 10, 12 | 18, 28, 38, 58 | 75, 115, 150 | Treatment of peripheral vessels stenosis |
| iVascular | Restorer | Cobalt chromium (CoCr L605) | 0.035 | 6 | 5, 6, 7, 8, 9, 10 | 18, 28, 38, 58 | 80, 140 | For the treatment of de novo or restenotic atherosclerotic lesions in protected peripheral arteries located under the aortic arch, and for palliation of biliary tract malignant stenosis with a nominal diameter ranging from 5–10 mm |
| Medtronic | Hippocampus Renal Rx Stent | Stainless steel | 0.014 | 5 | 4, 5, 5.5, 6, 6.5, 7 | 10, 15, 20, 24 | 80, 145 | Renal, peripheral |
| Medtronic | Visi-Pro Stent System | 316 L stainless steel | 0.035 | 7 | 9, 10 | 17, 27, 37, 57 | 80, 135 | Iliac |
| Medtronic | Visi-Pro Stent System | 316 L stainless steel | 0.035 | 6 | 6–8 | 12 (except 8-mm diameter), 17, 27, 37, 57 | 80, 135 | Iliac |
| Meril Life Sciences Pvt. Ltd. | Cogent BMS - Balloon Expandable Renal and Biliary Stent System | Cobalt chromium L605 | 0.014 | 5 | 5, 6, 7 | 12, 15, 18 | 150 | Indicated for use in patients with atherosclerotic disease of the renal arteries following suboptimal percutaneous transluminal renal angioplasty of a de novo or restenotic atherosclerotic lesion and for palliation of malignant neoplasms in the biliary tree with reference vessel diameter 5–7 mm in patients eligible for PTA and stenting procedures |
| Meril Life Sciences Pvt. Ltd. | Myra BMS - Balloon Expandable Peripheral Stent System | Cobalt chromium L605 | 0.035 | 6, 7, 8 | 5, 6, 7, 8, 9, 10 | 17, 27, 37, 47, 57 | 80, 135 | Intended for use in the treatment of atherosclerotic diseases of peripheral arteries below the aortic arch, with reference vessel diameter of 5–10 mm for Iliac/subclavian and for the other protected peripheral arteries in patients eligible for PTA and stenting procedures |
| Q3 Medical Group | Peripheral Balloon-Expandable Stent System (PBX) | Carbon-ion inert stainless steel | 0.035 | 6 (5–6-mm diameter), 7 (7–8-mm diameter), 8 (9–12-mm diameter) | 5, 6, 7, 8, 9, 10, 12 | 18, 28, 38, 48, 58 | 75, 115, 150 | Peripheral arteries |
| Q3 Medical Group | Peripheral Balloon-Expandable Stent System (QBX) | Cobalt chromium | 0.018, 0.035 | 5, 7 | 5, 6, 7, 8, 9, 10 | 17, 26, 36, 57 | 80, 120 (7 F); 80, 135 (5 F) | Peripheral arteries |
| Rontis AG | Zeus CC | Cobalt chromium MP35N | 0.035 | 6 | 5, 6, 7, 8, 9 | 20, 30, 40, 50, 60, 80 | 80, 120 | Peripheral arteries |
| Terumo Europe | Tsunami Peripheral Balloon-Expandable Stent | Stainless steel | 0.018 | 5, 6, 7 | 5, 6, 7 | 12, 18 | 90, 150 | Intended to be used for the treatment of stenotic lesions in various arteries excluding coronary, cervical, and cerebral vessel, to improve the blood flow |
Stents / Carotid Artery Stenting Systems
View Chart| Company Name | Product Name | Tapered Stent Diameters (Proximal/Distal) (mm) | Tapered Stent Lengths (mm) | Straight Stent Diameters (mm) | Straight Stent Lengths (mm) | Embolic Protection Device | Type | Position | CE Mark Indications |
|---|---|---|---|---|---|---|---|---|---|
| Abbott | RX Acculink Carotid Stent System | 8/6, 10/7 | 30, 40 | 5–10 | 20, 30, 40 | Emboshield Nav6 Embolic Protection Systems | Filter; BareWire filter delivery wire | Distal | Indicated for use in patients with atherosclerotic disease of the carotid arteries |
| Abbott | X.Act Carotid Stent System | 8/6, 9/7, 10/8 | 30, 40 | 7–10 | 20, 30 | Emboshield Nav6 Embolic Protection System | Filter; BareWire filter delivery wire | Distal | Indicated for use in patients with atherosclerotic disease of the carotid arteries; indicated for use in conjunction with Abbott Vascular's Emboshield family of embolic protection systems |
| Balton | Mer | 7/5, 8/6, 9/7, 10/7, 10/8 | 20, 30, 40, 50 | 4, 5, 6, 7, 8, 9, 10 | 20, 30, 40, 50 | Robin | Filter | Distal | Carotid artery stenting |
| Boston Scientific Corporation | Carotid Wallstent Monorail | – | – | 6, 8, 10 (unconstrained) | 36, 48, 49, 59, 62 | FilterWire EZ Embolic Protection System | Filter | Distal | Used in conjunction with the Boston Scientific Embolic Protection System, it is indicated for the treatment of patients at high risk for adverse events from carotid endarterectomy due to either anatomic or comorbid conditions who require carotid revascularization in the treatment of ipsilateral or bilateral carotid artery disease and meet the criteria outlined: patients with neurological symptoms and ≥ 50% stenosis of the common, internal carotid artery and/or the bifurcation by ultrasound or angiography of patients without neurological symptoms and ≥ 80% stenosis of the common, internal carotid artery and/or the bifurcation by ultrasound or angiogram, and patients with a reference vessel diameter within the range of 4–9 mm at the target lesion |
| Cordis | Precise Pro RX Carotid Stent System | Autotapering | 20, 30, 40 | 5–10 | 20, 30, 40 | Angioguard RX Emboli Capture Guidewire | Filter | Distal | Indicated for treatment of patients at high risk for adverse events from carotid endarterectomy who require carotid revascularization and meet the following criteria: patients with neurological symptoms and ≥ 50% stenosis of the common or internal carotid artery by ultrasound or angiography, or patients without neurological symptoms and ≥ 80% stenosis of the common or internal carotid artery by ultrasound or angiography, and patients must have a vessel diameter of 4–9 mm at the target lesion; the vessel distal to the target lesion must be within the range of 3–7.5 mm to allow for placement of Cordis Angioguard RX Guidewire |
| InspireMD | CGuard Carotid Embolic Prevention Stent System | – | – | 6, 7, 8, 9, 10 | 20, 30, 40, 60 | Compatible with both distal and proximal embolic protection devices | – | – | Indicated for improving carotid luminal diameter in patients at high risk for adverse events from carotid endarterectomy who require carotid revascularization and meet the following criteria: patients with neurological symptoms and > 50% stenosis of the common or internal carotid artery by either ultrasound or angiogram or patients without neurological symptoms and > 80% stenosis of the common or internal carotid artery by either ultrasound or angiogram; patients having a vessel with reference diameters between 4.8–9 mm at the target lesion |
| Medtronic | Protégé RX Carotid Stent System | 8/6, 10/7 | 30, 40 | 6–10 | 20, 30, 40, 60 | SpiderFX Embolic Protection Device | Filter; guidewire of choice | Distal | Indicated for treatment of stenoses of the common carotid artery, internal carotid artery, and carotid bifurcation |
| Terumo Neuro | Casper RX | In vivo tapering | In vivo tapering | 5–10 | 25, 37, 47; 22, 33, 40; 25, 35, 40; 25, 35, 40, 47; 33, 40; 35, 43 | EmPro Embolic Protection System | Dual-layer braided stent | Sustained embolic protection | Indicated for use in patients with carotid arterial atherosclerotic disease |
| Terumo Europe | Roadsaver Carotid Artery Stent | – | – | 5–10 | 16–40 | Nanoparasol Embolic Protection System | Filter, concentric nitinol micromesh, guidewire of choice | Distal | Indicated for use in patients with carotid arterial atherosclerotic disease; indicated for use as a guidewire to contain and remove embolic material (thrombus/debris) while preforming angioplasty and stenting procedures in carotid arteries |
Stents / Cerebral Stents
View Chart| Company Name | Product Name | Materials Used | Stent Diameters (mm) | Stent Lengths (mm) | Recommended Guidewire Size (inch) | Recommended Guide Catheter Size (inch) |
|---|---|---|---|---|---|---|
| Acandis GmbH & Co. KG | Acclino Stent System | Nitinol; laser-cut, closed-cell design | 3.5, 4.5 | 15, 25, 35 | 0.010–0.014 | 1.9-F microcatheter (ID: 0.0165) included |
| Cerenovus | Codman Enterprise 2 Vascular Reconstruction Device | Nitinol; laser-cut, closed-cell design with platinum markers | 5 (for vessels 2–4) | 16, 23, 30, 39 | No guidewire | 5- or 6-F guiding catheter for a 0.021 delivery microcatheter |
| Cerenovus | Codman Enterprise Vascular Reconstruction Device | Nitinol | 4.5 (for vessels 2–4) | 14, 22, 28, 37 | No guidewire | 5- or 6-F guiding catheter for a 0.021 delivery microcatheter |
| Terumo Neuro | LVIS EVO Intraluminal Support Device | Nitinol with platinum core (DFT wire) | 2.5, 3, 3.5, 4 | 12–34 | 0.014 | 0.0165, 0.017 |
| Terumo Neuro | LVIS Intraluminal Support Device | Nitinol, tantalum | 3.5, 4, 4.5, 5.5 | Various | 0.014 | ID: 0.021 |
| Terumo Neuro | LVIS Jr. Intraluminal Support Device | Nitinol, tantalum | 2.5, 3.5 | Various | 0.014 | 0.0165, 0.017 |
| Stryker | Neuroform Atlas Stent System | Nitinol; laser-cut, open-cell design | 3, 4, 4.5 | 15, 21, 24, 30 | 0.014 | 0.0165 |
| Stryker | Neuroform EZ Stent System | Nitinol; laser-cut, open-cell design | 2.5, 3, 3.5, 4, 4.5 | 10, 15, 20, 30 | 0.014 | ID: 0.027 |
| Stryker | Wingspan Stent System | Nitinol | 2.5, 3, 3.5, 4, 4.5 | 9, 15, 20 | 0.014 | Minimum ID: 0.064 |
Stents / Drug-Eluting Stents
View Chart| Company Name | Product Name | Drug Delivered | Material Used | Polymer Type | Maximum Guidewire Size (inch) | Introducer Size (F) | Stent Diameter (mm) | Stent Length (mm) | Delivery System Length (cm) | CE Mark Indications |
|---|---|---|---|---|---|---|---|---|---|---|
| Alvimedica | Cre8 BTK | Amphilimus (sirolimus + fatty acid) | Cobalt chromium | Polymer free | 0.014 | 4 | 2.25–4.5 | 8–46 | 142 | Peripheral/BTK |
| Biosensors International | BioMatrix Flex BTK Drug-Eluting Peripheral Stent | Biolimus A9 pharmaceutical ingredient | Stainless steel | Biodegradable polymer coating 15.6 μg/mm stent length | 0.014 | 5, 6 | 2.25, 2.5, 2.75, 3, 3.5, 4 | 8, 11, 14, 18, 24, 28, 33, 36 | 142 | Indicated for improving infrapopliteal luminal diameter for the treatment of occlusive lesions BTK and above the ankle that lead to severe claudication or CLI; treated infrapopliteal arteries must have a reference diameter ranging between 2.25–4 mm |
| Boston Scientific Corporation | Eluvia Drug-Eluting Vascular Stent System | Paclitaxel | Nitinol | Polymer-based technology with proven biocompatibility | 0.035 | 6 | 6–7 | 40, 60, 80, 100, 120, 150 | 75, 130 | SFA and/or PPA |
| Concept Medical | Abluminus DES+ | Sirolimus | Cobalt chromium alloy L605 | Customized biodegradable polymer matrix | 0.014 | 5 | 2.25, 2.50, 2.75, 3, 3.50, 4, 4.50, 5 | 8, 12, 16, 20, 24, 28, 32, 36, 40, 44, 48, 52 | RX 140 | Indicated for DM and AMI |
| Concept Medical | Abluminus NP | Sirolimus | Cobalt chromium alloy L605 | Polymer free | 0.014 | 5 | 2.25, 2.50, 2.75, 3, 3.50, 4 | 8, 12, 16, 20, 24, 28, 32, 36, 40 | 140 | Indicated for improving luminal diameter in patients, including those with bleeding risks or those who have to undergo DAPT interruption in the near future for any surgery and who have associated risks, such as diabetes mellitus, symptomatic coronary artery disease, stable angina, unstable angina, or documented silent ischemia due to atherosclerotic lesions in native coronary arteries with a reference vessel diameter 2.25–4 mm and lesion length of ≤ 36 mm |
| Cook Medical | Zilver PTX | Paclitaxel | Nitinol | Polymer free | 0.035 | 6 | 5–8 | 40, 60, 80, 100, 120, 140 | 80, 125 | Above-the-knee femoropopliteal arteries |
| iVascular | Angiolite BTK | Sirolimus | Cobalt chromium (CoCr L605) | Biostable fluorinated acrylate | 0.014 | 5 | 2, 2.25, 2.5, 2.75, 3, 3.5, 4, 4.5 | 9, 14, 16, 19, 24, 29, 34, 39 | 142 | Indicated for treating chronic and acute arterial lesions in the lower limbs below the knee, as well as popliteal and infrapopliteal lesions with reference vessel diameters between 2–4.5 mm, with the aim of increasing the internal diameter of an artery and consequently improving blood flow in the following cases: severe claudication and critical limb ischemia; also indicated for the treatment of erection-related arterial lesions in patients with arteriogenic erectile dysfunction to restore arterial flow to the corpora cavernosa |
Stents / Ostial Stent Positioning Systems
View Chart| Company Name | Product Name | Device Size (mm) | Working Length (cm) | Wire Diameters (inch) | Minimum Guiding Catheter (F) | Comments |
|---|---|---|---|---|---|---|
| AndraTec GmbH Germany | Optimus Bare and Optimus PTFE Covered Stent | 8–28 | 110 | 0.035 | 10 | Extra-large cobalt chromium stents as bare and PTFE covered |
| AndraTec GmbH Germany | Optimus CVS PTFE Covered Stent | 8–28 | 110 | 0.035 | 10 | PTFE-covered, large, balloon-expandable stent |
| Merit Medical Systems, Inc. | Ostial Pro Stent Positioning System | 15-mm leg span | 127 | 0.014 (distal: 4 cm), 0.018 (proximal: 123 cm) | 6 ID (0.070 inch), 7 ID (0.078 inch), 8 ID (0.088 inch) | A guidewire system designed to provide consistent and precise stent implantation in aorto-ostial lesions during coronary or peripheral interventional procedures |
Stents / Self-Expanding Stents
View Chart| Company Name | Product Name | Material Used | Introducer Size (F) | Guidewire Compatibility (inch) | Stent Diameter (mm) | Stent Length (mm) | Delivery System Length (cm) | CE Mark Indications |
|---|---|---|---|---|---|---|---|---|
| Abbott | Absolute Pro LL Peripheral Stent | Nitinol | 6 | 0.035 | 5–8 | 120, 150 | 80, 135 | Peripheral arteries as an adjunct to PTA and for the palliation of malignant strictures in the biliary tree |
| Abbott | Absolute Pro Peripheral Stent | Nitinol | 6 | 0.035 | 5–10 | 20, 30, 40, 60, 80, 100 | 80, 135 | Peripheral arteries as an adjunct to PTA and for the palliation of malignant strictures in the biliary tree |
| Abbott | Supera Peripheral Stent System | Interwoven nitinol wires | 6 | 0.018 | 4.5, 5, 5.5, 6, 6.5, 7, 7.5 | 20, 30, 40, 60, 80, 100, 120, 150, 180, 200 | 80, 120 | Peripheral vascular |
| Alvimedica | Easy Flype | Nitinol | 6 | 0.035 | 6–8 | 20–150 | 85, 135 | Peripheral |
| Alvimedica | Easy HiFlype | Nitinol | 6 | 0.035 | 9–12 | 20–100 | 85, 135 | Peripheral |
| amg International GmbH | ClaudEX Peripheral Self-Expandable Stent | Nitinol | 1.9 | 0.014 | 3.5, 4.5 | 15, 20, 25, 30, 35 | 200 | Intended for use in the treatment of peripheral artery obstruction or in cases of insufficient results after PTA (eg, residual stenosis or dissection due to arteriosclerotic plaque material or restenosis) |
| amg International GmbH | Facile Self-Expandable Stent System | Nitinol | 6 | 0.035 | 6–11 | 20, 40, 60, 80, 100, 120, 150 | 80, 120 | Peripheral arteries |
| amg International GmbH | Facile-pp Self-Expandable Stent System | Nitinol | 6 | 0.035 | 6–11 | 20, 40, 60, 80, 100, 120, 150, 175, 200 | 80, 120 | Peripheral arteries |
| Andramed GmbH | U-Flex Nitinol Stent | Nitinol | 5 | 0.018 | 5–10 | 15, 30, 40, 50, 60, 80, 100, 120, 150, 180, 200 | 80, 120 | Peripheral |
| Andramed GmbH | U-Flex Nitinol Stent | Nitinol | 6 | 0.035 | 5–10 | 20, 30, 40, 50, 60, 80, 100, 120, 150, 180, 200 | 80, 130 | Peripheral |
| Balton | Jaguar | Nitinol wire | 6, 7, 8 | 0.018, 0.035 | 4–14 | 15–150 | 80, 135 | Peripheral |
| BD Interventional | LifeStent Solo Vascular Stent System | Nitinol | 6 | 0.035 | 6, 7 | 200 | 80, 135 | Intended to improve luminal diameter in the treatment of symptomatic de novo or restenotic lesions in the native superficial femoral artery and proximal popliteal artery |
| BD Interventional | E-Luminexx Biliary Stent | Nitinol | 6 | 0.035 | 8, 10 | 40, 60, 80, 100 | 60 | Treatment of biliary strictures resulting from malignant neoplasms |
| BD Interventional | E-Luminexx Vascular Stent | Nitinol | 6 | 0.035 | 6, 7, 8, 9, 10, 12, 14 | 20, 30, 40, 50, 60, 80, 100, 120 | 80, 135 | Residual stenosis with impaired perfusion (pressure gradient) following balloon dilatation, especially in stages III and IV according to Fontaine; dissection; detached arteriosclerotic plaque material and luminal obstruction following balloon dilatation; occlusion after thrombolysis or after aspiration and before dilatation; restenosis or reocclusion |
| BD Interventional | LifeStar Vascular Stent System | Nitinol | 6 | 0.035 | 6, 7, 8, 9, 10, 12, 14 | 20, 30, 40, 50, 60, 80, 100, 120 | 80, 135 | Residual stenosis with impaired perfusion (pressure gradient) following balloon dilatation, especially in stages III and IV according to Fontaine; dissection; detached arteriosclerotic plaque material and luminal obstruction following balloon dilatation; occlusion after thrombolysis or after aspiration and before dilatation; restenosis or reocclusion |
| BD Interventional | LifeStent 5F Vascular Stent System | Nitinol | 5 | 0.035 | 5, 6, 7 | 20, 30, 40, 60, 80, 100, 120, 150, 170 (diameter dependent) | 80, 135 | Intended to improve luminal diameter in the treatment of symptomatic de novo or restenotic lesions in the native superficial femoral artery and popliteal artery |
| BD Interventional | LifeStent Vascular Stent System | Nitinol | 6 | 0.035 | 8, 9, 10, 12, 14 | 20, 30, 40, 60, 80 (diameter dependent) | 80, 130 | Intended for primary stenting of de novo or restenotic lesions of the peripheral arteries (20–170 mm); primary stenting of the SFA and/or the PPA (200 mm) |
| BD Interventional | LifeStent XL Vascular Stent System | Nitinol | 6 | 0.035 | 6, 7 | 200 | 80, 135 | Intended for primary stenting of de novo or restenotic lesions of the peripheral arteries (20–170 mm); primary stenting of the SFA and/or the PPA (200 mm) |
| Teleflex | Astron | Nitinol | 6 | 0.035 | 7, 8, 9, 10 | 30, 40, 60, 80 | 70, 120 | Iliac artery |
| Teleflex | Astron Pulsar | Nitinol | 4 | 0.018 | 4, 5, 6, 7 | 20, 30, 40, 60, 80 | 70–75, 120–135 | Femoral and infrapopliteal arteries |
| Teleflex | Pulsar-18 | Nitinol | 4 | 0.018 | 4, 5, 6, 7 | 20, 30, 40, 60, 80, 100, 120, 150, 170, 200 | 90, 135 | Femoral and infrapopliteal arteries |
| Teleflex | Pulsar-18 T3 | Nitinol | 4 | 0.018 | 4, 5, 6, 7 | 20, 30, 40, 60, 80, 100, 120, 150, 170, 200 | 90, 135 | Superficial femoral proximal popliteal and infrapopliteal arteries |
| Teleflex | Pulsar-35 | Nitinol | 6 | 0.035 | 5, 6, 7 | 30, 40, 60, 80, 100, 120, 150, 170, 200 | 90, 135 | Femoral and proximal popliteal arteries |
| Boston Scientific Corporation | Epic Self-Expanding Nitinol Vascular Stent | Nitinol | 6 | 0.035 | 6–10, 12 | 20, 30, 40, 50, 60, 70, 80, 100, 120 | 75, 120 | Iliac |
| Boston Scientific Corporation | Innova Self-Expanding Stent System | Nitinol | 6 | 0.035 (0.89 mm) | 5–8 | 20, 40, 60, 80, 100, 120, 150, 180, 200 | 75, 130 | SFA, proximal popliteal |
| Boston Scientific Corporation | Wallstent Endoprosthesis | Elgiloy | 6 (2 mm) | 0.035 (0.89 mm) | 6–10 | 18, 20, 23, 24, 34, 35, 36, 38, 39, 46, 47, 49, 52, 55, 59, 61, 66, 67, 69 | 75, 135 | Iliac |
| Boston Scientific Corporation | Wallstent Endoprosthesis | Elgiloy | 6 (2 mm)–12 (4 mm) | 0.035 (0.89 mm) | 5–8, 10, 12, 14, 16, 18, 20, 22, 24 | 20, 35, 40, 42, 45, 55, 60, 68, 70, 80, 90, 94 | 75, 135 (up to 12-mm diameter); 75 (≥ 14-mm diameter) | Tracheobronchial |
| Boston Scientific Corporation | Wallstent Endoprosthesis | Elgiloy | 6 (2 mm)–9 (3 mm) | 0.035 (0.89 mm) | 8, 10, 12 | 20, 40, 42, 60, 68, 80, 90, 94 | 75 | Transhepatic biliary |
| Boston Scientific Corporation | Wallstent Endoprosthesis | Elgiloy | 7 (2.33 mm)–9 (3 mm) | 0.035 (0.89 mm) | 10, 12 | 40, 42, 60, 68, 90, 94 | 75 | TIPS |
| Boston Scientific Corporation | Wallstent Endoprosthesis | Elgiloy | 6 (2 mm)–10 (3.33 mm) | 0.035 (0.89 mm) | 10, 12, 14, 16 | 20, 40, 42, 60, 68, 90, 94 | 75 | Central venous |
| Cook Medical | Zilver 518 Vascular Self-Expanding Stent | Nitinol | 5 | 0.018 | 4–10 | 4 mm: 20, 40, 80 mm; 5–9 mm: 40, 60, 80 mm; 10 mm: 40, 60 mm | 80, 125 | Iliac arteries |
| Cook Medical | Zilver 635 Biliary Self-Expanding Stent | Nitinol | 6 | 0.035 | 6, 8, 9, 10, 12 | 40, 60, 80, 100, 120 | 40, 135 | Yes |
| Cook Medical | Zilver 635 Vascular Self-Expanding Stent | Nitinol | 6 | 0.035 | 12, 14 | 12 mm: 40, 60, 80 mm; 14 mm: 40, 60, 80 mm | 80, 125 | Iliac arteries |
| Cook Medical | Zilver Flex Vascular Self-Expanding Stent | Nitinol | 6 | 0.035 | 5–10 | 20, 30, 40, 60, 80, 100, 120, 140; 170, 200 (only available in diameters 5, 6, 7, 8 mm) | 80, 125 | Iliac and above-the-knee femoropopliteal arteries |
| Cordis | Precise Pro RX | Nitinol | 5 (5–8-mm diameter), 6 (9–10-mm diameter) | 0.014 | 5–10 | 20, 30, 40 | 135 | Carotid |
| Cordis | SMART Control | Nitinol | 6 | 0.035 | 6–10, 12, 14 | 20, 30, 40, 60, 80, 100 | 80, 120 | Vascular |
| Cordis | SMART Flex | Nitinol | 6 | 0.035 | 5–8 | 30, 40, 60, 80, 100, 120, 150, 200 | 80, 120 | SFA, proximal popliteal |
| eucatech AG | Resistant | Nitinol | – | 0.035 | 4, 5, 6, 7, 8, 9, 10, 12 | 20, 30, 40, 60, 80, 100 | 85, 135 | Treatment of SFA and popliteal artery stenosis |
| eucatech AG | Resistant Camouflage | Nitinol with camouflage nanocoating | – | 0.035 | 5, 6, 7, 8 | 40, 60, 80, 100 | 135 | Treatment of stenosis of peripheral vessels |
| iVascular | iVolution pro | Nitinol | 6 | 0.035 | 5, 6, 7, 8, 9, 10 | 40, 60, 80, 100, 150, 200 | 80, 130 | Treatment of de novo or restenotic atherosclerotic lesions of peripheral arteries below the iliac crest (ie, iliac, femoral and popliteal arteries with nominal diameters between 4.5 and 9.5 mm) |
| Medtronic | EverFlex Self-Expanding Peripheral Stent With Entrust Delivery System | Nitinol | 5 | 0.035 | 5–8 | 20, 40, 60, 80, 100, 120, 150 | 80, 120, 150 | Peripheral |
| Medtronic | Protégé EverFlex Self-Expanding Stent System | Nitinol | 6 | 0.035 | 5–8 | 20, 30, 40, 60, 80, 100, 120, 150, 200 | 80, 120 | Peripheral |
| Medtronic | Protégé GPS Self-Expanding Stent System | Nitinol | 6 | 0.035 | 9, 10, 12 | 20, 30, 40, 60, 80 | 80, 120 | Iliac |
| Micro Medical Solutions | MicroStent | Nitinol | 4 | 0.014 | 3, 3.5, 4, 4.5 | 8, 15, 25, 40, 60 | 120 | Indicated for treatment of peripheral artery disease and critical limb ischemia |
| Natec Medical Ltd | Marina | Nitinol | 6 | 0.035 | 5–10 | 30–200 | 80, 130 | Peripheral and biliary |
| optimed Medizinische Instrumente GmbH | sinus-Repo-Visual 6F | Nitinol | 6 | 0.035 | 6–10, 12, 14 | 20, 30, 40, 60, 80, 100 | 75, 120 | Peripheral arteries |
| optimed Medizinische Instrumente GmbH | sinus-SuperFlex-535 | Nitinol | 5 | 0.035 | 4–10 | 30, 40, 60, 80 | 75, 120 | Peripheral arteries, biliary |
| optimed Medizinische Instrumente GmbH | sinus-SuperFlex-635 | Nitinol | 6 | 0.035 | 6–10, 12 | 30, 40, 60, 80, 100, 120, 150 | 75, 120 | Peripheral arteries, biliary |
| optimed Medizinische Instrumente GmbH | sinus-SuperFlex-DS | Nitinol | 4 | 0.018 | 4–9 | 12, 15, 18, 20, 22, 24 | 85 | Ductal stenting |
| optimed Medizinische Instrumente GmbH | sinus-XL | Nitinol | 10 | 0.035 | 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36 | 30, 40, 60, 80, 100 | 100 | Aorta and vena cava |
| optimed Medizinische Instrumente GmbH | sinus-XL 6F | Nitinol | 6 | 0.035 | 14, 16 | 30, 40, 60, 80, 100 | 100 | Aorta and vena cava |
| optimed Medizinische Instrumente GmbH | sinus-XL Flex | Nitinol | 10 | 0.035 | 14, 16, 18, 20, 22, 24 | 40, 60, 80, 100, 120, 150, 160 | 100 | Aorta, vena cava, and symptomatic obstructions of iliofemoral veins |
| optimed Medizinische Instrumente GmbH | Tentos 4F | Nitinol | 4 | 0.018 | 3–8 | 20, 30, 40, 60, 80, 100, 120, 150, 170 | 85, 135 | Femoral and infrapopliteal arteries |
| Q3 Medical Group | Peripheral Vascular Self-Expanding Stent System (PS) | Nitinol | 6 | 0.035 | 6–11 | 20, 40, 60, 80, 100, 120, 150 | 80, 120 | Peripheral arteries |
| Q3 Medical Group | Peripheral Vascular Self-Expanding Stent System (PSpp) | Nitinol | 6 | 0.035 | 6–11 | 20, 40, 60, 80, 100, 120, 150, 175, 200 | 80, 120 | Peripheral arteries |
| Q3 Medical Group | Self-Expandable Stent (BTK) | Nitinol | 1.9 | 0.014 | 3.5, 4.5 | 15, 20, 25, 30, 35 | 200 | Intended for use in the treatment of peripheral artery obstruction or in cases of insufficient results after PTA (eg, residual stenosis or dissection due to arteriosclerotic plaque material or restenosis) |
| Rontis AG | Zeus SX | Nickel titanium alloy (nitinol) | 6 | 0.035 | 6, 7, 8, 9, 10, 11 | 20, 40, 60, 80, 100, 120, 150 | 80, 120 | Peripheral arteries |
| Veryan Medical | BioMimics 3D Self-Expanding Stent System | Nitinol | 6 | 0.035 | 5, 6, 7 | 60, 80, 100, 125, 150 | 113 | SFA, proximal popliteal |
Stents / Self-Expanding Stent Grafts
View Chart| Company Name | Product Name | Materials Used | Introducer Size (F) | Guidewire Compatibility (inch) | Stent Diameter (mm) | Stent Length (mm) | Delivery System Length (cm) | CE Mark Indications | Comments |
|---|---|---|---|---|---|---|---|---|---|
| BD Interventional | Covera Plus Vascular Covered Stent | Nitinol | 8, 9 | 0.035 | 6, 7, 8, 9, 10 | 30, 40, 60, 80, 100 | 80, 120 | Indicated for the treatment of stenoses in the upper extremity venous outflow of patients dialyzing with an AV access graft or fistula and for the treatment of atherosclerotic lesions in iliac and femoral arteries with a reference vessel diameter of 4.5–9 mm | – |
| BD Interventional | Covera Vascular Covered Stent | Nitinol, ePTFE-covered stent | 8, 9 | 0.035 | 6, 7, 8, 9,10 | 30, 40, 60, 80, 100 | 80, 120 | Indicated for use in hemodialysis patients for the treatment of stenoses in the venous outflow of an arterio-venous (AV) fistula and at the venous anastomosis of an ePTFE or other synthetic AV graft | – |
| BD Interventional | Fluency Plus Endovascular Stent Graft | Nitinol/ePTFE | 8, 9, 10 | 0.035 | 5, 6, 7, 8, 9, 10, 12, 13.5 | 20, 30, 40, 60, 80, 100, 120 | 80, 117 | Residual stenosis with impaired perfusion (pressure gradient) after balloon dilatation, especially in stages III and IV according to Fontaine; dissection; detached arteriosclerotic plaque material and luminal obstruction after balloon dilatation; occlusion after thrombolysis or after aspiration and before dilatation; restenosis or reocclusion | – |
| Boston Scientific Corporation | Wallgraft Endoprosthesis With Unistep Plus Delivery System | Superalloy wire/polyethylene terephthalate graft material | 9–12 | 0.035 | 6–10, 12, 14 | 20, 30, 50, 70 | – | Indicated for use for treatment of complex iliac artery stenoses (lesions ≥ 3 cm in length or calcified or eccentric lesions < 3 cm in length) and iliac occlusions in vessels 7–12 mm in diameter; the exclusion of atherosclerotic arterial aneurysms and traumatic vessel disruptions in peripheral vessels 5–12 mm in diameter | – |
| Gore & Associates | Gore Viabahn Endoprosthesis With Propaten Bioactive Surface | Nitinol/ePTFE, gold | 6–10 | 0.018/0.014 (5–8 mm), 0.035 (5–13 mm) | 5, 6, 7, 8, 9, 10, 11, 13 | 25, 50, 75, 100, 150, 250 | 75 (0.035-inch system only), 120 | Indicated for the treatment of de novo or restenotic lesions in the iliac arteries; de novo or restenotic lesions in the superficial femoral artery and proximal popliteal artery; in-stent restenotic lesions in the superficial femoral artery and proximal popliteal artery; stenosis or thrombotic occlusion at the venous anastomosis of synthetic arteriovenous (AV) access grafts and in the venous outflow of dialysis access circuits, including the central veins; popliteal artery aneurysms and isolated visceral artery aneurysms; traumatic or iatrogenic vessel injuries in arteries that are located in the chest cavity, abdominal cavity, or pelvis (except for aorta, coronary, innominate, carotid, vertebral, and pulmonary arteries) | – |
| Gore & Associates | Gore Viabil Biliary Endoprosthesis | Nitinol/ePTFE | 8.5 (endoscopic), 10 (percutaneous) | 0.035 | 8, 10 | 40, 60, 80, 100 | 40 (percutaneous), 200 (endoscopic) | Benign* and malignant biliary strictures† | *Devices without transmural drainage holes; †Contraindicated for all cardiovascular applications |
| Gore & Associates | Gore Viatorr TIPS Endoprosthesis With Controlled Expansion | Nitinol/ePTFE | 10 | ≤ 0.035 | 8–10 | 60, 70, 80, 90, 100 | 75 | Indicated for use in the treatment of portal hypertension and its complications such as variceal bleeding and refractory ascites | TIPS, transjugular intrahepatic portosystemic shunt |
| Merit Medical Systems, Inc. | Merit Wrapsody Cell-Impermeable Endoprosthesis | Nitinol, ePTFE, PTFE | 8, 9, 10, 11, 12, 14 | 0.035 | 6, 7, 8, 9, 10, 12, 14, 16 | 30, 40, 50, 60, 70, 75, 80, 100, 125 | 80, 120 | Flexible self-expanding endoprosthesis indicated for use in hemodialysis patients for the treatment of stenosis or occlusion within the dialysis outflow circuit of an arteriovenous (AV) fistula or AV graft | The 6-10-mm-diameter stents come in lengths of 50, 75, 100, and 125 mm; the 12-, 14-, and 16-mm-diameter stents come in lengths of 30, 40, 50, 60, 70, and 80 mm |
| Scitech Medical | Solaris | Nitinol/PTFE | 9 | 0.035 | 6–9 | 40, 60, 80 | 130 | In the treatment of in-stent restenosis in the venous outflow of hemodialysis patients dialyzing by either an arteriovenous (AV) fistula or AV graft; in the treatment of stenosis in the venous outflow of hemodialysis patients dialyzing by an AV graft; restenosis or reocclusion (except vessels on the central circulatory system and central nervous system); dissection (except vessels on the central circulatory system and central nervous system); residual stenosis with impaired perfusion (pressure gradient) following balloon dilatation, especially in stages III and IV according to Fontaine (except vessels on the central circulatory system and central nervous system); detached arteriosclerotic plaque material and luminal obstruction following balloon dilatation (except vessels on the central circulatory system and central nervous system); occlusion after thrombolysis or after aspiration and before dilatation (except vessels on the central circulatory system and central nervous system) | Precise deployment, high flexibility, minimal shortening, balanced radial strength |
Stents / Venous Stents
View Chart| Company Name | Product Name | Stent Material | Cell Design | Introducer Size (F) | Guidewire Compatibility (inch) | Stent Diameter (mm) | Stent Length (mm) | Delivery System | Delivery System Length (cm) |
|---|---|---|---|---|---|---|---|---|---|
| BD Interventional | Venovo Venous Stent System | Nitinol | Open-cell | 8, 9, 10 | 0.035 | 10, 12, 14, 16, 18, 20 | 40, 60, 80, 100, 120, 140, 160 | Triaxial, thumbwheel | 80, 120 |
| Boston Scientific Corporation | Vici | Nitinol | Closed-cell | 9 | 0.035 | 12, 14, 16 | 60, 90, 120 | Coaxial | 100 |
| Boston Scientific Corporation | Wallstent-Uni Endoprosthesis (Iliac-Vein Indication) | Elgiloy | Closed-cell | 7-10 | 0.035 | 10, 12, 14, 16, 18, 20 | 40, 60, 90 | Unistep Plus | 75, 135 |
| Cook Medical | Zilver Vena Venous Self-Expanding Stent | Nitinol | Open-cell | 7 | 0.035 | 14, 16 | 60, 100, 140 | Pin and pull | 80, 120 |
| Medtronic | Abre Venous Self-Expanding Stent System | Nitinol | Open-cell | 9 | 0.035 | 10, 12, 14, 16, 18, 20 | 40, 60, 80, 100, 120, 150 | Triaxial, thumbwheel | 90 |
| optimed Medizinische Instrumente GmbH | sinus-Obliquus | Nitinol | Hybrid | 10 | 0.035 | 14, 16, 18 | 80, 100, 150 | Pin-pull | 100 |
| optimed Medizinische Instrumente GmbH | sinus-Venous | Nitinol | Hybrid | 10 | 0.035 | 10, 12, 14, 16, 18 | 60, 80, 100, 120, 150 | Pin-pull | 100 |
| optimed Medizinische Instrumente GmbH | sinus-XL | Nitinol | Closed-cell | 10 | 0.035 | 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36 | 30, 40, 60, 80, 100 | Pin-pull | 100 |
| optimed Medizinische Instrumente GmbH | sinus-XL Flex | Nitinol | Open-cell | 10 | 0.035 | 14, 16, 18, 20, 22, 24 | 40, 60, 80, 100, 120, 150, 160 | Pin-pull | 100 |
| Bentley InnoMed GmbH | BeYond venous | Nickel-titanium alloy (nitinol) | Open cell design; closed cell stent ends | 10 | 0.035 | 10–18 | 60–150 | Pull-back technique; radiopaque marker on catheter tip | 100 |
| optimed Medizinische Instrumente GmbH | sinus-XL 6F | Nitinol | Closed cell | 6 | 0.035 | 14, 16 | 30, 40, 60, 80, 100 | Pin pull | 100 |
Wires / Coiled Stainless Steel Guidewires
View Chart| Company Name | Product Name | Type | Diameter (inch) | Length (cm) | Tip Type | Antithrombogenic | Comments |
|---|---|---|---|---|---|---|---|
| Abbott | .035 LOC Guide Wire Extension | – | 0.035 | 115 | – | PTFE | – |
| Abbott | GuideRight | J-tip: fixed core | 0.021, 0.028, 0.030 | 150 | 3-mm J | PTFE coated | – |
| Abbott | GuideRight | J-tip: fixed core | 0.065 | 150 | 6-mm J | PTFE coated | – |
| Abbott | GuideRight | J-tip: movable core; double distal: fixed core | 0.035, 0.038 | 150 | 3-mm J | PTFE coated | – |
| Abbott | GuideRight | Straight: movable core | 0.035, 0.038 | 150 | Straight | PTFE coated | – |
| Abbott | GuideRight | Super stiff: fixed core | 0.032 | 180 | 3-mm J | PTFE coated | – |
| Abbott | GuideRight | Super stiff: fixed core | 0.038 | 180, 260 | Straight | PTFE coated | – |
| Abbott | GuideRight | Heparin coated: fixed core | 0.035 | 150, 180, 260 | J or straight | Heparin coated | – |
| Abbott | GuideRight | Heparin coated: fixed core | 0.038 | 150 | J or straight | Heparin coated | – |
| Abbott | GuideRight | Heparin coated: movable core | 0.035, 0.038 | 150 | 3-mm J | Heparin coated | – |
| Abbott | GuideRight | Steerable | 0.035 | 150 | Modified J or straight | PTFE coated | – |
| Abbott | GuideRight | TigerWire: steerable | 0.035 | 150 | Straight or angled | PTFE coated | – |
| Abbott | GuideRight | TigerWire: steerable | 0.035 | 180, 260, 300 | Angled | PTFE coated | – |
| Abbott | GuideRight | Introducer | 0.021 | 50 | DDS | PTFE coated | – |
| Abbott | GuideRight | Introducer | 0.038 | 80 | 3-mm J | PTFE coated | – |
| Abbott | GuideRight | Introducer | 0.025, 0.032, 0.035, 0.038 | 50 | DDJ: 3-mm J | PTFE coated | – |
| Abbott | GuideRight | Straight: fixed core | 0.035, 0.038 | 150, 260 | Straight | PTFE coated | – |
| Abbott | GuideRight | Straight: fixed core | 0.021, 0.025, 0.032 | 150 | Straight | PTFE coated | – |
| Abbott | GuideRight | J-tip: fixed core | 0.025 | 150, 180, 260 | 3-mm J | PTFE coated | – |
| Abbott | GuideRight | J-tip: fixed core | 0.032 | 150, 260 | 3-mm J | PTFE coated | – |
| Abbott | GuideRight | J-tip: fixed core | 0.035, 0.038 | 150, 180, 260 | 1.5-, 3-, 6-, 15-mm J | PTFE coated | – |
| Abbott | Hi-Torque Spartacore 14 Guide Wire | Core to tip | 0.014 | 130, 190, 300 | – | PTFE | – |
| Abbott | Hi-Torque Steelcore 18 Guide Wire | Core to tip | 0.018 | 190, 300 | Straight | PTFE | – |
| Abbott | Hi-Torque Steelcore 18 LT Guide Wire | Core to tip | 0.018 | 190, 300 | J-curved, straight | PTFE | – |
| Abbott | Hi-Torque Supra Core 35 Guide Wire | Core to tip | 0.035 | 145, 190, 300 | Straight | PTFE | – |
| Abbott | Hi-Torque Versacore Guide Wire | Core to tip | 0.035 | 145, 175, 260, 300 | Modified J, standard, floppy | PTFE | – |
| Abbott | HT Command | Hybrid stainless steel and nitinol | 0.014 | 190, 250, 300 | Shapeable/reshapeable nitinol | – | – |
| Abbott | HT Command 018 LT (long tapper) | Hybrid stainless steel and nitinol | 0.018 | 210, 300 | Shapeable/reshapeable nitinol | – | – |
| Abbott | HT Command 018 ST (short tapper) | Hybrid stainless steel and nitinol | 0.018 | 210, 300 | Shapeable/reshapeable nitinol | – | – |
| Abbott | HT Command ES | Hybrid stainless steel and nitinol | 0.014 | 190, 250, 300 | Shapeable/reshapeable nitinol | – | – |
| Abbott (distributed by OrbusNeich) | ViperWire Advance Guide Wire | Stainless-steel core | 0.014/0.014 tip, 0.014/0.017 tip | 335 | Straight | No | Designed specifically for use with CSI orbital atherectomy devices |
| Abbott (distributed by OrbusNeich) | ViperWire Advance Guide Wire With Flex Tip | Stainless-steel core | 0.014/0.014 tip, 0.014/0.018 tip | 335 | Straight with nitinol support coil | No | Designed specifically for use with CSI orbital atherectomy devices |
| AndraTec GmbH Germany | Lokum Amplatz Stiff | Fixed core | 0.035 | 180, 260, 320, 360 | 5-cm flexible tip, straight, 3-mm J, 6-mm | PTFE coated | – |
| AndraTec GmbH Germany | Lokum L-Quest Extra Stiff Type Guide Wire | Fixed core | 0.035 | 90, 150, 180, 260 | 5-, 10-, 15-cm flexible tip, straight, 3-mm J, 6-mm | PTFE coated | – |
| AndraTec GmbH Germany | Lokum L-Quest Extra Stiff Type Guide Wire | Extra stiff type stainless steel guidewire PTFE coated | 0.025, 0.035 | 90–260 | Straight, 3-, 6-mm J-tip | High performance PTFE coating | – |
| Argon Medical Devices, Inc. | Amplatz 3 mm J Curve | Amplatz | 0.035 | 90, 150 | Soft tip | – | – |
| Argon Medical Devices, Inc. | Amplatz Straight | Amplatz | 0.035 | 80, 90, 150, 180, 260 | Soft tip | – | – |
| Argon Medical Devices, Inc. | Bentson PTFE-Coated Guide Wire | Fixed core | 0.035, 0.038 | 150, 180, 260 | Straight | PTFE | – |
| Argon Medical Devices, Inc. | Nitinol Mandrel Wires for Micro-Puncture Technique | Straight | 0.018 | 80 | – | – | – |
| Argon Medical Devices, Inc. | PTFE-Coated Exchange Wire J-Tip | Fixed core | 0.025, 0.035 | 200, 260 | 3-mm J | PTFE | – |
| Argon Medical Devices, Inc. | PTFE-Coated Exchange Wire Straight | Fixed core | 0.025, 0.035, 0.038 | 260 | Straight | PTFE | – |
| Argon Medical Devices, Inc. | PTFE-Coated Guide Wire Double Ended J-Tip | Fixed core | 0.035 | 50, 150 | Double-ended J tip | PTFE | – |
| Argon Medical Devices, Inc. | PTFE-Coated Guide Wire J-Tip | Movable core | 0.032, 0.035, 0.038 | 145, 150 | J tip | PTFE | – |
| Argon Medical Devices, Inc. | PTFE-Coated Guide Wire J-Tip | Fixed core | 0.021, 0.025, 0.032, 0.035, 0.038 | 150, 175 | J tip | PTFE | – |
| Argon Medical Devices, Inc. | PTFE-Coated Guide Wire Straight | Fixed core | 0.025, 0.035, 0.038 | 150 | Straight | PTFE | – |
| Argon Medical Devices, Inc. | Stainless Steel Guide Wire Double Ended | Movable core | 0.025, 0.032, 0.035 | 45, 65, 80 | Double ended (straight and 3-mm J) | – | – |
| Argon Medical Devices, Inc. | Stainless Steel Guide Wire J-Tip | Fixed core | 0.021, 0.025, 0.035 | 40, 50, 75 | 3-mm J | – | – |
| Argon Medical Devices, Inc. | Stainless Steel Guide Wire Straight | Fixed core | 0.018, 0.021, 0.025, 0.035 | 25, 40, 75, 80, 100, 125, 150 | Straight | – | – |
| Argon Medical Devices, Inc. | Worker Standard Straight | Fixed core | 0.035, 0.038 | 80, 150, 180, 300, 400 | Soft tip | – | – |
| Argon Medical Devices, Inc. | Worker Standard With J Curve | Fixed core | 0.035, 0.038 | 80, 150, 180, 260 | Soft tip | – | – |
| Asahi Intecc Co Ltd. | Asahi Chikai | Stainless steel, Act One | 0.014 | 200, 300 | Straight, round curve | – | – |
| Asahi Intecc Co Ltd. | Asahi Chikai 008 | Stainless steel, Act One | 0.008 | 200 | Straight | – | – |
| Asahi Intecc Co Ltd. | Asahi Chikai 10 | Stainless steel, Act One | 0.010 | 200, 300 | Straight | – | – |
| Asahi Intecc Co Ltd. | Asahi Chikai X010 | Stainless steel, Act One | 0.010 | 200 | Round curve | – | – |
| Boston Scientific Corporation | Amplatz Super Stiff Guidewire | Delivery support/spring coil stainless steel | 0.035 (0.89 mm), 0.038 (0.97 mm) | 75, 145, 180, 260 | 3-mm J, straight, short taper | PTFE | – |
| Boston Scientific Corporation | Back-up Meier | Delivery support/spring coil stainless steel | 0.035 (0.89 mm) | 185, 300 | C-tip or J-tip styles | PTFE proximal coating | – |
| Boston Scientific Corporation | Platinum Plus Guidewire | Delivery support/spring coil stainless steel core | 0.014 (0.36 mm), 0.018 (0.46 mm), 0.025 (0.64 mm) | 145, 180, 260, 300 | Straight; long and short taper | Available with Mediglide silicone coating or Glidex hydrophilic coating | – |
| Boston Scientific Corporation | Starter Bentson | Access guidewire: fixed core | 0.035, 0.038 | 150, 180, 260 | Straight | PTFE proximal coating and two options: heparin or nonheparin distal coating | – |
| Boston Scientific Corporation | Starter J-Curve | Access guidewire: fixed core | 0.025, 0.035, 0.038 | 80, 125, 150, 180, 260 | J-tip | PTFE proximal coating and two options: heparin or nonheparin distal coating | – |
| Boston Scientific Corporation | Starter J-Curve | Access guidewire: movable core | 0.035, 0.038 | 125, 150, 260 | J-tip | PTFE proximal coating and two options: heparin or nonheparin distal coating | – |
| Boston Scientific Corporation | Starter Newton | Access guidewire: fixed core | 0.035, 0.038 | 150 | Straight, J-tip | PTFE proximal coating and two options: heparin or nonheparin distal coating | – |
| Boston Scientific Corporation | Starter Rosen | Access guidewire: fixed core | 0.035, 0.038 | 150, 180, 260 | J-tip | PTFE proximal coating and two options: heparin or nonheparin distal coating | – |
| Boston Scientific Corporation | Starter Straight | Access guidewire: movable core | 0.035, 0.038 | 150 | Straight | PTFE proximal coating and two options: heparin or nonheparin distal coating | – |
| Boston Scientific Corporation | Starter Straight | Access guidewire: fixed core | 0.025, 0.035, 0.038 | 80, 150, 260 | Straight | PTFE proximal coating and two options: heparin or nonheparin distal coating | – |
| Boston Scientific Corporation | Thruway | Navigating (access and crossing)/spring coil stainless steel | 0.014 (0.36 mm), 0.018 (0.46 mm) | 130, 190, 300 | J-tip, straight, short, long, and extra-long taper | Silicone and PTFE proximal coating | – |
| Cook Medical | Amplatz Extra Stiff | Fixed core | 0.025, 0.032, 0.035 | 80, 145, 180, 260, 300 | J-curved (3 mm), or straight, and short or long floppy tip | PTFE coating | – |
| Cook Medical | Amplatz Stiff | Fixed core | 0.035 | 145, 180, 260 | Straight | PTFE coating | – |
| Cook Medical | Amplatz Ultra Stiff | Fixed core | 0.035 | 60, 90, 145, 180, 260 | J-curved (3 mm) or straight, and short or long floppy tip | PTFE coating | – |
| Cook Medical | Classic Bentson | Fixed core | 0.018, 0.025, 0.035 | 145, 100, 180, 260 | Straight or J-curve (1.5 or 3 mm), with 6-cm floppy tip | PTFE coating | – |
| Cook Medical | Classic Double Flexible Tip | Fixed core | 0.018, 0.025, 0.035, 0.038 | 50, 60, 110, 145, 180 | Both J-curved (2 or 3 mm) and straight | PTFE coating or no coating | – |
| Cook Medical | Classic Fixed Core | Fixed core | 0.018, 0.021, 0.025, 0.032, 0.035, 0.038 | 50, 80, 145, 180, 220, 260 | J-curved (3 or 15 mm) or straight | PTFE coating | – |
| Cook Medical | Classic Movable Core | Movable core | 0.035, 0.038 | 145, 180 | J-curved (1.5 or 3 mm) or straight | PTFE coating | – |
| Cook Medical | Classic Newton | Fixed core | 0.035 | 145 | J-curve (15 mm) or straight, and 10 or 15 cm taper | PTFE coating | – |
| Cook Medical | Classic Rosen | Fixed core | 0.035 | 145, 180, 260 | J-curved (1.5 mm) | PTFE coating | – |
| Cook Medical | Lunderquist | Mandril | 0.035 | 90, 145, 180, 260, 300 | J-curved (3 or 7 mm), double curved, extra long double curved, or straight | PTFE coating | – |
| Cordis | Emerald | Fixed and movable core | 0.018, 0.021, 0.025, 0.032, 0.035, 0.038, 0.065 | 80, 125, 150, 175, 180, 220, 260 | Wide variety | – | – |
| Galt | Specialty Wires | Mandril | 0.008, 0.010, 0.014, 0.018 | 20, 40, 45, 60, 65, 80, 130 | Straight, angled | – | Available in stainless/stainless, nitinol/stainless, and nitinol/gold; featuring reference markers, angled tips, flexible tips |
| Medcomp | Spring Coiled Wires | Floppy tip guidewire | 0.035 | 150 | Floppy tip | – | PTFE coating |
| Medcomp | Spring Coiled Wires | Straight tip guidewire | 0.035 | 70 | Straight tip | – | – |
| Medcomp | Spring Coiled Wires | J/flex tip guidewire | 0.035 | 150 | J/flex tip | – | PTFE coating |
| Medcomp | Spring Coiled Wires | J/flex tip guidewire | 0.038 | 70 | J/flex tip | – | – |
| Medcomp | Spring Coiled Wires | J/flex tip guidewire | 0.035 | 45, 70 | J/flex tip | – | – |
| Medcomp | Spring Coiled Wires | Straight tip guidewire | 0.038 | 70 | Straight tip | – | – |
| Medcomp | Spring Coiled Wires | Straight tip guidewire | 0.038 | 120 | Straight tip | – | PTFE coating |
| Medtronic | Wholey Guidewire System | Stainless steel core, shapeable, optional extension system connector | 0.035 | 145, 175, 260, 300 | Modified J, shapeable | Hydrophobic green PTFE-coated coil | – |
| Medtronic | Wholey Guidewire System | Stainless steel core, shapeable, optional extension system connector | 0.035 | 145, 155, 175, 260, 300 | Straight, shapeable | Hydrophobic green PTFE-coated coil | – |
| Merit Medical Systems, Inc. | InQwire PTFE Coated | J-tip fixed core, straight-tip fixed core, J-tip movable core, straight-tip movable core | 0.014, 0.018, 0.021, 0.025, 0.035, 0.038 | 80, 150, 180, 260 | Straight; Bentson 23-cm flex, Bentson 15 cm, Bentson short taper 10-cm flex; Newton LT, LLT, LLLT flex tips; super stiff straight tip; Rosen/1.5 mm; 1.5-, 3-, 6-, 15-mm J; double-flex ended; exchange 260-cm straight and J-tip | PTFE coating with and without heparin coating | – |
| Merit Medical Systems, Inc. | Prelude Sheath Wire | Stainless steel coils or plastic jacketed | 0.018, 0.021, 0.025, 0.035, 0.038 | 45, 50, 80 | Straight, angled, or double ended (3-mm J; floppy) | – | – |
| optimed Medizinische Instrumente GmbH | PTFE-Coated Guidewires | Amplatz | 0.035 | 180, 260 | Straight, J-curved | PTFE | – |
| optimed Medizinische Instrumente GmbH | PTFE-Coated Guidewires | Double ended | 0.035 | 150 | 3-mm J-curved | PTFE | – |
| optimed Medizinische Instrumente GmbH | PTFE-Coated Guidewires | Movable core | 0.035 | 150 | Straight | PTFE | – |
| optimed Medizinische Instrumente GmbH | PTFE-Coated Guidewires | Fixed core | 0.035 | 150, 180, 260 | Straight, 1.5-mm J-curved, 3-mm J-curved | PTFE | – |
| optimed Medizinische Instrumente GmbH | PTFE-Coated Guidewires | Heavy duty | 0.035 | 150 | Straight | PTFE | – |
Wires / Hydrophilic Guidewires
View Chart| Company Name | Product Name | Type | Diameter (inch) | Length (cm) | Tip Type |
|---|---|---|---|---|---|
| Abbott | Hi-Torque Command | Hybrid stainless steel and nitinol | 0.014 | 190, 300 | Shapeable tip |
| Abbott | Hi-Torque Command ES | Hybrid stainless steel and nitinol | 0.014 | 190, 300 | Shapeable tip |
| Abbott | HT Command 018 LT (long tapper) | Hybrid stainless steel and nitinol | 0.018 | 210, 300 | Shapeable/reshapeable nitinol |
| Abbott | HT Command 018 ST (short tapper) | Hybrid stainless steel and nitinol | 0.018 | 210, 300 | Shapeable/reshapeable nitinol |
| Abbott | HydroSteer | Nitinol | 0.035, 0.038 | 150, 180, 260 | Angled, straight, J-tip |
| Abbott | HydroSteer | Nitinol | 0.018 | 150, 180 | Angled, straight |
| Asahi Intecc Co Ltd. | Asahi Chikai black | Stainless steel, Act One | 0.014 | 200 | 25°, 90° |
| Asahi Intecc Co Ltd. | Asahi Chikai black 14 soft tip | Stainless steel, Act One | 0.014 | 200 | 25° |
| Asahi Intecc Co Ltd. | Asahi Chikai black 18 | Stainless steel, Act One | 0.018/0.014 reverse tapered | 200 | 25° |
| Asahi Intecc Co Ltd. | Asahi Chikai black 18 soft tip | Stainless steel, Act One | 0.018/0.014 | 200 | 25° |
| Asahi Intecc Co Ltd. | Asahi Gladius | Stainless steel, Act One | 0.014, 0.018 | 200, 235, 300 | Straight, 1 mm preshaped |
| Asahi Intecc Co Ltd. | Asahi Meister 16 | Stainless steel, Act One | 0.016 | 165, 180 | 45°, double angle, round curve |
| Balton | Enter | Nitinol core, polymer coated | 0.025, 0.032, 0.035, 0.038 | 150–260 | Straight, 45° angle |
| Boston Scientific Corporation | Fathom-14 Guidewire | Hybrid stainless steel and nitinol | 0.014 (0.36 mm) | 200, 300 | 10 cm with 2-cm shapeable or angled tip |
| Boston Scientific Corporation | Fathom-16 Guidewire | Hybrid stainless steel and nitinol | 0.016 (0.41 mm) | 140, 180 | 10, 20 cm with 2-cm shapeable tip |
| Boston Scientific Corporation | Transend-14 Steerable Guidewire | Hydrophilic coating with scitanium core | 0.014 (0.36 mm) | 135, 165, 190 | 2-cm shapeable tip |
| Boston Scientific Corporation | Transend-18 Steerable Guidewire | Hydrophilic coating with scitanium core | 0.018 (0.46 mm) | 135, 165 | 2-cm shapeable tip |
| Boston Scientific Corporation | ZIPwire | Hydrophilic coating (full length), nitinol core | 0.018 (0.46 mm), 0.035 (0.89 mm), 0.038 (0.97 mm) | 80, 150, 180, 260 | Straight, angled, J-tip, and long-taper for accessing and navigating various anatomies |
| BrosMed Medical | Conger | Nitinol core | 0.025, 0.032, 0.035, 0.038 | 45, 80, 150, 180, 230, 260 | Straight, angled |
| Cerenovus | Agility 10 Steerable Guidewire | Stainless steel with hydrophilic coating | 0.010 | 195 | Shapeable tip |
| Cerenovus | Agility 14 Steerable Guidewire | Stainless steel with hydrophilic coating | 0.014 | 205, 350 | Shapeable tip |
| Cerenovus | Agility 16 Steerable Guidewire | Stainless steel with hydrophilic coating | 0.016 | 175, 205 | Shapeable tip |
| Cerenovus | Neuroscout 14 Steerable Guidewire | Stainless steel with hydrophilic coating | 0.014 | 205, 300 | Shapeable tip |
| Cook Medical | Roadrunner PC | Nitinol core with platinum coils, polyurethane jacket | 0.035, 0.038 | 80, 145, 180, 260 | Angled |
| Cook Medical | Roadrunner UniGlide | Nitinol core, polyurethane jacket | 0.018, 0.035, 0.038 | 80, 150, 180, 260, 320 | Straight, angled |
| Medcomp | Coated Mandrel Guidewires | Straight with hydrophilic coating | 0.010 | 60, 80 | Platinum coil tip |
| Medcomp | Coated Mandrel Guidewires | Straight with hydrophilic coating | 0.018 | 70, 80, 130 | Radiopaque tip |
| Medtronic | Cougar LS | Nitinol | 0.014 | 190, 300 | J-curved, straight |
| Medtronic | Cougar XT | Nitinol | 0.014 | 190, 300 | J-curved, straight |
| Medtronic | Intuition | Stainless steel | 0.014 | 180, 300 | Straight |
| Medtronic | Kitewire Deep | Polymer | 0.014 | 195, 250, 300 | Straight, shapeable |
| Medtronic | ProVia 12 | Stainless steel | 0.014 | 180, 300 | Straight with a tapered distal tip of 0.009 inch |
| Medtronic | ProVia 3 | Stainless steel | 0.014 | 180, 300 | Straight |
| Medtronic | ProVia 6 | Stainless steel | 0.014 | 180, 300 | Straight |
| Medtronic | ProVia 9 | Stainless steel | 0.014 | 180, 300 | Straight with a tapered distal tip of 0.009 inch |
| Medtronic | Zinger Light | Stainless steel | 0.014 | 180, 300 | J-curved, straight |
| Medtronic | Zinger Marker | Stainless steel | 0.014 | 180, 300 | J-curved, straight |
| Medtronic | Zinger Medium | Stainless steel | 0.014 | 180, 300 | J-curved, straight |
| Medtronic | Zinger Support | Stainless steel | 0.014 | 190, 300 | J-curved, straight |
| Merit Medical Systems, Inc. | Splash Hydrophilic Coated Guide Wire | Nitinol | 0.018, 0.025, 0.035, 0.038 | 80, 150, 180, 220, 260 | Straight, angled, and straight long taper; tip flexibility 5 cm; available in standard and stiff configurations |
| Merit Medical Systems, Inc. | True Form Reshapable Guide Wire | Stainless steel | 0.014 | 145, 165, 180 | Straight, angled |
| Terumo Neuro | Glidewire Gold Neuro Guidewire | Hydrophilic nitinol guidewire | 0.011, 0.014, 0.016, 0.018 | 180 | 45°, 70° angle |
| Terumo Neuro | Headliner Guidewire | Hydrophilic nitinol guidewire | 0.016 | 200 | 1.5-mm J tip, 90° angle, 90°/150° double angle |
| Terumo Neuro | Headliner Guidewire | Hydrophilic nitinol guidewire | 0.014 | 200 | 45°, 70° angle, STR (shapeable) |
| Terumo Neuro | Headliner Guidewire | Hydrophilic nitinol guidewire | 0.012 | 200 | 1.5-mm J tip, 45°, 90° angle, 90°/150° double angle |
| Terumo Neuro | Traxcess 14 | Soft | 0.014 | 200 | STR, shapeable |
| Terumo Neuro | Traxcess 14 EX | Support | 0.014 | 200 | STR, shapeable |
| Terumo Neuro | Traxcess 7 Mini | Soft | 0.007 | 210 | Soft |
| Terumo Neuro | Traxcess Docking Wire | Docking | 0.014 | 115 | – |
| Pediavascular | Spring Wire | Spring wire | 0.030 | 140 | Straight, J-tip |
| phenox GmbH | pORTAL Steerable Hydrophilic Guidewire | Steerable hydrophilic guidewire | 0.014 | 205 | Straight, shapeable |
| Rontis AG | Lotus II | Stainless steel core-to-tip, normal or extra support | 0.014 | 195, 300 | 30-mm radiopaque, straight (shapeable), J-curved |
| Rontis AG | Lotus XP | CTO stainless steel core-to-tip | 0.014 | 195, 300 | Domed tip or 0.005-inch wedged tip, 30-mm radiopaque, straight (shapeable) or J-curved |
| Stryker | Synchro 10 | Nitinol | 0.010 | 200, 300 | Shapeable |
| Stryker | Synchro 14 | Nitinol | 0.014 | 200, 300 | Shapeable |
| Stryker | Synchro Select Soft | Nitinol | 0.014 | 215, 300 | Shapeable, preshaped |
| Stryker | Synchro Select Standard | Nitinol | 0.014 | 215, 300 | Shapeable, preshaped |
| Stryker | Synchro Select Support | Nitinol | 0.014 | 215, 300 | Shapeable, preshaped |
| Stryker | Synchro2 Soft | Nitinol | 0.014 | 200, 300 | Shapeable, preshaped |
| Stryker | Synchro2 Standard | Nitinol | 0.014 | 200, 300 | Shapeable, preshaped |
| Stryker | Synchro2 Support | Nitinol | 0.014 | 215, 300 | Shapeable, preshaped |
| Stryker | Transend .010 | Stainless steel | 0.010 | 205 | Shapeable |
| Stryker | Transend 14 EX | Stainless steel | 0.014 | 182 | Shapeable |
| Stryker | Transend 14 Floppy | Stainless steel | 0.014 | 205 | Shapeable |
| Stryker | Transend 14 Platinum | Stainless steel with platinum coil tip | 0.014 | 205 | Shapeable |
| Stryker | Transend 14 Soft Tip | Stainless steel | 0.014 | 205 | Shapeable |
| Stryker | Transend 300 Extra Support | Stainless steel | 0.014 | 300 | Shapeable |
| Stryker | Transend 300 Floppy | Stainless steel | 0.014 | 300 | Shapeable |
| Terumo Europe | Radifocus Glidewire Advantage | Nitinol core with proximal PTFE and distal hydrophilic M COAT | 0.014, 0.018 | 180, 300 | Straight, 45° angle |
| Terumo Europe | Radifocus Glidewire Advantage | Nitinol core with proximal PTFE and distal hydrophilic M COAT | 0.035 | 180, 260 | Straight, 45° angle |
| Terumo Europe | Radifocus Glidewire Advantage Track | Proximal stainless steel with spiral PTFE; distal nitinol with hydrophilic M COAT | 0.014, 0.018 | 180, 300 | 35° angle |
| Terumo Europe | Radifocus Guide Wire GT | Gold coil | 0.012, 0.016 | 180, 200 | 45° angle, 90° angle X 4 mm, 1.5-mm J curve, double angulation 90° + 150° |
| Terumo Europe | Radifocus Guide Wire M | Stiff | 0.020, 0.025, 0.035, 0.038 | 80, 150, 180, 260, 300 | Straight, 45° angle |
| Terumo Europe | Radifocus Guide Wire M | Nonvascular type | 0.018, 0.020, 0.025, 0.032, 0.035, 0.038 | 80, 120, 150, 180, 260, 400, 450 | Straight, angled |
| Terumo Europe | Radifocus Guide Wire M | Half stiff | 0.035 | 180, 300 | 1.5–2, 3-mm J shape |
| Terumo Europe | Radifocus Guide Wire M | Standard | 0.018, 0.025, 0.032, 0.035, 0.038 | 50, 80, 120, 150, 180, 220, 260, 300 | Straight, 45° angle, 1.5-, 3-mm J shape, double angulation (Bolia curve) |
| Rapid Medical | Drivewire 24 Guidewire | Stainless steel with an inner nitinol braided flexible coil and hydrophilic coating on the distal segment of the wire | 0.024 | 202 | Steerable |
Wires / Mandril/Specialty Guidewires
View Chart| Company Name | Product Name | Type | Diameter (inch) | Length (cm) | Tip Type | Coating Type |
|---|---|---|---|---|---|---|
| Abbott | Hi-Torque Connect | Workhorse | 0.018 | 145, 195, 300 | Straight shapeable tip | Hydrophilic |
| Abbott | Hi-Torque Connect 250T | High tip load | 0.018 | 145, 195, 300 | Tapered | Hydrophilic |
| Abbott | Hi-Torque Connect Flex | Workhorse | 0.018 | 145, 195, 300 | Floppy | Hydrophilic |
| Abbott | Hi-Torque Proceed | High tip load | 0.014 | 190, 300 | Tapered and preshaped; unique micro textured tip | Distal hydrophilic, proximal hydrophobic |
| Abbott | Hi-Torque Winn 200 | High tip load | 0.014 | 190, 300 | Bare tapered | Hydrophilic |
| Abbott | Hi-Torque Winn 40 | Moderate tip load | 0.014 | 190, 300 | Bare tapered | Hydrophilic |
| Abbott | Hi-Torque Winn 80 | Moderate tip load | 0.014 | 190, 300 | Bare tapered | Hydrophilic |
| Argon Medical Devices, Inc. | Access Wires | Stainless steel and nitinol | 0.018 | 80 | Flexible, radiopaque tip | – |
| Argon Medical Devices, Inc. | Pointer Nitinol Guidewire | Flexible coil | 0.018 | 210, 260, 300 | Straight | Hydrophilic-coated radiopaque tip |
| Asahi Intecc Co Ltd. | Asahi Gaia PV | Stainless steel, Act One | 0.018 | 200, 235, 300 | Straight, 1-mm preshaped | Hydrophilic, uncoated tip |
| Asahi Intecc Co Ltd. | Asahi Gladius MG PV | Stainless steel, Act One | 0.014, 0.018 | 200, 300 | Straight, 1-mm preshaped | Polymer jacket, hydrophilic coating |
| Asahi Intecc Co Ltd. | Asahi Halberd | Stainless steel, Act One | 0.014, 0.018 | 200, 235, 300 | Straight, 1-mm preshaped | Hydrophilic, uncoated tip |
| Asahi Intecc Co Ltd. | Astato 30 | Stainless steel with hydrophilic coating | 0.018 tapered to 0.013 | 180, 300 | Straight | Hydrophilic |
| Asahi Intecc Co Ltd. | Astato XS 20 | Stainless steel with hydrophilic coating | 0.014 tapered to 0.008 | 180, 300 | Straight | Hydrophilic |
| Asahi Intecc Co Ltd. | Astato XS 40 | Stainless steel with hydrophilic coating | 0.014 tapered to 0.009 | 200, 300 | Straight | Hydrophilic |
| Teleflex | Cruiser-18 | Stainless steel | 0.018 | 195, 300 | Coil | Hydrophilic tip, hydrophobic shaft |
| Boston Scientific Corporation | V-14 ControlWire Guidewire | Crossing stenosed lesions: scitanium stainless steel core and hydrophilic coating | 0.014 (0.36 mm) | 182, 300 | Straight, angled (shapeable) | Polymer sleeve tip with ICE hydrophilic coating and PTFE proximal coating |
| Boston Scientific Corporation | V-18 ControlWire Steerable Guidewire | Crossing stenosed lesions: scitanium stainless steel core and hydrophilic coating | 0.018 (0.46 mm) | 110, 150, 200, 300 | Straight (shapeable) | Polymer sleeve tip with ICE hydrophilic coating and PTFE proximal coating |
| Boston Scientific Corporation | Victory Guidewire | Dedicated guidewires for intraluminal technique to cross calcified lesions or tight plaque or CTOs | 0.014 (0.36 mm), 0.018 (0.46 mm) | 195, 300 | Straight (shapeable)/tip load: 12, 18, 25, 30 grams | Polymer sleeve tip with 35 cm hydrophilic coating facilitates lesion crossing and PTFE proximal coating enables smooth device tracking |
| Cook Medical | Approach CTO | Microwire | 0.014 | 135, 190, 300 | Straight (shapeable) | PTFE |
| Cook Medical | Approach Hydro ST | Microwire | 0.014 | 135, 190, 300 | Straight (shapeable) | Hydrophilic distal tip, PTFE shaft |
| Cook Medical | Roadrunner Extra-Support | Microwire | 0.014, 0.018 | 180, 270, 300 | Angled | PTFE |
| Cordis | ATW | Intermediate support wire | 0.014 | 195 | Straight, J-curve | Duraglide/PTFE |
| Cordis | ATW Eco Pacs | Intermediate support wire | 0.014 | 195, 300 | Straight, J-curve | Duraglide/PTFE |
| Cordis | ATW Marker Wire | Intermediate support wire | 0.014 | 195 | Straight, J-curve | Duraglide/PTFE |
| Cordis | Jindo Steerable Guidewires | – | 0.035–0.022 | 180, 300 | Straight, shapeable, radiopaque tip | Distal part covered with PTFE sleeves |
| Cordis | Stabilizer | Balanced performance steerable guidewire | 0.014 | 180, 300 | Straight | Duraglide/PTFE |
| Cordis | Storq Steerable Guidewires | Stainless steel core wire | 0.035 | 180, 300 | Straight, angled, modified J | SLX coating is hydrophobic |
| Cordis | SV Wire | – | 0.018 | 180, 300 | Straight, shapeable | Proximal shaft coated with blue PTFE spray |
| Galt | Specialty Wires | Mandril | 0.008, 0.010, 0.014, 0.018 | 20, 40, 45, 60, 65, 80, 130 | Straight, angled | Silicone |
| Galt | Torx | Nitinol | 0.014, 0.018, 0.025 | 60, 80, 180, 260, 300 | Straight, angled | Silicone |
| Medcomp | Mandrel Wires | Stainless steel mandrel wire | 0.010 | 60, 80 | Platinum coil tip | Hydrophilic coating |
| Medcomp | Mandrel Wires | Nitinol wire | 0.018 | 70, 80, 130 | Radiopaque tip | Hydrosilk coating |
| Medcomp | Mandrel Wires | Nitinol wire | 0.010 | 40 | Straight | – |
| Medcomp | Mandrel Wires | Nitinol wire | 0.018 | 45 | Radiopaque tip | – |
| Medcomp | Mandrel Wires | Stainless steel mandrel guidewire | 0.018 | 65, 80 | Platinum coil tip | Silicone coating |
| Medcomp | Mandrel Wires | Stainless steel wire | 0.018 | 45 | Radiopaque tungsten tip | – |
| Medtronic | Avigo | Optimized balance between torque control and catheter trackability | 0.014 | – | 5-cm platinum coil tip | Hydrophilic coating |
| Medtronic | Babywire Double-Ended Nitinol Guidewire | Nitinol | 0.012 | 18, 50 | Straight | – |
| Medtronic | Nitrex Guidewire | Nitinol | 0.014, 0.018, 0.025 | 0.014-inch: 80, 180, 300; 0.018-inch: 60, 80, 180, 300; 0.025-inch: 180, 260 | Straight, angled | Silicone |
| Medtronic | Nitrex Guidewire With Flexible Shaft | Nitinol | 0.035 | 145, 180, 260, 400 | Straight, angled | Silicone |
| Medtronic | Nitrex Guidewire With Stiff Shaft | Nitinol | 0.035 | 80, 145, 180, 260, 300, 400 | Straight, angled | Silicone |
| Medtronic | SilverSpeed-10 | Stainless steel guidewire with radiopaque, platinum distal coil | 0.010 | – | 5-cm platinum coil tip | Hydrophilic coating |
| Medtronic | SilverSpeed-14 | Stainless steel guidewire with radiopaque, platinum distal coil | 0.014 | – | 5-cm platinum coil tip | Hydrophilic coating |
| Medtronic | SilverSpeed-16 | Stainless steel guidewire with radiopaque, platinum distal coil | 0.016 | – | 5-cm platinum coil tip | Hydrophilic coating |
| Merit Medical Systems, Inc. | InQwire: Marker Wire | Fixed core | 0.018 | 80, 120 | Straight 20-cm nitinol | Hydrophilic |
| Merit Medical Systems, Inc. | MAK (Mini Access Kits) Wires | Mandrel, nitinol with platinum tip, stainless steel, or nitinol core | 0.018 | 40, 60, 80 | Stainless steel, platinum, or palladium coil tips; stainless steel or nitinol mandrel; straight | – |
| Merit Medical Systems, Inc. | Prelude Sheath Wire | Stainless steel coils | 0.035, 0.038 | 50, 80 | Double ended: straight and 3-mm J | – |
Other Devices / Aneurysm Neck Bridging Devices
View Chart| Company Name | Product Name | Device Shape | Parent Vessel Diameter (mm) | Arch Width (mm) |
|---|---|---|---|---|
| Cerenovus | PulseRider Aneurysm Neck Bridging Device | T shape, Y shape | 2.7–3.5, 3.4–4.5 | 8.6, 10.6 |
| Perflow Medical | Cascade M Non-Occlusive Remodeling Net | Straight, compliant braid | 2–4 | 35 |
Other Devices / Aneurysm Neck Bridging Devices (Continued)
View Chart| Company Name | Product Name | Shaft Diameter (mm) | Shaft Length (mm) | Crown Diameter (mm) | Minimum Microcatheter (inch) | Parent Vessel Diameter (mm) |
|---|---|---|---|---|---|---|
| phenox GmbH | pCANVAS Bifurcation Aneurysm Flow Modulating Implant | 4 | 20, 25 | 5, 6, 8, 10 | 0.027 | 2.5 (minimum), 3.5 (maximum) |
| phenox GmbH | pCONUS 2 Bifurcation Aneurysm Implant | 4 | 15 | 5, 6, 7, 8, 10, 12, 15 | 0.021 | 2.5 (minimum), 3.7 (maximum) |
| phenox GmbH | pCONUS Bifurcation Aneurysm Implant | 3, 4 | 20, 25 | 4, 5, 6, 8, 10, 12, 15 | 0.021 | 2.2 (minimum), 3.9 (maximum) |
Other Devices / Assisted Compression Devices
View Chart| Company Name | Product Name | Type | Puncture Size (F) | Maximum Wire Compatibility | Comments |
|---|---|---|---|---|---|
| Abbott | FemoStop Gold | Mechanical compression device | All | All | Fully integrated femoral compression system allows for greater ease of use, precise placement, and pressure management; improves staff efficiency and reduces risk of cross-contamination |
| Abbott | FemoStop II Plus | Mechanical compression device | All | All | Femoral compression system allows for precise placement and pressure management, and improves staff efficiency; reusable device arch and manometer to save on product and packaging materials |
| Abbott | RadiStop | Mechanical compression device | All | All | Sturdy support plate provides comfortable and efficient positioning of the wrist before, during, and after the procedure; transparent material allows for easy and correct placement |
| Advanced Vascular Dynamics | ComfortPress | Femoral hemostasis: compression assist | All | – | Disposable, sterile external compression system used by medical professionals to aid in the practice of manual compression |
| Advanced Vascular Dynamics | CompressAR StrongArm SuperComfort | Femoral hemostasis: adjustable compression | All | – | Indicated for use by medical professionals to provide hemostasis of the femoral vascular access site following femoral artery catheterization procedures |
| Advanced Vascular Dynamics | mBrace 4200 | Wrist support for use with radial compression | All | – | Used for stabilizing and extending the wrist to 40° when inserting lines or catheters in the radial artery or other arteries in the wrist and can be used with radial hemostasis wristbands |
| Advanced Vascular Dynamics | RadAR 4160 | Radial hemostasis: adjustable compression | All | – | The disposable, sterile device is indicated for use by medical professionals to promote hemostasis at a puncture site into a blood vessel in a patient’s arm, following a cannulation procedure |
| Advanced Vascular Dynamics | Zephyr Model 9100 Vascular Compression Device | Radial hemostasis: inflatable, single balloon adjustable compression band | 7 | – | Enhances patient comfort while letting operators use the same technique employed for other inflatable radial compression devices; although the Zephyr syringe helps operators more easily control compression adjustment, any luer syringe may be used; indicated for use by medical professionals to promote hemostasis following a catheterization or other puncture into a blood vessel in a patient’s arm or leg including: radial, brachial, dorsalis pedis, or tibial blood vessels, arterial or venous line or sheath removal, hemodialysis, and in anticoagulation therapy |
| Advanced Vascular Dynamics | Zephyr-Dual Model 9200 Vascular Compression Device | Radial hemostasis: inflatable, dual balloon (radial and ulnar), adjustable compression band | 7 | – | Enhances patient comfort while letting operators use the same technique employed for other inflatable radial compression devices; although the Zephyr syringe helps operators more easily control compression adjustment, any luer syringe may be used; by compressing the ulnar artery together with radial artery compression, it reduces distal resistance to antegrade radial blood flow by limiting ulnar blood flow into the hand; this helps enhance postprocedure antegrade radial blood flow during vascular compression to facilitate patent hemostasis; indicated for use by medical professionals to promote hemostasis following a catheterization or other puncture into a blood vessel in a patient’s arm or leg, including: radial, brachial, dorsalis pedis, or tibial blood vessels, arterial or venous line or sheath removal, hemodialysis, and in anticoagulation therapy |
| Argon Medical Devices, Inc. | V+Pad | Topical hemostasis pad | All | – | Double-stitched, woven gauze pad with D-glucosamine-enriched fibers that stimulate the body's natural clotting cascade for the local management of bleeding wounds such as vascular access sites; use in conjunction with manual pressure |
| Forge Medical, Inc. | VasoStat Hemostasis Device | Radial artery and pedal/tibial artery hemostasis device | 4–7 | – | Designed for patent hemostasis through focused, adjustable pressure applied precisely over radial or pedal/tibial artery access site using unique ratcheting mechanism; transparent window allows continuous puncture site monitoring; no constricting bands or wrist immobilization needed; optimizes patient comfort and satisfaction |
| Galt | Galt Radial Artery Compression Band | Radial artery compression band | All | All | Clear, inflatable hemostasis device for a controlled, safe, and comfortable closure available in three sizes including universal to fit most patient wrist sizes |
| Merit Medical Systems, Inc. | PreludeSYNC | Radial compression device | All | All | Personal, effective, and comfortable radial compression; available in two sizes and two inflation luer options |
| Merit Medical Systems, Inc. | PreludeSYNC EZ | Radial compression device | All | All | Personal, effective, and comfortable radial compression; available in two sizes and two inflation luer options |
| Merit Medical Systems, Inc. | Safeguard (12, 24 cm) | Pressure-assisted device | All | – | Assists manual compression and maintains hands-free pressure; adjustable pressure is applied to wound and access site via an inflatable bulb contained within an adhesive bandage, allowing visibility of the site; available in two sizes |
| Merit Medical Systems, Inc. | Safeguard Radial | Radial hemostasis | All | – | Provides direct compression on the radial artery; excellent site visibility through clear window; soft, nonlatex adhesive band for increased patient comfort |
| Terumo Europe | TR Band | Radial artery compression device | All | All | A compression device designed to assist hemostasis of the radial artery after a transradial procedure |
| Tricol Biomedical Inc. | HemCon Patch | Hemostatic bandage | 6–8 | – | Designed specifically for use in diagnostic and interventional catheterizations; simple to administer and quickly controls bleeding from catheter access sites; available in multiple sizes; it safely and effectively reduces the direct pressure protocol with improved patient ambulation times; working independently from the clotting cascade, it is able to control severe bleeding quickly and provides an antibacterial barrier |
| Z-Medica, LLC | QuikClot 10 X 10, Hemostatic Dressing | Topical hemostatic dressing | All, including up to 12 | – | Nonwoven hemostatic gauze measuring 10 X 10 cm; impregnated with an inert mineral, kaolin, that is both safe and effective in promoting clotting and does not contain any animal or human proteins; packaged in a sterile, peelable, foil pouch and is indicated for the temporary control of moderate external bleeding and it should be used in conjunction with direct manual pressure; contains an x-ray identifiable strip for easy detection |
| Z-Medica, LLC | QuikClot 5 X 5, Hemostatic Dressing | Topical hemostatic dressing | All, including up to 12 | – | Nonwoven hemostatic gauze measuring 5 X 5 cm; impregnated with an inert mineral, kaolin, that is both safe and effective in promoting clotting and does not contain any animal or human proteins; packaged in a sterile, peelable, foil pouch and is indicated for the temporary control of moderate external bleeding and it should be used in conjunction with direct manual pressure |
| Z-Medica, LLC | QuikClot Interventional Hemostatic Bandage | Topical hemostatic bandage | All, including up to 12 | – | A kaolin-based hemostatic pad and 3M Tegaderm adhesive bandage, applied topically as an adjunct to manual compression and indicated for the local management and control of surface bleeding from vascular access sites; double packaged in a blister package and in a foil pouch for aseptic use |
| Z-Medica, LLC | QuikClot Radial Hemostatic Bandage | Topical hemostatic bandage for radial punctures | All, including up to 12 | – | Soft, white hydrophilic roll dressing impregnated with kaolin; does not contain animal or human proteins; packaged with a unique direct pressure dressing to hold the bandage in place and provide compression |
Other Devices / Atherectomy Devices
View Chart| Company Name | Product Name | Minimum Vessel Diameter (mm) | Sheath Compatibility (F) | Crossing Profile (inch) | Working Length (cm) | Tip Length (cm) |
|---|---|---|---|---|---|---|
| Abbott | Stealth 360 Orbital Atherectomy System 1.25 mm Micro Crown | – | 4 | 0.052 (1.32 mm) | 145 | 0.7 |
| Abbott | Stealth 360 Orbital Atherectomy System 1.25 mm Solid Crown | – | 6 | 0.069 (1.75 mm) | 145 | 0.7 |
| Abbott | Stealth 360 Orbital Atherectomy System 1.50 mm Classic Crown | – | 6 | 0.069 (1.75 mm) | 145 | 1.5 |
| Abbott | Stealth 360 Orbital Atherectomy System 1.50 mm Solid Crown | – | 6 | 0.069 (1.75 mm) | 145 | 1 |
| Abbott | Stealth 360 Orbital Atherectomy System 2.00 mm Classic Crown | – | 6 | 0.079 (2 mm) | 145 | 2 |
| Abbott | Stealth 360 Orbital Atherectomy System 2.00 mm Solid Crown | – | 6 | 0.079 (2 mm) | 145 | 3 |
| BD Interventional | RotarexS Rotational Atherothrombectomy System | 3 | 6 | 0.079 (2 mm) | 110, 135 | – |
| BD Interventional | RotarexS Rotational Atherothrombectomy System | 7 | 10 | 0.131 (3.33 mm) | 85 | – |
| BD Interventional | RotarexS Rotational Atherothrombectomy System | 5 | 8 | 0.105 (2.67 mm) | 85, 110 | – |
| Boston Scientific Corporation | Jetstream SC 1.6 mm | 2.5 | 7 | 0.063 (1.6 mm) | 145 | – |
| Boston Scientific Corporation | Jetstream SC 1.85 mm | 2.75 | 7 | 0.073 (1.85 mm) | 145 | – |
| Boston Scientific Corporation | Jetstream XC 2.1/3 mm | Blades down: 3; blades up: 4 | 7 | Blades down: 0.083 (2.1 mm); blades up: 0.118 (3 mm) | 135 | – |
| Boston Scientific Corporation | Jetstream XC 2.4/3.4 mm | Blades down: 3.5; blades up: 4.5 | 7 | Blades down: 0.094 (2.4 mm); blades up: 0.134 (3.4 mm) | 120 | – |
| Invamed | Paragon | 3 | 7 | 0.090 | 150 | – |
| Medtronic | HawkOne LS Directional Atherectomy System | 3.5–7 | 7 | 0.104 (2.6 mm) | 114 | 6.6 |
| Medtronic | HawkOne LX Directional Atherectomy System | 3.5–7 | 7 | 0.104 (2.6 mm) | 114 | 9.6 |
| Medtronic | HawkOne M Directional Atherectomy System | 3–7 | 6 | 0.085 (2.2 mm) | 135 | 5.9 |
| Medtronic | HawkOne S Directional Atherectomy System | 2–4 | 6 | 0.085 (2.2 mm) | 151 | 5.9 |
| Philips | Phoenix Atherectomy System 1.5 mm Tracking | 2 | 4 | 0.059 (1.5 mm) | 149 | – |
| Philips | Phoenix Atherectomy System 1.8 mm Tracking | 2.5 | 5 | 0.070 (1.8 mm) | 130, 149 | – |
| Philips | Phoenix Atherectomy System 2.2 mm Auto-Deflected | 3 | 6 | 0.087 (2.2 mm) | 130 | – |
| Philips | Phoenix Atherectomy System 2.2 mm Tracking | 3 | 6 | 0.087 (2.2 mm) | 130, 149 | – |
| Philips | Phoenix Atherectomy System 2.4 mm Deflecting | 3 | 7 | 0.095 (2.4 mm) | 127 | – |
| Philips | Turbo-Elite Laser Atherectomy 0.9 mm Catheter OTW | 1.4 | 4 | 0.047 | 150 | – |
| Philips | Turbo-Elite Laser Atherectomy 0.9 mm Catheter RX | 1.4 | 4 | 0.049 | 150 | – |
| Philips | Turbo-Elite Laser Atherectomy 1.4 mm Catheter OTW | 2.1 | 5 | 0.056 | 150 | – |
| Philips | Turbo-Elite Laser Atherectomy 1.4 mm Catheter RX | 2.1 | 5 | 0.062 | 150 | – |
| Philips | Turbo-Elite Laser Atherectomy 1.7 mm Catheter OTW | 2.6 | 5 | 0.069 | 150 | – |
| Philips | Turbo-Elite Laser Atherectomy 1.7 mm Catheter RX | 2.6 | 6 | 0.072 | 150 | – |
| Philips | Turbo-Elite Laser Atherectomy 2.0 mm Catheter OTW | 3 | 6 | 0.081 | 150 | – |
| Philips | Turbo-Elite Laser Atherectomy 2.0 mm Catheter RX | 3 | 7 | 0.080 | 150 | – |
| Philips | Turbo-Elite Laser Atherectomy 2.3 mm Catheter OTW 0.018-inch Guidewire | 3.5 | 7 | 0.091 | 120 | – |
| Philips | Turbo-Elite Laser Atherectomy 2.3 mm Catheter OTW 0.035-inch Guidewire | 3.5 | 7 | 0.091 | 125 | – |
| Philips | Turbo-Elite Laser Atherectomy 2.5 mm Catheter OTW 0.018-inch Guidewire | 3.8 | 8 | 0.102 | 110 | – |
| Philips | Turbo-Elite Laser Atherectomy 2.5 mm Catheter OTW 0.035-inch Guidewire | 3.8 | 8 | 0.102 | 112 | – |
| AngioDynamics | Auryon Atherectomy System Hydrophilic Catheter 0.9mm CE Marked | 1.4 | 4 | 0.040 | 150 | – |
| AngioDynamics | Auryon Atherectomy System Hydrophilic Catheter 1.5 mm | 2.25 | 5 | 0.061 | 150 | - |
| AngioDynamics | Auryon Atherectomy System Hydrophilic Catheter 1.7 mm | 2.6 | 5 | 0.069 | 150 | - |
| AngioDynamics | Auryon Atherectomy System Hydrophilic Catheter 2.0 mm | 3 | 6 | 0.081 | 135 | - |
| AngioDynamics | Auryon Atherectomy System Hydrophilic Catheter 2.35 mm | 3.6 | 7 | 0.095 | 110 | - |
| AngioDynamics | Auryon Atherectomy System Hydrophilic Catheter 0.9 mm XL | 1.4 | 4 | 0.043 | 225 | - |
| AngioDynamics | Auryon Atherectomy System Hydrophilic Catheter 1.5 mm XL | 2.25 | 5 | 0.061 | 225 | - |
Other Devices / Closure Devices
View Chart| Company Name | Product Name | Type | Puncture Size (F) | Maximum Wire Compatibility (inch) | Comments |
|---|---|---|---|---|---|
| Abbott | Perclose ProGlide | Suture | Common femoral artery 5–21 (max OD 26), common femoral vein 5–24 (max OD 29) | 0.038 | Provides secure repair with pre-tied polypropylene monofilament suture, ability to maintain wire access, minimal intravascular footprint with no re-access restrictions; broadest indication for both femoral arterial and venous access |
| Abbott | Perclose ProStyle | Suture | Common femoral artery 5–21 (max OD 26), common femoral vein 5–24 (max OD 29) | 0.038 | Provides secure repair with pre-tied polypropylene monofilament suture, ability to maintain wire access, minimal intravascular footprint with no re-access restrictions; broadest indication for both femoral arterial and venous access |
| Abbott | Prostar XL | Suture | 8.5–24 | 0.038 | Provides secure repair with two braided sutures, ability to maintain wire access with minimal intravascular footprint |
| Abbott | StarClose SE | Nitinol clip | 5–6 | 0.038 | Utilizes an extravascular nitinol clip to provide immediate repair, simple to use; hemostasis can be challenged and confirmed on the table |
| Cordis | Exoseal | Extravascular plug | 5, 6, 7 | – | Deployed through existing procedural sheath (up to 12 cm) with two visual indicators that provide precise and secure extravascular femoral artery closure; polyglycolic acid (PGA) plug material, deployed without impeding arterial blood flow and fully absorbable within 60–90 days; maximum sheath length compatibility: 12 cm |
| Cordis | Mynx Control Vascular Closure Device | Extravascular sealant | 5, 6, 7 | – | A next-generation deployment system designed for predictability and ease of use with two-button streamlined procedural steps, a sheath catch compatible with the procedural sheath, tension indicator providing visual confirmation of device position for proper extravascular polyethylene glycol (PEG) sealant deployment dissolved within 30 days; available in 5-, 6-, and 7-F sizes; indicated for antegrade and retrograde punctures; leaves nothing behind but a healed artery; maximum sheath length compatibility: 12 cm |
| Cordis | MynxGrip Vascular Closure Device | Extravascular sealant | 5, 6, 7 | – | Indicated for closure of 5- to 7-F femoral arteries and veins; provides secure mechanical closure with the safety of an extravascular polyethylene glycol (PEG) sealant; the Grip sealant actively adheres to and seals the arteriotomy or venotomy while expanding to fill the tissue tract; offers a patient-friendly closure option with no sutures, clamping, or metal implants and dissolves within 30 days, leaving nothing behind but a healed artery or vein; maximum sheath length compatibility: 12 cm |
| Haemonetics | Vascade MVP Venous Vascular Closure System (VVCS) | Extravascular, bioabsorbable closure device | 6–12 inner diameter (up to 15 maximum outer diameter) | Utilizes existing procedural sheath | Fully integrated, extravascular, bioabsorbable femoral venous closure system that is easy to use, leaves no permanent components behind, and has demonstrated safety and efficacy in the AMBULATE trial, a prospective, multicenter, randomized clinical trial comparing Vascade MVP to manual compression; the system combines proprietary collapsible disc technology and a thrombogenic resorbable collagen patch in an integrated design |
| Haemonetics | Vascade Vascular Closure System (VCS) | Extravascular closure device | 5, 6, 7 | Utilizes existing procedural sheath | Indicated for 5 to 7 F femoral arterial and venous access site closure; fully integrated, extravascular, bioabsorbable femoral access closure system that is easy to use, leaves no permanent components behind and has demonstrated safety and efficacy in the RESPECT trial, a prospective, multicenter, randomized clinical trial comparing Vascade to manual compression; the system combines proprietary collapsible disc technology and a thrombogenic resorbable collagen patch in an integrated design; it enables rapid hemostasis while minimizing complications |
| Invamed | AngioBlock | Embolization seal | 5, 6, 7, 8 | 0.035 (5/6 F), 0.038 (7/8 F) | Developed for achieving rapid, reliable, and safe homeostasis after angiography entry; the delivery sheath allows the system to detect the artery and deliver the polymer compound over the adventitia of the artery |
| Teleflex | Manta Vascular Closure Device | Bioresorbable implant | Following the use of 10–20 F device or sheaths (12–25 F OD) | 0.035 | Designed specifically for closure of large bore femoral artery access sites; easy positioning without the need for preclosure; simple deployment with help from auditory and visual cues and a reliable closure using a single device; the 14-F device is indicated for closure of femoral arterial access sites after the use of 10- to 14-F devices or sheaths (maximum OD/profile of 18 F), and the 18-F device is indicated for closure of femoral arterial access sites after the use of 15- to 18-F devices or sheaths (maximum OD/profile of 25 F) |
| Terumo Europe | Angio-Seal Evolution Vascular Closure Device | Mechanical seal, fully bioabsorbable components | ≤ 6, ≤ 8 | 0.035 (≤ 6 F), 0.038 (≤ 8 F) | Automated collagen compaction and enhanced ease-of-use design; suture, collagen, and anchor sandwich of the arteriotomy; all components reabsorb within 60 to 90 days; FDA labeling for immediate restick; FDA labeling for 20-minute ambulation and 60-minute discharge for diagnostic cases with a 6-F sheath or smaller procedural sheath |
| Terumo Europe | Angio-Seal VIP Vascular Closure Device | Mechanical seal, fully bioabsorbable components | ≤ 6, ≤ 8 | 0.035 (≤ 6 F), 0.038 (≤ 8 F) | Suture, collagen, and anchor sandwich of the arteriotomy; all components reabsorb within 60 to 90 days; FDA labeling for immediate restick; FDA labeling for 20-minute ambulation and 60-minute discharge for diagnostic cases with a 6-F sheath or smaller procedural sheath |
| Terumo Europe | FemoSeal Vascular Closure Device | Mechanical seal, fully bioabsorbable components | ≤ 7 | 0.038 | Suture and polymer discs sandwich the arteriotomy; all components reabsorb within 90 days |
Other Devices / CTO Crossing Devices
View Chart| Company Name | Product Name | Catheter Size (F) | Wire Size (inch) | Working Length (cm) | Minimum Guiding Catheter ID (inch) | Comments |
|---|---|---|---|---|---|---|
| Avinger, Inc. | Kittycat 2 | 5 | 0.014 | 150 | 0.065 | Peripheral OTW CTO crossing catheter; catheter shaft is preshaped for better steerability in the most tortuous anatomy; Juicebox compatible |
| Avinger, Inc. | Ocelot | 6 | 0.014 | 110 | 0.079 | Peripheral OTW CTO crossing catheter with onboard real-time OCT intravascular imaging for precise catheter navigation |
| Avinger, Inc. | Ocelot Pixl | 5 | 0.014 | 135 | 0.067 | Peripheral OTW CTO crossing catheter with onboard real-time OCT intravascular imaging for precise catheter navigation |
| Avinger, Inc. | Wildcat | 6 | 0.035 | 110 | 0.079 | Peripheral OTW CTO crossing catheter with three different modes of operation to cross any lesion; Juicebox compatible |
| Bentley InnoMed GmbH | BeBack crossing catheter | 2.9, 4 | 0.014, 0.018 | 80, 120 | 2.9 (crossover 4), 4 (crossover 6) | A low-profile support catheter that has a crossing and targeted re-entry capability due to the steerable nitinol needle at the tip; a radiopaque marker indicates the direction in which the curved needle will protrude from the catheter’s tip; antegrade, retrograde, and crossover are possible for intraluminal and subintimal approach on 0.014- and 0.018-inch wire platform |
| Cook Medical | TriForce Peripheral Crossing Set | Inner catheter: 4, outer sheath: 5, tapering to 4 (0.035-inch wire) | 0.035 | 65, 100 | 0.052 | Coaxial peripheral crossing set; both inner catheter and outer sheath are hydrophilically coated; inner catheter is braided with radiopaque tip; outer sheath is coil reinforced to provide exceptional tracking through tortuous anatomy; a tungsten-loaded tip on the outer sheath aids pushability and radiopacity; outer sheath is tapered down to inner catheter to provide additional support, strength, and pushability across challenging lesions |
| Cordis | Outback Elite Re-Entry Catheter | 6 | 0.014 | 80, 120 | – | Enables re-entry of a guidewire from the subintimal space back into the true lumen via re-entry cannula and highly visible L and T markers |
| EndoCross | Enabler-P Catheter System | 5 | 0.035 | 107 | 0.070 | Peripheral OTW balloon catheter system enabling true luminal crossing of peripheral CTOs; the Enabler-P catheter system provides increased tip force, distal pushability, and controlled advancement of a standard guidewire |
| Medtronic | Enteer Re-entry System, Catheter | 5 | 0.018 | 135, 150 | 0.066 | Re-entry catheter designed with a unique flat balloon to self-orient in the subintimal space and easily target the true lumen using the Enteer Guidewire; catheter available in two sizes for above- and below-the-knee use |
| Medtronic | Enteer Re-entry System, Guidewire | – | 0.014 | 300 | – | Specialized guidewire designed to target Enteer catheter exit ports and engage and penetrate tissue for re-entry into the true lumen from a subintimal position; available in three levels of stiffness (flexible, standard, stiff) for use across a range of peripheral vessels |
| Medtronic | Viance Crossing Catheter | 5 | 0.014 | 150 | 0.066 | Low-profile peripheral CTO crossing catheter with atraumatic distal tip; device operates via physician-controlled torque handle for fast manual spinning; the spinning motion created by the torque device allows the catheter tip to find its way through the lesion; available in flexible and standard stiffness |
| Merit Medical Systems, Inc. | Spinr High-Performance Guidewire Controller | – | 0.014–0.038 | – | 0.014 | Used to maneuver guidewires in the coronary and peripheral vasculature during interventional or diagnostic procedures; assists in accessing distal anatomy, navigating tortuous vessels, crossing old lesions, and working through fresh blockages |
| Philips | Pioneer Plus IVUS-Guided Re-Entry Catheter | 6 | 0.014 | 120 | – | Peripheral re-entry catheter that utilizes IVUS guidance to precisely target re-entry into the true lumen |
| Philips | Quick-Cross Extreme Support Catheter | 5 | – | 65, 90, 135, 150 | – | Low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, and pushability to track through complex anatomy |
| Philips | Quick-Cross Extreme Support Catheter | 4 | – | 90, 135, 150 | – | Low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, and pushability to track through complex anatomy |
| Philips | Quick-Cross Extreme Support Catheter | 4 | – | 135, 150 | – | Low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, and pushability to track through complex anatomy |
| Philips | Quick-Cross Select Support Catheter | 4 | – | 90, 135, 150 | – | Angled and low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, pushability, and allows the ability to navigate through complex anatomy |
| Philips | Quick-Cross Select Support Catheter | 4 | – | 135, 150 | – | Angled and low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, pushability, and allows the ability to navigate through complex anatomy |
| Philips | Quick-Cross Select Support Catheter | 5 | – | 65, 90, 135, 150 | – | Angled and low-profile tip, hydrophilic coating, and stainless steel braid provide increased strength, torque, pushability, and allows the ability to navigate through complex anatomy |
| Philips | Quick-Cross Support Catheter | 5 | – | 65, 90, 135, 150 | – | Low-profile, hydrophilic-coated, tapered-tip catheter provides seamless catheter-to-guidewire transition to facilitate crossing of challenging lesions and tracking through tortuous anatomy |
| Philips | Quick-Cross Support Catheter | 4 | – | 90, 135, 150 | – | Low-profile, hydrophilic-coated, tapered-tip catheter provides seamless catheter-to-guidewire transition to facilitate crossing of challenging lesions and tracking through tortuous anatomy |
| Philips | Quick-Cross Support Catheter | 4 | – | 135, 150 | – | Low-profile, hydrophilic-coated, tapered-tip catheter provides seamless catheter-to-guidewire transition to facilitate crossing of challenging lesions and tracking through tortuous anatomy |
| Reflow Medical, Inc | Wingman14 CTO Crossing Catheter | 2.7 | 0.014 | 65, 135, 150 | 0.039 | A beveled (needle) tip recanalization device intended to provide additional support to a steerable guidewire when accessing discrete regions of the peripheral vasculature; the Wingman CTO Crossing Catheter consists of a support catheter, with a user controlled radiopaque guide tip (5-mm extendable needle tip) and activating handle |
| Reflow Medical, Inc | Wingman18 CTO Crossing Catheter | 3.8 | 0.018 | 90, 135, 150 | 0.052 | A beveled (needle) tip recanalization device intended to provide additional support to a steerable guidewire when accessing discrete regions of the peripheral vasculature; the Wingman CTO Crossing Catheter consists of a support catheter, with a user controlled radiopaque guide tip (5-mm extendable needle tip) and activating handle |
| Reflow Medical, Inc | Wingman35 CTO Crossing Catheter | 4.6 | 0.035 | 65, 90, 135 | 0.066 | A beveled (needle) tip recanalization device intended to provide additional support to a steerable guidewire when accessing discrete regions of the peripheral vasculature; the Wingman CTO Crossing Catheter consists of a support catheter, with a user controlled radiopaque guide tip (5-mm extendable needle tip) and activating handle |
| Reflow Medical, Inc | Wingman 14C CTO Crossing Catheter | 2.7 | 0.014 | 90, 135, 150 | 0.039 | A beveled (needle) tip recanalization device intended to provide additional support to a steerable guidewire when accessing discrete regions of the peripheral vasculature; the Wingman CTO Crossing Catheter consists of a support catheter, with a user controlled radiopaque guide tip (5-mm extendable needle tip) and activating handle |
Other Devices / Dialysis Catheters
View Chart| Company Name | Product Name | Size (F) | Tip-to-Cuff Insertion Length (cm) | Tip Type | Number of Lumens | Sideholes (Yes/No) | Coated (Yes/No) | Acute or Chronic |
|---|---|---|---|---|---|---|---|---|
| Argon Medical Devices, Inc. | UltraStream | 15.5 | 19, 23, 27, 31, 35 | Step | Three (two arterial, one venous) | Yes | No | Chronic |
| Balton | Dialysis Catheter | 6.5–12 | – | – | Three | Yes | No | Acute |
| Bard Access Systems, Inc | Niagara | 13.5 | 15, 20, 24 (straight); 12.5, 15, 20 (AlphaCurve) | Step tip | Two | Yes | No | Acute |
| Bard Access Systems, Inc | Niagara Slim | 12 | 15, 20, 24 (straight); 12.5, 15, 20 (AlphaCurve) | Step tip | Two | Yes | No | Acute |
| Bard Access Systems, Inc | PowerTrialysis | 13 | 15, 20, 24, 30 (straight); 12.5, 15, 20, 24 (AlphaCurve) | Symmetric | Three | Yes | No | Acute |
| BD Interventional | EquiStream Long-Term Hemodialysis Catheter | 14.5 | 15, 19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, 31 (AlphaCurve) | Split tip | Two | Yes | No | Chronic |
| BD Interventional | EquiStream XK Long-Term Hemodialysis Catheter | 16 | 19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, 31 (alphacurve) | Split tip | Two | Yes | No | Chronic |
| BD Interventional | GlidePath Long-Term Dialysis Catheter | 14.5 | 15, 19, 23, 27, 31, 35, 42, (straight); 19, 24, 28, 31 (alphacurve) | Symmetric | Dual | Yes | No | Chronic |
| BD Interventional | HemoSplit Long-Term Hemodialysis Catheter | 14.5 | 15, 19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, 31 (AlphaCurve) | Split tip | Two | Yes | No | Chronic |
| BD Interventional | HemoSplit XK Long-Term Hemodialysis Catheter | 16 | 19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, (alphacurve) | Split tip | Two | Yes | No | Chronic |
| BD Interventional | HemoStar Long-Term Hemodialysis Catheter | 14.5 | 15, 19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, 31 (AlphaCurve) | Staggered | Two | Yes | No | Chronic |
| BD Interventional | HemoStar XK Long-Term Hemodialysis Catheter | 16 | 19, 23, 27, 31, 35, 42 (straight); 19, 24, 28, (alphacurve) | Staggered | Two | Yes | No | Chronic |
| Medcomp | Canaud Long Term Hemodialysis Catheter | 10 | 40 (tip-to-hub) | Single round | 2 | Yes | No | Chronic |
| Medcomp | Duo Flow 400XL Short Term Hemodialysis Catheter | 14 | 12, 15, 20, 24 (tip-to-hub) | Tapered | 2 | Yes | No | Acute |
| Medcomp | Duo Flow III Short Term Hemodialysis Catheter | 13 | 15, 17.5, 20, 25 (tip-to-hub) | Step | 2 | No | No | Acute |
| Medcomp | Duo-Flow Short Term Hemodialysis Catheter | 9, 11.5 | 12, 15, 20, 24 (tip-to-hub) | Tapered | 2 | Yes | No | Acute |
| Medcomp | Duo-Flow Side x Side Short Term Hemodialysis Catheter | 9, 11, 12, 14 | 12, 13, 13.5, 15, 20, 24 (tip-to-hub) | Tapered | 2 | Yes | No | Acute |
| Medcomp | Duo-Split Short Term Hemodialysis Catheter | 13 | 12, 15, 20, 24, 30 (tip-to-hub) | Split | 2 | Yes | No | Acute |
| Medcomp | Femoral Short Term Hemodialysis Catheter | 6.5, 7, 8.5, 9 | 13.3, 14, 15, 25 (tip-to-hub) | Tapered | 1 | Yes | No | Acute |
| Medcomp | Free Flow Short Term Hemodialysis Catheter | 12.5, 15.5 | 12, 15, 20, 24, 28 (tip-to-hub) | Coaxial | 2 | No | No | Acute |
| Medcomp | Hemo-Cath Long Term Hemodialysis Catheter | 8, 10, 12.5 | 15, 18, 20, 22, 24, 28, 32 (tip-to-hub) | Step | 2 | Yes | No | Chronic |
| Medcomp | Hemo-Cath Short Term Hemodialysis Catheter | 8, 10, 11.5, 13.5 | 12, 15, 20, 24, 27, 28, 35 (tip-to-hub) | Tapered | 2 | Yes | No | Acute |
| Medcomp | Hemo-Flow Long Term Hemodialysis Catheter | 14.5 | 24, 28, 32, 36, 40, 55 (tip-to-hub) | Step | 2 | Yes | No | Chronic |
| Medcomp | Hemo-Flow XF Long Term Hemodialysis Catheter | 15.5 | 20, 22, 24, 28, 32, 36, 40, 55 (tip-to-hub) | Step | 2 | Yes | No | Chronic |
| Medcomp | Soft-Line Short Term Hemodialysis Catheter | 7, 9, 11.5 | 7, 10, 12, 15, 20, 24 (tip-to-hub) | Tapered | 2 | Yes | No | Acute |
| Medcomp | Split Cath Long Term Hemodialysis Catheter | 10, 14, 16 | 15, 18, 20, 22, 24, 28, 32, 36, 40, 55 (tip-to-hub) | Split | 2 | Yes | No | Chronic |
| Medcomp | Split Stream Long Term Hemodialysis Catheter | 14, 16 | 24, 28, 32, 36, 40 (tip-to-hub) | Split | 2 | Yes | No | Chronic |
| Medcomp | Subclavian Short Term Hemodialysis Catheter | 8 | 12, 15, 20 (tip-to-hub) | Tapered | 1 | Yes | No | Acute |
| Medcomp | Symetrex Long Term Hemodialysis Catheter | 15.5 | 19, 23, 28, 33, 37, 42 | Symmetrical | 2 | Yes/No (options with and without sideholes) | No | Chronic |
| Medcomp | T-3 CT Short Term Hemodialysis Catheter | 15.5 | 15, 20, 24, 28, 32 (tip-to-hub) | Step | 3 | No | No | Acute |
| Medcomp | Tesio Long Term Hemodialysis Catheter | 6.5, 10, 12 | 29, 40, 52, 60, 70 (tip-to-hub) | Independent round | 2 | No | No | Chronic |
| Medcomp | Titan HD Long Term Hemodialysis Catheter | 15.5 | 24, 28, 32, 36, 40, 55 (tip-to-hub) | Step | 2 | With or without | No | Chronic |
| Medcomp | Tri-Flow Short Term Hemodialysis Catheter | 11.5, 12 | 12, 15, 20, 24 (tip-to-hub) | Tapered | 3 | Yes | No | Acute |
| Medcomp | Trio-CT Short Term Hemodialysis Catheter | 13.5 | 12, 15, 20, 24, 30 (tip-to-hub) | Tapered | 3 | Yes | No | Acute |
| Medtronic | Palindrome Precision Heparin Coated Dialysis Catheter | 14.5 | 19, 23, 28, 33 | Symmetric | Dual | Yes, side slots | Yes, heparin | Chronic |
| Medtronic | Palindrome Precision Symmetric Tip Dual Lumen Catheter | 14.5 | 19, 23, 28, 33, 44, 55 | Symmetric | Dual | Yes, side slots | No | Chronic |
| Medtronic | Palindrome Precision Symmetric Tip Dual Lumen Catheter With VenaTrac Insertion Stylets | 14.5 | 19, 23, 28, 33 | Symmetric | Dual | Yes, side slots | No | Chronic |
| Merit Medical Systems, Inc. | BioFlo DuraMax Catheter | 16 | 15–50 | Curved step-tip | 2 | Yes | Yes | Chronic |
| Merit Medical Systems, Inc. | CentrosFLO Long-Term Hemodialysis Catheter | 16 | 15, 17, 19, 23, 27, 31 | Self-centering split tip | Two | Yes | No | Chronic |
| Merit Medical Systems, Inc. | Flex-Neck Peritoneal Dialysis Catheter | 15 | 1.5, 4.5, 6.5, 9.5, 13.5, 14, 15.5 | Coil, straight | One | Yes | No | Chronic |
| Merit Medical Systems, Inc. | ProGuide | 14.5 | 19, 23, 27, 31, 35 | Step-tip | Two | Yes | No | Chronic |
| Teleflex | Arrow Arrowgard Blue Hemodialysis Catheterization Kits | 14 | 15, 20, 25 | Staggered tip | Two | Yes | No | Acute |
| Teleflex | Arrow Arrowgard Blue Hemodialysis Catheterization Kits | 12 | 15, 20 | Staggered tip | Two | Yes | Yes, Arrowgard Blue antimicrobial protection | Acute |
| Teleflex | Arrow Cannon II Plus Hemodialysis Catheterization Sets (Retrograde Catheters) | 15 | 19, 23, 27, 31, 50 | V-tip | Two | Yes | No | Chronic |
| Teleflex | Arrow Edge Hemodialysis Catheterization Sets (Antegrade Catheters) | 15 | 19, 23, 27, 31, 50 | V-tip | Two | Yes | No | Chronic |
| Teleflex | Arrow Hemodialysis Catheterization Kits | 12 | 16, 20, 25 | Staggered tip | Two | Yes | No | Acute |
| Teleflex | Arrow NextStep Hemodialysis Catheterization Sets (Antegrade Catheters) | 15 | 19, 23, 27, 31, 42, 50 | Step tip | Two | Yes | No | Chronic |
| Teleflex | Arrow NextStep Hemodialysis Catheterization Sets (Retrograde Catheters) | 15 | 19, 23, 27, 31 | Step tip | Two | Yes | No | Chronic |
| Teleflex | Arrow Pediatric Hemodialysis Catheterization Kits | 8, 9 | 11, 13 | Staggered tip | Two | Yes | No | Acute |
| Teleflex | Arrow Precurved Arrowgard Blue Hemodialysis Catheterization Kits | 14 | 15, 20 | Staggered tip | Two | Yes | Yes, Arrowgard Blue antimicrobial protection | Acute |
| Teleflex | Arrow Three Lumen Pressure Injectable Hemodialysis Catheterization Kits | 12 | 15, 20, 25 | Staggered tip | Three | Yes | No | Acute |
| Teleflex | Arrow You-Bend Arrowgard Blue Hemodialysis Catheterization Kits | 12 | 13, 16, 20 | Staggered tip | Two | Yes | Yes, Arrowgard Blue antimicrobial coating | Acute |
| Teleflex | Arrow-Clark VectorFlow Hemodialysis Catheterization Sets (Antegrade and Retrograde) | 15 | 19, 23, 27, 31, 42, 55 | Symmetric tip | Two | Yes | No | Chronic |
| Joline GmbH & Co. KG | High Flow Double Lumen Catheter | 11 , 13 | 15, 17.5, 20, 25, 30 | Step tip | 2 | No | No | Acute |
| Joline GmbH & Co. KG | High Flow Triple Lumen Catheter | 13.5 | 15, 17.5, 20, 25 | Tapered tip | Three | No | No | Acute |
| Joline GmbH & Co. KG | Extra Flow Pediatric Catheter | 6.5, 8 | 6.5 F: 7.5, 10, 12.5; 8 F: 10, 12.5, 15 | Special step tip | Two | No | No | Acute |
| Joline GmbH & Co. KG | Silicone Double Lumen Catheter Anterograde Implantation | Outer-Ø (oval): 6.4 X 3.7 mm | 19, 24, 29, 34 | Step tip | Two | No | No | Chronic |
| Joline GmbH & Co. KG | Silicone Double Lumen Catheter Retrograde Implantation | Outer-Ø (oval): 6.1 X 3.5 mm | 19, 24, 29, 34 | Step tip | Two | No | No | Chronic |
| Joline GmbH & Co. KG | Silicone Single Lumen Catheter | 14.4, 15 | 14.4 F: 45, 50, 55; 15 F: 25, 30 | Standard tip | One | No | No | Chronic |
| Joline GmbH & Co. KG | Evolution Flow Retrograde | 15.5 | 19, 23, 28, 33, 55 | Symmetric tip | Two | No | No | Chronic |
| Joline GmbH & Co. KG | Smooth Flow Double Lumen Catheter | 15.5 | 19, 23, 28, 33 | Symmetric tip | Two | No | No | Chronic |
| Joline GmbH & Co. KG | Double Lumen Catheter | 11 | 12.5, 15, 17.5, 20, 25 | Tapered tip | Two | Yes | No | Acute |
| Joline GmbH & Co. KG | Triple Lumen Catheter | 12 | 15, 17.5, 20, 25 | Tapered tip | Three | Yes | No | Acute |
Other Devices / Embolic Protection Devices
View Chart| Company Name | Product Name | Type | Position | CE Mark Indications |
|---|---|---|---|---|
| Abbott | Emboshield Nav6 | Barewire filter delivery wire | Distal | The system is designed to reduce distal embolization while maintaining blood flow during interventional procedures; indicated for use during percutaneous transluminal angioplasty, and stenting procedures in saphenous vein grafts and carotid arteries and percutaneous transluminal angioplasty, atherectomy and stenting procedures in the lower extremity arteries |
| Balton | Robin RX/OTW | Nitinol filter basket | Distal | Distal neuroprotection system is used to seize embolic material during performance of angioplasty procedure on carotid artery and during stent implementation in carotid arteries; recommended vessel diameter from 3 to 7.5 mm |
| Boston Scientific Corporation | FilterWire EZ Embolic Protection System | Filter | Distal | Indicated for use as a guidewire and EPS to contain and remove embolic material (thrombus/debris) while performing angioplasty and stenting procedures in coronary saphenous vein bypass grafts and carotid arteries; the diameter of the vessel at the site of filter loop placement should be between 2.25–5.5 mm for coronary saphenous vein bypass graft procedures and between 3.5–5.5 mm for carotid procedures |
| Boston Scientific Corporation | Sentinel Cerebral Protection System | Dual filter | Utilizes an embolic filter delivered to the brachiocephalic artery (proximal filter) and a second embolic filter delivered to the left common carotid artery (distal filter) | Indicated for use as an embolic protection device to capture and remove embolic material (thrombus/debris) that may enter the cerebral vascular system during endovascular procedures; the diameters of the arteries at the site of filter placement should be between 9–15 mm for the brachiocephalic and 6.5–10 mm in the left common carotid |
| Contego Medical LLC | Paladin Carotid Post-Dilation Balloon System With Integrated Embolic Protection | Carotid postdilation balloon with integrated embolic protection filter (40 µm) | Distal | Indicated for postdilation of a deployed self-expanding stent in the carotid artery |
| Contego Medical LLC | Vanguard IEP Peripheral Balloon Angioplasty System With Integrated Embolic Protection | Angioplasty balloon with integrated embolic protection filter (150 µm) | Distal | Indicated for peripheral vascular percutaneous transluminal angioplasty and the capture and removal of embolic material during angioplasty for the femoral, iliac, popliteal, and profunda arteries |
| Cordis | Angioguard RX Emboli Capture Guidewire System | Filter | Distal | Indicated for use as a guidewire and EPS to contain and remove embolic material (thrombus/debris) while performing carotid artery angioplasty and stenting procedures in carotid arteries; the diameter of the artery at the site of the filter basket placement should be from 3 to 7.5 mm (see instructions for use for basket/vessel sizing) |
| Invamed | Inca | Protective filter | Distal | Indicated for use as a guidewire and EPS to contain and remove embolic material while performing DVT carotid artery angioplasty, stenting procedures in carotid arteries; suitable for acute PE, VTE, and ICU thrombectomy |
| Medtronic | Mo.Ma Ultra Proximal Cerebral Protection Device | Proximal protection | Proximal | Indicated as an EPS to contain and remove embolic material (thrombus/debris) while performing angioplasty and stenting procedures involving lesions of the internal carotid artery and/or the bifurcation; the reference diameter of the external carotid artery should be between 3–6 mm and the reference diameter of the common carotid artery should be between 5–13 mm |
| Medtronic | SpiderFX Embolic Protection Device | Filter; guidewire of choice | Distal | Indicated for distal embolization protection during peripheral, coronary, and carotid interventions; indications, contraindications, warnings, and Instructions for Use can be found in the product labeling supplied with each device |
| Terumo Europe | Nanoparasol | Filter; concentric nitinol micromesh; guidewire of choice | Distal | Indicated for use in patients with carotid arterial atherosclerotic disease; indicated for use as a guidewire to contain and remove embolic material (thrombus/debris) while performing angioplasty and stenting procedures in carotid arteries |
Other Devices / Endovenous Ablation
View Chart| Company Name | Product Name | Technology | Wavelength (nm) | Sheath Size (F) | Sheath Length (cm) | CE Mark Indications |
|---|---|---|---|---|---|---|
| AngioDynamics | 400 Micron Perforator & Accessory Vein Ablation Kit (PVAK) | Procedure kit | All | 400 µm | 10 | Indicated for use in the treatment of superficial vein reflux of greater saphenous vein associated with varicosities, for treatment of incompetence and reflux of superficial veins in the lower extremity, and for the treatment of incompetent (ie, refluxing) perforator veins |
| AngioDynamics | NeverTouch | Procedure kit | All | 4 | 25, 45, 65, 90 | Endovascular coagulation of the great saphenous vein in patients with superficial vein reflux, for the treatment of varicose veins and varicosities associated with superficial reflux of the great saphenous vein, and for the treatment of incompetence and reflux of superficial veins of the lower extremity |
| AngioDynamics | NeverTouch Direct | Procedure kit | All | 600 µm | 10 | Treatment of varicose veins and varicosities associated with superficial vein reflux of the great saphenous vein and for the treatment of incompetent refluxing veins in the superficial venous system in the lower limb |
| AngioDynamics | Spotlight OPS | Procedure kit | All | 4 | 25, 55, 80 | Treatment of varicose veins and varicosities associated with superficial vein reflux of the great saphenous vein and with the treatment of incompetent refluxing veins in the superficial venous system in the lower limb |
| AngioDynamics | VenaCure 1470 | Laser | 1,470 | – | – | Treatment of varicose veins and varicosities with superficial reflux of the greater saphenous vein and in the treatment of incompetent refluxing veins in the superficial venous system in the lower limb |
| BD Interventional | Venclose Radiofrequency Generator | Radiofrequency | – | – | – | Intended for endovascular coagulation of blood vessels in patients with superficial vein reflux |
| BD Interventional | Venclose RF Ablation System | Radiofrequency | Adjustable heating length (2.5 cm/10 cm) | 6 (with working length of 60 cm and 100 cm) | 7, 12 | Intended for endovascular coagulation of blood vessels in patients with superficial vein reflux |
| Biolas | Endosealer | Polymer-based agent | – | – | – | Treatment of varicose veins (superficial and tributary veins) by a simple ablative polymerization method; small amount of polymer-based agent injected endovenously by a small injector system |
| Biolas | Evlas Circular | Laser | 1,470 | – | – | Endovenous laser treatment method depends on the principle of closing the damaged vein by generating laser energy inside the vein with minimally invasive surgery, rather than removing the leaking vessel with traditional surgery; after surgery, there won't be any leakage into the varicose veins and visible varicose veins will shrink and disappear; as soon as the damaged vein is treated, healthy veins will provide venous circulation |
| Biolas | VariClose | Vein sealing system | – | 6 | 90 | Embolization polymer that is indicated for ablation by polymerization of saphenous vein (vena saphena magna, valve saphenous parva) or perforator veins in endovenous treatment of incompetent lower-extremity varicose veins |
| Dornier MedTech GmbH | FlexiPulse | Laser | 940 | – | – | – |
| Dornier MedTech GmbH | LiteBeam + | Laser | 1,470 | – | – | – |
| F Care Systems | EVRF | Radiofrequency | – | 1 (gauge 20, 24) | 14, 120 | CR45- GSV; CR12- Reticular Perforator Colaterall up to 2 mm and up to 6 mm for C4 30 |
| iMS GmbH | AntiStick | Laser fiber 600 µm | 1,940 | 6 | 260 | Designed to direct laser energy at soft tissue during contact and noncontact surgical procedures, including in applications that involve the use of rigid and flexible endoscopes; they are suitable for use in vascular surgery |
| iMS GmbH | AntiStick | Laser fiber 400 µm | 1,940 | 4 (17 G) | 260 | Designed to direct laser energy at soft tissue during contact and noncontact surgical procedures, including in applications that involve the use of rigid and flexible endoscopes; they are suitable for use in vascular surgery |
| iMS GmbH | AntiStick Pro | Laser fiber 400 µm | 1,940 | 4 (16G) | 250 | The intended use of the optical fiber probes is to deliver laser radiation from its source to the treatment site of the patient in the context of a medical laser surgery; the optical fiber probes are indicated in laser surgery application of different disciplines in minimally invasive surgery |
| iMS GmbH | AntiStick Pro | Laser fiber 600 µm | 1,940 | 6 | 250 | The intended use of the optical fiber probes is to deliver laser radiation from its source to the treatment site of the patient in the context of a medical laser surgery; the optical fiber probes are indicated in laser surgery application of different disciplines in minimally invasive surgery |
| iMS GmbH | simLa6 | Laser | 1,940 | – | – | A surgical laser system for endovenous laser treatment (treatment of varicosis) in phlebology/vascular surgery; used in conjunction with the approved applicator fibers which are typically introduced directly into the veins/varicose veins to be treated using so-called introducers; indicated for the coagulation of the soft tissue/the denaturing of collagen in the vein (wall); the objective is the permanent sclerosing/occlusion of constricted leg veins; minimally invasive thermal treatment of varicose veins using primarily glass fibers applicators of varying external diameters that emit radially |
| Invamed | Filler | Polymer (n-BCA) | – | 6 | 90 | Treatment of iliac artery aneurysms, AAAs, and endoleaks using polymer n-BCA |
| Invamed | ThermaBlock | Handheld endovenous radiofrequency ablation catheter (without generator) | All | 6 | 100 | Treatment of the great saphenous vein and the small saphenous vein; no generator is needed; disposable |
| Invamed | Veinoff | Polymer | – | – | – | Treatment of varicose veins (tributary veins) by a simple ablative polymerization method; small amounts of polymer (OCA) injected endovenously by a butterfly catheter and small injector system |
| Invamed | VenaBlock | Delivery system | – | 6 | 90 | Treatment of venous insufficiency; indicated for use in the permanent closure of lower extremity superficial truncal veins, such as the great saphenous vein and perforator vein, continuously while applying pressure over the target vein segment |
| Invamed | VenaBlock Automated System | Delivery system | – | 6 | 200 | Treatment of venous insufficiency; indicated for use in the permanent closure of lower extremity superficial truncal veins, such as the great saphenous vein and perforator vein, continuously while applying pressure over the target vein segment automatically |
| Medtronic | ClosureFast 3 cm Radiofrequency Ablation Catheter | Radiofrequency ablation | Heating length (3 cm); working length of 60 cm | 7 | 7, 11 | Intended for endovascular coagulation of blood vessels in patients with superficial venous reflux |
| Medtronic | ClosureFast 7 cm Radiofrequency Ablation Catheter | Radiofrequency ablation | Heating length (7 cm); working lengths of 60 and 100 cm | 7 | 7, 11 | Intended for endovascular coagulation of blood vessels in patients with superficial venous reflux |
| Medtronic | ClosureFast 8 cm Radiofrequency Ablation Catheter | Radiofrequency ablation | Heating length (8 cm); working lengths of 60 and 100 cm | 6 | 7, 11 | Intended for endovascular coagulation of blood vessels in patients with superficial venous reflux |
| Medtronic | ClosureRFG Radiofrequency Generator (Model 3) | Radiofrequency | – | – | – | Intended for use with the ClosureFast catheter (7, 3 cm) and ClosureRFS products |
| Medtronic | ClosureRFS Endovenous Radiofrequency Stylet | Radiofrequency | – | 6 (with 12-cm working length) | – | Perforator veins |
| Medtronic | VenaSeal Closure System | Nonthermal, nontumescent: cyanoacrylate-based medical adhesive | – | Access with 5-F microintroducer; blue introducer (ID: 5, OD: 7) included in kit | 80 (blue introducer included) | Intended for the permanent, complete, endovascular adhesive closure of the great saphenous vein and associated varicosities in the treatment of venous reflux disease |
| Merit Medical Systems, Inc. | ClariVein OC | Mechanochemical | – | 4, 5 | – | Indicated for infusion of physician-specified agents in the peripheral vasculature including for endovascular occlusion of incompetent veins in patients with superficial venous reflux |
| STARmed Co., Ltd. | VeniStar 3 cm Endovenous Radiofrequency Ablation (RFA) Electrode | Radiofrequency | 0–3 cm active tip length | 7 (with 65 cm working length) | 7, 11 | Disposable hand-held electrode for electrosurgical instrument is intended for coagulation of tissue and blood vessel during endoscopic, percutaneous, laparoscopic, and intraoperative surgical procedures |
| STARmed Co., Ltd. | VeniStar 7 cm Endovenous Radiofrequency Ablation (RFA) Electrode | Radiofrequency | 3–7 cm active tip length | 7 (with 65 cm working length) | 7, 11 | Disposable hand-held electrode for electrosurgical instrument is intended for coagulation of tissue and blood vessel during endoscopic, percutaneous, laparoscopic, and intraoperative surgical procedures |
| STARmed Co., Ltd. | VVR RF System | Radiofrequency | – | – | – | Intended for use with the VeniStar electrode (3, 7 cm) |
| Total Vein Systems | Introducer Kits | Introducer kit | – | 4, 5, 6, 7 | 7, 11, 20, 25, 35, 45, 55, 65, 85 | Arterial and venous procedures requiring percutaneous introduction of intravascular devices |
| Total Vein Systems | Laser Fibers | Laser | Argon, KTP/532, Ho:YAG, Nd:YAG, 1.44Y AG, and Diode (532–2,100 nm) | – | – | Deliver laser light to soft tissue in the contact and noncontact mode during surgical procedures including via endoscopes and cystoscopes |
| Total Vein Systems | TVS 1470 | Laser | 1,470 (15 watt) | – | – | Surgical applications requiring the vaporization, incision, excision, ablation, cutting, and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment |
| Total Vein Systems | TVS 1470 Nano | Laser | 1,470 (7 watt) | – | – | Surgical applications requiring the vaporization, incision, excision, ablation, cutting, and hemostasis, or coagulation of soft tissue in conjunction with endoscopic equipment |
Other Devices / FFR Technologies
View Chart| Company Name | Product Name | Type (Fixed or Movable Core) | Diameter (inch) | Length (cm) | Tip Type | Antithrombogenic (Yes/No) | Comments |
|---|---|---|---|---|---|---|---|
| Abbott | PressureWire X Guidewire | Fixed core | 0.014 | 175 | Straight | Yes, PTFE coated | Fully integrated, wireless PressureWire system when used with compatible hemodynamic systems; provides FFR measurement on Ilumien, Ilumien Optis, Optis Mobile, and Optis Integrated systems |
| Infraredx, A Nipro Company | TVC Insight | – | 0.014 | 160 | – | – | High-resolution rotational IVUS image with precision automated pullback; excellent deliverability with a durable hydrophilic coating; catheter provides additional information with lipid core plaque detection (also see Intravascular Ultrasound) |
| Opsens Medical | OptoWire | Nitinol core with free-floating technology | 0.014 | 174 | 0.65-g tip load | Yes | A second-generation fiber-optic pressure guidewire; accurate pressure measurements can be repeated with consistency, and fiber optic enables unique concentric guidewire design with improved torqueability; operators can access complex anatomies while saving time and cost by delivering a stent over the same guidewire; the wire is designed to provide low drift |
| Philips | ComboWire Guidewire | Fixed core | 0.014 | 185 | Straight | Yes | Measures both pressure and flow, using Doppler ultrasound, on one wire; 1.5-cm sensor spacing and 0-cm sensor spacing available |
| Philips | FloWire Doppler Guidewire | Fixed core | 0.014 | 175, 300 | Straight, J-shaped | Yes | Measures flow using pulsed-wave Doppler technology |
| Philips | Verrata Plus Pressure Guidewire | Fixed core | 0.014 | 185, 300 | Straight, J-shaped | Yes | Integrated iFR, FFR, and IVUS on s5i, Core, and IntraSight systems; integrates to measure FFR with compatible hemodynamic systems |
| Philips | Verrata Pressure Guidewire | Fixed core | 0.014 | 185, 300 | Straight, J-shaped | Yes | Integrated iFR, FFR, and IVUS on s5i, Core, and IntraSight systems; integrates to measure FFR with compatible hemodynamic systems |
Other Devices / Hybrid Vascular Grafts
View Chart| Company Name | Product Name | Materials Used | Nitinol Reinforced Section Diameter (mm) | Nitinol Reinforced Section Length (cm) | Vascular Graft Section Introducer Size (F) | Vascular Graft Section Recommended Guidewire (inch) | Introducer Size (F) | Recommended Guidewire (inch) | CE Mark Indications |
|---|---|---|---|---|---|---|---|---|---|
| BD Interventional | Carboflo Vascular Graft | ePTFE with carbon impregnated into the inner portions of the graft wall | 4, 5, 6, 7, 8, 10 | 1, 2, 3, 4, 5, 6, 7, 8 | – | – | – | – | Indicated for use as vascular prostheses |
| BD Interventional | Distaflo Bypass Graft | ePTFE with carbon impregnated into the inner portions of the graft wall; graft is also modified with a proprietary cuff at the distal end | 6, 7, 8 | 50, 60, 70, 80 | – | – | – | – | Intended for bypass or reconstruction of peripheral arterial blood vessels |
| BD Interventional | Venaflo II Vascular Graft | Vascular ePTFE grafts for haemodialysis | 4-7 | 1, 2 , 2.5, 3, 3.5, 4, 4.5, 5 | – | – | – | – | – |
| Merit Medical Systems, Inc. | Hero Graft | Nitinol, silicone, barium sulfate, tantalum, ePTFE, PTFE, and titanium | 5 ID | 40 (customizable length) | – | 0.035 for over-the-wire | 20 peelaway for over-the-wire | 59 (minimum length) | Indicated for end-stage renal disease patients on hemodialysis who have exhausted all other access options; see Instructions for Use for full indication, contraindication, and caution statements; Rx only |
| Getinge | Flixene Vascular Graft | ePTFE | 6, 7, 4–6, 4–7 | 10, 30, 35, 40, 45, 50 | – | – | – | – | Flixene vascular grafts are intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access |
Other Devices / Intravascular Lithotripsy
View Chart| Company Name | Product Name | Diameter (mm) | Length (mm) | Guidewire Compatibility (inch) | Working Length (cm) | Max Pulses/Max Cycles (pulses per cycle) | Crossing Profile (mm) | Sheath Compatibility (F) | CE Mark Indication |
|---|---|---|---|---|---|---|---|---|---|
| Shockwave Medical, Inc. | Shockwave M5+ Peripheral IVL Catheters | 3.5, 4, 4.5, 5, 5.5, 6, 6.5, 7, 8 | 60 | 0.014 | 135 | 300/10 (30) | - | 6–7 | Indicated for lithotripsy-enhanced, low-pressure balloon dilatation of lesions, including calcified lesions, in the peripheral vasculature, including the iliac, femoral, ilio-femoral, popliteal, infra-popliteal, and renal arteries; this device is not intended for use in coronary, carotid, or cerebrovascular arteries |
| Shockwave Medical, Inc. | Shockwave S4 Peripheral IVL Catheters | 2.5, 3, 3.5, 4 | 40 | 0.014 | 135 | 160/8 (20) | - | 5 | Indicated for lithotripsy-enhanced, low pressure balloon dilatation of calcified, stenotic peripheral arteries in patients who are candidates for percutaneous therapy |
| Shockwave Medical, Inc. | Shockwave L6 Peripheral IVL Catheters | 8, 9, 10, 12 | 30 | 0.018 | 110 | 300/10 (30) | - | 7–8 | Indicated for lithotripsy-enhanced, low-pressure balloon dilatation of lesions, including calcified lesions, in the peripheral vasculature, including the iliac, femoral, ilio-femoral, popliteal, and infra-popliteal arteries; this device is not intended for use in coronary, carotid, or cerebrovascular arteries |
| Shockwave Medical, Inc. | Shockwave E8 Peripheral IVL Catheters | 2.5, 3, 3.5, 4, 5, 6 | 80 | 0.014 | 150 | 400/10 (40) | - | 5–6 | Indicated for lithotripsy-enhanced balloon dilatation of lesions, including calcified lesions, in the peripheral vasculature, including the iliac, femoral, iliofemoral, popliteal, infrapopliteal, and renal arteries; not for use in the coronary, carotid or cerebral vasculature |
| Shockwave Medical, Inc. | Shockwave Javelin Peripheral IVL Catheter | – | – | 0.014 | 150 | 120/12 (10) | 1.5 | 5 | Indicated for lithotripsy-enabled modification and crossing of calcified lesions in the peripheral vasculature, including the iliac, femoral, iliofemoral, popliteal, and infrapopliteal arteries, prior to final treatment; not for use in coronary, carotid, or cerebral vasculature; additionally, not for use in pulmonary vasculature in the United States and New Zealand |
Other Devices / Intravascular Spectroscopy
View Chart| Company Name | Product Name | Catheter Usable Length (cm) | Maximum Guidewire (inch) | Minimum Guide Catheter ID (F) | Shaft Distal Section (F) | Spectroscopic Method | Algorithm Target | Comments |
|---|---|---|---|---|---|---|---|---|
| Infraredx, A Nipro Company | TVC Insight | 160 | 0.014 | 6 (ID ≥ 0.067 inch) | 3.2 | Near infrared diffuse reflectance | Intramural cholesterol/necrotic core | High-resolution rotational IVUS image with precision automated pullback; excellent deliverability with a durable hydrophilic coating; catheter provides additional information with lipid core plaque detection (also see Intravascular Ultrasound) |
Other Devices / Intravascular Ultrasound
View Chart| Company Name | Product Name | Imaging Diameter (mm) | Catheter Usable Length (cm) | Maximum Guidewire (inch) | Minimum Guide Catheter ID (F) | Shaft Distal Section (F) | Minimum Sheath Diameter (F) | Comments |
|---|---|---|---|---|---|---|---|---|
| Infraredx, A Nipro Company | TVC Insight | 16 | 160 | 0.014 | 6 (ID ≥ 0.067 inch) | 3.2 | 6 | High-resolution rotational image with precision automated pullback; excellent deliverability with a durable hydrophilic coating; catheter provides additional information with lipid core plaque detection (see Intravascular Spectroscopy) |
| Philips | Eagle Eye Platinum Digital IVUS (coronary or peripheral) | 20 | 150 | 0.014 | 5 (ID ≥ 0.056 inch) | – | 5 | Highly deliverable plug-and-play IVUS with GlyDx hydrophilic, three radiopaque markers, VH IVUS, and ChromaFlo imaging |
| Philips | Eagle Eye Platinum ST Digital IVUS (coronary or peripheral) | 20 | 150 | 0.014 | 5 (ID ≥ 0.056 inch) | – | 5 | Short-tip model: highly deliverable plug-and-play IVUS with GlyDx hydrophilic, three radiopaque markers, VH IVUS, and ChromaFlo imaging |
| Philips | Refinity ST Rotational IVUS (coronary) | 14 | 135 | 0.014 | 5 (ID ≥ 0.056 inch) | – | 5 | High frequency (45 MHz) rotational IVUS |
| Philips | Visions PV .014P RX (small peripheral) | 20 | 150 | 0.014 | 5 (ID ≥ 0.056 inch) | – | 5 | Highly deliverable plug-and-play IVUS with hydrophilic coating, three radiopaque markers, and ChromaFlo imaging |
| Philips | Visions PV .018 (small peripheral) | 24 | 135 | 0.018 | 6 | – | 5 | Plug-and-play; digital IVUS with ChromaFlo imaging |
| Philips | Visions PV .035 (large peripheral) | 60 | 90 | 0.035 | 8.5 | – | 8.5 | Plug-and-play; digital IVUS with centimeter markers |
Other Devices / Mechanical Thrombectomy/Thrombolysis (Peripheral/Venous)
View Chart| Company Name | Product Name | Sheath Compatibility (F) | Guidewire Compatibility (inch) | Working Length (cm) | Mode of Operation | CE Mark Indications |
|---|---|---|---|---|---|---|
| Argon Medical Devices, Inc. | Cleaner 15 | 7 | – | 65, 135 | Battery-operated, handheld drive unit initiates the mechanical rotation of an atraumatic, wall-contacting, 15-mm sinusoidal vortex wire for effective thrombus maceration | Indicated for mechanical declotting and controlled and selective infusion of physician-specified fluids, including thrombolytics, in the peripheral vasculature; also indicated for mechanical declotting of native vessel dialysis fistulas and synthetic dialysis access grafts |
| Argon Medical Devices, Inc. | Cleaner XT | 6 | – | 65, 135 | Battery-operated, handheld drive unit initiates the mechanical rotation of an atraumatic, wall-contacting, 9-mm sinusoidal vortex wire for effective thrombus maceration | Indicated for mechanical declotting and controlled and selective infusion of physician-specified fluids, including thrombolytics, in the peripheral vasculature; also indicated for mechanical declotting of native vessel dialysis fistulas and synthetic dialysis access grafts |
| BD Interventional | AspirexS: Mechanical Aspiration Thrombectomy System | 8 | 0.018 | 85, 110 | Aspirex S catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of fresh thrombotic or thromboembolic material from blood vessels outside the cardiopulmonary, coronary, and cerebral circulations | Native blood vessels or vessels fitted with stents, stent grafts, or native or artificial bypasses outside the cardiopulmonary, coronary, and cerebral circulations |
| BD Interventional | AspirexS: Mechanical Aspiration Thrombectomy System | 10 | 0.025 | 110 | Aspirex S catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of fresh thrombotic or thromboembolic material from blood vessels outside the cardiopulmonary, coronary, and cerebral circulations | Native blood vessels or vessels fitted with stents, stent grafts, or native or artificial bypasses outside the cardiopulmonary, coronary, and cerebral circulations |
| BD Interventional | AspirexS: Mechanical Aspiration Thrombectomy System | 6 | 0.018 | 110, 135 | Aspirex S catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of fresh thrombotic or thromboembolic material from blood vessels outside the cardiopulmonary, coronary, and cerebral circulations | Native blood vessels or vessels fitted with stents, stent grafts, or native or artificial bypasses outside the cardiopulmonary, coronary, and cerebral circulations |
| BD Interventional | RotarexS Rotational Atherothrombectomy System | 8 | 0.018 | 85, 110 | RotarexS catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of thrombotic, thromboembolic and atherothrombotic material from fresh, subacute and chronic occlusions of blood vessels outside the cardiopulmonary, coronary and cerebral circulations | Native blood vessels or vessels fitted with stents, stent grafts or native or artificial bypasses outside the cardiopulmonary, coronary and cerebral circulations |
| BD Interventional | RotarexS Rotational Atherothrombectomy System | 10 | 0.025 | 85 | RotarexS catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of thrombotic, thromboembolic and atherothrombotic material from fresh, subacute and chronic occlusions of blood vessels outside the cardiopulmonary, coronary and cerebral circulations | Native blood vessels or vessels fitted with stents, stent grafts or native or artificial bypasses outside the cardiopulmonary, coronary and cerebral circulations |
| BD Interventional | RotarexS Rotational Atherothrombectomy System | 6 | 0.018 | 110, 135 | RotarexS catheters in combination with the Straub Medical Drive System (REF SRS-Set/80300) are intended for the percutaneous transluminal removal of thrombotic, thromboembolic and atherothrombotic material from fresh, subacute and chronic occlusions of blood vessels outside the cardiopulmonary, coronary and cerebral circulations | Native blood vessels or vessels fitted with stents, stent grafts or native or artificial bypasses outside the cardiopulmonary, coronary and cerebral circulations |
| Boston Scientific Corporation | AngioJet AVX Thrombectomy Set | 6 | 0.035 | 50 | High-velocity water jets enclosed in catheter utilize the Bernoulli principle for capture, microfragmentation, and removal | Breaking apart and removing thrombus from AV access conduits ≥ 3 mm in diameter |
| Boston Scientific Corporation | AngioJet Distaflex Thrombectomy Set | 4 | 0.014 | 145 | High-velocity water jets enclosed in catheter utilize the Bernoulli principle for capture, microfragmentation, and removal | Removing thrombus in the treatment of patients with symptomatic coronary artery or saphenous vein graft lesions prior to balloon angioplasty or stent placement and use in breaking apart and removing thrombus from infrainguinal peripheral arteries ≥ 2 mm in diameter |
| Boston Scientific Corporation | AngioJet Solent Dista Thrombectomy Set | 4 | 0.014 | 145 | High-velocity water jets enclosed in catheter utilize the Bernoulli principle for capture, microfragmentation, and removal (PowerPulse enabled) | Breaking apart and removing thrombus from upper and lower extremity peripheral arteries ≥ 1.5 mm in diameter |
| Boston Scientific Corporation | AngioJet Solent Omni Thrombectomy Set | 6 | 0.035 | 120 | High-velocity water jets enclosed in catheter utilize the Bernoulli principle for capture, microfragmentation, and removal (PowerPulse enabled) | Breaking apart and removing thrombus from upper and lower extremity peripheral arteries, upper extremity peripheral veins, iliofemoral and lower extremity veins, and AV access conduits ≥ 3 mm in diameter |
| Boston Scientific Corporation | AngioJet Solent Proxi Thrombectomy Set | 6 | 0.035 | 90 | High-velocity water jets enclosed in catheter utilize the Bernoulli principle for capture, microfragmentation, and removal (PowerPulse enabled) | Breaking apart and removing thrombus from upper and lower extremity peripheral arteries, upper extremity peripheral veins, iliofemoral and lower extremity veins, and AV access conduits ≥ 3 mm in diameter |
| Boston Scientific Corporation | AngioJet Spiroflex Thrombectomy Set | 5 | 0.014 | 135 | High-velocity water jets enclosed in catheter utilize the Bernoulli principle for capture, microfragmentation, and removal | Removing thrombus in the treatment of patients with symptomatic coronary artery or saphenous vein graft lesions prior to balloon angioplasty or stent placement and use in breaking apart and removing thrombus from infrainguinal peripheral arteries ≥ 2 mm in diameter |
| Boston Scientific Corporation | AngioJet SpiroflexVG Thrombectomy Set | 6 | 0.014 | 135 | High-velocity water jets enclosed in catheter utilize the Bernoulli principle for capture, microfragmentation, and removal | Removing thrombus in the treatment of patients with symptomatic coronary artery or saphenous vein graft lesions prior to balloon angioplasty or stent placement and use in breaking apart and removing thrombus from infrainguinal peripheral arteries ≥ 3 mm in diameter |
| Boston Scientific Corporation | AngioJet Ultra PE Thrombectomy Set | 6 | 0.035 | 120 | High-velocity water jets enclosed in catheter utilize the Bernoulli principle for capture, microfragmentation, and removal | Breaking apart and removing thrombus from main pulmonary and lobar arteries ≥ 6 mm in diameter |
| Boston Scientific Corporation | AngioJet XMI Thrombectomy Set | 4 | 0.014 | 135 | High-velocity water jets enclosed in catheter utilize the Bernoulli principle for capture, microfragmentation, and removal | Removing thrombus in the treatment of patients with symptomatic coronary artery or saphenous vein graft lesions prior to balloon angioplasty or stent placement and use in breaking apart and removing thrombus from infrainguinal peripheral arteries ≥ 2 mm in diameter |
| Boston Scientific Corporation | AngioJet ZelanteDVT Thrombectomy Set | 8 | 0.035 | 105 | High-velocity water jets enclosed in catheter utilize the Bernoulli principle for capture, microfragmentation, and removal (PowerPulse enabled) | Intended for use with the AngioJetUltra Console to break apart and remove thrombus, including DVT, from: Iliofemoral and lower extremity veins ≥ 6 mm in diameter and upper extremity peripheral veins ≥ 6 mm in diameter; also intended for use with the AngioJet Ultra Power Pulse technique for the controlled and selective infusion of physician specified fluids, including thrombolytic agents, into the peripheral vascular system |
| Boston Scientific Corporation | EkoSonic Endovascular System | 6 | 0.035 | 106 catheter length (treatment areas: 6, 12, 18, 24, 30, 40, 50), 135 catheter length (treatment areas: 12, 30, 40, 50) | The treatment offers a minimally invasive system for the acceleration of thrombus dissolution; the ultrasonic core generates a localized acoustic field that targets the entire thrombus; this greatly accelerates lytic dispersion by driving the drug deeper into the clot and unwinding the fibrin to expose plasminogen receptor sites | Intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral vasculature; for the treatment of pulmonary embolism with a ≥ 50% clot burden in one or both main pulmonary arteries or lobar pulmonary arteries, and evidence of right heart dysfunction based on right heart pressures (mean pulmonary artery pressure ≥ 25 mm Hg) or echocardiographic evaluation |
| Control Medical Technology | Control 10F Mechanical Thrombectomy System | 10 | 0.035 | 90 | Mechanical thrombectomy with mechanical aspirator, OTW catheter, and dilator | Mechanical thrombectomy to remove soft fresh emboli and thrombi from the peripheral vasculature |
| Control Medical Technology | Control 5F Mechanical Thrombectomy System | 5 | 0.035 | 135 | Mechanical thrombectomy | Mechanical thrombectomy to remove soft fresh emboli and thrombi from the peripheral vasculature |
| Control Medical Technology | Control 6F Mechanical Thrombectomy System | 6 | 0.035 | 135 | Mechanical thrombectomy | Mechanical thrombectomy to remove soft fresh emboli and thrombi from the peripheral vasculature |
| Control Medical Technology | Control 8F Mechanical Thrombectomy System | 8 | 0.035 | 90 | Mechanical thrombectomy with mechanical aspirator, OTW catheter, and dilator | Mechanical thrombectomy to remove soft fresh emboli and thrombi from the peripheral vasculature |
| Control Medical Technology | Control Mechanical Aspirator | Any sheath | Any guidewire | Any length | Mechanical aspirator | Mechanical thrombectomy and to remove fluids from the body |
| Inari Medical | ClotTriever Thrombectomy System | 13, 16 | 0.035 | 80 | Mechanical coring, collection, and retrieval of emboli and thrombi | The nonsurgical removal of thrombi and emboli from blood vessels; injection, infusion, and/or aspiration of contrast media and other fluids into or from a blood vessel; intended for use in the peripheral vasculature including deep vein thrombosis |
| Inari Medical | FlowTriever Catheter (disks) - FlowTriever Retrieval/Aspiration System | 20, 22 | 0.035 | 115 | Mechanical and aspirational disruption, fragmentation, maceration, and retrieval of emboli and thrombi | The nonsurgical removal of emboli and thrombi from blood vessels, and injection, infusion and/or aspiration of contrast media and other fluids into or from a blood vessel; the FlowTriever System is intended for use in the peripheral vasculature and for the treatment of pulmonary embolism; Triever catheters are intended for use in treating clot in transit in the right atrium, but not in conjunction with FlowTriever catheters |
| Inari Medical | FlowTriever2 Catheter (disks) - FlowTriever Retrieval/Aspiration System | 20, 22, 24, 26 | 0.035 | 120 | Mechanical and aspirational disruption, fragmentation, maceration, and retrieval of emboli and thrombi | The nonsurgical removal of emboli and thrombi from blood vessels, and injection, infusion and/or aspiration of contrast media and other fluids into or from a blood vessel; FlowTriever2 is intended for use in the peripheral vasculature |
| Inari Medical | Triever16 - FlowTriever Retrieval/Aspiration System | 20, 22, 24 | 0.035 | 113 | Mechanical and aspirational disruption, fragmentation, maceration, and retrieval of emboli and thrombi | The nonsurgical removal of emboli and thrombi from blood vessels, and injection, infusion and/or aspiration of contrast media and other fluids into or from a blood vessel; the FlowTriever System is intended for use in the peripheral vasculature and for the treatment of pulmonary embolism; Triever catheters are intended for use in treating clot in transit in the right atrium, but not in conjunction with FlowTriever catheters |
| Inari Medical | Triever20 - FlowTriever Retrieval/Aspiration System | 20, 22, 24 | 0.035 | 90 | Mechanical and aspirational disruption, fragmentation, maceration, and retrieval of emboli and thrombi | The nonsurgical removal of emboli and thrombi from blood vessels, and injection, infusion, and/or aspiration of contrast media and other fluids into or from a blood vessel; the FlowTriever System is intended for use in the peripheral vasculature and for the treatment of pulmonary embolism; Triever catheters are intended for use in treating clot in transit in the right atrium but not in conjunction with FlowTriever catheters |
| Inari Medical | Triever24 - FlowTriever Retrieval/Aspiration System | 24, 26 | 0.035 | 90 | Mechanical and aspirational disruption, fragmentation, maceration, and retrieval of emboli and thrombi | The nonsurgical removal of emboli and thrombi from blood vessels, and injection, infusion and/or aspiration of contrast media and other fluids into or from a blood vessel; the FlowTriever System is intended for use in the peripheral vasculature and for the treatment of pulmonary embolism; Triever Catheters are intended for use in treating clot in transit in the right atrium, but not in conjunction with FlowTriever catheters |
| Invamed | Mantis | 7 | – | 90 | Battery-operated, handheld drive unit initiates the mechanical rotation of an atraumatic unique loop shape with aspiration | DVT pharmacomechanical declotting and controlled and selective infusion of physician-specified fluids, including thrombolytics, in the peripheral vasculature; double engine volume, low and high speed options; hydrophilic tip |
| Invamed | Viper | 5 | 0.035 | 200 | Designed for controlled infusion of tPA along with mechanical vibrations | Over the guidewire system and 200 cm catheter length allows safe access to closed target vessels including pulmonary artery in PE cases |
| Penumbra, Inc. (Peripheral Vascular) | Indigo System Catheter, Lightning 12, Lightning 7, CAT7D, CAT8, CATD, CAT6, CAT5, and CAT3 | 5 (CAT3), 6 (CAT6, CAT5), 8 (CAT8, CATD), 7 (Lightning 7, CAT7D), 12 (Lightning 12) | 0.014–0.038 | 50–150 | The Indigo System with Lightning Aspiration Tubing is computer aided mechanical aspiration powered by the Penumbra ENGINE which utilizes a unique mechanism of action to help optimize thrombus removal procedures by differentiating between thrombus and blood. Lightning comes packaged as Lightning 7 and Lightning 12 | As part of the Indigo Aspiration System, the Indigo aspiration catheters and separators are indicated for the removal of fresh, soft emboli and thrombi from vessels of the peripheral arterial and venous systems, and for the treatment of pulmonary embolism |
| Penumbra, Inc. (Peripheral Vascular) | Indigo System Separator, SEP12, SEP7, SEP7D, SEP8, SEPD, SEP6, SEP5, and SEP3 | – | – | 90–190 | The device is advanced and retracted through the Indigo catheter at the proximal margin of the primary occlusion to facilitate clearing of the thrombus from the catheter tip, as needed | As part of the Indigo Aspiration System, the Indigo aspiration catheters and separators are indicated for the removal of fresh, soft emboli and thrombi from vessels of the peripheral arterial and venous systems, and for the treatment of pulmonary embolism |
| AngioDynamics | AlphaVac F18 System | 22 | 0.038 | 105 | Multipupose mechanical aspiration | The cannula is indicated for the nonsurgical removal of thrombi or emboli from the pulmonary arteries; aspiration of contrast media and other fluids from the pulmonary arteries; the cannula is intended for the treatment of pulmonary embolism The handle is indicated as a vacuum source for the AlphaVac Multipurpose Mechanical Aspiration System |
| Penumbra, Inc. (Peripheral Vascular) | Indigo System Catheters: Lightning Bolt 7 | 7 | 0.014–0.038 | 130 | Lightning Bolt Aspiration Tubing is designed to serve as a conduit to assist in thrombus removal, facilitating transfer of vacuum between the Penumbra Aspiration Pump and the INDIGO Aspiration Catheter while providing intermittent, continuous, or modulated aspiration; modulated aspiration is provided when the Lightning Bolt Aspiration Tubing alternates between connecting the INDIGO Aspiration Catheter to the Penumbra Aspiration Pump and a sterile saline intravenous (IV) bag at ambient pressure | The Indigo Aspiration Catheters and Separators are indicated for the removal of fresh, soft emboli and thrombi from vessels of the peripheral arterial and venous systems and for the treatment of pulmonary embolism. As part of the INDIGO Aspiration System, the INDIGO Sterile Aspiration Tubing is indicated to connect the INDIGO Aspiration Catheters to the Penumbra Aspiration Pump. |
Other Devices / Occlusion Devices
View Chart| Company Name | Product Name | Type | Position | CE Mark Indications |
|---|---|---|---|---|
| Invamed | ICT Paravalvular Leak Closure Device | Hard gel | Deliverable by the delivery system | Temporarily occlude and close valvular leaks in deep venous insufficiency |
| LeMaitre Vascular, Inc. | Pruitt Aortic Occlusion Catheter | Occlusion balloon | Distal | Designed for the purpose of obtaining rapid control of in-flow blood in the abdominal aorta in cases of ruptured aortic aneurysm or in other conditions when dissection of the neck of the aneurysm for different reasons may be especially difficult; this application of direct internal balloon occlusion is in lieu of external, proximal cross-clamping of the abdominal aorta and may prevent technical complications from special physiological situations; intraluminal balloon occlusion may be accomplished by direct insertion through the wall of the aneurysm |
| LeMaitre Vascular, Inc. | Pruitt Irrigation Occlusion Catheter | Occlusion balloon | Distal | To temporarily occlude vessels for the control of bleeding and to access the vessel lumen distal to the point of occlusion |
| LeMaitre Vascular, Inc. | Pruitt Occlusion Catheter | Occlusion balloon | Distal | The occlusion of vessels both arterial and venous for the control of bleeding |
| Penumbra, Inc. (Peripheral Vascular) | Packing Coil | Detachable | High-flow microcatheter deliverable | Indicated for arterial and venous embolizations in the peripheral vasculature |
| Penumbra, Inc. (Peripheral Vascular) | POD | Detachable with dedicated anchor segment for high flow vessel sacrifice | High-flow microcatheter deliverable | Indicated for arterial and venous embolizations in the peripheral vasculature |
| Penumbra, Inc. (Peripheral Vascular) | Ruby Coil | Detachable | High-flow microcatheter deliverable | Indicated for arterial and venous vessel embolizations in the peripheral vasculature |
| Front Line Medical Technologies Inc. | COBRA-OS | REBOA (large vessel balloon occlusion device; 4-F; 25-mm-diameter balloon; guidewire-free) | Aortic | Temporary occlusion of large blood vessels and/or circulatory support |
Other Devices / Optical Coherence Tomography
View Chart| Company Name | Product Name | Imaging Diameter (mm) | Catheter Usable Length (cm) | Maximum Guidewire (inch) | Minimum Guide Catheter ID (F) | Shaft Distal Section (F) |
|---|---|---|---|---|---|---|
| Abbott | Dragonfly Intravascular Imaging Catheter | 2–3.5 | 135 | 0.014 | 6 | 2.7 |
| Terumo Europe | Fastview-Coronary Imaging Catheter | 8–10 | 137 | 0.014 | 3.2 | 2.6 |
| Terumo Europe | Lunawave-OFDI Optical | – | – | – | – | – |
Other Devices / Percutaneous Arteriovenous Fistula Creation
View Chart| Company Name | Product Name | Size (F) | Maximum Guidewire Compatibility (inch) | Catheter Working Length (cm) | Recommended Introducer Size (F) | Fistula Site(s) | Outflow | Access | Mechanism of Action | AV Connection | Energy Source | Imaging Guidance | Adjunctive Procedures |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| BD Interventional | WavelinQ EndoAVF System | 4 | 0.014 | 43 (venous catheter); 50 (arterial catheter) | 5 | (1) Concomitant ulnar artery and ulnar vein; or (2) concomitant radial artery and radial vein | Split-flow fistula (cephalic or basilic vein) | Venous and arterial | Radiofrequency ablation | Platelet deposition and endothelium development of fistula tract | Electrosurgical unit (BD ESU-1) | Fluoroscopy and ultrasound | Recommended embolization of a brachial vein at index procedure |
Other Devices / Renal Denervation Systems
View Chart| Company Name | Product Name | Modality | Recommended Vessel (mm) | Electrode Design | Firing Scheme | Number of Catheter Sizes | Balloon Diameter (mm) | Balloon Working Length (mm) | Wire Compatibility | Minimum Guide Catheter ID (inch/mm) | Length (cm) | Guide Catheter Compatibility (F) | Safety Mechanisms | CE Mark Indication |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Medtronic | Symplicity Spyral | Radiofrequency | – | Quadrantic | – | One | – | – | – | – | 108 | 6 | Integrated into generator | Hypertension |
| Recor Medical | Paradise | Ultrasound | – | Circumferential | – | Three (5, 6, 7 mm) | – | – | 0.014 inch | – | 85 | 7 | Integrated into generator, circulating cooling fluid through balloon | Renal denervation |
Other Devices / Snares
View Chart| Company Name | Product Name | Catheter Size/Length (F/cm) | Working Diameters (mm) | Snare Length (cm) | Snare Type |
|---|---|---|---|---|---|
| ALN | ALN 2-in-1 Removal System (designed for the removal and/or repositioning of the ALN filters [with and without hook], however, the ALN filters with hook can also be removed using a snare) | – | – | – | – |
| ALN | ALN Precurved Removal System (designed for the removal and/or repositioning of the ALN filters [with and without hook], however, the ALN filters with hook can also be removed using a snare) | – | – | – | – |
| ALN | ALN Straight Removal System (designed for the removal and/or repositioning of the ALN filters [with and without hook], however, the ALN filters with hook can also be removed using a snare) | – | – | – | – |
| Andramed GmbH | AndraSnare | 4, 5/50, 110, 135 | 5, 10, 15, 20, 25, 30, 35 | 65/125/150 | Atraumatic nitinol loop with gold coating and X-Marker for better visualization and safer retrieval |
| Andramed GmbH | AndraSnare Micro | 2.3–3 | 2–7 | 175 | Atraumatic nitinol loop with gold coating and X-Marker for better visualization and safer retrieval |
| Andramed GmbH | Loopmaster-Sochman Snare | 8/150 | 25 | 130/150 | Atraumatic nitinol loop with guidewire with atraumatic tip for a safer retrieval |
| AndraTec GmbH Germany | Exeter Snare | 5/50 and 135 | 25 | 65, 150 | Exeter single open loop snare |
| AndraTec GmbH Germany | Exeter Snare | 4, 5/110 | 5–35 | 125 | Exeter single open loop snare |
| AndraTec GmbH Germany | Exeter Snare Micro | 3-3.2/150 | 2, 4, 7 | 175 | Single open loop design |
| Argon Medical Devices, Inc. | Atrieve | 3.2/150 | 2–4, 4–8 | 175 | Three noninterwoven loops with platinum strands |
| Argon Medical Devices, Inc. | Atrieve | 6/100 | 6–10, 9–15, 12–20 | 120 | Three noninterwoven loops with platinum strands |
| Argon Medical Devices, Inc. | Atrieve | 7/100 | 18–30, 27–45 | 120 | Three noninterwoven loops with platinum strands |
| BD Interventional | Bard Snare Retrieval Kit | 6/9/11 | 20 | 58 | Convenient all-in-one, easy-to-use kit; the snare catheter and helical loop are provided together with the dual sheath and the dilator |
| Cook Medical | CloverSnare 4-Loop Vascular Retriever | 6/90, 8/85, 10/80 | 32 | 90 | Four-loop nitinol snare with tantalum core coaxial sheath system with radiopaque markers at each distal tip |
| Cook Medical | Dotter Intravascular Retriever Set | 8/95 | 30-mm basket | 7-cm basket | Consists of a four-wire helical loop basket with a pin-vise handle, a catheter, and a Check-Flo Introducer Set |
| Cook Medical | Gunther Tulip Vena Cava Filter Retrieval Set | 6.3/80, 9, 11 (coaxial sheath set) | 20-mm snare loop | 80 | The GTRS jugular approach consists of a retrieval loop system with a braided platinum wire loop, a coaxial retrieval sheath system, an entry needle, a wire guide, and a dilator; a radiopaque band provided on the outer sheath identifies precise location of the distal tip of the sheath for positioning accuracy |
| Cook Medical | Indy OTW Vascular Retriever | 8/55, 8/100 | 40-mm basket | 55- or 100-cm catheter | Four-loop 40-mm radiopaque metal OTW vascular retriever snare with Flexor sheath and Tuohy-Borst hemostatic valve (55 and 100 cm); compatible with 0.035-inch guidewires |
| Medtronic | Amplatz GooseNeck Microsnare Kit | 2.3–3/150 | 2, 4, 7 | 175 | Engineered for precise retrieval and manipulation; features a highly radiopaque snare loop that is 90° to shaft of the snare; other features include a nitinol shaft for kink resistance and gold tungsten loop for enhanced visualization |
| Medtronic | Amplatz GooseNeck Microsnare Kit | 2.3–3/175 | 2, 4, 7 | 200 | Engineered for precise retrieval and manipulation; features a highly radiopaque snare loop that is 90° to shaft of the snare; other features include a nitinol shaft for kink resistance and gold tungsten loop for enhanced visualization |
| Medtronic | Amplatz GooseNeck Snare Kit | 4/48, 102 | 5, 10 | 65, 120 | Engineered for precise retrieval and manipulation; features a highly radiopaque snare loop that is 90° to shaft of the snare; other features include a nitinol shaft for kink resistance and gold tungsten loop for enhanced visualization |
| Medtronic | Amplatz GooseNeck Snare Kit | 6/48, 102 | 15, 20, 25, 30, 35 | 65, 120 | Engineered for precise retrieval and manipulation; features a highly radiopaque snare loop that is 90° to shaft of the snare; other features include a nitinol shaft for kink resistance and gold tungsten loop for enhanced visualization |
| Merit Medical Systems, Inc. | EN Snare Endovascular Snare System | 3.2/150, 6, 7/100 | 2–4, 4–8, 6–10, 9–15, 12–20, 18–30, 27–45 | 120, 175 | Incorporates an interlaced triple-loop design which conforms to vessel walls to promote accurate and reliable foreign body retrieval; the super elastic nitinol provides kink resistance and torque control; the platinum strands around the loops provide excellent fluoroscopic visualization |
| Merit Medical Systems, Inc. | One Snare Endovascular Snare System | 4/48, 4/100, 6/48, 6/100 | 5, 10, 15, 20, 25, 30, 35 | 65, 120 | Single 90° angle loop to optimize retrieval and manipulation of foreign objects; nitinol loop wrapped with gold-plated tungsten provides strength and shape retention and enhances visibility under fluoroscopy |
| Merit Medical Systems, Inc. | One Snare Microsnare System | 2.3–3/150, 175 | 2, 4, 7 | 175, 200 | Single 90° loop configuration and gold tungsten coils (for enhanced visualization) |
| Merit Medical Systems, Inc. | One Snare Petite Snare System | 4, 6 | 48 | 65 | Single 90° loop configuration and gold tungsten coils (for enhanced visualization) |
Other Devices / Therapeutic Infusion Systems
View Chart| Company Name | Product Name | Sheath Compatibility (F) | Guidewire Compatibility (inch) | Working Length (cm) | Mode of Operation | CE Mark Indications |
|---|---|---|---|---|---|---|
| Medtronic | Cragg-McNamara Valved Infusion Catheter | 4, 5 | 0.035, 0.038 | 40, 65, 100, 135 | Consists of catheters with radiopaque markers proximal and distal to the infusion segments; a Cragg-MicroValve at the distal tip provides endhole occlusion | Indicated for use in the controlled selective infusion of physician-specified pharmacological agents or radiopaque contrast media into the general vasculature |
| Merit Medical Systems, Inc. | Fountain Infusion Catheter With Squirt Fluid Delivery System | 4, 5 | 0.035 (0.89 mm) | 45, 90, 135 | Fluid delivery system with consistent, forceful, pulsed injections for optimal thrombolysis procedures | Intended to administer infusions of various therapeutic solutions into the peripheral vasculature of a patient |
| Merit Medical Systems, Inc. | Fountain Infusion System | 4, 5 | 0.035 | 45, 90, 135 | – | Intended to administer infusions of various therapeutic solutions into the peripheral vasculature of a patient |
| Merit Medical Systems, Inc. | Fountain Infusion System: Catheter, Occluding Wire, and AcessPLUS Hemostasis Valve | 4, 5 | 0.035 | 45, 90, 135 | – | Intended to administer infusions of various therapeutic solutions into the peripheral vasculature of a patient |
| Merit Medical Systems, Inc. | Fountain Occluding Wire | 4, 5 | – | 45, 90, 135 | Can be used for slow, continuous infusion, or pulse infusion | Intended to administer infusions of various therapeutic solutions into the peripheral vasculature of a patient |
| Merit Medical Systems, Inc. | Mistique Infusion Catheter | 5 | 0.035 | 45, 90, 135 | Can be used for slow, continuous infusion, or pulse infusion | Intended to administer infusions of various therapeutic solutions into the peripheral vasculature of a patient |
| RenalGuard Solutions, Inc. | RenalGuard | – | – | – | Protects patients from contrast-induced acute kidney injury by safely inducing higher rates of urine than are possible with standard diuretics alone; urine rates are achieved by matching the patient’s urine output milliliter-for-milliliter, minute-by-minute; reduces the risk of over- or under hydration relative to standard infusion | Indicated for temporary replacement of urine output by infusion of a matched volume of sterile replacement solution to maintain a patient’s intravascular fluid volume; not intended for infusion of blood, blood components, medications, or nutritional fluids |
| ThermopeutiX, Inc. | TAPAS Targeted Adjustable Drug Delivery System | 7 | 0.014 | 15–300 mm (adjustable) | Dual occlusive balloon technology to target, deliver, dwell, and aspirate any drug or therapeutic agent | Intended for use in peripheral arteries ≥ 1.8 mm for infusion of diagnostic or therapeutic agents |
| Translational Research Institute | ND Infusion Catheter | 6 | 0.014 | 135 | Expandable balloon to control blood flow during infusion through a multilumen spray tip | Intended to isolate a specific coronary or peripheral vascular treatment region from blood flow while allowing infusion of physician-specified fluids into the target region |
Other Devices / Thrombus Aspiration Devices
View Chart| Company Name | Product Name | Type | Maximum Tip Diameter (mm) | Minimum Guide Catheter Size (F) | Catheter Length (cm) |
|---|---|---|---|---|---|
| amg International GmbH | Isolv Aspiration Catheter | Preloaded stylet, available on different configurations, short (30 mm) or long (75 mm) rapid-exchange for improved flexibility or pushability, outside or inside arranged guidewire lumens for improved low-profile or large aspiration volume | 0.5 | 5, 6, 7 | 135, 141 |
| Arthesys | Pegase | Aspiration catheter, hydrophilic coating, preloaded stylet, low profile, rapid exchange | 0.5 | 6 | 145 |
| Control Medical Technology | Aspire Aspirator | Mechanical aspirator drive unit/pump | – | – | – |
| Control Medical Technology | Aspire Max 5 | 5-F braided large-lumen OTW | 1.65 | 6 | 55, 135 |
| Control Medical Technology | Aspire Max 6 | 6-F braided large-lumen OTW | 1.91 | 7 | 55, 135 |
| Control Medical Technology | Aspire RX-LP6 | Rapid-exchange low-profile coronary | 1.7 | 6 | 136 |
| eucatech AG | Euca AC | Aspiration catheter with hydrophilic coating | 0.53 | 6, 7 | 145 |
| Invamed | Dovi | Aspiration catheter with mechanical aspirator | 0.5 | 7 | 90 |
| iVascular | Capturer 6F | Thrombus extractor (RX) | 0.5334 | 6 | 140 |
| iVascular | Capturer 7F | Thrombus extractor (RX) | 0.635 | 7 | 140 |
| Medtronic | Diver CE Aspiration Catheter | Low-profile, rapid-exchange, hydrophilic coating with and without side holes | 1.58 | 6 | 145 |
| Medtronic | Export AP Catheter | Full-wall variable hub to tip braiding; hydrophilic coating; short, soft tip | 1.73 | 6 | 140 |
| Medtronic | Export Catheter | Guide catheter braid technology | 1.73, 1.98 | 6, 7 | 145 |
| Medtronic | Export XT Catheter | Full-wall variable hub to tip braiding; hydrophilic coating; short, soft tip | 1.73 | 6 | 140 |
| Meril Life Sciences Pvt. Ltd. | Aspiron-Aspiration Catheter | Manual aspiration thrombectomy device | 1 | 6 | 140 |
| Merit Medical Systems, Inc. | ASAP Aspiration Catheter Kit | Manual aspiration catheter and kit | 1.73 | Guiding catheter ID: 6 (≥ 0.070 inch) | 140 |
| Merit Medical Systems, Inc. | ASAPLP Aspiration Catheter Kit | Low-profile manual aspiration catheter and kit | 1.40 | Guiding catheter ID: 6 (≥ 0.066 inch) | 145 |
| Terumo Neuro | Sofia Plus Aspiration Catheter | Aspiration catheter | Distal OD: 2.; ID: 0.070 inch | 6 | 125, 131 |
| Natec Medical Ltd | Dyson | Thrombectomy coronary catheter | 1.7 | 6 | 140 |
| optimed Medizinische Instrumente GmbH | BigLumen Aspiration Catheter | Aspiration device | 1.25, 1.43, 1.64, 1.88 | 5, 6, 7, 8 | 70, 80, 90, 100, 120 |
| optimed Medizinische Instrumente GmbH | BigLumen Aspiration Catheter Set | Aspiration device | 1.43 | 6 | 100 |
| Q3 Medical Group | Aspiration Catheter (VX) | Preloaded stylet, available on different configurations, short (30 mm) or long (75 mm) rapid exchange for improved flexibility or pushability, outside or inside arranged guidewire lumens for improved low-profile or large aspiration volume | 0.5 | 5, 6, 7 | 135, 141 |
| Stryker | AXS Catalyst 5 Distal Access Catheter | Aspiration catheter | Distal OD: 1.76; ID: 0.058 inch | 6 (≥ 0.078 in) | 132 |
| Stryker | AXS Catalyst 6 Distal Access Catheter | Aspiration catheter | Distal OD: 1.81; ID: 0.060 inch | 6 (≥ 0.084 inch) | 132 |
| Stryker | AXS Catalyst 7 Distal Access Catheter | Aspiration catheter | Distal OD: 2.08; ID: 0.068 inch | 6 (≥ 0.084 inch) | 125, 132 |
| Stryker | AXS Universal Aspiration Set | Vacuum pump + aspiration tubing + disposable canister liner | – | – | – |
| Stryker | AXS Vecta 71 Aspiration Catheter | Aspiration catheter | Distal OD: 2.09; ID: 0.071 inch | 6 (≥ 0.088 inch) | 115, 125, 132 |
| Stryker | AXS Vecta 74 Aspiration Catheter | Aspiration catheter | Distal OD: 2.11; ID: 0.074 inch | 6 (≥ 0.091 inch) | 115, 125, 132 |
| Teleflex | Pronto .035 Extraction Catheter | Large-vessel thrombus aspiration catheter; full-length braided shaft; patented Silva tip | 3.25 | 10 (sheath) | 115 |
| Teleflex | Pronto LP 5 F Extraction Catheter | Low-profile; hydrophilic coating; patented Silva tip; delivery stylet; 5-F guide catheter compatibility | 1.35 | 5 | 138 |
| Teleflex | Pronto LP Extraction Catheter | Low-profile; hydrophilic coating; patented Silva tip; round, braided shaft; delivery stylet | 1.35 | 6 | 140 |
| Teleflex | Pronto V3 Extraction Catheter | Full-length braided shaft; hydrophilic coating; patented Silva tip; maximized extraction lumen and force | 1.65 | 6 | 140 |
| Teleflex | Pronto V4 Extraction Catheter | Embedded longitudinal wire; hydrophilic coating; patented Silva tip; maximized extraction lumen and force; 5.5, 6, 7, 8 F | 1.64–2.2 | 6, 7, 8 | 138 |
| Terumo Europe | Eliminate | Preloaded stylet, fully-braided shaft, and 23-cm-long rapid exchange segment for improved deliverability | – | 6, 7, 8 | 140 |
Other Devices / Valvulotomy Devices
View Chart| Company Name | Product Name | Type | Size (F) | Blade Range (mm) | Shaft Length (mm) | Guidewire Compatibility (inch) | Comments |
|---|---|---|---|---|---|---|---|
| Andramed GmbH | AndraValvulotome | Over-the-wire system | 4 | 2–8 | 900 | 0.014 | Utilizes self-sizing and self-centering technology |
| Andramed GmbH | AndraValvulotome | Over-the-wire system | 5 | 3–8 | 1,000 | 0.018 | Utilizes self-sizing and self-centering technology |
Other Devices / Vena Cava Filters
View Chart| Company Name | Product Name | Indicated Caval Diameter (mm) (based on average caval diameter) | Maximum Deployed Length (mm) | Catheter Carrier System ID (F) | Material | Design | Approach | Permanent/Retrievable |
|---|---|---|---|---|---|---|---|---|
| ALN | ALN Optional Filter | 32 | 55 | 7 | Stainless steel | Conical | Femoral/jugular/brachial/popliteal | Optional (permanent or temporary) |
| ALN | ALN Optional Filter With Hook | 32 | 59 | 7 | Stainless steel | Conical | Femoral/jugular/brachial/popliteal | Optional (permanent or temporary) |
| Argon Medical Devices, Inc. | OptionElite | Up to 32 | 56.5 | 5 | Nitinol | Conical | Femoral/jugular, standard or over-the-wire, from a single kit | Optional (permanent or retrievable) |
| B. Braun Melsungen AG | VenaTech Convertible | 14–28 | 60 | 7 | Cobalt-chromium alloy | Conical, self centering | Brachial, femoral, jugular, subclavian | Permanent, enables filter conversion to open configuration |
| B. Braun Melsungen AG | VenaTech LP | ≤ 35 | 43 | 7 | Cobalt-chromium alloy | Conical, self centering | Brachial, femoral, jugular, subclavian | Permanent |
| B. Braun Melsungen AG | VenaTech Retrievable | 14–28 | 53 | 7 (implantation), 10 (explantation) | Cobalt-chromium alloy | Conical | Brachial, femoral, jugular, subclavian | Retrievable |
| BD Interventional | Denali Vena Cava Filter | Up to 28 | 51 | 8.4 | Nitinol | Conical, two-level filtration | Femoral/jugular | Optional (permanent or retrievable) |
| Boston Scientific Corporation | Sentry | 16–28 | 57.7 | 7 (max OD of 9.75) | Nitinol frame with a bioabsorbable filament composed of poly-p-dioxanone (PPDO) | Self-expanding cylindrical frame designed to hold the filter in place along with conical filter arms held in place by a bioabsorbable filament; indicated for the prevention of recurrent pulmonary embolism (PE) via percutaneous placement in the inferior vena cava in patients with a transient risk of PE, in the following situations: pulmonary thromboembolism when anticoagulants are contraindicated; failure of anticoagulant therapy in thromboembolic diseases; emergency treatment following massive pulmonary embolism where anticipated benefits of conventional therapy are reduced; recurrent pulmonary embolism where anticoagulant therapy has failed or is contraindicated; patients at high risk of pulmonary embolism, not receiving medical thromboprophylaxis due to either increased risk of bleeding, active bleeding or heparin induced thrombocytopenia | Designed for access via left or right femoral vein or right jugular vein | Convertible |
| Cook Medical | Celect Platinum | 15–30 | 0–49 | 7 | Conichrome | Conical | Femoral/jugular | Optional (permanent or temporary) |
| Cook Medical | Günther Tulip Filter | 0–30 | 50 | 7 | Conichrome | Conical | Femoral/jugular | Optional (permanent or temporary) |
| Cordis | OptEase Retrievable Vena Cava Filter | Up to 30 | – | 6 | Nitinol | Double basket | Femoral/jugular/antecubital | Optional (permanent or retrievable) |
| Invamed | Keeper | 33 | 50 | 8 | Nitinol/MRI compatible | Self centering | Femoral/jugular | Optional (permanent or retrievable) |
| Mermaid Medical | Angel Catheter | 15–30 | 50 | ID: 8; OD: 9 | Nitinol | Conical | Femoral | Retrievable |
Other Devices / Venous Drainage Cannula and Circuits
View Chart| Company Name | Product Name | Sheath Compatibility (F) | Guidewire Compatibility (inch) | Cannula Size (F) | CE Mark Indications |
|---|---|---|---|---|---|
| AngioDynamics | AngioVac Cannula and Circuit | 26, 22 | 0.038 | 22, 18 | Intended for use as a venous drainage cannula during extracorporeal bypass for up to 6 hours; for use in procedures requiring extracorporeal circulatory support for periods of up to 6 hours |
Embolization / Intrasaccular Flow Disruptor
View Chart| Company Name | Product Name | Materials Used | Device Diameter (mm) | Device Height (mm) |
|---|---|---|---|---|
| Terumo Neuro | WEB Aneurysm Embolization System—Single Layer | Nitinol-platinum | 3–11 | 2–9 |
| Terumo Neuro | WEB Aneurysm Embolization System—Single Layer Sphere | Nitinol-platinum | 4–11 | 2.6–9.6 |
Other Devices / Mechanical Thrombectomy (Neurovascular)
View Chart| Company Name | Product Name | Sheath Compatibility (F) | Guidewire Compatibility (inch) | Working Length (cm) | Mode of Operation | CE Mark Indications |
|---|---|---|---|---|---|---|
| Acandis GmbH & Co. KG | Aperio 1.9 F Thrombectomy Device | – | 0.010–0.014 | 30 mm | Thrombectomy device for the mechanical extraction of clots from cerebral vessels with a diameter > 2 and ≤ 4 mm | Intended for use of restoration of the arterial flow for patients diagnosed with ischemic stroke due to large intracranial vessel occlusion (ie, internal carotid artery, M1 and M2 segments of the MCA); patients who fail intravenous thrombolytic therapy or who are ineligible for thrombolysis may be suited for treatment with the Aperio device |
| Acandis GmbH & Co. KG | Aperio 3 F Thrombectomy System | – | 0.010–0.014 | 40 mm | Thrombectomy system (includes microcatheter) for the mechanical extraction of clots from cerebral vessels with a diameter > 2 and ≤ 4 mm | Intended for use of restoration of the arterial flow for patients diagnosed with ischemic stroke due to large intracranial vessel occlusion (ie, internal carotid artery, M1 and M2 segments of the MCA); patients who fail intravenous thrombolytic therapy or who are ineligible for thrombolysis may be suited for treatment with the Aperio device |
| Cerenovus | ReVive SE Thrombectomy Device | 5 or larger | – | 205 | Mechanical thrombectomy (stent retriever) | Indicated to restore blood flow in patients with acute ischemic stroke secondary to intracranial occlusive vessel disease by providing temporary bypass across the occlusion and/or by the nonsurgical removal of emboli and thrombi; it may be used with aspiration and with the injection or infusion of contrast media and other fluids; the close-ended basket captures clots and large fragments |
| Terumo Neuro | Eric Retrieval Device | 0.017- and 0.021-inch microcatheter | 0.014 | 15, 20, 24, 30, 35, 44 | Clot retriever device with intraluminal clot capture surface | Intended for use in the revascularization of acute ischemic stroke caused by the intracranial occlusive vessels of patients who are not eligible for intravenous tissue plasminogen activator (IV tPA) or who fail IV tPA therapy |
| Terumo Neuro | Sofia Plus Aspiration Catheter | 6 | – | 125, 131 | Aspiration catheter | Indicated for general intravascular use, including the peripheral and neurovasculatures; can be used to facilitate introduction of diagnostic or therapeutic agents; not intended for use in coronary arteries; intended for use in the removal/aspiration of emboli and thrombi from selected blood vessels in the arterial system, including the peripheral and neurovasculatures |
| Penumbra, Inc. (Neuro) | 3D Revascularization Device | 6 (long sheath [Neuron MAX]) | 0.020 | 200 (delivery wire; compatible with Velocity delivery microcatheter [160 cm] and 3MAX reperfusion catheter [153 cm]) | Designed for use in combination with ACE and Penumbra JET 7 reperfusion catheters; the architecture enables maximum clot capture capability through four intraluminal chambers and is optimized for use with aspiration delivered by ACE reperfusion catheters or Penumbra JET 7 | As part of the Penumbra System, this device is indicated for use in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral–M1 and M2 segments) within 8 hours of symptom onset; patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment |
| Penumbra, Inc. (Neuro) | Penumbra System RED 43, RED 62 Reperfusion Catheter RED 68 Reperfusion Catheter, RED 72 Reperfusion Catheter, RED 72 with SENDit Technology, RED 78 | 6 (RED 72, RED 72 with SENDit Technology, RED 68, RED 62, RED 43 require 8-F short sheath or 6-F long sheath) | 0.014–0.016 | 132–153 | The Penumbra System is designed to remove thrombus and restore blood flow in the neurovasculature using aspiration | Indicated for use in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral – M1 and M2 segments, basilar, and vertebral arteries) within 8 hours of symptom onset; patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment |
| Penumbra, Inc. (Neuro) | Penumbra System Reperfusion Catheter ACE, 5MAX, 4MAX, 3MAX | 6 (ACE and 5MAX require 8 F short sheath or 6 F long sheath) | 0.014–0.016 | 132–160 | Direct aspiration and separator-assisted clot debulking if needed | As part of the Penumbra System, the reperfusion catheters and separators are indicated for use in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral – M1 and M2 segments, basilar, and vertebral arteries) within 8 hours of symptom onset; patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment |
| Penumbra, Inc. (Neuro) | Penumbra System Separator and Separator Flex 5MAX, 4MAX, 3MAX | – | – | Separator and separator flex length: 175–200 | Separator-assisted clot debulking, if needed | As part of the Penumbra System, the reperfusion catheters and separators are indicated for use in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral – M1 and M2 segments, basilar, and vertebral arteries) within 8 hours of symptom onset; patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment |
| phenox GmbH | Preset Lite Thrombectomy Device | 0.0165 inch (ID) | – | 180 (insertion wire) | Introduced into the target vessel through a suitable microcatheter and deployed inside the thrombus or distal to the thrombus; after complete deployment the slow withdrawal of the instrument occurs under continuous aspiration via the guiding catheter or aspiration catheter | Designed for mechanical clot retrieval from intracranial arteries as acute ischemic stroke treatment for patients who are ineligible for intravenous thrombolysis or for patients who failed thrombolysis therapy and as a supplement treatment of an initiated thrombolysis therapy |
| phenox GmbH | Preset Thrombectomy Device | 0.021 inch (ID) | – | 180 (insertion wire) | Introduced into the target vessel through a suitable microcatheter and deployed inside the thrombus or distal to the thrombus; after complete deployment the slow withdrawal of the instrument occurs under continuous aspiration via the guiding catheter or aspiration catheter | Designed for mechanical clot retrieval from intracranial arteries as acute ischemic stroke treatment for patients who are ineligible for intravenous thrombolysis or for patients who failed thrombolysis therapy and as a supplement treatment of an initiated thrombolysis therapy |
| Stryker | Trevo NXT ProVue Retriever; 3 X 25, 4 X 21, 4 X 35, and 6 X 30 mm | 8, 9 (balloon guide catheter) | 0.014 | 200 for all stent sizes | Mechanical thrombectomy; 360° of consistently large cells, a soft distal tip, and full-length radiopacity | (1) Indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of acute ischemic stroke to reduce disability in patients with a persistent, proximal anterior circulation, large vessel occlusion, and smaller core infarcts who have first received intravenous tissue plasminogen activator (IV t-PA); endovascular therapy with the device should start within 6 hours of symptom onset; (2) intended to restore blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stroke within 8 hours of symptom onset; patients who are ineligible for IV t-PA or who fail IV t-PA therapy are candidates for treatment; (3) indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of acute ischemic stroke to reduce disability in patients with a persistent, proximal anterior circulation, large vessel occlusion of the internal carotid artery (ICA) or middle cerebral artery (MCA)-M1 segments with smaller core infarcts (0-50 mL for age < 80 years, 0-20 mL for age ≥ 80 years); endovascular therapy with the device should start within 6 to 24 hours of time last seen well in patients who are ineligible for IV t-PA or who fail IV t-PA therapy |
| Stryker | Trevo XP ProVue Retriever; 3 X 20, 4 X 20, 4 X 30, 6 X 25 mm | 8, 9 (balloon guide catheter) | 0.014 | 190 for 3 X 20 mm; 180 for 4 X 20 mm, 4 X 30 mm, and 6 X 25 mm | Mechanical thrombectomy; 360° of consistently large cells, a soft distal tip and full-length radiopacity | Indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of acute ischemic stroke to reduce disability in patients with a persistent, proximal anterior circulation, large-vessel occlusion, and smaller core infarcts who have first received intravenous tissue plasminogen activator (IV t-PA); endovascular therapy with the device should start within 6 hours of symptom onset; intended to restore blood flow in the neurovasculature by removing thrombus in patients experiencing ischemic stroke within 8 hours of symptom onset; patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment Indicated for use to restore blood flow in the neurovasculature by removing thrombus for the treatment of acute ischemic stroke to reduce disability in patients with a persistent, proximal anterior circulation, large-vessel occlusion of the internal carotid artery (ICA) or middle cerebral artery (MCA)-M1 segments with smaller-core infarcts (0–50 mL for age < 80 years, 0–20 mL for age ≥ 80 years); endovascular therapy with the device should start within 6–24 hours of time last seen well in patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy |
| Vesalio Inc. | NeVa Thrombectomy System 4.0 X 22 mm | Minimum microcatheter ID: 0.021 (1.6 F) | Max: 0.018 | Basket working length: 22 mm, basket full length: 39 mm, pusher wire length: 200 cm | 2 drop zones for clot retrieval in acute ischemic stroke | Endovascular temporary use to restore blood flow in patients who are experiencing symptoms of acute ischemic stroke caused by an embolus in a cerebral vessel; Indicated for vessels with diameter > 2.0 mm and ≤ 3.5 mm |
| Vesalio Inc. | NeVa Thrombectomy System 4.5 X 29 mm | Minimum microcatheter ID: 0.021 (1.6 F) | Max: 0.018 | Basket working length: 29 mm, basket full length: 46 mm, pusher wire length: 200 cm | 3 drop zones for clot retrieval in acute ischemic stroke | Endovascular temporary use to restore blood flow in patients who are experiencing symptoms of acute ischemic stroke caused by an embolus in a cerebral vessel; Indicated for vessels with diameter > 2.0 mm and ≤ 4.5 mm |
| Vesalio Inc. | NeVa Thrombectomy System 5.5 X 37 mm | Minimum microcatheter ID: 0.027 (2.06 F) | Max: 0.018 | Basket working length: 37 mm, basket full length: 56 mm, pusher wire length: 200 cm | 3 drop zones for clot retrieval in acute ischemic stroke | Endovascular temporary use to restore blood flow in patients who are experiencing symptoms of acute ischemic stroke caused by an embolus in a cerebral vessel; Indicated for vessels with diameter > 3.5 mm and ≤ 5.5 mm |
| Vesalio Inc. | NeVa NET Thrombectomy System 4.0 X 30 mm | Minimum microcatheter ID: 0.021 (1.6 F) | Max: 0.018 | Basket working length: 30 mm; basket full length: 49 mm; pusher-wire length: 200 cm | 3 drop zones for clot retrieval in acute ischemic stroke; incorporates a braided net on the inside at the distal end of the expandable tip | Endovascular temporary use to restore blood flow in patients who are experiencing symptoms of acute ischemic stroke caused by an embolus in a cerebral vessel; indicated for vessels with diameter > 2.0 mm and ≤ 3.5 mm |
| Vesalio Inc. | NeVa NET Thrombectomy System 5.5 X 37 mm | Minimum microcatheter ID: 0.027 (2.06 F) | Max: 0.018 | Basket working length: 37 mm; basket full length: 56 mm; pusher-wire length: 200 cm | 3 drop zones for clot retrieval in acute ischemic stroke; incorporates a braided net on the inside at the distal end of the expandable tip | Endovascular temporary use to restore blood flow in patients who are experiencing symptoms of acute ischemic stroke caused by an embolus in a cerebral vessel; Indicated for vessels with diameter > 3.5 mm and ≤ 5.5 mm |
| Rapid Medical | Tigertriever XL | 0.021 inch (ID) | – | 220 | Incorporates a manually expandable braided distal segment designed to conform to vessel anatomy and thrombus morphology, enabling atraumatic engagement; controlled expansion via the handle allows precise thrombus capture while relieving vascular tension prior to retrieval, promoting safe and effective clot removal | Designed for use in flow restoration of patients with ischemic stroke due to large intracranial vessel occlusion; patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment |
| Rapid Medical | Tigertriever 13 | 0.0165/0.013 inch (ID) | – | 230 | Adjusts to the vasculature and clot providing an atraumatic approach; precise control to capture the thrombus and remove the tension from the vasculature before removal leading to safe and effective procedure; the user can control the manual expansion of the braided distal portion into the clot using the handle component of the device | Designed for use in flow restoration of patients with ischemic stroke due to large intracranial vessel occlusion; patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment; designed for use in flow restoration of patients with ischemic stroke due to distal vessel occlusions with a diameter of 1-2 mm |
| Rapid Medical | Tigertriever 17 | 0.017 inch (ID) | – | 220 | Adjusts to the vasculature and clot providing an atraumatic approach; unique operation changes these procedures from a passive to an active user approach that accelerates clot capture and potentially reduces the risk of vascular injury during removal; the user can control the manual expansion of the braided distal portion into the clot using the handle component of the device | Designed for use in flow restoration of patients with ischemic stroke due to large intracranial vessel occlusion; patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment |
| Rapid Medical | Tigertriever 25 | 0.025 inch (ID) | – | 220 | Incorporates a manually expandable braided distal segment designed to conform to vessel anatomy and thrombus morphology, enabling atraumatic engagement; controlled expansion via the handle allows precise thrombus capture while relieving vascular tension prior to retrieval, promoting safe and effective clot removal | Designed for use in flow restoration of patients with ischemic stroke due to large intracranial vessel occlusion; patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment |
| Rapid Medical | Tigertriever | 0.021 inch (ID) | – | 220 | Incorporates a manually expandable braided distal segment designed to conform to vessel anatomy and thrombus morphology, enabling atraumatic engagement; controlled expansion via the handle allows precise thrombus capture while relieving vascular tension prior to retrieval, promoting safe and effective clot removal | Designed for use in flow restoration of patients with ischemic stroke due to large intracranial vessel occlusion; patients who are ineligible for intravenous tissue plasminogen activator (IV t-PA) or who fail IV t-PA therapy are candidates for treatment |
| Vesalio Inc. | enVast 4.0 X 30 | – | Max: 0.018 | 30 mm | 2 drop zones for clot retrieval; includes a flow restoration zone; indicated for vessels with diameter > 2 mm and ≤ 4 mm; maximal diameter: 4 mm; minimum microcatheter compatibility: 0.021-inch ID | Endovascular temporary use to restore blood flow in patients who are experiencing symptoms of thrombosis in the coronary vasculature |
Other Devices / Inflation Devices
View Chart| Company Name | Product Name | Color | Pressure Range (atm) | Barrel Volume (mL) | Luminescent Gauge (Yes/No) | Gauge | Latch Type | Threads |
|---|---|---|---|---|---|---|---|---|
| B. Braun Melsungen AG | AI25 | Transparent/blue | 30 | 20 | No | Luer lock | Click and go | Without |
| BD Interventional | Presto Inflation Device | Blue/white | 0–40 | 30 | No | Angled | – | – |
| Merit Medical Systems, Inc. | basix Touch | White/blue handle | 35 | 30 | Yes | Yes | Squeeze handle/one-handed prep | Yes |
| Merit Medical Systems, Inc. | basixCompak | White/clear | 30 | 20 | Yes | Yes | Squeeze handle | Yes |
| Merit Medical Systems, Inc. | Diamond Touch | White/blue handle | 35 | 30 | Yes | Digital | Squeeze handle/one-handed prep | Yes |
Catheters / Multifunctional Catheters
View Chart| Company Name | Product Name | Sheath Compatibility (F) | Recommended Guidewire Size (inch) | Balloon Diameters (mm) | Balloon Lengths (cm) | Working Length (cm) | Support Catheter Construction | Dilator Construction | Balloon Nominal Pressure (atm) | Balloon Rated Burst Pressure (atm) | Comments |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Teleflex | Oscar Peripheral Multifunctional Catheter | 4 | 0.014 | 2, 2.5, 3, 3.5 | Variable from 2-18 | 127 | Reinforced shaft, polymer braid with straight tip and platinum-iridium marker | Straight with olive-shaped stainless steel tip | 8 | 14 (ø 3.5 mm), 16 (ø 2, 2.5, 3 mm) | Multicomponent system (support catheter, dilator, and PTA balloon) indicated for percutaneous transluminal interventions in the peripheral vasculature to provide support during access into and to dilate stenoses in femoral, popliteal and infrapopliteal arteries; also intended for injection of radiopaque contrast media for the purpose of angiography |
| Teleflex | Oscar Peripheral Multifunctional Catheter | 6 | 0.018 | 4, 5, 6, 7 | Variable from 2-18, 2-10 (ø 7 mm) | 72 (ø 7 mm), 80, 128 | Reinforced shaft, polymer braid with straight tip and platinum-iridium marker | Straight with olive-shaped stainless steel tip | 6 | 12 (ø 7 mm), 14 (ø 4, 5, 6 mm) | Multicomponent system (support catheter, dilator, and PTA balloon) indicated for percutaneous transluminal interventions in the peripheral vasculature to provide support during access into and to dilate stenoses in femoral, popliteal, and infrapopliteal arteries; also intended for injection of radiopaque contrast media for the purpose of angiography |
Other Devices / Retrievable Scaffold Therapy
View Chart| Company Name | Product Name | Material Used | Introducer Size (F) | Guidewire Compatibility (inch) | Device Diameter (mm) | Device Length (mm) | Delivery System Length (cm) | CE Mark Indications |
|---|---|---|---|---|---|---|---|---|
| Reflow Medical, Inc | Spur | Nitinol | 6 | 0.014 | 3, 4 | 60, 65 | 135 | Indicated for treatment of de novo or restenotic infrapopliteal lesions, with a reference vessel diameters ranging from 2.5 to 4.5 mm, prior to treatment with a commercially available drug-coated balloon; intended to treat de novo or restenotic lesions in the infrapopliteal arteries to prepare the vessel for treatment with a commercially available drug-coated balloon to enhance drug absorption |
Other Devices / Assist Devices
View Chart| Company Name | Product Name | Assisting/Supporting Part Diameter (mm) | Assisting/Supporting Part Length (mm) | Distal Tip Length (mm) | Minimum Microcatheter ID Compatibility (inch) | Total Length (cm) |
|---|---|---|---|---|---|---|
| Rapid Medical | Comaneci | 2.3 | 32 | 7 | 0.021 | 224 |
| Rapid Medical | Comaneci Petit | 1.9 | 24 | 7 | 0.021 | 223 |
| Rapid Medical | Comaneci 17 | 1.85 | 223 cm | 7 | 0.017 | 223 |
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