Advertisement
Advertisement
Bentley InnoMed GmbH
Lotzenäcker 3 , 72379 Hechingen, Germany
PHONE: +49 (0) 7471 984 995 10
Catheters / Specialty Catheters
View Chart| Company Name | Product Name | Catheter Size (F) | Working Length (cm) | Minimum Guiding Catheter ID (inch) | Comments |
|---|---|---|---|---|---|
| Bentley InnoMed GmbH | BeBack Crossing & Re-Entry 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 with a length-adjustable and 360° rotational nitinol needle; the C-shaped radiopaque marker indicates in which direction the curved needle protrudes from the tip of the catheter; antegrade, retrograde, and crossover are possible for intraluminal and subintimal approach on 0.014- and 0.018-inch wire platform; indicated for use in conjunction with guidewires to pass occluded regions of the peripheral vasculature; It may be used to facilitate placement and exchange of guidewires |
Advertisement
Advertisement
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 |
|---|---|---|---|---|---|---|---|---|
| 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 | 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 a bridging stent graft in patients requiring endovascular abdominal aortic aneurysm repair with a fenestrated 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 18 mm, 22 mm, 28 mm, 38 mm, and 58 mm; Ø 7 mm in lengths of 18 mm, 23 mm, 27 mm, 37 mm, and 57 mm; Ø 8 mm - 10 mm in lengths of 27 mm, 37 mm, and 57 mm; sizes approved when used as a bridging stent graft for FEVAR: Ø 5 mm and 6 mm in lengths of 22 mm, 28 mm, and 38 mm; Ø 7 mm in lengths of 23 mm, 27 mm, and 37 mm; Ø 8 mm -10 mm in lengths of 27 mm and 37 mm |
| 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 | Indicated for implantation in the native and/or recurrent coarctation of the aorta on adolescent or adult patients; restoring and improving 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 | Indicated for 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 | 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 arteries 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 | Indicated for 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 | Double cobalt chromium (L605), double ePTFE (unique stent-in-stent design) | 0.035 | 7/8 F for Ø 5 - 7 mm (depending on indication and access site), 8 F for Ø 8 mm, 8/9/10 F for Ø 9 and 10 mm (depending on indication and access site) | 5, 6, 7, 8, 9, 10 | ~28, ~38, ~58, ~78 | 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 |
|---|---|---|---|---|---|---|---|---|
| Bentley InnoMed GmbH | BeSmooth Peripheral | Cobalt chromium (L605) | 0.035 | 6 | 5, 6, 7, 8, 9, 10 | 18, 23, ~27, 38, ~57 | 75, 120 | Indicated for the treatment of de novo or restenotic atherosclerotic lesions in protected peripheral arteries (ie, iliac arteries: common, external, internal; visceral arteries: renal arteries, superior mesenteric artery, inferior mesenteric artery, celiac trunk) |
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) |
|---|---|---|---|---|---|---|---|---|---|
| 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 |
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 |
|---|---|---|---|---|---|---|
| Bentley InnoMed GmbH | BeBack Crossing & Re-Entry Catheter | 2.9, 4 | 0.014, 0.018 | 80, 120 | 2.9 F (crossover 4 F), 4 F (crossover 6 F) | A low-profile support catheter that has a crossing and targeted re-entry capability with a length-adjustable and 360° rotational nitinol needle; the C-shaped radiopaque marker indicates in which direction the curved needle protrudes from the tip of the catheter; antegrade, retrograde, and crossover are possible for intraluminal and subintimal approach on 0.014- and 0.018-inch wire platform; indicated for use in conjunction with guidewires to pass occluded regions of the peripheral vasculature; It may be used to facilitate placement and exchange of guidewires |
More Categories:
Aortic (AAA) Aortic (TAA) Balloons Catheters Embolization Sheaths Stents Wires Other Devices View AllAdvertisement