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Penumbra, Inc. (Neuro)
1351 Harbor Bay Parkway, Alameda, CA 94502
PHONE: (510) 748-3200 | FAX: (510) 748-3232
Catheters / Guiding Catheters
View Chart| Company Name | Product Name | Type | Size (F) | Length (cm) | Internal Diameter (inch) | Radiopaque Tip (Yes/No) | Hydrophilic Coated |
|---|---|---|---|---|---|---|---|
| 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 |
| 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 |
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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) |
|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
Embolization / Cerebral Coils
View Chart| Company Name | Product Name | Materials Used | Coil Type | Method of Detachment | CE Mark Indications | Comments |
|---|---|---|---|---|---|---|
| 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 |
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 |
|---|---|---|---|---|---|---|
| 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 |
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