IN-DATE
ESBF2314C103E: Medtronic Endurant IIs Stent Graft System, Bifurcated 23mm / 14mm / 103mm
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| Price: | $2,139.00 per box of 1 |
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| Quantity: | |
| In Stock: | 1 box of 1 |
| Status: | expired |
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Additional Details
Medtronic ESBF2314C103E Endurant™ IIs Bifurcated Stent Graft, 23 mm x 14 mm x 103 mm
Medtronic product code ESBF2314C103E is an Endurant™ IIs bifurcated stent graft designed for endovascular aneurysm repair (EVAR) of infrarenal abdominal aortic and aortoiliac aneurysms. The implantable graft has a 23 mm proximal graft diameter, 14 mm distal graft diameter, and 103 mm total covered length and is delivered through an 18 Fr delivery system.
Product Code: ESBF2314C103E
- Manufacturer: Medtronic
- Product Name: Endurant™ IIs Bifurcated Stent Graft
- Brand: Endurant™ IIs
- Device Type: Bifurcated abdominal aortic stent graft
- Proximal Graft Diameter: 23 mm (0.91 in)
- Distal Graft Diameter: 14 mm (0.55 in)
- Total Covered Length: 103 mm (4.06 in)
- Distal Design: C
- Delivery System: E
- Catheter Outer Diameter: 18 Fr
- Clinical Application: Endovascular treatment of infrarenal abdominal aortic and aortoiliac aneurysms
- Procedure Type: Endovascular aneurysm repair (EVAR)
- Specialty: Vascular Surgery, Interventional Radiology
- Anatomical Application: Infrarenal abdominal aorta and aortoiliac vasculature
- MR Status: MR Conditional
- Implantable: Yes
Features
- Bifurcated configuration provides the main aortic component for modular endovascular aneurysm repair
- Designed for use with compatible Endurant™ iliac limb components
- May be used with the Heli-FX™ EndoAnchor™ System when augmented radial fixation or sealing is required in approved anatomies
- 18 Fr delivery profile supports endovascular introduction through compatible iliac or femoral access
Sterilization
- Device Packaged as Sterile: Yes
- Requires Sterilization Prior to Use: No
- Single-Use, Disposable
AccessGUDID Info
- FDA Product Code: MIH
- FDA Product Code Name: SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- GMDN Term Code: 46777
- GMDN Term Name: Abdominal aorta endovascular stent-graft
- GMDN Term Description: A non-bioabsorbable tubular device typically implanted at the junction of the abdominal aorta and the common iliac arteries to reduce pressure on an abdominal aortic aneurysm (AAA) [includes aortoiliac aneurysm]; it does not contain anticoagulants or pharmaceuticals. It is percutaneously inserted via the femoral artery to the site of implantation where it self-expands. It is typically made of a metallic outer mesh structure with an inner polymer tube (endovascular graft) and is typically available as a: 1) single tube for insertion into the aorta and/or one iliac artery; or 2) two-part bifurcation design (e.g., Y-shaped tube) for insertion through both iliac arteries.
Manufacturer
Medtronic Cardiovascular Therapies offers a broad range of solutions for treating peripheral artery disease, aortic aneurysms, deep vein thrombosis, and other vascular conditions. Key technologies include the Endurant II and Endurant IIs stent graft systems for abdominal aortic aneurysms, the IN.PACT Admiral drug-coated balloon for femoropopliteal disease, and the Abre venous self-expanding stent system for iliofemoral venous outflow obstruction. With a commitment to advancing minimally invasive therapies, Medtronic’s vascular innovations help restore blood flow, reduce procedural risk, and improve quality of life for patients with complex vascular disease.
There is no valid manufacturer warranty on the products that Synergy Surgical sells. Any services provided by the original manufacturer of the products we sell are not available. However, eSutures offers a 100% money back guarantee (less shipping) on every item we sell within 30 days of purchase. For details, please see our Return Policy.
