IN-DATE
1012631-39: Abbott Omnilink Elite Vascular Balloon-Expandable Stent System 8mm x 39mm x 135cm
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| Price: | $699.00 per box of 1 |
|---|---|
| In Stock: | 0 box of 1 |
| Expiration: | In-Date |
We currently do not have this item in stock, but we can email you as soon as it is available.
Additional Details
Abbott Omnilink Elite Vascular Balloon-Expandable Stent System
Strength and flexibility that provides superb results in the iliacs.
The Omnilink Elite™ Stent System is indicated for the treatment of atherosclerotic iliac artery lesions with reference vessel diameters of ≥ 5.0 mm and ≤ 11.0 mm, and lesion lengths up to 50 mm.
- Cobalt chromium multi-link technology that allows for thin struts without sacrificing strength for flexibility and vessel conformability
- Superb accuracy with minimal impact to stent length
- Thin struts to minimize vessel wall injury
- Dual-layer balloon for a low profile system to treat difficult-to-reach lesions
Sterilization
- Device Packaged as Sterile: Yes
- Requires Sterilization Prior to Use: No
Contents
- (1) Abbott Omnilink Elite Vascular Balloon-Expandable Stent System
Additional Details
- Company Name: Abbott Vascular
- FDA Product Code: NIO
- FDA Product Code Name: Stent, Iliac
- GMDN Term Code: 47932
- GMDN Term Name: Peripheral artery stent, bare-metal
- GMDN Term Definition: A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.
AccessGUDID Info
- FDA Product Code: NIO
- FDA Product Code Name: STENT, ILIAC
- GMDN Term Code: 47932
- GMDN Term Name: Peripheral artery stent, bare-metal
- GMDN Term Description: A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.
Manufacturer
Abbott’s surgical innovations deliver advanced solutions that enhance precision, safety, and outcomes in the operating room. Building on the legacy of St. Jude Medical, Abbott offers a diverse portfolio of cutting-edge technologies, including structural heart devices like MitraClip™ for mitral valve repair and Amplatzer™ occluders for congenital heart defect closure. Their ProGlide™ vascular closure system and TactiCath™ ablation catheters further demonstrate Abbott’s commitment to empowering surgeons with reliable tools for minimally invasive procedures. By combining innovation with trusted expertise, Abbott continues to shape the future of surgical care. Browse Synergy Surgical's selection of Abbott surgical products, including Balloons, Stents, Vascular Closures and more.
