IN-DATE
C07150ML: Cordis SMART Vascular Stent System for SFA 7mm x 150mm, 120cm
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| Price: | $249.00 per box of 1 |
|---|---|
| Quantity: | |
| In Stock: | 1 box of 1 |
| Status: | expired |
The item listed above is expired and may be used for educational, training, and non-clinical research purposes only. Any product information appearing below, including the product indication statement, pertains to an in date item only.
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Additional Details
Cordis S.M.A.R.T. Vascular Stent System
S.M.A.R.T.® Vascular Stent systems, for superficial femoral artery (SFA) and iliac lesions, are proven reliable in over 3,000 patients and provide consistent outcomes
The S.M.A.R.T.® Vascular Stent System offers:
- Longitudinal stability: Greater stability minimizes stretching at deployment, thereby increasing placement accuracy.
- Radial force: The stent’s ability to resist compression maintains luminal gain.
- Uniform scaffolding: Smaller cell size and uniform coverage can help prevent vessel prolapse.
Product Code: C07150ML
- Stent Diameter: 7.0mm
- Stent Length: 150mm
- Shaft Length: 120cm
- Sheath Compatibility: 6F
- Guidewire Compatibility: 0.035"
Sterilization
- Device Packaged as Sterile: Yes
- Requires Sterilization Prior to Use: No
- Single-Use
- Disposable
Additional Details
- Company Name: Cordis Corporation
- FDA Product Code: NIP
- FDA Product Code Name: Stent, Superficial Femoral Artery
- 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 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: NIP
- FDA Product Code Name: STENT, SUPERFICIAL FEMORAL ARTERY
- 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.
- GMDN Term Code: 43691
- GMDN Term Name: Bare-metal biliary stent
- GMDN Term Description: A non-bioabsorbable tubular device intended to be implanted in an obstructed biliary duct (e.g., common bile duct) to maintain luminal patency; it is not intended for vascular implantation. It may be a mesh structure or a continuous tube and is made entirely of metal [e.g., high-grade stainless steel, cobalt-chrome (Co-Cr), nickel-titanium alloy (Nitinol)]. It may be expandable in situ (e.g., with a balloon catheter or self-expands) and disposable devices intended to assist implantation may be included.
Manufacturer
Cordis is a global leader in interventional cardiovascular technologies, with a strong legacy in developing minimally invasive solutions for the treatment of coronary and peripheral vascular disease. Their portfolio includes diagnostic and interventional catheters, guidewires, and balloon angioplasty systems, as well as stents like the SMART Control and S.M.A.R.T. Flex for peripheral use. Cordis also offers radial access products and closure devices to support efficient and safe procedures. With a renewed focus on innovation and global expansion, Cordis continues to provide trusted tools that help physicians deliver effective, streamlined care in both coronary and endovascular interventions.
