C06150ML

Cordis SMART Vascular Stent System for SFA 6mm x 150mm, 120cm

$249.00 box of 1

In Stock: 1 Each

Expiration: Expired

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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.

Description

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: C06150ML

  • Stent Diameter: 6.0mm
  • 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.

Additional information

Size

6.00mm

Arms

N/A

Manufacturer

Stent Length

150mm

Unit

box of 1

Usable Length

120cm

  • FDA Product Code: NIP
  • FDA Product Code Name: Stent, Superficial Femoral Artery
  • GMDN Term Code: 43691 47932
  • GMDN Term Name: Bare-metal biliary stent / Peripheral artery stent, bare-metal
  • 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. / 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

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