Device typeCentral/peripheral venous endovascular stent-graft: A non-bioabsorbable tubular device designed to be implanted in a central and/or peripheral vein (e.g., subclavian, brachiocephalic) to maintain vessel lumen patency, typically to treat stenosis in the outflow of an arteriovenous fistula (AVF) or graft used for haemodialysis; it is not intended for coronary or intracranial venous stenting. It is a mesh structure made of metal [e.g., nickel-titanium alloy] that is covered with a synthetic polymer [e.g., polytetrafluoroethylene (ePTFE)] membrane (endovascular graft), and contains an inner carbon coating to help prevent platelet adhesion. It is typically expanded in situ and disposable devices associated with implantation may be included.
FDA categoryStent Graft, Bypass, Superficial Femoral Artery
Device ID00850032145077
Catalog numberTSG-6.7X200
AvailabilityPrescription
Single useYes
SterileYes
MRI safetyMR Conditional
Size6.7mm