Device typePeripheral artery endovascular stent-graft, non-medicated: A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to maintain patency and improve luminal diameter, typically in patients with symptomatic peripheral vascular disease or following the recanalization of a total occlusion. It may be intended for implantation in an artery adjacent to the aorta (e.g., iliac, renal), however it is not a dedicated component of an aortoiliac stent-graft assembly; it may additionally be intended for venous implantation. It is a metallic mesh-like structure with a synthetic polymer tube (endovascular graft); it does not include pharmaceuticals.
FDA categoryIliac covered stent, arterial
Device ID05391522081185
Catalog numberLSMU0800837
AvailabilityPrescription
Single useYes
SterileYes
LatexNot made with natural rubber latex
MRI safetyMR Conditional
SizeImplant Length, 37 Millimeter
SizeBalloon Diameter, 8 Millimeter
SizeCatheter Length, 80 Centimeter