MONOFILAMENT MESH HIGH FLEXIBILITY AND OPTIMAL RADIAL FORCE FLARED ENDS
(+8 mm) to limit migration
SILICONE COVERAGE AND ROUNDED ENDS
Reduces the risk of intramural cellular infiltration
and hyperplastic reaction due to stent placement GREEN REMOVAL THREAD
for easier removal
RADIOPAQUE MARKERS:
Four at each end and two in the center
ON 0.038” or 0.035” STIFF GUIDE WIRE
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This product is a Class IIa, IIb, or III device, developed by a manufacturer ensuring CE conformity assessment by a certified notified body. The manufacturer guarantees compliance with current markings and standards under French regulations. Indications, contraindications, warnings, and instructions for use are listed in the user manual supplied with each product. Please refer to it before any use.