Venous stent E-LUMINEXX®

Features: Designed for exceptional visibility under fluoroscopy, which significantly enhances stent placement accuracy The proprietary interlocking Puzzle® Tantalum marker assures permanent attachment Dimensional design changes facilitate harmonization of radial force across the range of product diameters Open cell, flexible mesh design with minimal length change during deployment 2 mm flared stent ends designed to resist migration and compensate for lumen tapering Read the BARD ® ELUMINEXX ® Vascular Stent IFU thoroughly. Also, thoroughly read the IFUs supplied with any other interventional devices to be used in conjunction with the system. • Please use the product illustration at the beginning of this booklet to guide you through the device description. • Please use the fold-out, step-by-step procedure illustrations at the end of this booklet to guide you through the procedure description. The device is supplied in sterile condition. All materials inside the sterile barrier pouch (the delivery system and stent as well as the carrier tube and pouchliner) are sterile. The external surface of the sterile pouch and the product carton should not be considered sterile. Federal (U.S.A) law restricts this device to sale by or on the order of a physician. 1.0 DEVICE NAME • The brand name of the device is BARD ® ELUMINEXX ® Vascular Stent. • The Stent (Implant) is equipped with four highly visible radiopaque PUZZLE ® Tantalum Markers on both the proximal and distal end