GORE VIABAHN® Endoprosthesis

GORE VIABAHN® Endoprosthesis


Endoluminal Bypass for treating Peripheral Vascular Disease (PVD) in the superficial femoral and iliac arteries


Interventionalists treating patients suffering from Peripheral Vascular Disease (PVD) in the Superficial Femoral Artery (SFA) require a flexible stent-graft capable of re-lining tortuous arteries.

The GORE VIABAHN® Endoprosthesis is constructed with a durable, reinforced, biocompatible, expanded polytetrafluoroethylene (ePTFE) liner attached to an external nitinol stent structure. The flexibility of the GORE VIABAHN® Endoprosthesis enables it to traverse tortuous areas of the SFA and conform closely to the complex anatomy of the artery. W. L. Gore & Associates has now added a heparin-bonded surface to the GORE VIABAHN® Endoprosthesis.

The GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface is the only device of its kind approved for both the SFA and iliac artery. The latest interventional product offering from W. L. Gore & Associates, the stent-graft features the addition of proprietary heparin-bonded technology to the proven combination of ePTFE and Nitinol. End-point covalent bonding keeps heparin anchored to the endoprosthesis surface while the bioactive site remains free to interact with the blood.

With a new lower-profile, streamlined delivery system, the GORE VIABAHN® Endoprosthesis with Heparin Bioactive Surface makes it easier to reach and treat challenging SFA lesions.

Attention, see Instructions for Use


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