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The VBX Stent Graft is made with advanced technology and a unique design to offer unmatched versatilitya,1–8

What could you achieve in your complex endovascular aortic repair procedures with the VBX Stent Graft?


a Across indications and configurations of covered stents.

  1. Gore Medical Products Instructions for Use (IFU). W. L. Gore & Associates, Inc. Accessed July 26, 2025.https://eifu.goremedical.com/
  2. BeGraft Peripheral Stent Graft System [Instructions for Use]. Bentley InnoMed GmbH; 2018.
  3. BeFlared FEVAR Stent Graft System [Instructions for Use] Bentley InnoMed GmbH; 2024. 406725-001e/002.
  4. BeGraft Peripheral Plus Stent Graft System [Instructions for Use]. Bentley InnoMed GmbH; 2019. #401797-001/005.
  5. BeFlow Iliac Covered Stent System [Instructions for Use] Bentley InnoMed GmbH; 2024. 404742-001e/002.
  6. BD® LifeStream™ Balloon Expandable Vascular Covered Stent [Instructions for Use]. Clearstream Technologies, Ltd;2020. PK1299800. Rev. 5. 05/20.
  7. Advanta V12 Balloon Expandable Covered Stent [Instructions for Use]. Atrium Medical Corporation; 2019. AW011076. Rev AB.
  8. iVascular® iCover Balloon Expandable Stent System [Instructions for Use]. iVascular S.L.U.; 2021. MP45030Ed.0. March 2021.
  9. W. L. Gore & Associates, Inc. CBAS® Heparin Surface. Accessed Accessed August 8, 2025. https://www.goremedical.com/en-emea/cbas-material-technology
IFU Consult instructions

Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the markets where this product is available. RXOnly

INDICATIONS FOR USE IN EUROPE: The GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis is indicated for the treatment of: 

  • de novo or restenotic lesions found in iliac arteries, including lesions at the aortic bifurcation;
  • de novo or restenotic lesions in the visceral arteries;
  • isolated visceral, iliac, and subclavian artery aneurysms; or
  • traumatic or iatrogenic vessel injuries in arteries that are located in the chest cavity, abdominal cavity, or pelvis (except for aorta, coronary, innominate, carotid, vertebral, and pulmonary arteries).

The GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis is indicated for use as a bridging stent in branched and fenestrated endovascular aortic aneurysm repair with the followingb:

  • Approved for use branched aortic endovascular grafts constructed of polyester fabric, stainless steel stents, and polypropylene suture with branch diameters of 6/8 mm and lengths of 18/21 mm.
  • Approved for use fenestrated aortic endovascular grafts constructed of polyester fabric, stainless steel stents, and fenestrations with polypropylene suture ranging in diameter from 6–8 mm.

CONTRAINDICATIONS: Do not use the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis in patients with known hypersensitivity to heparin, including those patients who have had a previous incident of Heparin-Induced Thrombocytopenia (HIT) type II.

b Not applicable to Reduced Profile GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (BXB catalogue numbers).  

Product may not be available in all countries. Please check with your Gore representative for availability.