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Catalogue numberLabeled device 
diameter (mm)
Available device 
lengths (mm)
Recommended vessel 
diameter (mm)
Introducer 
sheath size (Fr)a
Guidewire 
diameter (Stiff)
VNS100502A10507-9100.035” (0.889 mm)
VNS100702A10757-9100.035” (0.889 mm)
VNS101002A101007-9100.035” (0.889 mm)
VNS101502A101507-9100.035” (0.889 mm)
VNS120502A12509-11110.035” (0.889 mm)
VNS120702A12759-11110.035” (0.889 mm)
VNS121002A121009-11110.035” (0.889 mm)
VNS121502A121509-11110.035” (0.889 mm)
VNS140502A145011-13110.035” (0.889 mm)
VNS140702A147511-13110.035” (0.889 mm)
VNS141002A1410011-13110.035” (0.889 mm)
VNS141502A1415011-13110.035” (0.889 mm)
VNS160502A165013-15110.035” (0.889 mm)
VNS160702A167513-15110.035” (0.889 mm)
VNS161002A1610013-15110.035” (0.889 mm)
VNS161502A1615013-15110.035” (0.889 mm)
VNS180502A185015-17120.035” (0.889 mm)
VNS180702A187515-17120.035” (0.889 mm)
VNS181002A1810015-17120.035” (0.889 mm)
VNS181502A1815015-17120.035” (0.889 mm)
VNS200502A205017-19120.035” (0.889 mm)
VNS200702A207517-19120.035” (0.889 mm)
VNS201002A2010017-19120.035” (0.889 mm)
VNS201502A2015017-19120.035” (0.889 mm)
VNS240502A245018-22140.035” (0.889 mm)
VNS240702A247518-22140.035” (0.889 mm)
VNS241002A2410018-22140.035” (0.889 mm)
VNS241502A2415018-22140.035” (0.889 mm)
VNS280502A285022-26140.035” (0.889 mm)
VNS280702A 287522-26140.035” (0.889 mm)
VNS281002A2810022-26140.035” (0.889 mm)
VNS281502A2815022-26140.035” (0.889 mm)

a See Instructions for Use (IFU) for sheath compatibility.

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

Products listed may not be approved in all markets.

INDICATIONS FOR USE IN THE U.S.: The GORE® VIABAHN® FORTEGRA Venous Stent is indicated for use in the treatment of symptomatic inferior vena cava obstruction with or without combined iliofemoral obstruction.

CONTRAINDICATIONS: The GORE® VIABAHN® FORTEGRA Venous Stent is contraindicated for use in patients with lesions where expansion of an angioplasty balloon catheter to minimum GORE® VIABAHN® FORTEGRA Venous Stent recommended vessel diameters was not achieved during pre-dilatation, or where lesions cannot be dilated sufficiently to allow passage of the delivery system.

GORE® VIABAHN® FORTEGRA Venous Stent is not authorized for use in Canada.