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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)
VNS100502E10507-9100.035” (0.889 mm)
VNS100702E10757-9100.035” (0.889 mm)
VNS101002E101007-9100.035” (0.889 mm)
VNS101502E101507-9100.035” (0.889 mm)
VNS120502E12509-11110.035” (0.889 mm)
VNS120702E12759-11110.035” (0.889 mm)
VNS121002E121009-11110.035” (0.889 mm)
VNS121502E121509-11110.035” (0.889 mm)
VNS140502E145011-13110.035” (0.889 mm)
VNS140702E147511-13110.035” (0.889 mm)
VNS141002E1410011-13110.035” (0.889 mm)
VNS141502E1415011-13110.035” (0.889 mm)
VNS160502E165013-15110.035” (0.889 mm)
VNS160702E167513-15110.035” (0.889 mm)
VNS161002E1610013-15110.035” (0.889 mm)
VNS161502E1615013-15110.035” (0.889 mm)
VNS180502E185015-17120.035” (0.889 mm)
VNS180702E187515-17120.035” (0.889 mm)
VNS181002E1810015-17120.035” (0.889 mm)
VNS181502E1815015-17120.035” (0.889 mm)
VNS200502E205017-19120.035” (0.889 mm)
VNS200702E207517-19120.035” (0.889 mm)
VNS201002E2010017-19120.035” (0.889 mm)
VNS201502E2015017-19120.035” (0.889 mm)
VNS240502E24b5018-22140.035” (0.889 mm)
VNS240702E24b7518-22140.035” (0.889 mm)
VNS241002E24b10018-22140.035” (0.889 mm)
VNS241502E24b15018-22140.035” (0.889 mm)
VNS280502E28b5022-26140.035” (0.889 mm)
VNS280702E28b7522-26140.035” (0.889 mm)
VNS281002E28b10022-26140.035” (0.889 mm)
VNS281502E28b15022-26140.035” (0.889 mm)

a. All devices are compatible with the GORE® DRYSEAL Sheath at the profiles noted in the table. If necessary, sheaths may be upsized by ≥1 Fr.

  • GORE® VIABAHN® FORTEGRA Venous Stent 10-20 mm devices are not compatible with the Cook CHECK-FLO® FLEXOR® sheath or the Abbott FAST-CATH™ Introducer sheath at the profiles noted above.
  • The 16 mm diameter device is not compatible with the Cordis AVANTI® Sheath Introducer or the Cordis BRITE TIP® Sheath Introducer at the profile noted above.
  • Do not use any introducer sheath that does not have an atraumatic tip (e.g., Inari Protrieve™ Sheath). 

b. Parallel balloons may be used: two 14-16 mm balloons in a 24 mm GORE® VIABAHN® FORTEGRA Venous Stent, or two 14–18 mm balloons in a 28 mm GORE® VIABAHN® FORTEGRA Venous Stent.

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 THE EMEA: The GORE® VIABAHN® FORTEGRA Venous Stent is indicated for use in the treatment of symptomatic inferior vena cava and iliofemoral venous outflow 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.

Products listed may not be approved in all markets.