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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)
VNS100502E
10
50
7-9
10
0.035” (0.889 mm)
VNS100702E
10
75
7-9
10
0.035” (0.889 mm)
VNS101002E
10
100
7-9
10
0.035” (0.889 mm)
VNS101502E
10
150
7-9
10
0.035” (0.889 mm)
VNS120502E
12
50
9-11
11
0.035” (0.889 mm)
VNS120702E
12
75
9-11
11
0.035” (0.889 mm)
VNS121002E
12
100
9-11
11
0.035” (0.889 mm)
VNS121502E
12
150
9-11
11
0.035” (0.889 mm)
VNS140502E
14
50
11-13
11
0.035” (0.889 mm)
VNS140702E
14
75
11-13
11
0.035” (0.889 mm)
VNS141002E
14
100
11-13
11
0.035” (0.889 mm)
VNS141502E
14
150
11-13
11
0.035” (0.889 mm)
VNS160502E
16
50
13-15
11
0.035” (0.889 mm)
VNS160702E
16
75
13-15
11
0.035” (0.889 mm)
VNS161002E
16
100
13-15
11
0.035” (0.889 mm)
VNS161502E
16
150
13-15
11
0.035” (0.889 mm)
VNS180502E
18
50
15-17
12
0.035” (0.889 mm)
VNS180702E
18
75
15-17
12
0.035” (0.889 mm)
VNS181002E
18
100
15-17
12
0.035” (0.889 mm)
VNS181502E
18
150
15-17
12
0.035” (0.889 mm)
VNS200502E
20
50
17-19
12
0.035” (0.889 mm)
VNS200702E
20
75
17-19
12
0.035” (0.889 mm)
VNS201002E
20
100
17-19
12
0.035” (0.889 mm)
VNS201502E
20
150
17-19
12
0.035” (0.889 mm)
VNS240502E
24b
50
18-22
14
0.035” (0.889 mm)
VNS240702E
24b
75
18-22
14
0.035” (0.889 mm)
VNS241002E
24b
100
18-22
14
0.035” (0.889 mm)
VNS241502E
24b
150
18-22
14
0.035” (0.889 mm)
VNS280502E
28b
50
22-26
14
0.035” (0.889 mm)
VNS280702E
28b
75
22-26
14
0.035” (0.889 mm)
VNS281002E
28b
100
22-26
14
0.035” (0.889 mm)
VNS281502E
28b
150
22-26
14
0.035” (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.