Catalogue Numbers for GORE® VIABAHN® FORTEGRA Venous Stent

Catalogue number	Labeled device diameter (mm)	Available device lengths (mm)	Recommended vessel diameter (mm)	Introducer sheath size (Fr)^a	Guidewire diameter (Stiff)
VNS100502A	10	50	7-9	10	0.035” (0.889 mm)
VNS100702A	10	75	7-9	10	0.035” (0.889 mm)
VNS101002A	10	100	7-9	10	0.035” (0.889 mm)
VNS101502A	10	150	7-9	10	0.035” (0.889 mm)
VNS120502A	12	50	9-11	11	0.035” (0.889 mm)
VNS120702A	12	75	9-11	11	0.035” (0.889 mm)
VNS121002A	12	100	9-11	11	0.035” (0.889 mm)
VNS121502A	12	150	9-11	11	0.035” (0.889 mm)
VNS140502A	14	50	11-13	11	0.035” (0.889 mm)
VNS140702A	14	75	11-13	11	0.035” (0.889 mm)
VNS141002A	14	100	11-13	11	0.035” (0.889 mm)
VNS141502A	14	150	11-13	11	0.035” (0.889 mm)
VNS160502A	16	50	13-15	11	0.035” (0.889 mm)
VNS160702A	16	75	13-15	11	0.035” (0.889 mm)
VNS161002A	16	100	13-15	11	0.035” (0.889 mm)
VNS161502A	16	150	13-15	11	0.035” (0.889 mm)
VNS180502A	18	50	15-17	12	0.035” (0.889 mm)
VNS180702A	18	75	15-17	12	0.035” (0.889 mm)
VNS181002A	18	100	15-17	12	0.035” (0.889 mm)
VNS181502A	18	150	15-17	12	0.035” (0.889 mm)
VNS200502A	20	50	17-19	12	0.035” (0.889 mm)
VNS200702A	20	75	17-19	12	0.035” (0.889 mm)
VNS201002A	20	100	17-19	12	0.035” (0.889 mm)
VNS201502A	20	150	17-19	12	0.035” (0.889 mm)
VNS240502A	24	50	18-22	14	0.035” (0.889 mm)
VNS240702A	24	75	18-22	14	0.035” (0.889 mm)
VNS241002A	24	100	18-22	14	0.035” (0.889 mm)
VNS241502A	24	150	18-22	14	0.035” (0.889 mm)
VNS280502A	28	50	22-26	14	0.035” (0.889 mm)
VNS280702A	28	75	22-26	14	0.035” (0.889 mm)
VNS281002A	28	100	22-26	14	0.035” (0.889 mm)
VNS281502A	28	150	22-26	14	0.035” (0.889 mm)

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

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. R_XOnly

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.