Catalogue Numbers for GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface* and GORE® VIABAHN® Endoprosthesis - U.S. 

GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface

.035" Guidewire 

Catalogue Number Endoprosthesis Labeled 
Diameter† (mm) 		Endoprosthesis 
Length† (cm) 		Catheter 
Length‡ (cm) 		Recommended 
Vessel Diameter§ (mm) 		Device Profile (Fr) Recommended 
Balloon Diameter 
for Device Touch-up‖

 (mm) 
VBHR050202A 
5 
2.5 
120 
4.0–4.7 
7 
5 
VBHR050502A 
5 
5.0
120
4.0–4.7 
7
5
VBHR050702A 
5
7.5
120
4.0–4.7 
7
5
VBHR051002A 
5
10.0
120
4.0–4.7 
7
5
VBHR051502A 
5 
15.0
120
4.0–4.7 
7
5
VBHR052502A 
5
25.0
120
4.0–4.7 
7
5
VBHR060201A 
6
2.5
75
4.8–5.5 
7
6
VBHR060202A 
6
2.5
120
4.8–5.5 
7
6
VBHR060501A 
6
5.0
75
4.8–5.5 
7
6
VBHR060502A 
6
5.0
120
4.8–5.5 
7
6
VBHR060702A 
6
7.5
120
4.8–5.5 
7
6
VBHR061001A 
6
10.0
75
4.8–5.5 
7
6
VBHR061002A 
6
10.0
120
4.8–5.5 
7
6
VBHR061501A 
6
15.0
75
4.8–5.5 
7
6
VBHR061502A 
6
15.0
120
4.8–5.5 
7
6
VBHR062502A 
6
25.0
120
4.8–5.5 
7
6
VBHR070201A 
7
2.5
75
5.6–6.5 
8
7
VBHR070202A 
7
2.5
120
5.6–6.5 
8
7
VBHR070501A 
7
5.0
75
5.6–6.5 
8
7
VBHR070502A 
7
5.0
120
5.6–6.5 
8
7
VBHR070702A 
7
7.5
120
5.6–6.5 
8
7
VBHR071001A 
7
10.0
75
5.6–6.5 
8
7
VBHR071002A 
7
10.0
120
5.6–6.5 
8
7
VBHR071501A 
7
15.0
75
5.6–6.5 
8
7
VBHR071502A 
7
15.0
120
5.6–6.5 
8
7
VBHR072502A 
7
25.0
120
5.6–6.5 
8
7
VBHR080201A 
8
2.5
75
6.6–7.5 
8
8
VBHR080202A 
8
2.5
120
6.6–7.5 
8
8
VBHR080501A 
8
5.0
75
6.6–7.5 
8
8
VBHR080502A 
8
5.0
120
6.6–7.5 
8
8
VBHR080702A 
8
7.5
120
6.6–7.5 
8
8
VBHR081001A 
8
10.0
75
6.6–7.5 
8
8
VBHR081002A 
8
10.0
120
6.6–7.5 
8
8
VBHR081501A 
8
15.0
75
6.6–7.5 
8
8
VBHR081502A 
8
15.0
120
6.6–7.5 
8
8
VBHR082502A 
8
25.0
120
6.6–7.5 
8
8
VBHR090502A 
9
5.0
120
7.6–8.5 
8
9
VBHR090702A 
9
7.5
120
7.6–8.5 
8
9
VBHR091002A 
9
10.0
120
7.6–8.5 
8
9
VBHR091502A 
9
15.0
120
7.6–8.5 
8
9
VBHR100502A 
10
5.0
120
8.6–9.5 
8
10
VBHR101002A 
10
10.0
120
8.6–9.5 
8
10
VBHR101502A 
10
15.0
120
8.6–9.5 
8
10
VBHR110502A 
11
5.0
120
9.6–10.5 
10
12
VBHR111002A 
11
10.0
120
9.6–10.5 
10
12
VBHR130502A 
13
5.0
120
10.6–12.0 
10 
14
VBHR131002A 
13
10.0
120
10.6–12.0 
10 
14

GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface

.014 / .018" Guidewire 

Catalogue Number Endoprosthesis Labeled 
Diameter† (mm) 		Endoprosthesis 
Length† (cm) 		Catheter 
Length‡ (cm) 		Recommended 
Vessel Diameter§ (mm) 		Device Profile (Fr) Recommended 
Balloon Diameter 
for Device Touch-up (mm) 
VBJR050202A 
5
2.5
120
4.0–4.7 
6
5
VBJR050502A 
5
5.0
120
4.0–4.7 
6
5
VBJR050702A 
5
7.5
120
4.0–4.7 
6
5
VBJR051002A 
5
10.0
120
4.0–4.7 
6
5
VBJR051502A 
5
15.0
120
4.0–4.7 
6
5
VBJR052502A 
5
25.0
120
4.0–4.7 
6
5
VBJR060202A 
6
2.5
120
4.8–5.5 
6
6
VBJR060502A 
6
5.0
120
4.8–5.5 
6
6
VBJR060702A 
6
7.5
120
4.8–5.5 
6
6
VBJR061002A 
6
10.0
120
4.8–5.5 
6
6
VBJR061502A 
6
15.0
120
4.8–5.5 
6
6
VBJR062502A 
6
25.0
120
4.8–5.5 
6
6
VBJR070202A 
7
2.5
120
5.6–6.5 
7
7
VBJR070502A 
7
5.0
120
5.6–6.5 
7
7
VBJR070702A 
7
7.5
120
5.6–6.5 
7
7
VBJR071002A 
7
10.0
120
5.6–6.5 
7
7
VBJR071502A 
7
15.0
120
5.6–6.5 
7
7
VBJR072502A
7
25.0
120
5.6–6.5 
7
7
VBJR080202A
8
2.5
120
6.6–7.5 
7
8
VBJR080502A 
8
5.0
120
6.6–7.5 
7
8
VBJR080702A 
8
7.5
120
6.6–7.5 
7
8
VBJR081002A 
8
10.0
120
6.6–7.5 
7
8
VBJR081502A 
8
15.0
120
6.6–7.5 
7
8
VBJR082502A 
8
25.0
120
6.6–7.5 
7**
8

GORE® VIABAHN® Endoprosthesis

.035" Guidewire 

Catalogue Number Endoprosthesis Labeled 
Diameter† (mm) 		Endoprosthesis 
Length† (cm) 		Catheter 
Length‡ (cm) 		Recommended 
Vessel Diameter§ (mm) 		Device Profile (Fr) Recommended 
Balloon Diameter for 
Device Touch-up‖ (mm) 
VBCR050202A 
5
2.5
120
4.0–4.7 
7
5
VBCR050502A 
5
5.0
120
4.0–4.7 
7
5
VBCR051002A 
5
10.0
120
4.0–4.7 
7
5
VBCR051502A 
5
15.0
120
4.0–4.7 
7
5
VBCR060202A 
6
2.5
120
4.8–5.5 
7
6
VBCR060501A 
6
5.0
75
4.8–5.5 
7
6
VBCR060502A 
6
5.0
120
4.8–5.5 
7
6
VBCR061001A 
6
10.0
75
4.8–5.5 
7
6
VBCR061002A 
6
10.0
120
4.8–5.5 
7
6
VBCR061501A 
6
15.0
75
4.8–5.5 
7
6
VBCR061502A 
6
15.0
120
4.8–5.5 
7
6
VBCR070202A 
7
2.5
120
5.6–6.5 
8
7
VBCR070501A 
7
5.0
75
5.6–6.5 
8
7
VBCR070502A 
7
5.0
120
5.6–6.5 
8
7
VBCR071001A 
7
10.0
75
5.6–6.5 
8
7
VBCR071002A 
7
10.0
120
5.6–6.5 
8
7
VBCR071501A 
7
15.0
75
5.6–6.5 
8
7
VBCR071502A 
7
15.0
120
5.6–6.5 
8
7
VBCR080202A 
8
2.5
120
6.6–7.5 
8
8
VBCR080501A 
8
5.0
75
6.6–7.5 
8
8
VBCR080502A 
8
5.0
120
6.6–7.5 
8
8
VBCR081001A 
8
10.0
75
6.6–7.5 
8
8
VBCR081002A 
8
10.0
120
6.6–7.5 
8
8
VBCR081501A 
8
15.0
75
6.6–7.5 
8
8
VBCR081502A 
8
15.0
120
6.6–7.5 
8
8
VBCR090502A 
9
5.0
120
7.6–8.5 
8
9
VBCR091002A 
9
10.0
120
7.6–8.5 
8
9
VBCR091502A 
9
15.0
120
7.6–8.5 
8
9
VBCR100502A 
10
5.0
120
8.6–9.5 
8
10
VBCR101002A 
10
10.0
120
8.6–9.5 
8
10
VBCR101502A 
10
15.0
120
8.6–9.5 
8
10
VBCR110502A 
11
5.0
120
9.6–10.5 
10
12
VBCR111002A 
11
10.0
120
9.6–10.5 
10
12
VBCR130502A 
13
5.0
120
10.6–12.0 
10 
14
VBCR131002A 
13
10.0
120
10.6–12.0 
10 
14

* As used by Gore, Heparin Bioactive Surface refers to Gore’s proprietary CBAS® Heparin Surface.

† Labeled device diameters and lengths are nominal.

‡ Ensure the guidewire is the appropriate size (see Instructions for Use) and has a length at least twice that of the delivery catheter.

§ Recommended endoprosthesis compression within the vessel is approximately 5 - 20%.

‖ For the 11 and 13 mm diameter devices, balloon inflation pressure should not exceed 8 atm.

The 13 mm diameter device is not compatible with the 10 Fr COOK® FLEXOR® CHECK-FLO® Sheath.

** The 8 mm x 25 cm device is not compatible with the 7 Fr COOK® CHECK-FLO® Sheath. 

Sizing, availability and pricing varies by country.

Please check with your Gore representative for availability. 

Catalogue Numbers for GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface* - Canada 

GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface

.014 / .018" Guidewire  

Catalogue Number Endoprosthesis Labeled 
Diameter† (mm) 		Endoprosthesis 
Length† (cm) 		Catheter 
Length‡ (cm) 		Recommended 
Vessel Diameter§ (mm) 		Device Profile (Fr) Recommended 
Balloon Diameter for 
Device Touch-up (mm) 
PAJR050202B 
5
2.5
120
4 – 4.7 
6
5
PAJR050502B 
5
5
120
4 – 4.7 
6
5
PAJR051002B 
5
10
120
4 – 4.7 
6
5
PAJR051502B 
5
15
120
4 – 4.7 
6
5
PAJR052502B 
5
25
120
4 – 4.7 
6
5
PAJR060202B 
6
2.5
120
4.8 – 5.5 
6
6
PAJR060502B 
6
5
120
4.8 – 5.5 
6
6
PAJR061002B 
6
10
120
4.8 – 5.5 
6
6
PAJR061502B 
6
15
120
4.8 – 5.5 
6
6
PAJR062502B 
6
25
120
4.8 – 5.5 
6
6
PAJR070202B 
7
2.5
120
5.6 – 6.5 
7
7
PAJR070502B 
7
5
120
5.6 – 6.5 
7
7
PAJR071002B 
7
10
120
5.6 – 6.5 
7
7
PAJR071502B 
7
15
120
5.6 – 6.5 
7
7
PAJR072502B 
7
25
120
5.6 – 6.5 
7
7
PAJR080202B 
8
2.5
120
6.6 – 7.5 
7
8
PAJR080502B 
8
5
120
6.6 – 7.5 
7
8
PAJR081002B 
8
10
120
6.6 – 7.5 
7
8
PAJR081502B 
8
15
120
6.6 – 7.5 
7
8
PAJR082502B 
8
25
120
6.6 – 7.5 
7¶ 
8

GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface

.035" Guidewire 

Catalogue Number Endoprosthesis Labeled 
Diameter† (mm) 		Endoprosthesis 
Length† (cm) 		Catheter 
Length‡ (cm) 		Recommended 
Vessel Diameter§ (mm) 		Device Profile (Fr) Recommended 
Balloon Diameter for 
Device Touch-up‖ (mm) 
PAHR090502B 
9
5
120
7.6 – 8.5 
8
9
PAHR091002B 
9
10
120
7.6 – 8.5 
8
9
PAHR091502B 
9
15
120
7.6 – 8.5 
8
9
PAHR100502B 
10
5
120
8.6 – 9.5 
8
10
PAHR101002B 
10
10
120
8.6 – 9.5 
8
10
PAHR101502B 
10
15
120
8.6 – 9.5 
8
10
PAHR110502B 
11
5
120
9.6 – 10.5 
10
12
PAHR111002B 
11
10
120
9.6 – 10.5 
10
12
PAHR130502B 
13
5
120
10.6 – 12 
10**
14
PAHR131002B 
13
10
120
10.6 – 12 
10**
14

* As used by Gore, PROPATEN Bioactive Surface refers to Gore's proprietary CBAS® Heparin Surface.

† Labeled device diameters and lengths are nominal.

‡ Ensure the guidewire is the appropriate size (see Instructions for Use) and has a length at least twice that of the delivery catheter.

§ Recommended endoprosthesis compression within the vessel is approximately 5–20%. 
‖ For the 11 and 13 mm diameter devices, balloon inflation pressure should not exceed 8 atm.

The 8 mm x 25 cm device is not compatible with the 7 Fr COOK® CHECK-FLO® Introducer.

** The 13 mm diameter device is not compatible with the 10 Fr COOK® FLEXOR® CHECK-FLO® Introducer.

COOK, CHECK-FLO and FLEXOR are trademarks of Cook Medical, Inc.

CBAS is a trademark of Carmeda AB, a wholly owned subsidiary of W. L. Gore & Associates, Inc. 

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 U.S.: The GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface is indicated for improving blood flow in patients with symptomatic peripheral arterial disease in superficial femoral artery de novo and restenotic lesions up to 270 mm in length with reference vessel diameters ranging from 4.0 – 7.5 mm. The GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface is indicated for improving blood flow in patients with symptomatic peripheral arterial disease in superficial femoral artery in-stent restenotic lesions up to 270 mm in length with reference vessel diameters ranging from 4.0 – 6.5 mm. The GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface is indicated for improving blood flow in patients with symptomatic peripheral arterial disease in iliac artery lesions up to 80 mm in length with reference vessel diameters ranging from 4.0 – 12 mm. The GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface is also indicated for the treatment of stenosis or thrombotic occlusion at the venous anastomosis of synthetic arteriovenous (AV) access grafts.  

CONTRAINDICATIONS: The GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface is contraindicated for non-compliant lesions where full expansion of an angioplasty balloon catheter was not achieved during pre-dilatation, or where lesions cannot be dilated sufficiently to allow passage of the delivery system. Do not use the GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface in patients with known hypersensitivity to heparin, including those patients who have had a previous incident of Heparin-Induced Thrombocytopenia (HIT) type II. 

24PL1080-EN02 MAT-0144-1