GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (Reduced Profile)      
BXB Codes

Catalogue 

Number 

Stent 
Labeled/Nominal 
Diameter (mm) 		Maximum 
Post-Dilated Stent 
Diameter (mm)* 

Stent 

Length (mm) 

Catheter 

Length (cm) 

Guidewire 

Diameter (in) 

Introducer 

Sheath Size (Fr) 

BXB051502E
5
8
15
135
.035
6
BXB051902E 
5
8
19
135
.035
6
BXB052902E
5
8
29
135
.035
6
BXB053902E 
5
8
39
135
.035
6
BXB055902E 
5
8
59
135
.035
6
BXB057902E 
5
8
79
135
.035
6
BXB061502E
6
8
15
135
.035
6
BXB061902E 
6
8
19
135
.035
6
BXB062902E 
6
8
29
135
.035
6
BXB063902E 
6
8
39
135
.035
6
BXB065902E 
6
8
59
135
.035
6
BXB067902E 
6
8
79
135
.035
6
BXB071502E 
7
11
15
135
.035
6
BXB071902E 
7
11
19
135
.035
6
BXB072902E 
7
11
29
135
.035
6
BXB073902E 
7
11
39
135
.035
6
BXB075902E 
7
11
59
135
.035
6
BXB077902E 
7
11
79
135
.035
6
BXB082902E 
8
11
29
135
.035
7
BXB083902E 
8
11
39
135
.035
7
BXB085902E 
8
11
59
135
.035
7
BXB087902E 
8
11
79
135
.035
7
BXB092902E 
9
13
29
135
.035
7
BXB093902E 
9
13
39
135
.035
7
BXB095902E 
9
13
59
135
.035
7
BXB097902E 
9
13
79
135
.035
7
BXBL082902E 
8
16
29
135
.035
7
BXBL083902E 
8
16
39
135
.035
7
BXBL085902E 
8
16
59
135
.035
8
BXBL087902E 
8
16
79
135
.035
8

GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis                                        
BXA Codes

Catalogue 

Number 

Stent 
Labeled/Nominal 
Diameter (mm) 		Maximum 
Post-Dilated Stent 
Diameter (mm)* 

Stent 

Length (mm) 

Catheter 

Length (cm) 

Guidewire 

Diameter (in) 

Introducer 

Sheath Size (Fr) 

BXA051502E
5
8
15

135

.035
7
BXA051902E
5
8
19

135

.035
7
BXA052902E
5
8
29

135

.035
7
BXA053902E
5
8
39

135

.035
7
BXA055902E
5
8
59

135

.035
7
BXA057902E
5
8
79

135

.035
7
BXA061502E
6
8
15

135

.035
7
BXA061902E
6
8
19

135

.035
7
BXA062902E
6
8
29

135

.035
7
BXA063902E
6
8
39

135

.035
7
BXA065902E
6
8
59

135

.035
7
BXA067902E
6
8
79

135

.035
7
BXA071502E
7
11
15

135

.035
7
BXA071902E
7
11
19

135

.035
7
BXA072902E
7
11
29

135

.035
7
BXA073902E
7
11
39

135

.035
7
BXA075902E
7
11
59

135

.035
7
BXA077902E
7
11
79

135

.035
7
BXA082902E
8
11
29

135

.035
7
BXA083902E
8
11
39

135

.035
7
BXA085902E
8
11
59

135

.035
7
BXA087902E
8
11
79

135

.035
8
BXA092902E
9
13
29

135

.035
8
BXA093902E
9
13
39

135

.035
8
BXA095902E
9
13
59

135

.035
8
BXA097902E
9
13
79

135

.035
8
BXA102902E
10
13
29

135

.035
8
BXA103902E
10
13
39

135

.035
8
BXA105902E
10
13
59

135

.035
8
BXA107902E
10
13
79

135

.035
8
BXA112902E
11
16
29

135

.035
8
BXA113902E
11
16
39

135

.035
8
BXA115902E
11
16
59

135

.035
8
BXA117902E
11
16
79

135

.035
8
BXAL082902E
8
16
29

135

.035
7
BXAL083902E
8
16
39

135

.035
7
BXAL085902E
8
16
59

135

.035
8
BXAL087902E
8
16
79

135

.035
8

* Secondary balloon required to post-dilate the stent beyond its nominal deployed diameter (secondary balloon not included). 

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

GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis:
INDICATIONS FOR USE IN EUROPE: The GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis is indicated for the treatment of:

  • de novo or restenotic lesions in the iliac arteries, including lesions at the aortic bifurcation;  
  • de novo or restenotic lesions in the visceral arteries;  
  • isolated visceral, iliac, and subclavian artery aneurysms; or
  • traumatic or iatrogenic vessel injuries in arteries that are located in the chest cavity, abdominal cavity, or pelvis (except for aorta, coronary, innominate, carotid, vertebral, and pulmonary arteries).

The GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis is indicated for use as a bridging stent in branched and fenestrated endovascular aortic aneurysm repair with the following:

  • Approved for use branched aortic endovascular grafts constructed of polyester fabric, stainless steel stents, and polypropylene suture with branch diameters of 6/8 mm and lengths of 18/21 mm.
  • Approved for use fenestrated aortic endovascular grafts constructed of polyester fabric, stainless steel stents, and fenestrations with polypropylene suture ranging in diameter from 6–8 mm.

CONTRAINDICATIONS: Do not use the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis in patients with known hypersensitivity to heparin, including those patients who have had a previous incident of Heparin-Induced Thrombocytopenia (HIT) type II.

 

GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (Reduced Profile):
INDICATIONS FOR USE IN EUROPE: The GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis is indicated for the treatment of:

  • de novo or restenotic lesions in the iliac arteries, including lesions at the aortic bifurcation;  
  • de novo or restenotic lesions in the visceral arteries;  
  • isolated visceral, iliac, and subclavian artery aneurysms; or
  • traumatic or iatrogenic vessel injuries in arteries that are located in the chest cavity, abdominal cavity, or pelvis (except for aorta, coronary, innominate, carotid, vertebral, and pulmonary arteries). 

CONTRAINDICATIONS: Do not use the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis in patients with known hypersensitivity to heparin, including those patients who have had a previous incident of Heparin-Induced Thrombocytopenia (HIT) type II.

Product may not be available in all countries. Please check with your Gore representative for availability.
25PL2128-EN01