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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) 

BXB051502E5815135.0356
BXB051902E 5819135.0356
BXB052902E5829135.0356
BXB053902E 5839135.0356
BXB055902E 5859135.0356
BXB057902E 5879135.0356
BXB061502E6815135.0356
BXB061902E 6819135.0356
BXB062902E 6829135.0356
BXB063902E 6839135.0356
BXB065902E 6859135.0356
BXB067902E 6879135.0356
BXB071502E 71115135.0356
BXB071902E 71119135.0356
BXB072902E 71129135.0356
BXB073902E 71139135.0356
BXB075902E 71159135.0356
BXB077902E 71179135.0356
BXB082902E 81129135.0357
BXB083902E 81139135.0357
BXB085902E 81159135.0357
BXB087902E 81179135.0357
BXB092902E 91329135.0357
BXB093902E 91339135.0357
BXB095902E 91359135.0357
BXB097902E 91379135.0357
BXBL082902E 81629135.0357
BXBL083902E 81639135.0357
BXBL085902E 81659135.0358
BXBL087902E 81679135.0358

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) 

BXA051502E5815

135

.0357
BXA051902E5819

135

.0357
BXA052902E5829

135

.0357
BXA053902E5839

135

.0357
BXA055902E5859

135

.0357
BXA057902E5879

135

.0357
BXA061502E6815

135

.0357
BXA061902E6819

135

.0357
BXA062902E6829

135

.0357
BXA063902E6839

135

.0357
BXA065902E6859

135

.0357
BXA067902E6879

135

.0357
BXA071502E71115

135

.0357
BXA071902E71119

135

.0357
BXA072902E71129

135

.0357
BXA073902E71139

135

.0357
BXA075902E71159

135

.0357
BXA077902E71179

135

.0357
BXA082902E81129

135

.0357
BXA083902E81139

135

.0357
BXA085902E81159

135

.0357
BXA087902E81179

135

.0358
BXA092902E91329

135

.0358
BXA093902E91339

135

.0358
BXA095902E91359

135

.0358
BXA097902E91379

135

.0358
BXA102902E101329

135

.0358
BXA103902E101339

135

.0358
BXA105902E101359

135

.0358
BXA107902E101379

135

.0358
BXA112902E111629

135

.0358
BXA113902E111639

135

.0358
BXA115902E111659

135

.0358
BXA117902E111679

135

.0358
BXAL082902E81629

135

.0357
BXAL083902E81639

135

.0357
BXAL085902E81659

135

.0358
BXAL087902E81679

135

.0358

* 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.