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Catalogue Numbers for GORE® VIABAHN® Endoprosthesis – Australia, New Zealand

GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface

Tip to Hub Deployment 0.035" 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)
PAH090502B 9 5.0 120 7.6 - 8.5 9 9
PAH091002B 9 10.0 120 7.6 - 8.5 9 9
PAH091502B 9 15.0 120 7.6 - 8.5 9 9
PAH100502B 10 5.0 120 8.6 - 9.5 11§ 10
PAH101002B 10 10.0 120 8.6 - 9.5 11§ 10
PAH101502B 10 15.0 120 8.6 - 9.5 11§ 10
PAH110502B 11 5.0 120 9.6 - 10.5 11 12II 
PAH111002B 11 10.0 120 9.6 - 10.5 11 12II
PAH130502B 13 5.0 120 10.6 - 12.0 12 14II
PAH131002B 13 10.0 120 10.6 -12.0 12 14II
GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface

Tip to Hub Deployment 0.018" 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 4.0 - 4.7 6 5
PAJR050502B 5 5.0 120 4.0 - 4.7 6 5
PAJR051002B 5 10.0 120 4.0 - 4.7 6 5
PAJR051502B 5 15.0 120 4.0 - 4.7 6 5
PAJR052502B 5 25.0 120 4.0 - 4.7 6 5
PAJR060202B 6 2.5 120 4.8 - 5.5 6 6
PAJR060502B 6 5.0 120 4.8 - 5.5 6 6
PAJR061002B 6 10.0 120 4.8 - 5.5 6 6
PAJR061502B 6 15.0 120 4.8 - 5.5 6 6
PAJR062502B 6 25.0 120 4.8 - 5.5 6 6
PAJR070202B 7 2.5 120 5.6 - 6.5 7 7
PAJR070502B 7 5.0 120 5.6 - 6.5 7 7
PAJR071002B 7 10.0 120 5.6 - 6.5 7 7
PAJR071502B 7 15.0 120 5.6 - 6.5 7 7
PAJR072502B 7 25.0 120 5.6 - 6.5 7 7
PAJR080202B 8 2.5 120 6.6 - 7.5 7 8
PAJR080502B 8 5.0 120 6.6 - 7.5 7 8
PAJR081002B 8 10.0 120 6.6 - 7.5 7 8
PAJR081502B 8 15.0 120 6.6 - 7.5 7 8
PAJR082502B 8 25.0 120 6.6 - 7.5 7 8


Consult Instructions for Use.

 

* 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%.

 § The 10 mm diameter device is compatible with the following 10 Fr introducer sheaths: Cordis AVANTI® Sheath Introducer, Boston Scientific SUPER SHEATH Introducer Sheath, B. Braun INTRADYN Tear-Away Introducer Sheath.

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

Sizing, availability and pricing varies by country.
Please check with your Gore representative for availability.