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

GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface

Indicated for use in the endovascular grafting of peripheral arteries
.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

Indicated for use in the endovascular grafting of peripheral arteries
.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.

Refer to Instructions for Use at eifu.goremedical.com for complete description of all indications, warnings, precautions and contraindications for the markets where this product is available.

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.

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