GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface* - Argentina, Chile, Colombia, Costa Rica, Mexico and Panama
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) |
---|---|---|---|---|---|---|
VBHR050202H | 5 | 2.5 | 120 | 4.0 – 4.7 | 7 | 5 |
VBHR050502H | 5 | 5 | 120 | 4.0 – 4.7 | 7 | 5 |
VBHR051002H | 5 | 10 | 120 | 4.0 – 4.7 | 7 | 5 |
VBHR051502H | 5 | 15 | 120 | 4.0 – 4.7 | 7 | 5 |
VBHR052502H | 5 | 25 | 120 | 4.0 – 4.7 | 7 | 5 |
VBHR060202H | 6 | 2.5 | 120 | 4.8 – 5.5 | 7 | 6 |
VBHR060502H | 6 | 5 | 120 | 4.8 – 5.5 | 7 | 6 |
VBHR061002H | 6 | 10 | 120 | 4.8 – 5.5 | 7 | 6 |
VBHR061502H | 6 | 15 | 120 | 4.8 – 5.5 | 7 | 6 |
VBHR062502H | 6 | 25 | 120 | 4.8 – 5.5 | 7 | 6 |
VBHR070202H | 7 | 2.5 | 120 | 5.6 – 6.5 | 8 | 7 |
VBHR070502H | 7 | 5 | 120 | 5.6 – 6.5 | 8 | 7 |
VBHR071002H | 7 | 10 | 120 | 5.6 – 6.5 | 8 | 7 |
VBHR071502H | 7 | 15 | 120 | 5.6 – 6.5 | 8 | 7 |
VBHR072502H | 7 | 25 | 120 | 5.6 – 6.5 | 8 | 7 |
VBHR080202H | 8 | 2.5 | 120 | 6.6 – 7.5 | 8 | 8 |
VBHR080502H | 8 | 5 | 120 | 6.6 – 7.5 | 8 | 8 |
VBHR081002H | 8 | 10 | 120 | 6.6 – 7.5 | 8 | 8 |
VBHR081502H | 8 | 15 | 120 | 6.6 – 7.5 | 8 | 8 |
VBHR082502H | 8 | 25 | 120 | 6.6 – 7.5 | 8 | 8 |
VBHR090502H | 9 | 5 | 120 | 7.6 – 8.5 | 8 | 9 |
VBHR091002H | 9 | 10 | 120 | 7.6 – 8.5 | 8 | 9 |
VBHR091502H | 9 | 15 | 120 | 7.6 – 8.5 | 8 | 9 |
VBHR100502H | 10 | 5 | 120 | 8.6 – 9.5 | 8 | 10 |
VBRH101002H | 10 | 10 | 120 | 8.6 – 9.5 | 8 | 10 |
VBHR101502H | 10 | 15 | 120 | 8.6 – 9.5 | 8 | 10 |
VBHR110502H | 11 | 5 | 120 | 9.6 – 10.5 | 10 | 12 |
VBHR111002H | 11 | 10 | 120 | 9.6 – 10.5 | 10 | 12 |
VBHR130502H | 13 | 5 | 120 | 10.6 – 12.0 | 10¶ | 14 |
VBHR131002H | 13 | 10 | 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® Introducer.