GORE® VIABAHN® Endoprosthesis with PROPATEN Bioactive Surface* - Brazil
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) |
---|---|---|---|---|---|---|
PAHR050202K | 5 | 2.5 | 120 | 4.0 – 4.7 | 7 | 5 |
PAHR050502K | 5 | 5 | 120 | 4.0 – 4.7 | 7 | 5 |
PAHR051002K | 5 | 10 | 120 | 4.0 – 4.7 | 7 | 5 |
PAHR051502K | 5 | 15 | 120 | 4.0 – 4.7 | 7 | 5 |
PAHR052502K | 5 | 25 | 120 | 4.0 – 4.7 | 7 | 5 |
PAHR060202K | 6 | 2.5 | 120 | 4.8 – 5.5 | 7 | 6 |
PAHR060502K | 6 | 5 | 120 | 4.8 – 5.5 | 7 | 6 |
PAHR061002K | 6 | 10 | 120 | 4.8 – 5.5 | 7 | 6 |
PAHR061502K | 6 | 15 | 120 | 4.8 – 5.5 | 7 | 6 |
PAHR062502K | 6 | 25 | 120 | 4.8 – 5.5 | 7 | 6 |
PAHR070202K | 7 | 2.5 | 120 | 5.6 – 6.5 | 8 | 7 |
PAHR070502K | 7 | 5 | 120 | 5.6 – 6.5 | 8 | 7 |
PAHR071002K | 7 | 10 | 120 | 5.6 – 6.5 | 8 | 7 |
PAHR071502K | 7 | 15 | 120 | 5.6 – 6.5 | 8 | 7 |
PAHR072502K | 7 | 25 | 120 | 5.6 – 6.5 | 8 | 7 |
PAHR080202K | 8 | 2.5 | 120 | 6.6 – 7.5 | 8 | 8 |
PAHR080502K | 8 | 5 | 120 | 6.6 – 7.5 | 8 | 8 |
PAHR081002K | 8 | 10 | 120 | 6.6 – 7.5 | 8 | 8 |
PAHR081502K | 8 | 15 | 120 | 6.6 – 7.5 | 8 | 8 |
PAHR082502K | 8 | 25 | 120 | 6.6 – 7.5 | 8 | 8 |
PAHR090502K | 9 | 5 | 120 | 7.6 – 8.5 | 8 | 9 |
PAHR091002K | 9 | 10 | 120 | 7.6 – 8.5 | 8 | 9 |
PAHR091502K | 9 | 15 | 120 | 7.6 – 8.5 | 8 | 9 |
PAHR100502K | 10 | 5 | 120 | 8.6 – 9.5 | 8 | 10 |
PAHR101002K | 10 | 10 | 120 | 8.6 – 9.5 | 8 | 10 |
PAHR101502K | 10 | 15 | 120 | 8.6 – 9.5 | 8 | 10 |
PAHR110502K | 11 | 5 | 120 | 9.6 – 10.5 | 10 | 12 |
PAHR111002K | 11 | 10 | 120 | 9.6 – 10.5 | 10 | 12 |
PAHR130502K | 13 | 5 | 120 | 10.6 – 12.0 | 10¶ | 14 |
PAHR131002K | 13 | 10 | 120 | 10.6 – 12.0 | 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 13 mm diameter device is not compatible with the 10 Fr COOK® FLEXOR® CHECK-FLO® Introducer.