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.