Catalogue Numbers for GORE® VIATORR® TIPS Endoprosthesis
GORE® VIATORR® TIPS Endoprosthesis with Controlled Expansion | ||||||
|---|---|---|---|---|---|---|
| Catalogue Number | Endoprosthesis Internal Diameter (mm)* | Graft Lined Length (cm) | Graft Unlined Length (cm) | Maximum Guidewire Diameter (in) | Hemostatic Introducer Sheath (Fr) | Maximum Dilatation Balloon Diameter (mm)* |
| PT8104275 | 8–10 | 4 | 2 | 0.035 | 10 | 10 |
| PT8105275 | 8–10 | 5 | 2 | 0.035 | 10 | 10 |
| PT8106275 | 8–10 | 6 | 2 | 0.035 | 10 | 10 |
| PT8107275 | 8–10 | 7 | 2 | 0.035 | 10 | 10 |
| PT8108275 | 8–10 | 8 | 2 | 0.035 | 10 | 10 |
* The selected balloon diameter may be 8, 9, or 10 mm, and should not exceed 10 mm. A balloon which can reach an inflation pressure of 10 ATM must be selected, and should be inflated to a minimum of 10 ATM.
Sizing, availability and pricing varies by country.
Refer to Instructions for Use at eifu.goremedical.com for a complete description of all applicable indications, warnings, precautions and contraindications for the markets where this product is available. RXOnly
INDICATIONS FOR USE IN EUROPE: The GORE® VIATORR® TIPS Endoprosthesis with Controlled Expansion is indicated for use in the treatment of portal hypertension and its complications such as variceal bleeding and refractory ascites.
CONTRAINDICATIONS: There are no known contraindications for this device.