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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)* 

PTB81042758–10 420.0351010
PTB81052758–10520.0351010
PTB81062758–10620.0351010
PTB81072758–10720.0351010
PTB81082758–10820.0351010

* 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.

Please check with your Gore representative for availability. 

IFU Consult instructions

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

INDICATIONS FOR USE IN THE U.S.: The GORE® VIATORR® TIPS Endoprosthesis is indicated for use in the de novo and revision treatment of portal hypertension and its complications such as variceal bleeding, gastropathy, refractory ascites, and / or hepatic hydrothorax.

INDICATIONS FOR USE IN CANADA: The GORE® VIATORR® TIPS Endoprosthesis with Controlled Expansion is indicated for the treatment of portal hypertension and its complications such as variceal bleeding and refractory ascites.

CONTRAINDICATIONS: There are no known contraindications for this device.