Arteriovenous shunt

País: Australia

Idioma: inglés

Fuente: Department of Health (Therapeutic Goods Administration)

Disponible desde:

Emergo Asia Pacific Pty Ltd T/a Emergo Australia

clase:

Class I

Fabricado por:

LeMaitre Vascular Inc 63 2nd Avenue, Burlington, Massachusetts, 01803 United States Of America

Área terapéutica:

13586 - Arteriovenous shunt

indicaciones terapéuticas:

Intended for the creation of a bridge graft for vascular access subsequent to at least one previously failed prosthetic access graft. A surgically-implanted device designed to provide a passage for blood to flow between an artery typically located in an arm, and a peripheral vein, central vein or right atrium, creating a graft fistula that provides blood access for external procedures, especially hemodialysis. It is a synthetic vascular graft/graft assembly with a thin wall and appropriate size (commonly 6 mm diameter) and configuration to facilitate vessel puncturing. It is typically used when it is not possible or convenient to create a direct arteriovenous fistula or for patients who have exhausted peripheral venous access. Disposable devices associated with implantation may be included. Storage solution is buffered saline. This is a single-use device.

Estado de Autorización:

A

Fecha de autorización:

2018-04-17