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Peripheral venous endovascular stent-graft

Access comprehensive regulatory information for Peripheral venous endovascular stent-graft in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Bard Australia Pty Ltd, manufactured by Angiomed GmbH & Co Medizintechnik KG in Germany. The device registration started on August 08, 2019.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.

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TGA ARTG Official Data
Class IIb
Class IIb
Peripheral venous endovascular stent-graft
Australia TGA ARTG Registered Device
Good Name: Bard Australia Pty Ltd - Peripheral venous endovascular stent-graft
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Intended Purpose

Intended for the treatment of stenoses in the upper extremity venous outflow of patients dialyzing with an arterio-venous (AV) access graft or fistula.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
August 08, 2019
Effective Date
August 08, 2019
Manufacturer
Country
Germany
Address
Wachhausstrasse 6, KARLSRUHE, 76227