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VENOVO Venous Stent System - Iliofemoral vein stent - ARTG 409902

Access comprehensive regulatory information for VENOVO Venous Stent System - Iliofemoral vein stent in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 409902 and sponsored by Bard Australia Pty Ltd, manufactured by Angiomed GmbH & Co Medizintechnik KG in Germany. The device registration started on June 01, 2023.

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 III
ARTG 409902
Class III
VENOVO Venous Stent System - Iliofemoral vein stent
ARTG ID: 409902
Good Name: Bard Australia Pty Ltd - VENOVO Venous Stent System - Iliofemoral vein stent
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Intended Purpose

The Venovo Venous Stent System is indicated for the treatment of symptomatic Iliofemoral venous outflow obstruction.

Device Classification
Risk Class
Class III
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
409902
Start Date
June 01, 2023
Effective Date
June 01, 2023
Manufacturer
Country
Germany
Address
Wachhausstrasse 6, KARLSRUHE, 76227