ARTG 409902VENOVO Venous Stent System - Iliofemoral vein stent
ARTG ID: 409902 · Bard Australia Pty Ltd · Angiomed GmbH & Co Medizintechnik KG · Class III · Started June 01, 2023
Good Name: Bard Australia Pty Ltd - VENOVO Venous Stent System - Iliofemoral vein stent
- Risk Class
- Class III
- Product Type
- Medical device system
- ARTG Category
- General
- ARTG ID
- 409902
- Start Date
- June 01, 2023
- Effective Date
- June 01, 2023
- Country
- Germany
- Address
- Wachhausstrasse 6, KARLSRUHE, 76227
The Venovo Venous Stent System is indicated for the treatment of symptomatic Iliofemoral venous outflow obstruction.
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.