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4DVENTRAL Semi-resorbable parietal reinforcement implant - Abdominal hernia surgical mesh, composite-polymer

Access comprehensive regulatory information for 4DVENTRAL Semi-resorbable parietal reinforcement implant - Abdominal hernia surgical mesh, composite-polymer in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Alliance Surgical Pty Ltd, manufactured by Cousin Biotech SAS in France. The device registration started on February 08, 2021.

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
Class III
4DVENTRAL Semi-resorbable parietal reinforcement implant - Abdominal hernia surgical mesh, composite-polymer
Australia TGA ARTG Registered Device
Good Name: Alliance Surgical Pty Ltd - 4DVENTRAL Semi-resorbable parietal reinforcement implant - Abdominal hernia surgical mesh, composite-polymer
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Intended Purpose

4DVentralยฎ is a midweight hydrophilic partially resorbable implant designed for the repair of ventral hernia or other fascial defects that require the addition of an extraperitoneal reinforcing or bridging material to obtain the desired surgical result. The 4D Ventralยฎ implant is designed for extraperitoneal implantation only.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
February 08, 2021
Effective Date
February 08, 2021
Manufacturer
Country
France
Address
8 Rue De L'Abbe Bonpain, Wervicq-Sud, 59117