Australia TGA ARTG record

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

Australia TGA ARTG Registered Device · Alliance Surgical Pty Ltd · Cousin Biotech SAS · Class III · Started February 08, 2021

Good Name: Alliance Surgical Pty Ltd - 4DVENTRAL Semi-resorbable parietal reinforcement implant - Abdominal hernia surgical mesh, composite-polymer

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

Sponsor

Name: Alliance Surgical Pty Ltd

Manufacturer

Name: Cousin Biotech SAS
Country: France
Address: 8 Rue De L'Abbe Bonpain, Wervicq-Sud, 59117

Intended purpose

4DVentral® 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 Ventral® implant is designed for extraperitoneal implantation only.

About this record

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.