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4DMesh โ€“ Pre-shaped - Abdominal hernia surgical mesh, composite-polymer - ARTG 283655

Access comprehensive regulatory information for 4DMesh โ€“ Pre-shaped - 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 registered under ARTG number 283655 and sponsored by Alliance Surgical Pty Ltd, manufactured by Cousin Biotech SAS in France. The device registration started on December 15, 2016.

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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Class III
ARTG 283655
Class III
4DMesh โ€“ Pre-shaped - Abdominal hernia surgical mesh, composite-polymer
ARTG ID: 283655
Good Name: Alliance Surgical Pty Ltd - 4DMesh - Pre-shaped - Abdominal hernia surgical mesh, composite-polymer
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Intended Purpose

The pre-shaped 4Dmeshes (Biomesh SR) are for laparoscopic treatment designed for the repair and reinforcement of inguinal and femoral hernias.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
283655
Start Date
December 15, 2016
Effective Date
May 09, 2018
Manufacturer
Country
France
Address
8 Rue De L'Abbe Bonpain, Wervicq-Sud, 59117