ARTG 474145Healix Advance BR Anchor with Orthocord - Fixation anchor, soft-tissue, biodegradable
ARTG ID: 474145 · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · Medos International SARL · Class III · Started December 19, 2024
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Healix Advance BR Anchor with Orthocord - Fixation anchor, soft-tissue, biodegradable
- Risk Class
- Class III
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 474145
- Start Date
- December 19, 2024
- Effective Date
- December 19, 2024
- Country
- Switzerland
- Address
- Chemin-Blanc 38, Le Locle, CH-, 2400
The HEALIX ADVANCE BIOCRYL RAPIDE (BR) Anchor with Orthocord are intended for fixation of soft tissue to bone in the following procedures: Shoulder: Rotator Cuff Repair, Biceps Tenodesis Foot/Ankle Achilles: Tendon Repair Knee: Medial Collateral Ligament Repair
Access comprehensive regulatory information for Healix Advance BR Anchor with Orthocord - Fixation anchor, soft-tissue, biodegradable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 474145 and sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by Medos International SARL in Switzerland. The device registration started on December 19, 2024.
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.