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Healix Advance BR Anchor with Orthocord, with Needle - Fixation anchor, soft-tissue, biodegradable - ARTG 474146

Access comprehensive regulatory information for Healix Advance BR Anchor with Orthocord, with Needle - 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 474146 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.

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TGA ARTG Official Data
Class III
ARTG 474146
Class III
Healix Advance BR Anchor with Orthocord, with Needle - Fixation anchor, soft-tissue, biodegradable
ARTG ID: 474146
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Healix Advance BR Anchor with Orthocord, with Needle - Fixation anchor, soft-tissue, biodegradable
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Intended Purpose

The HEALIX ADVANCE BIOCRYL RAPIDE (BR) Anchor with Orthocord areintended 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

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
474146
Start Date
December 19, 2024
Effective Date
December 19, 2024
Manufacturer
Country
Switzerland
Address
Chemin-Blanc 38, Le Locle, CH-, 2400