Shoulder glenoid fossa trial prosthesis
ARTG ID: 467428 · Zimmer Biomet Pty Ltd · Zimmer Inc · Class IIa · Started November 06, 2024
Good Name: Zimmer Biomet Pty Ltd - Shoulder glenoid fossa trial prosthesis
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 467428
- Start Date
- November 06, 2024
- Effective Date
- November 06, 2024
- Name
- Zimmer Inc
- Country
- United States of America
- Address
- 1800 W Center Street, WARSAW , INDIANA, 46580
The glenoid trial is copy of a final shoulder glenoid prosthesis designed for use before implantation to validate the size of the implant and to ensure correct orientation and positioning. It is available in different sizes.
Access comprehensive regulatory information for Shoulder glenoid fossa trial prosthesis in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 467428 and sponsored by Zimmer Biomet Pty Ltd, manufactured by Zimmer Inc in United States of America. The device registration started on November 06, 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.