Pure Global

Shoulder glenoid fossa trial prosthesis - ARTG 467428

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.

Free Database
Powered by Pure Global AI
TGA ARTG Official Data
Class IIa
ARTG 467428
Class IIa
Shoulder glenoid fossa trial prosthesis
ARTG ID: 467428
Good Name: Zimmer Biomet Pty Ltd - Shoulder glenoid fossa trial prosthesis
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Intended Purpose

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.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
467428
Start Date
November 06, 2024
Effective Date
November 06, 2024
Manufacturer
Country
United States of America
Address
1800 W Center Street, WARSAW , INDIANA, 46580