Pure Global

Surgical implant template, reusable

Access comprehensive regulatory information for Surgical implant template, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Zimmer Biomet Pty Ltd, manufactured by Biomet Trauma in United States of America. The device registration started on July 23, 2018.

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 I
Class I
Surgical implant template, reusable
Australia TGA ARTG Registered Device
Good Name: Zimmer Biomet Pty Ltd - Surgical implant template, reusable
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Intended Purpose

A device designed to determine the appropriate size.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General-Export
Registration Information
Start Date
July 23, 2018
Effective Date
July 23, 2018
Manufacturer
Country
United States of America
Address
56 East Bell Drive, Warsaw, IN, 46581