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Fixation device, external, system

Access comprehensive regulatory information for Fixation device, external, system 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 December 17, 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
Fixation device, external, system
Australia TGA ARTG Registered Device
Good Name: Zimmer Biomet Pty Ltd - Fixation device, external, system
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Intended Purpose

An assembly of devices designed to stabilize fractured bones, other than those in the vertebral column, to promote treatment and healing.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General-Export
Registration Information
Start Date
December 17, 2018
Effective Date
December 17, 2018
Manufacturer
Country
United States of America
Address
56 East Bell Drive, Warsaw, IN, 46581