Australia TGA ARTG record

Cannulated surgical drill

Australia TGA ARTG Registered Device · Zimmer Biomet Pty Ltd · Biomet UK Ltd · Class IIa · Started November 22, 2016

Good Name: Zimmer Biomet Pty Ltd - Cannulated surgical drill

Device classification

Risk Class: Class IIa
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: November 22, 2016
Effective Date: November 22, 2016

Sponsor

Name: Zimmer Biomet Pty Ltd

Manufacturer

Name: Biomet UK Ltd
Country: United Kingdom
Address: Waterton Industrial Estate, Bridgend, South Glamorgan, CF31 3XA

Intended purpose

A drill that is cannulated, intended to be used in orthopaedic surgery for drilling into bone, and clearing of intramedullary channel.

About this record

Access comprehensive regulatory information for Cannulated surgical drill in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Zimmer Biomet Pty Ltd, manufactured by Biomet UK Ltd in United Kingdom. The device registration started on November 22, 2016.

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.