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Cannulated surgical drill

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 ConMed Linvatec Australia Pty Ltd, manufactured by ConMed Corporation in United States of America. The device registration started on June 23, 2023.

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 IIa
Class IIa
Cannulated surgical drill
Australia TGA ARTG Registered Device
Good Name: ConMed Linvatec Australia Pty Ltd - Cannulated surgical drill
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Intended Purpose

A sterile reusable device in the form of a shaft of metal that is mounted into an appropriate surgical power tool (e.g., a reamer or drilling system handpiece) and rotated to bore into hard/tough tissues (e.g., bone, cartilage) to clear a channel of the same dimension as the diameter of the shaft. The device is cannulated, having a hollow centre, for use with a guide wire/pin that has been placed into the correct position prior to operation. This device is typically used in orthopaedic surgery, such as Anterior Cruciate Ligament (ACL) and Posterior Cruciate Ligament (PCL) reconstruction, prior to the insertion of a prosthetic device. It is designed to be cleaned and re-sterilised before every reuse.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
June 23, 2023
Effective Date
June 23, 2023
Manufacturer
Country
United States of America
Address
525 French Road, Utica, New York, 13502