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Orthopaedic bone distractor

Access comprehensive regulatory information for Orthopaedic bone distractor in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by Depuy Orthopaedics Inc in United States of America. The device registration started on June 24, 2019.

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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TGA ARTG Official Data
Class I
Class I
Orthopaedic bone distractor
Australia TGA ARTG Registered Device
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Orthopaedic bone distractor
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Intended Purpose

A hand-held manual surgical instrument designed to distract two bone surfaces to enable a surgical procedure. This is a reusable device.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
June 24, 2019
Effective Date
June 24, 2019
Sponsor
Manufacturer
Country
United States of America
Address
700 Orthopaedic Drive, Warsaw, IN, 46582