Australia TGA ARTG record

Orthopaedic bone distractor

Australia TGA ARTG Registered Device · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · Depuy Orthopaedics Inc · Class I · Started June 24, 2019

Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Orthopaedic bone distractor

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

Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes

Manufacturer

Name: Depuy Orthopaedics Inc
Country: United States of America
Address: 700 Orthopaedic Drive, Warsaw, IN, 46582

Intended purpose

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

About this record

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.