Australia TGA ARTG record

Wound retractor, intermediate/deep

Australia TGA ARTG Registered Device · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · Depuy Orthopaedics Inc · Class I · Started May 23, 2023

Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Wound retractor, intermediate/deep

Device classification

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

Registration information

Start Date: May 23, 2023
Effective Date: May 23, 2023

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

Used to separate/draw aside the margins of an incision or injury during a surgical intervention.

About this record

Access comprehensive regulatory information for Wound retractor, intermediate/deep 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 May 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.