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Wound retractor, intermediate/deep

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.

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TGA ARTG Official Data
Class I
Class I
Wound retractor, intermediate/deep
Australia TGA ARTG Registered Device
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Wound retractor, intermediate/deep
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Intended Purpose

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

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
Manufacturer
Country
United States of America
Address
700 Orthopaedic Drive, Warsaw, IN, 46582