Australia TGA ARTG record

Wound retractor, intermediate/deep

Australia TGA ARTG Registered Device · Stryker Australia Pty Ltd · Stryker Spine · Class Im · Started January 24, 2020

Good Name: Stryker Australia Pty Ltd - Wound retractor, intermediate/deep

Device classification

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

Registration information

Start Date: January 24, 2020
Effective Date: January 24, 2020

Sponsor

Name: Stryker Australia Pty Ltd

Manufacturer

Name: Stryker Spine
Country: United States of America
Address: 2 Pearl Court, Allendale, NJ, 07401

Intended purpose

Manual medical tools designed solely for use in the fitting of STRYKER Spine implants.

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 Im is sponsored by Stryker Australia Pty Ltd, manufactured by Stryker Spine in United States of America. The device registration started on January 24, 2020.

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.