Australia TGA ARTG recordNerve-locating probe, single-use
Australia TGA ARTG Registered Device · Stryker Australia Pty Ltd · Stryker Spine · Class IIa · Started January 24, 2020
Good Name: Stryker Australia Pty Ltd - Nerve-locating probe, single-use
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- January 24, 2020
- Effective Date
- January 24, 2020
- Name
- Stryker Spine
- Country
- United States of America
- Address
- 2 Pearl Court, Allendale, NJ, 07401
Indicated for use during surgery of the spine to deliver an electrical stimulus to the tissues and nerves at the operative site to assist in locating those nerves at risk during the surgical procedure.
Access comprehensive regulatory information for Nerve-locating probe, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa 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.