ARTG 384809Arthroscopic access cannula obturator
ARTG ID: 384809 · Zimmer Biomet Pty Ltd · Biomet Orthopedics · Class I · Started February 28, 2022
Good Name: Zimmer Biomet Pty Ltd - Arthroscopic access cannula obturator
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 384809
- Start Date
- February 28, 2022
- Effective Date
- February 28, 2022
- Country
- United States of America
- Address
- 56 East Bell Drive, Airport Industrial Park, Warsaw, IN, 46581
A non-sterile instrument designed to facilitate the insertion of an arthroscopic access cannula into a joint (e.g., shoulder, knee) during arthroscopic examination or surgery by filling out the cannula's lumen (open end). It is typically cannulated, made of metal, and supplied in a variety of sizes. This is a reusable device that must be sterilized prior to use.
Access comprehensive regulatory information for Arthroscopic access cannula obturator in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 384809 and sponsored by Zimmer Biomet Pty Ltd, manufactured by Biomet Orthopedics in United States of America. The device registration started on February 28, 2022.
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.