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Arthroscopic access cannula obturator - ARTG 384809

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.

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Class I
ARTG 384809
Class I
Arthroscopic access cannula obturator
ARTG ID: 384809
Good Name: Zimmer Biomet Pty Ltd - Arthroscopic access cannula obturator
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Intended Purpose

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.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
384809
Start Date
February 28, 2022
Effective Date
February 28, 2022
Manufacturer
Country
United States of America
Address
56 East Bell Drive, Airport Industrial Park, Warsaw, IN, 46581