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Arthroscopic access cannula obturator

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 sponsored by Zimmer Biomet Pty Ltd, manufactured by Santa Barbara Imaging Systems Inc in United States of America. The device registration started on May 21, 2021.

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
Class I
Arthroscopic access cannula obturator
Australia TGA ARTG Registered Device
Good Name: Zimmer Biomet Pty Ltd - Arthroscopic access cannula obturator
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Intended Purpose

Intended for the arthroscopic diagnosis and treatment of the skeletal system

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
May 21, 2021
Effective Date
May 21, 2021
Manufacturer
Country
United States of America
Address
Suite 101 340 Storke Road, Goleta, CA, 93117