Suture Insertion Devices - Suture kit, non-medicated - ARTG 418391

Access comprehensive regulatory information for Suture Insertion Devices - Suture kit, non-medicated in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 418391 and sponsored by Actis Medical Pty Ltd, manufactured by CANWELL MEDICAL CO LTD in China. The device registration started on August 17, 2023.

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.