ARTG 418391Suture Insertion Devices - Suture kit, non-medicated
ARTG ID: 418391 · Actis Medical Pty Ltd · CANWELL MEDICAL CO LTD · Class IIa · Started August 17, 2023
Good Name: Actis Medical Pty Ltd - Suture Insertion Devices - Suture kit, non-medicated
- Risk Class
- Class IIa
- Product Type
- Medical device system
- ARTG Category
- General
- ARTG ID
- 418391
- Start Date
- August 17, 2023
- Effective Date
- August 17, 2023
- Country
- China
- Address
- No 466 South Xianhua Street High-Tech Industrial Zone Jinhua, Zhejiang, 321016
Single use instruments intended to pass sutures in arthroscopic & open surgery. It includes needles, guides and wires.
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.