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Suture Insertion Devices - Suture kit, non-medicated

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 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.

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TGA ARTG Official Data
Class IIa
Class IIa
Suture Insertion Devices - Suture kit, non-medicated
Australia TGA ARTG Registered Device
Good Name: Actis Medical Pty Ltd - Suture Insertion Devices - Suture kit, non-medicated
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Intended Purpose

Single use instruments intended to pass sutures in arthroscopic & open surgery. It includes needles, guides and wires.

Device Classification
Risk Class
Class IIa
Product Type
Medical device system
ARTG Category
General
Registration Information
Start Date
August 17, 2023
Effective Date
August 17, 2023
Manufacturer
Country
China
Address
No 466 South Xianhua Street High-Tech Industrial Zone Jinhua, Zhejiang, 321016