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Suturing needle, single-use - ARTG 418392

Access comprehensive regulatory information for Suturing needle, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 418392 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.

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TGA ARTG Official Data
Class IIa
ARTG 418392
Class IIa
Suturing needle, single-use
ARTG ID: 418392
Good Name: Actis Medical Pty Ltd - Suturing needle, single-use
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Intended Purpose

An orthopaedic manual surgical instrument designed to pass surgical sutures through tissue in either arthroscopic or open surgery.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
418392
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