ARTG 460047Bone nail guidewire, single-use
ARTG ID: 460047 · Actis Medical Pty Ltd · Actis Medical Pty Ltd · Class I · Started August 19, 2024
Good Name: Actis Medical Pty Ltd - Bone nail guidewire, single-use
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 460047
- Start Date
- August 19, 2024
- Effective Date
- August 19, 2024
- Country
- Australia
- Address
- 1/18 Dequetteville Terrace, Kent Town, SA, 5067
A non-implantable metallic rod intended to aid with the insertion of a cannulated orthopaedic implant or drill bit during an orthopaedic procedure. Wires may be available in a variety of sizes, lengths, and designs. This is a reusable device.
Access comprehensive regulatory information for Bone nail guidewire, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 460047 and sponsored by Actis Medical Pty Ltd, manufactured by Actis Medical Pty Ltd in Australia. The device registration started on August 19, 2024.
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.