ARTG 407232Bone nail guidewire, single-use
ARTG ID: 407232 · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · Depuy Mitek (a Johnson & Johnson Company) · Class IIa · Started April 03, 2023
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Bone nail guidewire, single-use
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 407232
- Start Date
- April 03, 2023
- Effective Date
- April 03, 2023
- Country
- United States of America
- Address
- 325 Paramount Drive, Raynham, MA, 02767
A sterile, long, thin, rod designed to guide intramedullary canal devices for performing the implantation of an intramedullary nail to treat damaged bone.
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 IIa is registered under ARTG number 407232 and sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by Depuy Mitek (a Johnson & Johnson Company) in United States of America. The device registration started on April 03, 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.