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Bone nail guidewire, single-use - ARTG 407232

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.

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TGA ARTG Official Data
Class IIa
ARTG 407232
Class IIa
Bone nail guidewire, single-use
ARTG ID: 407232
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Bone nail guidewire, single-use
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Intended Purpose

A sterile, long, thin, rod designed to guide intramedullary canal devices for performing the implantation of an intramedullary nail to treat damaged bone.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
407232
Start Date
April 03, 2023
Effective Date
April 03, 2023
Manufacturer
Country
United States of America
Address
325 Paramount Drive, Raynham, MA, 02767