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Orthopaedic prosthesis implantation instrument, reusable - ARTG 482213

Access comprehensive regulatory information for Orthopaedic prosthesis implantation instrument, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 482213 and sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by Viant Medical LLC in United States of America. The device registration started on March 11, 2025.

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 I
ARTG 482213
Class I
Orthopaedic prosthesis implantation instrument, reusable
ARTG ID: 482213
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Orthopaedic prosthesis implantation instrument, reusable
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Intended Purpose

A hand-held surgical instrument intended to be used during implantation of an orthopaedic prosthesis , to aid in the navigation/placement of the prosthesis or other instruments

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
482213
Start Date
March 11, 2025
Effective Date
March 11, 2025
Manufacturer
Country
United States of America
Address
4545 Kroemer Rd, Fort Wayne, IN, 46818