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Femoral stem centralizer - ARTG 322160

Access comprehensive regulatory information for Femoral stem centralizer in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 322160 and sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by Depuy (Ireland) in Ireland. The device registration started on August 22, 2019.

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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Class IIb
ARTG 322160
Class IIb
Femoral stem centralizer
ARTG ID: 322160
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Femoral stem centralizer
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Intended Purpose

A sterile implantable device used during the implantation of a cemented femoral stem prosthesis to centralize and stabilize the prosthesis tip within the femoral medullary canal.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
322160
Start Date
August 22, 2019
Effective Date
August 22, 2019
Manufacturer
Country
Ireland
Address
Loughbeg Ringaskiddy, COUNTY CORK