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Femoral stem end cap, non-bioabsorbable - ARTG 322161

Access comprehensive regulatory information for Femoral stem end cap, non-bioabsorbable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 322161 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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TGA ARTG Official Data
Class IIb
ARTG 322161
Class IIb
Femoral stem end cap, non-bioabsorbable
ARTG ID: 322161
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Femoral stem end cap, non-bioabsorbable
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Intended Purpose

A sterile implantable device intended to be used during the implantation of a cemented femoral stem prosthesis to cushion the prosthesis tip against the cement within the femoral medullary canal.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
322161
Start Date
August 22, 2019
Effective Date
August 22, 2019
Manufacturer
Country
Ireland
Address
Loughbeg Ringaskiddy, COUNTY CORK