Australia TGA ARTG recordFemoral stem end cap, non-bioabsorbable
Australia TGA ARTG Registered Device · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · Depuy (Ireland) · Class IIb · Started August 22, 2019
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Femoral stem end cap, non-bioabsorbable
- Risk Class
- Class IIb
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- August 22, 2019
- Effective Date
- August 22, 2019
- Name
- Depuy (Ireland)
- Country
- Ireland
- Address
- Loughbeg Ringaskiddy, COUNTY CORK
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.
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 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.