ARTG 363212BI-MENTUM Dual Mobility System Cup PE Liner - Non-constrained polyethylene acetabular liner
ARTG ID: 363212 · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · Serf · Class III · Started April 23, 2021
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - BI-MENTUM Dual Mobility System Cup PE Liner - Non-constrained polyethylene acetabular liner
- Risk Class
- Class III
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 363212
- Start Date
- April 23, 2021
- Effective Date
- April 23, 2021
- Name
- Serf
- Country
- France
- Address
- 85 Avenue des Bruyeres, Decines, 69153
BI-MENTUM PE Liners are intended to be used with the whole BI-MENTUM dual mobility cups range. Therefore, medical conditions in which PE liners can be used is depending on BI-MENTUM dual mobility cups.
Access comprehensive regulatory information for BI-MENTUM Dual Mobility System Cup PE Liner - Non-constrained polyethylene acetabular liner in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 363212 and sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by Serf in France. The device registration started on April 23, 2021.
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.