ARTG 363151BI-MENTUM Dual Mobility System Revision Cementless Acetabular Cup - Acetabular shell
ARTG ID: 363151 · 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 Revision Cementless Acetabular Cup - Acetabular shell
- Risk Class
- Class III
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 363151
- Start Date
- April 23, 2021
- Effective Date
- April 23, 2021
- Name
- Serf
- Country
- France
- Address
- 85 Avenue des Bruyeres, Decines, 69153
Acetabular cups combining a "Revision Cup" and a "PE Liner" are intended for the treatment of the following conditions: surgical revision (including recurrent dislocation and loosening) if the bone reconstruction allows, Paprosky type IIA, IIB and IIC.
Access comprehensive regulatory information for BI-MENTUM Dual Mobility System Revision Cementless Acetabular Cup - Acetabular shell in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 363151 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.