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BI-MENTUM Dual Mobility System Cup PE Liner - Non-constrained polyethylene acetabular liner

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 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.

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Class III
Class III
BI-MENTUM Dual Mobility System Cup PE Liner - Non-constrained polyethylene acetabular liner
Australia TGA ARTG Registered Device
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - BI-MENTUM Dual Mobility System Cup PE Liner - Non-constrained polyethylene acetabular liner
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Intended Purpose

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.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
April 23, 2021
Effective Date
April 23, 2021
Manufacturer
Name
Serf
Country
France
Address
85 Avenue des Bruyeres, Decines, 69153