ATLAS Cross linked PE Trianon Flat Edge Insert - Non-constrained polyethylene acetabular liner - ARTG 296213
Access comprehensive regulatory information for ATLAS Cross linked PE Trianon Flat Edge Insert - 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 296213 and sponsored by Perios Pty Ltd, manufactured by FH Industrie in France. The device registration started on November 13, 2017.
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.
The insert component of the ATLAS hip system, designed for first-line use, or revision surgery and intended to restore the joint function and withstand the usual stresses associated with this joint. INDICATIONS FOR USE: The prostheses from FH ORTHOPEDICS are designed for specific indications detailed in the sales literature, such as: a) Primary, dysplasic or protruding coxarthrosis b) Rheumatoid coxitis c) Coxarthrosis with necrosis of the femoral head d) Revision surgery in a septic or aseptic environment e) Congenital dislocation f ) Traumatic injuries g) Femoral neck fracture h) Osteonecrosis of the femoral head