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balanSys vitamys UC Inlay - Bicompartmental knee prosthesis

Access comprehensive regulatory information for balanSys vitamys UC Inlay - Bicompartmental knee prosthesis in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is sponsored by Mathys Orthopaedics Pty Ltd, manufactured by Mathys Ltd Bettlach in Switzerland. The device registration started on December 14, 2018.

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
balanSys vitamys UC Inlay - Bicompartmental knee prosthesis
Australia TGA ARTG Registered Device
Good Name: Mathys Orthopaedics Pty Ltd - balanSys vitamys UC Inlay - Bicompartmental knee prosthesis
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Intended Purpose

The balanSys Bicondylar prosthesis is intended for treating degenerative joint diseases of the knee joint in skeletally mature patients. Indications include: - Painful and / or disabling joint disease of the knee resulting from osteoarthritis, avascular necrosis, inflammatory arthritis or post-traumatic arthritis - Revision of previous knee replacement - Fracture of the distal femur and / or proximal tibia that cannot be stabilized by standard fracture management techniques

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
December 14, 2018
Effective Date
December 14, 2018
Manufacturer
Country
Switzerland
Address
Robert Mathys Strasse 5 Bettlach, 2544