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ShockMaster 500 - Electromechanical orthopaedic extracorporeal shock wave therapy system

Access comprehensive regulatory information for ShockMaster 500 - Electromechanical orthopaedic extracorporeal shock wave therapy system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Axis Medical & Rehabilitation, manufactured by GymnaUniphy NV in Belgium. The device registration started on December 09, 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 IIa
Class IIa
ShockMaster 500 - Electromechanical orthopaedic extracorporeal shock wave therapy system
Australia TGA ARTG Registered Device
Good Name: Axis Medical & Rehabilitation - ShockMaster 500 - Electromechanical orthopaedic extracorporeal shock wave therapy system
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Intended Purpose

The ShockMaster is a compressed air operated ballistic shockwave generator. It generates a high energy sound wave for the treatment of muscular and some orthopaedic disorders to alleviate pain and increase functionality and mobility.

Device Classification
Risk Class
Class IIa
Product Type
Medical device system
ARTG Category
General
Registration Information
Start Date
December 09, 2021
Effective Date
December 09, 2021
Manufacturer
Country
Belgium
Address
Pasweg 6A, Bilzen, 3740