Australia TGA ARTG record

Shoulder continuous passive motion exerciser

Australia TGA ARTG Registered Device · Axis Medical & Rehabilitation · Kinetec SAS · Class IIa · Started May 06, 2021

Good Name: Axis Medical & Rehabilitation - Shoulder continuous passive motion exerciser

Device classification

Risk Class: Class IIa
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: May 06, 2021
Effective Date: May 06, 2021

Sponsor

Name: Axis Medical & Rehabilitation

Manufacturer

Name: Kinetec SAS
Country: France
Address: Rue Maurice, Perin ZI de Tournes, Tournes, 08090

Intended purpose

Intended to provide passive motion exercise for the a variety of joints specifically shoulder and elbow

About this record

Access comprehensive regulatory information for Shoulder continuous passive motion exerciser 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 Kinetec SAS in France. The device registration started on May 06, 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.