Australia TGA ARTG record

STENDO V3 - Compression unit, sequential

Australia TGA ARTG Registered Device · Macquarie Medical Systems Pty Ltd · Stendo · Class IIa · Started September 27, 2018

Good Name: Macquarie Medical Systems Pty Ltd - STENDO V3 - Compression unit, sequential

Device classification

Risk Class: Class IIa
Product Type: Medical device system
ARTG Category: General

Registration information

Start Date: September 27, 2018
Effective Date: September 27, 2018

Sponsor

Name: Macquarie Medical Systems Pty Ltd

Manufacturer

Name: Stendo
Country: France
Address: 17 Rue Du Port, BP 119, Louviers, Cedex, 27401

Intended purpose

Sequential Venous Compression System: Compression/Non-Compression Non-Invansive device for the lower part of the body (legs, thighs and abdomen) to reproduce and / or stimulate the natural physiological pulsations and the physical sheer stress forces.

About this record

Access comprehensive regulatory information for STENDO V3 - Compression unit, sequential in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Macquarie Medical Systems Pty Ltd, manufactured by Stendo in France. The device registration started on September 27, 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.