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STENDO V3 - Compression unit, sequential

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.

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TGA ARTG Official Data
Class IIa
Class IIa
STENDO V3 - Compression unit, sequential
Australia TGA ARTG Registered Device
Good Name: Macquarie Medical Systems Pty Ltd - STENDO V3 - Compression unit, sequential
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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.

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