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Multi-chamber venous compression system garment, reprocessed - ARTG 409174

Access comprehensive regulatory information for Multi-chamber venous compression system garment, reprocessed in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 409174 and sponsored by Arjo Australia Pty Ltd, manufactured by Arjo Australia Pty Ltd in Australia. The device registration started on May 18, 2023.

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 I
ARTG 409174
Class I
Multi-chamber venous compression system garment, reprocessed
ARTG ID: 409174
Good Name: Arjo Australia Pty Ltd - Multi-chamber venous compression system garment, reprocessed
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Intended Purpose

A non-sterile inflatable device in the form of a stocking, sleeve, or suit intended to be applied to the limbs externally to promote venous blood flow. As part of a compression system, the device applies pressure to the extremities through the sequential inflation of several chambers. The resulting increased venous blood flow may help to treat/prevent oedema, deep vein thrombosis (DVT) and pulmonary embolism (PE) in non-ambulatory patients or patients at risk. This is a previously used single-use device that has been processed for an additional single-use patient application.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
409174
Start Date
May 18, 2023
Effective Date
May 18, 2023
Manufacturer
Country
Australia
Address
Level 3 Building B 11 Talavera Road, Macquarie Park, NSW, 2113