Single-chamber venous compression system garment, reprocessed - ARTG 409171
Access comprehensive regulatory information for Single-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 409171 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.
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 intermittent inflation of a single-chamber. 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