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Compression system stocking/sleeve/suit, <specify>

Access comprehensive regulatory information for Compression system stocking/sleeve/suit, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Medline International Two Australia Pty Ltd, manufactured by Medline Industries LP in United States of America. The device registration started on February 07, 2024.

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
Class I
Compression system stocking/sleeve/suit, <specify>
Australia TGA ARTG Registered Device
Good Name: Medline International Two Australia Pty Ltd - Compression system stocking/sleeve/suit, <specify>
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Intended Purpose

An inflatable device applied to the limbs externally in the form of a stocking, sleeve, or suit to promote venous blood flow. As part of a compression system, the device applies pressure to the extremities. 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. The device may have one or several chambers, and be single-use or reusable.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General-Export
Registration Information
Start Date
February 07, 2024
Effective Date
February 07, 2024
Manufacturer
Country
United States of America
Address
Three Lakes Drive, Northfield, Illinois, 60093