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Humidifier, heated

Australia TGA ARTG Registered Device · Lowenstein Medical Australia Pty Ltd · Wilamed GmbH · Class IIb · Started September 28, 2018

Good Name: Lowenstein Medical Australia Pty Ltd - Humidifier, heated

Device classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration information
Start Date
September 28, 2018
Effective Date
September 28, 2018
Sponsor
Manufacturer
Country
Germany
Address
Aurachhohe 5-7, Kammerstein, 91126
Intended purpose

The respiratory humidifier is a device for heating and humidifying respiratory gases such as medical oxygen and/or compressed air or room air during artificial respiration or respiratory therapy in both clinical and non-clinical settings.

About this record

Access comprehensive regulatory information for Humidifier, heated in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Lowenstein Medical Australia Pty Ltd, manufactured by Wilamed GmbH in Germany. The device registration started on September 28, 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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