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Filter, humidifier, heat/moisture exchanger

Access comprehensive regulatory information for Filter, humidifier, heat/moisture exchanger in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Hospital Products Australia Pty Ltd, manufactured by Vadi Medical Technology Co Ltd Yangmei in Taiwan. The device registration started on August 14, 2020.

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
Filter, humidifier, heat/moisture exchanger
Australia TGA ARTG Registered Device
Good Name: Hospital Products Australia Pty Ltd - Filter, humidifier, heat/moisture exchanger
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DJ Fang

DJ Fang

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Intended Purpose

dedicated filter device that is inserted into an appropriate humidifier (reusable artificial nose), see: Humidifier, heat/moisture exchanger, reusable, so that when used together with this and connected in-line with a patient's artificial airway the unit will capture the patient's exhaled heat and moisture and use them to warm and humidify the inspired gases. The device is single use.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
August 14, 2020
Effective Date
August 14, 2020
Manufacturer
Country
Taiwan
Address
No 198 Lane 298 Huandong Road, ZhongShan Village Yangmei District, Taoyuan City, 32665