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Nebulizer, non-heated - ARTG 323489

Access comprehensive regulatory information for Nebulizer, non-heated in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 323489 and sponsored by Air Liquide Healthcare Pty Ltd, manufactured by Apex Medical Corp in Taiwan. The device registration started on September 16, 2019.

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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Class IIa
ARTG 323489
Class IIa
Nebulizer, non-heated
ARTG ID: 323489
Good Name: Air Liquide Healthcare Pty Ltd - Nebulizer, non-heated
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Intended Purpose

To provide a source of compressed air for aerosol therapy. It is used in conjunction with a jet (pneumatic) nebuliser to produce medicated aerosols for inhalation by pediatric and adult patients with respiratory symptoms.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
323489
Start Date
September 16, 2019
Effective Date
September 16, 2019
Manufacturer
Country
Taiwan
Address
No 9 Min Sheng St Tu-cheng, New Taipei City, 23679