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Inhaler, aerosol, portable - ARTG 315987

Access comprehensive regulatory information for Inhaler, aerosol, portable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 315987 and sponsored by GlaxoSmithKline Australia Pty Ltd, manufactured by GSK Consumer Healthcare (GMDT) in Ireland. The device registration started on April 01, 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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TGA ARTG Official Data
Class I
ARTG 315987
Class I
Inhaler, aerosol, portable
ARTG ID: 315987
Good Name: GlaxoSmithKline Australia Pty Ltd - Inhaler, aerosol, portable
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Intended Purpose

The Haleraid is a device designed to place over the GlaxoSmithKline range of metered dose inhalers as an aid to operation by patients with impaired strength in their hands (e.g. arthritis). Specifically for use with GlaxoSmithKline's 120 Dose and 200 Dose metered dose inhalars (MDI's).

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
315987
Start Date
April 01, 2019
Effective Date
April 01, 2019
Manufacturer
Country
Ireland
Address
Clocherane Youghal Road, Dungarvan, Co Waterford