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Dentifrice - ARTG 313241

Access comprehensive regulatory information for Dentifrice in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 313241 and sponsored by Haleon Australia Pty Ltd, manufactured by GSK Consumer Healthcare (GMDT) in Ireland. The device registration started on January 14, 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 IIa
ARTG 313241
Class IIa
Dentifrice
ARTG ID: 313241
Good Name: Haleon Australia Pty Ltd - Dentifrice
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Intended Purpose

Dentifrice for the relief of Dentine Hypersensitivity

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
313241
Start Date
January 14, 2019
Effective Date
January 14, 2019
Manufacturer
Country
Ireland
Address
Clocherane Youghal Road, Dungarvan, Co Waterford