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Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system - ARTG 459230

Access comprehensive regulatory information for Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 459230 and sponsored by Aussie Medi Tech Pty Ltd, manufactured by Quanta System SPA in Italy. The device registration started on August 12, 2024.

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 IIb
ARTG 459230
Class IIb
Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system
ARTG ID: 459230
Good Name: Aussie Medi Tech Pty Ltd - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system
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Intended Purpose

Device used for Dermatological vascular lesions, benign cutaneous lesions, benign pigmented lesions, tattoo removal, removal or lightening of unwanted hair, skin resurfacing / rejuvenation, scars, inflammatory acne, acne vulgaris, hair reduction, dermatological foot conditions (skin and nail), Fractional Skin resurfacing (wrinkle and fine line removal, deeper wrinkle correction, sun and age spot's reduction, acne and traumatic scar's removal, dyschromia removal.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
459230
Start Date
August 12, 2024
Effective Date
August 12, 2024
Manufacturer
Country
Italy
Address
Via Acquedotto 109, Samarate, VA, 21017