Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system - ARTG 464388
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 464388 and sponsored by Aussie Medi Tech Pty Ltd, manufactured by Quanta System SPA in Italy. The device registration started on October 14, 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.
SUPREMA Series medical devices are intended for use in medical specialties including plastic surgery, aesthetic medicine, dermatology and podiatry. SUPREMA Series medical devices are indicated for all skin types Fitzpatrick I-VI, including tanned skin. For treatment of: • Dermatological vascular lesions treatment • Benign pigmented lesions treatment • Benign cutaneous lesions treatment Plastic Surgery / Dermatology/Aesthetic Medicine / Podiatry: • Benign cutaneous lesions treatment 1064 nm (Nd:YAG laser) • Scars treatment • Inflammatory acne, acne vulgaris treatment • Permanent hair reduction / Removal or lightening of unwanted hair • Skin resurfacing / rejuvenation • Dermatological foot conditions (skin and nail) treatment 532 nm (Nd:YAG laser) Plastic Surgery / Dermatology/Aesthetic Medicine: