Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system - ARTG 343230
Access comprehensive regulatory information for Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system - 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 343230 and sponsored by Cutera Australia Pty Ltd, manufactured by Cutera Inc in United States of America. The device registration started on September 10, 2020.
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.
Intended for use in aesthetic and cosmetic applications in the medical specialties of dermatology and plastic surgery. Specific indications: • Tattoo removal • Treatment of benign pigmented lesions • Treatment of acne scars and wrinkles