Australia TGA ARTG recordDermatological Nd:YAG/frequency-doubled Nd:YAG laser system - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system
Australia TGA ARTG Registered Device · Cutera Australia Pty Ltd · Cutera Inc · Class IIb · Started September 10, 2020
Good Name: Cutera Australia Pty Ltd - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system
- Risk Class
- Class IIb
- Product Type
- Medical device system
- ARTG Category
- General
- Start Date
- September 10, 2020
- Effective Date
- September 10, 2020
- Name
- Cutera Inc
- Country
- United States of America
- Address
- 3240 Bayshore Boulevard, Brisbane, California, 94005
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
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 sponsored by Cutera Australia Pty Ltd, manufactured by Cutera Inc in United States of America. The device registration started on September 10, 2020.
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