Australia TGA ARTG recordDermatological Nd:YAG/frequency-doubled Nd:YAG laser system
Australia TGA ARTG Registered Device · Laseraid International Pty Ltd · Laseroptek Co Ltd · Class IIb · Started October 13, 2020
Good Name: Laseraid International Pty Ltd - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system
- Risk Class
- Class IIb
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- October 13, 2020
- Effective Date
- October 13, 2020
- Country
- South Korea
- Address
- #114 #116 #117 #203 #204 Hyundai I Valley 31, Galmachi-ro 244beon-gil Jungwon-gu, Seongnam-si Gyeonggi-do, Korea, 13212
The device is generally intended for use in surgical applications requiring incision, excision, ablation, vaporization and coagulation of body soft tissues in the medical specialties of dermatology, general, plastic and oral surgery as follows: treatment of benign pigmented lesions, wrinkles, acne scars and for hair, and the incision, excision, ablation, vaporization of soft tissue for general dermatology, but not limited to treatment.
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 sponsored by Laseraid International Pty Ltd, manufactured by Laseroptek Co Ltd in South Korea. The device registration started on October 13, 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.