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Hironic Q-Switched Nd:YAG Picosecond Laser - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system

Access comprehensive regulatory information for Hironic Q-Switched Nd:YAG Picosecond Laser - 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 CSHE Australia Pty Ltd, manufactured by Hironic Co Ltd in South Korea. The device registration started on August 04, 2022.

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
Class IIb
Hironic Q-Switched Nd:YAG Picosecond Laser - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system
Australia TGA ARTG Registered Device
Good Name: CSHE Australia Pty Ltd - Hironic Q-Switched Nd:YAG Picosecond Laser - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system
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Intended Purpose

Hironic Q-Switched Nd:YAG Picosecond Laser is intended to be used to treat scars through coagulation and vaporization, and to break pigments like tattoo ink or treat pigmentation and pigmented lesions such as nevus of Ota, freckles, Melasma and skin rejuvenation.

Device Classification
Risk Class
Class IIb
Product Type
Medical device system
ARTG Category
General
Registration Information
Start Date
August 04, 2022
Effective Date
August 04, 2022
Manufacturer
Country
South Korea
Address
19F 767 Sinsu-ro Suji-gu Yongin-si, Gyeonggi-do, 16827