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Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system

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 Wear Nothing Pty Ltd, manufactured by Dana Corp in South Korea. The device registration started on June 19, 2015.

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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Class IIb
Class IIb
Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system
Australia TGA ARTG Registered Device
Good Name: Wear Nothing Pty Ltd - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system
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Intended Purpose

Nd:YAG Surgical Laser instrument with handpiece to be used in dermatologic therapy or surgery by using laser light with wavelengths of 1064nm and 532nm for selective destruction to the pigmented lesions and tattoo particle such as inflammatory acne, large pores, blemishes, tattoos, freckles: to improvement for skin tone and skin pigmentation

Device Classification
Risk Class
Class IIb
Product Type
Medical device system
ARTG Category
General
Registration Information
Start Date
June 19, 2015
Effective Date
July 17, 2017
Manufacturer
Country
South Korea
Address
1206 Samsung IT Valley 27 Digital-ro 33-gil, Guro-gu, Seoul, 152-743