Australia TGA ARTG record

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

Australia TGA ARTG Registered Device · Laseraid International Pty Ltd · Laseroptek Co Ltd · Class IIb · Started August 05, 2022

Good Name: Laseraid International Pty Ltd - Helios IV - Dermatological Nd:YAG/frequency-doubled Nd:YAG laser system

Device classification

Risk Class: Class IIb
Product Type: Medical device system
ARTG Category: General

Registration information

Start Date: August 05, 2022
Effective Date: August 05, 2022

Sponsor

Name: Laseraid International Pty Ltd

Manufacturer

Name: Laseroptek Co Ltd
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

Intended purpose

Removal or lightening of unwanted hair, tattoo removal, treatment of vascular lesions, telangiectaias, spider angioma, cherry angioma, spider nevi, treatment of pigmented lesions.

About this record

Access comprehensive regulatory information for Helios IV - 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 August 05, 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.