Australia TGA ARTG record

HELIOSIII - Surgical frequency-doubled Nd:YAG laser system

Australia TGA ARTG Registered Device · Laseraid International Pty Ltd · Laseroptek Co Ltd · Class IIb · Started December 10, 2019

Good Name: Laseraid International Pty Ltd - HELIOSIII - Surgical frequency-doubled Nd:YAG laser system

Device classification

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

Registration information

Start Date: December 10, 2019
Effective Date: December 10, 2019

Sponsor

Name: Laseraid International Pty Ltd

Manufacturer

Name: Laseroptek Co Ltd
Country: South Korea
Address: 203 204 Hyundai I valley 31 Galmachi-ro 244beon-gil Jungwon-gu Seongnam-si, Gyeonggi-do, 13212

Intended purpose

Incision, excision, ablation, vaporization of soft tissue for general dermatology / Removal or lightening of unwanted hair with or without adjuvant preparation / Tattoo removal / Port wine birthmarks / Telangiectasias / Spider angioma / Cherry angioma / Spider nevi / Cafe-au-lait birthmarks / Solar lentiginos / Senile lentiginos / Backer's nevi / Freckles / Nevus spilus / Nevus of ota

About this record

Access comprehensive regulatory information for HELIOSIII - Surgical 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 December 10, 2019.

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.