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HELIOSIII - Surgical frequency-doubled Nd:YAG laser system - ARTG 327275

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 registered under ARTG number 327275 and 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.

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Class IIb
ARTG 327275
Class IIb
HELIOSIII - Surgical frequency-doubled Nd:YAG laser system
ARTG ID: 327275
Good Name: Laseraid International Pty Ltd - HELIOSIII - Surgical frequency-doubled Nd:YAG laser system
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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

Device Classification
Risk Class
Class IIb
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
327275
Start Date
December 10, 2019
Effective Date
December 10, 2019
Manufacturer
Country
South Korea
Address
203 204 Hyundai I valley 31 Galmachi-ro 244beon-gil Jungwon-gu Seongnam-si, Gyeonggi-do, 13212