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V-Laser - Surgical frequency-doubled Nd:YAG laser system - ARTG 301215

Access comprehensive regulatory information for V-Laser - 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 301215 and sponsored by Ebos Medical Devices Australia Pty Ltd, manufactured by WON Tech Co Ltd in South Korea. The device registration started on March 23, 2018.

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 301215
Class IIb
V-Laser - Surgical frequency-doubled Nd:YAG laser system
ARTG ID: 301215
Good Name: Ebos Medical Devices Australia Pty Ltd - V-Laser - Surgical frequency-doubled Nd:YAG laser system
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Intended Purpose

V-Laser laser system is intended for the non-invasive incision, excision, ablation and vaporisation of soft tissue for general surgical procedures.

Device Classification
Risk Class
Class IIb
Product Type
Medical device system
ARTG Category
General
Registration Information
ARTG ID
301215
Start Date
March 23, 2018
Effective Date
March 23, 2018
Manufacturer
Country
South Korea
Address
64 Techno 8-ro, Yuseong-gu, Daejeon, 34028