Pure Global

“LASEROPTEK” Helios II Q-switched Nd:YAG Laser - Taiwan Registration 46c065c69fc144bad601844a76d0db6a

Access comprehensive regulatory information for “LASEROPTEK” Helios II Q-switched Nd:YAG Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46c065c69fc144bad601844a76d0db6a and manufactured by LASEROPTEK Co., Ltd.. The authorized representative in Taiwan is WOH MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
46c065c69fc144bad601844a76d0db6a
Registration Details
Taiwan FDA Registration: 46c065c69fc144bad601844a76d0db6a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“LASEROPTEK” Helios II Q-switched Nd:YAG Laser
TW: “雷射歐普克”海力歐斯Q開關式釹雅鉻雷射
Risk Class 2
MD

Registration Details

46c065c69fc144bad601844a76d0db6a

Ministry of Health Medical Device Import No. 033628

DHA05603362806

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

May 08, 2020

May 08, 2025