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“LASEROPTEK” Helios IV 785 Q-switched Nd:YAG Laser - Taiwan Registration bf4ad4574138c5ade835f03b5657f16f

Access comprehensive regulatory information for “LASEROPTEK” Helios IV 785 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 bf4ad4574138c5ade835f03b5657f16f 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.

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bf4ad4574138c5ade835f03b5657f16f
Registration Details
Taiwan FDA Registration: bf4ad4574138c5ade835f03b5657f16f
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Device Details

“LASEROPTEK” Helios IV 785 Q-switched Nd:YAG Laser
TW: “雷射歐普克”第四代海力歐神Q開關式釹雅鉻雷射
Risk Class 2
MD

Registration Details

bf4ad4574138c5ade835f03b5657f16f

Ministry of Health Medical Device Import No. 035849

DHA05603584906

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Sep 15, 2022

Sep 15, 2027