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“LASEROPTEK” LOTUS III Multi-Pulsed Er:YAG Laser System - Taiwan Registration 0072081a817e866cd9cf7fe5233b1c57

Access comprehensive regulatory information for “LASEROPTEK” LOTUS III Multi-Pulsed Er:YAG Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0072081a817e866cd9cf7fe5233b1c57 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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0072081a817e866cd9cf7fe5233b1c57
Registration Details
Taiwan FDA Registration: 0072081a817e866cd9cf7fe5233b1c57
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Device Details

“LASEROPTEK” LOTUS III Multi-Pulsed Er:YAG Laser System
TW: “雷射歐普克”戀神第三代鉺雅鉻雷射儀
Risk Class 2
MD

Registration Details

0072081a817e866cd9cf7fe5233b1c57

Ministry of Health Medical Device Import No. 036668

DHA05603666807

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

Jul 07, 2023

Jul 07, 2028