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“Ilooda” CuRAS Q-switched Nd:YAG Laser system - Taiwan Registration 82786712387f4c370d4afd85f05f9163

Access comprehensive regulatory information for “Ilooda” CuRAS Q-switched Nd: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 82786712387f4c370d4afd85f05f9163 and manufactured by ILOODA CO., LTD.. The authorized representative in Taiwan is COLLAMATRIX 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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82786712387f4c370d4afd85f05f9163
Registration Details
Taiwan FDA Registration: 82786712387f4c370d4afd85f05f9163
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Device Details

“Ilooda” CuRAS Q-switched Nd:YAG Laser system
TW: “伊路達”庫雷斯Q開關釹雅各雷射
Risk Class 2
MD

Registration Details

82786712387f4c370d4afd85f05f9163

Ministry of Health Medical Device Import No. 035903

DHA05603590302

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 16, 2022

Sep 16, 2027