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“EunSung” Clearlight LD 808 - Taiwan Registration 001e087e2dcfa9380eb43ccc39d01226

Access comprehensive regulatory information for “EunSung” Clearlight LD 808 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 001e087e2dcfa9380eb43ccc39d01226 and manufactured by EUNSUNG GLOBAL CORP.. The authorized representative in Taiwan is MAVIS MEDICAL ENTERPRISE CO., LTD..

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001e087e2dcfa9380eb43ccc39d01226
Registration Details
Taiwan FDA Registration: 001e087e2dcfa9380eb43ccc39d01226
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Device Details

“EunSung” Clearlight LD 808
TW: “恩尚”二極體雷射
Risk Class 2
MD

Registration Details

001e087e2dcfa9380eb43ccc39d01226

Ministry of Health Medical Device Import No. 035397

DHA05603539700

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

Apr 20, 2022

Apr 20, 2027