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“LaMeditech” Handy Ray - Taiwan Registration 2999ecc43f8ae984164e5af0f181e442

Access comprehensive regulatory information for “LaMeditech” Handy Ray in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2999ecc43f8ae984164e5af0f181e442 and manufactured by LaMeditech Co., Ltd. The authorized representative in Taiwan is Y.H. BIOTEK CO., LTD..

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2999ecc43f8ae984164e5af0f181e442
Registration Details
Taiwan FDA Registration: 2999ecc43f8ae984164e5af0f181e442
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Device Details

“LaMeditech” Handy Ray
TW: “拉美迪克”採血器
Risk Class 2
MD

Registration Details

2999ecc43f8ae984164e5af0f181e442

Ministry of Health Medical Device Import No. 032502

DHA05603250205

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

Apr 10, 2019

Apr 10, 2024