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Esther Debridement Gel (Sterilized) - Taiwan Registration 41a5b91ef14910b189a64d0f25f12392

Access comprehensive regulatory information for Esther Debridement Gel (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 41a5b91ef14910b189a64d0f25f12392 and manufactured by Oriental Innovation Development Co., Ltd. Biomedical Factory. The authorized representative in Taiwan is ESTHER MATERIAL TECHNOLOGY CO., LTD..

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41a5b91ef14910b189a64d0f25f12392
Registration Details
Taiwan FDA Registration: 41a5b91ef14910b189a64d0f25f12392
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Device Details

Esther Debridement Gel (Sterilized)
TW: ใ€ไปฅๆ–ฏๅธ–ใ€žๆธ…ๅ‰ตไฟฎ่ญทๅ‡่† (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

41a5b91ef14910b189a64d0f25f12392

Company Information

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".

I General, Plastic Surgery and Dermatology

I.4018 ่ฆชๆฐดๆ€งๅ‰ตๅ‚ท่ฆ†่“‹ๆ

QMS/QSD;; ๅœ‹็”ข;; ๅง”่จ—่ฃฝ้€ 

Dates and Status

Apr 20, 2012

Apr 20, 2017

Dec 13, 2019

Cancellation Information

Logged out

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