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"Fushen" hydrophilic wound patch (sterilized) - Taiwan Registration 23d2ff24f8525244af98c29147d8a4db

Access comprehensive regulatory information for "Fushen" hydrophilic wound patch (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 23d2ff24f8525244af98c29147d8a4db and manufactured by DECORTEC CO., LTD.. The authorized representative in Taiwan is FORTUNE CROESUS 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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23d2ff24f8525244af98c29147d8a4db
Registration Details
Taiwan FDA Registration: 23d2ff24f8525244af98c29147d8a4db
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Device Details

"Fushen" hydrophilic wound patch (sterilized)
TW: โ€œๅฏŒ่–โ€่ฆชๆฐดๆ€งๅ‚ทๅฃ่ฒผๅธƒ (ๆป…่Œ)
Risk Class 1

Registration Details

23d2ff24f8525244af98c29147d8a4db

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of the classification and grading management measures for medical equipment "hydrophilic trauma covering materials (I.4018)".

I General, Plastic Surgery and Dermatology

I.4018 ่ฆชๆฐดๆ€งๅ‰ตๅ‚ท่ฆ†่“‹ๆ

ๅง”่จ—่ฃฝ้€ ;; ๅœ‹็”ข;; QMS/QSD

Dates and Status

Jun 09, 2010

Jun 09, 2025