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Cenefom otolaryngology foam (sterilized) - Taiwan Registration 672a83f4abf6877f402bd971ef43fd18

Access comprehensive regulatory information for Cenefom otolaryngology foam (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 672a83f4abf6877f402bd971ef43fd18 and manufactured by CENEFOM CORP.. The authorized representative in Taiwan is CENEFOM CORP..

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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672a83f4abf6877f402bd971ef43fd18
Registration Details
Taiwan FDA Registration: 672a83f4abf6877f402bd971ef43fd18
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Device Details

Cenefom otolaryngology foam (sterilized)
TW: Cenefom่€ณ้ผปๅ–‰็ง‘็”จๆณกๆฃ‰(ๆป…่Œ)
Risk Class 1

Registration Details

672a83f4abf6877f402bd971ef43fd18

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of classification and grading management of medical devices "external use of non-absorbent gauze or sponge balls (I.4014)" identification range.

I General, Plastic Surgery and Dermatology

I.4014 Non-absorbent cloth or sea balls are used externally

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Mar 26, 2014

Mar 26, 2029