Taiwan FDA registration 672a83f4abf6877f402bd971ef43fd18

Cenefom otolaryngology foam (sterilized)

TW: Cenefom耳鼻喉科用泡棉(滅菌)

Taiwan·Risk Class 1·CENEFOM CORP.·Registered Mar 26, 2014 – Mar 26, 2029Active

Registration details

Analysis ID: 672a83f4abf6877f402bd971ef43fd18

Company information

Manufacturer: CENEFOM CORP.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: CENEFOM CORP.

Product details

Intended Use: 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.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4014 Non-absorbent cloth or sea balls are used externally
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Mar 26, 2014
Expiry Date: Mar 26, 2029

About this record

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..

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