Taiwan FDA registration b0c0b6df5d70619d9603ed3d13ac8c68

Cenefom foam for nasal hemostasis (sterilized)

TW: Cenefom 鼻止血用泡棉 (滅菌)

Taiwan·Risk Class 1·CENEFOM CORP.·Registered Jan 24, 2017 – Jan 24, 2027Active

Registration details

Analysis ID: b0c0b6df5d70619d9603ed3d13ac8c68

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: 國產;; QMS/QSD

Dates and status

Registration Date: Jan 24, 2017
Expiry Date: Jan 24, 2027

About this record

Access comprehensive regulatory information for Cenefom foam for nasal hemostasis (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b0c0b6df5d70619d9603ed3d13ac8c68 and manufactured by CENEFOM CORP.. The authorized representative in Taiwan is CENEFOM CORP..

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