Taiwan FDA registration 85ffe05966dbe359fe947ce5b7c5e8b5

"KIMA" Manual blood cell counting device (Non-Sterile)

TW: "奇馬" 手動血球計數裝置 (未滅菌)

Taiwan·Risk Class 1·MD·KIMA S.A.S.·Registered Apr 19, 2016 – Apr 19, 2021Expired

Registration details

Analysis ID: 85ffe05966dbe359fe947ce5b7c5e8b5
License Form: Ministry of Health Medical Device Import No. 016418
Customs Code: DHA09401641805

Company information

Manufacturer: KIMA S.A.S.
Manufacturer Country: Italy
Authorized Representative: RAFA INTERNATIONAL CORP.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Manual Blood Cell Counting Device (B.6160)".
Product Type (Level 1): B Hematology and pathology devices
Product Type (Level 2): B6160 Manual blood counting device
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 19, 2016
Expiry Date: Apr 19, 2021

About this record

Access comprehensive regulatory information for "KIMA" Manual blood cell counting device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 85ffe05966dbe359fe947ce5b7c5e8b5 and manufactured by KIMA S.A.S.. The authorized representative in Taiwan is RAFA INTERNATIONAL CORP..

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