Taiwan FDA registration a4427d2da2004237f66179e1b8279d68

"Bioken" mumps virus test reagent (unsterilized)

TW: "生研" 腮腺炎病毒檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·DENKA CO., LTD·Registered Mar 22, 2013 – Mar 22, 2028Active

Registration details

Analysis ID: a4427d2da2004237f66179e1b8279d68
Customs Code: DHA04401282900

Company information

Manufacturer: DENKA CO., LTD
Manufacturer Country: Japan
Authorized Representative: TUNYEN ENTERPRISE CORPORATION

Product details

Intended Use: It is limited to the first-level identification scope of the "Mumps Virus Serum Reagent (C.3380)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3380 腮腺炎病毒血清試劑
Import Information: import

Dates and status

Registration Date: Mar 22, 2013
Expiry Date: Mar 22, 2028

About this record

Access comprehensive regulatory information for "Bioken" mumps virus test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a4427d2da2004237f66179e1b8279d68 and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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