Taiwan FDA registration 57748e34999876ff6f066d4de3a4b424

"Rapid Test" Adenovirus (Respiratory) Rapid Test Reagent (Unsterilized)

TW: "速測" 腺病毒(呼吸道)快速檢驗試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·CERTEST BIOTEC S.L.·Registered Jan 02, 2012 – Jan 02, 2017Cancelled
Registration details
Analysis ID
57748e34999876ff6f066d4de3a4b424
Customs Code
DHA04401126004
Company information
Manufacturer Country
Spain
Authorized Representative
JOLEX INTERNATIONAL CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Adenovirus Serological Reagent (C.3020)".
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.3020 腺病毒血清試劑
Import Information
import
Dates and status
Registration Date
Jan 02, 2012
Expiry Date
Jan 02, 2017
Cancellation Date
Mar 14, 2017
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Rapid Test" Adenovirus (Respiratory) Rapid 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 57748e34999876ff6f066d4de3a4b424 and manufactured by CERTEST BIOTEC S.L.. The authorized representative in Taiwan is JOLEX INTERNATIONAL CO., LTD..

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