Taiwan FDA registration c1476ba47ccfc39b9971e8094c678c7b

Abbott Clinical Biochemical Integrative Microchip Technology Urine Corrector

TW: 亞培臨床生化整合晶片技術尿液校正劑
Taiwan flagTaiwan·Risk Class 2·ABBOTT GMBH;; SEKISUI DIAGNOSTICS P.E.I. INC.·Registered Dec 22, 2006 – Dec 22, 2026Active
Registration details
Analysis ID
c1476ba47ccfc39b9971e8094c678c7b
Customs Code
DHA00601785200
Company information
Manufacturer Country
Canada;;Germany
Product details
Intended Use
For correction of sodium, potassium and chlorine analysis in urine.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1150 Calibrated Products
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Dec 22, 2006
Expiry Date
Dec 22, 2026
About this record

Access comprehensive regulatory information for Abbott Clinical Biochemical Integrative Microchip Technology Urine Corrector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c1476ba47ccfc39b9971e8094c678c7b and manufactured by ABBOTT GMBH;; SEKISUI DIAGNOSTICS P.E.I. INC.. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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