Taiwan FDA registration ec162c9afcee9f24aa0fc56980018956

Abbott clinical biochemical second-generation alkaline phosphatase assay group

TW: 亞培臨床生化第二代鹼性磷酸酶檢驗試劑組
Taiwan flagTaiwan·Risk Class 2·ABBOTT IRELAND DIAGNOSTICS DIVISION·Registered Sep 30, 2022 – Sep 30, 2027Active
Registration details
Analysis ID
ec162c9afcee9f24aa0fc56980018956
Customs Code
DHA05603585603
Company information
Manufacturer Country
Ireland
Product details
Intended Use
This product is used on the ARCHECT c system to quantify alkaline phosphatase in human serum or plasma.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1050 Alkaline phosphatase or isoenzyme testing system
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Sep 30, 2022
Expiry Date
Sep 30, 2027
About this record

Access comprehensive regulatory information for Abbott clinical biochemical second-generation alkaline phosphatase assay group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ec162c9afcee9f24aa0fc56980018956 and manufactured by ABBOTT IRELAND DIAGNOSTICS DIVISION. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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