Taiwan FDA registration 954ffcb268635ac6f7fcb8b5a64fd12c

Abbott albumin BCP test group

TW: 亞培白蛋白BCP檢驗試劑組
Taiwan flagTaiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH·Registered Jan 24, 2019 – Jan 24, 2029Active
Registration details
Analysis ID
954ffcb268635ac6f7fcb8b5a64fd12c
Customs Code
DHA05603214303
Company information
Manufacturer Country
United States;;Germany
Product details
Intended Use
This product can be used to quantify albumin in human serum or plasma on the Alinity c analyzer.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1035 Albumin Testing System
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Jan 24, 2019
Expiry Date
Jan 24, 2029
About this record

Access comprehensive regulatory information for Abbott albumin BCP test group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 954ffcb268635ac6f7fcb8b5a64fd12c and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).

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