Taiwan FDA registration 3657a12d46336747d55e3e2dfb204333

Apex urea nitrogen assay set

TW: 亞培尿素氮檢驗試劑組
Taiwan flagTaiwan·Risk Class 2·FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A PART OF THERMO FISHER SCIENTIFIC INC.;; ABBOTT GMBH·Registered Dec 28, 2018 – Dec 28, 2028Active
Registration details
Analysis ID
3657a12d46336747d55e3e2dfb204333
Customs Code
DHA05603199803
Company information
Manufacturer Country
United States;;Germany
Product details
Intended Use
This product can be used to quantify urea nitrogen in human serum, plasma or urine on the Alinity c analyzer.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1770 尿素氮試驗系統
Import Information
Contract manufacturing;; input
Dates and status
Registration Date
Dec 28, 2018
Expiry Date
Dec 28, 2028
About this record

Access comprehensive regulatory information for Apex urea nitrogen assay set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3657a12d46336747d55e3e2dfb204333 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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