貝克曼庫爾特亞瑟斯黃體脂酮 II 校正液 - Taiwan Registration d35aa34afa8af5a310f90f5f247d3a12
Access comprehensive regulatory information for 貝克曼庫爾特亞瑟斯黃體脂酮 II 校正液 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d35aa34afa8af5a310f90f5f247d3a12 and manufactured by Beckman Coulter, Inc.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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Device Details
Product Details
This product is used to calibrate Beckman Coulter Arthurs Lutebolone II Reagent for the quantitative determination of progesterone concentrations in human serum and plasma (lithium heparin) in conjunction with the automated Access 2 Immunoassay System and the DxI 9000 Access Immunoassay Analyzer.
A Clinical chemistry and clinical toxicology
A.1150 Calibrated Products
QMS/QSD;; 輸入
Dates and Status
Sep 09, 2024
Sep 09, 2029

