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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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d35aa34afa8af5a310f90f5f247d3a12
Registration Details
Taiwan FDA Registration: d35aa34afa8af5a310f90f5f247d3a12
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Device Details

貝克曼庫爾特亞瑟斯黃體脂酮 II 校正液
Risk Class 2

Registration Details

d35aa34afa8af5a310f90f5f247d3a12

DHA05603750306

Company Information

United States

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