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貝克曼庫爾特雌三醇試劑組(未滅菌) - Taiwan Registration 729f6aa2bbd84af7e4e750ba9a18e157

Access comprehensive regulatory information for 貝克曼庫爾特雌三醇試劑組(未滅菌) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 729f6aa2bbd84af7e4e750ba9a18e157 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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729f6aa2bbd84af7e4e750ba9a18e157
Registration Details
Taiwan FDA Registration: 729f6aa2bbd84af7e4e750ba9a18e157
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Device Details

貝克曼庫爾特雌三醇試劑組(未滅菌)
Risk Class 1

Registration Details

729f6aa2bbd84af7e4e750ba9a18e157

DHA09402354605

Company Information

United States

Product Details

Limited to the first level of identification scope of the "Estriol Test System (A.1265)" of the Administrative Measures for the Classification and Grading of Medical Devices.

A Clinical chemistry and clinical toxicology

A.1265 雌三醇試驗系統

Input;; QMS/QSD

Dates and Status

Jul 17, 2024

Jul 17, 2029