貝克曼庫爾特庫爾特 DxH 稀釋液(未滅菌) - Taiwan Registration 20c43421e37aa82292bc639ecb9bd418
Access comprehensive regulatory information for 貝克曼庫爾特庫爾特 DxH 稀釋液(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 20c43421e37aa82292bc639ecb9bd418 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
It is limited to the first level of identification of "blood cell thinners (B.8200)" in the management measures for the classification and grading of medical devices.
B Hematology, pathology, and genetics
B.8200 Hemocytodilant
Input;; QMS/QSD
Dates and Status
Nov 19, 2024
Nov 19, 2029