"BECKMAN COULTER" DxH 500 Series Diluent (Non-Sterile) - Taiwan Registration 0888e74c0316cdace47a7f8362c442bd
Access comprehensive regulatory information for "BECKMAN COULTER" DxH 500 Series Diluent (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0888e74c0316cdace47a7f8362c442bd and manufactured by BECKMAN COULTER GmbH. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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Device Details
Registration Details
0888e74c0316cdace47a7f8362c442bd
Ministry of Health Medical Device Import No. 017674
DHA09401767402
Product Details
Limited to the first level identification range of blood cell thinners (B.8200) of the management methods for medical devices.
B Hematology and pathology devices
B8200 Blood cell thinner
Imported from abroad
Dates and Status
Mar 31, 2017
Mar 31, 2027

