"BECKMAN COULTER" DxH 500 Diluent (Non-Sterile) - Taiwan Registration 53050e34591c735e07ba9eb5d2c34c65
Access comprehensive regulatory information for "BECKMAN COULTER" DxH 500 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 53050e34591c735e07ba9eb5d2c34c65 and manufactured by BECKMAN COULTER GmbH. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Registration Details
53050e34591c735e07ba9eb5d2c34c65
Ministry of Health Medical Device Import No. 016508
DHA09401650806
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
May 09, 2016
May 09, 2021

