Beckman Coulter Flow-Check Pro Fluorospheres - Taiwan Registration 74e305fd3d5d01a6796204fd31b4cb15
Access comprehensive regulatory information for Beckman Coulter Flow-Check Pro Fluorospheres in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 74e305fd3d5d01a6796204fd31b4cb15 and manufactured by Beckman Coulter, Inc.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BECKMAN COULTER, INC., and 1 recent registrations in the same category. 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
74e305fd3d5d01a6796204fd31b4cb15
Ministry of Health Medical Device Import No. 030501
DHA05603050106
Product Details
This product is a fluorescent bead suspension for the calibration and validation of daily optical and fluid systems by Navios, Navios EX or FC500 flow cytometers.
B Hematology and pathology devices
B5220 automatically differentiates cell counters
Imported from abroad
Dates and Status
Feb 06, 2018
Feb 06, 2028

