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Beckman Coulter Flow-Check Pro Fluorospheres - Taiwan Registration 42762979c9c844dc5bda315aef42d1e8

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 42762979c9c844dc5bda315aef42d1e8 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.

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42762979c9c844dc5bda315aef42d1e8
Registration Details
Taiwan FDA Registration: 42762979c9c844dc5bda315aef42d1e8
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Device Details

Beckman Coulter Flow-Check Pro Fluorospheres
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น่žขๅ…‰ๅพฎ็ƒๆ‡ธๆตฎๆถฒ
Risk Class 2
MD
Cancelled

Registration Details

42762979c9c844dc5bda315aef42d1e8

Ministry of Health Medical Device Import No. 027219

DHA05602721903

Company Information

United States

Product Details

B Hematology and pathology devices

B5220 automatically differentiates cell counters

Imported from abroad

Dates and Status

Apr 24, 2015

Apr 24, 2020

Aug 05, 2022

Cancellation Information

Logged out

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