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Beckman Coulter Flow-Set Pro Fluorospheres - Taiwan Registration 078a67b4eccd3f755e9616762c92294b

Access comprehensive regulatory information for Beckman Coulter Flow-Set 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 078a67b4eccd3f755e9616762c92294b 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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078a67b4eccd3f755e9616762c92294b
Registration Details
Taiwan FDA Registration: 078a67b4eccd3f755e9616762c92294b
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Device Details

Beckman Coulter Flow-Set Pro Fluorospheres
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰นๆตๅผ็ดฐ่ƒžๅ„€ๆจ™ๆบ–ๅŒ–่žขๅ…‰็ƒ
Risk Class 2
MD

Registration Details

078a67b4eccd3f755e9616762c92294b

Ministry of Health Medical Device Import No. 030500

DHA05603050004

Company Information

United States

Product Details

This product is a suspension of fluorescent beads for the correction of forward scattered light, side-scattered light and fluorescence channel detector with flow cytometry FC500 (FL1-5), NAVIOS and NAVIOS EX flow cytometry (FL1-10).

B Hematology and pathology devices

B8625 Hematological Quality Management Mixture

Imported from abroad

Dates and Status

Feb 06, 2018

Feb 06, 2028

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