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Beckman Coulter Flow-Set Pro Fluorospheres - Taiwan Registration e6eaac22d586c0eadff7343f2106f264

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 e6eaac22d586c0eadff7343f2106f264 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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e6eaac22d586c0eadff7343f2106f264
Registration Details
Taiwan FDA Registration: e6eaac22d586c0eadff7343f2106f264
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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
Cancelled

Registration Details

e6eaac22d586c0eadff7343f2106f264

Ministry of Health Medical Device Import No. 026085

DHA05602608503

Company Information

United States

Product Details

B Hematology and pathology devices

B8625 Hematological Quality Management Mixture

Imported from abroad

Dates and Status

May 22, 2014

May 22, 2019

Aug 05, 2022

Cancellation Information

Logged out

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