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Beckman Coulter UniCel DxH 900 Cellular Analysis System - Taiwan Registration 4ef9b66b69b9092a3b0780da9857c43e

Access comprehensive regulatory information for Beckman Coulter UniCel DxH 900 Cellular Analysis System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ef9b66b69b9092a3b0780da9857c43e and manufactured by Beckman Coulter, Inc.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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4ef9b66b69b9092a3b0780da9857c43e
Registration Details
Taiwan FDA Registration: 4ef9b66b69b9092a3b0780da9857c43e
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Device Details

Beckman Coulter UniCel DxH 900 Cellular Analysis System
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น่ก€ๆถฒๅˆ†ๆž็ณป็ตฑ
Risk Class 2
MD

Registration Details

4ef9b66b69b9092a3b0780da9857c43e

Ministry of Health Medical Device Import No. 031441

DHA05603144106

Company Information

United States

Product Details

This product provides laboratory automation to perform quantitative analysis of multiple parameters of hematology.

B Hematology and pathology devices

B5220 automatically differentiates cell counters

Imported from abroad

Dates and Status

Aug 30, 2018

Aug 30, 2028