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HEMOCHRON Whole Blood Microcoagulation Analyzer - Taiwan Registration 85cf30b2adb299a48016b629a8c441ec

Access comprehensive regulatory information for HEMOCHRON Whole Blood Microcoagulation Analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 85cf30b2adb299a48016b629a8c441ec and manufactured by Accriva Diagnostics Inc.. The authorized representative in Taiwan is Werfen Taiwan Limited.

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85cf30b2adb299a48016b629a8c441ec
Registration Details
Taiwan FDA Registration: 85cf30b2adb299a48016b629a8c441ec
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Device Details

HEMOCHRON Whole Blood Microcoagulation Analyzer
TW: ๆผข่Žซๅ…‹ๅพฎ้‡ๅ‡่ก€ๆ™‚้–“ๆธฌๅฎšๅ„€
Risk Class 2
MD

Registration Details

85cf30b2adb299a48016b629a8c441ec

Ministry of Health Medical Device Import No. 025093

DHA05602509300

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

B Hematology and pathology devices

B5425 Multifunctional equipment for in vitro agglutination research

Imported from abroad

Dates and Status

Jul 24, 2013

Jul 24, 2028