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HemosIL UF Heparin Controls - Taiwan Registration 1f2ee118d93ce125ffbef67778ce3e03

Access comprehensive regulatory information for HemosIL UF Heparin Controls in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1f2ee118d93ce125ffbef67778ce3e03 and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is Werfen Taiwan Limited.

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1f2ee118d93ce125ffbef67778ce3e03
Registration Details
Taiwan FDA Registration: 1f2ee118d93ce125ffbef67778ce3e03
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Device Details

HemosIL UF Heparin Controls
TW: ๅธŒๆ‘ฉ่ฅฟ็ˆพๆœชๅˆ†ๆฎต่‚็ด ๅ“็ฎกๆถฒ
Risk Class 2
MD

Registration Details

1f2ee118d93ce125ffbef67778ce3e03

Ministry of Health Medical Device Import No. 025256

DHA05602525602

Company Information

United States

Product Details

This product is used with IL blood coagulation instrument system (ACL TOP series, ACL ELITE/ELITE PRO/8/9/10000, and ACL Futura/ACL Advance) as a liquid heparin reagent for unfractionated heparin (UFH) quality control.

B Hematology and pathology devices

B5425 Multifunctional equipment for in vitro agglutination research

Imported from abroad

Dates and Status

Aug 07, 2013

Aug 07, 2028