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HemosIL Heparin Calibrators - Taiwan Registration 09978cc291f8decc24f809ff68aee325

Access comprehensive regulatory information for HemosIL Heparin Calibrators in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 09978cc291f8decc24f809ff68aee325 and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is Werfen Taiwan Limited.

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09978cc291f8decc24f809ff68aee325
Registration Details
Taiwan FDA Registration: 09978cc291f8decc24f809ff68aee325
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Device Details

HemosIL Heparin Calibrators
TW: ๅธŒๆ‘ฉ่ฅฟ็ˆพ่‚็ด ๆ กๆญฃๆถฒ
Risk Class 2
MD

Registration Details

09978cc291f8decc24f809ff68aee325

Ministry of Health Medical Device Import No. 025258

DHA05602525803

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 correction solution for liquid heparin reagent.

A Clinical chemistry and clinical toxicology

A1150 calibrate

Imported from abroad

Dates and Status

Aug 07, 2013

Aug 07, 2028