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HemosIL Liquid Heparin - Taiwan Registration 77af61bdda9f1b3d8b879d23c0790685

Access comprehensive regulatory information for HemosIL Liquid Heparin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77af61bdda9f1b3d8b879d23c0790685 and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is Werfen Taiwan Limited.

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77af61bdda9f1b3d8b879d23c0790685
Registration Details
Taiwan FDA Registration: 77af61bdda9f1b3d8b879d23c0790685
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Device Details

HemosIL Liquid Heparin
TW: ๅธŒๆ‘ฉ่ฅฟ็ˆพๆถฒๆ…‹่‚็ด ่ฉฆๅŠ‘
Risk Class 2
MD

Registration Details

77af61bdda9f1b3d8b879d23c0790685

Ministry of Health Medical Device Import No. 025280

DHA05602528009

Company Information

United States

Product Details

This product uses IL blood coagulation instrument system (ACL TOP series, ACL ELITE/ELITE PRO/8/9/10000, and ACL Futura/ACL Advance) to quantitatively measure unfractionheparin (UFH) and low molecular weight heparin in human citrate acidated plasma by automated colorimetric quantitation, LMWH).

B Hematology and pathology devices

B7525 Heparin analysis

Imported from abroad

Dates and Status

Sep 10, 2013

Sep 10, 2023