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Cimosir Apixaban correction liquid and quality control fluid - Taiwan Registration 367d12bc083643acbeca2a03cbb41c09

Access comprehensive regulatory information for Cimosir Apixaban correction liquid and quality control fluid in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 367d12bc083643acbeca2a03cbb41c09 and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is Werfen Taiwan Limited.

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367d12bc083643acbeca2a03cbb41c09
Registration Details
Taiwan FDA Registration: 367d12bc083643acbeca2a03cbb41c09
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Device Details

Cimosir Apixaban correction liquid and quality control fluid
TW: ๅธŒๆ‘ฉ่ฅฟ็ˆพ Apixabanๆ กๆญฃๆถฒๅŠๅ“็ฎกๆถฒ
Risk Class 2

Registration Details

367d12bc083643acbeca2a03cbb41c09

DHA05603133507

Company Information

United States

Product Details

This product calibration solution can be used for correction by ACL TOP Family when performing Apixaban's Liquid Anti-Xa test. This product quality control liquid can be used for quality control when ACL TOP Family conducts Apixaban's Liquid Anti-Xa test.

A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical); A.1150 calibration

import

Dates and Status

Jul 18, 2018

Jul 18, 2028