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Cimosir protein S reagent - Taiwan Registration 11c1945c49d777ca81fa9288b2d7b735

Access comprehensive regulatory information for Cimosir protein S reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 11c1945c49d777ca81fa9288b2d7b735 and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is Werfen Taiwan Limited.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including INSTRUMENTATION LABORATORY CO., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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11c1945c49d777ca81fa9288b2d7b735
Registration Details
Taiwan FDA Registration: 11c1945c49d777ca81fa9288b2d7b735
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Device Details

Cimosir protein S reagent
TW: ๅธŒๆ‘ฉ่ฅฟ็ˆพ่›‹็™ฝS่ฉฆๅŠ‘
Risk Class 2

Registration Details

11c1945c49d777ca81fa9288b2d7b735

DHA00602432000

Company Information

United States

Product Details

The concentration of protein S in human citrate acidated plasma was determined in the IL automatic coagulation instrument system (ACL TOP Family, ACL ELITE/ELITE PRO/8/9/1000, ACL Advance and ACL classic (100-7000)).

B Hematology, pathology, and genetics

B.7290 factor deficiency test

import

Dates and Status

Jan 18, 2013

Jan 18, 2028

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