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Cimosir protein S reagent - Taiwan Registration 21da739a2f2eb42b7b9e732832b37ea4

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 21da739a2f2eb42b7b9e732832b37ea4 and manufactured by INSTRUMENTATION LABORATORY CO.. The authorized representative in Taiwan is GRANT TECHNOLOGY CO., LTD..

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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21da739a2f2eb42b7b9e732832b37ea4
Registration Details
Taiwan FDA Registration: 21da739a2f2eb42b7b9e732832b37ea4
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Device Details

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

Registration Details

21da739a2f2eb42b7b9e732832b37ea4

DHA00601628400

Company Information

United States

Product Details

The concentration of Protein S in human citric plasma is determined by colorimetric method in the IL blood coagulation instrument system.

B Hematology, pathology, and genetics

B.5425 Versatile system for in vitro agglutination studies

Dates and Status

Mar 31, 2006

Mar 31, 2016

May 10, 2018

Cancellation Information

Logged out

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