"Siemens" C-reactive protein test kit - Taiwan Registration 1c6b859730e6e9d8eac2e838c4f49f8b
Access comprehensive regulatory information for "Siemens" C-reactive protein test kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1c6b859730e6e9d8eac2e838c4f49f8b and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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Device Details
Product Details
This product is intended for in vitro diagnostic use and is used with the Atellica CH Analyzer to quantify C-reactive protein (CRP) in human serum and plasma (lithium heparin).
C Immunology and microbiology
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Dates and Status
Dec 01, 2023
Dec 01, 2028