"Leica" Bond Ready-to-Use Primary Antibody Cytokeratin 20 (Ks20.8) (Non-Sterile) - Taiwan Registration 698d4fe8a3b1eaffe9ff180936557fc9
Access comprehensive regulatory information for "Leica" Bond Ready-to-Use Primary Antibody Cytokeratin 20 (Ks20.8) (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 698d4fe8a3b1eaffe9ff180936557fc9 and manufactured by LEICA BIOSYSTEMS NEWCASTLE LTD.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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Device Details
Registration Details
698d4fe8a3b1eaffe9ff180936557fc9
Ministry of Health Medical Device Import No. 020252
DHA09402025202
Product Details
Limited to the first level identification range of immunopathological histochemical reagents and kits (B.1860) of the Measures for the Administration of Medical Devices.
B Hematology and pathology devices
B1860 Immunopathological histochemical reagents and kits
Imported from abroad
Dates and Status
Mar 29, 2019
Mar 29, 2024

