Armas Automated D Duplex Test Set - Taiwan Registration 7de2bc6fdcb3ca0100d3752664935426
Access comprehensive regulatory information for Armas Automated D Duplex Test Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7de2bc6fdcb3ca0100d3752664935426 and manufactured by TRINITY BIOTECH PLC. The authorized representative in Taiwan is BioChain Co., Ltd..
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Device Details
Product Details
Quantification of fibrin schizome products containing D-dimers in human plasma using an automated coagulation analyzer.
B Hematology, pathology, and genetics
B.7320 Fibrinogen/Fibrinolysis Product Analysis
import
Dates and Status
Nov 22, 2006
Nov 22, 2011
Nov 09, 2012
Cancellation Information
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