K-Arthur Fibrinogen Analysis Reagent - Taiwan Registration 3349393d3250fe698806d29d04c9589f

Access comprehensive regulatory information for K-Arthur Fibrinogen Analysis Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3349393d3250fe698806d29d04c9589f and manufactured by KAMIYA BIOMEDICAL COMPANY. The authorized representative in Taiwan is REDOX BIOMEDICINE CO., LTD..

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