RAMP D-dimer Assay - Taiwan Registration 73323c6332e221e4ffdc5f3fab3e0ac1
Access comprehensive regulatory information for RAMP D-dimer Assay in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 73323c6332e221e4ffdc5f3fab3e0ac1 and manufactured by RESPONSE BIOMEDICAL CORPORATION. The authorized representative in Taiwan is RECHI CO., LTD..
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Device Details
Registration Details
73323c6332e221e4ffdc5f3fab3e0ac1
Ministry of Health Medical Device Import No. 027885
DHA05602788501
Product Details
This product is used for the quantitative detection of human fiber degradation product (FDP) dimer in EDTA anticoagulant whole blood collection blood collection blood collection blood spectrum blood plasma plasma quantitative coagulation blood spectrum blood plasma blood plasma quantitative coagulation blood collection blood plasma This product is an in vitro diagnostic reagent.
B Hematology and pathology devices
B7320 Fibrinogen Fibrinogen Breakdown Product Analysis
Imported from abroad
Dates and Status
Oct 20, 2015
Oct 20, 2025

