DirectCHECK Whole Blood Control - Taiwan Registration 670170a433c3a65761a4ff7f8170874f
Access comprehensive regulatory information for DirectCHECK Whole Blood Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 670170a433c3a65761a4ff7f8170874f and manufactured by Accriva Diagnostics Inc.. The authorized representative in Taiwan is Werfen Taiwan Limited.
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Device Details
Registration Details
670170a433c3a65761a4ff7f8170874f
Ministry of Health Medical Device Import No. 030087
DHA05603008709
Product Details
Quality control materials for monitoring Hammock microcoagulation time analyzers.
A Clinical chemistry and clinical toxicology
A1660 Quality Control Materials (Analytical and Non-Analytical)
Imported from abroad
Dates and Status
Oct 24, 2017
Oct 24, 2027

