PakPlus - Taiwan Registration 0d1ea35fa01e6c5cef6b3119cb87e4ae
Access comprehensive regulatory information for PakPlus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0d1ea35fa01e6c5cef6b3119cb87e4ae and manufactured by IMMUCOR GTI DIAGNOSTICS, INC.. The authorized representative in Taiwan is METEK LAB INC..
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Device Details
Registration Details
0d1ea35fa01e6c5cef6b3119cb87e4ae
Ministry of Health Medical Device Import No. 028495
DHA05602849506
Product Details
Solid phase enzyme immunoassay was used to screen for type I HLA and platelet glycoprotein IV. antibodies, and platelet glycoprotein II.b/III.a, I.B/I.X, I.A/II.A PLEOMORPHIC ANTIGEN DETERMINANT ANTIBODIES.
B Hematology and pathology devices
B4020 Analyze specific reagents
Imported from abroad
Dates and Status
Sep 21, 2016
Sep 21, 2026