Reagent for the A-site typing of LFD, human leukocyte antigen - Taiwan Registration 7ce53c74c006d56b95b58c4ba9e31f3b
Access comprehensive regulatory information for Reagent for the A-site typing of LFD, human leukocyte antigen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7ce53c74c006d56b95b58c4ba9e31f3b and manufactured by GEN-PROBE TRANSPLANT DIAGNOSTICS, INC.. The authorized representative in Taiwan is METEK LAB INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including IMMUCOR GTI DIAGNOSTICS, INC., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Device Details
Product Details
็ฌฌไธๅ่็ฌฌไบๅไบบ้ก็ฝ่ก็ๆๅ(HLA)ๅฐๅถๅบๅ (allele)ๅปๆฐงๆ ธ็ณๆ ธ้ ธ(DNA)ๅๅ.
B Hematology, pathology, and genetics
B.0001 Human leukocyte antigen typing test system
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Dates and Status
Feb 06, 2007
Feb 06, 2017
Jul 21, 2016
Cancellation Information
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