Reagent for the A-site typing of LFD, human leukocyte antigen - Taiwan Registration 2560d5303da34653a886734f22fe6abd
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 2560d5303da34653a886734f22fe6abd and manufactured by IMMUCOR GTI 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 GEN-PROBE TRANSPLANT 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
The determination of DNA typing of human leukocyte antigen dual gene A by specific sequence oligonucleoacid fragment analysis (SSO) is used with a Luminex instrument.
B Hematology, pathology, and genetics
B.0001 Human leukocyte antigen typing test system
import
Dates and Status
Apr 09, 2015
Apr 09, 2030

