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LFCO type 2 human leukocyte antibody identification reagent - Taiwan Registration 9728ec423ba61c6235d9e382782ebf30

Access comprehensive regulatory information for LFCO type 2 human leukocyte antibody identification reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9728ec423ba61c6235d9e382782ebf30 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.

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9728ec423ba61c6235d9e382782ebf30
Registration Details
Taiwan FDA Registration: 9728ec423ba61c6235d9e382782ebf30
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Device Details

LFCO type 2 human leukocyte antibody identification reagent
TW: ่ŠๅฏŒๅฏๅพท็ฌฌไบŒๅž‹ไบบ้กž็™ฝ่ก€็ƒๆŠ—้ซ”้‘‘ๅฎš่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

9728ec423ba61c6235d9e382782ebf30

DHA00602363504

Company Information

Product Details

Microbead qualitative immunoassay for detection of human leukocyte population reactive IgG antibodies (PRAs) type II.

B Hematology, pathology, and genetics

B.0001 Human leukocyte antigen typing test system

import

Dates and Status

May 24, 2012

May 24, 2017

Jul 21, 2016

Cancellation Information

Logged out

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