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LFCO type 2 human leukocyte antibody identification reagent - Taiwan Registration 652f6c83d0a8063cce77438ed863a8d6

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 652f6c83d0a8063cce77438ed863a8d6 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.

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652f6c83d0a8063cce77438ed863a8d6
Registration Details
Taiwan FDA Registration: 652f6c83d0a8063cce77438ed863a8d6
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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

Registration Details

652f6c83d0a8063cce77438ed863a8d6

DHA00602469909

Company Information

United States

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, 2013

May 24, 2028

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