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Levercord Human White Blood Cell Antibody Screening Reagent - Taiwan Registration aa440da30ffab4ec8da3e3c8b1e75e03

Access comprehensive regulatory information for Levercord Human White Blood Cell Antibody Screening Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa440da30ffab4ec8da3e3c8b1e75e03 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. 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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Registration Details
Taiwan FDA Registration: aa440da30ffab4ec8da3e3c8b1e75e03
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Device Details

Levercord Human White Blood Cell Antibody Screening Reagent
TW: ่ŠๅฏŒๅฏๅพทไบบ้กž็™ฝ่ก€็ƒๆŠ—้ซ”็ฏฉๆชข่ฉฆๅŠ‘
Risk Class 2

Registration Details

aa440da30ffab4ec8da3e3c8b1e75e03

DHA00602308903

Company Information

United States

Product Details

This product is a qualitative reagent for the detection of human type I and type II HLA antibodies.

B Hematology, pathology, and genetics

B.0001 Human leukocyte antigen typing test system

import

Dates and Status

Jan 16, 2012

Jan 16, 2027