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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.

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2560d5303da34653a886734f22fe6abd
Registration Details
Taiwan FDA Registration: 2560d5303da34653a886734f22fe6abd
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Device Details

Reagent for the A-site typing of LFD, human leukocyte antigen
TW: ่ŠๅฏŒๅฏๅพทไบบ้กž็™ฝ่ก€็ƒๆŠ—ๅŽŸAไฝ้ปžๅˆ†ๅž‹่ฉฆๅŠ‘
Risk Class 2

Registration Details

2560d5303da34653a886734f22fe6abd

DHA05602720100

Company Information

United States

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

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