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LFCO Human Leukocyte DRB 3, 4, 5 Site Typing Reagent - Taiwan Registration 16d44fddc8489b336e556e8b7ad46960

Access comprehensive regulatory information for LFCO Human Leukocyte DRB 3, 4, 5 Site Typing Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 16d44fddc8489b336e556e8b7ad46960 and manufactured by IMMUCOR GTI DIAGNOSTICS, INC.. The authorized representative in Taiwan is METEK LAB INC..

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16d44fddc8489b336e556e8b7ad46960
Registration Details
Taiwan FDA Registration: 16d44fddc8489b336e556e8b7ad46960
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Device Details

LFCO Human Leukocyte DRB 3, 4, 5 Site Typing Reagent
TW: ่ŠๅฏŒๅฏๅพทไบบ้กž็™ฝ่ก€็ƒๆŠ—ๅŽŸDRB 3,4,5ไฝ้ปžๅˆ†ๅž‹่ฉฆๅŠ‘
Risk Class 2

Registration Details

16d44fddc8489b336e556e8b7ad46960

DHA05602720202

Company Information

United States

Product Details

DNA typing of human leukocyte antigen dual genes DRB 3,4,5 is determined by sequence-specific oligonucleoacid fragment analysis (SSO), which 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