"Neo-Kehua" Myris human T-lymphotropic virus type 1 and type 2 antibody test reagent - Taiwan Registration 2be58bffce1614e695dc4a95acc3007b
Access comprehensive regulatory information for "Neo-Kehua" Myris human T-lymphotropic virus type 1 and type 2 antibody test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2be58bffce1614e695dc4a95acc3007b and manufactured by DIASORIN S.P.A. UK BRANCH. The authorized representative in Taiwan is NEW SCIENTIFIC EQUIPMENT CO., LTD..
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.
Device Details
Product Details
Enzyme immunoassay for human T-lymphophilic virus type I and type II antibodies (HTLV-I and HTLV-II) in human serum or plasma for screening.
B Hematology, pathology, and genetics
B.4020 Analysis of specific tests
import
Dates and Status
Jul 19, 2012
Aug 12, 2022
Apr 12, 2024
Cancellation Information
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