"Neoscienceization" Myorest Human Immunodeficiency Virus Antibody Reagent - Taiwan Registration bbffe771c150f6a154cedd8a562bd0b9
Access comprehensive regulatory information for "Neoscienceization" Myorest Human Immunodeficiency Virus Antibody Reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bbffe771c150f6a154cedd8a562bd0b9 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 statutory testing of human immunodeficiency virus type 1 (HIV-1, HIV-1O subtype) and type II (HIV-2) antibodies in human serum or plasma for screening.
B Hematology, pathology, and genetics
B.4020 Analysis of specific tests
import
Dates and Status
Jul 16, 2012
Aug 08, 2022
Apr 12, 2024
Cancellation Information
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