Abbott "Marisi" human immunodeficiency virus antibody test reagent - Taiwan Registration 532c7c29bb287f5fcc5d9fbd20fb10e7
Access comprehensive regulatory information for Abbott "Marisi" human immunodeficiency virus 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 532c7c29bb287f5fcc5d9fbd20fb10e7 and manufactured by DIASORIN S.P.A. UK BRANCH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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 and type 2 antibodies in human serum or plasma for screening.
B Hematology, pathology, and genetics
import
Dates and Status
Aug 08, 2005
Aug 08, 2027

