"Neo-branched" human immunodeficiency virus antibody Western ink dot method 2.2 test reagent - Taiwan Registration 0c60f1c32c1bea4537d9118bd3aded83
Access comprehensive regulatory information for "Neo-branched" human immunodeficiency virus antibody Western ink dot method 2.2 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 0c60f1c32c1bea4537d9118bd3aded83 and manufactured by MP BIOMEDICALS ASIA PACIFIC PTE. LTD.. 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
Western ink dot testing for HIV-1 and HIV-2 antibodies in human serum or plasma can be used as a confirmation reagent for HIV-1, and HIV-2 positive patients should be confirmed with other reagents.
B Hematology, pathology, and genetics
B.4020 Analysis of specific tests
import
Dates and Status
Aug 16, 2012
Apr 07, 2014
Nov 15, 2016
Cancellation Information
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