HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 AND TYPE 2 (HIV) ANTIGEN AND ANTIBODY - ANVISA Registration 10009010470

Access comprehensive regulatory information for HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 AND TYPE 2 (HIV) ANTIGEN AND ANTIBODY in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10009010470 and manufactured by LABTEST DIAGNOSTICA S/A. The registration is held by LABTEST DIAGNOSTICA S/A with validity until Oct 21, 2034.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including ABBOTT GMBH, Eco Diagnostica Ltda, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.