ANTIBODY FOR HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 AND TYPE 2 (HIV 1 AND HIV 2) - ANVISA Registration 81077790013

Access comprehensive regulatory information for ANTIBODY FOR HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 AND TYPE 2 (HIV 1 AND HIV 2) in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 81077790013 and manufactured by REM INDUSTRIA E COMERCIO SOCIEDADE UNIPESSOAL LTDA. The registration is held by REM INDUSTRIA E COMERCIO SOCIEDADE UNIPESSOAL LTDA with validity until Apr 30, 2028.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including WAMA PRODUTOS PARA LABORATORIO LTDA, 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.