CONFIRMATORY ANTIBODY FOR HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 (HIV 1) - ANVISA Registration 80020690099
Access comprehensive regulatory information for CONFIRMATORY ANTIBODY FOR HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 (HIV 1) in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80020690099 and manufactured by BIO-RAD. The registration is held by BIO-RAD LABORATORIOS BRASIL LTDA with validity until Oct 14, 2027.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 1 companies making the same product including MP BIOMEDICALS ASIA PACIFIC PTE LTD, and 2 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.
Related Devices (2)
Registration Details
80020690099
253510380720115
03188198000177
Company Information
Dates and Status
Oct 14, 2002
14/10/2027
09/18/2025 19:00:01
ANTICORPO CONFIRMATÓRIO PARA VÍRUS DE IMUNODEFICIÊNCIA HUMANA TIPO 1 (HIV 1)
HIV-1 BLOT 1.3 TESTE WESTERN BLOT
Not specified
80313210023
Jun 01, 2020
ANTICORPO CONFIRMATÓRIO PARA VÍRUS DE IMUNODEFICIÊNCIA HUMANA TIPO 1 (HIV 1)
HIV-1 BLOT 1.3 TESTE WESTERN BLOT
MP BIOMEDICALS ASIA PACIFIC PTE LTD
80313210023
Jun 01, 2020