CONFIRMATORY ANTIBODY FOR HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 (HIV 1) - ANVISA Registration 80313210023
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 80313210023 and manufactured by manufacturer not specified. The registration is held by MP BIOMEDICALS DO BRASIL LTDA with validity until Jan 30, 2027.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 1 companies making the same product including BIO-RAD, 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
80313210023
25351348241202030
07776689000190
Company Information
Dates and Status
Jun 01, 2020
30/01/2027
09/18/2025 19:00:01
ANTICORPO CONFIRMATÓRIO PARA VÍRUS DE IMUNODEFICIÊNCIA HUMANA TIPO 1 (HIV 1)
NEW LAV BLOT I
BIO-RAD
80020690099
Oct 14, 2002
ANTICORPO CONFIRMATÓRIO PARA VÍRUS DE IMUNODEFICIÊNCIA HUMANA TIPO 1 (HIV 1)
NEW LAV BLOT I
Not specified
80020690099
Oct 14, 2002

