INFLUENZA A VIRUS - ANVISA Registration 80464810603
Access comprehensive regulatory information for INFLUENZA A VIRUS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80464810603 and manufactured by manufacturer not specified. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until Oct 08, 2028.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including R-BIOPHARM AG, NOVATEC IMMUNDIAGNOSTICA GMBH TECHNOLOGIE & WALDPARK, 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.
Related Devices (2)
Registration Details
80464810603
25351239332201861
09377976000152
Company Information
Dates and Status
Oct 08, 2018
08/10/2028
09/18/2025 19:00:01
VÍRUS INFLUENZA A
MICROPARTÍCULAS INFLUENZA A IgM (CLIA)
Not specified
80102513476
Jul 14, 2025
VÍRUS INFLUENZA A
MICROPARTÍCULAS INFLUENZA A IgM (CLIA)
AUTOBIO DIAGNOSTICS CO., LTD
80102513476
Jul 14, 2025
VÍRUS INFLUENZA A
Família VIASURE Flu Typing II Real Time PCR Detection Kit
CERTEST BIOTEC, S.L.
82149920029
Jun 12, 2023
VÍRUS INFLUENZA A
Família VIASURE Flu Typing II Real Time PCR Detection Kit
Not specified
82149920029
Jun 12, 2023
VÍRUS INFLUENZA A
Família Kit de Detecção por PCR em Tempo Real VIASURE Flu Tipo I
Not specified
82149920047
Jun 12, 2023

