INFLUENZA A VIRUS - ANVISA Registration 81905510052
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 81905510052 and manufactured by INSTITUT VIRION\SERION GMBH. The registration is held by GMRB COMÉRCIO DE PRODUTOS MÉDICOS E DIAGNÓSTICOS LTDA with validity until Mar 10, 2034.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including NOVATEC IMMUNDIAGNOSTICA GMBH TECHNOLOGIE & WALDPARK, R-BIOPHARM AG, 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
81905510052
25351249731202216
34255136000164
Company Information
Dates and Status
Nov 28, 2022
10/03/2034
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

