INFLIXIMAB (IFX) - ANVISA Registration 80464810919
Access comprehensive regulatory information for INFLIXIMAB (IFX) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80464810919 and manufactured by IMMUNDIAGNOSTIK AG. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 4 companies making the same product including PROGENIKA BIOPHARMA S.L., BIOSYNEX SA, and 4 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.
Device Details
Registration Details
80464810919
25351040334202523
09377976000152
Company Information
Dates and Status
May 05, 2025
VIGENTE
09/18/2025 19:00:01
INFLIXIMAB (IFX)
LISA-TRACKER INFLIXIMAB
BIOSYNEX SA
10338930321
Aug 05, 2024
INFLIXIMAB (IFX)
Família AFIAS Infliximab
BODITECH MED INC.
10350840426
Oct 20, 2022
INFLIXIMAB (IFX)
PROMONITOR IFX
PROGENIKA BIOPHARMA S.L.
80134860242
Jul 03, 2017
INFLIXIMAB (IFX)
Quantum Blue® Infliximab
BUHLMANN LABORATORIES AG
80102511760
Mar 27, 2017

