INFLIXIMAB (IFX) - ANVISA Registration 10338930321
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 10338930321 and manufactured by BIOSYNEX SA. The registration is held by EUROIMMUN BRASIL MEDICINA DIAGNOSTICA 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 IMMUNDIAGNOSTIK AG, PROGENIKA BIOPHARMA S.L., 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
10338930321
25351369552202466
93741726000166
Company Information
Dates and Status
Aug 05, 2024
VIGENTE
09/18/2025 19:00:01
INFLIXIMAB (IFX)
IDKmonitorยฎ Infliximab drug level ELISA
IMMUNDIAGNOSTIK AG
80464810919
May 05, 2025
INFLIXIMAB (IFX)
Famรญlia AFIAS Infliximab
BODITECH MED INC.
10350840426
Oct 20, 2022
INFLIXIMAB (IFX)
PROMONITOR IFX
PROGENIKA BIOPHARMA S.L.
80134860242
Jul 03, 2017
INFLIXIMAB (IFX)
Quantum Blueยฎ Infliximab
BUHLMANN LABORATORIES AG
80102511760
Mar 27, 2017

