ANTI-INFLIXIMAB (IFX) ANTIBODIES - ANVISA Registration 10338930315
Access comprehensive regulatory information for ANTI-INFLIXIMAB (IFX) ANTIBODIES in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 10338930315 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, 2 companies making the same product including BODITECH MED INC., 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
10338930315
25351369547202453
93741726000166
Company Information
Dates and Status
Jul 22, 2024
VIGENTE
09/18/2025 19:00:01
ANTICORPOS ANTI-INFLIXIMAB (IFX)
Famรญlia AFIAS Total Anti-Infliximab
BODITECH MED INC.
10350840430
Nov 07, 2022
ANTICORPOS ANTI-INFLIXIMAB (IFX)
Famรญlia AFIAS Free Anti-Infliximab
BODITECH MED INC.
10350840427
Oct 27, 2022
ANTICORPOS ANTI-INFLIXIMAB (IFX)
Quantum Blueยฎ Anti-Infliximab
Not specified
80102512585
Sep 24, 2020
ANTICORPOS ANTI-INFLIXIMAB (IFX)
PROMONITOR ANTI-IFX
PROGENIKA BIOPHARMA S.L.
80134860239
Jul 03, 2017

