ANTI-ADALIMUMAB ANTIBODIES (ADL) - ANVISA Registration 80134860235
Access comprehensive regulatory information for ANTI-ADALIMUMAB ANTIBODIES (ADL) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80134860235 and manufactured by PROGENIKA BIOPHARMA S.L.. The registration is held by GRIFOLS BRASIL LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 3 companies making the same product including IMMUNDIAGNOSTIK, BODITECH MED INC., 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
80134860235
25351310767201695
02513899000171
Company Information
Dates and Status
Jul 03, 2017
VIGENTE
09/18/2025 19:00:01
ANTICORPOS ANTI-ADALIMUMAB (ADL)
Famรญlia AFIAS Free Anti-Adalimumab
BODITECH MED INC.
10350840429
Nov 07, 2022
ANTICORPOS ANTI-ADALIMUMAB (ADL)
Quantum Blueยฎ Anti-Adalimumab
BUHLMANN LABORATORIES AG
80102512669
Jun 10, 2021
ANTICORPOS ANTI-ADALIMUMAB (ADL)
IDKmonitorยฎ Adalimumab free ADA ELISA
IMMUNDIAGNOSTIK
80464810759
Feb 11, 2021
ANTICORPOS ANTI-ADALIMUMAB (ADL)
IDKmonitorยฎ Adalimumab total ADA ELISA
IMMUNDIAGNOSTIK
80464810760
Feb 11, 2021

