ADALIMUMAB (ADL) - ANVISA Registration 10350840428
Access comprehensive regulatory information for ADALIMUMAB (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 10350840428 and manufactured by BODITECH MED INC.. The registration is held by BIOSYS LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 3 companies making the same product including BUHLMANN LABORATORIES AG, PROGENIKA BIOPHARMA S.A., and 3 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.

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Registration Details
10350840428
25351406589202211
02220795000179
Company Information
Dates and Status
Oct 27, 2022
VIGENTE
09/18/2025 19:00:01
ANTI-ADALIMUMAB ANTIBODIES (ADL)
FamĂlia AFIAS Free Anti-Adalimumab
BODITECH MED INC.
10350840429
Nov 07, 2022
INFLIXIMAB (IFX)
FamĂlia AFIAS Infliximab
BODITECH MED INC.
10350840426
Oct 20, 2022
ANTI-INFLIXIMAB (IFX) ANTIBODIES
FamĂlia AFIAS Free Anti-Infliximab
BODITECH MED INC.
10350840427
Oct 27, 2022
ANTI-INFLIXIMAB (IFX) ANTIBODIES
FamĂlia AFIAS Total Anti-Infliximab
BODITECH MED INC.
10350840430
Nov 07, 2022
INTERLEUKINS
FamĂlia AFIAS IL-6
BODITECH MED INC.
10350840459
Jul 08, 2024
ADALIMUMAB (ADL)
IDKmonitor® Adalimumab drug level ELISA
IMMUNDIAGNOSTIK
80464810758
Feb 04, 2021
ADALIMUMAB (ADL)
BÜHLMANN Quantum Blue® Adalimumab
BUHLMANN LABORATORIES AG
80102512062
Jun 25, 2018
ADALIMUMAB (ADL)
PROMONITOR-ADL
PROGENIKA BIOPHARMA S.A.
80134860240
Jul 03, 2017