ADALIMUMAB (ADL) - ANVISA Registration 80102512062
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 80102512062 and manufactured by BUHLMANN LABORATORIES AG. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS 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 PROGENIKA BIOPHARMA S.A., BODITECH MED INC., 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
80102512062
25351167716201874
04718143000194
Company Information
Dates and Status
Jun 25, 2018
VIGENTE
09/18/2025 19:00:01
INFLIXIMAB (IFX)
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80102511760
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ANTI-INFLIXIMAB (IFX) ANTIBODIES
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Not specified
80102512585
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ANTI-GANGLIOSIDE ANTIBODIES
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80102512136
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IMMUNOGLOBULIN G
IgG MONO
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80115310068
Aug 14, 2006
KAPPA/LAMBDA CHAIN
N ANTISORO Ig HUMANO/CADEIA L, TIPO LAMBDA
SIEMENS HEALTHCARE DIAGNÓSTICOS LTDA
10345161269
Aug 10, 2009
ADALIMUMAB (ADL)
Família AFIAS Adalimumab
BODITECH MED INC.
10350840428
Oct 27, 2022
ADALIMUMAB (ADL)
IDKmonitor® Adalimumab drug level ELISA
IMMUNDIAGNOSTIK
80464810758
Feb 04, 2021
ADALIMUMAB (ADL)
PROMONITOR-ADL
PROGENIKA BIOPHARMA S.A.
80134860240
Jul 03, 2017