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Medical device registration with ANVISA
Search by number, product, registration holder or CNPJ. The data comes from ANVISA's open data publications and is updated here daily.
Registrations held by MICO BIOMED DO BRASIL LTDAremove
6 registrations
| Product | Registration holder | Class | Validity |
|---|---|---|---|
| Kit de Detecção Multiplex COVID-19 - nCoV-VM82202950005 | MICO BIOMED DO BRASIL LTDA | III | 30/05/2032 |
| Kit de detecção multiplex A/B de COVID-19 e gripe82202950010 | MICO BIOMED DO BRASIL LTDA | III | 11/07/2032 |
| VERI-Q PCR 316 - MTB-QS - Mycobacterium tuberculosis Detection Kit82202950012 | MICO BIOMED DO BRASIL LTDA | III | 08/08/2032 |
| Teste Rápido de Anticorpo Neutralizante VERI-Q SARS-CoV-2 rCoV-RN82202950014 | MICO BIOMED DO BRASIL LTDA | III | 22/05/2033 |
| Covid-19 Ag Rapid Test - MIS-COV-0282202950015 | MICO BIOMED DO BRASIL LTDA | III | 22/05/2033 |
| Kit Veri-Q pan-Dengue virus Detection82202950024 | MICO BIOMED DO BRASIL LTDA | III | 02/10/2033 |
Source: ANVISA open data, medical device file. The database provides registration validity, rather than registration status: a registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.
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HSC manages medical device registration with ANVISA, from risk classification to monitoring the application.
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