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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 CELER BIOTECNOLOGIA S/Aremove
58 registrations
| Product | Registration holder | Class | Validity |
|---|---|---|---|
| Finecare T3 Teste Quantitativo80537410042 | CELER BIOTECNOLOGIA S/A | II | Valid |
| Finecare T4 Teste Quantitativo80537410043 | CELER BIOTECNOLOGIA S/A | II | Valid |
| Finecare TSH Teste Quantitativo80537410044 | CELER BIOTECNOLOGIA S/A | II | Valid |
| POLARIS80537410002 | CELER BIOTECNOLOGIA S/A | II | Valid |
| ROTAVÍRUS TESTE RÁPIDO CELER80537410127 | CELER BIOTECNOLOGIA S/A | II | Valid |
| SPECTRUM80537410001 | CELER BIOTECNOLOGIA S/A | II | Valid |
| UCARE 6000 ANALISADOR AUTOMÁTICO DE GASES SANGUÍNEOS80537410116 | CELER BIOTECNOLOGIA S/A | II | Valid |
| UCARE 6000 SOLUTION PACK80537410117 | CELER BIOTECNOLOGIA S/A | II | Valid |
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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