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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 ROCHE DIAGNÓSTICA BRASIL LTDAremove
306 registrations
| Product | Registration holder | Class | Validity |
|---|---|---|---|
| cobas® 4800 HPV - Amplification/Detection Kit10287410898 | ROCHE DIAGNÓSTICA BRASIL LTDA | III | 04/10/2035 |
| cobas® 4800 HPV Controls Kit10287410894 | ROCHE DIAGNÓSTICA BRASIL LTDA | III | 21/09/2035 |
| cobas® EGFR Mutation Test10287410970 | ROCHE DIAGNÓSTICA BRASIL LTDA | III | 12/03/2027 |
| cobas® KRAS Mutation Test10287410969 | ROCHE DIAGNÓSTICA BRASIL LTDA | III | 02/01/2037 |
| cobas® PIK3CA Mutation Test10287411578 | ROCHE DIAGNÓSTICA BRASIL LTDA | III | 12/07/2031 |
| mySugr Glucose Insights10287411797 | ROCHE DIAGNÓSTICA BRASIL LTDA | III | 15/06/2036 |
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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