ANVISA registration
PLEXA DF-1 - ELETRODO DE FIXAÇÁO ATIVA PARA CARDIOVERSOR DESFIBRILADOR IMPLANTÁVEL condicional para Ressonância Magnética (ProMRI).
Registration 80224390267. CABO/ELETRODO PARA DESFIBRILAÇÃO ENDOCARDÍACA
Registration details
| Registration number | 80224390267 |
|---|---|
| Application number | 25351537615201601 |
| Technical name | CABO/ELETRODO PARA DESFIBRILAÇÃO ENDOCARDÍACA |
| Risk class | IV |
| Published on | 30/01/2017 |
| Validity | Valid until 30/01/2037 |
Registration holder
| Legal name | BIOTRONIK COMERCIAL MÉDICA LTDA. |
|---|---|
| CNPJ | 50.595.271/0001-05 |
Manufacturer
- BIOTRONIK SE & CO KG ALEMANHA
Other registrations held by BIOTRONIK COMERCIAL MÉDICA LTDA.view all
Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this 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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