ANVISA registration
AeroDR Maxmove
Registration 80101380025. Sistema de raios-X de diagnóstico multimodalidade, móvel
Registration details
| Registration number | 80101380025 |
|---|---|
| Application number | 25351354162202491 |
| Technical name | Sistema de raios-X de diagnóstico multimodalidade, móvel |
| Risk class | III |
| Published on | 19/08/2024 |
| Validity | Valid until 19/08/2034 |
Registration holder
| Legal name | KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDA |
|---|---|
| CNPJ | 71.256.283/0001-85 |
Manufacturer
- SEDECAL - SOCIEDAD ESPANOLA DE ELETROMEDICINA Y CALIDADE S.A ESPANHA
Other registrations held by KONICA MINOLTA HEALTHCARE DO BRASIL INDUSTRIA DE EQUIPAMENTOS MEDICOS LTDAview 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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