ANVISA registration
Sistema Automático de Extração do Ácido Nucleico VERI-Q B16
Registration 82202950022. Instrumento para preparo e processamento de amostras fase pré-analítica
Registration details
| Registration number | 82202950022 |
|---|---|
| Application number | 25351099166202400 |
| Technical name | Instrumento para preparo e processamento de amostras fase pré-analítica |
| Risk class | I |
| Published on | 25/03/2024 |
| Validity | Indefinite validity |
Registration holder
| Legal name | MICO BIOMED DO BRASIL LTDA |
|---|---|
| CNPJ | 40.749.573/0001-37 |
Manufacturer
- MICO BIOMED CO.,LTD. CORÉIA DO SUL
Other registrations held by MICO BIOMED DO BRASIL LTDAview all
Veri-Q PCR 316 - QD-P100 - Equipamento para Amplificação de Material Genético
82202950001Veri-Q PREP M16 - 16TU-CV19
82202950002KIT DE COLETA DE SALIVA - VERI-Q
82202950003Veri-Q PREP M16 - G2-16TU - Dispositivo Extrator de Ácido Nucleico
82202950004Kit de Detecção Multiplex COVID-19 - nCoV-VM
82202950005VERI-Q PREP M16 16TU-DWB
82202950006Source: 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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