ANVISA registration
Kit de Detecção Multiplex COVID-19 - nCoV-VM
Registration 82202950005. CORONAVÍRUS
Registration details
| Registration number | 82202950005 |
|---|---|
| Application number | 25351531115202214 |
| Technical name | CORONAVÍRUS |
| Risk class | III |
| Published on | 30/05/2022 |
| Validity | Valid until 30/05/2032 |
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
82202950004VERI-Q PREP M16 16TU-DWB
82202950006Veri Q PREP M16 16TU-DST
82202950007Source: 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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