ANVISA registration

Teste Rápido de Anticorpo Neutralizante VERI-Q SARS-CoV-2 rCoV-RN

Registration 82202950014. CORONAVÍRUS

Registration details

Registration number82202950014
Application number25351178303202200
Technical nameCORONAVÍRUS
Risk classIII
Published on22/05/2023
ValidityValid until 22/05/2033

Registration holder

Legal nameMICO BIOMED DO BRASIL LTDA
CNPJ40.749.573/0001-37

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

82202950001

Veri-Q PREP M16 - 16TU-CV19

82202950002

KIT DE COLETA DE SALIVA - VERI-Q

82202950003

Veri-Q PREP M16 - G2-16TU - Dispositivo Extrator de Ácido Nucleico

82202950004

Kit de Detecção Multiplex COVID-19 - nCoV-VM

82202950005

VERI-Q PREP M16 16TU-DWB

82202950006

Source: ANVISA

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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