ANVISA registration

Família Tell Me Fast Teste para Detecção de Anticorpos IgG/IgM do Novo Coronavírus (COVID-19)

Registration 81325990122. CORONAVÍRUS

Registration details

Registration number81325990122
Application number25351910386202062
Technical nameCORONAVÍRUS
Risk classIII
Published on17/09/2020
ValidityValid until 17/09/2030

Registration holder

Legal nameQR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA
CNPJ19.933.144/0001-29

Manufacturer

  • BIOCAN DIAGNOSTICS INC. CANADÁ

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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Medical device registration with ANVISA

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