ANVISA registration

COVID-19-CHECK-1 ANTIGEN® Self -Testing

Registration 81086830047. AUTOTESTE PARA ANTÍGENO DO SARS-COV-2 (CORONAVÍRUS)

Registration details

Registration number81086830047
Application number25351052652202294
Technical nameAUTOTESTE PARA ANTÍGENO DO SARS-COV-2 (CORONAVÍRUS)
Risk classIII
Published on30/03/2022
ValidityValid until 30/03/2032

Registration holder

Legal nameFASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA
CNPJ20.037.992/0001-39

Manufacturer

  • VEDALAB FRANÇA

Other registrations held by FASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDAview all

GLIADIN IgM ELISA

81086830002

C- PEPTIDE CHECK 1

81086830003

COVID-19-CHECK -1

81086830004

DUO INFLUENZA A+B -CHECK-1

81086830005

STREP B CHECK-1

81086830006

STREP A CHECK-1

81086830007

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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