ANVISA registration

Família de Teste Rápido do Antígeno SARS-CoV-2 (Swab Nasal) para Autoteste

Registration 81325990203. AUTOTESTE PARA ANTÍGENO DO SARS-COV-2 (CORONAVÍRUS)

Registration details

Registration number81325990203
Application number25351052638202291
Technical nameAUTOTESTE PARA ANTÍGENO DO SARS-COV-2 (CORONAVÍRUS)
Risk classIII
Published on18/04/2022
ValidityValid until 18/04/2032

Registration holder

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

Manufacturer

  • ACRO BIOTECH, INC. (MONTCLAIR) ESTADOS UNIDOS DA AMÉRICA

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.

Next step

Medical device registration with ANVISA

HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.

Speak to a specialist