ANVISA registration

QuickPROFILE COVID-19 Antigen Test Card

Registration 80464810788. CORONAVÍRUS

Registration details

Registration number80464810788
Application number25351021124202293
Technical nameCORONAVÍRUS
Risk classIII
Published on21/02/2022
ValidityValid until 21/02/2032

Registration holder

Legal nameARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA
CNPJ09.377.976/0001-52

Manufacturer

  • LUMIQUICK DIAGNOSTICS 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