ANVISA registration

QuickProfile Zika Virus IgG/IgM Combo Test

Registration 80464810706. IMUNOGLOBULINA IgM/IgG PARA VÍRUS ZIKA

Registration details

Registration number80464810706
Application number25351524379202041
Technical nameIMUNOGLOBULINA IgM/IgG PARA VÍRUS ZIKA
Risk classIV
Published on08/09/2020
ValidityValid until 08/09/2030

Registration holder

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

Manufacturer

  • LUMIQUICK DIAGNOSTICS, INC. 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