ANVISA registration

ZIKA VIRCLIA® IgM MONOTEST

Registration 81816720068. IMUNOGLOBULINA M (IgM) PARA VÍRUS ZIKA

Registration details

Registration number81816720068
Application number25351754353202379
Technical nameIMUNOGLOBULINA M (IgM) PARA VÍRUS ZIKA
Risk classIV
Published on23/09/2024
ValidityValid until 23/09/2034

Registration holder

Legal nameALIFAX BRASIL COMER., EXP., IMP., DIST. DE EQUIPAMENTOS E REAGENTES PARA DIAGNOSTICO IN VITRO LTDA
CNPJ31.167.508/0001-02

Manufacturer

  • VIRCELL S.L. ESPANHA

Other registrations held by ALIFAX BRASIL COMER., EXP., IMP., DIST. DE EQUIPAMENTOS E REAGENTES PARA DIAGNOSTICO IN VITRO LTDAview all

FAMÍLIA DE ANALISADORES AUTOMÁTICOS PARA CULTURA DE MICRO-ORGANISMOS

81816720000

Família de Teste de Suscetibilidade Antimicrobiana CLSI

81816720001

Família de Teste de Suscetibilidade Antimicrobiana EUCAST

81816720002

FAMÍLIA DE ANALISADORES AUTOMÁTICOS PARA VELOCIDADE DE HEMOSSEDIMENTAÇÃO (VHS)

81816720003

HB & L CULTURE KIT

81816720004

G-NF AST BROTH KIT

81816720005

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