ANVISA registration

VIDAS® TBI (GFAP, UCH-L1)

Registration 10158120751. PARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE II

Registration details

Registration number10158120751
Application number25351397013202417
Technical namePARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE II
Risk classII
Published on07/10/2024
ValidityIndefinite validity

Registration holder

Legal nameBIOMERIEUX BRASIL COMERCIO DE PRODUTOS LABORATORIAIS LTDA
CNPJ33.040.635/0001-71

Manufacturer

  • BIOMERIEUX SA FRANÇA

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