ANVISA registration

FAMÍLIA A2+F CONTROLE E CALIBRADOR

Registration 81733730025. HEMOGLOBINA SUBTIPO

Registration details

Registration number81733730025
Application number25351137963202575
Technical nameHEMOGLOBINA SUBTIPO
Risk classIII
Published on24/11/2025
ValidityValid until 24/11/2035

Registration holder

Legal nameTRINITY BIOTECH DO BRASIL COMERCIO E IMPORTACAO LTDA
CNPJ15.648.426/0002-04

Manufacturer

  • TRINITY BIOTECH PRIMUS CORPORATION DBA TRINITY BIOTECH 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