ANVISA registration

Família de Teste rápido combinado em cassete para GDH + Toxina A + Toxina B da Clostridium difficile (Fezes)

Registration 81325990402. PARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE III

Registration details

Registration number81325990402
Application number25351103898202584
Technical namePARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE III
Risk classIII
Published on13/10/2025
ValidityValid until 13/10/2035

Registration holder

Legal nameQR CONSULTING, IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS LTDA
CNPJ19.933.144/0001-29

Manufacturer

  • ACRO BIOTECH, INC. (MONTCLAIR) 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