ANVISA registration

Família ProGRP

Registration 10287411800. PEPTÍDEO DE LIBERAÇÃO DE GASTRINA

Registration details

Registration number10287411800
Application number25351091958202690
Technical namePEPTÍDEO DE LIBERAÇÃO DE GASTRINA
Risk classIII
Published on29/06/2026
ValidityValid until 29/06/2036

Registration holder

Legal nameROCHE DIAGNÓSTICA BRASIL LTDA
CNPJ30.280.358/0001-86

Manufacturer

  • ROCHE DIAGNOSTICS GMBH ALEMANHA

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