ANVISA registration

CATETER SISTEMA FECHADO DE ASPIRAÇÃO TRAQUEAL MEDIPLUS

Registration 80480059013. Tubo Endobronquial

Registration details

Registration number80480059013
Application number25351055905202524
Technical nameTubo Endobronquial
Risk classII
Published on05/05/2025
ValidityIndefinite validity

Registration holder

Legal nameATUAL COMERCIO E REPRESENTACOES DE PRODUTOS MEDICOS LTDA
CNPJ08.955.615/0001-83

Manufacturer

  • SHREE UMIYA SURGICAL PVT. LTD. ÍNDIA

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