ANVISA registration

CATETER BALÃO DE DILATAÇÃO PARA PTA

Registration 81576620030. CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA

Registration details

Registration number81576620030
Application number25351103536202321
Technical nameCATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Risk classIII
Published on06/03/2023
ValidityValid until 23/06/2035

Registration holder

Legal nameCORDIS MEDICAL BRASIL LTDA
CNPJ27.548.227/0001-22

Manufacturing sites

  • CORDIS CASHEL IRLANDA
  • CORDIS US CORP. 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