ANVISA registration

ACUITY PRO - CATETER GUIA DE 9FR

Registration 10341350798. CATETER GUIA INTRAVASCULAR

Registration details

Registration number10341350798
Application number25351086451201444
Technical nameCATETER GUIA INTRAVASCULAR
Risk classIV
Published on18/02/2015
ValidityValid until 18/02/2035

Registration holder

Legal nameBOSTON SCIENTIFIC DO BRASIL LTDA
CNPJ01.513.946/0001-14

Manufacturing sites

  • BOSTON SCIENTIFIC CORPORATION - MARLBOROUGH ESTADOS UNIDOS DA AMÉRICA
  • CARDIAC PACEMAKERS INC., A SUBSIDIARY OF BOSTON SCIENTIFIC CORPORATION 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.

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