ANVISA registration

CATETER BALÃO DE PRÉ-DILATAÇÃO PERIFÉRICO PARA FIO-GUIA DE 0.035" - OCEANUS 35

Registration 80102511147. CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA

Registration details

Registration number80102511147
Application number25351171514201397
Technical nameCATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Risk classII
Published on29/07/2013
ValidityIndefinite validity

Registration holder

Legal nameVR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
CNPJ04.718.143/0001-94

Manufacturer

  • LIFE VASCULAR DEVICES BIOTECH S.L ESPANHA

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