ANVISA registration

CARTO VIZIGO 8,5F BI-DIRECTIONAL GUIDING SHEATH

Registration 80145901916. KIT PARA INTRODUÇÃO DE CATETER VASCULAR, DIRIGÍVEL

Registration details

Registration number80145901916
Application number25351699902201959
Technical nameKIT PARA INTRODUÇÃO DE CATETER VASCULAR, DIRIGÍVEL
Risk classIV
Published on23/12/2019
ValidityValid until 23/12/2029

Registration holder

Legal nameJOHNSON & JOHNSON DO BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS PARA SAÚDE LTDA
CNPJ54.516.661/0001-01

Manufacturing sites

  • BIOSENSE WEBSTER, INC. - (IRVINE) ESTADOS UNIDOS DA AMÉRICA
  • BIOSENSE WEBSTER, INC. - IRVINE ESTADOS UNIDOS DA AMÉRICA

Other registrations held by JOHNSON & JOHNSON DO BRASIL INDÚSTRIA E COMÉRCIO DE PRODUTOS PARA SAÚDE LTDAview all

SUTURA CIRURGICA ABSORVIVEL SINTETICA DE PDS II

10132590004

NUROLON*

10132590015

MERSILENE*

10132590021

VICRYL

10132590022

FITA CARDÍACA

10132590023

FITA UMBILICAL

10132590026

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