ANVISA registration

SISTEMA DE FILTRO PARA VEIA CAVA OPTEASE

Registration 81576620021. FILTRO INTRAVASCULAR E DISPOSITIVOS ASSOCIADOS

Registration details

Registration number81576620021
Application number25351103378202318
Technical nameFILTRO INTRAVASCULAR E DISPOSITIVOS ASSOCIADOS
Risk classIV
Published on06/03/2023
ValidityValid until 20/08/2034

Registration holder

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

Manufacturing sites

  • CORDIS CASHEL IRLANDA
  • CORDIS CORPORATION ESTADOS UNIDOS DA AMÉRICA

Other registrations held by CORDIS MEDICAL BRASIL LTDAview all

CATETERES GUIA CORDIS VISTA BRITE TIP 8F

81576620000

FIO GUIA DIRIGÍVEL CORDIS STORQ

81576620001

Catéter Balão Kaneka PTCA

81576620002

DISPOSITIVO DE ENCERRAMENTO VASCULAR MYNX CONTROL

81576620003

CATETER BALÃO PTCA NEON

81576620004

Cateter Balão PTCA NEON NC

81576620005

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.

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