ANVISA registration

CATETER DE DILATAÇÃO PARA ANGIOPLASTIA TRANSLUMINAL PERCUTÂNEA (PTA) SABERX 0.014

Registration 81576629022. CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA

Registration details

Registration number81576629022
Application number25351794695202321
Technical nameCATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Risk classII
Published on11/12/2023
ValidityIndefinite validity

Registration holder

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

Manufacturer

  • CORDIS US CORP. 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.

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