ANVISA registration

CATETER PARA ANGIOPLASTIA TRANSLUMINAL PERCUTANEO (PTA) SLEEK

Registration 81576620015. CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA

Registration details

Registration number81576620015
Application number25351102953202357
Technical nameCATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Risk classIII
Published on06/03/2023
ValidityValid until 05/05/2028

Registration holder

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

Manufacturer

  • CLEARSTREAM TECHNOLOGIES LTD IRLANDA

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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