ANVISA registration

STENT FRED X 3.5/5.5 - DISPOSITIVO ENDOLUMINAL DE REDIRECIONAMENTO DE FLUXO

Registration 80583400035. STENT VASCULAR INTRACRANIANO

Registration details

Registration number80583400035
Application number25351228843202403
Technical nameSTENT VASCULAR INTRACRANIANO
Risk classIV
Published on03/08/2026
ValidityValid until 03/08/2036

Registration holder

Legal nameENDOTEC PRODUTOS MEDICOS S/A
CNPJ09.586.279/0001-01

Manufacturer

  • MICROVENTION EUROPE SARL FRANÇA

Other registrations held by ENDOTEC PRODUTOS MEDICOS S/Aview all

BeGraft Stent Graft System

80583400003

BeGraft Coronary Stent Graft System

80583400004

STENT CASPER - STENT PARA ARTÉRIA CARÓTIDA

80583400005

HYDROFILL- SISTEMA EMBÓLICO HYDROCOIL ® (HES)

80583400006

HIDROCOIL HYDROSOFT

80583400007

STENT FRED - DISPOSITIVO ENDOLUMINAL DE REDIRECIONAMENTO DE FLUXO

80583400008

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