ANVISA registration

BeGraft Aortic Stent Graft System (BGA)

Registration 80583400031. Endoprotese Vascular

Registration details

Registration number80583400031
Application number25351602007202225
Technical nameEndoprotese Vascular
Risk classIV
Published on11/12/2023
ValidityValid until 11/12/2033

Registration holder

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

Manufacturer

  • BENTLEY INNOMED GMBH ALEMANHA

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.

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