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Vascular Endoprosthesis - ANVISA Registration 80583400029

Access comprehensive regulatory information for Vascular Endoprosthesis in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80583400029 and manufactured by BENTLEY INNOMED GMBH. The registration is held by ENDOTEC PRODUTOS MEDICOS S/A with validity until Sep 26, 2032.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BENTLEY INNOMED GMBH, BOLTON MEDICAL, INC., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80583400029
2 Related Devices
Registration Details
ANVISA Registration Number: 80583400029
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Related Devices (2)

BeGraft Aortic Stent Graft System (BGA)
Risk Class IV

Registration Details

80583400029

25351065705202237

09586279000101

Company Information

Germany
PT: ALEMANHA

Dates and Status

Sep 26, 2022

26/09/2032

09/18/2025 19:00:01

BeGraft Aortic Stent Graft System (BGA)
Risk Class IV

Registration Details

80583400029

25351065705202237

09586279000101

Company Information

Dates and Status

Sep 26, 2022

26/09/2032

09/18/2025 19:00:01