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ANVISA registration 80583400031Valid until Dec 11, 2033

Vascular Endoprosthesis

ANVISA Registration Number: 80583400031ENDOTEC PRODUTOS MEDICOS S/ABENTLEY INNOMED GMBHRisk Class IV
Verified
Device names
Technical name
Vascular Endoprosthesis
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PT: Endoprotese Vascular
Commercial name
BeGraft Aortic Stent Graft System (BGA)
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Risk class
Class IV
Registration details
Registration Number
80583400031
Process Number
25351602007202225
CNPJ
09586279000101
Company information
Registration Holder
ENDOTEC PRODUTOS MEDICOS S/A
Manufacturer
BENTLEY INNOMED GMBH
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Dec 11, 2023
Validity
11/12/2033
Last Updated
08/18/2026 19:00:00
About this record

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 80583400031 and manufactured by BENTLEY INNOMED GMBH. The registration is held by ENDOTEC PRODUTOS MEDICOS S/A with validity until Dec 11, 2033.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.