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Stent System, BeGraft, Aortic - Argentina Medical Device Registration

Access comprehensive regulatory information for Stent System, BeGraft, Aortic in the Argentina medical device market through Pure Global AI's free database. This Revalidation of Registration I-II-III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on December 11, 2023.

This page provides complete registration details including product code (416-130), brand name (Bentley InnoMed GmbH), authorized representative information, registration type, and regulatory compliance data from the official Argentina ANMAT medical device database. Pure Global AI offers free access to Argentina's medical device registry, helping global MedTech companies navigate Argentina regulations efficiently.

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Argentina ANMAT Data
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Revalidation of Registration I-II-III-IV
Stent System, BeGraft, Aortic
Sistema de endoprรณtesis, BeGraft, Aรณrtico
Argentina Medical Device Registration
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Product Information

BGA1912_1; BGA1914_1; BGA1916_1; BGA2912_1; BGA2914_1; BGA2916_1; BGA3912_1; BGA3914_1; BGA3816_1; BGA4912_1; BGA4914_1; BGA4816_1; BGA5912_1; BGA5914_1; BGA5816_1; BGA1912_2; BGA1914_2; BGA 1916_2; BGA 2912_2; BGA2914_2; BGA2916_2; BGA2918_2; BGA2720_2; BGA3912_2; BGA3914_2; BGA3816_2; BGA3816_2; BGA3818_2; BGA3720_2; BGA3722_2; BGA3724_2; BGA4912_2; BGA4914_2; BGA4816_2; BGA4818_2; BGA4820_2; BGA4822_2; BGA4824_2; BGA5912_2; BGA5914_2; BGA5816_2.

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
416-130
Brand Name
Bentley InnoMed GmbH
Product Name
Stent System, BeGraft, Aortic
Sistema de endoprรณtesis, BeGraft, Aรณrtico
Registration Information
Registration Date
December 11, 2023
Database ID
cmhaytq4c07fjekuzel7zca0l
Authorized Representative