416-130Stent System, BeGraft, Aortic
Argentina Medical Device Registration · Bentley InnoMed GmbH · ANGIOCOR S.A. · Registered December 11, 2023
Revalidation of Registration I-II-III-IV- Registration Type
- Revalidation of Registration I-II-III-IV
- Reválida de Registro I-II-III-IV
- Product Code
- 416-130
- Brand Name
- Bentley InnoMed GmbH
- Product Name
- Stent System, BeGraft, Aortic
- Sistema de endoprótesis, BeGraft, Aórtico
- Registration Date
- December 11, 2023
- Database ID
- cmhaytq4c07fjekuzel7zca0l
- Name
- ANGIOCOR S.A.
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.
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.