416-166Aortic arch stent graft system
Argentina Medical Device Registration · NEXUS · ANGIOCOR S.A. · Registered February 14, 2024
Registration modification (non-agile) Class III-IV- Registration Type
- Registration modification (non-agile) Class III-IV
- Modificación de Registro (no ágil) Clase III-IV
- Product Code
- 416-166
- Brand Name
- NEXUS
- Product Name
- Aortic arch stent graft system
- Sistema de injerto de stent de arco aórtico
- Registration Date
- February 14, 2024
- Database ID
- cmhaytp5r06j1ekuznumg18rn
- Name
- ANGIOCOR S.A.
Arc module, ASC module, DE Module
Módulo de arco, Módulo ASC, Módulo DE
Access comprehensive regulatory information for Aortic arch stent graft system in the Argentina medical device market through Pure Global AI's free database. This Registration modification (non-agile) Class III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on February 14, 2024.
This page provides complete registration details including product code (416-166), brand name (NEXUS), 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.