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Aortic arch stent graft system - Argentina Medical Device Registration

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.

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Argentina ANMAT Data
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Registration modification (non-agile) Class III-IV
Aortic arch stent graft system
Sistema de injerto de stent de arco aórtico
Argentina Medical Device Registration
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Product Information

Arc module, ASC module, DE Module

Spanish:

Módulo de arco, Módulo ASC, Módulo DE

Device Classification
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 Information
Registration Date
February 14, 2024
Database ID
cmhaytp5r06j1ekuznumg18rn
Documents
Authorized Representative