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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 Class III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on April 29, 2024.

This page provides complete registration details including product code (416-165), brand name (Nexus DUO), 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 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

Nexus DUO Aortic Arch Stent Grafting System (Custom Medical Product)

Spanish:

Sistema de injerto de stent de arco aórtico Nexus DUO (Producto médico personalizado)

Device Classification
Registration Type
Registration Class III-IV
Registro Clase III-IV
Product Code
416-165
Brand Name
Nexus DUO
Product Name
Aortic arch stent graft system
Sistema de injerto de stent de arco aórtico
Registration Information
Registration Date
April 29, 2024
Database ID
cmhayu0e30ewrekuzulxmsjpd
Documents
Authorized Representative