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Stent System - Argentina Medical Device Registration

Access comprehensive regulatory information for Stent System 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 April 09, 2024.

This page provides complete registration details including product code (1991-167), brand name (AlturaTM), 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
Sistema de endoprotesis
Argentina Medical Device Registration
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Product Information

AA, AI Endoprótesis aórtica: 01-AA-24-090; 01-AA-27-090, 01-AA-30-090 Endoprótesis Ilíaca: 01-AI-13-065; 01-AI-17-065; 01-A-A-21-065

Spanish:

AA, AI Endoprótesis aórtica: 01-AA-24-090; 01-AA-27-090, 01-AA-30-090 Endoprótesis ilíaca: 01-AI-13-065; 01-AI-17-065; 01-AI-21-065

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Reválida de Registro I-II-III-IV
Product Code
1991-167
Brand Name
AlturaTM
Product Name
Stent System
Sistema de endoprotesis
Registration Information
Registration Date
April 09, 2024
Database ID
cmhayu26d0h1jekuzersjb0ya
Authorized Representative