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Carotid Stent System - Argentina Medical Device Registration

Access comprehensive regulatory information for Carotid 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 March 22, 2024.

This page provides complete registration details including product code (310-138), brand name (RX ACCULINK), 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
Carotid Stent System
Sistema de stent carotídeo
Argentina Medical Device Registration
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Product Information

1011337-20 1011338-20 1011339-20 1011340-20 1011341-20 1011342-20 1011337-30 1011338-30 1011339-30 1011340-30 1011341-30 1011342-30 1011343-30 1011344-30 1011337-40 1011338-40 1011339-40 1011340-40 1011341-40 1011342-40 1011343-40 1011344-40

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Reválida de Registro I-II-III-IV
Product Code
310-138
Brand Name
RX ACCULINK
Product Name
Carotid Stent System
Sistema de stent carotídeo
Registration Information
Registration Date
March 22, 2024
Database ID
cmhaytn4s0440ekuzqwu869m2
Documents
Authorized Representative