Argentina flag310-139

Carotid Stent System

Sistema de stent carotídeo

Argentina Medical Device Registration · X.ACT · BIOSUD S.A. · Registered April 12, 2024

Revalidation of Registration I-II-III-IV
Device classification
Registration Type
Revalidation of Registration I-II-III-IV
Reválida de Registro I-II-III-IV
Product Code
310-139
Brand Name
X.ACT
Product Name
Carotid Stent System
Sistema de stent carotídeo
Registration information
Registration Date
April 12, 2024
Database ID
cmhaytks50223ekuzce67hs9o
Authorized representative
Documents
Product information

XRX 020 07S XRX 020 08S XRX 020 09S XRX 020 10S XRX 030 07S XRX 030 08S XRX 030 09S XRX 030 10S XRX 030 08T XRX 030 09T XRX 030 10T XRX 040 08T XRX 040 09T XRX 040 10T

About this record

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 April 12, 2024.

This page provides complete registration details including product code (310-139), brand name (X.ACT), 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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