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Sirolimus Coronary Elution Stent System - Argentina Medical Device Registration

Access comprehensive regulatory information for Sirolimus Coronary Elution 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 June 28, 2024.

This page provides complete registration details including product code (954-168), brand name (Biomime™ Morph), 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
Sirolimus Coronary Elution Stent System
Sistema de stent coronario de elución de Sirolimus
Argentina Medical Device Registration
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Product Information

Biomime™ Morph Sirolimus Elution Coronary Stent System

Spanish:

Sistema de stent coronario de elución de Sirolimus Biomime™ Morph

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Reválida de Registro I-II-III-IV
Product Code
954-168
Brand Name
Biomime™ Morph
Product Name
Sirolimus Coronary Elution Stent System
Sistema de stent coronario de elución de Sirolimus
Registration Information
Registration Date
June 28, 2024
Database ID
cmhaytq4e07kbekuzw134u2m6
Authorized Representative