Sirolimus Coronary Elution Stent System
Argentina Medical Device Registration · Biomime™ Morph · UNIFARMA S.A. · Registered June 28, 2024
Revalidation of Registration I-II-III-IV- 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 Date
- June 28, 2024
- Database ID
- cmhaytq4e07kbekuzw134u2m6
- Name
- UNIFARMA S.A.
Biomime™ Morph Sirolimus Elution Coronary Stent System
Sistema de stent coronario de elución de Sirolimus Biomime™ Morph
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.