Peremo-Everolimus Eluting Coronary Stent System - EUDAMED Registration 18904224939018

Access comprehensive regulatory information for Peremo-Everolimus Eluting Coronary Stent System in the European Union medical device market through Pure Global AI's free database. This Class III device is registered with EU EUDAMED under Primary DI 18904224939018 and manufactured by Meril Life Sciences Pvt. Ltd. in India.

This page provides complete registration details including trade name (Peremo™ ), manufacturer information, authorized representative details, competent authority (Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.