EnVeo™ PRO Delivery Catheter System - FDA Registration MDR-07972C

Access comprehensive regulatory information for EnVeo™ PRO Delivery Catheter System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07972C and manufactured by Medtronic International Limited (Singapore Branch)- 50 Pasir Panjang Road, #04-51 Mapletree Business City Singapore 117384 mfd by: Medtronic Ireland - Parkmore Business Park West Galway, Ireland for Medtronic CoreValve LLC- Santa Ana, CA, USA in USA. The device was registered on June 13, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Medtronic Philippines, Inc), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.