EGIDA™ DR DIGITAL DUAL CHAMBER IMPLANTABLE CARDIOVERTER DEFIBRILLATOR - FDA Registration MDR-01614

Access comprehensive regulatory information for EGIDA™ DR DIGITAL DUAL CHAMBER IMPLANTABLE CARDIOVERTER DEFIBRILLATOR in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01614 and manufactured by Medtronic International Ltd. in Switzerland. The device was registered on April 01, 2020.

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.