Philippines FDA registration MDR-01614

EGIDA™ DR DIGITAL DUAL CHAMBER IMPLANTABLE CARDIOVERTER DEFIBRILLATOR

Philippines flagPhilippines·Medtronic International Ltd.·Switzerland·Issued April 01, 2020 – November 25, 2024
Device information
Product Name
EGIDA™ DR DIGITAL DUAL CHAMBER IMPLANTABLE CARDIOVERTER DEFIBRILLATOR
Registration Number
MDR-01614
Manufacturer details
Country of Origin
Switzerland
Importer & distribution
Importer/Distributor
Medtronic Philippines, Inc.
Registration dates
Issuance Date
April 01, 2020
Expiry Date
November 25, 2024
About this record

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.

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