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Protégé GPS Self-Expanding Peripheral Stent System - FDA Registration MDR-07456

Access comprehensive regulatory information for Protégé GPS Self-Expanding Peripheral Stent System in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07456 and manufactured by Medtronic International Limited (Singapore Branch) - 50 Pasir Panjang Road, #04-51, Mapletree Business City, Singapore 117384 mfd. by: ev3, Inc. - 4600 Nathan Lane North, Plymouth, Minnesota 55442, USA in USA. The device was registered on July 10, 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.

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MDR-07456
Protégé GPS Self-Expanding Peripheral Stent System
Registered medical device in Philippines
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Device Information
Product Name
Protégé GPS Self-Expanding Peripheral Stent System
Registration Number
MDR-07456
Importer & Distribution
Importer/Distributor
Medtronic Philippines Inc.
Registration Dates
Issuance Date
July 10, 2025
Expiry Date
November 16, 2029