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Cool-tip™ RFA High Power Patient Return Electrode (Grounding Pad) - FDA Registration MDR-00626

Access comprehensive regulatory information for Cool-tip™ RFA High Power Patient Return Electrode (Grounding Pad) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-00626 and manufactured by Covidien Private Limited - 50 Pasir Panjang Road, #04-51 Mapletree Business City, Singapore mfd. by: Covidien LLC - 6044 Longbow Court Boulder Colorado 80301 USA For Covidien LLC - 15 Hampshire Street, Mansfeld, MA 02048 USA in USA. The device was registered on May 14, 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-00626
Cool-tip™ RFA High Power Patient Return Electrode (Grounding Pad)
Registered medical device in Philippines
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Device Information
Product Name
Cool-tip™ RFA High Power Patient Return Electrode (Grounding Pad)
Registration Number
MDR-00626
Importer & Distribution
Importer/Distributor
Medtronic Philippines, Inc.
Registration Dates
Issuance Date
May 14, 2025
Expiry Date
May 23, 2029