Philippines FDA registration MDR-01841

CAPSURE SP NOVUS® STEROID-ELUTING BIPOLAR, IMPLANTABLE, TINED, VENTRICULAR, TRANSVENOUS LEAD

Philippines flagPhilippines·Medtronic International Ltd.·USA·Issued April 01, 2020 – February 25, 2025
Device information
Product Name
CAPSURE SP NOVUS® STEROID-ELUTING BIPOLAR, IMPLANTABLE, TINED, VENTRICULAR, TRANSVENOUS LEAD
Registration Number
MDR-01841
Manufacturer details
Country of Origin
USA
Importer & distribution
Importer/Distributor
Medtronic Philippines, Inc.
Registration dates
Issuance Date
April 01, 2020
Expiry Date
February 25, 2025
About this record

Access comprehensive regulatory information for CAPSURE SP NOVUS® STEROID-ELUTING BIPOLAR, IMPLANTABLE, TINED, VENTRICULAR, TRANSVENOUS LEAD in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01841 and manufactured by Medtronic International Ltd. in USA. 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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