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Implantable Cardioverter Defibrillator - India CDSCO Medical Device Registration

Implantable Cardioverter Defibrillator is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000379_63ffdcb9385a83321e1699c5fde5ad69_67944b81abcdb7769f2de4226f873a47. This device is marketed under the brand name Cobalt™ XT DR MRI SureScan . The license holder is India Medtronic Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class D
Implantable Cardioverter Defibrillator
UID: IMP/MD/2021/000379_63ffdcb9385a83321e1699c5fde5ad69_67944b81abcdb7769f2de4226f873a47

Brand Name

Cobalt™ XT DR MRI SureScan

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Evera S DR system is intended to provide atrial and/or ventricular antitachycardia pacing, cardioversion, and defibrillation for automated treatment of atrial and/or life-threatening ventricular tachyarrhythmias

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