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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_866529248cf6cc6601abe0428155ee87. 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_866529248cf6cc6601abe0428155ee87

Brand Name

Cobalt™ XT DR MRI SureScan

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Visia AF MRI SureScan system is intended to provide ventricular antitachycardia pacing and ventricular defibrillation for automated treatment of life-threatening ventricular tachyarrhythmias

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