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Single-chamber implantable defibrillator - India CDSCO Medical Device Registration

Single-chamber implantable defibrillator is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000217_ef3df0cf5600998fa6383bb82fe25425_fcb3362e38291163ec3a5fd584b5a845. This device is marketed under the brand name ORIGEN ICD. The license holder is Boston Scientific India Pvt. Ltd.,, 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
Single-chamber implantable defibrillator
UID: IMP/MD/2021/000217_ef3df0cf5600998fa6383bb82fe25425_fcb3362e38291163ec3a5fd584b5a845

Brand Name

ORIGEN ICD

Device Class

Class D

Approving Authority

CDSCO

Product Information

The S-ICD System is intended to provide defibrillation therapy for the treatment of life-threatening ventricular tachyarrhythmias in patients who do not have symptomatic bradycardia, incessant ventricular tachycardia, or spontaneous, frequently recurring ventricular tachycardia that is reliably terminated with anti-tachycardia pacing

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