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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/2021/000217_8ea86474d70bba5a51d8f1e0d0a754c0_29e2c5224d63886213eb06694322adfe. 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
Implantable Cardioverter Defibrillator
UID: IMP/MD/2021/000217_8ea86474d70bba5a51d8f1e0d0a754c0_29e2c5224d63886213eb06694322adfe

Brand Name

ORIGEN ICD

Device Class

Class D

Approving Authority

CDSCO

Product Information

Boston Scientific implantable cardioverter defibrillators (ORIGEN ICD) are intended to provide ventricular antitachycardia pacing (ORIGEN ICD) and ventricular defibrillation for automated treatment of life-threatening ventricular arrhythmias

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