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Defibrillator - India CDSCO Medical Device Registration

Defibrillator is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000585_573af448e4733b7079213ab73a413dcb_b8b817b87e9962386795543c4ef833af. This device is marketed under the brand name LIFEPAK 20e Monitor/Defibrillator and accessories. The license holder is M/s Stryker India Private Ltd.,, and it is classified as Device Class Class C. 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 C
Defibrillator
UID: IMP/MD/2021/000585_573af448e4733b7079213ab73a413dcb_b8b817b87e9962386795543c4ef833af

Brand Name

LIFEPAK 20e Monitor/Defibrillator and accessories

Device Class

Class C

Approving Authority

CDSCO

Product Information

The LIFEPAK CR2 defibrillator is indicated for use on patients of all ages in cardiopulmonary arrest. The patient must be unresponsive (LIFEPAK 20e Monitor/Defibrillator and accessories), not breathing normally, and showing no signs of circulation (LIFEPAK 20e Monitor/Defibrillator and accessories)

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