Pure Global

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_df5c91534592eeb5e84d3878432224fa. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
Defibrillator
UID: IMP/MD/2021/000585_573af448e4733b7079213ab73a413dcb_df5c91534592eeb5e84d3878432224fa

Brand Name

LIFEPAK 20e Monitor/Defibrillator and accessories

Device Class

Class C

Approving Authority

CDSCO

Product Information

The LIFEPAK 15 monitor/defibrillator is intended for use by trained medical personnel. For information about training options, contact your local Physioโ€Control representative. The LIFEPAK 15 monitor/defibrillator can be used in outโ€ofโ€doors and indoor emergency care settings within the environmental conditions specified. The monitor/defibrillator is designed to be used during ground transportation. Monitoring and therapy functions may only be used on one patient at a time. Manual mode monitoring and therapy functions are intended for use on adult and pediatric patients. Automated external defibrillation mode is intended for use on patients eight years of age and older.

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing