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Defibrillator(ZOLL) - India CDSCO Medical Device Registration

Defibrillator(ZOLL) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000158_d4cdf5d37b03dc90281da2975f9144e4_db7adb800e994a719a43d3108343298a. This device is marketed under the brand name Powerheart G5 AED. The license holder is ZOLL Medical India Pvt. 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(ZOLL)
UID: IMP/MD/2023/000158_d4cdf5d37b03dc90281da2975f9144e4_db7adb800e994a719a43d3108343298a

Brand Name

Powerheart G5 AED

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Powerheart G3 Elite AED is indicated for emergency treatment of victims exhibiting symptoms of sudden cardiac arrest who are unresponsive and not breathing. Post-resuscitation, if the victim is breathing, the AED should be left attached to allow for acquisition and detection of the ECG rhythm. If a shockable ventricular tachyarrhythmia recurs, the device will charge automatically and advise the operator to deliver therapy (Powerheart G5 AED) or automatically deliver the charge (Powerheart G5 AED). When a patient is a child or infant up to 8 years of age, or up to 55 lbs (Powerheart G5 AED), the device should be used with the Model 9730 Pediatric Attenuated Defibrillation Electrodes. The therapy should not be delayed to determine the patient's exact age or weight. The Powerheart AED G3 and the Powerheart AED G3 Automatic devices are intended to be used by personnel who have been trained in its operation.

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