Defibrillator
- UID
- IMP/MD/2021/000585_573af448e4733b7079213ab73a413dcb_0442471e8ef6a81af603b922bde0b1d6
- Device class
- Class C
- Brand name
- LIFEPAK 20e Monitor/Defibrillator and accessories
- License holder
- M/s Stryker India Private Ltd.,
- Approving authority
- CDSCO
- Product information
- The intended use for the LIFEPAK 1000 Defibrillator is emergency treatment of patients in cardiac arrest. It can operate in manual or semiautomatic mode. A lesser trained emergency responder can use the device in the semi-automated mode; the device analyzes the cardiac rhythm and indicates “shock advised” if it detects a shockable rhythm. If the device is in the manual mode a person trained in cardiac rhythm interpretation such as a paramedic can deliver a defibrillation shock without relying on the automated analysis of the device
Defibrillator is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000585_573af448e4733b7079213ab73a413dcb_0442471e8ef6a81af603b922bde0b1d6. 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.
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