Resuscitation System
- UID
- IMP/MD/2021/000505_6c0614722c285e48bc9b449c9a1395fb_9bd4a3be4300b96515cebfddb86919d7
- Device class
- Class C
- Brand name
- Neopuff
- License holder
- Fisher & Paykel Healthcare India Pvt Ltd
- Approving authority
- CDSCO
- Product information
- The Fisher and Paykel Healthcare Neopuff Infant Resuscitator is a manually operated, gas powered resuscitator which provides assisted respiratory breaths to newborn babies in delivery suites, nurseries and neonatal intensive care units. This device is designed for use in the hospital environment and must be prescribed by a physician. The intended population for use of the Neopuff Infant Resuscitator is neonates and infants up to 10kg
Resuscitation System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_6c0614722c285e48bc9b449c9a1395fb_9bd4a3be4300b96515cebfddb86919d7. This device is marketed under the brand name Neopuff. The license holder is Fisher & Paykel Healthcare India Pvt Ltd, and it is classified as Device Class Class C. The approving authority is CDSCO.
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