Respiratory Support System
- UID
- IMP/MD/2021/000505_49cb9eef6ab40b2051a8f42a4e41115b_afad8e9e11dc9c7a6811193a527dd02b
- Device class
- Class C
- Brand name
- Neopuff
- License holder
- Fisher & Paykel Healthcare India Pvt Ltd
- Approving authority
- CDSCO
- Product information
- For the treatment of spontaneously breathing patients who would benefit from receiving high flow warmed and humidified respiratory gases. This includes patients who have had upper airways bypassed
Respiratory Support System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_49cb9eef6ab40b2051a8f42a4e41115b_afad8e9e11dc9c7a6811193a527dd02b. 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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