Switch Nasal Interfaces
- UID
- IMP/MD/2021/000505_db20b9bc022e8251cc4e5cee51454346_51cfde77522e004409841b17ab956376
- Device class
- Class B
- Brand name
- 850 Family
- License holder
- Fisher & Paykel Healthcare India Pvt Ltd
- Approving authority
- CDSCO
- Product information
- This product is a single-patient-use device that delivers respiratory gases to adult patients in hospitals and medical facilities. Spontaneously Breathing Patients: This product is indicated for the delivery of Nasal High Flow (850 Family) and Low Flow Oxygen to spontaneously breathing patients by appropriately qualified healthcare professionals. Apneic Patients: This product is indicated for the delivery of Transnasal Humidified Rapid Insufflation Ventilatory Exchange (850 Family) to apneic patients in operating and procedure rooms, under the direction of an appropriately qualified anesthetist, anesthesiologist, or medical professional. This product facilitates switching between the delivery of NHF/THRIVE and the delivery of anesthesia mask ventilation
Switch Nasal Interfaces is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_db20b9bc022e8251cc4e5cee51454346_51cfde77522e004409841b17ab956376. This device is marketed under the brand name 850 Family. The license holder is Fisher & Paykel Healthcare India Pvt Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.
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