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Switch Nasal Interfaces - India CDSCO Medical Device Registration

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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CDSCO Registered
Class Class B
Switch Nasal Interfaces
UID: IMP/MD/2021/000505_db20b9bc022e8251cc4e5cee51454346_51cfde77522e004409841b17ab956376

Brand Name

850 Family

Device Class

Class B

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

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