Respiratory Humidification System - India CDSCO Medical Device Registration

Respiratory Humidification System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_cf28636ee3be798b4b84583ad531aa76_39f8a3cca39155e258f4cc1500a62302. 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

Respiratory Humidification System

UID: IMP/MD/2021/000505_cf28636ee3be798b4b84583ad531aa76_39f8a3cca39155e258f4cc1500a62302

Brand Name

850 Family

License Holder

Fisher & Paykel Healthcare India Pvt Ltd

Device Class

Class B

Approving Authority

CDSCO

Product Information

The myAIRVO 2 is 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. The flow may be from 2 - 60L/min depending on the patient interface. The myAIRVO 2 is for patients in homes and long- term care facilities

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Brand: 850 Family

Fisher & Paykel Healthcare India Pvt Ltd

Respiratory Humidification System - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

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