Respiratory Humidification System
- UID
- IMP/MD/2021/000505_cf28636ee3be798b4b84583ad531aa76_85ebf9ea49e2409a8c0637649e036377
- Device class
- Class B
- Brand name
- 850 Family
- License holder
- Fisher & Paykel Healthcare India Pvt Ltd
- Approving authority
- CDSCO
- Product information
- The AIRVO™ 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 AIRVO™ 2 is for patients in hospitals and long-term care facilities
Respiratory Humidification System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_cf28636ee3be798b4b84583ad531aa76_85ebf9ea49e2409a8c0637649e036377. 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.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.