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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_2269aa5404a26272382782378b26f9cf_fbf30a121397d3872f56f2d64b66d031. 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.

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CDSCO Registered
Class Class B
Respiratory Humidification System
UID: IMP/MD/2021/000505_2269aa5404a26272382782378b26f9cf_fbf30a121397d3872f56f2d64b66d031

Brand Name

850 Family

Device Class

Class B

Approving Authority

CDSCO

Product Information

The MR810 System is intended to provide therapeutic levels of heat and humidity to a patient's inspired respiratory gases, when using a continuous or intermittent ventilator system.

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