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F&P Reusable Humidification Chambers - India CDSCO Medical Device Registration

F&P Reusable Humidification Chambers is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_cf5be1991fd79044757c0b0d136a4fc4_9ad01e83b3729038ccdd8bbbd7bda92c. 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
F&P Reusable Humidification Chambers
UID: IMP/MD/2021/000505_cf5be1991fd79044757c0b0d136a4fc4_9ad01e83b3729038ccdd8bbbd7bda92c

Device Class

Class B

Approving Authority

CDSCO

Product Information

The MR340 is a reusable chamber for heating and humidifying respiratory gases for paediatric and neonate patients requiring respiratory support. This is intended for use with Fisher & Paykel Healthcare MR850 humidifiers in hospital or clinical environments and should only be prescribed by a physician. The MR370 is a reusable humidificaion chamber for use with F&P heater bases and is for adult applications. It is used to provide humidification for intubated or nonintubated patients

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