Flow Diverter - India CDSCO Medical Device Registration

Flow Diverter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_47bc40c912a2339e61755d8d17329f17_9d0f01a57aad49c8e20f66d5d6aeb6f8. 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

Flow Diverter

UID: IMP/MD/2021/000505_47bc40c912a2339e61755d8d17329f17_9d0f01a57aad49c8e20f66d5d6aeb6f8

Brand Name

850 Family

License Holder

Fisher & Paykel Healthcare India Pvt Ltd

Device Class

Class B

Approving Authority

CDSCO

Product Information

This product is intended for use as an in-line pressure relief device, designed to limit the system pressure when used with approved F&P breathing circuits and interfaces. This product is indicated for adult patients in hospitals and medical facilities

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Brand: 850 Family

Fisher & Paykel Healthcare India Pvt Ltd

Flow Diverter - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

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