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Breathing Circuit - India CDSCO Medical Device Registration

Breathing Circuit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_2daa881a8276b71ce18fdb18cb40c0c9_39f148030b06663d24229796e9460b96. 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
Breathing Circuit
UID: IMP/MD/2021/000505_2daa881a8276b71ce18fdb18cb40c0c9_39f148030b06663d24229796e9460b96

Brand Name

850 Family

Device Class

Class B

Approving Authority

CDSCO

Product Information

It is designed to be used for infant resuscitation to deliver appropriate PEEP and PIP with a flow rate from 5-15L/min. Designed to connect to the F&P Neopuff Infant Resuscitator or a gas resuscitator compliant to ISO 10651-5:2006

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