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Filtered Nasal Interfaces - India CDSCO Medical Device Registration

Filtered Nasal Interfaces is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_6e26ddbff32a69b721e02d2e0bdbb64f_883bbcee2cd67217d8af5991a3bca9a0. 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
Filtered Nasal Interfaces
UID: IMP/MD/2021/000505_6e26ddbff32a69b721e02d2e0bdbb64f_883bbcee2cd67217d8af5991a3bca9a0

Brand Name

850 Family

Device Class

Class B

Approving Authority

CDSCO

Product Information

This product is a single-patient-use device that delivers respiratory gases to adult patients in hospitals and medical facilities

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