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Single Use Breathing Circuits - India CDSCO Medical Device Registration

Single Use Breathing Circuits is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_53ca28a4a9bae9e3798c562284242f37_aa86e36cbd134dcd4fa7db1e9228088f. 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
Single Use Breathing Circuits
UID: IMP/MD/2021/000505_53ca28a4a9bae9e3798c562284242f37_aa86e36cbd134dcd4fa7db1e9228088f

Brand Name

850 Family

Device Class

Class B

Approving Authority

CDSCO

Product Information

For the delivery of heated, humidified breathing gases to spontaneously breathing adult patients requiring respiratory support. This breathing set is suitable for use with Fisher & Paykel Healthcare MR850 Humidifiers in hospital and long-term care environments

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