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F&P Single Use Humidification Chambers - India CDSCO Medical Device Registration

F&P Single Use Humidification Chambers is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000505_89b214ed8ee873c75b70192d8bf35e3e_cf8b0432f73fdccfdd5004dbc7b1a817. 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 Single Use Humidification Chambers
UID: IMP/MD/2021/000505_89b214ed8ee873c75b70192d8bf35e3e_cf8b0432f73fdccfdd5004dbc7b1a817

Device Class

Class B

Approving Authority

CDSCO

Product Information

The chamber is designed for humidifying gas with Fisher & Paykel Healthcare Breathing Circuits. Compatible with Fisher & Paykel Healthcare humidifiers

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