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Humidification Chambers - India CDSCO Medical Device Registration

Humidification Chambers is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000098_9ff695628ccca06682546c814aaf9541_9b7f4f73ee408e12415d42c421be8a5b. This device is marketed under the brand name Flexicare. The license holder is FLEXICARE MEDICAL (INDIA) PRIVATE LIMITED, 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
Humidification Chambers
UID: IMP/MD/2019/000098_9ff695628ccca06682546c814aaf9541_9b7f4f73ee408e12415d42c421be8a5b

Brand Name

Flexicare

Device Class

Class B

Approving Authority

CDSCO

Product Information

The Flexicare Auto-fill Humidification Chamber is intended for use with Flexicare Invasive and Non-Invasive ventilation, Heated Wire, Non-Heated Wire and High Flow Heated Wire Circuits. It is part of a complete system to connect a patientโ€™s airway to a ventilator, providing warmed and humidified inspired respiratory gases to ventilated patients and those receiving respiratory support. The Humidification Chamber is intended for use to hold sterile water required to humidify the air being delivered to patients. Intended for any patient requiring active humidification within a hospital environment. For use with FL-9000. Compatible with Fisher & Paykel MR850 Respiratory Gas Humidifier

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