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Non-heated respiratory humidifier - India CDSCO Medical Device Registration

Non-heated respiratory humidifier is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000098_80ce5707bd1bc28fc0089c7e9f5d412d_239279ed8206892b4b3f7210c5cf78f1. 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.

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CDSCO Registered
Class Class B
Non-heated respiratory humidifier
UID: IMP/MD/2019/000098_80ce5707bd1bc28fc0089c7e9f5d412d_239279ed8206892b4b3f7210c5cf78f1

Brand Name

Flexicare

Device Class

Class B

Approving Authority

CDSCO

Product Information

Flexicareโ€™s Bubble Humidifiers are designed to moisten dry oxygen that is being administered to the patient for inhalation via the nose or mouth. The humidified oxygen reduces the loss of moisture from the mucous membranes and other tissues throughout the patientโ€™s respiratory tract. Sterile water is placed in the bowl of the bubble humidifier. The unit is connected to an oxygen supply and a nasal cannula or similar device, fitted to the patient. A prescribed flow of oxygen is set and bubbled through the sterile water, then passes to the patient. The device is used in both hospital and home environments

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