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CDSCO UID IMP/MD/2022/000573_c14b8d431bb7f32a7b18cd69545781c2_7d20be917e24c0ffeb4e8b8add992fb2

Respiratory Humidifier

FLEXICARE MEDICAL (INDIA) PRIVATE LIMITED·Device Class Class B·India CDSCO·Brand: FL-9000
Registration details
UID
IMP/MD/2022/000573_c14b8d431bb7f32a7b18cd69545781c2_7d20be917e24c0ffeb4e8b8add992fb2
Device class
Class B
Brand name
FL-9000
License holder
FLEXICARE MEDICAL (INDIA) PRIVATE LIMITED
Approving authority
CDSCO
Product information
A mains electricity (FL-9000) device designed to heat and humidify air/oxygen inspired by a patient to help maintain the mucous membranes of the respiratory tract typically during periods of prolonged respiratory support/therapy (FL-9000). The heated/humidified gases are delivered to the patient's airway and lungs via the nose/mouth or a tracheostoma in association with a parent respiratory device (FL-9000). The humidifier typically includes a heating element and provisions for attaching a humidification chamber and tubing set.
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About this record

Respiratory Humidifier is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000573_c14b8d431bb7f32a7b18cd69545781c2_7d20be917e24c0ffeb4e8b8add992fb2. This device is marketed under the brand name FL-9000. 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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