Respiratory Humidifier - India CDSCO Medical Device Registration
Respiratory Humidifier is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2023/000132_c14b8d431bb7f32a7b18cd69545781c2_d68dbbfdf174f472439b33df2f7a98ae. This device is marketed under the brand name HekaFlo. The license holder is Heka Medicals India Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Kerala.
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Brand Name
HekaFlo
License Holder
Heka Medicals India Pvt LtdDevice Class
Approving Authority
Kerala
Product Information
The HekaFlo is for the treatment of spontaneously breathing patients who will be benefited by supplying high flow warmed and humidified respiratory gases. Based on the patient interface the flow may be set between 2- 60 L/min. The device is intended to provide the heated and humidified respiratory gases via a breathing circuit and nasal cannula.
