NASOPHARYANGEL AIRWAY TUBE – SILICONE - India CDSCO Medical Device Registration
NASOPHARYANGEL AIRWAY TUBE – SILICONE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2021/000136_796873351cf888fce0b199126556aff2_2fd40891f50a62bd05d0c6903fe52710. The license holder is Meditec Devices, and it is classified as Device Class Class A. The approving authority is Kokan Division.
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License Holder
Meditec DevicesDevice Class
Approving Authority
Kokan Division
Product Information
when a patient becomes unconscious, the muscles in the jaw commonly relax and can allow the tongue to slide back and obstruct the airway. the purpose of the flared end is to prevent the device from becoming lost inside the patient's nose. a catheter is passed through nasopharyngeal the nares and advanced to the depth of the nasopharynx to remove air choke or obstruction. A resuscitator
