A closed suction system module is provided. In one embodiment, the closed suction system module includes a coupling member configured to couple to a suction port of a multi-port manifold or endotracheal tube adapter (e.g., dual-port or tri-port adapter). In one embodiment, the closed suction system module includes a suction catheter configured to clean the interior surfaces of body-inserted tubes or artificial airways (alone or in addition to suctioning natural airways or portions of the respiratory tract or other body lumens). The suction catheter may include a cleaning portion at a distal portion of the suction catheter (e.g., near the distal end or tip of the suction catheter). In some embodiments, the cleaning portion includes at least one expandable cleaning member (e.g., balloon, sleeve, wiper).

The Invention of a method of Closing an Orifice located right behind the Epiglottis under the vocal cords unlocks the keys of Immune System and adjusts the Endocrine system. This Orifice is responsible of letting Saliva streaming abnormally into capillaries to imbue them with extra water and inhibiting digested nutrients of Plasma to enter capillaries due to deregulation of Starling Forces. A phenomenon that damages capillaries membranes by creating perforations and reducing the functioning capacity of the lymphatic system and T, B and NK Cells, responsible of enhancing the Immune System. Closing this Orifice will drain out Extra water (Saliva) of capillaries and regulate Starling forces to enable nutrients to enter bloodstream and to increase cells Metabolism, regulate hormones secretion, enable the maturation of NK cells to kill cancers, regulate blood sugar, regulate blood pressure, repair brain's neurons and reproduce new cells to replace defected ones.

One aspect of the present disclosure relates to a reversible airway device. The reversible airway device (10) can include: a supra-glottic airway support (12) comprising a multi-lumen tubular guide (14) and an optional sealing member (16); an endotracheal tube (26); and at least one seal (42). The multi-lumen tubular guide has a distal end portion (18), a proximal end portion (22), a first passageway (20) extending between the distal and proximal end portions, and a second passageway (24) that is non-concentric with the first passageway and also extends between the distal and proximal end portions. The at least one seal is disposed within the first passageway, the second passageway, or both, so as to occlude the flow of a gas through the first passageway and/or the second passageway. The endotracheal tube can be inserted into the first or second passageway and can traverse the seal.

Devices and methods for allowing for improved assisted ventilation of a patient. The methods and devices provide a number of benefits over conventional approaches for assisted ventilation. For example, the methods and devices described herein permit blind insertion of a device that can allow ventilation regardless of whether the device is positioned within a trachea or an esophagus. In addition, the methods and device allow for timed delivery of ventilations based on a condition of a thoracic cavity to increase the amount and efficiency of blood flow during a resuscitation procedure.

Enteral tubes, tube tip detection systems, and methods for detecting tube misplacement are provided. For example, a tube tip detection system comprises an enteral tube having a tip and a first light disposed at the tip that is illuminated as the enteral tube is inserted into a patient to indicate to a user of the system whether the tip is misplaced in the patient's airway. Similarly, enteral tubes are provided that comprise a tip, a length, and a light that is continuously illuminated as the enteral tube is inserted into a patient. Methods for detecting a tube misplacement in a patient's airway include embedding a light into an enteral tube, inserting the enteral tube into the patient through the patient's nose or mouth, and monitoring a location of the light as the enteral tube is inserted into the patient to determine if the tube is traveling into the patient's airway.

An endotracheal tube (ETT) system and methods are provided. In at least one example, an ETT system may comprise, a tube, inflatable cuff coupled to the tube, and a restrictor. In at least one example the restrictor may comprise one more cavities. In a further example, a restrictor drainage assembly may be coupled to the restrictor, the restrictor drainage assembly configured to drain secretions that may be collected at a collection point formed by the restrictor when the ETT system is positioned in an airway of a patient and in an inflated state.

Airway devices, systems, and methods are disclosed that can achieve ventilation of lungs through a mask that seals around the glottis and connects to a flexible airway channel, while also providing evacuation of gastric and/or pharyngeal body fluid and/or blood during upper airway surgeries or procedures.

Devices and methods for allowing for improved assisted ventilation of a patient. The methods and devices provide a number of benefits over conventional approaches for assisted ventilation. For example, the methods and devices described herein permit blind insertion of a device that can allow ventilation regardless of whether the device is positioned within a trachea or an esophagus. In addition, the methods and device allow for timed delivery of ventilations based on a condition of a thoracic cavity to increase the amount and efficiency of blood flow during a resuscitation procedure.

A reversible airway device can include a tubular guide, a laryngeal mask, and an endotracheal tube. The tubular guide can have a distal end portion, a proximal end portion, and a first passageway extending between the distal and proximal end portions. The tubular guide can further include a first longitudinal seam. The laryngeal mask can be attached to the distal end portion of the tubular guide. The laryngeal mask can include an opening in fluid communication with the first passageway. The laryngeal mask can further include a second longitudinal seam. The endotracheal tube can be slidably disposed within the first passageway and have a second passageway. The first and second longitudinal seams can be adapted to permit ingress and egress of the tubular guide from the airway without detaching the endotracheal tube from a ventilation source.

An effectively-support-type oxygen inhalation and sputum aspiration oropharyngeal airway device, comprising an inner airway body provided from a proximal end to a distal end, and a support plate parallel tongue surface and having -a-certain width; the support plate comprises a proximal end positioned on the front face of inner airway body and constituting the wall of duct, and a distal bending portion with bending angle of 0-180; the front face of distal bending portion is provided with at least two evenly distributed projections, recesses, or through holes; the surfaces of the projections facing to teeth are smooth and the surfaces of facing to pharynx have a height of 1-2 mm, or the recessing depth of recesses is 0.5-1 mm, or the diameter of through holes is 1-3 mm; the inner airway body provided from a proximal end to a distal end integrates a sputum aspiration duct and an oxygen inhalation duct.