A tracheostoma device for cooperation with a tracheostoma device holder superimposed on a tracheostoma of a person includes a tubular body and a container. The tubular body is at the proximal end of the tracheostoma device. The tubular body includes at least one inlet upon exhalation through the tracheostoma device, and is adapted for cooperation with the tracheostoma device holder. The container being at the distal end of the tracheostoma device, includes at least one outlet upon exhalation through the tracheostoma device and is adapted for housing a heat and moisture exchanging foam. The tubular body and the container have a hardness of 100 Shore A or less.

The mucus-removing device is adapted for use with a patient. The patient is further defined with a tracheostomy tube. The mucus-removing device is configured for use with the tracheostomy tube. The mucus-removing device generates a vacuum at the tracheostomy tube such that mucus is withdrawn from the pulmonary system through the tracheostomy tube and into the mucus-removing device. The mucus-removing device generates the vacuum at the tracheostomy for a fixed period of time. The periodic nature of the generation of the vacuum allows the patient to breath comfortably during the removal process. The mucus-removing device comprises a pump, a hose, a tracheostomy tube connector, and a control system. The hose attaches the pump to the tracheostomy tube connector. The tracheostomy tube connector attaches the mucus-removing device to the tracheostomy tube of the patient. The control system regulates the operation of the pump.

The present invention provides an improved visual laryngeal mask comprising a snorkel, an end of the snorkel is provided with a fixing seat. The fixing seat is provided with an airbag, and the fixing seat has a recess which is provided with an airway opening. The inner wall of the snorkel longitudinally extends an imaging cavity and a cleaning channel. The imaging cavity has a built-in imaging device, and the imaging cavity and the cleaning channel protrude forward relative to the airway opening to form a stopper which prevents an epiglottis from blocking the imaging device.

A mouthpiece for interfacing a subject to a respiratory measurement apparatus incorporates bite blocks and a tongue depressor such that when the bite blocks are clamped between teeth of the user's upper and lower jaws, the tongue depressor forces the user's tongue downward so as not to inhibit gas flow through a lumen of the mouthpiece. Also disclosed are cheek supports that can be coupled to the mouthpiece and where the space between adjacent cheek supports is selectively adjustable to fit the subject involved.

An oral appliance for increasing oxygenation including: an upper component configured to fit onto at least a portion of upper teeth of a user and including an upper locking mechanism; and a lower component configured to fit onto at least a portion of lower teeth of the user and including a lower locking mechanism configured to engage the upper locking mechanism in at least one position of the lower component relative to the upper component corresponding to at least one protrusion position of a mandible of the user of 50% of maximum protrusion to set an oxygenation capacity of the user; wherein the upper locking mechanism and the lower locking mechanism are configured to be lockable or unlockable or both by a pressure of a tongue the user or the mandible or both.

A wearable suction catheter that can be used without clinician control. The suction catheter attaches on or near the patient with a patient interface configured for the shape of the nose, mouth or tracheostomy tube. The patient interface includes at least two radial duct openings and each end of the interface is connected to airway tubing ending in a wye. The wye end of the catheter includes a cleaning access port and is attached to a suction source that provides continuous or intermittent suction.

The invention relates to a tracheostoma protection device for covering a tracheostoma, comprising an open-cell foam cloth, an adhesive strip and an air-impermeable region arranged distally on the foam cloth and associated with the tracheostoma, the tracheostoma being concealable by means of the air-impermeable region. During use of the tracheostoma protection, the foam cloth can by moved at least to some degree outwardly from a contact surface about the tracheostoma.

Techniques for emergency apneic oxygenation include a cannula having a longitudinal inner passage with an inner diameter. A distal portion has a first outer diameter greater than the inner diameter, and is made of shape memory material shaped to bend in a first direction along the inner passage. A cannula base has a second outer diameter greater than the first outer diameter. A distance from a distal end of the cannula to a proximal end of the distal portion of the cannula is less than a distance from a surface of a throat of a subject to a distal surface of an airway of the subject. The inner passage is configured to pass a catheter connected at a proximal end to an oxygen source. In various embodiments, the cannula is used with a trocar and, optionally, a system base, or supplied in a kit with a catheter.

Implementations of a tracheostomy plate decorative cover are provided. In some implementations, the tracheostomy plate decorative cover comprises a front surface, a back surface, a left side, a right side, a top side, a bottom side, a tracheostomy tube opening, a first neck strap opening, and a second neck strap opening.

In some implementations, a method for using the tracheostomy plate decorative cover comprises positioning and/or attaching the tracheostomy plate decorative cover to a tracheostomy plate. In some implementations, the method may also comprise attaching the tracheostomy plate to a tracheostomy tube. In some implementations, the method may also comprise attaching a neck strap to the tracheostomy plate.

An aspect of the disclosure is related to a medical device for providing an air passageway through a neck of a patient. In one embodiment, the medical device may include: a neckband configured to extend around the neck of the patient, the neckband including a connector positioned along a length of the neckband for positioning along an anterior part of the neck of the patient, the connector including a connector through hole; a cannula having an elongated tube extending from a connecting head, the elongated tube being configured to extend into a trachea of the patient and including an inner passageway, the connecting head having a through hole that is continuous with the inner passageway of the elongated tube thereby allowing air to pass through the cannula into the trachea, the connecting head having an outer diameter that is sized to have a friction fit with the connector through hole.