Breathing tubes for use with a spirometer. The breathing tubes include a body having an oval interior cross-sectional shape and are configured to engage interior surfaces of the spirometer, so as to ensure the proper orientation of the body within the spirometer.

Laryngeal airway devices for human and veterinary use include an airway tube having a distal end and a proximal end. The distal end of the airway tube is provided with a pre-formed and non-inflatable peri-pharyngeal bowl. The peri-pharyngeal bowl has a posterior bowl portion having a back dorsal portion and a side wall extending around and depending from the periphery of the back dorsal portion to define an internal space, and further having a resiliently deformable flange extending laterally from the side wall of the back dorsal portion which defines an extended internal space, the resiliently deformable flange has inner and outer surfaces that extend to a circumferential edge.

A laryngeal mask airway device (20, 320) is provided including an inflatable balloon (30, 330), which is (a) shaped so as to define at least an inflatable annular cuff (32, 332) and a proximal inflatable pharyngeal portion (34, 334), and (b) insertable through an anterior opening of a patients oral cavity. The inflatable balloon (30, 330) is configured such that when an inflatable chamber (56) thereof is filled with air at a pressure of 10 cm H2O and unconstrained, a volume of the air in a proximal one-third (60) of the inflatable chamber (56) equals at least 200% of a volume of the air in a distal one-third (62) of the inflatable chamber (56). Other embodiments are also described.

Described is a system including an air pressure supply arrangement, a sensor and a titration device. The air pressure supply arrangement provides air pressure to a patient's airways. The sensor detects input data corresponding to a patient's breathing patterns of a plurality of breaths. The titration device receives and analyzes the input data to determine existence of breathing disorder and corresponding characteristics. The titration device generates output data for adjusting the air pressure supplied to the patient as a function of an index of abnormal respiratory events included in the input data.

An expandable inter-vivos tube that allows for the use in medical procedures while limiting known complications arising from conventional inter-vivos tubes is presented, wherein the expandable inter-vivos tube comprises a slit formed longitudinally within a tube and a plurality of nipples extending from an outer surface of the tube that are insertable within a corresponding one of a plurality of slides within an outer slidable element that is slidable within the slit. A position of the nipples within the slots causes a distance between the edges of the to increase; thus, increasing a circumference of the inter-vivos tube as the outer element is slide from a proximal end of the tube element to a distal end of the tube.

An expandable inter-vivos tube that allows for the use in medical procedures while limiting known complications arising from conventional inter-vivos tubes is presented, wherein the expandable inter-vivos tube comprises a slit formed longitudinally within a tube and a plurality of nipples extending from an outer surface of the tube that are insertable within a corresponding one of a plurality of slides within an outer slidable element that is slidable within the slit. A position of the nipples within the slots causes a distance between the edges of the to increase; thus, increasing a circumference of the inter-vivos tube as the outer element is slide from a proximal end of the tube element to a distal end of the tube.

The invention relates to a device for the dynamically adapting sealing of an organ or a body cavity, e.g. the windpipe (trachea) of an intubated and ventilated patient, wherein the sealing balloon element is produced via particularly rapid shifting of filling medium from an extracorporeal reservoir or an extracorporeal source to the sealing balloon, and wherein, in the dynamic sealing of the trachea according to the example case, a balloon-type foil body preferably formed with residual material in the diameter, i.e. exceeding the tracheal diameter, is in contact with the inner wall of the trachea in a sealing manner and with a pressure that is as constant as possible, wherein fluctuations in the balloon volume, caused by fluctuations in the intrathoracic pressure relating to the mechanics of breathing, are compensated as quickly as possible by supplying volume from an extracorporeal reservoir or an extracorporeal source, and the tracheal secretion sealing of the balloon is thereby kept continuous. This is both made possible by a sufficiently high-volume supply of the balloon filling medium to the cuff, and also prevents steps, gaps or ridges in the supply system, whereby volume flow directed towards the balloon can be minimised, which is crucial for a rapid-as-possible stabilising of the filling volume in the balloon, in particular with small pressure differences between 15 and 30 mbar that are driving the volume flow.

An airway management device comprising a body having a proximal end for receiving an oxygen supply tube and an distal end for insertion into a trachea of a patient; said body including a linear portion adjacent to the proximal end and a curved portion adjacent to the distal end; said body including an external shell and having a first bore through said shell for receiving the oxygen supply tube; wherein flexural strength for said airway management device is provided by said shell.

An endotracheal device for mechanical ventilation of a patient includes a ventilation tube and a barrier. The ventilation tube includes a distal part, with a distal end, intended to be inserted into an airway of a patient, and a proximal part, with a proximal end, intended to be connected to a ventilation machine. The barrier is made of solid viscoelastic material, covers the ventilation tube in the distal area, and is configured to occupy, when inserted, the subglottic region, as well as the glottic region and also the supraglottic region of the larynx of the patient, for which reason the barrier has a variable cross section along the length thereof. The device provides greater safety and a lower incidence of complications in mechanical ventilation of patients.

An oropharyngeal airway device includes an elongated hollow body having proximal and distal ends, and a collar secured to the proximal end of the elongated hollow body. The device also includes an aspiration tube and an adapter where the adapter has a first open end and an opposing second open end. The first and second open ends are each coupled to the aspiration tube. In addition, the device includes a delivery conduit coupled to the adapter and positioned within the elongated hollow body in order to deliver gas from a gas supply to the distal end of the elongated hollow body and into an airway of a patient. The device includes at least one fastener within the collar for removably securing the adapter to the collar.