Abstract: Disclosed is a touch-sensitive user interface intended to interact with a tracheobronchial-air stimulation device including: —a touch-sensitive display screen for providing the user with information about the use of the tracheobronchial-air stimulation device, —a communication module for communicating data between the touch-sensitive user interface and the tracheobronchial-air stimulation device, —a memory in which biofeedback software and data, referred to as input data, may be saved, and —a data processing unit configured by the biofeedback software.

Abstract: A tracheal tube assembly includes an outer cannula configured to be positioned in a patient airway and an inner cannula configured to be disposed inside the outer cannula. The tracheal tube assembly includes a removable neck flange bracket with trach tie adapter points secured about the outer cannula, and a connector coupled to a proximal end of the outer cannula. The connector can include a swivel design feature and a flexible tubing connector may be formed with the connecter. The connector is constructed and arranged to provide a view of the inner cannula, and the inner cannula and the connector form a contiguous passageway for exchanging fluid with the patient airway in operation.

Abstract: An adjustable tracheostoma valve is disclosed. The adjustable tracheostoma valve includes a passageway for connecting the trachea with the surroundings. A valve disk is provided in the passageway. The disk is moveable to allow for inhalation and exhalation through the passageway and is configured to close in response to pressure to direct air to the patient's pharynx, esophagus, sinuses, and mouth for speech following surgical removal of the larynx.

Abstract: An endotracheal tube insertion device includes an insertion member, a flexible optical assembly member movably mounted to the insertion member, an endotracheal tube, and an endotracheal tube attachment member attached to the insertion member and configured to receive and retain the endotracheal tube.

Abstract: A cushion for a breathing mask and a breathing mask. The cushion includes a connection portion for connecting to a frame or an elbow assembly of the breathing mask; a face contact portion for getting in contact with the face of a patient, wherein the face contact portion is formed by a thin membrane; and a support portion which is connected between the connection portion and the face contact portion, wherein the face contact portion has an external extension portion which extends from the support portion to the exterior of the cushion and an internal extension portion which extends from the outer circumference side of the external extension portion to the interior of the cushion in at least partial area.

Abstract: A headgear assembly for retaining a respiratory mask on a user's face includes arrangements or components that allow for variation in a size of the headgear assembly. In some configurations, the headgear assembly includes one or more hubs, each of which are configured to connect a top and rear strap together. The size of the headgear assembly can be determined by the size or configuration of the hub. In other configurations, the headgear assembly comprises one or more spacer elements within one or more straps of the headgear. The size of the headgear assembly can be determined by the size of the spacer element or a relative position between the strap and the spacer element.

Abstract: An oxygen mask configured for CO2 sampling and oxygen delivery, the oxygen mask having an oxygen inlet, a nasal breath-sampling element and a breath sampling port configured to receive breath samples, sampled by the breath-sampling element, wherein the breath-sampling element is configured to reduce dilution of exhaled breath by the delivered oxygen.

Abstract: A fluid coupling conduit is for a patient interface device. The fluid coupling conduit includes a body including: an inlet end structured to receive a flow of breathing gas, an outlet end fluidly coupled to the inlet end, and a middle portion disposed between the inlet end and the outlet end, the middle portion including a rim defining a relief aperture provided in an aperture plane. The fluid coupling conduit further includes a blocking member substantially disposed in the relief aperture, a number of openings being formed between the blocking member and the rim. The rim includes a number of protrusions extending transversely to the aperture plane.

Abstract: Some embodiments of the invention include a tracheal humidification device. The tracheal humidification device may include a first body portion and a second body portion. The first body portion may include a tracheostomy connection port formed to couple with a tracheostomy connection tube; and a heat moisture exchanger port formed to couple with a heat moisture exchanger. The second body portion may be coupled with the first body portion, for example, rotatably coupled. The second body portion may include a nebulizer port formed to couple with a nebulizer and having a closable seal that is closable when the nebulizer is not coupled with the nebulizer port; and a suction port having a closable cap.

Abstract: Several embodiments of exhalation ports for use respiratory systems are described. Some of the embodiments provide an elongate body defining a lumen through which gases may flow. A plurality of tapered openings is arranged on a portion of the elongate body and configured to vent gases. A shroud extends from the elongate body and surrounds one or more of the plurality of tapered openings. The exhalation port is arranged to removably connect in-line with a circuit for delivering gases to a patient.

Abstract: The present invention provides a new inhaler device for the storage and administration of inhalable liquids to a patient offering one or more advantages or improvements over known inhalers, particularly inhalers for the delivery of halogenated volatile liquids such as methoxyflurane for use as an analgesic.

Abstract: A pneumatic system for delivering oxygen to a subject, including an oxygen supply channel having an inlet, a patient delivery outlet and an exhaust; and a flow control element configured to control the flow from the oxygen inlet to the patient delivery outlet, or to the exhaust; wherein inhalation by the patient causes the flow control element to assume a first position, allowing oxygen to flow from the oxygen inlet to the patient delivery outlet; and wherein exhalation by the patient causes the flow control element to assume a second position, directing oxygen flow from the oxygen inlet to the exhaust.

Abstract: An embodiment of the utility model disclosed a sleep-aiding apparatus, which comprises a surface case of the body and a bottom case of the body fastened with each other.

Abstract: The present disclosure relates to a technology for a sensor network, machine to machine (M2M), machine type communication (MTC) and internet of things (IoT). The present disclosure can be utilized for intelligent services (smart homes, smart buildings, smart cities, smart cars or connected cars, health care, digital education, retail trading, security and safety-related services, etc.) based on the technology. A control method of a control device for managing a user's sleep environment according to the present invention may comprise the steps of: obtaining sleep-related information of the user on the basis of user sensing data sensed by a sensor; and controlling, on the basis of the sleep-related information, a first wavelength band output of at least one electronic device comprising a light source. The present invention may also include other embodiments, not limited to the above embodiment.

Abstract: A novel aromatherapy vaporization device is disclosed having a heating chamber first portion for receiving of phyto material and a heating chamber second portion. In a first mode of operation phyto material is loaded into the heating chamber first portion having a first conductive heating element disposed therein and in a second mode of operation an angle of a hinge is varied that brings the heating chamber second portion in proximity to the heating chamber first portion. In the second mode of operation electrical current flows from a first battery to a first conductive heating element and the phyto material is heated to a predetermined temperature and vapor is emitted from the heating of the phyto material and is captured in the heating chamber second portion and flows through a heating chamber first portion aperture and propagates through a fluid pathway for inhalation from an inhalation aperture.

Abstract: Disclosed herein are expandable introducer sheaths and methods of making and using the same. The sheaths minimize trauma to a patient's vasculature by allowing for temporary expansion of a portion of the sheath to accommodate passage of a delivery system for a cardiovascular device, then return to a non-expanded state after the passage of the device. The sheath includes an elongated annular member having longitudinally extending channels that facilitate the sheath's temporary expansion. The channels are positioned in such a way that, upon expansion, they enable the movement of protruding contact surfaces toward the inner and outer surfaces of the annular member, reducing friction between the surface and the passing device. Some embodiments of the expandable sheath include an elastic outer layer that pushes the protruding contact surfaces back towards their original positions after the passage of the device.

Abstract: Sliding friction between a catheter and a guiding core is reduced by a rotating inner catheter member (12), introduced between the guiding core (13) and an outer catheter member (11). The inner catheter member (12) is rotated in the outer catheter member (11) by a motor (14), which may be controlled by a control unit (2). A lower catheter friction with respect to the guidewire allows the physician improved assessment of the forces resulting from collisions of the outer catheter member (11) and the vascular wall.

Abstract: A system for aspirating thrombus includes an aspiration catheter including a supply lumen and an aspiration lumen each extending within an elongate shaft, and an opening at or near the distal end of the supply lumen, the opening configured to allow the injection of pressurized fluid into the aspiration lumen at or near the distal end of the aspiration lumen when the pressurized fluid is pumped through the supply lumen, a tubing set including tubing and having a distal end configured to couple to the aspiration lumen of the aspiration catheter and a proximal end configured to couple to a vacuum source, a tubing compression element configured to externally engage the tubing of the tubing set, and an activation interface configured to activate the tubing compression element to compress the tubing at a location between the proximal end of the tubing set and the distal end of the tubing set.

Abstract: Methods and devices are configured for accessing an umbilical vein of a human. The umbilical vein catheter includes a proximal access port that is closed with a septum. The septum provides a closed system to reduce the risk of air embolism and intraluminal infection via the catheter.

Abstract: A rapid exchange microcatheter for accessing the intracranial neurovasculature. A side opening through the sidewall is located a first distance proximal to the distal-most tip. A proximal opening located proximal to the side opening is a second distance from the distal-most tip. A distal, reinforced catheter portion extends between a distal end region to a point near the side opening. A proximal, reinforced catheter portion extends a distance from a point near the side opening towards the proximal end of the catheter body. The side opening is positioned within a gap between a proximal end of the distal reinforced catheter portion and a distal end of the proximal reinforced catheter portion. A payload of a cerebral treatment device is housed within the lumen proximal to the side opening. Related devices, systems, and methods are disclosed.

Abstract: A catheter for ablation, mapping, injection, and directional control by an external magnetic system has a catheter body, an intermediate section, and a tip section having a tip electrode with an omnidirectional distal end and a concentric needle port. The tip electrode houses a magnetic device and a position sensor in an integrated configuration that facilitates a path in the tip section for extension and retraction of a component, including an injection needle, with reduced stress and friction. The integrated configuration is an efficient use of space in the tip electrode that allows the tip section to carry both the position sensor and the necessary volume of magnetic or magnetizable material to accomplish magnetic navigation. The catheter also includes a very soft and flexible intermediate section and an even softer and more flexible distal transitional section carrying additional magnetic members to facilitate remote magnetic navigation.

Abstract: A tracheoscope pull wire control mechanism includes a rotating wheel pivotally arranged inside a handle; a holding cavity is formed on an upper portion of the rotating wheel; a spring and a brake block are arranged in the groove, such that a connection rod of the control piece above the handle passes through a long slotted hole at a position opposite to the handle, and is clamped and linked with the brake block; and the near ends of the two pull wires are extended and are combined on the rotating wheel of the control mechanism. The positioning structure can be operated with a single hand, which is different from the conventional two-hand control manner; and the operation efficiency and the convenience are improved.

Abstract: An elongate medical device with independently-deflectable segments and a handle for manually deflecting those segments can include a shaft having a distal segment and proximal segment, at least one proximal segment deflection wire adapted to deflect the proximal segment, at least one distal segment deflection wire adapted to deflect the distal segment independent of the proximal segment, and a handle portion. The handle portion may comprise a first manual actuation mechanism coupled to the at least one distal segment deflection wire and a second manual actuation mechanism coupled to the at least one proximal segment deflection wire. Actuation of the first manual actuation mechanism may impart a tensile force on the distal segment deflection wire to cause the distal segment to deflect, and actuation of the second manual actuation mechanism may impart a tensile force on the proximal segment to cause the proximal segment to deflect.

Abstract: A tracheoscope includes a handle having a control mechanism; one end of the handle is connected with a plug-in type screen, and the other end of the handle is combined with a catheter; the far end of the catheter is provided with a hose part including a main elastic spring ring inside, and the farthest end of the catheter is combined with a probe provided with a shooting module and luminophors inside; two pull wires are arranged in the catheter; and the near ends of the two pull wires are extended and are combined on the control mechanism, and the far ends of the two pull wires are respectively arranged in two small elastic spring rings in a penetration manner and are fixed. The probe can be stably combined with the shooting module and the luminophors, so the shooting stability is improved.

Abstract: A catheter for mapping and/or ablating a region of the heart includes an intermediate section that is connected to a tip assembly at a preset angle by a flexible preshaped section that is more flexible than the intermediate section. The flexible section may absorb displacement force applied to the tip assembly, such as when the tip assembly encounters uneven tissue surface, without displacing the intermediate section. The flexible section prevents excessive force from being applied to the tip assembly, reducing the risk of any of the following: a) mechanical perforation, b) steam pop, c) burying the tip assembly in the myocardium resulting in high temperatures, low energy delivery, thrombus formation and char formation.

Abstract: Some embodiments of a medical device anchor system include an anchor device that receives a medical instrument (such as a catheter or the like) and secures the instrument in place relative to a skin penetration point. In some circumstances, the anchor device may allow the anchor device to be used after medical instrument is already in place without the need for a second penetration point for the anchor device.

Abstract: A catheter assembly includes: a catheter; a hollow inner needle that is removably disposed in the catheter and has a lumen through which a guide wire is insertable; a needle hub that is fixed to a proximal end portion of the inner needle; and a guide member that is attachable to a proximal end portion of the needle hub and configured to guide the guide wire towards the inner needle.

Abstract: A guide wire has an elongated core portion, a resin coating layer including a resin material and covering a distal portion of the core portion, and a metallic tubular member that has a lumen into which the core portion is inserted, and that is disposed so as to be in contact with at least a portion of a proximal end of the resin coating layer. The tubular member is formed in a state where the lumen is reduced in diameter by cold forging, and at least a portion of an inner surface forming the lumen has a compressive bonding surface which is compressively bonded to an outer surface of the core portion.

Abstract: An apparatus for performing a medical procedure includes a balloon with a variable profile. The balloon includes at least one inflatable chamber occupied by a fluid, such as air, and solids, such as generally spherical balls. When the chamber is inflated, the solids are spaced apart as a result of their ability to move or flow, but when the chamber is evacuated, the solids become compacted and prevent it from fully collapsing. The balloon may have a plurality of inflatable chambers with solids in different arrangements to achieve different objectives during the medical procedure, such as for example stent deployment. For example, one chamber may be expanded while the other is restrained to alter the balloon geometry, such as for providing focused force or permitting perfusion.

Abstract: There is provided a cervical canal dilator device having a hollow shaft having proximal and distal ends. The shaft is covered on an end portion of the distal end by a slidable protective sleeve. There is at least one inflatable dilating balloon formed on the distal end of the shaft. There is at least one tube extending internally along the shaft and connected to the at least one balloon for inflation thereof, the tube having a connection port on the proximal end of the shaft. A camera is situated at the tip of the distal end of the shaft and a plurality of ejection orifices are formed on the shaft, adjacent to the camera, and anywhere else along it.

Abstract: A balloon wrapping apparatus and a balloon wrapping method are disclosed by which a balloon can be accurately positioned in relation to a pleating section and to a folding section. The balloon wrapping apparatus for wrapping a balloon of a balloon catheter provided with the balloon at a distal portion of an elongated shaft includes: a pleating section having a plurality of blades aligned with space parts therebetween in a circumferential direction, and forms the balloon with wing shapes projecting in radial directions by clamping the balloon in the space parts by moving rotationally the blades; and a folding section having a plurality of blades aligned in a circumferential direction, and that folds the wing shapes formed in the balloon in the circumferential direction by moving rotationally the blades; and a support base that supports a part of the shaft which part is on a proximal side of the balloon.

Abstract: An inflation system having two pressure vessels integrated into a balloon catheter. A pressurized chamber and a vacuum chamber are integrally attached to proximal end of the balloon catheter and activated by a common valve or switch. Pressure or vacuum is selectively transmitted to the balloon depending on the valve/switch position. The working fluid may be air, or a combination of air and saline with an intermediate piston/cylinder assembly. The balloon catheter may be a part of a heart valve delivery system with a balloon-expandable heart valve crimped onto the balloon.

Abstract: Systems and methods for implanting an endovascular shunt in a patient is disclosed. The system having an expandable anchor configured for being deployed in a dural venous sinus of a patient at a location distal to a curved portion of a wall of an inferior petrosal sinus (IPS) of the patient; an elongate guide member coupled to, and extending proximally from, the anchor; a shunt delivery catheter having a first lumen configured to receive the guide member, and a second lumen extending between respective proximal and distal openings in the shunt delivery catheter, the shunt delivery catheter further having a penetrating element coupled to a distal end of the catheter; and the system further having a guard at least partially disposed over, and movable relative to, the penetrating element.

Abstract: A topical applicator of the propel/repel type includes a reservoir, an attachable applicator cap, and a metered dosing system. The reservoir is suitable for mixing a topical formulation of multiple constituents using an electronic mortar and pestle and is closed using the applicator cap. Alternatively, the reservoir may be prefilled with a ready-to-use cream and medicament formulation, then sealed with a removable seal. The topical applicator can include a fast purge feature that overrides the metered dosing system to facilitate removal of air from the reservoir. The topical applicator can also include a one-way ratcheting feature to prevent reverse movement (repel) of the metered dosing system. Metered doses can be dispensed through holes in the applicator cap by rotating a knob, which has detent positions that correspond to discrete doses, and which provides audible and tactile feedback.

Abstract: The present invention provides a nail penetration device for delivery of an antifungal treatment. Also provided are methods for introducing an antifungal treatment to an infected tissue, along with nail fungus treatment kits. Such a device is useful for treatment of fungal infection.

Abstract: The present disclosure relates to a method for manufacturing a microneedle enabling product quality and efficiency in production to be improved by reducing the time needed for spotting a viscous material. The method for manufacturing a microneedle, according to the present disclosure, comprises the steps of spotting a viscous material on a plurality of spots on a film by supplying the viscous material to the upper surface of the film by means of a plurality of through-holes provided on an injection plate, elongating the viscous material spotted on the film; and coagulating the elongated viscous material.

Abstract: A medical tubing organizer includes a base defining a longitudinal direction, a lateral direction being defined as substantially orthogonal to the longitudinal direction, and a vertical direction being defined as substantially orthogonal to the longitudinal and lateral directions. A tube retainer is positioned on a top of the base and configured to receive a medical tube that extends along the lateral direction. The tube retainer is further configured to adjust between a free flow state and a retention state, wherein, in the free flow state, the tube retainer is configured to enable movement of the medical tube in the lateral direction and resist movement in the longitudinal direction, and in the retention state, the tube retainer is configured to resist movement in the lateral, longitudinal, and vertical directions. A connector is positioned on the base for selectively coupling the medical tubing organizer to a structure.

Abstract: A self-aligning system for coupling a catheter to a rotational drive assembly includes a catheter and a drive assembly. The catheter includes an elongate catheter body, a rotatable driveshaft extending within the elongate catheter body, a connector at a proximal end of the elongate catheter body, and a keyed feature extending from an outer diameter of the connector. The drive assembly includes a motor configured to rotate the driveshaft, a receiving tube with a distal opening configured to receive the connector, and a channel on an inner surface of the receiving tube, the channel including two opposing curved walls that are angled towards a substantially straight section. The keyed feature is configured to slide against one of the opposing curved walls and into the substantially straight section to rotationally align the proximal end of the catheter with the drive assembly.

Abstract: A medical connector includes: a male connector portion that is connectable to a closed female connector portion of another medical connector, the closed female connector portion comprising an opening formed on a top wall, and a valve body blocking the opening and having a slit, an outer peripheral edge portion of the valve body being secured to the top wall; wherein the male connector portion includes: a tubular body having an outer diameter equal to or less than a length that is twice a distance between a center of a top surface of the valve body and an end of the slit that is radially furthest from the center, the tubular body being insertable into the slit, a limiting portion configured to limit an insertion depth of the tubular body, a sealing portion configured to surround the slit, and a locking portion.

Abstract: Devices, systems and methods are provided for stimulation of tissues and structures within a body of a patient. In particular, implantable leads are provided which are comprised of a flexible circuit. Typically, the flexible circuit includes an array of conductors bonded to a thin dielectric film. Example dielectric films include polyimide, polyvinylidene fluoride (PVDF) or other biocompatible materials to name a few. Such leads are particularly suitable for stimulation of the spinal anatomy, more particularly suitable for stimulation of specific nerve anatomies, such as the dorsal root (optionally including the dorsal root ganglion).

Abstract: A method and a device for treating at least a part of an individual's skin having a natural first polarization state. The method comprises the steps of applying at least two electrodes on the individual's skin at a distance from each other, and supplying a direct current to said electrodes to form an electrical potential difference between said electrodes on said part of the skin in order to bringing said part of the skin into a second polarization state, which is different from the first. The part of the skin is then suitable subjected to further treatment for example using cosmetics or pharmaceuticals. The invention can be utilized in the field of cosmetics and for therapy, and it can be used e.g. for accelerating skin care processes.

Abstract: The invention relates to a device (100) for radio-frequency (RF) skin treatment comprising an active electrode (1, 31) arranged on an operational side (15) of the device and having a first skin contact surface for electrical contact with a skin of a user during use. The device further comprises a return electrode (2, 32) arranged on the operational side (15) of the device and having a second skin contact surface for electrical contact with the skin of the user during use. The second skin contact surface is at least five times larger than the first skin contact surface. An RF generator (21) is arranged to supply an RF treatment voltage between the active electrode and the return electrode when the active electrode and the return electrode are in electrical contact with the skin, so as to heat the skin below the active electrode.

Abstract: The invention discloses an device for regulating vital energy—Zen Qi (), which relates to the field of biotechnology, which comprises two electrodes and an electronic circuit generating output, where the positive and negative electrode of the output are placed respectively close to or contact with the yin and yang sides of the organism; This device include: the power supply section, the current control section, the data storage and display section, the constant current section, the over-current protection section, the over-voltage protection section and the current detection section. By using real-time current detection and over-current and over-voltage protection, this device ensures the safety of organisms. The functions of the electronic circuit as described above can be achieved by discrete components or by integrated circuit. If it uses integrated circuit, it can greatly save a lot of discrete components, reducing the size of the device and improve its reliability.

Abstract: Disclosed is a method for processing asynchronous signals generated by a light sensor, the sensor having a matrix of pixels, the method including: —receiving the asynchronous signals, each signal being associated with a pixel in a group of pixels in the matrix, each signal including successive events issued by the associated pixel; —upon an occurrence of an event in one of the asynchronous signals, updating an integration value associated to the group by adding an additive value to the integration value; —if the integration value is greater than a predetermined threshold, generating an event in an outputted asynchronous signal.

Abstract: A device may include an implantable circuit and at least one pair of implantable electrodes, in electrical communication with the implantable circuit. The circuit and the electrodes may configured for implantation in a subject in the vicinity of a nerve. The circuit may be configured to deliver to the electrodes an electrical signal having a current less than about 1.6 milliamps, and the electrodes may be configured to emit an electric field such that a portion of the field lines extend along a length of the nerve such that the delivery of the electrical signal of less than about 1.6 milliamps causes modulation of the nerve.

Abstract: A computer implemented system and method facilitates a cycle of generation, sharing, and refinement of volumes related to stimulation of anatomical tissue, such as brain or spinal cord stimulation. Such volumes can include target stimulation volumes, side effect volumes, and volumes of estimated activation. A computer system and method also facilitates analysis of groups of volumes, including analysis of differences and/or commonalities between different groups of volumes.

Abstract: Methods and devices for configuring the use of a motion sensor in an implantable cardiac device. The electrical signals of the patient's heart are observed and may be correlated to the physical motion of the heart as detected by the motion sensor of the implantable cardiac device in order to facilitate temporal configuration of motion sensor data collection that avoids detecting cardiac motion in favor of overall motion of the patient.

Abstract: An electronics module for use in an Implantable Medical Device (IMD) may include a plurality of electrical components connected to form a circuit that includes a terminal and a potting material that supports the plurality of electrical components. The plurality of electrical components and the potting material together form a circuit sub-module in which the terminal is accessible from outside of the circuit sub-module. A metallic layer that conforms to an outer surface of the circuit sub-module is provided thereon such that the terminal is accessible from outside of the metallic layer.

Abstract: An encapsulated filtered feedthrough assembly for an implantable medical device including a ferrule, an electrical insulator coupled to the ferrule, a printed circuit board (PCB), a feedthrough conductor extending through the electrical insulator and the PCB, and a capacitor coupled to the PCB. The encapsulated filtered feedthrough assembly can include a mold defining an opening and located with respect to the printed circuit board such that at least a portion of the capacitor is positioned within the opening. A first non-conductive material can underfill the capacitor and a second non-conductive material can be backfilled into the mold to encapsulate the capacitor.

Abstract: In some examples, the disclosure describes an implantable medical device comprising a plurality of electrodes, sensing circuitry configured to sense a physiological electrical signal via the plurality of electrodes, and communication circuitry configured to transmit and/or receive a transconductance communication signal via the plurality of electrodes, wherein at least one electrode of the plurality of electrodes comprises a lower-capacitance portion and a higher-capacitance portion.