The present invention includes a system and device for aiding in the diagnosis of a physiological abnormality resulting in detectable, measurable variations in contents of breathed air. The system includes a handheld unit defining an airway, wherein the airway includes a plurality of sensors adapted to measure a plurality of parameters related to the presence of a physiological abnormality. The system further includes a control unit remotely connected to the handheld unit. The control unit includes a controller adapted to receive input signals from the handheld unit and remit output signals in response thereto. The output signals are usable by a user in determining the presence or absence of a physiological abnormality. The control unit further also can include a display adapted to display the output signals to a user thereby easing the determination of the physiological abnormality. The system further includes a mouthpiece selectively connectable to the handheld unit. The mouthpiece can include a filter adapted to substantially prohibit the passage of germs into the airway of the handheld unit.

The present invention is a holding case for an instrumented intra-oral appliance containing recorded data, which charges the intra-oral appliance while not in use and transmits recorded data to storage for review and analysis. The transferred data may be subjected to downloading, validation, storage, analysis, measuring, database fusion (with for example data from other devices), data output, and data recording. Output may be further transferred to a computer, processor, phone, tablet computer, or other hardware for review by a user or technical, research, medical, or other oversight personnel. The holding case can also send data to the appliance including firmware or other onboard operating instructions. The holding case can include additional features such as custom dentition of the user, UV light, or a visual user interface.

Embodiments of the present disclosure relate to reusable medical sensors. According to certain embodiments, the medical sensor may include a sensor housing, an emitter disposed in the sensor housing, the emitter being configured to direct light through the tissue of a patient, and a detector disposed in the sensor housing, the detector being configured to detect light from the emitter after the light has passed through the tissue of the patient and to convert the detected light to an electrical signal. The sensor may also include a dye disposed in the sensor housing, wherein the dye is configured to exit the sensor housing when the sensor housing is damaged and is within a solution.

Apparatus and methods related to an underbody support for supporting a body of a being, such as during surgery to prevent contact pressure injuries. In certain embodiments, the underbody support may include one or more inflatable chambers enclosing a volume. At least one of the inflatable chambers may include one or more compression sensitive switches for monitoring the volume of the inflatable chamber, and the one or more compression sensitive switches may be located within the inflatable chamber. In some embodiments the one or more compression sensitive switches are sized to close when the said inflatable chamber is deflated to a desired residual volume.

Apparatus and methods related to an underbody support for supporting a body of a being, such as during surgery to prevent contact pressure injuries. In certain embodiments, the underbody support may include one or more inflatable chambers enclosing a volume. At least one of the inflatable chambers may include one or more compression sensitive switches for monitoring the volume of the inflatable chamber, and the one or more compression sensitive switches may be located within the inflatable chamber. In some embodiments the one or more compression sensitive switches are sized to close when the said inflatable chamber is deflated to a desired residual volume.

Apparatus and methods related to an underbody support for supporting a body of a being, such as during surgery to prevent contact pressure injuries. In certain embodiments, the underbody support may include one or more inflatable chambers enclosing a volume. At least one of the inflatable chambers may include one or more compression sensitive switches for monitoring the volume of the inflatable chamber, and the one or more compression sensitive switches may be located within the inflatable chamber. In some embodiments the one or more compression sensitive switches are sized to close when the said inflatable chamber is deflated to a desired residual volume.

A disinfection system for use in cleansing one or more medical devices or components that are placed on, in, or in proximity to a patient during a medical procedure is disclosed. Non-limiting examples of a medical component that may be cleansed by the disinfection system include an ultrasound probe or a chest sensor of a catheter placement system. In one embodiment, therefore, a disinfection system for a medical device is disclosed, comprising a container configured for proximate placement with respect to the medical device and an array of light sources included with the container. Each light source is configured to produce disinfecting light in a high energy visible light wavelength range. Further, the light sources are arranged to impinge the disinfecting light upon a portion of the medical device so as to disinfect the impinged surfaces of the medical device.

A medical battery includes: a chargeable and dischargeable battery cell; a first electrode and a second electrode that are connected to the battery cell and are electrically connected to external electrodes in a non-contact state; a switching unit that is provided in a battery circuit including the battery cell, the first electrode, and the second electrode, the switching unit being configured to switch a current flowing through the battery circuit to an alternating current or a direct current; an insulating housing that seals and houses the battery cell, the first electrode, the second electrode, and the switching unit therein; and a heat storage unit arranged between an inner surface of the housing and the first electrode, and between the housing and the second electrode.

The present disclosure relates to an analyte sensor comprising a working electrode, a sensing layer disposed on at least a portion of the working electrode that comprises an analyte-responsive enzyme, and a polymer membrane overcoating at least the sensing layer. The polymer membrane comprises an antimicrobial agent disposed therein, a hydrogel coating disposed thereon, or both an antimicrobial agent disposed therein and a hydrogel coating disposed thereon. The presence of an antimicrobial agent, such as an antibiotic, a hydrogel coating, or both reduces early/late signal attenuation of the analyte sensor. The polymer membrane can further be combined with a metal-containing layer in electrochemical communication with a reference electrode, a counter electrode, and/or second working electrode.