Abstract: An automatic sensor inserter is disclosed for placing a transcutaneous sensor into the skin of a living body. According to aspects of the invention, characteristics of the insertion such as sensor insertion speed may be varied by a user. In some embodiments, insertion speed may be varied by changing an amount of drive spring compression. The amount of spring compression may be selected from a continuous range of settings and/or it may be selected from a finite number of discrete settings. Methods associated with the use of the automatic inserter are also covered.

Abstract: A spirometer comprises a housing defining a fluid flow pathway extending between a first end and a second end, a first opening along the pathway and a second opening longitudinally spaced along the pathway from the first opening. A flow chamber defining a fluid flow pathway is disposed within the housing between the first opening and the second opening, the flow chamber including an elongated resistive element along the central longitudinal axis of the flow chamber for defining a flow passage through the flow chamber between the resistive element and the inner surface of the flow chamber. The flow chamber conditions fluid flow for accurate sensing of the fluid flow over a range. A pressure sensor is disposed within the housing in fluid communication with the first opening and the second opening for sensing a pressure differential between the first opening and the second opening and producing an electric signal that corresponds with the rate of fluid flow through the housing.

Abstract: A magnetic field generating-apparatus for biostimulation including: a C-shaped annular core having a gap-portion; and coils wound around the core, wherein the core includes a pair of facing extended-portions which lie on the both sides of the gap-portion and which face each other by extending toward the adjacent directions, and includes a pair of opposite-side portions which are juxtaposed on the respective outsides of the pair of facing extended-portions, and wherein the coils are wound around the pair of opposite-side portions respectively.

Abstract: In accordance with embodiments of the present disclosure, a flexible and non-absorbent vaginal insert device shaped to be held securely in place in a vagina when inserted, so as to improve symptoms associated with pelvic organ prolapse or urinary incontinence or both, is provided. The device is designed to be relatively easy to insert and remove. An applicator may be used to aid with insertion. The vaginal insert device comprises an upper portion, having a cone-shaped body, having a circular transverse cross-section throughout its length, having a wall with an interior side and an exterior side, an upper open end, a lower end, and a hollow interior, wherein the upper open end of the upper portion is the innermost portion of the device during insertion, and wherein the wall of the upper portion can be squeezed to make the upper portion more compact for easier insertion of the device, and wherein after insertion the wall expands back to its original shape.

Abstract: A method for graphically displaying evoked potentials is disclosed herein. The method transforms each of an averaged evoked potentials into a single vertical line, wherein a first amplitude range is represented by a first color, a second amplitude range is represented by a second color, a third amplitude range is represented by a third color and a fourth amplitude range is represented by a fourth color.

Abstract: An analyzer for diagnosing pulmonary and abdominals including, a pulsed force generator for outputting a mechanical disturbance to generate vibrations and reflected/return waves/vibrations in a patient's torso, and sensors for detecting the vibration/return wave signals. The apparatus compares the detected electrical signals with pre-stored reference wave profiles and based on the compared data generates an output signal indicative of a potential presence or absence of a pulmonary disease and/or condition.

Abstract: The present embodiments relate generally to applicators of on-skin sensor assemblies for measuring an analyte in a host, as well as their method of use and manufacture. In some aspects, an applicator for applying an on-skin sensor assembly to a skin of a host is provided. The applicator includes an applicator housing, a needle carrier assembly comprising an insertion element configured to insert a sensor of the on-skin sensor assembly into the skin of the host, a holder releasably coupled to the needle carrier assembly and configured to guide the on-skin sensor assembly while coupled to the needle carrier assembly, and a drive assembly configured to drive the insertion element from a proximal starting position to a distal insertion position, and from the distal insertion position to a proximal retraction position.

Abstract: A medical device for narrowing or closing an anatomical channel includes a band part (1) which can be placed around the body tissue (2) surrounding the anatomical channel and which can be closed to form a ring that encloses a through-opening (6) for the body tissue, wherein the band part (1) has a hollow chamber (3), and wherein the through-opening (6) can be made smaller by introducing a fluid into the hollow chamber (3). The medical device moreover includes a pump unit (10) which serves to convey the fluid and which has an electric drive (15) controllable by an electronic control system of the device, wherein a pressure value corresponding to the pressure of the fluid in the hollow chamber (3) or dependent on this pressure can be detected by the electronic control system. The device moreover has an air pressure sensor (23) for detecting the atmospheric pressure.

Abstract: A fluid control device (10) includes a container (13), a pump (11), a solenoid valve (12), and a capacitor. The pump (11) is driven by a main power source, and is capable of pressurizing or depressurizing the inside of the container (13). A suction port and a discharge port of the pump (11) internally communicate with each other. The solenoid valve (12) is connected at both ends thereof to the container (13) and the pump (11). If the voltage of the main power source is reduced or lost, the solenoid valve (12) releases pressure in the container (13) by being driven by the power stored in the capacitor or secondary battery.

Abstract: A rectocele device having an inflatable balloon and extendable armature inside of the balloon as the balloon expands provides added stability when used to push on a rectocele. More specifically, a rectocele handle can include a rectocele paddle, which can extend in length, and balloon combination extending from the handle. A protective sheath that has a tubular body covers the balloon. The paddle, generally comprised by a piston and piston housing, can increase its length by way of a piston extending in and out of the piston housing. When the rectocele paddle and balloon combination is deployed in a vagina, to push on the rectocele, the balloon is inflated which causes the piston to extend from the piston housing with the balloon inflation. The piston and piston housing paddle provide stability for the inflated balloon.

Abstract: A ferrofluid chamber has a housing that is adapted to be coupled to a component that generates a magnetic field. The housing may be disposed around the component so as to insulate a noise-producing region of the component. The magnetic field may be of sufficient strength to stimulate anatomical tissue. In addition, a ferrofluid may be disposed within the housing for cooling the component.

Abstract: In accordance with embodiments of the present disclosure, a flexible and non-absorbent vaginal insert device shaped to be held securely in place in a vagina when inserted, so as to improve symptoms associated with pelvic organ prolapse or urinary incontinence or both, is provided. The device is designed to be relatively easy to insert and remove. An applicator may be used to aid with insertion. The vaginal insert device comprises an upper portion, having a cone-shaped body, having a circular transverse cross-section throughout its length, having a wall with an interior side and an exterior side, an upper open end, a lower end, and a hollow interior, wherein the upper open end of the upper portion is the innermost portion of the device during insertion, and wherein the wall of the upper portion can be squeezed to make the upper portion more compact for easier insertion of the device, and wherein after insertion the wall expands back to its original shape.

Abstract: A device for obtaining physiological information including plethysmographs of a medical patient and detecting a condition of pneumonia. The portable pneumonia screening device may include one or more sensors configured to obtain physiological information. The pneumonia screener may provide for methods of selecting and interfaces to assist selecting a patient's age group. The screener may match a selected age group from a set of programmed threshold level of oxygen saturation, respiratory, pulse rate, or other physiological parameters to assist pneumonia diagnosis. The pneumonia screener may provide one or more visual and/or audio stimuli, such as an animation, sound or music. The visual and/or audio stimuli may indicate initialization, diagnostic in progress, completion, or other events or progress of events. In some embodiments, the visual and/or auditory stimuli may be used to soothe or intrigue the patient such that patient agitation is reduced during the screening process.

Abstract: There is provided a system, system architecture, and method for neural cross-frequency coupling analysis. In an embodiment, the method includes: receiving neural signals; extracting a phase frequency signal and an amplitude frequency envelope signal from each of the neural signals; determining a first measure of cross-frequency coupling comprising a mean vector length modulation index (MVL-MI), determining the MVL-MI comprises determining a magnitude of an averaged complex-valued time series from a plurality of samples of the neural signals to extract a phase-amplitude coupling measure, each sample associated with a respective one of the amplitude frequency envelope signals and the phase frequency signals; and outputting at least one measure of the cross-frequency coupling.

Abstract: Systems for applying a transcutaneous monitor to a person can include a telescoping assembly, a sensor, and a base with adhesive to couple the sensor to skin. The sensor can be located within the telescoping assembly while the base protrudes from a distal end of the system. The system can be configured to couple the sensor to the base by compressing the telescoping assembly.

Abstract: This medical device measures blood flow rate through the renal artery after a kidney transplant in real time. The device utilizes a force sensing resistor (FSR) to detect the amount of blood and the given blood pressure at any instantaneous point in time. The FSR wraps around the renal artery after transplantation and should remain connected for five to seven days for optimal kidney blood flow and kidney functioning detection. This will be achieved by measuring the flow rate, estimating blood pressure, and beats per minute this device should alert doctors if irregular kidney function should occur for fast and immediate surgical or bedside intervention. Our goal is to detect post-transplant kidney rejection in real-time. The device is biocompatible and sterile, easily removed from the renal artery, and smaller than 5 mm in diameter.

Abstract: The disclosed systems and methods for monitoring a patient in a medical setting may include various types of sensors that obtain data indicative of one or more patient parameters and one or more environmental parameters. One or more processors may process the data to identify a correlation, or causal relationship, between the one or more patient parameters and the one or more environmental parameters. Thus, the systems and methods may be used to identify particular environmental parameters that affect a particular patient to facilitate creation of a suitable environment for the particular patient. The disclosed monitoring systems and methods may be especially useful for sensitive, high-risk, and/or non-verbal patients, such as infants in a neonatal intensive care unit (NICU).

Abstract: Some embodiments relate to a reconfigurable biosensor adapted for performing tests in a plurality of modes or a smartphone or wearable device comprising the reconfigurable biosensor.

Abstract: There is provided a method that includes receiving pulse-oximetry measurements (SpO2) of a patient's peripheral arterial blood oxygen saturation during a first time period, and receiving breathing samples of the patient. The method further includes determining, using breathing samples of the patient, oxygen partial pressure measurements (PAO2) and carbon dioxide partial pressure measurements (PACO2) from exhaled air of the patient during a steady-state breathing of the patient during the first time period.

Abstract: A method for administering tests using a regional antigen testing kit is provided. The method comprises providing the regional antigen testing kit, extracting a predetermined amount of concentrated antigen from one of a plurality of concentrated antigens, dispensing the predetermined amount of concentrated antigen into a corresponding one of a plurality of wells, as indicated by visual indicia, repeating the extracting and dispensing steps until a desired number of the plurality of wells contain concentrated antigen, providing a prick tester having a plurality of needles extending thereon, aligning the plurality of needles of the prick tester with the plurality of wells, inserting each of the plurality of needles of the prick tester into one of the plurality of wells, and applying the plurality of needles of the prick tester to the skin of a patient to elicit a potential response.