Abstract: An inventive medical device includes an implantable device, such as an electrochemical sensor. The implantable device has an implantable portion configured for insertion into a patient, a contact portion configured for connection to another device, and an interconnecting portion connecting the implantable portion and the contact portion. A housing is provided that has a first part that is removably connectable with a second part to form a sterile packaging to seal the implantable portion against a surrounding environment. The first part comprises a first sealing surface and the second part comprises a second sealing surface and the first and second sealing surfaces interact to form a sealing area. The interconnecting portion of the implantable device extends through the sealing area. An inventive method of producing the medical device is also disclosed.

Abstract: A device monitors circumferences of the leg, and estimates volume of a section of the leg, to detect edema, which can be indicative of CHF, and gauge the effectiveness of medication. The device sends the calculations to a database via BLUETOOTH™ for the patient's treating medical personnel to see.

Abstract: A blood sampling transfer device that includes a lancing tape having a flow channel and a transfer cartridge removably connected to the lancing tape is disclosed. The blood sampling transfer device provides a closed system that reduces the exposure of a blood sample to both skin and environment and provides fast mixing of a blood sample with a sample stabilizer.

Abstract: A skin pricking device includes a housing having an opening formed in a proximal end thereof; a spring mounted lancet including a needle within a casing having body and cap parts, interconnected by a separable coupling. The cap part has a cap projecting through the opening allow a user to grip and remove the cap. The device further includes a trigger for firing the lancet. Turning the cap part moves the entire lancet, engaging a trigger stop surface on the distal body part of the lancet with a trigger catch and further biasing the trigger to block the lancet. Further turning of the cap part over a second angle relative to the housing causes the cap part to move in a proximal direction by a further, second distance, thereby axially separating the cap part from the body part, whereby the cap part can then be removed from the device.

Abstract: A subject performs a sit-to-stand operation while wearing a device (SU) that contains an acceleration sensor (11) on the front of the chest. The present invention derives a muscular strength index representing the muscular strength of a human body by obtaining maximum acceleration value data from a signal expressing the size of an acceleration vector comprising a tri-axial component in detected acceleration, and using the maximum acceleration value data and the muscle mass or body fat mass of the subject. The present invention has the ability to derive a physical activity amount from the acceleration detection results, and on the basis of the activity amount (ACT) during a prescribed activity target period and the muscular strength index at the start and end times of the activity target period, obtains an activity efficiency index that corresponds to changes in the muscular strength index in response to the amount of activity.

Abstract: A body characteristic measurement method causing a computer to execute a process, the process includes: determining a gait of a quadruped based on accelerations, acquired from a multi-axis acceleration sensor attached to the chest of the quadruped, in multiple axial directions; and determining, if the determined gait is gallop or canter, an injury risk of the quadruped based on a waveform of a positive half-wave region of acceleration in a movement direction of the quadruped in the case where an increase in the acceleration in the movement direction of the quadruped is defined as positive.

Abstract: A nursing monitoring device includes an inlet conduit with an inlet opening to enable milk that is released from a nipple to enter the inlet conduit. An outlet conduit with an outlet opening enables milk from the outlet conduit to enter a mouth of a nursing child. A measurement unit connected to the inlet conduit and to the outlet conduit enables measurement of a property of the milk that flows from the inlet conduit to the outlet conduit via the measurement unit. The outlet conduit is sufficiently long to enable placement of the measurement unit laterally to the mouth.

Abstract: The invention relates to a device for posturography having a measuring platform, which comprises a standing surface for a test person having a base element on which the measuring platform is tiltably supported by means of a tilting apparatus, and having an air cushion means with which an air cushion bearing the base element is formed, wherein a damping member having a damping material is arranged between the measuring platform and the base element, by which damping member a tilting movement of the measuring platform is damped.

Abstract: A biopsy device includes a body, a needle, a cutter, an analysis area, a valve, and a tissue sample holder. The cutter is movable relative to the needle and in communication with the needle for transporting tissue samples. The analysis area is disposed proximally of the cutter and in communication with the needle to receive a tissue sample cut by the cutter for analysis by a user. The valve is disposed proximally of the analysis area and configured to alternate between an open configuration and a closed configuration. The tissue sample holder is disposed proximally of the valve and fixedly attached to the body. The valve is configured to permit analysis of the sample disposed in the analysis area when the valve is in the closed configuration and to permit the tissue sample to be passed into the tissue sample holder when the valve is in the open configuration configuration.

Abstract: A lancing device having improved charging features is disclosed. In one example embodiment, the charging mechanism generally includes a user actuated portion or charging member and a cam feature for engagement therewith. The charging member includes a finger projection or boss and the cam feature includes a ramped surface. Actuating the charging member causes the finger projection to movably engage the ramp surface of the cam feature and charge the drive mechanism.

Abstract: A pulse wave measuring device checks whether amplitude of a pulse signal satisfies a gain changing condition and, when the gain changing condition is satisfied, changes a gain. The pulse wave measuring device includes an amplitude storing unit and a mode progressing unit. The amplitude storing unit stores plural gain changing conditions, to which a series of order are assigned, respectively. A mode progressing unit 15 changes the gain changing condition to the next-ordered gain changing condition upon determination that the mode progress condition is satisfied. The gain changing condition is satisfied in case that Y1 or more number of pieces of X1 amplitudes are larger than an upper limit value U1 or smaller than a lower limit value L1. X1 is increased as the order of the set gain changing condition is higher.

Abstract: A system for measuring and monitoring physiologically relevant motion of a subject includes at least a motion sensor to measure movement of the subject and produce a series of movement data representing the movement of the subject over a period of time. The system also includes at least a biometric sensor to simultaneously measure biometrics of the subject and produce a series of biometric values of the subject over the period of time. The system is configured to determine a noise-to-signal ratio for the series of movement data as a function of biometric intervals in the series of biometric values and identify at least a portion of the series of movement data as corresponding to a physiologically relevant biorhythm. The system can be used to diagnose and monitor a disease or disorder, including a neurological disorder or a traumatic brain injury.

Abstract: A catheter includes a distal distension balloon and circumferentially arranged motility measurement balloons proximal of the distension balloon. A manifold includes balloon ports each configured to fluidly couple to a motility measurement balloon, pressure transducer ports, and a priming port. A port selector is coupled to the manifold and movable between different positions. Each port selector position causes the manifold to establish different fluidic couplings between the respective motility balloon, pressure transducer, and priming ports. A pressure sensing device includes pressure transducers each fluidly coupled to one of the pressure transducer ports. The pressure sensing device is configured to coordinate calibration of the pressure transducers at atmospheric pressure with the port selector in a first position and motility balloon pressure measurements with the port selector in a third position.

Abstract: An eye sensor, system and method for measuring fixational eye movements of an individual's eyeball (e.g., ocular microtremors and microsaccades) to provide a variable voltage biosignal for measuring the individual's brainstem activity is provided. The eye sensor comprises a sensor mounted on the individual's closed or opened eyelid so as to be deflected by the fixational eye movements of the eyeball. A shielded flexible ribbon assembly supplies the biosignal generated by the sensor to an amplifier located on the individual's skin where the biosignal is amplified. The amplifier is interconnected with a signal processor and a display by which graphical and numerical representations of the biosignal are made accessible to an anesthesiologist, intensivist or clinician. A method for analyzing the biosignal to determine the brainstem activity of a patient is also provided.

Abstract: The present invention concerns an elongated medical device (1) suitable for intravascular insertion. Said device comprising a flexible elongated body (2) having a distal portion (3) with a distal end (4) and a proximal portion (5) and an optic force sensing assembly (20) disposed within said flexible elongated body (2) proximate said distal end.

Abstract: The arterial health of an individual can be determined by: attaching a fingertip photopiethysmography device to a fingertip of the hand of the elevated arm of the individual; measuring the analog pulse contour of the individual using the fingertip photopiethysmography device; digitizing the analog pulse contour; analyzing the digitized pulse contour for stable waveforms; processing the stable waveforms of the digitized pulse contour using dynamic time warping; comparing the stable waveforms to a library of known disease state waveforms; and assigning a most probable disease state for the individual based on said comparison.

Abstract: Implementations are disclosed for monitoring a state or change in state of a physiological parameter based on measured impedance data. In certain implementations, no images are reconstructed from the impedance data. In certain implementations, a metric (e.g., distinguishability, likelihood ratios, and so forth) may be computed and compared to reference metrics or thresholds, such as for changes over time or in comparison to a standard to determine the presence or absence of a physiological state of interest or of a change in such state.

Abstract: Techniques and examples pertaining to evaluating a health condition of an aspect of a patient are described. A method for evaluating the health condition of the aspect of the patient may involve obtaining successive measurement readings of a vital sign concurrently from both a left arm and a right arm of the patient for a plurality of times. The method may also involve calculating a characteristic value based on the measurement readings. The method may also involve designating a health indicator based on the characteristic value and a standard value associated with the aspect of the patient, such that the health indicator serves as an indication of the health condition of the aspect of the patient. The aspect of the patient may be a body organ of the patient. The method may further involve diagnosing the patient based on the health indicator.

Abstract: An earpiece may include an earpiece housing, an intelligent control disposed within the earpiece housing, and a glucose sensor operatively connected to the intelligent control. The intelligent control may be configured to determine glucose levels associated with a user of the earpiece using the glucose sensor. The earpiece may further include a wireless transceiver disposed within the earpiece housing, the wireless transceiver operatively connected to the intelligent control. The glucose sensor may be a non-invasive glucose sensor such as a near infrared glucose sensor. The earpiece housing may be configured to position the glucose sensor against a wall of the external auditory canal.

Abstract: A method and device for identifying a human movement state that includes: determining according to acceleration signals that are collected by a three-axis acceleration sensor that a human is in a walking state, calculating a walking step number of the human, and calculating a walking step frequency according to the number; calculating a corresponding physical sign frequency during the walking process according to a physical sign signal that is collected; and comparing the walking step frequency and the physical sign frequency that are obtained by calculating respectively with a step frequency threshold and a physical sign frequency threshold, and if the walking step frequency is greater than the step frequency threshold, and the physical sign frequency is greater than the physical sign frequency threshold, determining that the human movement state is a running state, and recording the calculated walking step number to be a running step number.