Abstract: An apparatus and method for estimating bio-information are provided. The apparatus for estimating bio-information includes: a spectrometer configured to measure a spectrum from an object according to measurement conditions; and a processor configured to obtain signal-to-noise ratio (SNR) values for each wavelength of the spectrum measured by the spectrometer, generate a plurality of simulated absorbance spectra based on the SNR values for each wavelength of the spectrum, and determine an optimal wavelength combination for use in measuring the bio-information based on the plurality of simulated absorbance spectra.

Abstract: An apparatus and method of manufacture includes a helical wire coil and a core wire. The core wire has a first wire portion and a second wire portion. The first wire portion of the core wire extends through the helical wire coil. The second wire portion of the core wire is intertwined with the first helical wire coil to fixedly secure the core wire relative to the first helical wire coil. The core wire is formed from a first material that is non-extensible. The core wire is fixedly secured relative to a distal portion of the helical wire coil such that the core wire inhibits longitudinal elongation of the helical wire coil along a longitudinal coil axis.

Abstract: Athletic activity monitoring methods and systems are disclosed. In one embodiment, a sensor module is physically coupled to an object during an athletic activity conducted by a user. An athletic activity monitoring method for use with the sensor module includes detecting movement of the object; determining an initial spatial orientation of the object; and determining a change in the spatial orientation of the object. The method further includes wirelessly transmitting data relating to the change in spatial orientation to a computer, where the computer is remotely located from the user during the athletic activity; wirelessly receiving activity metric data from the remote computer, where the activity metric data is based on the transmitted data relating to the change in spatial orientation; and providing an output to the user that conveys an activity metric.

Abstract: The present technology is directed to respiratory therapy data management systems, device, and methods. The systems can collect, store, monitor, report, and/or analyze patient treatment data associated with patient use of one or more respiratory therapy devices. The patient treatment data can include therapy data related to the use of multiple respiratory therapies, such as ventilation, oxygen, cough-assistance, suction, and nebulization. The patient treatment data may be collected from a plurality of respiratory devices associated with a particular patient, or from a single respiratory device associated with a particular patient. The system can generate customizable reports detailing the patient treatment data. The reports can summarize patient use, illustrate therapy trends, and/or provide therapy recommendations.

Abstract: A patient monitoring system to help manage a patient that is at risk of falling is disclosed. The system includes a patient-worn wireless sensor that can be affixed to the patient's back that senses the patient's motion and wirelessly transmits information indicative of the sensed motion to a patient monitor. The patient monitor receives, stores, and processes the transmitted information to determine whether the patient has fallen or is about to fall. Upon such detection, the system can notify the patient's caretakers that the patient has fallen or is about to fall and therefore, is in need of immediate attention.

Abstract: Ophthalmological device including an applanation tonometer tip having a bi-curved cornea-contacting surface and method of using such device for measurement of intraocular pressure. The cornea-contacting surface includes a first rotationally symmetric portion a curvature of which is substantially adapted to that of a typical cornea and a second rotationally symmetric portion that is peripheral to and adjoining the first portion. In operation, the applanation of the cornea in an area corresponding to the first portion of the cornea-contacting surface is substantially negligible.

Abstract: A syringe is coupled to a biopsy needle through a coupling structure that includes a motor-driven element such as a gear to rotate the needle. The motor can oscillate back and forth to cause the needle to oscillate. Structures are described to permit one-handed operation of the device and automatic motor activation based on attaining a desired plunger position. Non-electric motors are described along with a mechanism for axial oscillation of the needle.

Abstract: A device and a method for taking up and handling a liquid sample and a substance are described. The device has a sample unit and a substance container. The substance container has a reservoir which is designed to keep a substance in the reservoir. The reservoir also has an opening which is closed by a sealing film or sealing plate so that substance kept in the reservoir is sealed with respect to the surroundings. The sample unit is equipped with a sample taker which is designed to take up and hold a liquid sample. It also has an opener which is designed to be at least partially inserted into the opening of the reservoir and to lift the sealing film or sealing plate from the opening.

Abstract: An apparatus includes a pre-sample reservoir, a diversion mechanism, and a flow metering mechanism. The diversion mechanism has an inlet port couplable to a lumen-defining device to receive bodily-fluids from a patient, a first outlet port fluidically couplable to the pre-sample reservoir, and a second outlet port fluidically couplable to a sample reservoir. The diversion mechanism defines a first fluid flow path and a second flow path that are configured to place the first outlet port and the second outlet port, respectively, in fluid communication with the inlet port. The flow metering mechanism is configured to meter a flow of a predetermined volume of bodily-fluid through the first fluid flow path into the pre-sample reservoir, to meter a flow of a second volume of bodily-fluid through the second fluid flow path into the sample reservoir, and to display a volumetric indicator associated with the predetermined volume and the second volume.

Abstract: Systems and methods for enhancing diagnostic evoked potential recordings of a nerve or nerve pathway of interest. A grid array of stimulating electrodes are placed on, over, or through skin in a location beneath which a nerve or nerve pathway is suspected to lie. A stimulator controls the grid array, where each electrode is independently controllable as active or inactive, as a cathode or anode, etc. A plurality of recording electrodes may record Somato-Sensory Evoked Potentials (SSEPs) and/or Transcranial Electrical Motor Evoked Potentials (TCeMEP) in response to activation of the stimulating electrodes. A processor controls stimulating the stimulating electrodes, and receives responses from the recording electrodes, in a general search mode and a focused search mode in order to use a minimum stimulation intensity at which a maximum response amplitude is detected to continually stimulate the nerve or the nerve pathway.

Abstract: A female insertion system is provided. The system includes a conformable insert shaped for insertion into one or more structures of a female human that are associated with at least one of reproduction and one or more erogenous zones; one or more sensors, at least one of the sensors included in the insert, and configured to measure and to relay data, wherein the data is acquired on one of a one-time basis and a multiple-time basis included one of a non-continuous period, a continuous period, and an intermittent temporal period; and a processor configured to: control the insert; generate a treatment for one of the structures of the female human; store the data; and based on the data, automatically affect one or more of the structures via the insert.

Abstract: An electronic device may include: an optical sensor configured to emit a reference light to a reference object and detect the reference light reflected from the reference object during calibration, and emit a measurement light to a target object and detect the measurement light reflected from the target object during a measurement; a display; and a processor configured to: when the electronic device is placed on a charger and is in a charging state, perform the calibration of the optical sensor based on the reference light reflected from the reference object; control the display to output guide information for estimating bio-information according to progress stages of the measurement after charging of the electronic device; and estimate the bio-information based on a light quantity of the measurement light that is reflected from the target object, and a light quantity of the reference light reflected from the reference object.

Abstract: Systems and method are described for determining if a decision support recommendation is to be presented to a user for treatment of a diabetic state, including receiving a plurality of input data items impacting a diabetic state of a user of continuous glucose monitor, the input data items serving as input data to a process for determining a decision support recommendation; assigning a reliability level to each of the input data items; calculating a reliability metric based on the reliability levels assigned to each of the input data items; determining a decision support recommendation based on the process and the input data and presenting the decision support recommendation to the user on a user interface only if the reliability metric exceeds a threshold.

Abstract: Systems, devices, and methods for performing precise treatment, mapping, and/or testing of tissues are disclosed. Systems, devices, and methods for administering an agent to one or more a precise regions within a tissue mass are disclosed. Systems, devices, and methods for treating targeted regions within a tissue mass are disclosed. Systems, devices, and methods for identifying, localizing, monitoring neural traffic in the vicinity of, quantifying neural traffic in the vicinity of, and mapping neural traffic near targeted regions within a tissue mass are disclosed.

Abstract: A method of operating a fitness tracking system includes generating movement data corresponding to movement of a user, sampling the generated movement data at a first sampling rate as first sampled data when operating the fitness tracking system in an activity detection mode, and sampling the generated movement data at a second sampling rate as second sampled data when operating the fitness tracking system in a workout mode. The second sampling rate is greater than the first sampling rate.

Abstract: There is provided a wheezing detection device, including: a wheezing determiner that performs processing of determining whether wheezing is included in the pulmonary sound of the subject, based on the signal of the pulmonary sound that is measured by a sound measurer after an instruction for starting wheezing detection processing is issued; and a controller that ends measurement of the signal of the pulmonary sound performed by the sound measurer and reports a result of the processing, in a case where an elapsed time period from a measurement start time point of the signal, which is firstly measured by the sound measurer after the instruction is issued, reaches a predetermined time period set in advance, or in a case where it is determined by the wheezing determiner that wheezing is included in the pulmonary sound of the subject.

Abstract: An orthopaedic surgical system includes a sensor module for determining the joint force of a patient's knee joint and an adaptor for coupling various tibial trialing components to the sensor module. The sensor module includes a tibial paddle to which the adaptor is configured to couple. The adaptor and tibial paddle include structures that control the orientation at which the adaptor is attachable to the tibial paddle. Some tibial trialing components may be positioned over the adaptor in a mobile orientation that facilities rotation of the tibial trialing component relative to the tibial paddle or a fixed orientation that restricts the rotation of the tibial trialing component.

Abstract: Examples of the disclosure relate to an apparatus for sensing biometric parameters. The apparatus may comprise heat transfer means configured to transfer heat from a first location to a location proximate to a subject's sweat glands. The apparatus may also comprise sweat transfer means configured to transfer sweat from the location proximate to a subject's sweat glands to one or more sensors wherein the one or more sensors are configured to sense one or more biometric parameters from the subject's sweat.

Abstract: The present invention generally relates to systems and methods for delivering and/or receiving a substance or substances such as blood from subjects. In one aspect, the present invention is directed to devices and methods for receiving or extracting blood from a subject, e.g., from the skin and/or from beneath the skin, using devices containing a substance transfer component (for example, one or more needles or microneedles) and a reduced pressure or vacuum chamber having an internal pressure less than atmospheric pressure prior to receiving blood. In some embodiments, the device may contain a “snap dome” or other deformable structure, which may be used, at least in part, to urge or move needles or other suitable substance transfer components into the skin of a subject. In some cases, for example, the device may contain a flexible concave member and a needle mechanically coupled to the flexible concave member such that the needle may be urged or moved into the skin using the flexible concave member.

Abstract: A method for measuring a neural response to a stimulus. Measurement circuitry is settled prior to a stimulus, by connecting a sense electrode to the measurement circuitry to allow the measurement circuitry to settle towards a bio-electrically defined steady state. Charge is recovered on stimulus electrodes by short circuiting the stimulus electrodes to each other. An electrical stimulus is then applied from the stimulus electrodes to neural tissue, while keeping the sense electrode disconnected from the measurement circuitry. After the stimulus, a delay is imposed during which the stimulus electrodes are open circuited and the sense electrode is disconnected from the measurement circuitry and from the stimulus electrodes. After the delay, a neural response signal present at the sense electrode is measured by connecting the sense electrode to the measurement circuitry.