A system for non-invasively measuring an analyte in a vehicle driver and controlling a vehicle based on a measurement of the analyte. At least one solid-state light source is configured to emit different wavelengths of light. A sample device is configured to introduce the light emitted by the at least one solid-state light source into tissue of the vehicle driver. One or more optical detectors are configured to detect a portion of the light that is not absorbed by the tissue of the vehicle driver. A controller is configured to calculate a measurement of the analyte in the tissue of the vehicle driver based on the light detected by the one or more optical detectors, determine whether the measurement of the analyte in the tissue of the vehicle driver exceeds a pre-determined value, and provide a signal to a device configured to control the vehicle.

A vital signs monitoring ring with integrated display includes a ring housing, the ring housing comprising at least two windows and a printed circuit board assembly (PCBA) layer configured to be attached to the ring housing. The PCBA layer includes a display section, a sensor section, a transmission mode oximetry measurement section configured to be in alignment with the at least two windows, a power supply, and a switch configured to power on the vital signs monitoring ring with integrated display via the power supply. The display section is configured to display physiological and action parameters associated with a user by sensing the physiological and action signals from a digit of user wearing the vital signs monitoring ring with integrated display using at least the sensor section and the transmission mode oximetry measurement section.

Indirect, oscillometric, digital blood pressure monitoring systems and methods enabling self-calibration to obtain absolute blood pressure values using algorithmic analysis of arterial pressure pulses to establish an oscillometric profile and compensate for intervening effects on digital arterial pressure. Proper algorithmic analysis is dependent upon proper positioning and maintained engagement of a digital cuff on the digit of a user and subsequent hydraulic coupling of the cuff to the arteries within the digit.

An exemplary hearing system that is configured to assist a user in hearing includes an in-the-ear (ITE) component configured to fit at least partially within an ear canal of the user while the hearing system is worn by the user, a first sensor electrode provided on a surface of the ITE component and configured to contact, while the hearing system is worn by the user, outer ear tissue of the user, and a second sensor electrode configured to be located, while the hearing system is worn by the user, at an entrance to or outside of the ear canal of the user. The first sensor electrode and the second sensor electrode may be configured to be used to detect a physiological attribute of the user while the hearing system is worn by the user. Corresponding methods and systems are also disclosed.

Systems, methods, and devices relating to a sensor array for use with a user's finger segment and which indirectly maps the topography of a surface under the finger segment. Each sensor array is worn on a user's finger segment and has multiple sensitive strain gauges as well a positioning sensor. The multiple strain gauges are deployed around the periphery or sides of the finger segment. Each strain gauge measures the deformation of the finger segment pad as the finger segment passes over the surface topography. The relative ratios of the deformation detected indicates the location of a feature or contact point on the topography relative to the group of strain gauges. The positioning sensor determines the array's orientation as well as its location relative to a predetermined global reference frame.

A monitoring device for measuring one or more physiological parameters of a medical patient can include a finger clip sensor connected to a monitor. A placement indicator helps the patient to properly position the sensor. The monitor can display a message alerting the patient to reposition the sensor. The device can delay measurement until the sensor is properly positioned.

The present invention concerns the field of medical technology and relates to a device for the measurement, diagnosis, and/or therapy of the strength of the human finger, hand, arm, and/or shoulder, as can for example be used to measure bending strength. The object of the invention is to specify a device with which a multi-functional measurement, diagnosis, and/or therapy of the strength of the human finger, hand, arm, and/or shoulder is possible on one device. The object is attained by a device composed at least of a base plate and force-measuring sensors, of which at least one sensor comprises a puller bolt passing therethrough and this force-measuring sensor is positioned in a stationary manner on one side of the base plate and is connected to an actuation part in a force-fit via the puller bolt, furthermore in the region of the base plate a guide for additional force-measuring sensors is present and movable auxiliary devices can also be present.

An optical fingerprint authentication device includes at least a light source and an image sensor and detects diffused light. The light source is an organic electroluminescence panel. The organic electroluminescence panel comprises a light emitting portion region and a light-transmitting non-light emitting portion, the light emitting portion region being shaped by an organic electroluminescence element. A fingerprint information reader having the image sensor arranged at a position adjacent to the non-light emitting portion is provided.

A device for detection of the tactile sensitivity of a user includes a base frame and a mechanical system joined to the base frame, the mechanical system being movable relative to the base frame and having a resting area for the fingertip of at least one finger of the user. The mechanical system includes a plurality of movable plate-shaped members arranged side by side to each other so that the resting area is defined by the thicknesses of at least part of the upper edges of the plate-shaped members. Each plate-shaped member is connected to an actuator, which can be operated to independently move each plate-shaped member from a minimum height position to a maximum height position, a control unit being further provided, which is adapted to operate the actuators.

A contact lens according to an embodiment of the present disclosure includes: a lens section that is worn on an eyeball; an acquisition section that is provided in the lens section and acquires biological information; and an output section that outputs the biological information acquired by the acquisition section to an external apparatus to be worn on a human body. The output section has one or a plurality of coil antennas extending along a front surface of the lens section, and a capacitor that is coupled to the one or the plurality of coil antennas in series or in parallel.