A method for checking a PPG sensor of a hearing apparatus that has a rechargeable battery. A charger has a receiving space for the hearing apparatus and a testing environment for testing the functionality of the PPG sensor. The hearing apparatus is placed in the receiving space and the test environment is used to perform a function test on the PPG sensor.

A physiological monitoring device is provided and includes a physiological sensing device, a first PPG sensor, a vital signs detector, and a PPG controller. The physiological sensing device senses at least one physiological feature of a subject to generate at least one sensing signal. The first PPG sensor senses pulses of a blood vessel of the subject to generate a first PPG signal when the first PPG sensor is activated. The vital signs detector obtains vital signs data according to the at least one sensing signal. The PPG controller detects whether a specific event is happening to the subject according to the vital signs data. In response to detecting that the specific event is happening to the subject, the PPG controller activates the first PPG sensor. The physiological monitoring apparatus obtains a blood oxygen level of the subject according to the first PPG signal.

Embodiments herein relate to reflective optical medical sensor devices. In an embodiment, a reflective optical medical sensor device including a central optical detector and a plurality of light emitter units disposed around the central optical detector is provided. A plurality of peripheral optical detectors can be disposed to the outside of the plurality of light emitter units. Each of the plurality of peripheral optical detectors can form a channel pair with one of the plurality of light emitter units. The reflective optical medical sensor device can also include a controller in electrical communication with the central optical detector, the light emitter units, and the peripheral optical detectors. The controller can be configured to measure performance of channel pairs; select a particular channel pair; and measure a physiological parameter using the selected channel pair. Other embodiments are also included herein.

The melanin bias reducing pulse oximeter system reduces melanin interference when obtaining pulse oximetry readings for individuals with higher skin concentrations of melanin. The system incorporates optics reducing the melanin bias through hardware and software designed using extensive testing, via a proprietary testing method. The physical pulse oximeter includes different mechanical designs, for example, finger clip, ring, and bracelet design for enhanced usage, accuracy, and comfort for those unable to wear traditional pulse oximeters. The user interface includes built-in UI, external and portable UI, bedside monitoring, and connection to patient monitoring systems, via wired and/or wireless means. Further systems include those with both melanin bias reducing pulse oximetry and heart telemetry in the same device, via either a wired or wireless compact waterproof system to be used for continuous monitoring including blood oxygen saturation as a 5.sup.th vital sign. Systems also include fall detection, bed alarm, and location services.

A cardiac activity measurement assembly for a sports equipment handle and the handle is disclosed, wherein the assembly includes an optical cardiac activity sensor configured to measure cardiac activity of a user, and an attachment element for floatingly attaching the optical cardiac activity sensor to a handle of sports equipment in order to reduce pressure on a measuring head of the sensor caused by a skin contact between the measuring head and at least one finger or a palm of the user when gripping the handle.

An apparatus for measuring blood pressure includes: a pulse wave measurer including a first light source configured to emit a first light, a second light source configured to emit a second light, and a photodetector configured to measure a pulse wave signal of an object based on the first light emitted by the first light source onto the object and returning from the object; a force measurer configured to measure a contact force between the object and the pulse wave measurer; and a processor configured to control emission of the second light from the second light source based on the measured contact force, and configured to estimate blood pressure of the object based on the measured pulse wave signal and the measured contact force.

The present invention is related to a biological data sensor for measuring biological data from a user. The biological data sensor comprises a sensing module and a wearable charging module. The sensing module is formed by flexible printed circuit (FPC) and attached to the user's skin. The sensing module includes light emitting units, at least one sensing unit, and a rechargeable battery. The light emitting unit emits a first sensing light onto the user's skin. The first sensing light is transmitted onto the user's skin and reflected from the user's skin as a second detecting light. The sensing unit receives the second sensing light and outputs the biological data. The rechargeable battery is electrically connected to the light emitting units and the sensing unit, and the rechargeable battery provides power to the light emitting units and the sensing unit. The wearable charging module is worn on a part of the user adjacent to the sensing module. The wearable charging module includes a charger and a first transmitter. The first transmitter is electrically connected to the charger, obtains power from the charger, wirelessly transmits the power to the rechargeable battery of the sensing module, and receives the biological data from the sensing module.

This document describes assessing cardiovascular function using an optical sensor, such as through sensing relevant hemodynamics understood by pulse transit times, blood pressures, pulse-wave velocities, and, in more breadth, ballistocardiograms and pressure-volume loops. The techniques disclosed in this document use various optical sensors to sense hemodynamics, such as skin color and skin and other organ displacement. These optical sensors require little if any risk to the patient and are simple and easy for the patient to use.

Systems and methods for measuring vitals in accordance with embodiments of the invention are illustrated. One embodiment includes a method for measuring vital signs. The method includes steps for identifying regions of interest (ROIs) from video data of an individual, generating temporal waveforms from the ROIs, analyzing the generated temporal waveforms to extract vital sign measurements, and generating outputs based on the analyzed temporal waveforms.

Embodiments herein relate to devices and methods for assessing deep tissue temperature using optical sensing. In an embodiment an optical temperature monitoring device is included having an optical emitter, wherein the optical emitter is configured to emit light at a first wavelength from 100 nm to 2000 nm. The optical temperature monitoring device also includes an optical detector configured to detect incident light. The optical temperature monitoring device can be configured so that the light from the optical emitter propagates at a depth of at least 1 cm through tissue as measured from a surface of the optical temperature monitoring device and back to the optical detector and the incident light detected by the optical detector is used to determine a temperature of the tissue at depths of at least 1 cm as measured from a surface of the optical temperature monitoring device. Other embodiments are also included herein.