A biological measuring device includes a light source that emits first light illuminating an area on a living body, an imaging device that detects second light returned from the living body and acquires a first image including at least part of the living body, and a control circuit that controls the light source. If a specific part of the living body is not located in a predetermined coordinate range in the first image, the control circuit restricts emission of the first light from the light source. The predetermined coordinate range is set outside the area.

Methods, systems, and coaptation measurement devices as described herein include an elongate sensor body at the end of a proximal connecting member, and a plurality of sensors in an array across a face of the sensor body, wherein each sensor of the plurality of sensors is configured to detect if a portion of a heart valve is in contact with the sensor.

A wearable electronic device includes a housing, and an electrode carrier attached to the housing and having a nonplanar surface. The wearable electronic device includes a set of electrodes, including electrodes positioned at different locations on the nonplanar surface. The wearable electronic device includes a sensor circuit and a switching circuit. The switching circuit is operable to electrically connect a number of different subsets of one or more electrodes in the set of electrodes to the sensor circuit.

An illustrative system may include a TDC configured to monitor for an occurrence of a photodetector output pulse during a measurement time window that is within and shorter in duration than a light pulse time period, the photodetector output pulse generated by a photodetector when the photodetector detects a photon from a light pulse having a light pulse time period; a PLL circuit for the TDC and having a PLL feedback period defined by a reference clock, the PLL circuit configured to: output a plurality of fine phase signals and output one or more signals representative of a plurality of feedback divider states during the PLL feedback period; and a precision timing circuit configured to adjust, based on one or more of the fine phase signals and/or the feedback divider states, a temporal position of the measurement time window within the light pulse time period.

A wearable biofluid volume and composition system includes a microfluidic flexible fluid capture substrate having a microfluidic channel configured as a sweat collection channel and is configured to be worn on a human body and to collect and analyze biofluid. The microfluidic flexible fluid capture substrate further has a plurality of conductive traces and electrodes. An electronic module is attached to the microfluidic flexible fluid capture substrate and is configured to measure and analyze data from the biofluid collected by the microfluidic flexible fluid capture substrate and to transmit the analyzed data to a smart device.

This relates to one or more integrated photodiodes on a back surface of a PPG device. The one or more integrated photodiodes can reduce the gap between one or more windows and the active area of the photodiode(s) to increase the PPG signal strength without affecting the depth of light penetration into skin tissue. In some examples, the photodiode stackup can contact the surface of the windows. In some examples, the photodiode stackups can exclude a separate substrate. In some examples, the photodiode stackup can be deposited on the inner surface of the windows opposite the outer surface of the device. In some examples, the photodiode stackup can be deposited on the back surface and/or outer surface of the device. In this manner, PPG sensors can be included in the device without the need for extra layers and measurement accuracy can be improved due to lower light loss.

According to some embodiments, a medical instrument (for example, an ablation device) comprises an elongate body having a proximal end and a distal end, an energy delivery member positioned at the distal end of the elongate body, a first plurality of temperature-measurement devices carried by or positioned within the energy delivery member, the first plurality of temperature-measurement devices being thermally insulated from the energy delivery member, and a second plurality of temperature-measurement devices positioned proximal to a proximal end of the energy delivery member, the second plurality of temperature-measurement devices being thermally insulated from the energy delivery member.

A system for determining muscle activation comprises a set of electrode adherable to a skin of a subject, and a processor in communication with the electrodes. The processor has a circuit configured for receiving locations of the electrodes and electrical signals detected by the electrodes, analyzing the signals to identify a section of an active muscle, identifying locations of at least a segment of active muscles and activation patterns of the active muscles based on the identified section, and constructing a displayable map of the locations and the activation patterns, wherein patterns corresponding to different active muscles are distinguishable on the map.

A method for determining a region in which the actual concentration is located, in a medium, of a substrate made up of any molecule likely to undergo catalysed oxidation-reduction by a catalyst. The method includes the following steps: taking at least one group of at least two biosensors, each biosensor having a calibration curve of the signal induced by the oxidation-reduction reaction and having identical initial portions of their calibration curves up to a concentration value of the substrate from which the measurement of the signal differ; and when more than one group is present, the biosensors in different groups having different calibration curves without identical initial portions; placing the biosensors in contact with the medium; measuring the signal induced by the oxidation or reduction reaction for each biosensor in the group/groups; comparing all the signal values produced by the biosensors and following the method described in the description.

Disclosed is a magnetoencephalography apparatus (100) and a method. The apparatus comprises a plurality of magnetic sensors, one or more processors and one or more memories. The method comprises obtaining a reference data, calculating from the reference data a reference basis, obtaining a source basis, obtain a source data, adding together the source basis and the reference basis to form a joint basis and determine an estimate for the magnetic brain activity of the source by parametrizing the source data in the joint basis.