A biological information detecting device or the like in which waterproof performance or the like is improved by a simple structure. The device includes a sensor unit which detects biological information of a test body, and a case portion in which the sensor unit is disposed. The case portion is provided with a light transmitting portion including a detection window which transmits light incident on the sensor unit, and a light blocking portion blocking light from being incident on an inner portion of the case portion. In a case where a direction towards the sensor unit from the test body at the time of mounting the biological information detecting device is set to a first direction, a joining portion between the light transmitting portion and the light blocking portion protrudes or is dented along a direction intersecting with the first direction.

A humidifier assembly is configured to humidify a pressurized flow of breathable gas from a flow generator of a CPAP unit and includes a base configured to be attached to the flow generator, the base including a recess portion. A water receptacle is configured to be received within the recess portion of the base and includes a floor and a flange around an opening at the top of the water receptacle. A lid is hingedly attached to the base and is configured to pivot between an open position and a closed position. This lid includes a top wall, an outer depending wall, an inner depending wall in the form of a double wall, and an outlet pipe. A lid seal is attached to an underside of the top wall of the lid by way of a tongue and groove structure. A catch is located on the base and configured to lock the lid in the closed position.

A method for measuring sound from vortices in the carotid artery comprising: a first and second quality control provisions, wherein the quality control compares detected sounds to pre-determined sounds, and upon confirmation of the quality control procedures, detecting sounds generated by the heart and sounds from vortices in the carotid artery for at least 30 seconds. A method for determining stenosis of the carotid artery in a human patient consisting of a first step of placing a sensing device comprising an array and three sensing elements onto the patient, wherein a first sensing element is placed near the heart and the two remaining sensing elements are placed adjacent to the carotid arteries; the sensing elements then measure sounds from each of the three sensing elements, resulting in sound from three channels. The sound is measured in analog and modified to digital format and then each of the three channels are analyzed before a power spectral density analysis is performed. The power spectral density graph reveals peaks that are not due to noise, that are then analyzed to provide for a calculation of percent stenosis or complete occlusion of the carotid artery.

A device includes a housing, an emitter, a detector, and a processor. The housing has a body contact surface configured for affixation to a tissue site of a body. The emitter is coupled to the housing and has an emission surface and an electrical terminal. The emission surface is configured to emit light proximate the body contact surface in response to a signal applied to the electrical terminal. The detector is coupled to the housing. The detector has a sense surface and an output terminal. The detector is configured to provide an output signal on the output terminal in response to light detected at the sensor surface. The processor is coupled to the electrical terminal and coupled to the output terminal. The processor is configured to implement an algorithm to monitor for an interruption between the body contact surface and the body and configured to generate an interrupt signal corresponding to the monitoring.

A detected signal of a heartbeat sensor and a detected signal of an inertial sensor are received by a processor. The processor estimates a heart rate in a case where an exercise intensity obtain from the detected signal of the inertial sensor is equal to or more than a threshold value, based on a relation between the exercise intensity and a heart rate obtained from the detected signal of the heartbeat sensor during a period in which the exercise intensity obtained from the detected signal of the inertial sensor is less than the threshold value.

A sensor which is adapted to attach to a head of a subject includes a first fastener that includes a first end portion and a second end portion and extends into an arc-shape, a first coupling portion that is disposed on an inner circumference side of the first fastener, a second fastener that has a first through hole and a second through hole, a second coupling portion that is disposed on a first side of the second fastener, and attachable to and detachable from the first coupling portion, a light emitter that is disposed on the first side of the second fastener, and opposed to the first through hole, and a light detector that is disposed on the first side of the second fastener, and opposed to the second through hole.

A vascular graft includes deformable sleeves that include an electrical component. The electrical component can be variable-resistance or piezoelectric, in embodiments, such that deformation of the sleeves due to pressure changes create or modify an electrical signal. A transponder can then transmit information relating to the pressure inside and outside of the vascular graft.

An electrode includes separate first and second electrical contacts to contact the skin of a subject. A charge-holding structure is electrically connected between the first and second contacts. An indicator is operatively coupled to the charge-holding structure so that the indicator changes visibly in response to a change in the charge stored in the charge-holding structure. The electrode can include a rectifier across the contacts. A container for electrodes includes an electrical supply and a plurality of receptacles for electrodes so that a voltage difference is maintained across conductors of each receptacle (and contacts of an electrode therein) for at least one week. A method of making electrodes includes arranging the contacts over a support, connecting the charge-holding structure between them, arranging the indicator over the support, and charging the charge-holding structure so that the indicator has a first visual appearance.

A distributed ultrasound system includes a portable ultrasound system comprising: one or more transmitters configured to transmit ultrasound waves into a subject region; one or more receivers configured to receive ultrasound waves from the subject region in response to the ultrasound waves transmitted into the subject region; and a portable ultrasound processing unit configured to perform ultrasound image processing for generating one or more ultrasound images of the subject region using, at least in part, the ultrasound waves received from the subject region by the one or more receivers, wherein the portable ultrasound system is handheld and capable of being moved over a patient's body to an area proximate to the subject region; and an external ultrasound docking unit configured to receive and electrically couple with the portable ultrasound system and offload at least a portion of the ultrasound image processing from the portable ultrasound system when the portable ultrasound system is coupled to the external ultrasound docking unit, wherein the portable ultrasound system determines whether to offload the at least a portion of the ultrasound image processing based at least one of a temperature or a battery level of portable ultrasound system.

Disclosed herein are left atrial appendage (LAA) occluders that include self-powered physiological sensors to monitor physiological parameters of a subject. The sensors can be powered by harvesting energy generated by the patient's body or using wireless power delivery technologies. The disclosed devices can be used to close the LAA and to provide self-powering sensors to wirelessly monitor physiological parameters such as heart rate, pressure, temperature, size of the atrium, and levels of biomarkers such as C-reactive protein (CRP) and B-type natriuretic peptide (BNP) (e.g., using biosensors). In addition to addressing the stroke risk for patients with non-valvular atrial fibrillation, the disclosed devices offer post-surgical connected care that can reduce hospital readmissions, provide superior medical management, and improve patient quality of life.