Abstract: A moveable shelf assembly is used within a dish treating appliance. The moveable shelf assembly includes a retaining body having at least one attachment arm. The at least one attachment arm is configured to be coupled to a dish rack. The moveable shelf assembly also includes a planar shelf body extending along a width. The planar shelf body is operably coupled to the retaining body for rotation between a storage position and a use position.

Abstract: Provided is a shoe care apparatus including a door capable of simplifying an assembly process while reducing material cost. The shoe care apparatus includes: a main body; a care room provided inside the main body and accommodating shoes; and a door opening and closing the care room, wherein the door includes: a front panel forming a front surface of the door, and including a side trim provided on a rear surface of the front panel or a magnet provided on the rear surface of the front panel; a rear body forming a rear surface of the door; and a reinforcement plate positioned between the front panel and the rear body, and detachably coupled with the front panel, and the reinforcement plate includes: a recess portion accommodating at least one portion of the side trim; and a magnet coupling portion coupled with the magnet by a magnetic force of the magnet, and arranged in parallel to the recess portion.

Abstract: A clothing care device includes an inner cabinet that has an accommodation space configured to accommodate clothing therein, an inlet defined at a first portion of the accommodation space and configured to supply air to the accommodation space, and an outlet defined at a second portion of the accommodation space and configured to suction air from the accommodation space. The shoe care device further includes a connection path configured to circulate air between the inlet and the outlet, a blowing fan disposed at the connection path and configured to blow air from the outlet toward the inlet, a dehumidifying material disposed at the connection path and configured to dehumidify the air blown by the blowing fan, a heater configured to heat the dehumidifying material, and a regeneration path configured to guide, to a location other than the inlet, the air having passed through the dehumidifying material heated by the heater.

Abstract: According to one embodiment of the present disclosure, there is disclosed a method of controlling an endoscope scope, which is performed by a computing device including at least one processor. The method includes: obtaining first data regarding the actual movement state of a motor included in an endoscope device and second data regarding the target movement state of a scope included in the endoscope device; and controlling the motor based on the obtained first data and second data.

Abstract: A system, method and apparatus to automatically perform endotracheal intubation in a patient comprising, inserting a blade inside an upper airway of a patient to retract an anatomical structure; inserting a bending portion and a tube arranged on the bending portion inside the airway of the patient; collecting airway data using at least one imaging sensor arranged on the bending portion; communicating collected airway data to a processing circuitry; predicting an intended path for insertion of the tube and generating control signals using the processing circuitry, wherein the intended path is predicted based on at least one anatomical structure recognized by the processing circuitry using the collected airway data; and communicating the control signals generated by the processing circuitry to at least one actuation unit to actuate the three-dimensional movement of the tube.

Abstract: An endoscopic image processing apparatus is configured to generate a display image including one main screen and one or more sub-screens smaller than the main screen for displaying an endoscopic image obtained by picking up an image of an object in a subject with an endoscope. The endoscopic image processing apparatus includes a processor. The processor receives the endoscopic image and detects one or more lesion candidate regions included in the endoscopic image, highlights a position of the lesion candidate region, and sets, based on any one of a state of the lesion candidate region, a work state of a user who performs work using the endoscope, or a display state of the display image, a highlighting method in highlighting a position of the lesion candidate region included in at least one of the main screen or the sub-screen.

Abstract: A medical support method includes: causing a trained model to generate certainty information in which a certainty of a lumen being present in each of a plurality of divided regions obtained by dividing a medical image or an image corresponding to the medical image in a circumferential direction is given to the plurality of divided regions; outputting first information indicating that the lumen is present in any of the plurality of divided regions on the basis of the certainty information; and outputting second information indicating that the lumen is present in a central region of the medical image in a case where the certainty information is information in which a value exceeding a threshold value is given as the certainty to two or more divided regions having a positional relationship exceeding 90 degrees in the circumferential direction among the plurality of divided regions.

Abstract: In the endoscopic examination support apparatus, the video acquisition means acquires an endoscopic video captured by an endoscope. The lesion detection means detects a lesion candidate from the endoscopic video. The heat map generation means generates a heat map which represents a lesion possibility of the lesion candidate included in the endoscopic video by a color. The display control means superimposes and displays an area where the lesion possibility is equal to or higher than a first threshold on the endoscopic video in a first display mode, and superimposes and displays an area where the lesion possibility is equal to or higher than a second threshold on the endoscopic video in a second display mode.

Abstract: A visualization system includes an observation apparatus having a first image recording device to observe an operation region with a first observation plane, and an endoscope having a probe and a second image recording device to observe the operation region with a second observation plane. A display device represents a first image recorded by the first image recording device in a first orientation and a second image recorded by the second image recording device in a second orientation. The visualization system further includes a tracking system to determine an orientation of the endoscope relative to the observation apparatus and a controller configured to transform the second image based on the orientation of the endoscope relative to the observation apparatus.

Abstract: Disclosed is a system for detecting bowing or looping events during a medical procedure, the system comprising: a medical device including: an insertion portion having a proximal portion and a distal end. A distal sensor may be disposed at the distal end of the insertion portion. The distal sensor is configured to measure an acceleration or a velocity of the distal end of the insertion portion or a distance traveled by the distal end of the insertion portion. A proximal sensor is configured to measure an acceleration or a velocity of the proximal portion of the insertion portion or a distance traveled by the proximal portion of the insertion portion.

Abstract: A central control apparatus that centrally controls a plurality of medical devices as controlled devices includes a processor. The processor is configured to: set a function allocated to one or more switches provided in the controlled devices, detect occurrence of an error of the controlled devices and a state of the occurred error, and change, based on a detection result of the error, the function allocated to the one or more switches to a function for restoration from the detected error.

Abstract: Devices, systems, and methods for a suction valve assembly for a medical device. The suction valve assembly includes a valve body, a sliding shaft, and a flap seal. The valve body has a central channel extending vertically between vent openings in the top and a working opening in the bottom and a side opening extending from the central channel to the side surface. The sliding shaft moves within the central channel between an upper position where its upper channels are adjacent the vent openings, and a lower position where it extends into the working opening and unseats the flap seal.

Abstract: A multi-working channel device with a cylindrical assembly having a distal end, a proximal end, an interior space, and an aperture. The multi-working channel device also has a longitudinally extending tube with a proximal end, a distal end that is coterminous with the distal end of the cylindrical assembly, and a balloon. The multi-working channel device also utilizes a stylet having a proximal end and a distal end that is connected to the balloon. The stylet can be adjusted between a home position and an active position. In the home position, the balloon is at least partially within the longitudinally extending tube. Alternatively, the active position deploys the balloon from the longitudinally extending tube. The stylet selectively urges the balloon to the active position, facilitating employment of the alimentary engagement device. In addition, the balloon is selectively inflated through the longitudinally extending tube.

Abstract: A coupler device for a forward viewing endoscope comprises a main body having a proximal end configured to attach to the distal end portion of the endoscope and a distal end portion that at least partially seals the distal end portion of the scope and allows for viewing of the surgical site. The coupler device may include a flexible working channel extension for attachment to the working channel of the endoscope. The coupler device provides a protective cover to reduce the ingress of debris, fluid, bacteria, or other unwanted matter from the working end of the endoscope which could lead to infection and decreased performance of the scope. A kit for use in an endoscopic procedure on a patient comprises the coupler device and an end viewing endoscope having a working channel, a light and a camera lens.

Abstract: A medical system may comprise an endoscope, including a handle and a sheath having a first illumination source, a second illumination source, and an imaging device at a distal tip of the sheath. The first illumination source may be configured to emit white light. The second illumination source may be configured to emit a non-white light. The system may also comprise a display device, a controller configured to interface with the endoscope and the display device, and a carrying case configured to contain the endoscope, the display device, and the controller.

Abstract: An actuation assembly for a medical device may include a first gear including: a first gear toothed region; and a first gear untoothed region; and a second gear including: a second gear toothed region; a second gear untoothed region; and an articulation wire coupled to the second gear. In a first portion of a rotational range of the first gear, the first gear toothed region may interact with the second gear toothed region, such that the second gear toothed region rotates upon rotation of the first gear. In a second portion of the rotational range, the first gear untoothed region may interact with the second gear untoothed region, such that the second gear remains stationary upon rotation of the first gear.

Abstract: A sealing device for endoscope intubation and an endoscope are provided in the present disclosure, which includes: a main body part, wherein the main body part has an axis, and is used for connecting to the catheter, at least a portion of the main body part is configured to be capable of being inserted into the tracheal intubation, and there is a gap between the main body part and the inner tube wall of the tracheal intubation; a sealing part, which is annularly arranged on the main body part, wherein the sealing part is configured to seal the gap; and a friction part, which is arranged on the main body part, wherein at least portion of the friction part is configured to abut against the inner wall of the tracheal intubation.

Abstract: A method includes forming, by atomic layer deposition, a first barrier layer on a surface of a printed circuit board (“PCB”) and on an outer surface of an electrical component attached to the surface of the PCB; forming an adhesion promotion layer on a surface of the first barrier layer; and forming, on the adhesion promotion layer, a second barrier layer including Parylene.

Abstract: The present disclosure relates generally to the field of medical instruments. In particular, the present disclosure relates to a biopsy cap and endoscope biopsy cap housing with improved stability and stress distribution to securely and removably attach to an endoscope biopsy port. In one example, a biopsy cap housing may include a first center-split half comprising a first half of an upper and lower chamber and first pivot member, and a second center-split half comprising a second half of an upper and lower chamber, and second pivot member, wherein mating surfaces of the first and second center-split halves may be configured to interlock to define the upper and lower chambers.

Abstract: Attachments for endoscopes as well as methods for making and using attachments are disclosed. An example attachment may include a housing. One or more angled locking members may extend from an inner surface of the housing. The angled locking members may be designed to engage a biopsy port of an endoscope. One or more stabilizing members may extend from the inner surface of the housing. A locking apparatus may be coupled to the housing. A sealing member may be disposed within the housing.

Abstract: A method for inserting a cannula of an endoscope into a cavity of a patient includes slidably coupling an inner sleeve of a sheath with an outer sleeve of the sheath and advancing an introducer, in a collapsed configuration and positioned at a distal end of the outer sleeve, through a cavity of the patient until the introducer is inserted into the internal space of the patient. The method includes translating the inner sleeve relative to the outer sleeve and towards the introducer to dilate the internal space, and placing the cannula of the endoscope within the inner sleeve of the sheath, proximal to the introducer at the distal end of the outer sleeve. The method includes advancing the cannula along the inner sleeve and through the introducer a desired distance within the cavity, and removing the cannula and sheath from the patient.

Abstract: A medical device includes a sheath extending longitudinally from a proximal end to a distal end and a handle coupled to the proximal end of the sheath. The handle includes a deflection lever coupled thereto. The deflection lever is rotatable proximally and distally along the handle to deflect a distal end of the shaft to which it is operably coupled and a locking mechanism movable between an locked configuration in which the locking mechanism engages an engagement feature on the outer surface of the handle, preventing the deflection lever from rotating and locking the distal end of the shaft in a desired position, and an unlocked configuration in which the locking mechanism releases the engagement feature to allow rotation of the deflection lever and deflection of the distal end of the shaft.

Abstract: An endoscope includes: a bending tube, the bending tube including: a plurality of bending pieces; a plurality of hinges linking two adjacent bending pieces of the plurality of bending pieces in a freely pivotable manner in a long axis direction; and at least one elastic member including a plurality of fixing regions, fixed to a circumferential region of the plurality of bending pieces, respectively, wherein a first length of the at least one elastic member between a pair of fixing regions in the long axis direction is greater than a second length between a respective pair of circumferential regions in the long axis direction.

Abstract: Systems and methods for a medical valve are disclosed. For example, the medical valve may include a valve body including a body outlet aperture and a body inlet aperture, and an inner shaft including an inner shaft outlet aperture and an inner shaft inlet aperture, wherein the inner shaft is configured to rotate such that the medical valve transitions to an active state whereby the body inlet aperture and the inner shaft inlet aperture are substantially in alignment.

Abstract: A surgical camera apparatus includes an elongated head assembly having a profile shape extending along a longitudinal axis. The elongated head assembly forms an angled distal tip oriented at a tip angle offset from the longitudinal axis. The angled distal tip may house a camera module and a light source in a stacked configuration.

Abstract: A light source device comprises a first light combination module and at least two light sources. The light source device is configured to be connected with a light guide module. The at least two light sources include a first light source and at least one second light source. The first light combination module includes a first light combination element. The first light combination element is disposed between the light guide module and the first light source and configured to transform a first beam into a first transmitted light, the first beam being related to the first light source. The first light combination element is further configured to generate a first reflected light from at least one second beam emitted by the at least one second light source, and combine the first reflected light and the first transmitted light into a combined light.

Abstract: An adapter for connecting a port of a channel of a surgical instrument to a cleaning fluid supply. The adapter including a rigid housing with a port interface and a connection interface for the cleaning fluid supply. Wherein the port interface comprises a gasket with a central opening for guiding the fluid into the port of the channel, the port interface with the gasket is configured to be pressed along a pressing direction on the port of the channel to establish a sealing and rinse the channel with the cleaning fluid, and the gasket is deformable along the pressing direction in order to fit differently configured ports.

Abstract: Methods and systems for providing a flow of fluid to an endoscope. An illustrative container and tube set arranged and configured to couple to an endoscope may comprise a first container configured to contain a fluid and having a first port in fluid communication with a bottom portion thereof and a pressure vessel system. The pressure vessel system may include a housing defining a first cavity, a sleeve disposed within the first cavity of the housing and defining a second cavity between an inner surface of a wall of the housing and the sleeve, a first fluid inlet in selective fluid communication with the first cavity, a second fluid inlet in fluid communication with the second cavity, and a first fluid outlet in fluid communication with the first cavity.

Abstract: Disclosed is a retractor mounting device for a surgery including a mounting unit, a main body provided at an end of the mounting unit, a retraction unit installed to be elevated on the main body, a sub-body disposed to be spaced apart from the main body, and an endoscope unit installed to be movable or rotatable on the sub-body.

Abstract: The perimeter includes a screen, a light source assembly, projection optics, and an adjustable beam deflector. The projection optics includes an adjustable lens having a focal length that can be changed by the control unit of the device. The projection optics further includes a projection lens element. The focal length of the adjustable lens is being changed as a function of the location of the stimulus light spot, thereby compensating for the location-dependent length of the optical path from the projection optics to the screen. The distance between the projection lens element and the adjustable lens is equal to the focal length of the projection lens element, which makes the spot size independent on the location.

Abstract: A sensory traits information collecting method includes: a first viewed-object presenting step of presenting one or more viewed objects (30) including a predetermined visibility element (31, etc.) to a subject in a white light environment in which white light (L0) is incident on a retina (R) of the subject; a predetermined light environment creating step of creating a predetermined light environment in which predetermined light (L1) different from the white light (L0) in at least one of spectral distribution and luminance is incident on the retina (R) of the subject; a second viewed-object presenting step of presenting the viewed object (30) to the subject again in the predetermined light environment; an information reception step of receiving sensory traits information related to the way of seeing of the viewed object (30) in the first viewed-object presenting step and the second viewed-object presenting step; and a collecting step of collecting the sensory traits information received from the subject.

Abstract: Blood flow information is extracted from speckle information of a time series of structural optical coherence tomography (OCT) images. Flow information can be determined from high-frequency information of the OCT images, a speckle density of the OCT images, from a co-occurrence matrix applied to the OCT image, from a machine learning analysis of an input OCT image, or the like. A flow profile analogous to a pulse waveform is then generated as a time series of the extracted flow information.

Abstract: An ophthalmic information processing apparatus includes an acquisition unit, a segmentation processor, and a display controller. The acquisition unit is configured to acquire an OCT image and one or more tomographic information images. The OCT image is a tomographic image of an eye to be examined. The one or more tomographic information images are generated using a method different from a method of generating the OCT image and represent tomographic information of the eye to be examined. The segmentation processor is configured to perform segmentation processing on the OCT image to identify a boundary of a layer region in a depth direction. The display controller is configured to display the OCT image, in which the boundary identified by the segmentation processor is distinguishably depicted, and the one or more tomographic information images on a display means.

Abstract: A map of a person's spatial vision abilities, including areas of low acuity and areas of high acuity, may be generated from medical records or from a calibration phase. During presentation of a computer simulation such as a computer game, the map is provided to a foveated renderer to optimize which areas should be rendered most crisply. Content placement may be optimized to ensure that any critical elements to the game, for instance, any text that needs to be seen or treasures or special pickups that need to be seen clearly can be moved into regions of the player's field of view that the person has higher acuity in.

Abstract: A system and method are provided for bimodal detection and/or imaging of macular pigments. Fundus autofluorescence spectroscopy is applied in a first and a second region of an eye to measure fluorescence values from the fluorescing pigment (e.g., lipofuscin). The first region can be a macula, which has a higher density of macular pigments, and the second region can be in the peripheral retina, which has a lower density of macular pigments. Fundus reflection spectroscopy is applied in the first and a second region of an eye, as a baseline image, to determine absorptions due to other pigments (e.g., melanin) than the macular pigments and the fluorescing pigment. The density of macular pigments is determined using the measures fluorescence values and the absorptions due to other pigments.

Abstract: A fundus imaging apparatus includes two or more curved mirrors, an illumination optical system, an image sensor, and a controller. The illumination optical system irradiates slit-shaped illumination light onto a fundus of an eye to be examined through the two or more curved mirrors, and illuminates the fundus while moving an illumination region. The image sensor is arrangeable at a fundus conjugate position substantially conjugate optically to the fundus, and receives returning light from the eye to be examined. The controller controls at least the illumination optical system. A longitudinal direction of an image formed by the illumination light on the fundus is approximately parallel to a plane including two or more focal points of the two or more curved mirrors. The controller controls the illumination optical system so that the image described above moves in a direction intersecting the longitudinal direction on the fundus.

Abstract: According to an aspect there is provided a device for analyzing a speckle pattern from biological tissue, the device comprising: a light source configured to generate light for illuminating the biological tissue, such that the light is scattered by the biological tissue and forms the speckle pattern; a Fourier transform element configured to collect the light scattered by the biological tissue and to transform the collected light into a spatial Fourier domain at a Fourier plane of the Fourier transform element; a spatial bandpass filter arranged at the Fourier plane, the spatial bandpass filter being configured to selectively transmit light at a spatial position of the Fourier plane, the spatial position corresponding to a band of speckle sizes of the speckle pattern; a photosensitive detector configured to detect the light transmitted though the bandpass filter, wherein a signal output from the photosensitive detector comprises information on contrast of the speckle pattern.

Abstract: A device for fluorescence-based imaging and monitoring of a target is provided. The device includes a light source emitting light for illuminating the target, the emitted light including at least one wavelength or wavelength band causing at least one biomarker associated with the target to fluoresce, and a light detector for detecting the fluorescence.

Abstract: A digital dermatoscope for skin examination, the digital dermatoscope being formed as a hand-held device, wherein the digital dermatoscope comprises a handle part which can be grasped by a hand and a head part adjoining the handle part and having an imaging unit, wherein the imaging unit has an imaging unit housing arranged on a lower side of the head part, an image sensor accommodated inside the imaging unit housing, and a lens, wherein an exchangeable spacer attachment contacting the skin to be examined during a skin examination is arranged at an end of the imaging unit housing, the digital dermatoscope further comprising a control unit and a first display arranged on an upper side of the head part, wherein the control unit is formed to drive the first display to display images of a skin section to be examined acquired by means of the imaging unit.

Abstract: Methods and apparatuses are disclosed for capturing and analyzing images of tissue, such as human skin, using variable polarization. Exemplary devices are described having a detection polarizer via which an area of tissue is imaged and one or more light sources whose emitted light is polarized with one or more source polarizers. In a first such device, one or more of the detection polarizer and a source polarizer is rotatable so as to allow the angle between their polarizations to be varied. An area of tissue can be imaged as the angle is varied. Another device has multiple fixed source polarizers of different polarization orientations, each source polarizer polarizing the light emitted by a corresponding group of light sources which can be selectively activated, thereby enabling the device to illuminate an area of tissue with polarized light of different orientations relative to the orientation of the detection polarizer.

Abstract: An imaging system for a patient comprises an imaging probe. The imaging probe comprises: an elongate shaft for insertion into the patient and comprising a proximal end, a distal portion, and a lumen extending between the proximal end and the distal portion; a rotatable optical core comprising a proximal end and a distal end, the rotatable optical core configured to optically and mechanically connect with an interface unit; a probe connector positioned on the elongate shaft proximal end and surrounding at least a portion of the rotatable optical core and an optical assembly positioned in the elongate shaft distal portion and proximate the rotatable optical core distal end, the optical assembly configured to direct light to tissue and collect reflected light from the tissue. A shear-thinning fluid can be provided between the elongate shaft and the rotatable optical core, such as to reduce undesired rotational variations of the rotatable optical core.

Abstract: An electric toothbrush includes an oscillating assembly and a driving assembly. The oscillating assembly has a plurality of tooth cleaning elements, a light emitting element, and a light receiving element. The drive assembly drives the oscillating assembly to oscillate at a first frequency. The light receiving element is fixed on an isolating member having a resonant frequency different from the first frequency.

Abstract: Disclosed is a magnetic imaging apparatus comprising a housing comprising a face, wherein a first axis extends through the face into a field of view, and an array of permanent magnets positioned in the housing, wherein an inherent gradient magnetic field extends from the array of permanent magnets relative to the first axis into the field of view. The magnetic imaging apparatus further comprises a gradient coil set, at least one radio frequency coil, a power circuit, a memory storing a relaxation model for a tissue type, and a control circuit. The control circuit is configured to obtain a T2 data set related to a structure positioned in the field of view, generate a T2-weighted image of the structure, and convert the T2-weighed image of the structure to a heat map based on the relaxation model for the tissue type.

Abstract: The invention generally relates to medical imaging systems that instantly and/or automatically detect borders. Embodiments of the invention provide an imaging system that automatically detects a border at a location within a vessel in response only to navigational input moving the image to that location. In some embodiments, systems and methods of the invention operate such that when a doctor moves an imaging catheter to a new location with in tissue, the system essentially instantly finds, and optionally displays, the border(s), calculates an occlusion, or both.

Abstract: A system and method utilizes optical depth sensors to estimate heart rate of one or more subjects. A method includes obtaining optical depth video data of at least one subject; identifying a region of interest of the subject(s) from optical depth video data; segmenting the region of interest into multiple areas; identifying pixel intensity with respect to time in the areas to produce a depth signal data matrix including multiple spatial channels; decomposing the depth signal data matrix into a low-rank spatial-temporal eigenvector matrix to produce refined depth signal data streams; and projecting the refined depth signal data streams onto a selected pulsatile direction and producing a cardiac pulse signal for the subject(s).

Abstract: Systems and methods for monitoring heart failure (HF) status in a patient are discussed. An exemplary system includes a gait analyzer circuit than can receive gait or balance information, and generate a gait feature such as gait speed or a gait pattern. The system includes a HF detector circuit that can detect patient HF status, or to predict patient risk of a future worsening heart failure (WHF) event, using the gait feature. In some examples, the system may trigger sensing physiologic information according to the detected gait, and detect patient HF status using the sensed physiologic information. The system can initiate or adjust a heart failure therapy according to the HF status or the WHF risk.

Abstract: A blood pressure measurement unit configured to measure blood pressure of a user based on a pulse wave signal superimposed on a cuff pressure signal detected when increasing or decreasing cuff pressure that indicates internal pressure of a cuff attached to the user; a pulse rate measurement unit configured to measure a pulse rate of the user based on the pulse wave signal; an interval calculation unit configured to calculate a data group of pulse wave intervals based on the pulse wave signal; a clustering unit configured to cluster the data group of the pulse wave intervals into one or more clusters by using a threshold; and a determination unit configured to determine, based on an index value indicating a magnitude of variation of the data group belonging to the cluster, whether atrial fibrillation occurs in the user. The clustering unit sets the threshold based on the pulse rate.

Abstract: A system and method for contactless predictions of one of vital signs, health risk for a disease or condition, blood biomarker values, and hydration status, the method executed on one or more processors, the method including: receiving a raw video capturing a human subject; determining one of vital signs, health risk for a disease or condition, blood biomarker values, and hydration status using a trained machine learning model, the machine learning model taking the raw video as input, the machine learning model trained using a plurality of training videos where ground truth values for the vital signs, the health risk for a disease or condition, the blood biomarker values, or the hydration status were known during the capturing of the training video; and outputting the predicted vital signs, health risk for a disease or condition, blood biomarker values, or hydration status.

Abstract: A multi-sensor remote patient monitoring platform combines multiple technologies on a patient's own device to dramatically reduce the number of devices a patient needs while also reducing device distribution logistics on health care providers. Continuous temperature monitors can be used to collect frequent temperature data over large periods of time. Additionally, a rPPG device can obtain at least one vital sign data by a remote photoplethysmogram (rPPG) comprising a plethysmogram that is optically obtained via a camera by detection of blood volume changes in the microvascular bed of tissue of the patient. The temperature data and vital sign data can be input into a remote server-side computer system that can analyze the received data for indication of a fever, and provide an alert to the patient or a clinician when the result of the analysis indicates the fever. Such alerts can be clinically beneficial for disease states in which fever can be fatal, particularly for those fevers having fast onset.

Abstract: A measurement device, a control method, and a control recording medium that can reduce a processing load of a processor and suppress a delay in processing such as measurement are provided. A measurement device according to one aspect of the present invention includes a main MCU that performs measurement based on biological data obtained by a sensor, a communication IC that performs wireless communication with an information terminal, and a nonvolatile memory connected to the communication IC. The main MCU specifies an address of a write destination in the nonvolatile memory and causes the communication IC to write the biological data into the nonvolatile memory, and specifies an address of a read source in the nonvolatile memory and causes the communication IC to read the biological data from the nonvolatile memory and transmit the biological data to the information terminal.