Abstract: A dishwasher appliance includes a tub. A leak pan is positioned below the tub. A leveling assembly is configured for adjusting a level of the tub. The leveling assembly includes a housing mounted to the leak pan. A leveling leg is positioned within the housing. The leveling leg has a foot. An axle is mounted to the leak pan. A gear set is positioned within the housing. The gear set is configured to transfer rotation of the axle through the gear set to the leveling leg to adjust the level of the tub. The foot of the leveling leg is spaced from a thread on an outer surface of the leveling leg such that the gear set unmeshes from the thread on the outer surface of the leveling leg when the leveling leg is fully retracted.

Abstract: Provided are a method performed by an appliance for washing and rinsing goods, where some of the goods loaded into the appliance are sensitive to process water temperature changes, and an appliance performing the method. The method may include receiving via a user interface, an instruction that an appliance, during execution of a general-type washing program, should take into account that goods sensitive to temperature changes are loaded into the appliance, measuring a temperature value in a washing compartment of the appliance upon executing a draining process, and supplying fresh water to the washing compartment of the appliance. The method may include measuring, when the fresh water has been supplied, whether the process water being accommodated in a sump of the appliance is at a target temperature value or not and if not adjusting the temperature of the process water in the sump to attain the target temperature value.

Abstract: A dosing device or system for dispensing tablets, which can include at least one active ingredient for an automatic washing process, into an automatic washing machine, wherein the dosing device or system is for dispensing one or more, but not all, of the tablets at once into the automatic washing machine, and wherein the dosing device or system can be for dispensing only one tablet at once.

Abstract: A dishwasher including a dish rack having a wire frame rack defining an interior and comprising a plurality of spaced wire frame elements defining a dish supporting surface forming at least a portion of the interior, and a bumper having a body and an elastic surface. The bumper can span at least two of the wire frame elements.

Abstract: An endoscope (1) having a handle (2), an insertion portion (3) arranged at the distal end of the handle, a bending portion (4) arranged at the distal end of the insertion portion, and two control wires (40, 41) used to control the bending of the bending portion via control inputs made at the handle. The handle includes at least one lever member (21) pivotable about a pivot axis (22), a pulley element (42) located between the proximal end of the handle and the pivot axis of the lever member.

Abstract: An endoscope (1) including a handle (2) arranged at a proximal end and an insertion tube (3) extending from said handle (2) towards a distal end, a bending section (7) arranged at the distal end and controllable by and operator via control input means (8) arranged at the handle (2); and at least one insertion tube part with at least one lumen, wherein the bending section (7) is displaceable in said lumen so as to be movable relative to the insertion tube (3) from a retracted position within said lumen to an extended position at least partially outside said lumen.

Abstract: A direct visualization catheter includes an elongate shaft defining a lumen and having a distal end portion and a proximal end portion and a transparent balloon attached to the distal end portion of the shaft. The balloon includes a first layer comprising a thermoset polymer and a plurality of polymeric fibers at least partially embedded in the thermoset polymer and a second layer disposed on the first layer and comprising a hydrogel.

Abstract: Provided is an endoscope that can easily perform the attachment and detachment work of a proximal end side of a wire without impairing the operability of an operating part.

Abstract: A visual oral scraping spoon of the present application includes an oral scraping spoon, an oral observation instrument and a connecting mechanism. The oral scraping spoon is detachably connected to the oral observation instrument through the connecting mechanism, and under the action of an observation system of the oral observation instrument, the oral scraping spoon can be used to scrape and clean the teeth or the tongue under direct vision, and the cleaning effect can be observed in real time, and the cleaning process can be shot and photographed. Furthermore, the oral observation instrument may also be provided with a flusher, the flusher is used in conjunction with the oral scraping spoon to thoroughly flush the removed dental calculus, dental plaque, coated tongue and the like in time, and the using process is more comfortable, convenient and efficient.

Abstract: A system includes a member having a lumen; and a stabilizer positioned at a distal end of the lumen, wherein: the stabilizer includes at least two radially-inward projections circumferentially spaced apart from one another at the distal end of the lumen; the at least two radially-inward projections defining an opening at the distal end of the lumen; and a cross-sectional area of the opening is less than a cross-sectional area of the lumen.

Abstract: A handheld endoscope has a disposable, single-use portion that includes a distal tip, cannula, housings, and a proximal port that is connected to a substantially straight working channel. The cannula is rotatable about the main longitudinal axis of the cannula. The endoscope also includes a re-usable portion that has a handle and display module. The single-use and re-usable portions mate and un-mate with each other via physical side-mounting arrangement as well as separate electrical connectors. The handle can house imaging system electronics that support manual and auto imaging modes which can be selected via touch screen control on the display module. The re-useable portion is sealed with various o-rings and/or gaskets and can be highly fluid resistant to facilitate disinfecting and/or sterilization.

Abstract: A cable for connecting a medical imaging device to a medical imaging controller includes a first connector located at a distal end of the cable for connecting to the imaging device, a second connector located at a proximal end for connecting to the medical imaging controller, a circuit board comprising at least one memory that stores at least authentication information associated with the cable. The circuit board is communicatively connected via a communication bus on the circuit board to the second connector for enabling access to the authentication information by the medical imaging controller. One or more imaging communication lines extend between the first connector and the second connector for communicating imaging data from the medical imaging device to the medical imaging controller. The one or more imaging communication lines bypass the communication bus on the circuit board.

Abstract: The present invention relates to an optical connection device for optically connecting a first connector (42) of a first optical fiber device (44) with a second connector (46) of a second optical fiber device (48) along an optical axis, which comprises a plug part (40) having an elongated shaft (58) having a longitudinal shaft axis (62) and a lumen (60) extending through the shaft (58) along the shaft axis (62) for receiving the first connector (42), the plug part (40) further having a cap (64) at a first end of the shaft (58) which has an insertion opening (66) for insertion of the first connector (42) into the lumen (60), the opening (66) being aligned and communicating with the lumen (60), the plug part (40) having an optical window (68) having a solid body element (69), wherein the plug part (40) is at least in part deformable; and a clamp part (18), wherein the plug part (40) is configured to be at least partially inserted into the clamp part (18), and the clamp part (18) is configured to, when the plug

Abstract: An endoscope system is provided. The system comprises an endoscope having a hollow tube formed therein; and an instrument for insertion through the hollow tube, wherein the instrument has a first end for operational control and a second distal end for instrument operation at a distal end of the endoscope, wherein the distal end of the endoscope has an illumination device and a vision device for providing illuminated vision at the distal end of the endoscope for operational control of the instrument operation at the distal end of the instrument, and wherein the distal end of the instrument and the distal end of the endoscope are interoperably coupled for rotational control of the instrument with respect to the endoscope.

Abstract: Various embodiments include an endoscopic device. A sheath may enclose the device and may thereby guard against environmental contamination. The sheath may include one or more channels for transmission of instruments and/or solution to and from the body. The sheath may be disposable. A stopper unit may reduce fluid leakage from inside a body cavity during a procedure. The stopper unit may include a serrated outer contour to assist in catching at a body orifice. The stopper unit may have a perforable inner barrier designed to reseal about a probing portion inserted through the stopper unit.

Abstract: The present invention relates to an intubation system comprising insertion unit to be connected to a bending section of a medical instrument comprising an inner elongated shaft structure being capable of torque transmission around its length axis and an outer elongated shaft structure surrounding the inner elongated shaft structure and having a continuous outer surface, and an orientation controller being attached to the inner elongated shaft, such that when the orientation controller rotates, the bending section turns around itself.

Abstract: Disclosed is a self-propelled soft robot body, including a tube which is internally and axially provided with a tube cavity, and at least one propelling structure, comprising a first driving unit, a second driving unit and a third driving unit, which are evenly fixed on a peripheral wall of the tube cavity, relative to an axis thereof, and along the axis of the tube; and the first driving unit, the second driving unit and the third driving unit are respectively telescopic along the axis of the tube; at least two support structures, with each two adjacent support structures having at least one propelling structure arranged therebetween, the support structures are fixedly connected with the propelling structure and arranged on the peripheral wall of the tube cavity.

Abstract: Portable surgical systems, methods, and kits are described. The surgical systems may include a camera configured to capture images, viewing equipment configured to receive and display the captured images, a processor, and a stand. The camera, the viewing equipment, the processor, and the stand are configured to be housed in a case. Surgery may be performed using the surgical system by retrieving surgical components from the case, assembling the retrieved surgical components into a surgical system, positioning a patient within the surgical system for surgery, configuring the surgical system, performing the surgery with the surgical system, reconfiguring the surgical system during the surgery, disassembling the surgical system after the surgery, and placing the components in the case.

Abstract: A medical imaging system includes multiple illuminating endoscopes with cameras having image sensors exposure control and a frame memory. The exposure control of each camera activates the frame memory and light source for collection of selected frame images by the frame memory. A data link among the endoscopes synchronizes exclusive initiation of the exposure controls in recurring serial order for activation of each respective frame memory and light source.

Abstract: A tip section of a multi-camera endoscope includes a front-pointing camera on a planar surface of a distal end of the tip section and two side-pointing cameras positioned on a cylindrical surface in proximity to the planar surface such that the side field of view provided by the two side-pointing cameras partially overlaps with the front field of view provided by the front-pointing camera. The tip section further includes a working channel configured for insertion of a surgical tool; and a pathway fluid injector for inflating and/or cleaning a body cavity into which the endoscope is inserted.

Abstract: An endoscope device includes: a light source configured to perform any one of simultaneous lighting and sequential lighting; an image sensor including a plurality of pixels; a plurality of filters including at least one type of primary filter and a complementary filter; and a processor including hardware, the processor being configured to cause the light source to switch between the simultaneous lighting and the sequential lighting, when the simultaneous lighting is performed, perform interpolation processing to generate an output image by using an imaging signal generated from a pixel corresponding to the complementary filter, and when the sequential lighting is performed, perform interpolation processing to generate an output image by using an imaging signal generated from a pixel corresponding to the complementary filter as an imaging signal generated from a pixel corresponding to the at least one type of primary filter.

Abstract: A subjective optometry apparatus has a projection optical system including a visual target presenting portion and an optical member to project a target light flux toward a subject eye, and causing the target light flux to be incident on the optical member with a deviation of the incident target light flux from an optical axis of the optical member, a housing accommodating the projection optical system, a presentation window for emitting the target light flux from the inside of the housing to the outside thereof, an eye refractive power measurement unit provided outside the housing, and holding means integrally connecting the housing to the eye refractive power measurement unit to hold the eye refractive power measuring unit. When using the eye refractive power measuring unit, a distance from the presentation window to the eye refractive power measurement unit in an optical path is equal to or less than 180 mm.

Abstract: A virtual reality-based ophthalmic inspection system includes a wearable unit, an electronic unit, and at least one detector. The wearable unit is available for an inspected object to wear the wearable unit on head. The electronic unit is assembled with the wearable unit and has a left-eye display zone and a right-eye display zone. A first visual acuity of the inspected object is identified according to a first eyesight information. The electronic unit performs a visual correction confirmation process, the at least one detector detects a condition value of corresponding the right eye and/or the left eye, and the electronic unit answers a first comparison result after comparing the condition value with a threshold value.

Abstract: Embodiments of the present invention provide a computer-implemented method of determining a parameter indicative of dark adaptation of an eye, comprising receiving threshold data from a dark adaptometer indicative of a perception threshold of the eye, fitting first and second models to the threshold data, wherein the first model is associated with a first dark adaptation mechanism and the second model is associated with the first dark adaption mechanism and a second dark adaptation mechanism, determining a confidence associated with the fitting of each of the first and second models to the received threshold data, iteratively repeating the steps of receiving the threshold data and fitting the first and second models in dependence on the determined confidence, and outputting an indication of one or more parameters indicative of dark adaptation of an eye associated with one or both of the first and second models.

Abstract: An ophthalmologic apparatus of embodiments includes an OCT unit, an acquisition unit, and a specifying unit. The OCT unit is configured to acquire a tomographic image of a subject's eye using optical coherence tomography. The acquisition unit is configured to acquire a front image of the subject's eye. The specifying unit is configured to specify shape of a tissue of the subject's eye based on the tomographic image acquired by the OCT unit and the front image acquired by the acquisition unit.

Abstract: An ophthalmologic information processing apparatus includes an acquisition unit, a tissue specifying unit, and a specifying unit. The acquisition unit is configured to acquire a tomographic image of a subject's eye. The tissue specifying unit is configured to acquire first shape data representing shape of a tissue of the subject's eye by performing segmentation processing on each of a plurality of tomographic images acquired by the acquisition unit. The specifying unit is configured to obtain second shape data representing shape of the tissue based on the plurality of first shape data acquired by the tissue specifying unit.

Abstract: An ophthalmologic information processing apparatus includes an acquisition unit, a tissue specifying unit, and a specifying unit. The acquisition unit is configured to acquire a tomographic image of a subject's eye formed based on scan data acquired using an optical system for performing optical coherence tomography on the subject's eye. The tissue specifying unit is configured to acquire first shape data representing shape of a tissue of the subject's eye by performing segmentation processing on the tomographic image. The specifying unit is configured to specify a low sensitivity component having a small variation with respect to a change in a position of the optical system with respect to the subject's eye from the first shape data, and to obtain second shape data representing shape of the tissue based on the specified low sensitivity component.

Abstract: Methods and apparatus, including computer program products, are provided for remote monitoring. In some example implementations, there is provided a method. The method may include receiving, at a remote monitor, a notification message representative of an event detected, by a server, from analyte sensor data obtained from a receiver monitoring an analyte state of a host; presenting, at the remote monitor, the notification message to activate the remote monitor, wherein the remote monitor is configured by the server to receive the notification message to augment the receiver monitoring of the analyte state of the host; accessing, by the remote monitor, the server, in response to the presenting of the notification message; and receiving, in response to the accessing, information including at least the analyte sensor data. Related systems, methods, and articles of manufacture are also disclosed.

Abstract: Methods and apparatus, including computer program products, are provided for remote monitoring. In some example implementations, there is provided a method. The method may include receiving, at a remote monitor, a notification message representative of an event detected, by a server, from analyte sensor data obtained from a receiver monitoring an analyte state of a host; presenting, at the remote monitor, the notification message to activate the remote monitor, wherein the remote monitor is configured by the server to receive the notification message to augment the receiver monitoring of the analyte state of the host; accessing, by the remote monitor, the server, in response to the presenting of the notification message; and receiving, in response to the accessing, information including at least the analyte sensor data. Related systems, methods, and articles of manufacture are also disclosed.

Abstract: In one aspect, a computerized method useful for implementing a language neutral virtual assistant includes the step of providing a set of digital medical devices. The set of digital medical devices obtains a specified medical sensor information from a patient and communicates the specified medical sensor information to one or more remote entities. The method includes the step of providing a set of tele-health devices. The set of tele-health devices communicates an audio-video data of a tele-health session to the one or more remote entities. The method includes the step of creating an open Device Integration Layer (DIL), wherein the DIL communicates with the set of digital medical devices. The DIL communicates with the set of tele-health devices in a tele-health session. The method includes the step of with the DIL, parsing and translating a digital output of the medical device data of the set of digital medical devices and the set of tele-health devices.

Abstract: A wearable medical device includes an electrode assembly having a plurality of ECG sensing electrodes configured to monitor a cardiac condition of a patient using the device, a call button to initiate a call with a remote location and a transceiver configured to communicate information to and from the wearable medical device. The device includes a memory and a controller having at least one processor configured to execute instructions stored in the memory. The instructions include receiving, via actuation of the call button, a request to initiate a communication link with the remote location, providing, via a user interface, a confirmatory prompt that the patient indicate confirmation to proceed with the request to initiate the communication link with the remote location, and initiating, via the transceiver, the communication link to the remote location responsive to the indication of the confirmation to proceed with the request to initiate the communication link.

Abstract: Embodiments of the present disclosure include a photodiode that can detect optical radiation at a broad range of wavelengths. The photodiode can be used as a detector of a non-invasive sensor, which can be used for measuring physiological parameters of a monitored patient. The photodiode can be part of an integrated semiconductor structure that generates a detector signal responsive to optical radiation at both visible and infrared wavelengths incident on the photodiode. The photodiode can include a layer that forms part of an external surface of the photodiode, which is disposed to receive the optical radiation incident on the photodiode and pass the optical radiation to one or more other layers of the photodiode.

Abstract: The present disclosure relates to gastrointestinal (GI) tract detection methods, devices and systems.

Abstract: According to a method for using near infrared spectroscopy to detect compartment syndrome, an optics array is placed around a body region of a patient that contains a vulnerable compartment of tissue. The optics array includes emitters that generate photons at NIR wavelengths and detectors that detect photons at NIR wavelengths. Photons are emitted from at least one of the emitters, and detected at more than one of the detectors after those photons traveled through the tissues of the body region of the patient. A cross-sectional measure of regional differences in absorption within a cross-section of the body region of the patient is displayed so as to allow detection of compartment syndrome. The method is carried out with a device for using near infrared spectroscopy to detect compartment syndrome.

Abstract: Systems for calculating extent of congestive heart failure (CHF) and/or identifying exacerbation of CHF. In one embodiment, a system includes smartglasses configured to be worn on a user's head, and an inward-facing camera and a sensor, both physically coupled to the smartglasses. The inward-facing camera is mounted more than 5 mm away from the head and captures images of an area comprising skin on the user's head, which is larger than 4 cm{circumflex over (?)}2. The sensor measures a signal indicative of a respiration rate of the user (respiration signal). The system also includes a computer that calculates the extent of CHF based on: a facial blood flow pattern recognizable in the images, and respiration rate recognizable in the respiration signal.

Abstract: Described herein are systems, devices, and methods for cardiac monitoring. In particular, the systems, devices, and methods described herein may be used to conveniently sense the presence of an intermittent arrhythmia in an individual. The systems, devices, and methods described herein may be further configured to sense an electrocardiogram.

Abstract: A method of computing a hear rate compensates for noise in data transmission that can lead to false R-peak detection or missed R-peak detection. The method computes an updated heart rate based on a window of approximately ten seconds of digitized ECG readings broadcast from a sensor. A new value is calculated approximately every second such that the window of ECG readings overlaps considerably between consecutive calculations. The method compensates for noisy data by discarding heart rate samples that differ by more than a threshold amount from a previously calculated heart rate value. The threshold is adjusted based on a standard deviation of differences between heart rate samples.

Abstract: A vital sign measurement device includes a belt to be worn around an upper limb of a living body, and a transmission and reception unit provided to the belt, capable of transmitting and receiving radio waves. The transmission and reception unit includes transmission and reception antenna units. The transmission antenna unit emits radio waves respectively toward an artery of the upper limb and a heart. The reception antenna unit receives radio waves respectively reflected by the artery and/or a tissue being displaced in accordance with a pulse wave of the artery and by the heart and/or a tissue being displaced in accordance a heartbeat of the heart. The vital sign measurement device includes a vital sign detection unit that acquires a pulse wave signal representing the pulse wave of the artery and a heartbeat signal representing the heartbeat of the heart based on the outputs from the reception antenna unit.

Abstract: An apparatus for estimating blood pressure, includes a pulse wave sensor configured to measure a first pulse wave signal from a user, and a processor configured to differentiate or integrate the measured first pulse wave signal to obtain a reference signal, correct the measured first pulse wave signal, based on the obtained reference signal, to obtain a second pulse wave signal, and estimate the blood pressure, based on the obtained second pulse wave signal.

Abstract: A display control device of the present disclosure is configured to present information for positioning a pulse wave sensor relative to a measurement site. A measurement device includes a belt wrapped around and attached to a measurement site for measuring a pulse transit time, a sensor unit provided on an inner peripheral surface of the belt that i toward the measurement site when the belt is attached, and a display provided on an outer peripheral surface of the belt opposite to the inner peripheral surface. The display is provided on the outer peripheral surface in a site configured to face a site where the sensor unit is positioned when the belt is attached, and the sensor unit includes a first pulse wave sensor and a second pulse wave sensor disposed spaced apart from each other in a width direction of the belt.

Abstract: A measurement device (1) performs filtering processing via an analog filter (403) with a predetermined transfer function on a first signal indicating a pulse wave of a subject and a second signal indicating a pulse wave or an electrocardiogram of the subject; performs filtering processing via a digital filter with the predetermined transfer function on third time series data, which is first time series data of the first signal arranged in reverse chronological order, and fourth time series data, which is second time series data of the second signal arranged in reverse chronological order; and calculates a pulse transit time on the basis of a signal indicated by fifth time series data, which is the third time series data post filtering processing arranged in chronological order, and a signal indicated by sixth time series data, which is the fourth time series data post filtering processing arranged in chronological order.

Abstract: An apparatus for estimating bio-information, includes a pulse wave sensor configured to measure a pulse wave signal from a user, and a processor configured to obtain two or more parameters among a maximum point, an average point, and an onset point, from a waveform of the measured pulse wave signal, and combine the obtained two or more parameters to generate a pulse wave analysis result.

Abstract: A myocardial excitation complementation/visualization apparatus includes an acquiring section that acquires intracardiac electrocardiograms of a subject, the intracardiac electrocardiograms being recorded by a recording unit having a plurality of electrodes, a processing section that performs a computation for completing and visualizing a state of excitation in a myocardium of the subject based on the intracardiac electrocardiograms, and a displaying section that displays the state of excitation in the myocardium of the subject based on an output of the processing section. The processing section includes a first generating section, a correcting section, a second generating section, and a third generating section. The displaying section displays a change of the state of excitation in the myocardium of the subject based on the visualized data.

Abstract: A living-body contact electrode used primarily in a garment for measuring living-body information, which is comfortable to wear, even during exercise, without rubbing between the electrode and the skin while acquiring a stable electrical signal in a dry state and a wet state. A living-body contact electrode can acquire a living-body electrical signal with decreased electrical noises by suppressing the displacement of the electrode without impairing feeling and feel of wearing by suppressing the skin irritation. This is achieved by limiting the coefficient of static friction of the surface of the electrode with respect to the skin, by decreasing the frictional coefficient of an electrical wiring part to be equal to or less than a predetermined value, and by combining the electrical wiring part with the electrode.

Abstract: A catheter comprising an elongated catheter body, and an electrode assembly distal of the catheter body, the assembly comprising a plurality of spines, wherein each spine has a distal end that is connected to the distal end of at least one other spine, wherein each spine has an electrode-carrying portion, the electrode-carrying portions of all spines of the assembly being in a single common plane, and wherein all spines of the assembly have a uniform exposed total length.

Abstract: A brain wave detection bioelectrode capable of improving adhesion is provided. The brain wave detection bioelectrode includes: a holder part that includes a plurality of through holes; an electrode part that is formed of at least one conductive elastic body including a base part extending to an outer peripheral side of a peripheral surface of each of the through holes and including at least one projecting part that projects from the base part and can penetrate the through hole; and a lid part having a conductive property that clamps the base part between itself and the holder part.

Abstract: A wearable sensing device includes a connector socket provided with contact pads connectable to sensing electrodes for sensing biological electrical signals. A supply module is provided with a battery, which is housed in a first casing configured for reversible coupling with the connector socket. A control module is housed in a second casing distinct from the first casing and configured for coupling with the supply module and with the connector socket. The control module is equipped with a processing unit configured to process biological electrical signals detectable through the contact pads. Mechanical-connection members couple the supply module to the connector socket. Electrical-connection members distinct from the mechanical-connection members are configured to connect the battery and the contact pads to the control module.

Abstract: A microelectronic sensor for non-invasive monitoring of glucose levels in blood is based on the combination of an open-gate pseudo-conductive high-electron mobility transistor and a Vivaldi antenna installed in the open gate area of the transistor. The sensor is capable of sensing sub-THz radiation produced by a body of a user, and comprises a heterojunction structure made of the layers of GaN/AlGaN single- or poly-crystalline semiconductor materials stacked alternately and a conducting channel comprising a two-dimensional electron gas (2DEG) or a two-dimensional hole gas (2DHG) formed at the interface between the GaN/AlGaN layers. The highest sensitivity of the sensor is achieved when the thickness of the top recessed layer (GaN or AlGaN) in the open gate area between the source and drain contacts is 5-9 nm and the surface roughness of this top layer is about 0.2 nm or less.

Abstract: A medical system (6000) includes an EIT module (30, 33, 8000), a ventilation module (7100), a dosing module (4), a data input module (50) and a control module (70). The control module (70) coordinates a breath-hold maneuver, which is carried out at the ventilation module (7100). The control module (70) coordinates a perfusion measurement and a data acquisition (50) of EIT data (3), which is carried out at the EIT module (30, 33, 8000). The control module (70) determines an indicator, which indicates a state of perfusion of the lungs, and makes this indicator of the state of perfusion of the lungs available.

Abstract: A method and system to assess data from a dielectric probe to determine the health of tissue by denoising the data and clustering the data points. The assessment is used to assist medical professionals in the care patients.