Abstract: An improved showerhead assembly is provided for facilitating the application of soap or shampoo upon a bather. The showerhead assembly is preferably handheld and includes an elongate handle, and a showerhead including a face having one or more nozzles for spraying water. In addition, the showerhead assembly includes a detachable reservoir for storing soap or shampoo. Preferably, the reservoir is detachable from the showerhead by a threaded coupling in which the reservoir includes male threads which can be capped. Preferably, the showerhead assembly includes a controller for allowing one to selectively dispense shampoo or soap from within the reservoir into the stream of water which is ejected from the showerhead nozzles.

Abstract: The present invention relates to the technical field of furniture items, in particular to a reusable fixed tissue holder including: a bar frame including a first bar frame and a second bar frame sleeving the first bar frame; a base fixed to one end of the first bar frame; a disc seat mounted in the base; a sucking disc body mounted on the disc seat, wherein a first channel is disposed on the disc seat, and a second channel connected with the channel is disposed on the sucking disc body; and a button structure mounted on the base and used for connecting the first channel and the second channel to the outer atmosphere. According to the present invention, a cavity is exhausted by using a pipe barrel to form a negative pressure, the tissue holder can be adsorbed on the wall surface without applying a great pressing force.

Abstract: In one aspect, an autonomous cleaning robot includes a drive configured to propel the robot along the floor surface and a tank assembly. The tank assembly includes a reservoir, left and right receptacles, and a handle extending across a cover of the tank assembly, the handle being moveable between a first position and a second position, wherein when the handle is in the second position, the tank assembly is locked in position. The tank assembly also includes left and right latch assemblies receivable by the left and right receptacles, respectively. Each latch assembly includes a moveable assembly configured to lock the tank assembly in position when the handle is in the second position.

Abstract: A surface cleaning head with a leading roller may be used to facilitate capturing of debris in the air flow into a suction conduit on the underside of the surface cleaning head. The leading roller is generally positioned adjacent to and in advance of the opening of the suction conduit. The surface cleaning head may have dual agitators—a leading roller and a rotating brush roll—with the leading roller being located in front of the brush roll. The leading roller may have a smaller diameter than the brush roll and may provide a softer cleaning element. The leading roller may also have a bottom portion exposed to the flow path to the suction conduit and at least a top half that is not exposed to that flow path. The leading roller may also float relative to the surface cleaning head and/or may be adjustable relative to the brush roll.

Abstract: Provided is a robot cleaner including a main body including a suction portion disposed therein, a main wheel for moving the main body, wherein a vertical level of the main wheel varies in a vertical direction with respect to the main body, an auxiliary wheel disposed at a front portion or a rear portion of the main body, wherein a vertical level of the auxiliary wheel is fixed with respect to the main body, and a driving member assembly disposed in the main body, wherein the driving member assembly varies a vertical level of the main body from a floor face while rotating in forward and rearward directions of the main body, wherein the driving member assembly has different hitting radii when rotating forward and rearward.

Abstract: Connector assemblies including a first subassembly having a recessed portion and a pair of locator tracks and a second subassembly having a pair of locator projections, vacuum assemblies including these connector assemblies, and methods of using the same are provided herein.

Abstract: A system of robotic cleaning devices and a method of a master robotic cleaning device of controlling at least one slave robotic cleaning device. The method performed by a master robotic cleaning device of controlling at least one slave robotic cleaning device includes detecting obstacles, deriving positional data from the detection of obstacles, positioning the master robotic cleaning device with respect to the detected obstacles from the derived positional data, controlling movement of the master robotic cleaning device based on the positional data, and submitting commands to the at least one slave robotic cleaning device to control a cleaning operation of said at least one slave robotic cleaning device, the commands being based on the derived positional data, wherein the cleaning operation of the slave robotic cleaning device is controlled as indicated by the submitted commands.

Abstract: There is provided a cleaning robot system including a charging station and a cleaning robot. The charging station includes multiple positioning beacons. The cleaning robot includes an image sensor and a processor. The image sensor is used to acquire light generated by the multiple positioning beacons on the charging station and generate an image frame. The processor is electrically connected to the image sensor, and used to calculate a relative position with respect to the charging station according to beacon images of the multiple positioning beacons in the image frame to determine a recharge path accordingly.

Abstract: Methods, systems, and devices for performing autonomous self-service are described. A robotic device may identify a status of a chamber associated with the robotic device based on sensor data received from a sensor of the robotic device and pause an autonomous debris collection process of the robotic device based on the identified status. The robotic device may automatically remove a first container from the chamber based on the identified status and discard the first container away from the robotic device. In some examples, the robotic device may discard the first container at a fixed position within a geo-boundary corresponding to the debris collection process. The robotic device may resume the autonomous debris collection process based on an introduction of a second container.

Abstract: A reservoir device includes: a liquid storage structure, configured to store liquid; a liquid feeding assembly, configured to feed the liquid into the liquid storage structure; a barrier assembly; a sensing field generator, configured to generate a sensing field; a sensor; and an electrical control assembly. The barrier assembly is arranged inside the liquid storage structure. The sensor is configured to sense the sensing field. The barrier assembly is configured to float under a buoyance action of the liquid, and to block the sensor from sensing the sensing field when the barrier assembly floats in a first liquid level position. The electrical control assembly is configured to control the liquid feeding assembly to stop feeding the liquid into the liquid storage structure when the barrier assembly blocks the sensor from sensing the sensing field.

Abstract: A robot cleaner includes a water tank forming a space to store water, a body forming an exterior and having a housing which forms a space in which the water tank is mounted, a pair of spin mops rotatably mounted at a lower side of the body, a first nozzle provided at the housing, a second nozzle provided at the tank and configured to couple to the first nozzle, and a fixing part generating a magnetic force when the tank is mounted in the housing to fix an arrangement of the tank mounted in the housing. The fixing part includes a fixing device (e.g., a magnet or metal) provided around a circumference of the second nozzle and a response fixing device (e.g., a magnet or metal) provided around a circumference of the first nozzle and having a shape corresponding to the fixing device. The first nozzle and the second nozzle are attached to each other by the fixing device and the response fixing device.

Abstract: A rack mounting assembly for supporting a third rack assembly within a tub of a dishwasher appliance is provided. The rack mounting assembly includes a mounting body positioned inside the wash chamber and having a mounting post and a support flange extending from the mounting body and being spaced apart to define a support slot. A roller includes a mounting sleeve having a rear lip that is received within the support slot when the roller is installed onto the mounting body.

Abstract: A dishwasher appliance including at least one upper rack assembly. Adjacent panels along a transverse direction of the dishwasher appliance form a pivotable connection at the longitudinal sides between adjacent panels that allow adjacent panels to collapse or fold towards each other such that the upper rack assembly may be selectively collapsed or extended along the transverse direction by movement of the plurality of panels towards or away from each other.

Abstract: An endoscopy system that includes a computer system with a high definition display monitor and a handheld portion. The handheld portion includes a re-usable handle portion and a single use portion that is configured to be disposed of following a single use. The single-use portion includes an elongated cannula with an imaging module and illumination modules at its distal tip. The handheld portion includes multiple sensors that can detect and measure rotation of the cannula relative to the handle portion, and rotation of the entire handheld portion. The sensor data is used to correctly orient and display images captured by the imaging module onto the high definition display monitor.

Abstract: Described herein are various method of using a direct drive system to perform procedures at a distance. One exemplary method include tying a knot or suturing at a distance with a first and second end effector. The direct drive system can enable sufficient end effector dexterity, including the ability to control various degrees of freedom of end effector movement, and allow a user to perform complicated task at a distance. In one aspect the direct drive system includes flexible tools that permit access to surgical site via a natural orifice.

Abstract: A tip part for an endoscope has a vision receptor having a vision sensor for providing an image from received light, a first lens, and a casing, the casing supporting the first lens so that the casing substantially maintains a position of the first lens in relation to the vision sensor; a first light source; an exterior housing; and a light shield positioned between the vision receptor and the first light source so as to prevent ingress of stray light from the first light source into the vision receptor by optically shielding the vision receptor; wherein the casing is formed integrally with the exterior housing so that the casing also substantially maintains the first lens in a position in relation to the exterior housing.

Abstract: An endoscope includes: a barrel having an opening of a through hole on an outer surface; a lens inserted into the through hole and having a distal end surface which protrudes from the outer surface; a first resin disposed between a wall surface of the through hole and a side surface of the lens; and a second resin disposed on a surface of the first resin, a portion of the barrel disposed around the opening, and an entire circumference of an outer peripheral portion of the distal end surface of the lens, the second resin forming a protruding portion which protrudes from the distal end surface of the optical member, containing light blocking particles, and having a larger fracture toughness value than the first resin.

Abstract: A working channel device is mountable on the outer circumference of an endoscope, such as an endoscope of the flexible shaft design. The device has a tubular or hose-like working channel and a distal fixing element that can be fixed to the working channel. The distal fixing element can engage around the endoscope in a clamping manner at the endoscope head of the endoscope. A proximal fixing element can be fixed to the working channel, which can engage around the endoscope, preferably at the endoscope grip of the endoscope. A preferably sleeve-like adapter can be mounted at the proximal end of the working channel of the working channel device. The adapter has or forms the proximal fixing element and additionally forms a connection point/interface for the connection of medical devices.

Abstract: A surgical robotic system automatically calibrates tubular and flexible surgical tools such as endoscopes. By compensating for unideal behavior of an endoscope, the surgical robotic system can accurately model motions of the endoscope and navigate the endoscope while performing a surgical procedure on a patient. During calibration, the surgical robotic system moves the endoscope to a target position and receives data describing an actual position and/or orientation of the endoscope. The surgical robotic system determines gain values based at least on the discrepancy between the target position and the actual position. The endoscope can include tubular components referred to as a sheath and leader. An instrument device manipulator of the surgical robotic system actuates pull wires coupled to the sheath and/or the leader, which causes the endoscope to articulate.

Abstract: Fluorescence videostroboscopy imaging is described. A system includes an emitter for emitting pulses of electromagnetic radiation and an image sensor comprising a pixel array for sensing reflected electromagnetic radiation. The system includes a controller configured to cause the emitter to emit the pulses of electromagnetic radiation at a strobing frequency determined based on a vibration frequency of vocal cords of a user. The system is such that at least a portion of the pulses of electromagnetic radiation emitted by the emitter comprises electromagnetic radiation having a wavelength from about 795 nm to about 815 nm.

Abstract: A medical imaging device in accordance with the present application includes a color separation prism, a fluorescence image sensor, a visible light image sensor, and a bandpass filter. The color separation prism splits light into first light belonging to a visible light wavelength band and second light belonging to a fluorescence wavelength band. The fluorescence image sensor is provided at an output side of the color separation prism and is configured to image at least part of the second light belonging to the fluorescence wavelength band separated by the dichroic film. The visible light image sensor is provided at the output side of the color separation prism and is configured to image at least part of the first light belonging to the visible light wavelength band separated by the dichroic film. The bandpass filter is disposed between the color separation prism and the fluorescence image sensor.

Abstract: An ear nose and throat (ENT) imaging and analysis system includes an endoscope usable to capture images of the nasal canal and other aspects of patient anatomy. Endoscopic images may be presented to a user via a touchscreen display, and the software may provide different imaging modes that aid in identifying particular anatomical structures or areas within the nasal canal. In one mode, the system uses an object recognition process to identify the nasal valve opening within the images at a relaxed state, and during forceful inhalation, and then calculates the difference between the two states, which may be suggestive of nasal valve collapse. In other modes, the system is configured to identify abnormalities of the inferior turbinate, septum, or other anatomy, as well as empty spaces within the nasal canal, as well as areas and volumes of empty space and user defined boundaries.

Abstract: An optical fiber bundle manufacturing apparatus includes: a winding member; a guide member movable in a direction parallel to a rotary axis, the guide member being configured to guide an optical fiber wire to any one of first winding positions, a converging winding position and second winding positions; and a processor configured to perform processing to move the guide member such that a first branching portion branching into p branches, a converging portion converging the first branching portion branching into p branches into one, a second branching portion branching into q branches, and a connecting portion connecting the first branching portion and the second branching portion are formed in this order by the optical fiber wire.

Abstract: Methods and diagnostic tools are provided for assessing contrast sensitivity in a subject in the presence and absence of luminance noise by: i) presenting to the subject a series of scenes, each scene comprising at least a first target having a preselected level of contrast superimposed on a uniform background and a second target having a preselected level of contrast superimposed on a luminance noise background, wherein in each successively presented scene the first and second targets that are superimposed on the uniform background and on the luminance noise background, respectively, have contrast levels that are different from the contrast levels of the first and second targets superimposed on the uniform background and on the luminance noise background, respectively, in the previously presented scene; ii) monitoring responses by the subject to step i); and iii) evaluating the contrast sensitivity of the subject based on the monitored responses.

Abstract: Predicting a non perfusion area. An enhancement image processing section performs enhancement image processing on a fundus image of a subject eye to enhance vascular portions (304). A prediction processing section predicts a non perfusion area in the fundus image that has been subjected to the enhancement image processing (306 to 312). A generation section generates a non perfusion area candidate image (314).

Abstract: Systems and methods for tracking eye movement during a diagnostic procedure include a retina imaging system configured to capture a first plurality of images of an eye and detect a presence of a fovea, an eye tracker configured to capture a second plurality of images of the eye and track a position and orientation of the eye; and a control processor configured to synchronize the first and second plurality of images, determine a time at which the fovea is detected in the first plurality of images, and determine one or more images from the second plurality of images to be classified as representative of fixation. The classified images are analyzed to determine eye fixation status during the diagnostic procedure based on eye tracking data.

Abstract: A system for testing and/or training the vision of a user is disclosed herein. The system includes at least one camera, a visual display device having an output screen, and a data processing device operatively coupled to the at least one camera and the visual display device. In one embodiment, the data processing device is programmed to determine a head position, head velocity, and/or head speed of a user during a vision test or vision training routine from a plurality of images of the head of the user captured by the at least one camera. In another embodiment, the data processing device is programmed to determine, based upon an input signal received from a user input device, a contrast display setting for a screen background relative to at least one visual target, the contrast display setting enabling the user to gradually adapt to increasing levels of visual stimulation.

Abstract: Disclosed is an eye examination apparatus that can be used in professional settings. The eye examination apparatus has a body having a first eye opening and a second eye opening for a user to see into the eye examination apparatus using two eyes. The eye examination apparatus also has a first camera coupled to the body and positioned to acquire ophthalmic images through the first eye opening, and a second camera coupled to the body and positioned to acquire ophthalmic images through the second eye opening. The eye examination apparatus also has at least one display coupled to the body and positioned to be viewable through the first eye opening and the second eye opening.

Abstract: An intraoral scanner comprises a light source, a moveable opto-mechanical module, an axial actuator, and an image sensor. The light source is configured to generate light that is to be output onto an object external to the intraoral scanner. The moveable opto-mechanical module comprises integrated projection/imaging optics and an exit pupil, the projection/imaging optics having an optical axis, wherein the projection/imaging optics are entirely integrated into the moveable opto-mechanical module. The axial actuator is coupled to the projection/imaging optics and configured to move the moveable opto-mechanical module comprising an entirety of the projection/imaging optics in the optical axis to achieve a plurality of focus settings. The image sensor is configured to receive reflected light that has been reflected off of the object external to the intraoral scanner for the plurality of focus settings.

Abstract: A system for measuring blood oxygenation levels and capillary refill time (CRT) of a user includes a camera configured to capture a video stream that includes a series of images representing a process of first squeezing a fingernail of the user to a blanched state, and then releasing to a resting state, and a Convolutional Neural Network (CNN) based processing unit configured to process an input image to create a two-dimensional representation of features, remove spatial relationships in the two-dimensional representation, generate non-spatial metadata, identify the fingernail in the resting state, and regions within a static image of the fingernail, and configured to generate a blood oxygenation value, and a measurement confidence level, and generate a CRT value of the user by applying the blood oxygenation value, and the measurement confidence level to a series of images captured by the camera over time.

Abstract: A sphygmomanometer includes: a first fluid bag that is to be worn around a measurement site; first and second pulse wave sensors that are mounted on first fluid bag, and detect pulse waves of respective opposing areas of an artery running along measurement site; pressing parts that locally presses areas corresponding to first and second pulse wave sensors from an outer circumference side, opposite of an inner circumference side of first fluid bag where first and second pulse wave sensors are mounted. Blood pressure is calculated based on pulse transit time obtained from outputs from first and second pulse wave sensors, with first fluid bag in an unpressurized state and first and second pulse wave sensors being pressed by a pressing force of the pressing part. Blood pressure is calculated, for oscillometric blood pressure measurement, based on pressure within first fluid bag with first fluid bag in a pressurized state.

Abstract: A method for synchronizing operation of a heart assist pump device to a patient's cardiac cycle includes obtaining a signal from a motor of a heart assist pump device and filtering the signal to remove noise. The method also includes determining a speed synchronization start point at which time the motor of the heart assist pump device will begin a change in speed of operation based on the filtered signal. The method further includes modulating a speed of the motor of the heart assist pump device to a target speed at the speed synchronization start point, thereby synchronizing the change in speed of operation with a patient's cardiac cycle.

Abstract: The present disclosure relates to a device, method and system for calculating, estimating, or monitoring the blood pressure of a subject based on physiological features and personalized models. At least one processor, when executing instructions, may perform one or more of the following operations. A first signal representing a pulse wave relating to heart activity of a subject may be received. A plurality of second signals representing time-varying information on a pulse wave of the subject may be received. A personalized model for the subject may be designated. Effective physiological features of the subject based on the plurality of second signals may be determined. A blood pressure of the subject based on the effective physiological features and the designated model for the subject may be calculated.

Abstract: An electromagnetic (EM) probe for monitoring at least one biological tissue. The EM probe comprises a spiral antenna conductor (not shown) and an EM radiation absorbing layer (92) mounted along the antenna. The EM radiation absorbing layer has a plurality of substantially concentric frame shaped regions (93A-C) corresponding to portions of said spiral antenna having equal surface of antenna conductor, any of said plurality of concentric frame shaped regions has an EM radiation absorption coefficient different than any other of said neighboring concentric frame shaped regions.

Abstract: The invention provides a sensor for measuring both impedance and ECG waveforms that is configured to be worn around a patient's neck. The sensor features 1) an ECG system that includes an analog ECG circuit, in electrical contact with at least two ECG electrodes, that generates an analog ECG waveform; and 2) an impedance system that includes an analog impedance circuit, in electrical contact with at least two (and typically four) impedance electrodes, that generates an analog impedance waveform. Also included in the neck-worn system are a digital processing system featuring a microprocessor, and an analog-to-digital converter. During a measurement, the digital processing system receives and processes the analog ECG and impedance waveforms to measure physiological information from the patient. Finally, a cable that drapes around the patient's neck connects the ECG system, impedance system, and digital processing system.

Abstract: A location of a number of fiducial points can be computed. The fiducial points can include impedance locations of an electrode disposed on a catheter in an impedance based coordinate system and magnetic locations of a magnetic position sensor disposed on the catheter in a magnetic based coordinate system. The impedance location of the electrode in the impedance based coordinate system can be transformed into a transformed impedance location of the electrode in the magnetic based coordinate system. A magnetic location of the electrode in the magnetic based coordinate system can be determined. A determination of whether an impedance shift exists between the transformed impedance location of the electrode in the magnetic based system and the magnetic location of the electrode in the magnetic based system can be made. An electromagnetic dynamic registration can be generated between the impedance based coordinate system and the magnetic based coordinate system based on the impedance shift.

Abstract: A method, including receiving, from electrodes positioned within a heart, first signals from at least three of the electrodes indicating electrical activity in tissue with which the at least three of the electrodes engage, and second signals indicating locations of the at least three electrodes. The second signals are processed to compute the locations of the at least three electrodes and to determine a geometric center of the locations. Based on the signals, an electroanatomical map is generated for an area of the tissue including the geometric center, and an arrhythmia focus is determined in the map. A circle is presented, and within the circle, a region of the map is presented including the geometric center and the focus so that the geometric center on the map aligns with a center of the circle, the region within the circle indicating a spatial relationship between the geometric center and the focus.

Abstract: Provided are systems and methods for displaying an estimated location of an instrument. In one aspect, the method includes determining a first location of the instrument based on first location data generated by a set of one or more location sensors for the instrument, the first location data corresponding to a first time period, and after the first time period, receiving a user command to move the instrument during a second time period. The method also includes estimating a second location of the instrument based on the first location and the received user command, the estimated second location corresponding to the second time period, and confirming the estimated second location based on second location data generated by the set of location sensors. The method further includes causing the estimated second location to be displayed prior to the confirmation of the estimated second location.

Abstract: The systems and methods provide for novel a triggering mode that allows the patient to trigger or initiate the delivery of a breath during ventilation on a ventilator. Further, the systems and methods provide for triggering ventilation utilizing a statistical trigger mode. Additionally, the systems and methods provide for analyzing and/or displaying information related to a potential change in a triggering threshold for a currently utilized breath type.

Abstract: A respiratory therapy device having a diagonal feedback array, and methods for the user thereof.

Abstract: The present invention relates to the field of medical monitoring, and in particular non-contact video monitoring to measure tidal volume of a patient. Systems, methods, and computer readable media are described for determining a region of interest of a patient and monitoring that region of interest to determine tidal volume of the patient. This may be accomplished using a depth sensing camera to monitor a patient and determine how their chest and/or other body parts are moving as the patient breathes. This sensing of movement can be used to determine the tidal volume measurement.

Abstract: Among other thing, the present invention provides solution to the problem, particularly, the present invention certain surfaces and certain sample holder to improve the sensitivity, speed, and easy-to-use of an optical signal based assays, such as colorimetric assays or fluorescence assays.

Abstract: A plantar pressure sensing system is located at a sole of shoe. The plantar pressure sensing system includes a first layer, a second layer a plurality of sensor, a plurality of convex portions, a plurality of connection portions, a processor and a storage. The processor is coupled with the storage and configured to be connected with the plurality of sensors. The plurality of sensors are configured to form the first layer. The plurality of convex portions and the plurality of connection portions are configured to form the second layer. Overall, the plantar pressure sensing system is able to detect pressure with the sensors by setting the alignment of the convex portions, thereby obtaining a more accurate pressure(s) reading from the sole of shoe. The data validity of the plantar pressure sensing system is improved.

Abstract: The present disclosure generally relates to user interfaces and more specifically to techniques for displaying user interfaces associated with physical activities. Exemplary user interfaces related to activity competitions are described. Exemplary user interfaces related to a friends list for activity sharing are described. Exemplary user interfaces associated with alerts presented to a user in response to automatically determining a boundary of a workout are described. Exemplary user interfaces associated with configuring a pace alert for a workout application are described.

Abstract: This disclosure generally relates to systems and methods for detecting, monitoring, and responding to abnormalities in an infant's breathing. One or more sensing devices may collect infant breathing related data, which may be filtered and converted to a frequency signal. The frequency signal may be monitored for irregularity or stoppage, and a processing module may determine whether the irregularity or stoppage is caused by an actual stoppage or irregularity in infant breathing. If infant breathing is determined to have stopped, a corrective action may be performed.

Abstract: Presented herein are systems, methods for collecting fluid from a surface (e.g., skin) and analyzing the fluid (e.g., to measure chemical, physical and/or biological properties of the fluid). For example, a system for fluid collection on a surface (e.g., skin) and fluid analysis includes at least one of the following modules: (i) a collection and delivery module to collect a fluid over a wet or partially wet surface and deliver it to (ii) a main sensing module to perform chemical, physical and/or biological analysis on the fluid. The system also includes (iii) a flow regulation module, for controlling fluid flow (e.g., transport) through the system and (iv) a waste module to collect and/or dispose of the fluid after analysis is complete.

Abstract: Multi-state engagement with continuous glucose monitoring (CGM) systems is described. Given the number of people that wear CGM systems and because CGM systems produce measurements continuously, a platform that provides a CGM system may have an enormous amount of data. This amount of data is practically, if not actually, impossible for humans to process. In implementations, a CGM platform includes a data analytics platform that obtains packages of glucose measurements provided by a CGM system and also obtains additional data associated with a user. The data analytics platform generates state information for the user by processing these CGM packages and the additional data, at least in part, by using one or more models. Based on this state information, the data analytics platform controls communication with the user, which may include generating intervention strategies to prevent users from transitioning to a negative state such as discontinuing use of the CGM system.

Abstract: One variation of the method for managing blood loss of a patient includes: receiving an image of a physical sample; extracting a feature from an area of the image corresponding to the physical sample; estimating a blood volume indicator of the physical sample according to the extracted feature; estimating a patient blood loss based on the blood volume indicator; estimating a euvolemic patient hematocrit based on an estimated patient blood volume and the estimated patient blood loss; receiving a measured patient hematocrit; and generating a volemic status indicator based on a comparison between the measured patient hematocrit and the estimated euvolemic patient hematocrit.

Abstract: An oximeter device has a replaceable probe tip. The probe tip can be removed or detached from the probe unit and discarded. A replacement probe tip can be attached to the probe tip. The replaceable probe tip allows the probe unit to be reused many times, each time with new sterile probe tip.

Abstract: The present disclosure relates to devices, systems and methods for extracting physiological information indicative of at least one vital sign of a subject. An embodiment of a device comprises a pre-treatment unit configured to derive at least three detection signals from electromagnetic radiation reflected from a skin region of a subject, wherein at least two detection signals comprise wavelength-dependent reflection information in a different wavelength channel and at least two detection signals comprise reflection information in different polarization channels having different polarization directions.