Abstract: The disclosure relates to an oximeter, including a blood oxygen collecting unit that has a first light emitting unit emitting a red light, a second light emitting unit emitting an infrared light, and a light receiving sensor receiving the red light emitted by the first light emitting unit and not absorbed by a human body and the infrared light emitted by the second light emitting unit and not absorbed by the human body, and converting them into an electrical signal, a storage unit that stores measurement data and/or a power-on startup screen, the power-on startup screen including the last measurement result of a blood oxygen saturation and/or previous measurement results of the blood oxygen saturation, a power-on button that is for power-on startup, a microprocessor that calculates a blood oxygen saturation of the human body based on the electrical signal detected by the light receiving sensor.

Abstract: Monitoring apparatus for measuring the respiratory rate of a subject comprises an upper arm unit attached to a subject's upper arm in use and containing at least one movement sensor and a photoplethysmograph configured to monitor blood volume within the subject's upper arm while the upper arm unit is worn on the subjects upper arm. The output from the photoplethysmograph and movement sensor(s) are processed to calculate and output an estimate of the rate of respiration of the subject. Respiratory cycle induced variations in the photoplethysmograph signal and movement sensor signals can be independently determined and there is a greater confidence in the calculated respiratory rate when these independent calculations give consistent readings. If there is insufficient confidence, no rate of respiration is displayed.

Abstract: A method and optode for determining a concentration of an analyte in a sample liquid is provided. The method comprises a radiation source, where excitation radiation is directed onto a carrier unit which is in contact with the sample liquid and has immobilized molecules of a sensor dye that is sensitive to the analyte. The excitation radiation induces luminescence radiation of the sensor dye. This radiation is detected by a radiation detector, which generates an output signal. The analyte concentration is ascertained from the detector output signal using an evaluation routine. This uses a property of the luminescence radiation on the interaction of the concentration of the analyte in the sample liquid used. The dependence of the examined property of the luminescence radiation on an indirect exchange interaction between the individual molecules of the sensor dye, which interact with each other over particles of the analyte.

Abstract: Coupler assemblies and methods are disclosed as the coupler assemblies may be used with a catheter. An exemplary coupler assembly includes a spherical linkage coupler for a catheter. The coupler comprises a first cylinder portion for connecting to a structure, and a second cylinder portion for connecting to a distal end of a body of the catheter. The coupler also comprises a spherical linkage including at least two link arms. Each of the two link arms are connected on one end to the first cylinder portion and on the other end to the second cylinder portion. The two link arms connect a portion of the structure to the distal end of the catheter and enable the structure to move relative to the distal end of the catheter in response to an external force exerted on the structure.

Abstract: An optical probe comprises three optical elements including at least one light source and at least one light detector. The three optical elements are positioned in a triangular configuration. Three optical fibers are each coupled to one of the three optical elements and have an exposed distal end portion. At least one light shroud is disposed radially around the exposed distal end portions of at least one of the optical fibers coupled to the at least one light source.

Abstract: A reusable sensor is disclosed for producing a signal indicative of at least one physiological parameter of tissue. The sensor can include a sensor housing that has a distal opening, a wire lumen, and a proximal opening. The distal opening can include a lumen extending through the body of the sensor housing and the wire lumen can be located on the outside of the sensor housing. The sensor can also include a first component located on a top surface of the sensor housing and along the pathway of the wire lumen. The sensor can also include a second component located on the bottom surface of the sensor housing opposite of the first component. The second component can also be located along the pathway of the wire lumen. The sensor can also include a wire coaxially disposed within the wire lumen and connecting the first component and second component.

Abstract: Embodiments herein relate to reflective optical medical sensor devices. In an embodiment, a reflective optical medical sensor device including a central optical detector and a plurality of light emitter units disposed around the central optical detector is provided. A plurality of peripheral optical detectors can be disposed to the outside of the plurality of light emitter units. Each of the plurality of peripheral optical detectors can form a channel pair with one of the plurality of light emitter units. The reflective optical medical sensor device can also include a controller in electrical communication with the central optical detector, the light emitter units, and the peripheral optical detectors. The controller can be configured to measure performance of channel pairs; select a particular channel pair; and measure a physiological parameter using the selected channel pair. Other embodiments are also included herein.

Abstract: A removable wearable device sleeve includes a sleeve body, one or more sensors, and an interface for operative communication with the wearable device. A removable sleeve includes a sleeve body having a front element having a first aperture, a back element having a second aperture, a tubular element having a first end and a second end with a third aperture, and one or more back elements define a cavity to encase an earpiece, an interface, and a sensor, wherein the sensor communicates sensor readings to the wearable device through the interface. A method of placing a sensor configured to communicate with a wearable device onto the wearable device includes providing a removable sleeve and inserting the wearable device through the first aperture of the front element into the cavity of the removable sleeve to provide a removable wearable device sleeve.

Abstract: A computer system for simultaneously sampling multiple light channels is configured to emit a first pulse-oximetry light signal from a first light source and to emit a second pulse-oximetry light signal from a second light source. The computer system then captures a combined pulse-oximetry signal from both the first pulse-oximetry light signal and the second pulse-oximetry light signal simultaneously at a photoreceptor sensor. The computer system identifies information within the combined pulse-oximetry signal, wherein the first light source and the second light source capture different attributes of the information.

Abstract: An ear-worn device includes a speaker, an optical emitter, an optical detector, a processor, and a housing configured to be positioned within an ear of a subject, wherein the housing encloses the speaker, optical emitter, optical detector, and processor. The housing includes at least one window that exposes the optical emitter and optical detector to the ear of the subject, and the housing includes at least one aperture through which sound from the speaker can pass. Light transmissive material is located between the optical emitter and the at least one window and is configured to deliver light emitted from the optical emitter to an ear region of the subject at one or more predetermined locations. Light transmissive material is positioned between the optical detector and the at least one window and is configured to collect light external to the housing and deliver the collected light to the optical detector.

Abstract: Devices and systems have a sensor probe configured to measure tissue oxygen saturation in the intestine or mesentery. The devices and systems can determine the oxygenation state of the entire thickness of the intestine or mesentery. Embodiments of the invention also include methods for inducing a temporary ischemic period in an intestine or mesentery tissue and analyzing changes in oxygen saturation of the tissue during the temporary ischemic period or during a recovery phase. The devices, systems, and methods can be applied in diagnosing intestinal ischemia in a patient, as well as in monitoring tissue oxygen saturation of the intestine or mesentery during or after a surgical procedure.

Abstract: Devices and systems have a sensor probe configured to measure tissue oxygen saturation in the intestine or mesentery. The devices and systems can determine the oxygenation state of the entire thickness of the intestine or mesentery. Embodiments of the invention also include methods for inducing a temporary ischemic period in an intestine or mesentery tissue and analyzing changes in oxygen saturation of the tissue during the temporary ischemic period or during a recovery phase. The devices, systems, and methods can be applied in diagnosing intestinal ischemia in a patient, as well as in monitoring tissue oxygen saturation of the intestine or mesentery during or after a surgical procedure.

Abstract: An physiological measurement device provides a device body having a base, legs extending from the base and an optical housing disposed at ends of the legs opposite the base. An optical assembly is disposed in the housing. The device body is flexed so as to position the housing over a tissue site. The device body is unflexed so as to attach the housing to the tissue site and position the optical assembly to illuminate the tissue site. The optical assembly is configured to transmit optical radiation into tissue site tissue and receive the optical radiation after attenuation by pulsatile blood flow within the tissue.

Abstract: Embodiments described herein generally relate to devices, systems and methods for measuring a volume or number of doses remaining in a drug delivery device that is used for delivering a dose to a patient. In some embodiments, a dose measurement system for measuring the liquid volume in a container includes a light guide disposed and configured to reflect electromagnetic radiation toward the container. The dose measurement system also includes a light guide disposed and configured to emit electromagnetic radiation into the light guide. A plurality of sensors are located in the apparatus that are optically coupleable to the light guide and are disposed and configured to detect the electromagnetic radiation emitted by at least a portion of the light guide. The apparatus also includes a processing unit configured to receive data representing the portion of the detected electromagnetic radiation from each of the plurality of sensors.

Abstract: A system and method are provided for diagnosis of animal respiratory diseases using auscultation techniques. Animal lung sounds are recorded and digitized. Lung sounds are obtained by an electronic digital stethoscope or a wireless audio digital recording unit. The sounds are stored as digital data, and one or more algorithms are applied to the data for producing an output to the user indicative of the health of the animal. The acoustic characteristics of the sound are compared with baseline data in the algorithms. One embodiment includes a digital stethoscope with an integral display. Another embodiment provides a system for gathering information about an animal to include not only auscultation data, but also information from other field devices such as temperature probes or weigh scales. The combined information can be analyzed by system software to generate detailed information to a user to include a diagnosis and recommended treatment options.

Abstract: A radio frequency (RF) current sensor for remotely activating a smoke evacuation device in an electrosurgical system includes a sensor body with a cable interfacing sidewall and a retaining member. The cable interfacing sidewall and the retaining member define a retention pocket for receiving a cable communicating RF current. The RF current sensor additionally includes a sensor element for detecting RF current in the cable and a sensor cable in electrical communication with the sensor element. The RF current sensor can operate in at least two modes, depending on whether the cable communicates RF current to a monopolar or bipolar electrosurgical instrument, but regardless of the operation mode, the sensor cable can communicate an activation signal and a current signal derived from the detected RF current to the smoke evacuation device, which activates or adjusts the period of time and/or the smoke evacuation flow rate of a vacuum source.

Abstract: Provided is a method for measuring blood glucose levels of a subject with a portable apparatus for noninvasively measuring blood glucose levels including at least one light receiving element for detecting light by using different light integration times, including: (a) switching on an LED for emitting light having wavelength absorbed in or scattered by glucose; (b) measuring a first signal value according to light which is reflected off the surface skin layer of the subject and enters in response to a first light integration time in the situation where the light is radiated; (c) adjusting a second light integration time for measuring light reflected off the inner skin layer of the subject based on the first signal value; (d) measuring a second signal value according to the light which is reflected off the inner skin layer of the subject and enters in response to the adjusted second light integration time; and (e) producing the blood glucose level of the subject by using a third signal value according to light

Abstract: The invention provides a pulse oximetry sensor for attachment to the lower half of the palm or the ulnar edge of the palm. The sensor may be portable, untethered and in some instances, disposable. The features of the sensor make it effective in stable, chronic or emergency medical settings.

Abstract: The disclosure includes a system for sensing physiologic data. The system can include a flexible configured to wrap around a finger of a user, a first electrode coupled to the flexible strap, and a second electrode coupled to the flexible strap. The system can also include a sensor housing comprising at least one sensor configured to detect physiologic data from the finger and a data receiving module communicatively coupled to the first electrode, the second electrode, and the at least one sensor. The data receiving module can be configured to receive physiologic data from the at least one sensor.

Abstract: An electronic device to be mounted around a finger includes: a top part on which a nail of the finger is located; a bottom part disposed opposite to the top part, where a fingerprint surface of the finger is located on the bottom part; and a side part connecting the top part and the bottom part to each other, where the top part generates a nail image by image-picking up the nail, and senses a movement of the finger, based on the nail image.

Abstract: A plethysmography (“PPG”) measurement system may include at least one source of PPG radiation and at least one auxiliary sensor for detection of PPG radiation. The radiation source emits a portion of the PPG radiation toward a subject and another portion along an optical path for direct communication between the PPG radiation source and the auxiliary sensor. The auxiliary sensor may develop a profile against which measurements from primary PPG sensors, which receive light returning from the subject, may be compared. From this comparison, new PPG signals may be generated that exhibit lower noise than the PPG signals output by PPG sensors. These noise mitigation techniques may be used advantageously by a PPG system to generate more accurate measurements and also to reduce power consumption by the radiation sources.

Abstract: A device for biorhythm detection, includes: a memory; and a processor coupled to the memory and configured to perform operations of: acquiring activity amount data indicating an amount of activity of a test subject which is measured by an activity amount meter configured to measure the amount of activity of the test subject; and detecting, as a frequency derived from a biorhythm of the test subject, a frequency that indicates peak power in a result which is obtained through frequency analysis of a first time waveform of the activity amount data.

Abstract: A fingerprint sensor device with built-in liveness detection capabilities includes: an area sensor disposed on a top surface of a substrate; a stiffener disposed below a bottom surface of the substrate; a printed circuit making electrical connection to the sensor disposed below the stiffener; and a light source and a photodetector. At least one of the light source and photodetector is disposed on the printed circuit below the area sensor. The stiffener includes at least one through-hole located with respect to the light source or photodetector to allow light from the light source to transmit through the stiffener towards a finger located on the area sensor or to allow light reflected from the finger to pass through the stiffener to the photodetector.

Abstract: A sensor device includes a first light emitter that emits light with a wavelength from a first spectral range, a second light emitter that emits light with a wavelength from a second spectral range, a first light detector configured to detect light with a wavelength from the first spectral range, but not to respond to light with a wavelength from the second spectral range, and a second light detector configured to detect light with a wavelength from the first spectral range and light with a wavelength from the second spectral range, wherein a distance between the first light emitter and the first light detector is smaller than a distance between the second light emitter and the second light detector.

Abstract: A biological information measurement device includes a correction unit that receives a first signal expressing a change in an amount of light of a first wavelength detected from a living body and a second signal expressing a change in an amount of light of a second wavelength detected from the living body, and corrects at least one of the first signal and the second signal to reduce a difference between an amount of change in the first signal and an amount of change in the second signal associated with a change in an amount of arterial blood of the living body, and a computing unit that computes a change in a blood oxygen concentration in the living body on a basis of the first signal and the second signal of which at least one is corrected by the correction unit.

Abstract: A method of non-invasively monitoring hematocrit levels includes monitoring a first emission response to the light provided at the first excitation wavelength, wherein the first emission response is monitored at a first wavelength and monitoring a second emission response to the light provided at the first excitation wavelength, wherein the second emission response is monitored at a second wavelength. A ratiometric value is calculated based on a ratio of the first emission response to the second emission response, wherein the ratiometric value corresponds with hematocrit level of the patient.

Abstract: A semiconductor device includes an antenna mounted on a wiring substrate. A holding member includes a first plate-shaped part having a first surface and a second surface, a second plate-shaped part having a third surface and a fourth surface, and a coupling part configured to couple the first plate-shaped part and the second plate-shaped part so that the second surface and the third surface have parts facing each other with a space therebetween. The one end of the wiring substrate is fixed to the holding member so that the antenna overlaps the coupling part, as seen from above. A part continuing to the one end of the wiring substrate is folded back so as to being arranged sequentially along the first surface, the second surface, the third surface, and the fourth surface. The other end of the wiring substrate extends in an elastically deformable state from the fourth surface.

Abstract: A glycated hemoglobin measurement device and method is disclosed. The device provides for measurement of glycated hemoglobin (A1c) without the need for blood sampling and the associated discomfort. The device uses a 400-540 nanometer light source and associated detection circuitry to convert light returned by the source into a waveform that is then processed into a patient specific value. The determined patient specific value is then multiplied by a calibration constant to yield a glycated hemoglobin (A1c) value which is then displayed or otherwise provided to the patient or a medical practitioner.

Abstract: A non-invasive measurement of biological tissue reveals information about the function of that tissue. Polarized light is directed onto the tissue, stimulating the emission of fluorescence, due to one or more endogenous fluorophors in the tissue. Fluorescence anisotropy is then calculated. Such measurements of fluorescence anisotropy are then used to assess the functional status of the tissue, and to identify the existence and severity of disease states. Such assessment can be made by comparing a fluorescence anisotropy profile with a known profile of a control.

Abstract: A method of estimating oxygen saturation includes illuminating a target site with light of three different wavelengths, for example green, red and infrared, and detecting light returned from the site at each of the wavelengths. The method distinguishes between cardiac pulsatility and nonpulsatility based on a parameter of the return light of the shortest wavelength. The method formulates an estimate of oxygen saturation as a function of a parameter of the light of the two longer wavelengths taken at both a period of pulsatility and at a period of nonpulsatility. An oximeter adapted to carry out the method is also disclosed. Aspects of the method and oximeter may be used to estimate other physiological parameters.

Abstract: Medical radar devices, including ultra-wideband (UWB) devices, for use in assisting and/or guiding cardiopulmonary resuscitation (CPR) by indicating one or more of: compression depth, compression frequency, and a return to spontaneous circulation. The devices and methods described herein may use reflected energy applied to a patient's chest to determine cardiac motion and/or chest compression and provide feedback to the person applying the CPR. In some variations the device is incorporated as a part of another resuscitation device, such as a defibrillator or automatic compression device.

Abstract: A blood pressure measurement apparatus includes a pressure controller that controls an internal pressure of a cuff, an oscillation acquiring section that acquires an oscillation corresponding to a pressure vibration, a pulse wave signal acquiring section that acquires a pulse wave signal of the subject from a probe, a processor, and a memory that stores instructions executable by the processor. In the apparatus, when the instructions are executed by the processor, the apparatus causes the pressure controller to inflate the internal pressure, determines whether a first condition is satisfied or not, determines whether a second condition is satisfied or not, and if the first condition and the second condition are satisfied, determines a mean blood pressure of the subject based on the internal pressure.

Abstract: Fetal tissue oxygenation may be performed transabdominally by, for example, receiving a plurality of detected electronic signals that correspond to light emitted from a pregnant mammal's abdomen and a fetus contained therein that has been detected by the detector and converted into the detected electronic signal. An indication of a depth of the fetus within the pregnant mammal's abdomen may be received and a portion of the detected electronic signals that correspond to light that was incident upon the fetus may be isolated responsively to the indication of the depth of the fetus using, for example, time of flight of photons that correspond to the detected electronic signals. A fetal tissue oxygen saturation level may then be determined using the isolated portion of the detected electronic signals that correspond to light that was incident upon the fetus.

Abstract: The invention relates to a biometric authentication device, comprising: a positioning module with measurement zone; a cryptographic calculation module; ultrasound module; a module for measuring heart rate and blood pressure; a photographic module configured to create a photograph of the venous network of the finger; a photograph of the fingerprint of the finger; a contrast light spectrometry of the finger; and a photograph of the venous network of the finger by infrared which would capture the intrinsic emission of the finger. The cryptographic module is configured to authenticate the user according to the vector image relating to said ultrasound of the venous and nervous networks of said finger, the measurement of a heart rate and the measurement of a blood pressure, the photograph of the venous network of said finger, the photograph of the fingerprint of said finger, and the spectrometry of said finger.

Abstract: Provided are sensors and articles of manufacture comprising one or more sensors. Also provided are uses of the sensors. The sensors have an elastomeric foam and one or more light sources and one or more light receivers. In various examples, the light source(s) and light receiver(s) are disposed on and/or disposed in and/or partially disposed in the elastomeric foam.

Abstract: The present disclosure describes embodiments of a patient monitoring system and methods that include the measure and display of hemoglobin statistics. In an embodiment, total hemoglobin trending is displayed over a period of time. Statistics can include frequency domain analysis, which may be unique for each patient monitored. The total hemoglobin trending and/or statistics can further be used to help control the treatment of a patient, such as being used to control IV administration.

Abstract: An oximeter sensor system includes a light source group having a plurality of LEDs including at least a first visible light LED, a second visible light LED and an infrared LED adjacent the first visible light LED and the second visible light LED, an infrared filter disposed in front of only the first visible light LED and the second visible light LED, a light source housing having a base, one or more sidewalls and a light-emitting end where the light source housing has a frustum shape where the light source group is disposed adjacent the base and facing the light-emitting end and where the one or more sidewalls has a reflective coating thereon, a light detector disposed opposite to, spaced from and facing the light-emitting end of the light source housing, and a cuvette disposed between the light-emitting end of the light source housing and the light detector.

Abstract: The present invention is directed to a bio-fluid detector such as a hemoglobin detector having the capability of receiving, storing and transmitting health information utilizing a portable transmitter and receiver including electronic PDAs such as cell phones. Further, the present invention utilizes a non-invasive hemoglobin detector that is connected to a portable transmitter-receiver such as PDAs including, but not limited to, cell phones.

Abstract: Disclosed herein is a ring-shaped wearable device for detecting biometrics with a light source and a photodetector directed towards a digit wearing the ring-shaped device. The ring can thus detect oxygen saturation of a wearer based on light transmitted through the wearer's finger. The ring can include power saving measures to extend the battery life. A motion sensor can help determine opportune moments for data collection such as when the wearer is still. The motion sensor can be used to remove noise from the data caused by motion. After data is collected or during data collection, the ring can wirelessly communicate the data to another portable electronic device such as a phone or watch.

Abstract: Apparatus for measuring sural nerve conduction velocity and amplitude, the apparatus including a housing; stimulation means for electrically stimulating a human sural nerve; a biosensor comprising a plurality of electrodes for detecting a sural nerve response evoked by the stimulation means; acquisition means electrically connected to the biosensor for electrically acquiring the sural nerve response detected by the biosensor; processing means electrically connected to the acquisition means for digitizing, processing and storing the acquired sural nerve response; calculation means electrically connected to the processing means for calculating the conduction velocity and amplitude of the processed sural nerve response; and display means for displaying the sural nerve conduction velocity and amplitude; wherein the stimulation means and the biosensor are designed to be placed on a patient's anatomy, in the vicinity of a sural nerve.

Abstract: Approaches to determining a sleep fitness score for a user are provided, such as may be based upon monitored breathing disturbances of a user. The system receives user state data generated over a time period by a combination of sensors provided via a wearable tracker associated with the user. A system can use this information to calculate a sleep fitness score, breathing disturbance score, or other such value. The system can classify every minute within the time period as either normal or atypical, for example, and may provide such information for presentation to the user.

Abstract: An optical device for the quantitative determination of the concentration of at least one analyte in a liquid sample comprises a housing (52) defining a first chamber (56) and a second chamber (60). A sample port (64) is defined in the first chamber (56). The sample port (64) receives light from a plurality of test regions of an assay device when the optical device is engaged with the assay device. The optical device further comprises a plurality of optical detectors (75, 76, 77) provided in the second chamber (60) and a mask member (66) interposed between the first chamber (56) and the second chamber (60) and having an aperture (68) defined therein and configured to direct light from the sample port (64) onto the optical detectors (75, 76, 77).

Abstract: A device for measuring a physiological parameter of a user carrying the device that includes a sensor having at least two sensor elements for detecting a sensor signal, a carrier configured to carry the sensor, and electrical contacts of the sensor elements that lead on, into or through the carrier. One or more frames carried by the carrier are formed around the sensor and/or the individual sensor elements, and an insulator material is filled between the one or more frames and the sensor and/or the sensor elements surrounded by a respective frame without covering a top surface of a respective sensor element facing away from the carrier.

Abstract: An optical vital signs sensor configured to measure or determine vital signs of a user comprises a light source configured to generate a light beam having an angular range of angles of incidence. The light beam is directed towards the skin of the user. A photo detector is provided and is configured to detect light which is indicative of a reflection of the light beam from the light source in or from the skin of the user. The light source and the photo detector are arranged adjacent to each other and on the same side of the skin of the user. A light shaping unit is configured to shape the light beam of the light source before the light beam enters the skin by limiting the angular range of angle of incidence to less than 20°.

Abstract: A method of evaluating characteristics of a work piece includes forming a photosensitive layer on the work piece. Then an ion implantation is performed on the work piece. The work piece is radiated, and an optical intensity of the photosensitive material on the work piece is calculated. The ion implantation pattern is evaluated according to the optical intensity. A chemical structure of the photosensitive material is changed upon the ion implantation. The work piece is recovered by reversing the chemical structure of the photosensitive material or removing the ion interrupted photosensitive material by chemicals.

Abstract: A sleeve includes a body having a top opening. The body covers a handheld oximeter probe or a portion of the probe. The sleeve has a shape that approximately matches the oximeter probe or portion of the probe, which is covered by the sleeve. The sleeve has a top opening that allows a user to slide the oximeter probe into the sleeve. The sleeve is transparent to radiation emitted and collected by the oximeter probe. The sleeve is formed of a material that prevents patient tissue, fluid, viruses, bacteria, and fungus from contacting the covered portions of the oximeter probe. The sleeve leaves the probe relatively sterile after use so that little or no clearing of the probe is required for a subsequent use, such as when the probe is covered with a new, unused sleeve.

Abstract: Embodiments of the invention relate to a method and apparatus for measuring at least one parameter that is (i) descriptive of stochastic motion of suspended particles within a fluid; and/or (ii) is a rheological property of the fluid or of the suspension; (iii) describes a concentration of suspended particles within the fluid; and/or (iv) is a diffusion coefficient of the suspended particles and/or (iv) is a viscosity of the fluid or of the suspension; and/or (v) is a food aging or spoilage parameter and/or (vii) is an in-vivo or in-vitro blood coagulation parameter.

Abstract: A system for measuring the blood loss comprises a measuring device that determines the hemoglobin concentration of fluid within a container utilizing a light source and a light detector. The container receives blood and other fluids from a patient during a medical procedure. Light from the light source is passed through the blood and other fluids in the container and is detected by the light detector. Based upon a magnitude of light detected, the hemoglobin concentration of the fluid in the container can be determined. A volume-measuring device determines the volume of blood and fluid in the container. Knowing the hemoglobin concentration and volume of fluid in the container, the volume of patient blood loss in the container can be determined. The blood loss measuring device in combination with infusion systems maintains a real-blood volume status so that proper infusion of blood, crystalloid and/or colloid solutions occurs.

Abstract: A LED switching system, including a multi-chip LED including first and second sets of LED chips, the first set of LED chips associated with a first wavelength band and the second set of LED chips associated with a second wavelength band; a first LED driver in communication with the first set of LED chips; a second LED driver in communication with the second set of LED chips; a LED controller configured to: receive input indicating a selection of one of the wavelength bands; identifying one of the first set and the second set of LED chips associated with the selected wavelength band; and providing a signal to one of the first and the second LED drivers that is in communication with the identified set of LED chips; wherein, in response to the signal, the one of the first and the second LED drivers activates the identified set of LED chips.

Abstract: A fingerprint sensor device with built-in liveness detection capabilities includes: an area sensor disposed on a top surface of a substrate; a stiffener disposed below a bottom surface of the substrate; a printed circuit making electrical connection to the sensor disposed below the stiffener; and a light source and a photodetector. At least one of the light source and photodetector is disposed on the printed circuit below the area sensor. The stiffener includes at least one through-hole located with respect to the light source or photodetector to allow light from the light source to transmit through the stiffener towards a finger located on the area sensor or to allow light reflected from the finger to pass through the stiffener to the photodetector.