Abstract: A system, transceiver, and method for calculating and correcting levels (e.g., analyte levels) in a first medium (e.g., blood) using measurements from a second medium (e.g., interstitial fluid). In some embodiments, a transceiver may calculate an initial second medium level. The transceiver may calculate an initial second medium level rate of change (“ROC”) using at least the initial second medium level and past second medium level(s). The transceiver may calculate a first medium level using at least the initial second medium level and the initial second medium level ROC. The transceiver may calculate a subsequent second medium level. The transceiver may calculate an updated second medium level ROC using at least the initial second medium level, the subsequent second medium level, and past second medium level(s). The transceiver may calculate a corrected first medium level using at least the initial second medium level and the updated second medium level ROC.

Abstract: The present invention relates generally to systems and methods for measuring an analyte in a host. More particularly, the present invention relates to systems and methods for transcutaneous measurement of glucose in a host.

Abstract: The present invention relates generally to systems and methods for measuring an analyte in a host. More particularly, the present invention relates to systems and methods for transcutaneous measurement of glucose in a host.

Abstract: Systems and methods for processing sensor analyte data are disclosed, including initiating calibration, updating calibration, evaluating clinical acceptability of reference and sensor analyte data, and evaluating the quality of sensor calibration. The sensor can be calibrated using a calibration set of one or more matched sensor and reference analyte data pairs. Reference data resulting from benchtop testing an analyte sensor prior to its insertion can be used to provide initial calibration of the sensor data. Reference data from a short term continuous analyte sensor implanted in a user can be used to initially calibrate or update sensor data from a long term continuous analyte sensor.

Abstract: A method for noninvasive analysis of subcutaneous tissue includes irradiating a surface of the tissue with short wave infrared (SWIR) radiation in a first spectral band that is strongly absorbed by water, and with SWIR radiation in a second spectral band such that an interaction of the radiation in both spectral bands with a component of the tissue other than water is substantially identical. An intensity of the radiation in each of the spectral bands that emerges from the tissue is measured. A relative absorption by the tissue of radiation in one of spectral bands relative to absorption by the tissue of radiation in the other of the spectral bands is calculated. A state of the tissue is determined in accordance with the calculated relative absorption.

Abstract: The present disclosure relates to noninvasive methods, devices, and systems for measuring various blood constituents or analytes, such as glucose. In an embodiment, a light source comprises LEDs and super-luminescent LEDs. The light source emits light at at least wavelengths of about 1610 nm, about 1640 nm, and about 1665 nm. In an embodiment, the detector comprises a plurality of photodetectors arranged in a special geometry comprising one of a substantially linear substantially equal spaced geometry, a substantially linear substantially non-equal spaced geometry, and a substantially grid geometry.

Abstract: An oximeter measures oxygen saturation for two or more different tissue depths and shows these results on a screen. A probe of the oximeter has multiple different distances between source and detector sensors. One probe implementation has fixed sensor positions. Other implementations include sensors on a moveable platform or openings to accept sensors, which allow a user to vary a distance between sensors.

Abstract: A system includes a mobile computing device, a sleeve, a contact surface, a sensor module, and a telemetry module. The mobile computing device has a first processor within a housing. The sleeve has an internal surface configured to fit the housing. The contact surface is disposed on an external surface of the sleeve. The sensor module is coupled to the contact surface and is configured to generate an electrical signal corresponding to a measured physiological parameter associated with tissue at the contact surface. The telemetry module is coupled to the sensor module and is configured to communicate data corresponding to the electrical signal to the mobile computing device.

Abstract: A needle assembly comprising a housing, a first needle hub provided by the housing, a first hollow needle portion mounted to the first needle hub and extending from the first needle hub in a distal direction. A second needle hub is provided by the housing. A second hollow needle portion is mounted to the second needle hub and extends from the second needle hub in a proximal direction, opposite to the distal direction, wherein a hollow flashback chamber is arranged within the housing between the first needle portion and the second needle portion. The flashback chamber communicates with the inner lumen provided within the first and second hollow needle portion and is connected to the atmosphere by a passage and wherein a filter is provided within the passage, which is designed such that it is permeable for air to pour out of the flashback chamber into the atmosphere.

Abstract: A blood separation device adapted to receive a blood sample having a whole blood portion and a plasma portion is disclosed. The blood separation device includes a housing defining a first chamber, a second chamber, and a separation member disposed therebetween. The blood separation device also includes an actuator, wherein actuation of the actuator draws the blood sample into the first chamber and the separation member is adapted to allow the plasma portion to pass through the separation member to the second chamber. The blood separation device matches the plasma chamber volume, the blood chamber volume, and the applied single pressure source so that the correct trans-membrane pressure and shear rate is obtained.

Abstract: One variation of a method for addressing psychological conditions of a patient through guided meditation includes: serving a first psychological test to the patient through a virtual patient portal; transforming results of the first psychological test into a set of psychological conditions of the patient; matching a first predefined meditation path to the patient based on a severity of each psychological condition in the set of psychological conditions; serving a first guided meditation track in the first meditation path to the patient through the virtual patient portal; serving a second psychological test to the patient through the virtual patient portal; calculating new intensities of each psychological condition in the set of psychological conditions of the patient based on results of the second psychological test; and matching a second predefined meditation path to the patient based on the new intensities of each psychological condition in the set of psychological conditions.

Abstract: According to one aspect of the inventive concept there is provided a system for monitoring incontinence comprising: a urine sensitive circuit arranged to present a changed electrical characteristic when exposed to urine; a measurement circuit arranged to perform a measurement on a urine bladder of a wearer to determine at least one parameter which varies with a fill level of the urine bladder; a sensor arranged to determine an orientation and/or a movement of the sensor; and a processing circuit arranged to: determine whether the urine sensitive circuit has been exposed to urine; estimate an amount of urine released on to the urine sensitive circuit; and in response to determining that the urine sensitive circuit has been exposed to urine, record data representing said at least one parameter determined by the measurement circuit, an estimated movement and/or posture of the wearer based on an orientation and/or a movement determined by the sensor, and an estimate of the amount of urine released on to the urine

Abstract: A fluid analysis device including a fluid receipt chamber, a first capacitive element for measuring fluid flow into the fluid receipt chamber and a controller operatively coupled to the first capacitive element, wherein the controller is configured to measure a first capacitance of the first capacitive element.

Abstract: There is provided a method of indirectly estimating muscle strength ratio, comprising: receiving images and associated body part locations of a target individual, wherein the images depict the target individual performing a first and a second defined movement, identifying first image(s) depicting the first defined movement, and obtaining an associated first set of body part locations, identifying second image(s) depicting the second defined movement, and obtaining an associated second set of body part locations, computing a first image-metric according to the first set of body part locations, computing a second image-metric according to the second set of body part locations, computing an image-parameter according to the first and second image-metrics, and converting the image-parameter to an estimate of a measured-parameter indicative of strength measurement ratio of the target muscle(s) obtained by a dynamometer, according to correlation between image-parameters and measured-parameters obtained based on the

Abstract: The present system is directed in various embodiments to devices, systems and methods for detection, evaluation and/or monitoring olfactory dysfunction by measuring and determining the patient's olfactory detection threshold for the left and the right nostril. In some cases, the present invention relates to devices, systems and methods for detecting an asymmetric differential in a patient's relative olfactory detection and/or identification threshold (left vs right nostril) which, when present, may be used as a device to detect, diagnose and/or monitor olfactory deterioration resulting from Alzheimer's disease, and/or the efficacy of treatment regimens therefor over time. Alternatively, general olfactory dysfunction may be evaluated and/or monitored without regard to the individual nostril's performance.

Abstract: The present invention relates to a system (10) for supporting an elderly, frail and/or diseased person (12), in particular a person suffering from Parkinson's disease, wherein the system (10) comprises: a detection unit (14) including (i) a brain activity sensor (20) for detecting a brain activity signal relating to the brain activity of the person (12) and (ii) a motion detection unit (22) for detecting a motion signal relating to a motion of one or more body parts of the person (12); an analysis unit (16) for determining, based on the detected brain activity signal and motion signal, an activity level of the person (12) which is indicative of the motoric and cognitive activity of the person (12); and a feedback unit (18) for providing a feedback to the person (12) if the activity level of the person (12) exceeds a predetermined threshold.

Abstract: A system for monitoring a joint of a patient includes multiple sensors to be disposed near a joint and to measure or observe actions or physical quantities associated with the joint; and at least one communications module coupled to the sensors to receive data from the sensors and to transmit sensor information to an external device. In some embodiments, the sensors are implantable near the joint. In other embodiments, the sensors are disposed in a sensor module that is positioned adjacent the skin of the patient near the joint.

Abstract: A closed loop, neural activity triggered rehabilitation device and method are provided for facilitating recovery of a patient from the effects of a sensory motor disability. The device includes a sensor system positionable adjacent the brain of the patient. The sensor system detects neural signals. A functional stimulation component is operatively connectable to at least one body part, such as a muscle or a nerve. The functional stimulation component stimulates the at least one body part in response to the neural signals detected. A sensory stimulation module is operatively connected to the patient to provide sensory feedback thereto.

Abstract: Methods, systems, and devices for signal analysis in an implanted cardiac monitoring and treatment device such as an implantable cardioverter defibrillator. In some examples, captured data including detected events is analyzed to identify likely overdetection of cardiac events. In some illustrative examples, when overdetection is identified, data may be modified to correct for overdetection, to reduce the impact of overdetection, or to ignore overdetected data. Several examples emphasize the use of morphology analysis using correlation to static templates and/or inter-event correlation analysis.

Abstract: A method and an apparatus for pulse signal analyzing are provided. The method includes: receiving a pulse signal; decomposing the pulse signal into a plurality of characteristics signal; generating a spectrum for each of the plurality of characteristics signal by using a spectrum projection; obtaining a plurality of quantized data for each of the plurality of characteristics signal by quantizing the spectrum corresponding to each of the plurality of characteristics signal; and determining a physiological condition corresponding to the pulse signal according to the plurality of quantized data of the plurality of characteristics signal.

Abstract: A wearable sensing device having a first and second opening, a first semipermeable membrane having a first surface and a second surface, and a second semipermeable membrane having a third and fourth surface, a ketone body sensor, and a void. The first opening is juxtaposed to the first surface and the second opening is juxtaposed to the third surface. The space between the first and second openings is the void and wherein the ketone body sensor is positioned within the void. Gasses may permeate through the first opening and into the void to contact the sensor and exit the void through the second opening. The sensor may be in direct skin contact with vapor dissipation being enabled through ventilation. Ventilation will be facilitated by microgrooves on the sensor surface or through vent openings in the encasement.

Abstract: A method, apparatus, and computer program for estimating user's physiological state from gait measurements carried out during a physical exercise are disclosed. The physiological state is computed from at least one of step interval variability and stride interval variability acquired from the gait measurements.

Abstract: A wrist-worn device heart-monitoring device is presented. The wrist-worn heart-monitoring device includes a radial tonometer configured to output a pressure signal indicating a pulse pressure wave at a user's wrist, two or more electrodes configured to output an electrical signal indicating a user's heart has been commanded to contract, and a microphone configured to output an audio signal indicating a closing of a user's aortic valve. The wrist-worn heart-monitoring device further includes a pulse transit time monitor configured to calculate a pre-ejection period of the user's heart based on at least the pressure, electrical, and audio signals, and calculate a pulse transit time based on at least the pre-ejection period, the pressure signal, and the electrical signal.

Abstract: Wearable heat flux devices are disclosed that can detect heat flux based on evaporative cooling for determining a core body temperature of a user, and that can heat or cool a surface of a user for reaching a steady-state heat flux to determine the core body temperature of the user. Exemplary heat flux devices can include a heat flux sensor and a wicking layer. The heat flux sensor can be configured to detect heat flux at a location on a user. The wicking layer can be configured to absorb moisture at the location and to transport the moisture above the heat flux sensor. The heat flux subsequently detected by the heat flux sensor includes the evaporative cooling from the evaporation of the moisture.

Abstract: Intravascular devices, systems, and methods are disclosed. In some embodiments, side-loading electrical connectors for use with intravascular devices are provided. The side-loading electrical connector has at least one electrical contact configured to interface with an electrical connector of the intravascular device. A first connection piece of the side-loading electrical connector is movable relative to a second connection piece between an open position and a closed position, wherein in the open position an elongated opening is formed between the first and second connection pieces to facilitate insertion of the electrical connector between the first and second connection pieces in a direction transverse to a longitudinal axis of the intravascular device and wherein in the closed position the at least one electrical contact is electrically coupled to the at least one electrical connector received between the first and second connection pieces.

Abstract: An electroencephalography (EEG) sensor is installed on a seat and configured to monitor brain activity of a user to generate a EEG signal. An electrocardiogram (ECG) sensor is installed on the seat and configured to monitor heart activity of the user to generate a ECG signal. A processor of the seat is in communication with the EEG sensor and the ECG sensor, and is configured to process the EEG signal and the ECG signal to determine a stress level of the user.

Abstract: Aspects relate to providing radio frequency components responsive to magnetic resonance signals. According to some aspects, a radio frequency component comprises at least one coil having a conductor arranged in a plurality of turns oriented about a region of interest to respond to corresponding magnetic resonant signal components. According to some aspects, the radio frequency component comprises a plurality of coils oriented to respond to corresponding magnetic resonant signal components. According to some aspects, an optimization is used to determine a configuration for at least one radio frequency coil.

Abstract: A monitoring device configured for insertion into a conduit of a subject includes a housing, at least one physiological sensor coupled to the housing, a transmitter coupled to the housing, an expandable element, inflatable element, stretched membrane or balloon coupled to the housing and configured to occlude at least a portion of the conduit, a power source attached to the housing, and a processor coupled to the housing and operatively coupled to memory containing computer instruction causing the monitoring device to obtain physiological information via the at least one physiological sensor where the physiological information includes one or more of pulse rate information, body temperature information, breathing rate information, blood pressure information, cardiac output information, or blood gas level information, and processing and analyzing the physiological information to provide a result.

Abstract: Example embodiments relate to systems and methods for heart rate detection with motion artifact reduction. One embodiment includes an electronic system for heart rate detection. The electronic system includes a random sampling sensor module. The random sampling sensor module includes a first sensor circuit configured to provide nonuniform random samples below a Nyquist rate of a photoplethysmographic signal. The random sample sensor module also includes a second sensor circuit configured to provided nonuniform random samples below a Nyquist rate of a motion signal. The motion signal and the photoplethysmographic signals are sampled with an equivalent pattern. The electronic system also includes a heart rate detection module. The heart rate detection module is configured to calculate a heart rave value based on frequencies corresponding to peak powers of calculated power spectral density value sets corresponding to the photoplethysmographic signals in a frequency range of interest.

Abstract: A system that detects heartbeats includes a sensor or a transducer and algorithms based on deep learning. The algorithms employ techniques of artificial intelligence that enable the system to extract heartbeat features under low signal-to-noise-ratio (SNR) conditions when a user is exercising. The algorithms can be applied to various technologies for heart rate monitoring such as ultrasound Doppler, photoplethysmogram (PPG), electrocardiogram (EKG), acoustic, pressure/force sensing and laser/RF Doppler, among other types of sensing methods.

Abstract: Body-mountable devices are provided to detect the presence or status of a tumor in a body by detecting probes associated with circulating cells of the tumor that travel to subsurface vasculature of the body. The probe enters a tumor and associates with cells of the tumor before the cells metastasize. A wearable body-mountable device can be worn for a protracted period of time to detect the probe associated with circulating tumor cells in the vasculature at low concentrations and/or at low rates. A body-mounted device could detect the presence of such released, tumor-cell-associated probes to determine a presence or status of a tumor in the body.

Abstract: Analyte sensor faults are detected. Datasets of glucose values sensor electronics are coupled to a glucose sensor in fluid contact with interstitial fluid under a skin surface. Baseline median glucose value and glucose variability values are computed, based on the first dataset. A baseline data point is stored. Evaluation median glucose value and variability are computed, based on the second dataset of glucose values. An evaluation data point is stored. A magnitude of a vector that extends between the baseline data point and the evaluation data point is computed. A component of the magnitude of the vector that is parallel to a hypoglycemia risk contour line is computed and compared to a predefined threshold value. An indication that a sensor fault has been detected if the component is greater than a threshold is displayed.

Abstract: Apparatus and methods for providing dynamic displays. In one embodiment, a method is provided wherein health parameters having goals associated therewith are displayed; data relating to the health parameters is received and the display is incremented according to a progress of the user toward the goal. When collection of the data is completed, it is determined whether a current value of a first one of the health parameters within a predetermined range of the goal associated therewith. When the current value of the first one of the health parameters is within the range, a portion of the display relating thereto is upgraded. When the current value of all of the health parameters is within the range, the entire display is upgraded. The display upgrades may comprise display of an animation and/or using color, light, and/or flashing to simulate a shining or shimmering of the display.

Abstract: A method and apparatus for automated reconstruction of a 3D computed tomography (CT) volume from a small number of X-ray images is disclosed. A sparse 3D volume is generated from a small number of x-ray images using a tomographic reconstruction algorithm. A final reconstructed 3D CT volume is generated from the sparse 3D volume using a trained deep neural network. A 3D segmentation mask can also be generated from the sparse 3D volume using the trained deep neural network.

Abstract: A radiation system (50), comprising a patient support platform (3). An X-ray radiation source (2a, 2b, 2c) is positioned beneath the patient support platform and enclosed by fixed radiation shielding. An X-ray radiation detector (22) is positioned above the patient support platform. A detector X-ray radiation shield (1, 11) comprising shield extension (7) is arranged on either side of the patient support platform, which extend from the X-ray radiation 5 detector to the fixed radiation shielding. The shield extensions are able to be moved relative to the source radiation shield to allow access to a patient on the support platform.

Abstract: A filter set of a CT scanning device and control method thereof are provided. An example of the CT scanning device includes a gantry, an X-ray generator, a filter set, a detector, and a drive motor. The filter set includes a disc, a filter disposed on the disc and having a substantially annular groove structure, and a drive shaft connected to the disc. A body thickness of the annular groove structure varies in a circumferential direction and a radial direction. A shaft axis of the drive shaft is parallel to a radiation direction of X-ray. As the drive shaft is driven by the drive motor, the disc rotates around the shaft axis, such that a region of the filter is aligned with the radiation direction of the X-ray, and a body thickness of the region corresponds to a respective X-ray attenuation for an examination region of a subject.

Abstract: A mobile X-ray apparatus includes: an X-ray radiation device; a controller configured to control the X-ray radiation device; a power supply configured to supply operating power to the X-ray radiation device and the controller via a lithium ion battery and control overcurrent occurring during X-ray emission by the X-ray radiation device; and a charger configured to charge the power supply. Each of the controller, the power supply, and the charger is embodied in a physically separate module, and each of the power supply and the charger is encased in a metal case.

Abstract: A medical imaging device is disclosed herein. The medical imaging device includes a user interface device for displaying information relevant to an imaging process to a user and/or receiving user input relevant to an imaging process and at least one component controllable according to a user command entered using the user interface device, wherein the user interface device includes at least one pair of mixed reality smart glasses.

Abstract: The disclosure provides a method and device for performing three-dimensional blood vessel reconstruction using angiographic images. The method includes an acquisition step that acquires a first two-dimensional image of the blood vessel in the first projection direction and a corresponding reconstructed three-dimensional model of the blood vessel.

Abstract: A non-invasive method to predict post-surgery vascular graft failure is provided. Computer Tomography Angiography (CTA) images are obtained of a patient post-surgery. A personalized three-dimensional computer model of the patient is derived from the obtained CTA images. The personalized three-dimensional computer model distinguishes a Computational Fluid Dynamics (CFD) model coupled with a closed-loop Lumped Parameter Network (LPN). Post-surgery vascular graft predictors are calculated from the personalized three-dimensional computer model indicative, i.e. predictors, of the post-surgery vascular graft failure or vascular stenosis.

Abstract: Provided are a radiography system, a radiography method, a radiography program, and a body thickness estimation apparatus that can estimate the body thickness of a subject using each of radiographic images generated by irradiation with radiations having different energy levels. A radiography system includes a radiography apparatus including two radiation detectors and a console including an estimation unit that estimates the body thickness of a subject on the basis of the ratio of pixel values in a region, which corresponds to a soft tissue of the subject and is a corresponding region of radiographic images generated by the two radiation detectors irradiated with radiations having different energy levels, and correspondence relationship information in which the ratio and the body thickness are associated with each other.

Abstract: A radiography system includes a radiography apparatus including two radiation detectors and a console that corrects a ratio of pixel values in a region, which corresponds to a soft tissue of a subject and is a corresponding region of radiographic images generated by the two radiation detectors irradiated with radiations having different energy levels, on the basis of correction data corresponding to a body thickness, and derives the bone density of the subject on the basis of a difference between a ratio of pixel values in a region corresponding to a bone tissue of the subject and the corrected ratio of the pixel values.

Abstract: A method of processing images for interventional imaging, wherein a region of interest is visualized, is provided. The method comprises acquiring a series of 2D images of the region of interest in a patient during at least one respiratory phase, acquiring an electrocardiographic signal which is synchronized with the acquisition of the series of 2D images, processing the electrocardiographic signal to estimate at least one deformation phase of the region of interest induced by the patient's respiratory movement, and registering the different successive 2D images in relation to the estimated deformation phase.

Abstract: A radiography support device that supports imaging of an object with a radiation detection panel in which a plurality of pixels are two-dimensionally arranged and which detects radiation emitted from a radiation source, includes: a first reading control unit that reads first pixel signals from at least some of the plurality of pixels in a state in which the radiation is not emitted from the radiation source and a state in which the object is placed on the radiation detection panel; a first arithmetic unit that calculates a position of the object with respect to the radiation detection panel based on the first pixel signals; and a notification processing unit that performs a notification process in a case in which the position of the object is out of a predetermined range.

Abstract: Disclosed is an X-ray CT radiographing apparatus capable of selecting various FOVs, simplifying radiographing motion, and reducing X-ray exposure dose, and a method thereof. An X-ray CT radiographing apparatus according to the present invention includes a rotation supporter rotating by a rotation driver, a generating unit including an X-ray generator emitting X-rays and a collimator so as to radiate a collimated X-ray beam, a sensing unit including a small width X-ray sensor moving in a tangential direction of a rotation trajectory, and a controller controlling operations of the rotation driver, the generating unit, and the sensing unit when performing X-ray radiographing, and configuring movement trajectories of an X-ray beam for radiographing FOVs different from each other to be the same, and controlling the generating unit to turn OFF the X-ray beam in sections different from each other of the movement trajectory of the X-ray beam according to the FOV.

Abstract: A radiography apparatus includes a radiation emitting device that irradiates a subject with radiation, a camera that captures an image of the subject to acquire a captured image of the subject, and a radiation detector that detects the radiation transmitted through the subject and generates a radiographic image of the subject. The driving state of at least one of the radiation emitting device or the radiation detector is controlled on the basis of whether the radiation detector is included in the captured image.

Abstract: Techniques for imaging protocol translation are described herein. The techniques may include data indicating a protocol for image capture of a first imaging device. The protocol includes parameters. The techniques may include translating the protocol of the first imaging device for use at a second imaging device by determining adjustments to be made to one or more of the parameters.

Abstract: A medical image diagnosis apparatus according to an embodiment includes an input circuitry, a scan control circuitry, and a reconstruction control circuitry. The input circuitry receives a specifying operation for specifying, from a region of a first medical image acquired such that the first medical image contains less noise, a region for which a second medical image that is a higher-definition image than the first medical image is acquired. The scan control circuitry adjusts an irradiation region of X-rays in a slice direction and a channel direction such that a part corresponding to the region on which the specifying operation is received by the input circuitry is irradiated with the X-rays. The reconstruction control circuitry performs reconstruction, on the first medical image as an initial image, by the successive approximation method by using projection data collected after the irradiation region of the X-rays is adjusted by the scan control circuitry.

Abstract: A method for conveying one or more predictive indicators of an imaging control parameter is provided. The method includes: obtaining an initial image acquisition via an imaging system based at least in part on an initial configuration of the imaging system; collecting data regarding the imaging control parameter during the initial image acquisition; and generating the one or more predictive indicators based at least in part on the collected data. Each of the one or more predictive indicators corresponds to a calculated value of the imaging control parameter associated with a potential configuration of the imaging system different from the initial configuration.

Abstract: A method of communicating between imaging components of an X-ray imaging system may include determining, by an initiator imaging component, whether a target imaging component is a primary manufacturer imaging component (PMIC). Responsive to the target imaging component not being the PMIC, the method may include generating a communication message including a communication packet according to a packet protocol. Responsive to the target imaging component not being the PMIC, the method may also include sending the communication message to the target imaging component as a secondary manufacturer imaging component. Responsive to the target imaging component being the PMIC, the method may include generating a message including a header packet and one or more data packets according to a message protocol. Responsive to the target imaging component being the PMIC, the method may also include sending the message to the target imaging component as the primary manufacturer imaging component.