Abstract: A method, including receiving a unipolar ECG signal from the location in the heart from a selected one electrode of a pair of electrodes, computing a local unipolar minimum derivative of the unipolar signal at a plurality of times of occurrences of the local unipolar minimum derivative, identifying candidate time of occurrences of the plurality of times of occurrences of the local unipolar minimum derivative as candidate annotations of the time of activation of the myocardium, extracting features for each of the candidate annotations, assigning a confidence level based on a feature value for each of the candidate annotations, eliminating candidate annotations that have a confidence level below a threshold and generating a local activation time map using the remaining candidate annotations.

Abstract: One variation of a method for modeling neurological development includes: aggregating electroencephalography (EEG) data that comprise multiple EEG signals of each user in a set of users, EEG signals of each user recorded on multiple distinct dates, the set of users comprising a plurality of users of various known neurological statuses; identifying a synchronization pattern trend within the EEG data of the set of users; and correlating the synchronization pattern trend with neurological development within the set of users.

Abstract: A medical testing apparatus and method of use for penetrating a patient's tissue with an agent, the apparatus comprises an arcuate rail having spaced first and second sides supported by upper and lower arcuate surfaces and an arcuate handle having first and second ends extending from the upper surface of the arcuate rail. A plurality of tips extend substantially from and normally outward as the lower arcuate surface. The plurality of tips comprises alternating blunt tips and reed tips.

Abstract: A detection device for fusion of tactile sensing and optical tomography includes a handheld probe, a controller for performing signal control and data acquisition on the handheld probe and communicating with a computer, and the computer for performing data analysis and image reconstruction and display on controller information. The handheld probe includes a probe front cover. A tactile sensor, a probe base, and a photoelectric sensor module disposed in sequence are sandwiched between a first probe side cover and a second probe side cover matching the probe front cover. An optical fiber connected to the photoelectric sensor module is interposed between the first probe side cover and the second probe side cover. A detection method based on the detection device comprises detecting tumors inside biological tissue, and detecting physical changes (i.e. local hardness) of the tissue and functional changes (i.e. blood supply distribution) of the tissue.

Abstract: The present invention is related to a vaginal drug delivery device and to a vaginal diagnostic device that comprises a first and second rigid member, wherein the first and/or second rigid member comprises a reservoir holding a medicament to be delivered, an opening, and a pump for pumping said medicament out of said opening, and/or wherein the first rigid member and/or second rigid member comprises a diagnostic device for performing an intravaginal diagnosis or measurement therefor. The device further comprises a first flexible member and flexible part, wherein at least one of the first flexible member and the flexible part is at least partially elastic having an elasticity such that the device can be squeezed from an extended shape to a collapsed shape. The device is pre-biased to assume the extended shape when little to no external force is being applied thereto.

Abstract: Disclosed herein is a joint evaluation device and corresponding systems and methods for evaluating ligaments and other soft tissue connections between, for example, a tibia and a femur at a knee joint. The joint evaluation device being arranged and configured to induce and measure forces while positions of the tibia and femur are monitored. Some embodiments use a computer assisted surgery device to track positions of the tibia and the femur, and may include a computing device configured to evaluate the forces measured between a first engagement portion and a second engagement portion of the joint evaluation device to output information related to the status of the ligament and other soft tissue connections prior to any bone resections being made to the tibia or the femur.

Abstract: Disclosed are systems, devices and methods for estimating blood glucose parameters, including blood glucose concentration glucose sensor signals.

Abstract: An example method is provided to include receiving a media bitstream comprising one or more media units and a first enhancement information message, wherein the first enhancement information message comprises at least two independently parsable structures, a first independently parsable structure comprising information about at least one purpose of one or more neural networks (NNs) to be applied to the one or more media units, and a second independently parsable structure comprising or identifying one or more neural networks; decoding the one or more media units; and using the one or more neural networks to enhance or filter one or more frames of the decoded the one or more media units, based on the at least one purpose. An example method includes. Corresponding apparatuses and computer program products are also provided.

Abstract: One aspect of the present disclosure relates a method of diagnosis and/or treatment of a solid tumor. The method includes directly measuring neural activity within a solid tumor for a time and determining a state of the solid tumor based on the neural activity. The diagnosis and/or treatment can be determined based on the state of the solid tumor. In some instances, the neural activity can be used in a closed loop to detect the neural activity, determine the state, determine the risk, apply treatment, check again for neural activity, and cease treatment when the neural activity is gone.

Abstract: An ostomy appliance system includes an ostomy appliance having a stoma opening and a first electrical interface, and at least one thermal sensor configured to detect at least one thermal property, such as temperature, at the ostomy appliance, the at least one temperature sensor connected to the first electrical interface with electrical circuitry. A wearable device may be removably connected to the ostomy appliance and operably connected to the at least one thermal sensor. The wearable device includes a housing, a second electrical interface configured for electrical connection to the first electrical interface, a power supply and a controller operably connected to the power supply. The controller is configured to determine a condition of the ostomy appliance based on the at least one thermal property detected at the at least one thermal sensor. The wearable device may also include a wireless transceiver configured to communicate with a personal communication device.

Abstract: Systems and methods for assessing compliance with position therapy. In an embodiment, position therapy is provided to a user while the user is wearing a position therapy device. The position therapy comprises, by the device, collecting positional data, determining positions of the user over a time period based on the positional data, and, when it is determined that the user is in a target position, providing feedback to the user to influence the user to change to a non-target position. In addition, the device stores a duration of use in its memory. The duration of use indicates a duration that the user has used the wearable position therapy device in each of one or more positions. An assessment of the user's compliance with the position therapy is then provided based, at least in part, on the duration of use.

Abstract: Methods and systems for generating physiological metrics for display on a computing device are disclosed herein. In some implementations, an exemplary system comprises a torso wearable device including a wireless transmitter and a sensor, and non-transitory computer-readable media (CRM). The CRM, when executed by a computing device in communication with the wireless transmitter, can perform operations comprising: receiving the input signals representing respiration of the user; displaying a graphical user interface to the user; receiving one or more user inputs associated with a desired metric; displaying on the graphical user interface a first visualization corresponding to the desired metric; and displaying on the graphical user interface a second visualization corresponding to a physiological metric based on the input signals generated from the sensor. The second visualization can change in real time based on real time angular displacement of the sensor in response to the respiration of the user.

Abstract: The wearable article 200 comprises a sensing component. The electronics module 100 is removably coupled to the wearable article 200. The electronics module comprises a housing and a processor disposed within the housing 101. An interface element 121, 123 interfaces with the sensing component so as to receive signals from the sensing component and provide the same to the processor. A sensor 105 is disposed within the housing 101. The sensor 105 monitors a property of the environment external to the electronics module 100 through the housing 101. The housing 101 is constructed such that the sensor 105 has line of sight through the housing 101.

Abstract: A sensor apparatus includes at least one substrate layer of an elastically deformable material, the substrate layer extending longitudinally between spaced apart ends thereof. A conductive layer is attached to and extends longitudinally between the spaced apart ends of the at least one substrate layer. The conductive layer includes an electrically conductive material adapted to form a strain gauge having an electrical resistance that varies based on deformation of the conductive layer in at least one direction.

Abstract: A subcutaneously implantable device includes a housing, a clip attached to the housing, and an electrode. The clip is configured to move between an open position and a closed position to increase or decrease an opening between the housing and the clip to anchor the device to a muscle, a bone, and/or a first tissue. The electrode is configured to contact an organ, a nerve, the first tissue, and/or a second tissue. Circuitry in the housing is in electrical communication with the electrode and is configured to provide monitoring, therapeutic, and/or diagnostic capabilities with respect to the organ, the nerve, the first tissue, and/or the second tissue.

Abstract: Apparatus, system and method for medical analysis of a seated individual, includes determining the aortic valve opening; the PTT; and calculating the PWV. Determining the aortic valve opening includes collecting BCG data while sitting on a seat and determining the timing of the aortic valve opening, taking into account posture. Measuring the aortic pulse wave transit time includes collecting BCG data while sitting on a seat capable of measuring changes in apparent weight; determining the timing of the aortic valve opening; detecting the arrival of the pulse wave at the end point; and measuring the relative timings of the two events. Calculating the PWV includes determining a length of the arterial segment through which a pulse wave is to be measured between a start point and an end point; and dividing the determined length of the arterial segment by the PTT.

Abstract: Methods and systems of catheterization include a flexible catheter adapted for insertion into a heart of a living subject. The catheter has a lumen for passing an electrically conductive fluid therethrough, which is propelled by a peristaltic pump. A fluid reservoir connected to the lumen supplies the fluid to the catheter. Electrocardiogram circuitry is connectable to the subject for monitoring electrical activity in the heart. An electrically conductive cable diverts induced charges in the fluid from the catheter electrodes, for example by shorting to a rotating element in the peristaltic pump.

Abstract: A system to generate images based on imaging data of a portion of a body and physiological event data associated with a physiological process of the body.

Abstract: A cabinet and multiple drawers are originally provided in a collapsed configuration with multiple separate walls, layers and plates connected together, such as through bendable creases. Folding along the creases causes a cabinet sheet to be reconfigured into a deployed cabinet with multiple recesses for receiving drawers therein. A topper can be placed on top of the cabinet. Wheel assemblies can be attached to a bottom of the cabinet. A drawer sheet including multiple separate layers and walls separated by creases can similarly be folded to be erected into a deployed drawer which fits into one of the recesses in the cabinet. A wheeled base can optionally be provided as a multi-wheel assembly upon which the bottom of the cabinet can rest. The cabinet and/or drawers can be partially pre-assembled and optionally spring-loaded to pop-up from a collapsed planar configuration to a deployed configuration.

Abstract: A holding apparatus for holding a sterilizable medical product and for storing the medical product before and/or after the cleaning process, and a product monitoring system featuring such a holding apparatus. The holding apparatus includes a data processing device connectable to at least one sensor in a signal-conducting manner. The sensor is a temperature sensor for determining a temperature during the cleaning process and/or a pressure sensor for determining a static and/or dynamic pressure of a cleaning fluid during the cleaning process. The data processing device processes the sensor signals to form cleaning information and is connectable to a memory apparatus in a data-conducting manner, on which memory apparatus the cleaning information is storable. The cleaning information is retrievable or readable from the memory apparatus by an evaluation device such that a cleaning profile of the medical product can be determined based on the cleaning information.

Abstract: A storage system, including: a lid; a bottom side of the storage system opposite the lid; a first plurality of medical implants stored in a rack, wherein first plurality of medical implants are oriented in a first direction from the lid to the bottom side; a first drawer located between a portion of the first plurality of medical implants and the bottom side of the storage system; a second plurality of medical implants stored in the first drawer, wherein the second plurality of medical implants are oriented in a second direction that is substantially perpendicular to the first direction; and a drawer locking mechanism configured to engage the first drawer when the lid is closed to prevent the first drawer from sliding out of the storage system and to disengage the first drawer when the lid is open to allow the first drawer to slide out of the storage system.

Abstract: The management system mounts rear upright instrument supports on the base of a tray. Each rear support holds the rear end of surgical instruments such as forceps or scissors with the finger holes spaced apart. The forward end of the instruments are held by a forward support. That support has a bar over the instruments, which is positioned to be horizontal when the forward support (and the rear support) is full.

Abstract: An information acquisition unit acquires at least one information item of subject information, imaging condition information, or positioning information. Next, a body movement feature derivation unit derives body movement feature information indicating a feature of body movement of a breast which occurs at the time of the tomosynthesis imaging. A storage stores correspondence information in which the derived body movement feature information corresponds to at least one information item of the subject information, the imaging condition information, or the positioning information.

Abstract: A radiation monitoring system includes a patient support apparatus. A radiation sensor assembly is operably coupled to the patient support apparatus. The radiation sensor assembly includes a radiation sensor and a first controller. The radiation sensor senses radiation data corresponding to a radiation dose received by a patient. A management system includes a second controller that stores a patient profile database. The second controller is communicatively coupled with the first controller. The first controller communicates the radiation data to the second controller for storage in the patient profile database to monitor the radiation dose received by the patient.

Abstract: A breast imaging apparatus includes a radiation source that irradiates a breast of a subject with radiation, a radiation detector that detects the radiation transmitted through the breast to output a radiographic image, an ultraviolet light source that performs irradiation of ultraviolet light, and a controller that controls an operation of the ultraviolet light source. The controller prohibits the irradiation of the ultraviolet light by the ultraviolet light source in a case where a predetermined set condition is satisfied. The controller determines that the set condition is satisfied, for example, in a case where a person is shown in a captured image of a camera.

Abstract: The present disclosure relates to a system and method with which an imaged range in the past can be reproduced with high precision. In accordance with certain embodiments, an X-ray CT apparatus includes a camera-image producing section for producing a first camera image of a patient, a landmark fixing section for fixing a landmark with reference to a chest of the patient, and an imaged-range defining section for defining a first imaged range in a first scan based on landmark data representing the landmark. The camera-image producing section acquires a second camera image of the patient in a follow-up examination, the landmark fixing section fixes a second landmark with reference to the chest of the patient contained in the second image, and the imaged-range defining section defines second imaged range in a second scan based on landmark data representing the landmarks, and imaged-range data representing the first imaged range.

Abstract: Systems and method for performing X-ray computed tomography (CT) that can improve spectral separation and decrease motion artifacts without increasing radiation dose are provided. The systems and method can be used with either a kVp-switching source or a single-kVp source. When used with a kVp-switching source, an absorption grating and a filter grating can be disposed between the X-ray source and the sample to be imaged. Relative motion of the filter and absorption gratings can by synchronized to the kVp switching frequency of the X-ray source. When used with a single-kVp source, a combination of absorption and filter gratings can be used and can be driven in an oscillation movement that is optimized for a single-kVp X-ray source. With a single-kVp source, the absorption grating can also be omitted and the filter grating can remain stationary.

Abstract: The X-ray imaging system according to the present embodiment includes an X-ray tube, a holding assembly, a flying object, an X-ray detector, and processing circuitry, The X-ray tube is configured to emit X-rays. The holding assembly is configured to hold the X-ray tube. The flying object is equipped with the holding assembly. The X-ray detector is configured to detect the X-rays emitted by the X-ray tube. The processing circuitry is configured to control a flight of the flying object, and to control the flight of the flying object such that the X-ray tube is arranged on a predetermined position with respect to the X-ray detector.

Abstract: Provided is a portable X-ray device powered by a power factor correction (PFC)-based inverter, which includes a body in which a plurality of wheels are mounted on a lower surface, an input/output device which extends from an installation ground to a predetermined height and outputs data acquired from an X-ray photographing part is mounted on one side, and a handle with a structure gripped by a hand of a user is mounted on one side; a variable support which is mounted on an upper portion of the body by a hinge structure; an X-ray photographing part which is mounted on one end portion of the variable support; and a power supply mounted inside the body and provided with a PFC-based inverter configured to remove noise from applied commercial AC power, and provide the high DC voltage to the X-ray photographing part.

Abstract: An imaging control device includes a hardware processor. The hardware processor generates second dynamic image data from first dynamic image data that is image data of a dynamic image having multiple frame images received from a radiographic image capturing device, the second dynamic image data being image data of a dynamic image having only a part of the multiple frame images; and transmits, to an external device, the second dynamic image data and information indicating a first radiation dose that is information corresponding to a radiation dose in imaging for obtaining the first dynamic image data.

Abstract: In a method for diagnosing and treating a patient having lesions in both arteries of left and right lower limbs. By determining that a lesion distal to an aortailiac bifurcation is to be treated first, catheters and an operation time can be reduced. The lesion to be treated first can be on a priority basis based on diagnostic data, deciding that a lesion proximal to the bifurcation is to be treated next, and then treating the lesions substantially continuously.

Abstract: The present disclosure relates to an artificial intelligence-based oral CT automatic color conversion device and a method for driving same. The artificial intelligence-based oral CT automatic color conversion device according to an embodiment of the present invention comprises: a storage unit which stores a color conversion image related to the bone density of an alveolar bone, which is previously prepared by a user; and a control unit which, when an oral CT input image of a patient is received, converts color of the received oral CT input image on the basis of a predetermined parameter value, and adjusts the predetermined parameter value by using an error value resulting from the converted oral CT input image and the (pre)stored color conversion image to automatically convert the color of an oral CT input image to be input later.

Abstract: An image processing apparatus generates a material characteristic image based on a plurality of radiation images corresponding to a plurality of radiation energies, and estimates at least one of the plurality of radiation energies at a second timing using a plurality of material characteristic images including a material characteristic image generated based on a plurality of radiation images acquired at a first timing and a material characteristic image generated based on a plurality of radiation images acquired at the second timing later than the first timing.

Abstract: A near field communication system according to an embodiment includes: a long coupler provided for a first device; a short coupler provided for a second device and configured to perform wireless communication based on electromagnetic field coupling, with the long coupler; and signal processing circuitry configured to vary gain for each of various frequencies of a signal transmitted and received between the long coupler and the short coupler, in accordance with the position of the short coupler with respect to the long coupler.

Abstract: A tubing assembly for electronic catheter guidance systems is provided and can include a catheter, an internal acoustic transducer and an external acoustic transducer. The catheter extends in a longitudinal direction and has proximal and distal ends that define a lumen therebetween. Further, the catheter is configured for placement within a patient's digestive or respiratory tract. The internal acoustic transducer can be located within the catheter's lumen, and the external acoustic transducer can be located on or outside the patient's body. The transducers can transmit and/or receive acoustic signals as directed by a processor and communicate with the processor to deliver sound data to a display device. The frequency response and/or attenuation of the signals can indicate placement of the catheter in the digestive tract compared to the respiratory tract. A catheter guidance system and method for accurately placing a catheter in the digestive or respiratory tract are also provided.

Abstract: There is provided a biological sound measuring device, including: a main body including: a first sound measuring instrument, a housing that has an opening, a second sound measuring instrument, and a controller that causes a sound generator to generate a sound in a state where the opening in the housing is not closed, that determines whether or not a relationship between a measurement sensitivity of the first sound measuring instrument and a measurement sensitivity of the second sound measuring instrument satisfies a condition set in advance, and that when it is determined that the relationship does not satisfy the condition, notifies that it is unable to ensure measurement accuracy of biological sound or adjusts the measurement sensitivity of one or both of the first sound measuring instrument and the second sound measuring instrument.

Abstract: A wireless system and method for measuring and analyzing blood in a user's body is provided. The system includes a processing, power, and communication component (PPC) having a hardware unit and first housing enclosing the hardware unit; a probe having a piezoelectric crystal and second housing enclosing the piezoelectric crystal; a dock having a sensor and third housing enclosing the sensor. The second housing is spaced apart from the first housing. The third housing is adapted to removably couple to the first housing. The piezoelectric crystal can transmit an ultrasound wave into the body, receive a return ultrasonic wave, convert the return wave into an electrical signal, and transmit the signal to the sensor. The sensor is configured to receive and then transmit the electronic signal to the hardware unit, which is configured to wirelessly transmit a data set based on the electronic signal to a computer device.

Abstract: Devices, systems, and methods for evaluating a vessel and tracking progression of an intravascular procedure are disclosed. In an embodiment, a medical system is disclosed. One embodiment of the medical system comprises a medical processing unit in communication with an intravascular device configured to obtain intravascular ultrasound (IVUS) data and with an external ultrasound device configured to obtain external ultrasound data. The medical processing unit is configured to receive the IVUS data from the intravascular device, wherein the intravascular device is positioned proximate to an aneurysm, receive the external ultrasound data from the external ultrasound device, wherein the external ultrasound device is positioned to image the aneurysm, and track progression of a coil embolization of the aneurysm based on the IVUS data and the external ultrasound data.

Abstract: The ultrasound diagnostic apparatus, ultrasound image generation apparatus and method transmit ultrasound waves to a subject into which a puncture tool is inserted, receive reflected waves reflected from the subject and the puncture tool, and generate echo signals of time-sequential frames based on the received reflected waves, and generate an ultrasound image of the subject based on the generated echo signals. These apparatus and method generate a differential echo signal between time-sequential frames from the echo signals, perform a tip detection process based on the differential echo signal to thereby detect at least one tip candidate including a tip end of the puncture tool, highlight a tip candidate of the puncture tool detected to thereby generate a tip image, and display the tip image of the highlighted puncture tool so as to be superimposed on the generated ultrasound image.

Abstract: In a transcatheter treatment support technique using a combination of a guide wire equipped with a photoacoustic technique and an ultrasonic imaging device, the ultrasonic imaging device estimates a front edge position of the guide wire using a difference between arrival times of photoacoustic waves arriving at an array of elements configuring an ultrasonic probe or a change of an image of the photoacoustic generation source, which depends on a distance of the photoacoustic generation source from an imaging region, and grasps a relationship between an imaging position and the front edge position of the guide wire using the estimation result. This enables visually grasping a relationship between a region (imaging region) from which an image is able to be obtained with reflective waves from a biological body with use of the ultrasonic probe and an insertion object present outside the region, particularly, the front edge of the guide wire.

Abstract: An ultrasonic diagnosis system includes a reaction force detection sensor that detects a reaction force acting on an ultrasonic probe when the ultrasonic probe is pressed against a body surface of a subject. Then, the ultrasonic diagnosis system estimates the push-in amount of the ultrasonic probe with respect to the subject by using the reaction force detection sensor during the ultrasonic diagnosis to output a display or a warning of the estimated push-in amount of the ultrasonic probe to the output device.

Abstract: Provided is an ultrasound diagnostic apparatus including an ultrasound probe, an imaging section that images the subject on the basis of a reception signal output from the ultrasound probe to generate an ultrasound image, an image analysis section that performs image analysis using the ultrasound image, a movement detection sensor that detects and outputs a movement of the ultrasound probe as a detection signal, a movement amount calculation section that calculates a movement amount of the ultrasound probe in a case where an imaging inspection portion that is currently being imaged among a plurality of inspection portions of the subject is inspected, using the detection signal output from the movement detection sensor, and a portion discrimination section that discriminates the imaging inspection portion on the basis of an image analysis result in the image analysis section and the movement amount calculated by the movement amount calculation section.

Abstract: A system and method for automatically setting an elevational tilt angle of a mechanically wobbling ultrasound probe is provided. The method includes acquiring, by a mechanically wobbling ultrasound probe of an ultrasound system, an ultrasound volume of a region of interest. The method includes analyzing, by at least one processor of the ultrasound system, the ultrasound volume to identify an ultrasound image slice depicting an anatomical object of interest. The ultrasound image slice corresponds with an elevational tilt angle. The method includes setting, by the at least one processor, the mechanically wobbling ultrasound probe to the elevational tilt angle corresponding with the ultrasound image slice depicting the anatomical object of interest. The method includes acquiring, by the mechanically wobbling ultrasound probe, a two-dimensional (2D) ultrasound image at the elevational tilt angle. The method includes causing, by the at least one processor, a display system to present the 2D ultrasound image.

Abstract: Ultrasound imaging apparatus for imaging a region of interest in a subject comprises a plurality of separate ultrasonic probes (2a-2c) each having at least one transducer (72) for transmitting and receiving ultrasonic waves and a communications unit. A control unit (1) controls the probes to coordinate their operation in sequence, and obtains ultrasonic images from the probes for generating a display of those images together in real time simultaneously. The control unit transmits control signals to at least one of the probes, and each probe receives control signals from the control unit and/or from an adjacent one of the probes. The control signals cause the probes to execute a scan sequentially in a predetermined probe sequence which is usually repeated, and the control unit generates a display by combining the image data from the probes.

Abstract: Systems and methods are provided for employing informational models trained using the Autoprogressive Algorithm to learn the mechanical behavior and internal structure of biological materials using a sparse sampling of force and displacement measurements. Forces are applied to the biological material and the force and displacement are measured and applied to the AutoP algorithm. Additionally, a coordinate based scaling factor is applied to the measured displacement.

Abstract: In one embodiment, the disclosure relates to a probe that a cylindrical marker band defining an inner surface, an outer surface, a first end and a second end and having a band length, the inner surface defining a marker band bore, the cylindrical marker band includes a radiopaque material; a molded unitary lens defining an elongate optical fiber receiving section having a fiber section length and a beam directing surface, wherein the fiber section length and the band length overlap along an overlap distance; and an optical fiber, wherein a first section of the optical fiber is disposed in the optical fiber receiving section, wherein a portion of the first section of the optical fiber is disposed within the marker band bore.

Abstract: A sternal compass includes a first scissor clamp arm having a first scissor clamp arm handle end and a first scissor clamp arm effector end; and a second scissor clamp arm having a second scissor clamp arm handle end and second scissor clamp arm effector end. The second scissor clamp arm crosses the first scissor clamp arm at a pivot point. A centerline alignment mechanism is located between the first scissor clamp arm and the second scissor clamp arm. The centerline alignment mechanism has a hinge point aligned with the pivot point. A center line frame extends in line with the hinge point and the pivot point toward the first scissor clamp arm effector end and the second scissor clamp arm effector end. The center line frame has a marking device to mark a centerline of a sternum of a patient.

Abstract: A medical instrument tray for supporting medical instruments and connecting to a medical vacuum hose and evacuating gases and debris from a procedure area to reduce spread of airborne bacteria, viruses, or other contaminates comprises an upper surface and a laminar air flow suction device. The upper surface supports the medical instruments. The laminar air flow suction device extends below the upper surface and comprises a first opening and a second opening. The first opening is configured to connect to the medical vacuum hose and has a first opening width. The second opening has a second opening width that is wider than the first opening width.

Abstract: The present application provides a sensor-based surgery set and a method for determining the position of a holding device for a surgical instrument. The surgery set includes at least one holding device, an initialization station, and a number of sensors. The initialization station has a number of sensor slots, wherein each sensor is assigned to one sensor slot and wherein the initialization station is coupled to a storage unit in which initialization information is assigned to each sensor slot. A number of sensor slots are arranged on the holding device, wherein each sensor slot is assigned to one sensor slot of the initialization station. In an initialization arrangement, a specific number of sensors is in engagement with the sensor slots of the initialization station and are coupled to the storage unit for initialization and data transmission. In use, however, the sensors are in engagement with the sensor slots.

Abstract: The present disclosure relates to a method for generating a dental product or an orthodontic product. The method may comprise (a) providing a mixture comprising (i) a latent ruthenium (Ru) complex; (ii) an initiator; (iii) a sensitizer that sensitizes said initiator; and (iv) at least one polymer precursor; and (b) exposing the mixture to electromagnetic radiation to activate the initiator, wherein upon activation, the initiator reacts with the latent Ru complex to generate an activated Ru complex, which activated Ru complex reacts with the at least one polymer precursor to generate at least a portion of a final product of the dental product or the orthodontic product, wherein the at least the portion of the final product of the dental product or the orthodontic product comprises a polymer generated from the at least one polymer precursor.