Abstract: One or more devices, systems, methods, and storage mediums for optical imaging medical devices, such as, but not limited to, Optical Coherence Tomography (OCT), single mode OCT, and/or multi-modal OCT apparatuses and systems, and methods and storage mediums for use with same, for triggering auto-pullback, including for devices or systems using blood clearing, are provided herein. Examples of applications include imaging, evaluating and diagnosing biological objects, such as, but not limited to, for Gastro-intestinal, cardio and/or ophthalmic applications, and being obtained via one or more optical instruments, such as, but not limited to, optical probes, catheters, capsules and needles (e.g., a biopsy needle). Techniques provided herein also improve processing and imaging efficiency while achieving images that are more precise.

Abstract: An intraluminal imaging device includes a flexible elongate member sized and shaped for insertion into a vessel of a patient, the flexible elongate member including a proximal portion and a distal portion; an imaging assembly positioned at the distal portion of the flexible elongate member; and a bridge member at electrical ground and in contact with at least a portion of the imaging assembly to maintain the at least portion of the imaging assembly at electrical ground, wherein the bridge member is disposed in cylindrical configuration. Associated devices, systems, and methods are also provided.

Abstract: A computer-implemented method for displaying a 3D model of a patient in a 3D scene, each voxel of the displayed 3D model being associated to a respective pixel of at least one corresponding cross-sectional image of the patient, the 3D scene further including a cursor and at least one display window. The method includes the steps of: computing a current position of the cursor in a scene coordinate system of the 3D scene based on a current position of a user point in user coordinate system; and for each active display window of the at least one display window, displaying a displayed image based on the cross-sectional image, which includes a pixel associated to the voxel that is the closest to the computed current position of the cursor and which has a corresponding image cross-section plane that matches a window cross-section plane of the active display window.

Abstract: A distributed fiber-optic acoustic sensing system and a signal processing method. The distributed fiber-optic acoustic sensing system is based on a high spatial resolution distributed fiber-optic acoustic sensor. The interval between adjacent sensing units is centimeter or millimeter level. Through specific digital signal processing, signal enhancement can be realized, noise in the system and environment are suppressed, at the same time, problems such as interference fading is solved, and the sensor signal-to-noise ratio of subunits can be increased by two to three orders of magnitude. Each subunit can serve as an independent high-sensitivity sensor for sensing. The multiple subunits can form one or more new sensor arrays. The azimuth estimation and spatial orientation of signal sources can be realized by the array signal processing method.

Abstract: The present disclosure provides a new concept of fusion imaging device for simultaneously providing anatomical information and functional/biochemical information of human bodies, to accurately localize lesions in the pre-operative process and measure in real time, thereby ensuring the stability of patients with lower radiation doses than the existing fusion imaging devices such as positron emission tomography (PET)/computed tomography (CT) and single photon emission computed tomography (SPECT)/CT, and includes: a transducer to transmit and receive an ultrasound; a matching layer positioned on top of the transducer to reduce a difference in acoustic resistance between the transducer and an affected part, to support an ultrasound beam to be smoothly transmitted into tissues and a reflected beam to be received with high sensitivity; a backing member to absorb the ultrasound on an opposite side of the affected part with respect to the transducer; and a scintillator to detect gamma rays which are radiation, wherei

Abstract: Surgical systems are provided. In one exemplary embodiment, a surgical system includes first and second port devices, that are each configured to be at least partially disposed within a body. The first port device includes a first housing defining a first plurality of ports each configured to allow a respective instrument of a first set of instruments to be inserted therethrough. The first port device is configured to interact with at least one respective instrument that is inserted through its respective port. The second port device is configured to interact with at least one respective instrument that is inserted through its respective port. The first and second port devices are each configured to allow at least a portion of the first set of instruments and at least a portion of the second set of instruments to work cooperatively together. Methods for using the same are also provided.

Abstract: Flexible catheters adapted to be inserted into a body to deliver high-voltage, fast (e.g., microsecond, sub-microsecond, nanosecond, picosecond, etc.) electrical energy to target tissue may include a plurality of conductive layers, that may be coaxial. These catheters and method of using them to treat tissue are configured to reduce or avoid arcing.

Abstract: An invasive medical device assembly includes an invasive medical device and a hub housing configured to surround a portion of the invasive medical device. The invasive medical device may be a needle or other invasive medical device, and the hub housing may be configured to surround a hub of the invasive medical device. In one aspect, the invasive medical device may include a transducer. The hub housing can include at least one integrated circuit embedded therein that is configured to contact the external surface of the needle to electrically connect the transducer to a power source. The hub housing can be configured to provide an ergonomic handle for a user.

Abstract: Needles are deployed in tissue under direct ultrasonic or other imaging. To aid in deploying the needle, a visual needle guide is projected on to the image prior to needle deployment. Once the needle guide is properly aligned, the needle can be deployed. After needle deployment, a safety boundary and treatment region are projected on to the screen. After confirming that the safety boundary and treatment regions are sufficient, the patient can be treated using the needle.

Abstract: For intraluminal ultrasound probes, the transducer is divided into multiple segments. The segments are connected in a way that allows them to slide relative to each other. This sliding arrangement allows for the transducer to be used in two different apertures at different times while in the patient. One aperture is shaped for insertion of the probe through a limited space, and the other aperture forms an array with a larger elevation extent, allowing greater quality imaging along the elevation dimension.

Abstract: A method of forming a stimulation lead includes forming an implantable lead body, including helically winding at least one cable about a mandrel to form a coiled cable assembly in a first, restrained state. Helically winding the at least one cable includes applying a tensile force to the at least one cable as the at least one cable is wound about the mandrel. Forming the lead body also includes releasing the tensile force from the at least one cable to allow the coiled cable assembly to release stored mechanical energy and transition from the restrained state to a second, relaxed state in which the coiled cable assembly is substantially free of stored mechanical energy. The method further includes subjecting the lead body to a reflow process by applying heat to the lead body, where the tensile force is released prior to the lead body being subjected to the reflow process.

Abstract: A method and system for ultrasonic fluid spectral Doppler imaging are disclosed. The system comprises: a transmission circuit for transmitting an ultrasonic beam to a detection object; a receiving circuit and a beam synthesis module for receiving an echo of the ultrasonic beam and obtaining an ultrasonic echo signal; an image processing module for obtaining an ultrasonic fluid flow state image of a region of interest in the detection object according to the ultrasonic echo signal, identifying a sampling position in the region of interest, respectively obtaining a Doppler spectrogram corresponding to each sampling position according to the ultrasonic echo signal, and generating position displaying marks for characterizing the sampling positions; and a display for displaying the position displaying marks in the ultrasonic fluid flow state image, and displaying the obtained Doppler spectrogram. The system may simultaneously display spectra of multiple locations on a same time axis.

Abstract: The current disclosure provides methods and systems for navigating among display panels and graphical elements of a user interface of a medical imaging system via controls of a handheld imaging device. In one embodiment, the current disclosure provides for a method comprising, in response to an operator of the medical imaging system adjusting one or more controls arranged on a control handle of a handheld ultrasound device of the medical imaging system, adjusting a focus of a user interface (UI) of the medical imaging system among a plurality of graphical control elements displayed in the UI; and in response to the operator selecting a graphical control element of the plurality of graphical control elements at a location of the focus of the UI via the one or more controls, executing an action of the medical imaging system associated with the selected graphical control element.

Abstract: A system for deploying needles in tissue includes a controller and a visual display. A treatment probe has both a needle and tines deployable from the needle which may be advanced into the tissue. The treatment probe also has adjustable stops which control the deployed positions of both the needle and the tines. The adjustable stops are coupled to the controller so that the virtual treatment and safety boundaries resulting from the treatment can be presented on the visual display prior to actual deployment of the system.

Abstract: A robotic catheter system includes a controller with a master input device. An instrument driver is in communication with the controller and has a guide instrument interface including a plurality of guide instrument drive elements responsive to control signals generated, at least in part, by the master input device. An elongate guide instrument has a base, distal end, and a working lumen, wherein the guide instrument base is operatively coupled to the guide instrument interface. The guide instrument includes a plurality of guide instrument control elements operatively coupled to respective guide drive elements and secured to the distal end of the guide instrument. The guide instrument control elements are axially moveable relative to the guide instrument such that movement of the guide instrument distal end may be controlled by the master input device.

Abstract: A reusable rotating ultrasound capsule for mounting to a distal end of a catheter. An exemplary device includes a motor compartment having a proximal face and a distal end. A sensor compartment includes a cap that seals with the motor compartment. A motor located within the motor compartment includes a drive component and a shaft rotatably coupled to the drive component and extending distally from the motor compartment into the sensor compartment. The shaft includes an ultrasound transducer. A plurality of electrical contacts are mounted on the proximal face. At least two of the electrical contacts are electrically coupled to the motor. A rotational electrical coupler includes a rotational component mechanically coupled to the shaft and electrically coupled to the ultrasound transducer and a stationary component mechanically coupled to the motor compartment and electrically coupled to one or more of the plurality of electrical contacts.

Abstract: The present disclosure provides a system and method for using widely available ultrasound imaging to overcome the limitations of imaging guidewires and other small objects that may be subwavelength in size relative to an ultrasound wavelength. The system and method can reduce the use of X-rays and exposure to the dangerous effects of radiation and avoids the expense of MRI technology. The subwavelength object, such as a guidewire, can be detected using several methods and associated systems described herein, including the object changing positions at a frequency that creates a brighter ultrasound image of the object as the object progresses across a scanned region of the ultrasound detector. In some embodiments, the movement of the small object causes a different speckle signature than the object itself would otherwise generate. Analysis of changes in speckle patterns due to progressive movement of an object can yield a detectable object.

Abstract: Methods, computer program products, and/or systems are provided that perform the following operations: setting a memory buffer having contiguous memory blocks; obtaining a decision tree comprising nodes including split nodes and leaf nodes, wherein each of the split nodes includes at least two child nodes that are ordered according to a likelihood of accessing a child node after each of the split nodes; mapping the nodes onto respective blocks of the memory blocks, each of the memory blocks storing attributes of a corresponding one of the nodes, wherein each of the split nodes and any child nodes of each split node are mapped onto successive blocks, wherein ordered child nodes of a same one of the split nodes are mapped onto successive blocks; executing the nodes by processing the attributes of the nodes as accessed from the memory according to an order of the memory blocks in the memory buffer.

Abstract: A robotic surgical system in which the system applies a scaling factor between user input from a user input device and corresponding movements of the robotic manipulator. Scaling factors may be applied or adjusted based on detected conditions such as the type of instrument being manipulated, detected distance between multiple instruments being manipulated, user biometric parameters.

Abstract: Methods and apparatus are provided for electrically addressing multiple ultrasonic transducers that are connected to a common electrical channel and housed within an imaging probe. An imaging probe may comprise an imaging ultrasonic transducer and a moveable element for controlling the direction of an emitted imaging beam, and an angle sensing ultrasonic transducer, where the angle sensing ultrasonic transducer is configured for determining the direction of an ultrasonic imaging beam. The angle-sensing transducer may be configured to direct an angle sensing ultrasonic beam towards an acoustically reflective substrate and provide a signal by detecting a reflected ultrasonic beam reflected from the acoustically reflective substrate, where the acoustically reflective substrate is positioned relative to the movable element such that motion of the movable element produces a change in the signal.

Abstract: A system and method for operating an ultrasonic treatment device includes generating an ultrasound electrical signal using an ultrasound signal generator; supplying the ultrasound electrical signal to an ultrasonic transducer to generate ultrasonic vibratory motion of an ultrasonic vibration transmission member; monitoring an electrical characteristic associated with the ultrasonic transducer; processing the monitored electrical characteristic to determine at least one of a type of material encountered by a distal end of the ultrasonic vibration transmission member and a type of vascular pathway that the ultrasonic catheter is traversing; and controlling at least one of a modulation frequency and a waveform of the ultrasound electrical signal based on the determined at least one of the type material encountered by the distal end of the ultrasonic vibration transmission member and the type of vascular pathway that the ultrasonic catheter is traversing.

Abstract: Systems and methods for utilizing a hybrid transmitter in an ultrasound system. A system can include a hybrid transmitter configured to transmit ultrasound waves toward a subject area. The hybrid transmitter can comprise a linear transmitter configured to generate linear transmitter output and a switching transmitter configured to generate switching transmitter output. The hybrid transmitter can also comprise a summer configured to sum the linear transmitter output and the switching transmitter output to generate hybrid transmitter output for driving a transducer load to generate the ultrasound waves transmitted towards the subject area. The ultrasound system can also comprise a receiver configured to receive one or more ultrasound waves from the subject area in response to the ultrasound waves transmitted toward the subject area for generating ultrasound images of the subject area.

Abstract: A catheter and catheter system includes a first lumen and a second lumen adjacent to the first lumen. The catheter occupies an arc around the first lumen, wherein the arc is greater than 180° and less than 360°, thus creating a lengthwise opening to the first lumen. The catheter material surrounds the second lumen in a cross-sectional dimension. Prior to a procedure, a sampling device is introduced into the second lumen prior and the probe is snapped into the first lumen prior to insertion into an endoscope.

Abstract: A catheter and guide wire assembly (10) for measurement of blood pressure in a living body, comprising: a proximal tube (11) having a distal end and a proximal end; a distal tube (12) having a distal end and a proximal end, which is connected to the distal end of the proximal tube (11); a fluid-permeable coil (13) having a distal end and a proximal end, which is connected to the distal end of the distal tube (12); a distal tip (14), in which the distal end of the fluid-permeable coil (13) is secured; and a core wire (16), which is attached in the proximal tube (11) and which extends through a portion of the proximal tube (11), the distal tube (12) and the fluid-permeable coil (13), and is secured in the distal tip (14), wherein the distal end of the proximal tube (11) and the proximal end of the distal tube (12) are connected by a butt joint and wherein the core wire (16) is glued or brazed to the inner wall of the proximal tube (11) at or close to the butt joint.

Abstract: A microscope may receive a fiber optic connector via a connector adapter of the microscope, wherein the connector adapter includes an opening and a shaped reflective surface surrounding the opening. The microscope may align a ferrule of the fiber optic connector with the opening of the connector adapter of the microscope, wherein the ferrule includes a ferrule chamfer or a ferrule radius. The microscope may transmit direct light onto the shaped reflective surface and may receive reflected light from the ferrule chamfer or the ferrule radius and with a camera of the microscope.

Abstract: An ultrasound diagnosis apparatus includes: a two-dimensional (2D) transducer array in which a plurality of transducers that transmit/receive an ultrasound signal to/from an object are arranged in two dimensions; an analog beamformer configured to perform analog beamforming in a first direction, and perform analog beamforming in a second direction perpendicular to the first direction on signals respectively received by the plurality of transducers; and a digital beamformer configured to perform digital beamforming on the signals that are analog-beamformed in the first direction, and perform digital beamforming on the signals that are analog-beamformed in the second direction.

Abstract: A transseptal system includes a needle, a guidewire, a handle, and a dilator. The handle defines a needle passage to slidably receive the needle, and a guidewire passage to slidably receive the guidewire. The dilator defines a lumen having a distal region and a proximal region. The dilator is coupled to the handle such that the lumen is open to the needle passage and the guidewire passage. The proximal region of the lumen is sized to simultaneously receive the needle body and the guidewire. The distal region is sized to slidably receive one of the needle and the guidewire on an individual basis. A transseptal puncture and access procedure can be performed, including puncturing tissue with the needle followed by immediate advancement of the guidewire into the accessed area, eliminating the need for multiple instrument exchanges during the procedure.

Abstract: An ultrasound system 1 includes an ultrasound probe 2 and an image display device 3. The ultrasound probe 2 includes a transducer array 11 including a plurality of transducers, a transmitting and receiving unit 14 that transmits and receives ultrasonic waves using an aperture transducer group consisting of some transducers to generate a sound ray signal, and an image information data generation unit 19 that generates image information data from the sound ray signal. The image display device 3 includes a display unit 34. One of the ultrasound probe 2 and the image display device 3 includes a display image region determination unit 22 that determines a display image region obtained by excluding a shallow image region from an ultrasound image on the basis of the width of all of the transducers, the width of the aperture transducer group, and a steering angle range of a scanning line. The display unit 34 displays the ultrasound image based on the image information data only in the display image region.

Abstract: Systems and methods are described for planning of catheter ablation procedures, and in particular for planning of the placement of lesions and/or parameters used in ablation. In some embodiments, planning is based on thermal and/or dielectric simulation of lesions, individualized to the anatomy of the particular patient. Optionally, a plan comprises planning of a path along which an ablation lesion is to be formed, the ablation lesion optionally comprising one or more sub-lesions. The plan is optionally optimized for one or more criteria including, for example: minimization of path length, minimization of sub-lesion number, simplification of catheter maneuvering, avoidance of collateral damage to non-target tissue, access to the target dependent on anatomy shape and/or catheter mechanics, and/or features of the target anatomy such as tissue wall thickness and/or fiber direction.

Abstract: An ultrasound patch may conform to a curved surface of a large, curvilinear part of a human body, and may capture ultrasound images of underlying tissue for detection of disease. The patch may comprise a flexible, elastomeric substrate, in which phased arrays of piezoelectric ultrasound transducers are embedded. The phased arrays may steer ultrasound beams through a wide angle to image a large volume of tissue. Mechanical deformation of the flexible substrate as it conforms to a curvilinear body part may change the relative 3D positions of the phase arrays. However, localization may be performed to detect these 3D positions. Data captured by the phased arrays may be processed, to create an ultrasound image of the underlying tissue. A semi-flexible, intermediate layer may partially encapsulate each phased array, to distribute stress at an interface between the rigid phased array and more flexible substrate.

Abstract: In part, the disclosure relates to intravascular data collection systems and the software-based visualization and display of intravascular data relating to detected side branches and side branch obstruction. An estimate of side branch diameter can be made based on a vessel profile or a maximum diameter of a vessel at a distal and proximal location relative to the side branch. A amount of side branch obstruction may be determined by comparing an observed side branch diameter with in the image data with the estimated side branch diameter. In addition, an amount of blood flow obstruction may also be determined.

Abstract: A robotic surgical system in which the system applies a scaling factor between user input from a user input device and corresponding movements of the robotic manipulator. Scaling factors may be applied or adjusted based on detected conditions such as the type of instrument being manipulated, detected distance between multiple instruments being manipulated, user biometric parameters.

Abstract: An apparatus having an implantable ultrasound generating treating device to induce brain disorder treatment, suitable for implantation in or under the skull bone of a patient, includes several ultrasound generating transducers, which are connectable by a common electrical connection circuit to a generator, and wherein the ultrasound generating transducers each have one or several operating frequencies. The transducers include the group of transducers having several transducers driven by a same electrical drive signal, and connected to the generator system by a common electrical connection circuit, where the electric drive signal serves both as power signal and as a control signal for operating selectively, within said group, at least one or the other of a first transducer or sub-group of transducers, and of a second transducer or sub-group of transducers. The apparatus is also used to treat brain disorders.

Abstract: Described herein are methods and apparatuses for detecting an obstructive material within a lumen of an aspiration catheter using one or more sensors with the lumen of the suction catheter to prevent excess blood loss and improve operation of the apparatus.

Abstract: Ultrasound image devices, systems, and methods are provided. In one embodiment, a method of automated medical examination, comprising receiving, from an imaging device, a first image representative of a subject's body while the imaging device is positioned at a first imaging position with respect to the subject's body; determining a first motion control configuration for repositioning the imaging device from the first imaging position to a second imaging position based on a first predictive network, the first image, and a target image view including a clinical property; and repositioning, by a robotic system coupled to the imaging device, the imaging device to the second imaging position based on the first motion control configuration.

Abstract: A bending neck comprising a plurality of pivotally connected hollow links is formed by machining a tube to form individual, pivotally connected links. A second tube may be located inside the first tube and simultaneously machined with the first tube. Grooves are formed on opposite sides of the outer surface of the second tube to provide a passageway for control cables which control the articulation of the links. In a second implementation indentations are formed in the side of the single tube to form ring-like projections into the inner lumen of each link, through which the control cables may pass.

Abstract: An ultrasound probe has an acoustic window (10) or lens (20) through which ultrasound is transmitted and received by a transducer array (30) located behind the lens or window inside a probe enclosure. The external, patient-contacting surface (24) of the acoustic lens or window is textured. The texturing of the surface of the lens or window better retains gel spread over the lens or window for an ultrasound procedure, reduces reverberation artifacts, and diminishes the appearance of scratches on the lens or window.

Abstract: The invention relates to an assisting apparatus (2) for assisting a user in moving an insertion element (11) like a catheter to a target element within, for instance, a person (8). A target element representation representing the target element within the object in its three-dimensional position and three-dimensional orientation and with its size is generated based on a provided target element image. Moreover, a three-dimensional position of the insertion element is tracked, while the insertion element is moved to the target element, and the target element representation and the tracked position of the insertion element are displayed. The three-dimensional position and orientation of the target element relative to the actual position of the insertion element can therefore be shown to the user, while the insertion element is moved to the target element, which allows the user to more accurately and faster move the insertion element to the target element.

Abstract: For active control of steering, one or more motors integrated into an intra-cardiac echocardiography catheter handle control the bending. Multiple sets of motors may be used to control steering wires anchored at different segments along the catheter, allowing steering with multiple bends in complex patterns controlled by a controller. The handle may be releasably separated into a reusable motor part and a disposable steering wire part so that the more complex and expensive motor part is not discarded and so that the number of motors may be matched to the number of steering wires.

Abstract: An imaging device positioning system for monitoring an anatomical region (10). The imaging device positioning system employs an imaging device (20) for generating an image (21) of an anatomical region (10). The imaging device positioning system further employs a imaging device controller (30) for controlling a positioning of the imaging device (20) relative to the anatomical region (10). During a generation by the imaging device (20) of the image (21) of the anatomical region (10), the imaging device controller (30) adapts the control of the positioning of the imaging device (20) relative to the anatomical region (10) to a physiological condition of the anatomical region (10) extracted from the image (21) of the anatomical region (10).

Abstract: Provided is a plasma guide wire including a core shaft, a coil, a tip, a coil-core shaft joining region, and first to third insulating resin tubes. The first insulating resin tube is disposed on the outer periphery of the coil, and extends proximally from the tip to beyond the coil-core shaft joining region. The second insulating resin tube is disposed on the outer periphery of the core shaft, is joined to the proximal end of the first insulating resin tube, and extends from the proximal end of the first insulating resin tube to the proximal side of the core shaft. The second insulating resin tube is harder than the first insulating resin tube. The third insulating resin tube is disposed on at least a portion of a region of the inner periphery of the first insulating resin tube, proximal to a location facing the proximal end of the coil.

Abstract: The invention discloses a three-dimensional atrial septal puncture method including positioning the heart from a body surface by a three-dimensional projection positioning method and displaying interventional instruments by the three-dimensional system and guiding the same into a heart cavity. The method also includes constructing a right atrium three-dimensional model by delivering a catheter with a positioning device to the right atrium and reconstructing and fusing pre-operative image data by the three-dimensional system. The method also includes setting parameters, connecting an interventional operating device with a pressure sensor tail wire and an electrode tail wire, and displaying a guidewire or a puncture needle. The method includes delivering and positioning the long sheath, analyzing and marking the fossa ovalis position by a structure and potential method.

Abstract: Aspects of the technology described herein relate to ultrasound transducer devices including capacitive micromachined ultrasonic transducers (CMUTs) and methods for forming CMUTs in ultrasound transducer devices. Some embodiments include forming a cavity of a CMUT by forming a first layer of insulating material on a first substrate, forming a second layer of insulating material on the first layer of insulating material, and then etching a cavity in the second insulating material. A second substrate may be bonded to the first substrate to seal the cavity. The first layer of insulating material may include, for example, aluminum oxide. The first substrate may include integrated circuitry. Some embodiments include forming through-silicon vias (TSVs) in the first substrate prior to forming the first and second insulating layers (TSV-Middle process) or subsequent to bonding the first and second substrates (TSV-Last process).

Abstract: A medical device control handle or catheter includes deflection assembly and at least one of the following: a disk actuator, a lever actuator and a ring actuator for actuating additional puller wires in manipulation of multiple features of the medical device or catheter independently of each other. The disk actuator has a common rotational axis with but is rotationally independent of the deflection assembly. The lever actuator has a separate rotational axis. The ring is mounted outside of the control handle and rotatable relative to the control handle to actuate another puller wire for manipulating another feature of the catheter. Each of the disk, lever and ring actuators are of a design that allows existing control handles and catheters to be readily modified to include these actuators.

Abstract: The present invention comprises methods, compositions, devices and systems for determining the status of, or treating, a body structure or conduit. An embodiment of the invention comprises a fluid pressure control device for pressure control of fluid introduced into a body structure or conduit.

Abstract: A device comprises a miniature transducer having an altered backing geometry that can be placed within different casing sizes of an imaging probe device. The backing geometry extends along a longitudinal axis of the imaging probe and provides an angle (e.g., 45-degree angle) configured to reflect ultrasound and/or light waves/signals in a direction perpendicular to the longitudinal axis of the imaging probe. This design is configured to enable ultrasound and/or light waves/signals to be redirected and dampened within the transducer to preserve a suitable signal to noise ratio while minimizing the required depth of the backing.

Abstract: A medical device includes an elongated medical device body; a first operating line and a second operating line inserted in an axial direction of the medical device body; and a bending operating part for performing a bending operation of a distal end part of the medical device body by pulling the first and second operating lines, at an intermediate part and a proximal end part in the axial direction of the medical device body, the first and second operating lines extending in parallel so as to be spaced apart from each other in a circumferential direction of the medical device body, and at the distal end part in the axial direction of the medical device body, the first and second operating lines being curved and joined together so as to approach each other in the circumferential direction of the medical device body gradually toward a distal end side.

Abstract: A medical device includes a medical device body, first and second operating lines inserted in axial direction of the device body, and a bending operating part that pulls the operating lines to perform bending operation of a distal end part of the device body. The device body has the distal end part in the axial direction such that the operating lines are gradually curved and approach each other in circumferential direction of the device body toward a distal end side in the distal end part. The device body has a curved region and a parallel region such that in the curved region, the operating lines gradually curve and approach each other in the circumferential direction toward the distal end side and that in a parallel region, the operating lines extend in parallel to each other between the distal end of the curved region and distal ends of the operating lines.

Abstract: A method of providing and processing an ultrasound capable endoscope assembly that uses an endoscope having a proximal and a distal end, and that has been used previously. The endoscope is cleansed to a level appropriate for re-use within a human body. The method also uses an unused ultrasound assembly, sealed in antiseptic packaging, and which includes a multiple signal pathway connector; an ultrasound transducer head including an ultrasound transducer; and a set of signal pathways, extending from the ultrasound transducer to the multiconductor electrical connector. In the method, the ultrasound assembly is to the endoscope, so that the set of signal pathways extends along the elongate body of the endoscope and the ultrasound transducer head is attached at the distal end. After use, the ultrasound assembly is detached from the endoscope and permanently disposed.

Abstract: An ultrasound diagnosis apparatus includes: a two-dimensional (2D) transducer array in which a plurality of transducers that transmit/receive an ultrasound signal to/from an object are arranged in two dimensions; an analog beamformer configured to perform analog beamforming in a first direction, and perform analog beamforming in a second direction perpendicular to the first direction on signals respectively received by the plurality of transducers; and a digital beamformer configured to perform digital beamforming on the signals that are analog-beamformed in the first direction, and perform digital beamforming on the signals that are analog-beamformed in the second direction.