Abstract: A catheter pump assembly is provided that includes a proximal a distal portion, a catheter body, an impeller, and a flow modifying structure. The catheter body has a lumen that extends along a longitudinal axis between the proximal and distal portions. The impeller is disposed at the distal portion. The impeller includes a blade with a trailing edge. The flow modifying structure is disposed downstream of the impeller. The flow modifying structure has a plurality of blades having a leading edge substantially parallel to and in close proximity to the trailing edge of the blade of the impeller and an expanse extending downstream from the leading edge. In some embodiments, the expanse has a first region with higher curvature and a second region with lower curvature. The first region is between the leading edge and the second region.

Abstract: A leg cutting system with a leg support clamp 2 with a height for maintaining a structural integrity of the leg 1 during and after the leg 1 is cut. The system includes at least two leg support clamp parts joined in at least one clamp structure joint 11 with releasable mechanical fasteners for joining or releasing the at least two leg support clamp parts along the at least one clamp structure joint. A wire saw 6 with a wire saw support frame 7 and longitudinal saw tracks 16 for longitudinal displacement of the sawing wire along said longitudinal saw tracks 16 can be fixed to the leg support clamp. A wire replacement unit 9 with a plurality of sawing wires with a joint allowing the wires to be joined is located adjacent the wire saw. The embodiment(s) furthermore relates to a leg support clamp.

Abstract: A computerized method for healthcare data management generally includes forming, using the healthcare data system computing device, a digital twin of the individual patient based on the health information related to the individual patient, the digital twin of the individual patient being a digital representation of at least one health state of the individual patient; forming, using the healthcare data system computing device, a digital twin of the population of patients based on the health information related to the population of patients, the digital twin of the population of patients being a digital representation of at least one health attribute of the population of patients; and presenting, at the healthcare data system computing device, to a user of the healthcare data system the digital twin of the patient and the digital twin of the population of patients.

Abstract: Methods, systems, and devices for a mechanical circulatory support system are disclosed herein. An implantable power supply can be part of a mechanical circulatory support system. The implantable power supply can include one or several energy storage components, a power source, a voltage converter, and an output bus. Power can be provided to the voltage converter from one or both of the power source and the first energy storage component. The voltage converter can convert the voltage of the power from a first voltage to a second voltage and can power the output bus.

Abstract: An eye-movement determination method includes providing an a touch display and a memory that stores an image that includes a point of interest, wherein the image is a stored image, and repeatedly executing a set of steps. The steps include determining a position of a contact point, locating a corresponding position in an image that is displayed on the touch display, generating a degraded image from the stored image, displaying the degraded image on the touch display, and recording successive positions of the contact point. The contact point is a point at which a user contacts the touch display. The degraded image is substantially identical to the stored image with a clear zone but degrades beyond the clear zone.

Abstract: In one embodiment, an apparatus is provided, comprising: at least one non-transitory memory; a touch screen; an actuator; and one or more processors in communication with the at least one non-transitory memory, the touch screen, and the actuator, wherein the one or more processors execute instructions stored in the at least one non-transitory memory, to cause the apparatus to: detect, via the touch screen, a touch on an object of a duration that is greater than a duration threshold; in response to detection of the touch of the duration that is greater than the duration threshold, display the object as being selected; detect, via the touch screen, another touch; in response to detection of the another touch: rotate the selected object, and open content associated with the selected object in a background virtual display layer.

Abstract: A cam phaser for a camshaft, the cam phaser including a stator that is operatively connected with a crankshaft through a drive wheel; a rotor that is connectable torque proof with a camshaft and rotatable relative to the stator, wherein the drive wheel is connected torque proof or integrally configured in one piece with a stator base element or with a stator cover that is connected to and sealed relative to the stator base element, wherein a vane of the rotor is arrangeable between two bars of the stator and an intermediary space that is configured between the two bars is divided by the vane into a first pressure cavity and a second pressure cavity.

Abstract: A switch valve for controlling a hydraulic fluid flow, the switch valve comprising: a capture element that is arranged in a valve housing and that is displaceable into a first switching position or a second switching position and interlockable by a spring loaded interlocking element in the first switching position or the second switching position, wherein a first hydraulic connection is connected with a relief connection in the first switching position and a second hydraulic connection is connected with the relief connection in the second switching position, wherein a switching travel of the capture element is limited, wherein the interlocking element is at least partially arranged in a recess of the capture element, and wherein the valve housing includes a first groove that is oriented in an axial direction and limited in the axial direction wherein the interlocking element is arranged axially movable in the first groove.

Abstract: The invention generally relates to improved medical blood pump devices, systems, and methods. For example, blood pumps may be provided that include a housing defining a blood flow path between an inlet and an outlet. A rotor may be positioned in the blood flow path. A motor stator may be driven to rotate the rotor to provide the blood flow through the pump. Axial and/or tilt stabilization components may be provided to increase an axial and/or tilt stabilization of the rotor within the blood flow path. In some embodiments, biasing forces are provided that urge the rotor toward a bearing component. The biasing force may be provided by adjusting drive signals of the motor stator. Additionally, or alternatively, one or more magnets (e.g., permanent/stator magnets) may be provided to bias the rotor in the upstream and/or downstream direction (e.g., toward a bearing (chamfer, step, conical), or the like).

Abstract: A kit including a cam phaser, including a central valve that is configured to distribute a pressure fluid, and an actuator that controls the central valve, a rotor that is rotatably supported in a stator, wherein the cam phaser is driven or drivable by a dry running traction drive, wherein a pressure fluid distribution chamber that is fillable with the pressure fluid through the central valve is provided between the cam phaser and the actuator, wherein the pressure fluid distribution chamber is connected with an armature chamber of the actuator and sealed towards an ambient, wherein the actuator includes at least one armature that is movable by a coil, a pole core and a pole tube that form a pole tube assembly, and wherein the pressure fluid distribution chamber is sealed by a bonded or friction locking and form locking connection of the actuator with the central valve.

Abstract: The present invention generally relates to heart treatment systems. In some aspects, methods and systems are provided for facilitating communication between implanted devices. For example, an implantable cardiac rhythm management device may be configured to communicate with an implantable blood pump. The implantable cardiac rhythm management device may deliver heart stimulation rate information in addition to information associated with any detected abnormalities in heart function. In response, the pump may be configured to adjust pumping by the pump to better accommodate a patient's particular needs.

Abstract: The present disclosure generally includes methods and systems for recommending a lab test for a patient is disclosed. The method includes obtaining a proposed prescription for the patient from an external data source. The method further includes obtaining patient attributes for the patient, including a diagnosis of the patient. The method also includes determining whether to recommend one or more different lab tests for the patient prior to the patient beginning the proposed prescription based on the proposed prescription and the patient attributes, and providing a testing recommendation to a customer relationship management system, wherein the testing recommendation indicates the one or more different tests that are recommended for the patient in response to determining to recommend one or more different lab tests for the patient, wherein the customer relationship management system transmits the testing recommendation to a healthcare system of a clinic of the patient.

Abstract: Hydrogen generation assemblies and methods of generating hydrogen are disclosed. In some embodiments, the method may include receiving a feed stream in a fuel processing assembly of the hydrogen generation assembly; and generating a product hydrogen stream in the fuel processing assembly from the received feed stream. Generating a product hydrogen stream may, in some embodiments, include generating an output stream in a hydrogen generating region from the received feed stream, and generating the product hydrogen stream in a purification region from the output stream. The method may additionally include receiving the generated product hydrogen stream in a buffer tank of the hydrogen generation assembly; and detecting pressure in the buffer tank via a tank sensor assembly. The method may further include stopping generation of the product hydrogen stream in the fuel processing assembly when the detected pressure in the buffer tank is above a predetermined maximum pressure.

Abstract: Hydrogen generation assemblies, hydrogen purification devices, and their components are disclosed. In some embodiments, the devices may include a permeate frame with a membrane support structure having first and second membrane support plates that are free from perforations and that include a plurality of microgrooves configured to provide flow channels for at least part of the permeate stream. In some embodiments, the assemblies may include a return conduit fluidly connecting a buffer tank and a reformate conduit, a return valve assembly configured to manage flow in the return conduit, and a control assembly configured to operate a fuel processing assembly between run and standby modes based, at least in part, on detected pressure in the buffer tank and configured to direct the return valve assembly to allow product hydrogen stream to flow from the buffer tank to the reformate conduit when the fuel processing assembly is in the standby mode.

Abstract: The present invention relates to a non-implantable medical device (1, 1?) intended to cover wounds and skin lesions, comprising a biosensor (3E, 3E?), characterised in that said biosensor (3E, 3E?) comprises a piece made of absorbent, hydrophilic material fixing, on the surface and/or within the thickness thereof, a composition of agglomerated powders comprising particles of ethylene vinyl acetate (EVA) having a surface in part covered with at least one orthophosphoric acid salt and a visual indicator of microbiological growth. In particular, the medical device (1, 1?) may comprise several layers in order to enable the guiding of a liquid. The present invention relates to a method for preparing such a medical device (1, 1?).

Abstract: A coupling system includes an applicator tool and an attachment ring mounted on the applicator tool. Clips are contained within the applicator tool and are deployed through the attachment ring in order to anchor the attachment ring to biological tissue. When deployed, tips of the clips follow a curved trajectory through an annular cuff of the attachment ring and through the underlying tissue. The tips loop back out of the tissue and to a location where they are later trapped or clamped by the attachment ring. While the tips are trapped or clamped, the applicator tool cinches the clips by pulling rear segments of the clips. Thereafter, the applicator tool disconnects from the attachment ring which remains anchored to the tissue and serves as a coupling for a cannula. The cannula can have movable lock members that secure it to the attachment ring.

Abstract: Systems, assemblies, and related modules for connecting components of medical devices employ connector cables with electrical conductors and optical fibers. A connector assembly for coupling a battery module with a medical system including an implanted or worn medical device includes an input connector and an output connector. The input connector includes metal contact plates, has no moving parts, and is sealed to prevent water or dust ingression into the housing. The output connector includes metal pins to electrically couple to the metal plates of the input connector, a connector cable including electrical conductors coupled to the metal pins configured to transmit electrical power and an optical fiber configured to transmit data, and a latching mechanism disposed at an end of the output connector configured to physically attach the output connector to the housing. The cable body has a substantially flat cross-section.

Abstract: Packaging machine of articles into containers, comprising a plurality of work stations, each work station comprising one or more working devices of the packaging machine; a conveyor of containers using movers and a linear motor, comprising a path and a plurality of independently controllable movers, wherein the control system of the machine is configured so as to dynamically vary a master/slave configuration between the motion control of the movers on the path, and the control of the working devices of the packaging machine.

Abstract: The present invention relates to an isolated bacterium from the genus Pseudoalteromonas for its use as a probiotic, the use of said strain as a preservative, cyclolipopeptides which may be obtained from this bacterium, a composition comprising at least such a cyclolipopeptide, as well as to their uses.