Abstract: A system for managing business to business communications may include an event generation unit configured to create a first event based on receiving a purchase order from a client. The system may also include an event detection unit in communication with the event generation unit, the event detection unit configured to detect the first event. The system may also include an action unit in communication with the event generation unit. The action unit may be configured to determine a first action to perform based on the detection of the first event, and perform the first action. The event generation unit may be further configured to create a second event based on the performance of the first action.

Abstract: A compression device is used to increase intra-luminal pressure within the upper esophageal sphincter of a patient in order relieve an impact of an abnormal or defective upper esophageal sphincter anatomy, physiology, or functionality. In one implementation, the compression device is used in conjunction with an external pressure sensing device to determine the external pressure that is to be applied to the cricoid for a specific patient. The compression device can be a means for the management and/or treatment of abnormal upper esophageal sphincter functionality, or a means for strengthening an esophageal sphincter of a subject, or a means for curing esophageal reflux disease of a subject, or a means for improving vocal function in a subject, or a means for managing lung aspiration, or a means for applying cricoid pressure during anesthesia intubation, or a means for stabilizing body structures such as during medical imaging or radiation treatment.

Abstract: An ankle brace, having a rear-entry ankle cuff adapted to be worn adjacently above lateral and medial malleoli of an ankle, and an open-heel, open-malleoli and open-toe midfoot member extending forwardly and downwardly from the ankle cuff.

Abstract: A compression device is used to increase intra-luminal pressure within the upper esophageal sphincter of a patient in order relieve an impact of an abnormal or defective upper esophageal sphincter anatomy, physiology, or functionality. In one implementation, the compression device is used in conjunction with an external pressure sensing device to determine the external pressure that is to be applied to the cricoid for a specific patient. The compression device can be a means for the management and/or treatment of abnormal upper esophageal sphincter functionality, or a means for strengthening an esophageal sphincter of a subject, or a means for curing esophageal reflux disease of a subject, or a means for improving vocal function in a subject, or a means for managing lung aspiration, or a means for applying cricoid pressure during anesthesia intubation, or a means for stabilizing body structures such as during medical imaging or radiation treatment.

Abstract: A compression device is used to increase intra-luminal pressure within the upper esophageal sphincter of a patient in order relieve an impact of an abnormal or defective upper esophageal sphincter anatomy, physiology, or functionality. In one implementation, the compression device is used in conjunction with an external pressure sensing device to determine the external pressure that is to be applied to the cricoid for a specific patient. The compression device can be a means for the management and/or treatment of abnormal upper esophageal sphincter functionality, or a means for strengthening an esophageal sphincter of a subject, or a means for curing esophageal reflux disease of a subject, or a means for improving vocal function in a subject, or a means for managing lung aspiration, or a means for applying cricoid pressure during anesthesia intubation, or a means for stabilizing body structures such as during medical imaging or radiation treatment.

Abstract: A compression device is used to increase intra-luminal pressure within the upper esophageal sphincter of a patient in order relieve an impact of an abnormal or defective upper esophageal sphincter anatomy, physiology, or functionality. In one implementation, the compression device is used in conjunction with an external pressure sensing device to determine the external pressure that is to be applied to the cricoid for a specific patient. The compression device can be a means for the management and/or treatment of abnormal upper esophageal sphincter functionality, or a means for strengthening an esophageal sphincter of a subject, or a means for curing esophageal reflux disease of a subject, or a means for improving vocal function in a subject, or a means for managing lung aspiration, or a means for applying cricoid pressure during anesthesia intubation, or a means for stabilizing body structures such as during medical imaging or radiation treatment.

Abstract: A compression device is used to increase intra-luminal pressure within the upper esophageal sphincter of a patient in order relieve an impact of an abnormal or defective upper esophageal sphincter anatomy, physiology, or functionality. In one implementation, the compression device is used in conjunction with an external pressure sensing device to determine the external pressure that is to be applied to the cricoid for a specific patient. The compression device can be a means for the management and/or treatment of abnormal upper esophageal sphincter functionality, or a means for strengthening an esophageal sphincter of a subject, or a means for curing esophageal reflux disease of a subject, or a means for improving vocal function in a subject, or a means for managing lung aspiration, or a means for applying cricoid pressure during anesthesia intubation, or a means for stabilizing body structures such as during medical imaging or radiation treatment.

Abstract: An ankle support, comprising a rear-entry ankle cuff adapted to be worn adjacently above lateral and medial malleoli of an ankle, and an open-heel, open-malleoli and open-toe midfoot member extending forwardly and downwardly from the ankle cuff.

Abstract: The present invention provides an encasement for preventing arthropods contamination of an object or for decontaminating an object contaminated with arthropods. The encasement comprises an enclosure defining an aperture, the enclosure being formed of an arthropod impervious material. The encasement also comprises a cover formed of an arthropod impervious material and shaped to cover the aperture, the cover being attachable to the enclosure to prevent arthropods from escaping or entering the encasement. The encasement also comprises a heating source linked to the encasement for heating an interior of the encasement and a heater control device connected to the heating source for controlling the temperature within the encasement. The aperture is sized to allow use of the object upon separation of the cover from the enclosure and the enclosure and cover are sized and shaped to completely house the object upon attachment between the cover and the enclosure.

Abstract: Embodiments relate to non-invasive medical devices, systems and methods for the detection of coronary artery disease. In an embodiment, a handheld coronary artery disease (CAD) detection device is used in a non-invasive manner to determine whether an internal coronary artery blockage is present. The CAD detection device can be used in conjunction with an identification element, such as scanning area identification pads or a scanning area guide, to aid in the proper placement of the CAD detection device while scanning a patient. Advantages of embodiments include non-invasive test procedures; quick results; and cost-effectiveness.

Abstract: The present invention provides an encasement for preventing arthropods contamination of an object or for decontaminating an object contaminated with arthropods. The encasement comprises an enclosure defining an aperture, the enclosure being formed of an arthropod impervious material. The encasement also comprises a cover formed of an arthropod impervious material and shaped to cover the aperture, the cover being attachable to the enclosure to prevent arthropods from escaping or entering the encasement. The encasement also comprises a heating source linked to the encasement for heating an interior of the encasement and a heater control device connected to the heating source for controlling the temperature within the encasement. The aperture is sized to allow use of the object upon separation of the cover from the enclosure and the enclosure and cover are sized and shaped to completely house the object upon attachment between the cover and the enclosure.

Abstract: An engine crankcase breather for oil segregation, from blow-by gases, in an engine. The engine crankcase breather includes a housing with an inlet located in a downstream direction of the blow-by gases and an outlet. The breather also includes a baffle within the housing which poses a tortuous path for the blow-by gases, in order to segregate oil particles from the blow-by gases. The baffle includes a hook-shaped portion, in which the oil segregation takes place. The engine crankcase breather further includes a trough extending within the housing.

Abstract: An oil mist detector test rig including an oil container, an aerosol generator, an oil mist detector, and a collection unit. The aerosol generator generates fluid aerosol in the oil container. The oil mist detector is configured to provide a first reading based on a concentration of the generated fluid aerosol in the oil container. Additionally, the collection unit is configured to provide a second reading based on the concentration of the generated fluid aerosol in the oil container.

Abstract: A method of and apparatus for growing single crystal silicon ingots is disclosed. The apparatus includes a charge structure with one or more charge units that are substantially multi-crystalline or single crystal silicon. The silicon charge structure is preferably coupled to a single crystal seed structure that can be used to grow a silicon ingot after the silicon charge unit is melted into a quartz growing crucible. The silicon charge units can be linked together through silicon linking structures that are threaded into or otherwise secured to the silicon charge units. In accordance with the method of the invention a crucible holding poly-silicon stock and the silicon charge structure are isolated within a process chamber. A process melt is formed and charged with the silicon charge structure, and a silicon ingot is formed without exposing the crystal growing chamber to an outside environment.

Abstract: A method and a sensor holding and positioning device. In one embodiment, the device includes a sensor base having two feet, the base forming a raised bridge between the two feet. The bridge has one or more cross members spanning all or part of the space between the two feet. A sensor suspension including a sensor holder and sensor-height-adjustment mechanism is coupled by a pivot-arm axle to the sensor base, such that the sensor suspension is able to rotate in an arc about the long axis of the axle. In one such embodiment, the device further includes a pressure sensor attached to the sensor holder of the sensor suspension. In another such embodiment, the sensor suspension is able to slide back and forth along a line parallel to the long axis of the axle. Another aspect is a method for positioning a sensor over the radial artery, for example in a human's wrist. Yet another aspect is a pulse-waveform acquisition system.

Abstract: A cover for an anchor system, for example a motor vehicle child safety seat anchor system, having an attachment point adjacent a base layer opening and a tether selectively detachably connected to the attachment point. The cover comprises a circumferential flange defining an opening therein, and operatively connected to the base layer opening. A cap is receivable within the circumferential flange opening, is rotatably attached to the circumferential flange, and selectively movable about a pivot point from a closed position to an open position. A notch is defined in at least one of the flange and the cap. The notch allows the tether to pass therethrough when the cap is in the closed position.

Abstract: A sensor holding and positioning device. In one embodiment, the device includes a sensor base having two feet, the base forming a raised bridge between the two feet. The bridge has one or more cross members spanning all or part of the space between the two feet. A sensor suspension including a sensor holder and sensor-height-adjustment mechanism is coupled by a pivot-arm axle to the sensor base, such that the sensor suspension is able to rotate in an arc about the long axis of the axle. In one such embodiment, the device further includes a pressure sensor attached to the sensor holder of the sensor suspension. In another such embodiment, the sensor suspension is able to slide back and forth along a line parallel to the long axis of the axle. Another aspect is for positioning the sensor over the radial artery, for example in a human's wrist. Yet another aspect is a pulse-waveform acquisition system.