Abstract: An electrical panelboard enclosure includes an enclosure housing with an interior equipment chamber accessible by way of a service entrance door. A service panel is adapted for connection to a main power source in order to receive main power therefrom. A power supply is operatively connected to receive main power from the service panel and deliver it to a load. The power supply is also adapted for connection to a backup power source in order to receive backup power therefrom and deliver it to the load in the event of a main power cutoff. A load disconnector is operatively connected between the power supply and the load. The load disconnector is manually operable to disconnect the load from the power supply to prevent the power supply from delivering either main or backup power to the load.

Abstract: An orifice plate carrier for positioning an orifice plate within an orifice fitting to measure fluid flow rate through a conduit is disclosed. In some embodiments, the plate carrier has an opening therethrough and an inner surface surrounding the opening. A lip extends radially from the inner surface to support an orifice plate assembly with an orifice plate disposed therein. At least one flow port extends through the body. Each flow port is configured to allow fluid therethrough and to reduce a pressure differential between fluid up and downstream of the orifice plate during installation and extraction. At least two notches, each notch extending radially from the inner surface, engage the orifice plate and maintain the concentric position of the orifice plate within the fitting.

Abstract: An apparatus for providing haptic feedback to an operator of a vehicle is described including a pedal, torque motor, actuator and controller. The pedal is rotatable between a closed position and an open position. The torque motor applies rotational force to the pedal. The actuator is rotatably positioned between the torque motor and pedal. The controller provides haptic feedback to the operator by sending a haptic signal via the torque motor, actuator and pedal in which rotational force is applied to the pedal to rotate the pedal toward the closed position.

Abstract: Pumps and plunger assemblies are provided. An exemplary pump can have or contain a cylinder mounted in a pump housing, a plunger assembly including a crosshead, a plunger, a stationary bushing having substantial portions fixedly mounted within a laterally extending bore of the crosshead, and a non-stationary pivotally rotating wrist pin mounted within the bushing. The pump can also include a power end seal assembly including a seal housing extending at least partially through an aperture in the sealed fluid end-facing side of the power end of the pump, a power end seal disposed therein in sealing contact with the power end section of the plunger and a splashguard assembly.

Abstract: An instrument gas conditioning system is provided. The system includes filtering, and optionally drying, a gas stream to obtain a filtered, and optionally dried, gas stream. The filtered, and optionally dried, gas stream is heated in a heater and then regulated through a regulator. The filtered, heated, regulated, and, optionally dried, gas stream may be used as instrumentation gas.

Abstract: Method and system of a flange seal ring. At least some of the illustrative embodiments are systems comprising a metallic ring and a plurality of cogs. The metallic ring comprises a central bore that defines an internal diameter, a first sealing face that defines a first plane, a second sealing face that defines a second plane, a first groove in the first sealing face, and a second groove in the second sealing face. The plurality of cogs couple to the metallic ring, each cog extends through the first plane, and the plurality of cogs positioned one each at a plurality of radial positions around the metallic ring. At least one of the plurality of cogs configured to have an adjustable position relative to the central bore, and the cogs configured to align the central bore to a corresponding bore of a flange.

Abstract: An electrical panelboard enclosure includes an enclosure housing with an interior equipment chamber accessible by way of a service entrance door. A service panel is configured to receive power from a main power source. A main power breaker has a main power breaker toggle switch and is positionable between a power-on state and a power-off state to selectively activate and deactivate the main power. A power cutoff switch mechanism is operable from outside the service entrance door and is positionable between a power-on state and a power-off state to mechanically engage and deactivate the main power breaker toggle switch and cutoff the main power without opening the service entrance door. A lockout system is operable to prevent the service entrance door from being secured in a closed position unless the main power breaker and the power cutoff switch mechanism are in the same state.

Abstract: A seal assembly is disposed in an annular recess in a cylinder chamber between a pump cavity and a pump exterior. The seal assembly includes a main seal and a back-up seal and seals to a pump plunger disposed within the cylinder chamber. The back-up seal includes an extrusion recess extending from a surface of the back-up seal adjacent the main seal along an inner or an outer diameter of the back-up seal. During pumping operations the plunger strokes through the cylinder chamber causing the main seal to extrude into the extrusion recess to form a seal between the plunger and the cylinder chamber.

Abstract: An electrically non-conductive back plate for supporting the back of a patient in a supine position comprises on its front face facing the back of the patient a pair or more of ECG electrodes capable of maintaining electrically conductive skin contact with the patient's back. The pair of ECG electrodes is disposed at a sharp angle with the mean heart vector, in particular so as to form an angle ? of about 45°±25° with the projection S of the patient's spine on the back plate. Also disclosed is an ECG electrode for mounting in a recess of the back plate and an apparatus for treating cardiac arrest by compression of the sternum comprising the back plate.

Abstract: A physical access control system is disclosed which includes a network, at least one access controller, a producer device, and a consumer device. Each access controller generates status and event information associated with a controlled physical barrier. The producer device includes producer logic which collects and stores the status and event information. The consumer device includes consumer logic which periodically polls the producer logic via the network to retrieve the status and event information from the producer device. The producer logic and the consumer logic communicate via the network according to a commonly accepted message syndication protocol, such as the RSS protocol or the Atom Publishing Protocol or the like. The use of a commonly accepted message syndication protocol simplifies communications, avoids proprietary configurations and facilitates integration, such as combining systems or adding new devices and the like.

Abstract: A window regulator assembly is described that comprises a window bracket that is in contact with the bottom edge of the window; a cable; a carrier plate that is in contact with the window bracket and both ends of the cable; a tension spring located on each end of the cable; an upper bracket assembly; a drum housing having a cable drum; a hollow conduit located between the upper bracket assembly and the drum housing; and a drive unit. The upper bracket assembly, cable drum, and conduit are capable of slideably receiving the cable, while the tension springs provide a predetermined amount of tension to the cable in order for the window regulator assembly to move the window between open and closed positions. Many of the components of the window regulator assembly may be formed from a thermoplastic material.

Abstract: Embodiments of the present concept are directed to medical devices. For example, a medical device including a display for providing feedback to a rescuer who is performing Cardio Pulmonary Resuscitation (CPR) chest compressions to a patient. The display is structured to graphically indicate an instantaneous value of a measured compression depth of the chest of the patient. The display includes an indicator range that corresponds at least in part to a compression depth range of some of the measured compression depths. An indicator is represented as progressing along the indicator range as the depth changes within the compression depth range to represent a value of the measured compression depth in relation to the indicator range. Depending on the measured compression depth, the indicator progresses at a variable rate relative to a difference in the measured compression depth.

Abstract: Apparatus and methods are described including at least one rigid structure configured to be inserted into a subject's fornix such that distal end of the rigid structure is at a site anterior to a perivascular adipose layer of at least one of the subject's left and right broad ligaments. At least one uterine artery compression device is placed posterior to the broad ligaments and compresses at least one of the subject's left and right uterine arteries by pressing the at least one broad ligament against the rigid structure. Other applications are also described.

Abstract: A medical device for use with a patient is described. The medical device includes a component for administering a treatment to the patient or receiving data of the patient. The component is configured to operate according to an internal setting. The medical device also includes a user interface through which a user can modify the internal setting, as well as a settings signature generator for generating a settings signature that represents a present state of the internal setting. A gateway is also provided for communicating a version of the settings signature out of the medical device.

Abstract: An ultrasonic flow meter for measuring the flow of a fluid through a pipeline. In some embodiments, the ultrasonic flow meter includes a spool piece, a transducer assembly, and a port cover assembly. The spool piece has a throughbore and a transducer port extending between the throughbore and an outer surface of the spool piece. The transducer assembly is disposed within the transducer port and includes a transformer, a piezoelectric element, and an electrical coupling therebetween. The port cover assembly is coupled to the transducer assembly. The port cover assembly receives a cable coupled to the transducer assembly and is spring-loaded to bias the port cover assembly toward the transducer assembly to resist the cable from being electrically uncoupled from the transducer assembly.

Abstract: A transducer assembly for an ultrasonic flow meter comprises a piezoelectric capsule. In an embodiment, the piezoelectric capsule includes a housing having a central axis, a first end, a second end opposite the first end, and a first inner chamber extending axially from the first end. In addition, the piezoelectric capsule includes a piezoelectric element disposed in the first inner chamber. Further, the piezoelectric element includes a plurality of spacers disposed in the first inner chamber between the piezoelectric element and the housing.

Abstract: Techniques for routing event data from a field device, such as an external defibrillator, to a selected subset of a plurality of possible destinations are described. The event data may include physiological data of the patient, such as a 12-lead electrocardiogram (ECG). The destinations may be associated with one of a plurality of patient treatment centers, and may include, as examples, computing device, printers, displays, personal digital assistants, or web-accessible accounts. In some examples, a server maintains user-configurable information or rules for at least some of the destinations, and uses the information or rules for determining whether event data received from a field device is routed to the destination. In some examples, the server may also make the routing determination based on an analysis of event data, such as a determination as to whether the event data indicates that the patient is suspected to be experiencing an acute myocardial infarction.

Abstract: In an embodiment, a medical device can be used with a power adapter system. In addition, it can receive a data set from the power adapter system, and examine the data set to determine whether the data set confirms or not an authentication of the power adapter for use with the medical device. If the authentication is not confirmed, the external medical device can operate differently than otherwise. For example, power can be drawn from the power adapter system only if an inside battery is not charged.

Abstract: In an embodiment, an ultrasonic flow meter comprises a spool piece including a throughbore and a transducer port extending from the outer surface of the spool piece to the throughbore. In addition, the ultrasonic flow meter comprises a transducer assembly disposed in the transducer port. The transducer assembly has a central axis and comprises a transducer holder having a first end proximal the throughbore of the spool piece, and a second end distal the throughbore of the spool piece. Further, the transducer assembly comprises a piezoelectric capsule including a piezoelectric element. The piezoelectric capsule is coupled to the transducer holder and extends generally axially from the first end of the transducer holder. Still further, the transducer assembly comprises a transformer capsule including a transformer. The transformer capsule is coupled to the transducer holder and is axially spaced apart from the piezoelectric capsule.

Abstract: In one embodiment, an external second medical device is capable of being attached to a patient. The second medical device includes an operation module that is capable of operating at different capacities, such as at a first capacity and a second capacity. The second medical device also includes a receiver for receiving a warning about an impending administration of a first treatment to the patient, by a first medical device that does not know about the second medical device being attached to the patient. In response to receiving the warning, the second medical device undertakes a defensive action, whereby the operation of the operation module is capable of being performed at the second capacity. This way, the first treatment, when administered, will impact the second medical device less or not at all.