Abstract: An embodiment of a piezoelectric assembly for an ultrasonic flow meter comprises a piezoelectric element including a first face and a second face. In addition, the piezoelectric assembly comprises a first electrode engaging the first face. Further, the piezoelectric assembly comprises a second electrode engaging the second face. Still further, the piezoelectric assembly comprises an electrically conductive shim connector attached to the first electrode. Moreover, the piezoelectric assembly comprises a first wire electrically coupled to the shim connector.

Abstract: An ultrasonic flow meter for measuring the flow of a fluid through a pipeline. In an embodiment, the flow meter comprises a spool piece including a throughbore and a transducer port extending to the throughbore. In addition, the flow meter comprises a transducer assembly disposed in the transducer port. The transducer assembly comprises a piezoelectric capsule including a piezoelectric element. Further, the transducer assembly comprises a transformer capsule including a transformer. The transformer capsule is coupled to the piezoelectric capsule. Still further, the transducer assembly comprises a receptacle capsule coupled to the transformer capsule. The receptacle capsule includes a receptacle housing and a receptacle coaxially disposed within the receptacle housing. The receptacle is electrically coupled to the transformer. Moreover, the receptacle is rotatable relative to the receptacle housing between a first position and a second position.

Abstract: The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates optical characteristics of light transmitted into a patient to ascertain physiological signals, such as pulsatile changes in general blood volume proximate a light detector module. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided.

Abstract: An improved dimensional detection system is portable and can be used to characterize a workpiece. The dimensional detection system employs as few as a single focused light source and as few as a single camera along with a calibration data set to convert the illuminated pixels of an image of a beam on the workpiece into a cloud of real world points in space on an outer surface of the workpiece. The cloud of points can be processed to characterize the workpiece, such as by determining the right hexahedron that would encompass all of the real world points in space and which could be used to determine a dimensional weight of the workpiece.

Abstract: Methods and apparatus are provided for determining a defibrillation treatment protocol in an external defibrillator using a measurement of elapsed time. The present invention provides a defibrillator with a timer function. Upon activation of the defibrillator, an internal timer begins to run. By closely associating the activation of the defibrillator with the onset of the patient's attack, and by making allowances for inherent time differences between these events, the timer provides a measure of the elapsed time between the onset of the patient's emergency and the presentation of the defibrillator at the patient's side. Using this measure of elapsed time, the defibrillator determines an appropriate treatment therapy, such as CPR or defibrillation therapy.

Abstract: A manifold for a liquid dispensing system has at least two layers. The first layer has multiple through holes along its thickness direction, and one or more fluid channels perpendicular to the thickness direction. The second layer has one or more through holes along its thickness direction, each communicating with one of the through holes of the first layer. The second layer also has one or more fluid channels perpendicular to the thickness direction. The fluid channels each have an inlet at the edge of the respective layer and an outlet at one of the through holes. The second layer also has one or more holes defining valve bores. A valve in each of the valve bores controls flow of a liquid to a respective one of the fluid channels of the second layer. Also provided are a liquid dispensing system and a method of manufacturing a manifold.

Abstract: A pipeline flow meter orifice fitting includes a first body, a flow bore through the first body, a chamber in the first body adjacent to the flow bore, an orifice plate supported in alignment with the flow bore by an orifice plate carrier, wherein the orifice plate carrier is exposed to the chamber and divides the flow bore into a first region to one side of the orifice plate and a second region to the other side of the orifice plate, a second body coupled to said first body, a first flow path fluidicly coupling the first region and the chamber through the second body, and a second flow path fluidicly coupling the second region and the chamber through the second body. In some embodiments, a three way valve is mounted on the first body, the three way valve selectably actuatable to open a first flow path between the first region and the chamber or a second flow path between the second region and the chamber.

Abstract: An information processing system in a computer network comprising an edge system, an identity provider, a relying party and a tracing service, in which the tracing service relays a queue of information of authorized user activity from a relying party to an identity provider, which then can provide that activity information to the user.

Abstract: A meter proving method and system. At lease some of the illustrative embodiments are methods comprising establishing a prover time by a prover device, measuring a flow rate of a fluid with a flow meter that uses multiple measurements taken over a period of time to produce each individual flow rate value (the flow meter electrically coupled to the prover device), and generating a meter volume over the prover time based on the flow rate. The generating the meter volume based on the flow rate does not involve: generating a pulse train output signal by the flow meter; and generating the meter volume based on an attribute of the pulse train.

Abstract: The invention may be embodied as a system or method of controlling DC power distribution using electronic power switches (“EPSs”) are disclosed. Current sensors may be used to monitor the performance of the electronic power switches. Load systems are electrically connected to outputs of the EPSs. An acceptable output current is determined for each EPS, and the EPSs are controlled to provide those acceptable currents. Operating parameters may be provided by a remote user via a network interface. Control power may be conditioned and isolated for proper operation of the DC power management system.

Abstract: Devices, methods, and software implementing those methods for providing communicating external chest compression (ECC) devices and defibrillation (DF) devices, where the ECC and DF devices can be physically separate from each other. Both ECC and DF devices are able to operate autonomously, yet able to communicate with and cooperate with another device when present. Some ECC and DF devices are adapted to be physically and/or electrically coupled to each other. One ECC device includes a backboard, a chest compression member, a communication module, controller, and at least one sensor, electrode lead or electrode. One DF device includes a defibrillator module, a controller, and a communication module that can communicate with the ECC communication module. The communicating ECC and DF devices may deliver ECC, pacing, defibrillation, ventilation, and cooling therapies, and may deliver instructions to human assistants, in a coordinated and cooperative fashion.

Abstract: Methods, devices, and business systems are provided for insuring those who might use a defibrillator against at least some of the costs of using the device in a medical emergency event. The insurance may be purchased in advance of an event occurrence, and then redeemed after an event where the defibrillator is used. In a further embodiment, the insurer may request reimbursement from a patient or patient's insurance company following defibrillator use with or without involving the owner of the defibrillator.

Abstract: An apparatus and techniques for determining whether a medical electrode, such as a defibrillation electrode coupled to an automated external defibrillator, is in a condition for replacement. The determination can be made as a function of one or more data. In one exemplary embodiment, the determination is a function of one or more measurements of an impedance of a hydrogel bridge in a test module. In another exemplary embodiment, the determination is a function of one or more environmental condition data from one or more environmental sensors.

Abstract: A battery state of health estimator and similar method, system and computer product is disclosed providing for a estimate of a state of health (SOH) of one or more batteries, comprising, estimating a sampling of internal resistances of the one or more batteries, generating a time history of the internal resistance over a predetermined amount of time, generating a cumulative internal resistance histogram from the time history, calculating a final estimate of internal resistance of one or more batteries which represents the calculated SOH of one or more batteries and comparing the calculated SOH to a predetermined critical resistance threshold. If the calculated SOH is less than the predetermined critical resistance threshold, the battery is in no worse than a “Blue Monday” condition, and if the calculated SOH is greater than the critical resistance threshold, then the one or more batteries has failed.

Abstract: The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates two or more different physiological signals, such as phonocardiogram (PCG) signals, electrocardiogram (ECG) signals, patient impedance signals, piezoelectric signals, and accelerometer signals for features indicative of the presence of a cardiac pulse. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided.

Abstract: The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates optical characteristics of light transmitted into a patient to ascertain physiological signals, such as pulsatile changes in general blood volume proximate a light detector module. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided.

Abstract: A method and apparatus for a defibrillating system is disclosed that monitors the patient during treatment and then uses the information it gathers to adjust treatment protocols during treatment based on the patient's response. The protocols may include adaptive rhythm analysis intervals, adaptive CPR intervals, and adaptive shock stacks. A method of operating a defibrillator may include the steps of: obtaining a data set on at least one physiological parameter of a patient in a first data gathering interval; performing an analysis of the data set; and determining a time interval between the analysis of the first data set and a second data set, or the duration of a CPR interval, or the number of shocks in a shock stack, based on the result of the analysis of the data set.

Abstract: The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates optical characteristics of light transmitted into a patient to ascertain physiological signals, such as pulsatile changes in general blood volume proximate a light detector module. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided.

Abstract: The presence of a cardiac pulse in a patient is determined by evaluating physiological signals in the patient. In one embodiment, a medical device evaluates two or more different physiological signals, such as phonocardiogram (PCG) signals, electrocardiogram (ECG) signals, patient impedance signals, piezoelectric signals, and accelerometer signals for features indicative of the presence of a cardiac pulse. Using these features, the medical device determines whether a cardiac pulse is present in the patient. The medical device may also be configured to report whether the patient is in a VF, VT, asystole, or PEA condition, in addition to being in a pulseless condition, and prompt different therapies, such as chest compressions, rescue breathing, defibrillation, and PEA-specific electrotherapy, depending on the analysis of the physiological signals. Auto-capture of a cardiac pulse using pacing stimuli is further provided.