Abstract: The medication delivery device is designed to receive a replaceable medication container (5) and to determine an adjusted medication dose AD for each medication container (5) received if the amount of medication contained in the medication container (5) is not a multiple of a prescribed dose D. The adjusted medication dose is the dose to be delivered instead of the prescribed dose at each use of the medication delivery device with the medication container (5) received. The adjusted dose is determined by selecting one of a first dose, that is higher than the prescribed dose, and of a second dose, that is lower than the prescribed dose, as a function of a variable B that cumulates the values nAD. (AD?D), where nAD is equal to INT (Cont/AD) and Cont is the amount of medication in the medication container received.

Abstract: A medical pump including an electromagnetic emitter and detector is provided. The emitter emits electromagnetic radiation of a predetermined wavelength. A pump set that is compatible with the medical pump modifies the emitted electromagnetic radiation when properly installed in the pump. The detector receives electromagnetic radiation, and a filter excludes electromagnetic radiation having a wavelength other than the predetermined wavelength. The pump monitors the filtered signal to determine whether the received electromagnetic radiation corresponds to the emitted electromagnetic radiation as modified by a properly loaded, compatible pump set and determines whether a compatible pump set is properly loaded in the pump as a function thereof.

Abstract: An apparatus comprising a pump configured to deliver insulin, an input configured to receive information related to managing diabetes of a user, a user interface, and a controller communicatively coupled to the pump, the input, and the user interface. The controller includes an insulin timing module configured to initiate delivery of insulin in a time relation to when a meal is to be consumed by the user and to adjust delivery of the insulin according to the received information. Other devices, systems, and methods are disclosed.

Abstract: This document discusses, among other things, an apparatus comprising a pump configured to deliver insulin, a wireless communication port, a controller, and a housing to enclose the apparatus. The controller is configured to communicate with a second device via the communication port using an open standard wireless communication protocol. The housing includes a mechanical coupling to slidably engage the second device which includes a second wireless communication port. Slidably engaging the second device positions the first and second communication ports opposite each other to allow communication via the first and second communication ports when slidably engaged.

Abstract: A method and system for detecting an inclusion within an infusion system. The method includes monitoring an output signal of a flowrate sensor as fluid flows through an infusion system. The output signal is then converted with a noise reduction filter to obtain a filtered output signal. The filtered output signal is compared to a threshold value and an alarm is activated if the filtered output signal falls below a desired threshold, thereby indicating an occlusion within the infusion system.

Abstract: A medical fluid machine includes a housing providing a first wall and a second wall, the first and second walls at least partially defining a pump chamber. A fluid receptacle is located within the pump chamber, the fluid receptacle including first and second flexible membranes configured to be moved apart to accept a medical fluid and moved together to dispel the fluid. A medical fluid outlet is in communication with the fluid receptacle. A first valve arrangement is configured to enable medical fluid in a sufficiently air-free condition to be delivered from the receptacle through the medical fluid outlet to a patient. A second valve arrangement is configured to enable medical fluid with entrained air to be delivered instead from the receptacle through the medical fluid outlet to an entrained air destination.

Abstract: Method and apparatus for providing retractable infusion tubing for an infusion device and a jog wheel user interface for an analyte monitoring system receiver and/or an infusion device control unit is provided.

Abstract: System for detecting and removing gas bubbles from a vascular infusion line, including a cassette adapted for disposition intermediate the fluid line, the cassette including a flexible tube having an inlet port for connection to a supply side of the fluid line, an outlet port configured for connection to a patient side of the fluid line, and a purge port intermediate the inlet and outlet ports, and a base unit adapted to receive the cassette and monitor fluid flow through the tube, the base unit including a sensor to detect the presence of a gas bubble in the fluid flow, a pinch valve adapted to stop the flow of fluid, and a control unit adapted to operate the base unit so that (i) fluid is permitted to flow past the pinch valve when no gas bubble is detected; and (ii) fluid flow is arrested when a gas bubble is detected.

Abstract: System for detecting and removing gas bubbles from a vascular infusion line, including a cassette adapted for disposition intermediate the fluid line, the cassette including a flexible tube having an inlet port for connection to a supply side of the fluid line, an outlet port configured for connection to a patient side of the fluid line, and a purge port intermediate the inlet and outlet ports, and a base unit adapted to receive the cassette and monitor fluid flow through the tube, the base unit including a sensor to detect the presence of a gas bubble in the fluid flow, a pinch valve adapted to stop the flow of fluid, and a control unit adapted to operate the base unit so that (i) fluid is permitted to flow past the pinch valve when no gas bubble is detected; and (ii) fluid flow is arrested when a gas bubble is detected.

Abstract: Methods and systems of patient treatment are disclosed. The methods and systems include use of medical device informatics to modify and validate therapies and drugs used in those therapies. In certain embodiments, a medical device, such as a medical infusion pump, interfaces with a server to administer the patient treatments. In one aspect, a method of tracking changed parameters in a medical infusion pump is disclosed. The method includes establishing a communication session between a medical infusion pump and a medical device server, and communicating an original parameter value, an updated parameter value, and a final parameter value from the medical infusion pump to the medical device server. The method further includes storing the original parameter value, the updated parameter value, and the final parameter value on the medical device server. Metadata associated with one or more of the parameter values identifies that parameter value to the medical device server and the medical infusion pump.

Abstract: Some embodiments of a portable infusion pump system can be configured to deliver medicine (e.g., insulin or the like) to a user and to deliver media content to a user. The media content can include, for example, MP3 music and other audio/video data stored in a memory device in the portable system. Thus, in particular embodiments, the portable infusion pump system can serve a dual purpose of providing medication and entertainment for the user from a compact and unobtrusive device.

Abstract: A method for delivering a target volume of fluid to a destination is provided. The method includes delivering a first volume of fluid to the destination in increments each having approximately a first incremental volume, the first volume of fluid being less than the target volume and delivering a second volume of fluid to the destination in increments each having approximately a second incremental volume, the second incremental volume being less than the first incremental volume, such that the sum of the first volume and the second volume is approximately equal to the target volume.

Abstract: A medical pump, for use with a cassette having a pumping chamber, includes a pumping element with a piston slider assembly which intermittently pressurizes the pumping chamber during a pumping cycle and has a piston head connected to a main body with a single pressure sensor positioned there between. A camshaft is associated with the pumping element, an inlet control element, and an outlet control element for closing the pumping chamber to flow when the pumping chamber is pressurized. A processing unit receives pressure and position data from the pressure sensor and a position sensor associated with the pumping element, and processes this data to determine the operating condition of the pump. The operating conditions determined include: blocked fluid flow, no fluid in the line, no cassette associated with the pump, proper pump priming, or proper valve sealing.

Abstract: A medical pump, for use with a cassette having a pumping chamber, includes a pumping element with a piston slider assembly which intermittently pressurizes the pumping chamber during a pumping cycle and has a piston head connected to a main body with a single pressure sensor positioned there between. A camshaft is associated with the pumping element, an inlet control element, and an outlet control element for closing the pumping chamber to flow when the pumping chamber is pressurized. A processing unit receives pressure and position data from the pressure sensor and a position sensor associated with the pumping element, and processes this data to determine the operating condition of the pump. The operating conditions determined include: blocked fluid flow, no fluid in the line, no cassette associated with the pump, proper pump priming, or proper valve sealing.

Abstract: Device for extracorporeal treatment of blood 1 intended to operate in a mode with a single needle 2, comprising: a treatment unit 3 having a first compartment 4 and a second compartment 5, which are separated by a semipermeable membrane 6, an extracorporeal blood circuit comprising a single needle 2, an intake line 7 in fluid communication with the first compartment 4 of the treatment unit 3, the first compartment 4, and a return line 8 in fluid communication with the first compartment 4 of the treatment unit 3, a purge line 9 at the outlet of the second compartment 5, a closure means (10, 11) acting on at least the intake line 7 and the return line 8 in order to generate the alternate sequence of blood intake and return, at least a first chamber 12 which is in fluid communication with the extracorporeal blood circuit and defines a first additional blood volume, the first chamber 12 having a variable total content; the first chamber 4 being rigid and including at least one wall capable of being moved, t

Abstract: A system and method for measuring fluid volume and changes in fluid volume over time, using a simple, low cost architecture is described.

Abstract: A device and a method for accurate and remote dispensing of a radioactive liquid are disclosed. A source of a radioactive liquid (1) and a source of a flushing liquid (5) are selectively connected to a fluid delivery path (7, 8, 10) by way of valve means (V1). An activity metering unit (9) is operable to determine a level of radioactivity in a metering section (8) of the fluid delivery path downstream from the valve means (V1). The device is operated by transporting a first amount of radioactive liquid (1) to the metering section (8), using the activity metering unit (9) to measure a reference level of radioactivity, calculating a second amount of the radioactive liquid still to be delivered such that the first and second amounts of radioactive liquid together have some predetermined level of radioactivity, and delivering the first and second amounts of radioactive liquid to the destination (11).

Abstract: The present invention consists of an implantable device with at least one package that houses electronics that receives input data or signals, and optionally power, from an external system through at least one coil attached to the at least one package, processes the input data and delivers electrical pulses to neural tissue through at least one array of multiple electrodes that is/are attached to the at least one package. The invention, or components thereof, is/are intended to be installed in the head, or on or in the cranium or on the dura, or on or in the brain.

Abstract: Medical device for administering a solution, said device comprising pumping means, a reservoir, means of communication between said reservoir and said pumping means, and a line for connecting the medical device to a patient, characterized in that it comprises means for determining the physical/chemical characteristics of the solution as a function of time by means of a mathematical model that takes account of the permeability of the reservoir walls as a function of time and the temperature of the solution.

Abstract: An insulin pump and an infusion set adapter having a membrane which can be acted upon by a liquid flow path associated with the pump, wherein the pump comprises a sensor by which a change in shape or location of at least a portion of the membrane caused by a change in the liquid pressure in the flow path can be detected in a contact-free manner to identify an occlusion in the flow path.

Abstract: A portable pumping system provides insulin or other drugs to a user. A shape memory element is used to actuate the pump and an intelligent system controls the actuator in order to minimize stresses within the system and provide accurate and reliable dosage delivery. The control system utilizes various types of feedback to monitor and optimize the position of the pumping mechanisms. Physical design aspects also minimize stress and the combination of the physical design aspects and the intelligent operation of the system results in a lightweight and cost effective pump that may be used in a disposable fashion if desired.

Abstract: An apparatus for delivering a fluid to a patient is provided. The apparatus includes an infusion pump for delivering the fluid, a control unit electrically connected to the infusion pump, a display operatively connected to the control unit, a communications interface operatively connected to the control unit and adapted for wireless communication, and an RFID reader operatively connected to the control unit. The control unit is configured for reading an RFID tag associated with an infusate container containing the fluid and reading an RFID tag associated with the patient.

Abstract: The invention relates to micropumps for infusing fluids. More specifically, the present disclosure describes and illustrates a micropump design that may be useful for infusing insulin into a diabetic patient. The disclosed design employs a pump chamber that has a diaphragm and a plurality of check valves that are configured to avoid leakage from the reservoir through the pump engine and into an infusion device and, also, to ensure the complete, accurate evacuation of the pump chamber.

Abstract: The present invention provides a device and a method for effectively processing epidural anesthesia by providing the needle-localization information in real time. The idea of this invention is derived from the concept that different tissues due to their different composition have different optical properties, such as absorbance and reflection, so we can discriminate the tissue types where the needle reaches by their distinctive optical properties. In this device, the inner solid needle of the puncture needle used before is replaced by a hollow needle which filled with optical fibers, and the distal end of those optical fibers are connected with two light sources of different wavelengths and a light analyzer. Thus, while qualifying and comparing the optical properties of those tissues, these device and method can be very helpful during epidural anesthesia and also reduce the risk of the surgery.

Abstract: A device for regulating the concentration of glucose in the blood of a diabetes patient includes a measuring component for measuring the concentration, a pump component for selectively introducing glucagon, or glucose instead, or insulin into the body of the patient, for instance by way of at least one hypodermic needle to be inserted into the body of the patient; and a control component which receives signals from the measuring component which are representative of the concentration and which control the pump component on the basis of at least one reference value for the concentration pre-entered into the control component and a program; wherein the device is embodied such that the measuring component and the pump component can be in substantially permanent contact with the bodily fluid or the blood of a patient.

Abstract: The invention relates to a self-parameterizable method for detecting occlusion and pulling out of a tubing for ad-ministering, by enteral route, physiological liquids and to a device for carrying out said method. The inventive device comprises, in essence: a pump (1); an administering tubing (2, 3); a tri-route tubular structure (4, 5, 7) provided with an occlusion detection area (7); a computer (14) and an electromagnetic detection means (8, 9) for detecting the presence of a fluid in said detection area (7) and for detecting a pulling out of said tri-route structure; an electromagnetic detection means (15, 16) for detecting the presence of air inside the dispensing tubing and the pulling out thereof.

Abstract: A programming device for an implantable drug pump includes a display device, a communication device, and a controller. The communication device is adapted to facilitate a communication link between the programming device and an implantable drug pump. The controller adapted to receive bolus data stored on the implantable drug pump when the communications link has been established, to process the bolus data, and to control the display device to generate a visual representation of numbers of bolus attempts for multiple periodic time intervals.

Abstract: A system and method to automatically initiate an injection procedure of a medicament into a patient. In the system, a delivery assembly includes an injector for infusing the medicament into the patient. Further, the system includes a monitor for detecting a parameter characteristic of the procedure, for instance, a pressure indicative of a partial vacuum between the injector and the injection site, a pressure exerted by the patient against the delivery assembly, a conductance, a capacitance, or an optical blood reading. Also, the system includes a timer for determining compliance of the parameter within a predetermined range during a first time interval. In response to the timer, an actuator initiates the injection procedure at the expiration of the first time interval. Further, the actuator may stop the injection procedure if the parameter is outside the predetermined range during a second time interval.

Abstract: A device for control of fluid flow with closed loop quasi static adjustment of in-line pressure-based resistance. The disclosed device and methods of using the device provide for the ability to control a flow rate with a highly portable device; the ability for an operator to safely use the device with minimal training; the ability to automatically switch between a primary and secondary fluid; the ability to maintain a flow rate through a tubing set even when the control device is removed; and the ability to measure fluids introduced with a manual bolus injection.

Abstract: Some embodiments of an infusion pump system can incorporate an accelerometer or other motion sensor to detect the user's activity level. If the user's activity level indicates that he or she is exercising or otherwise at an elevated level, the infusion pump device can be configured to automatically adjust the dispensation rate of a medicine such as insulin. Accordingly, an insulin delivery rate can be corrected to account for a user's activity level (e.g., an elevated activity level during exercise or the like).

Abstract: Some embodiments of a portable medical device, such as an infusion pump, can receive an external reference signal (e.g., a radio, cellular and/or satellite signal) to provide an automatic time-setting and maintenance operation. In these circumstances, the medical device can maintain accurate time and date information even in the event of a power interruption, a time-zone change and/or an internal clock error, for example. In this manner, the portable medical device provides safe operation and added convenience to the user.

Abstract: A power injector that incorporates at least one signal transmission connector in a movable joint (e.g., between a powerhead and a support or stand; between at least one adjacent pair of support sections of a support for the powerhead) is disclosed. Such a signal transmission connector may be in the form of a slip ring module, but in any case is part of the signal transmission link to the powerhead. At least that portion of a signal transmission conduit that is adjacent to the powerhead may be disposed within the interior of the corresponding portion of the support or stand, thereby reducing the potential that an individual will grab onto the signal transmission conduit when attempting to move at least part of the power injector, to change the position of the powerhead, or both.

Abstract: A pump system can include a pump device and a controller device removably attachable to the pump device. The controller device can be reusable, and one or more pump devices can be disconnected and reconnected to the controller device. As such, some pump usage data can be conveniently stored in the pump device itself. In such circumstances, the controller device can receive data related to the pump's history or other usage when the pump device is attached to the controller.

Abstract: The invention relates to: A medication delivery device (1) for delivering a specific dose comprising a medication cartridge (11) having an outlet (111) and a piston (112), and means (12) for holding said cartridge, and a piston rod (13) being operable to engage and displace said piston, and electrically driven actuating means (15), and driving means (161, 162) for transferring movement from said actuating means to said piston rod, and memory means (17) for storing data, and processing means (18) for evaluating said data and for controlling said actuating means. The object of the present invention is to provide a medication delivery system that combines a relatively high dose accuracy with the use of relatively low quality mechanical components and which enables compensation for built-in non-linearities.

Abstract: An expansion/compression mechanism of a piston rod assembly is composed of a bush shaft, a first cylindrical piston rod that is screwed with the bush shaft, a second cylindrical piston rod that is screwed with the first piston rod, and a piston rod holding member for housing the bush shaft and these piston rods. Therefore, the piston rods move linearly in multiple stages.

Abstract: The smart medical compliance method and system invention prevents adverse drug events through the use of protocols that uniquely identifies the patient, care provider, medication and/or medical device that is to be used with radio frequency identification (RFID). The RFID devices incorporate fail-safe locks or indicators that prevent the inadvertent or unauthorized use of medication, medical devices, or medical supplies. The system corroborates, patient, the care provider, the medical device, and the manner in which it is to be used, and authorizes the action to be undertaken through an interface on a personal digital assistant PDA over a wireless communication channel. The system also timestamps events in the equivalent of a medical black box such that records may be kept to further improve patient care and allow an analysis of procedures. In addition, the system includes interfaces to medication preparation and safe disposal. A number of smart devices that interact with the system are also described.

Abstract: In a peristaltic medical infusion pump unit, comprising a peristaltic assembly and a counter surface or anvil facing said peristaltic assembly and provided by the inner surface of a door (30) pivotally mounted on a housing (12) of the unit, the door (30) is readily non-destructively removable and replaceable. In use of the peristaltic pump unit, a flexible resilient tube (36) forming part of a medical fluid delivery line is extended between the peristaltic assembly and the counter surface or anvil provided by the door. The medical is fluid delivery line has first and second colour coded fittings (38, 40) spaced therealong upstream and downstream of the peristaltic assembly (26) and the region of the housing of the pump unit across which the infusion line is extended is provided, correspondingly spaced above and below the peristaltic assembly (26) with correspondingly colour coded support means (22, 24) for these fittings.

Abstract: An injector 20 that may be used to deliver radiographic contrast media and/or flushing solution into a patient's vascular system for the purposes such as obtaining enhanced diagnostic x-ray images. The injector includes the following features: (1) a syringe mount 26 for attachment of a syringe 28 to the injector 20; (2) display 34 and controls 90 for volume and flow rates; (3) automatic limiting of the operating pressure of the injector 20 as determined by the selection of a flow rate; (4) a syringe cradle 48 having a warming capability; (5) a purge/retract trigger 36 for control of the injection procedure having intuitive direction (i.e.

Abstract: A delivery device includes first and second housing portions that selectively engage and disengage. A reservoir on one housing portion operatively engages a drive device and/or a needle inserting device on the other housing portion. Upon proper engagement of the housing portions, the reservoir operatively couples to the drive device and/or the needle inserting device. A first magnet on the first housing portion and a second magnet (or a magnetically-attractive material) on the second housing portion are positioned to magnetically interact with each other, upon operative engagement of the housing portions. A third magnet on the second housing portion may be opposed to the first magnet to help align the housing portions for connection. A magnet-responsive device may be on one or both housing portions to detect alignment and/or connection of the housing portions.

Abstract: Self-injection system allows a user to inject a drug from a cartridge carrying unique identification information, into any one of a plurality of injection sites. Tissue at each injection site is associated with at least one injection parameter, such as flow-rate, that is different for each site. A scanner reads the identification information of the cartridge and cooperates with a central processing unit to determine the validity of the drug in order to permit an injection procedure to commence. The central processing unit has a memory for storing the different injection parameters and controls a drive unit for driving fluid from the cartridge and through a needle into the selected tissue, at the injection parameter that is associated with the user selected tissue for the injection.

Abstract: A patch pump device generally includes at least one fluid source, a fluid communicator, and an electrochemical actuator. The fluid communicator is in fluid communication with the fluid source. The electrochemical actuator is operative to cause fluid to be delivered from the fluid source into the fluid communicator.

Abstract: The present invention provides a user input device for operating a drug delivery system is provided, comprising display means adapted to simultaneously display a plurality of menu items, display means adapted to display at least one user settable drug delivery parameter, 5 and user input means allowing a user to directly select each of the simultaneously displayed menu items, wherein the user input means comprises a keyboard comprising at least one pair of user input keys, each pair allowing a user to bi-directionally set a user settable drug delivery parameter when user controllable settings are displayed. By this arrangement a compact and economical yet easy to use user interface is provided.

Abstract: The present invention provides a chemical liquid injection system in which a chemical liquid injector can detect whether or not the injection of a liquid from a liquid syringe into a patient is inappropriate for a personal reason such as the development of a side effect although the liquid is of an appropriate type for the injection system, and the chemical liquid injector can issue an alarm to notify the inappropriate injection. Chemical liquid injector 100 acquires a product ID of the liquid recorded on liquid chip 214 of liquid syringe 200 and an inappropriate ID recorded in a electric chart to output a notification when the product ID matches the inappropriate ID.

Abstract: An electric syringe according to the invention injects a dental anesthetic by pressing a rubber plug of a cartridge filled with an anesthetic. The electric syringe includes: a push member configured to press and move the rubber plug of the cartridge; a drive motor configured to generate a drive force; a transmission mechanism part configured to transmit the drive force to the push member; and a control unit configured to control a moving of the push member by controlling the drive motor, wherein the control unit controls the drive motor to move the push member to gradually increase an injection speed of the anesthetic in the beginning of the injection and to move the push member to inject the anesthetic in a constant injection speed after a predetermined time has elapsed.

Abstract: Disclosed is a medical infusion device including a dedicated processing unit for detecting abnormal operation of the operation of the device. Specifically, a watchdog controller is employed as an independent monitor of the functioning of microprocessors used in the medical infusion device for controlling things such as RF communication, insulin infusion, and system integrity. Through the use of an independently-powered watchdog control system, the accuracy and reliability of the device is enhanced, resulting in greater assurance to the patient receiving periodic or continuous infusion of a drug.

Abstract: The syringe pump comprises a receiving position for a syringe. The piston plate of the syringe is moved by a drive head which is fastened to a drive rod. For locking the piston rod prior to fixing the piston plate in the drive head, a braking element is provided on a syringe holding head. The syringe holding head further serves for determining the respective syringe size. After placing the syringe holding head against a syringe cylinder, the brake element is actuated to temporarily engage the piston rod and fix it relatively to the syringe cylinder.

Abstract: Disclosed is a system to deliver insulin to a user's body. The system includes a dispensing unit to deliver the insulin to the body, and a control mechanism to control delivery of basal insulin according to a predetermined basal infusion pattern, the basal infusion pattern selected from a plurality of predetermined basal infusion patterns. In some embodiments, selection of the basal infusion pattern may be based on one or more personal characteristics of the user.

Abstract: A fluid injecting device (30) generally including a fluid delivery assembly (32) and a needle-free injecting assembly (34). The fluid delivery assembly (32) delivers or transfers the fluid medicine from a cartridge (40) into the needle-free injecting assembly (34) for injecting into a patient. A drive train (112) applies a force to a piston (64) inside the cartridge (40) during the delivery of the fluid to the needle-free injecting assembly (34) to prevent adhesion or static friction between the piston (64) and the cartridge (40). In addition, sensors can be used to help ensure the proper amount of dosage is transferred to the needle-free injecting assembly, conserve power, reduce leakage during disassembly, among other functions.

Abstract: A disease management system, methods, and devices are shown and described. In one embodiment, the system includes an infusion pump and a remote controller with the ability to be paired to each other. A method to verify a wireless connection between an infusion pump and a remote controller is shown and described herein. In a further embodiment, a method to verify a wireless connection between an infusion pump and a remote controller is provided. In addition, a method of operating a diabetes management system is provided in which the system includes an infusion pump and at least a remote controller.

Abstract: A disease management system, methods, and devices are shown and described. In one embodiment, the system includes an infusion pump and a remote controller with the ability to be paired to each other. A method to verify a wireless connection between an infusion pump and a remote controller is shown and described herein. In a further embodiment, a method to verify a wireless connection between an infusion pump and a remote controller is provided. In addition, a method of operating a diabetes management system is provided in which the system includes an infusion pump and at least a remote controller.