Abstract: A machine state monitoring device is a machine state monitoring device that is intended for a motor drive device of a machine tool. The motor drive device includes: a motor; a converter and an inverter that adjust a power supply voltage; a power failure detection unit that acquires an input voltage of the motor drive device so as to detect a power failure in the motor drive device; and a communication unit that transmits, based on the result of the detection of the detection unit, a time when the power failure is started, and a time when the power failure is completed. The machine state monitoring device includes: a communication unit that receives information of the time when the power failure is started and the time when the power failure is completed from the communication unit of the motor drive device; and a storage unit that stores the information.

Abstract: Various embodiments provide an apparatus, system method for treating neurological conditions by delivering solid form medication to the ventricles or other areas of the brain. Particular embodiments provide an apparatus and method for treating epilepsy and other neurological conditions by delivering solid form medication to ventricles in the brain wherein the medication is contained in a diffusion chamber so as to allow the medication to dissolve in the cerebrospinal fluid of the brain and then diffuse out of the diffusion chamber to be delivered to the ventricles and brain tissue. In one or more embodiments, portions of apparatus have sufficient flexibility to conform to the shape of the ventricles of the brain when advanced into them and/or to not cause deformation of the ventricle sufficient to cause a significant physiologic effect.

Abstract: Disclosed is a method for controlling a fuel pump for a motor vehicle, including determining if a set amount of fuel to be compressed is less than the minimum volume that can be delivered by the pump and, if this is the case, determining a new set amount of fuel to be compressed equal to the product of a number of compressions of a volume equal to the set amount of fuel to be compressed required to achieve at least the minimum volume that can be delivered and the set amount of fuel to be compressed; transmitting the new set amount of fuel to be compressed to the fuel pump; and subsequently disabling the fuel pump for a number of occurrences of the set amount of fuel equal to the number of compressions of a volume equal to the set amount of fuel to be compressed.

Abstract: A connector retains a medicine reservoir in a housing. The connector snaps onto the reservoir, the connector and reservoir are inserted into an aperture in the housing, and the connector snaps into the aperture in the housing. The connector may have a tubing and needle fixed in it to insert into the reservoir. The connector does not require a particular orientation when snapped into the housing and some embodiments may rotate freely. When snapped into the housing, the connector provides an auditory cue. For removal of the connector and reservoir, the exposed portion of the connector is compressed from the side. The configuration of the connector solves several problems associated with threaded connectors or other similar connectors.

Abstract: A medical system for delivering treatment or therapy to a patient has a kill switch for interrupting the delivery. The kill switch, which can disrupt the delivery directly or can cause an error message to be generated that disrupts the delivery, can be activated by the operator or remotely. In an ablation catheter system, a kill switch mechanism immediately and abruptly terminates delivery of ablation treatment or therapy.

Abstract: The catheter device comprises a drive shaft connected to a motor, and a rotor mounted on the drive shaft at the distal end section. The rotor has a frame structure which is formed by a screw-like boundary frame and rotor struts extending radially inwards from the boundary frame. The rotor struts are fastened to the drive shaft by their ends opposite the boundary frame. Between the boundary frame and the drive shaft extends an elastic covering. The frame structure is made of an elastic material such that, after forced compression, the rotor unfolds automatically.

Abstract: A medical error reduction system may include a medical error reduction software for use in creating and revising at least one drug library. The software configured to provide one of a plurality of sets of privileges to each of a plurality of sets of users. Each of the plurality of sets of privileges arranged to allocate a degree of software functionality to one of the plurality of sets of users. The degree of software functionality configured to define the ability of a user to alter the at least one drug library. The medical error reduction system may include at least one server. The medical error reduction system may include at least one editor computer each of the at least one editor computer comprising a processor in communication with a display. The at least one editor computer and at least one server may be configured to communicate via a network in a client-server based model. Each of the at least one drug library may be for use in at least one medical device.

Abstract: Described is a medical adapter assembly comprising an end including a neuraxial fitting that is not directly connectable to a standard luer fitting, an opposing end including a standard luer fitting connectable to a standard luer fitting of an intravenous medical device, and a check valve that allows fluid flow from the end with the standard luer fitting to the end with the neuraxial fitting, but prevents fluid flow from the end with the neuraxial fitting to the end with the standard luer fitting. Methods of using the medical adapter assembly and kits containing the medical adapter assembly are also described.

Abstract: A system for maintaining drug information and communicating with medication delivery devices includes software designed for use in a hospital, pharmacy or biomedical technical service environments. The software may be provided on a computer readable medium. The software allows a facility to customize a drug library with both hard and soft drug limits and other parameters for use with an infuser having a plug and play module removably inserted into a slot within a housing, or for use with an infuser having a connectivity engine enclosed within the housing. The system supports data transfer to one or more infusers connected to one or more computers. The connection between the computer and the pump can be hard wired or wireless.

Abstract: A fluid pump includes a pump body with a manual operation bulb or a power supply unit provided on an upper end and an inlet and an outlet provided on both sides of a liquid passage. A suction pipe connected to the inlet of the pump body includes a bendable part between an upper suction pipe part and a lower suction pipe part which are formed in a rigid rod shape. A discharge hose shaped as a bellows tube is connected to the outlet of the pump body. A pipe sleeve has ends partially fitted into the upper suction pipe part and the lower suction pipe part. It is installed on the outer circumferential surface of the suction pipe and shaped as a cylinder or a “C” with one end cut out from the cylinder to facilitate moving its position from the bending part to the upper suction pipe part.

Abstract: Presented herein are implantable systems and methods for long-term delivery of treatment substance to a recipient.

Abstract: A communication device for a medicament delivery device is presented that includes at least one translation detection arrangement, configured to detect a translation of at least one physical part of the medicament delivery device by utilization of a resilience and an electrical conductivity for at least one spring of the medicament delivery device. Also included is at least one change of state detection unit, configured to detect at least one change of state for the medicament delivery device based on the detected translation. The communication device further includes at least one activation unit, configured to activate the at least one change of state detection unit based on the at least one detected translation. The communication device also includes at least one transmission unit configured to provide a wireless transmission of information related to the at least one change of state to an external receiving device.

Abstract: A syringe pump is disclosed that includes a body, a syringe seat, a syringe actuator, a memory, and one or more processors. The syringe seat is coupled to the body. The syringe actuator is configured to actuate a syringe secured within the syringe seat. The memory is configured to store a plurality of instructions. The one or more processors, in accordance with the plurality of instructions, is/are configured to: prime the syringe pump in a prime phase; determine if an occlusion exists during the prime phase using a first test; stop the prime phase; initiate fluid delivery into a patient; enter into a start-up phase; determine if an occlusion exists using a second test during the start-up phase; transition from the start-up phase into a steady-state phase; and determine if an occlusion exists during the steady-state phase using a third test.

Abstract: An engagement mechanism associated with a reciprocally movable piston of a fluid injector is configured for releasably engaging an engagement portion at a proximal end of a rolling diaphragm syringe having a flexible sidewall configured for rolling upon itself when acted upon by the piston. The engagement mechanism has a plurality of engagement elements reversibly and radially movable relative to the engagement portion of the syringe between a first position, where the plurality of engagement elements are disengaged from the engagement portion of the syringe, and a second position, where the plurality of engagement elements are engaged with the engagement portion of the syringe. The engagement mechanism further has a drive mechanism for moving the plurality of engagement elements between the first position and the second position.

Abstract: One or more embodiments of the disclosure relate, generally, to a replacement pen cap for a medication injection pen comprising at least one temperature sensor for monitoring a temperature of a medication, detect dosing events, and determine that medication may be denatured based on temperature data, received analyte measurement data prior, and the detected dosing events.

Abstract: An apparatus includes a body, a catheter, and a fluid connector assembly. The catheter extends distally from the body and includes at least one electrode and at least one irrigation port. A fluid conduit is in fluid communication with the at least one irrigation port. A fluid connector assembly extends proximally from the body and includes a fluid connector body and a grounding member. The fluid connector body is configured to couple with a complementary connector associated with a fluid source. A proximal end of the fluid conduit is positioned in an interior region of the fluid connector body. The grounding member is interposed between the proximal end of the fluid conduit and the fluid connector body. The grounding member is in communication with the interior region of the fluid connector body such that the grounding member provides an electrical ground to fluid communicated to the fluid conduit via the fluid connector body.

Abstract: A variety of location-based and/or proximity-based features related to diabetes management systems can be used to improve maintenance compliance and/or to provide important information to PWD designated assistance entities (e.g., family, friends, givers, HCPs, emergency medicine providers) under certain conditions. In some cases, a user's location can be tracked or determined to trigger and/or time alerts about upcoming maintenance tasks in a way that will increase the likelihood that the PWD will immediately perform the designated maintenance task. In some cases, methods, devices, and systems provided herein can use proximity to non-paired mobile computing devices to deliver data to PWD designated assistance entities.

Abstract: Disclosed herein is a medical device. The medical device includes a blade tube section, a motor, and a cotch yoke or slotted link mechanism. The blade tube section includes an outer blade tube, an inner blade tube, and a cutting window at a distal end of the blade tube section. The motor is spaced from the blade tube section. The scotch yoke or slotted link mechanism is between the inner blade tube and the motor.

Abstract: A wearable drug delivery device that can deliver a liquid drug stored in a container to a patient is provided. The container can be a prefilled cartridge that can be loaded into the drug delivery device by the patient or that can be preloaded within the drug delivery device when provided to the patient. A sealed end of the container is pierced to couple the stored liquid drug to a needle conduit that is coupled to a needle insertion component that provides access to the patient. A drive system of the drug delivery device can expel the liquid drug from the cartridge to the patient through the needle conduit. The drive system can be controlled to provide the liquid drug to the patient in a single dose or over multiple doses.

Abstract: Provided is a device for suctioning bodily fluids and for supplying a fluid substance to a human or animal body, in which the device includes a drive unit (1, 1?, 1?; 2) having a drive (20), a pump head (30, 30?, 30?) which is drivable by the drive (20) and a connecting part (5, 7?, 4?) which is releasably connectable to the drive unit (1, 1?, 1?; 2) and has a tube guide (555, 710?, 43?). The tube guide (555, 710?, 43?) is realized in such a manner for receiving a tube (I) that the tube, in combination with the pump head (30, 30?, 30?), forms a peristaltic pump (3) by way of which the fluid substance is conveyable through the tube (I) to the human or animal body. The pump head (30, 30?, 30?) is incorporated in the connecting part (5, 7?, 4?), and the drive unit (1, 1?, 1?; 2) includes a coupling element (24, 24?) which is connected to the drive (20) in order to couple the pump head (30, 30?. 30?) to the drive (20).

Abstract: Apparatus and methods of dispensing fluid intravenously to a subject, and of flushing a line of an intravenous fluid administration apparatus, are provided. The apparatus may include a chamber including a plurality of connector ports and be configured to operate in fluid communication with an upstream source via a first connector port and, during operation, pass therethrough to downstream tubing, under a first pressure condition, first fluid from the upstream source via a second connector port. A third connector port may be configured to connect to an end of tubing or a valve connector such that, during operation, the chamber is configured to, under a second, higher pressure condition, pass therethrough to the downstream tubing a second fluid from a second fluid source via the third and second connector ports, prevent first fluid flow into the downstream tubing, and prevent second fluid flow through the first connector port.

Abstract: Apparatus and methods of dispensing fluid intravenously to a subject, and of flushing a line of an intravenous fluid administration apparatus, are provided. The apparatus may include a reservoir pump configured to operate in fluid communication with an upstream source of a first fluid and a downstream pressure-operated valve. The apparatus may also include a port connector configured to operate in fluid communication with at least the pressure-operated valve. The reservoir pump may also be configured to, during operation, automatically refill itself with the first fluid from the first upstream source. The downstream pressure-operated valve may be configured to operate in fluid communication with the reservoir pump and a second fluid source upstream of the pressure-operated valve, and to, during operation, dispense the first fluid to tubing downstream of the pressure-operated valve based on a pressure condition within the pressure-operated valve exceeding a threshold pressure.

Abstract: An injection device for dispensing of a liquid medicament is disclosed. The device includes an elongated housing extending in an axial direction to accommodate a cartridge, a drive member axially displaceable inside the housing and being in sealed engagement with a side wall of the housing, wherein the drive member has an abutment face to axially abut with a proximal end of a barrel of the cartridge to displace the cartridge from the undeployed position towards the deployed position, wherein the drive member has an outlet located distally from the sealed engagement and further has an inlet located proximally from the sealed engagement, wherein the inlet and the outlet are in flow connection with each other via a flow path extending through the drive member and wherein at least one flow restrictor is arranged across or in the flow path.

Abstract: An irrigation system is disclosed that can be uses in, for example, rectal irrigation. The system comprises a reservoir for an irrigating liquid and a probe for arrangement in a user. The probe includes an inflatable balloon for fixing the catheter in a body cavity. A first pump is provided to pump irrigation liquid from the reservoir to the probe, and a second pump is provided to pump a fluid to the balloon for inflation. A control unit controls the transfer of the irrigation liquid and the fluid, and includes a valve for releasing fluid from the balloon for deflation. Tubing provides fluid communication between the reservoir, control unit and probe. The control unit and the first and second pumps are further arranged as an integrated unitary component, and the manually operable balloon control element is arranged in the vicinity of the second pump.

Abstract: An infusion monitoring device (IMD) for facilitating infusion pump medication treatment compliance. The IMD having at least one sensor to monitor data on a tube extending from an infusion pump. The IMD may be part of a compliance system. The IMD able to collect data and communicate data to a network for remote compliance analysis. The system provides compliance feedback to support the patient and improve compliance with the treatment process.

Abstract: Disclosed are various embodiments for identification of medical fluid treatment to a medical patient. Systems and their operations are disclosed to identify a fluidic treatment protocol among a plurality of medical infusion lines. The system includes medical infusion pumps, illuminating medical infusion lines, and computing resources to initiate identification. Fluidic medical treatment is prone to error, cognitive load is elevated in healthcare operations, the various embodiments disclosed herein are systems and methods to decrease error and reduce cognitive load by identifying as a visual cue the medical fluid treatment protocol.

Abstract: Systems and methods for providing sensitive and specific alarms indicative of glycemic condition are provided herein. In an embodiment, a method of processing sensor data by a continuous analyte sensor includes: evaluating sensor data using a first function to determine whether a real time glucose value meets a first threshold; evaluating sensor data using a second function to determine whether a predicted glucose value meets a second threshold; activating a hypoglycemic indicator if either the first threshold is met or if the second threshold is predicted to be met; and providing an output based on the activated hypoglycemic indicator.

Abstract: Enhanced confirmations for programming of touchscreen infusion pumps reduce the likelihood of users confirming pump parameters that have been mistakenly programmed. Following programming of a given pump parameter, an icon or image intuitively related to the pump parameter can be displayed on the touchscreen. To confirm programming of the parameter, the user can be required to trace the icon on the touchscreen. The user will therefore necessarily associate the confirmation step with the parameter being programmed and be far more likely to realize if a mistake has been made because the user was intending to program a different parameter than with simple confirmations involving the press of a confirmation button.

Abstract: A device includes: a first member comprising a first-member-side power transmission part; and a second member comprising a second-member-side power transmission part configured to be attachable to and detachable from the first member, the second member being a part of a medicinal-liquid administering device. The first-member-side power transmission part and the second-member-side power transmission part are configured to be engaged with each other for administering a medicinal liquid into a living body. The second member is configured to open a housing covering the first-member-side power transmission part to engage the second-member-side power transmission part with the first-member-side power transmission part at a time of attaching the first member to the second member.

Abstract: The present invention provides an interactive, electronic, knowledge-based ordering process for specialty/biotech pharmaceuticals (medically coded drugs) which results in less waste, improved procedural efficiencies, and greater cost savings than the current ordering systems. The knowledge-base of the system is based on the health plan's clinical policies as well as the status of the patient and their entitled benefits with the health plan, and it is applied in an interactive manner through a web-enabled system which provides a real-time, prospective examination and control over requests for authorization to dispense the medically coded drugs. The system also includes a feedback loop from the specialty pharmacies to provide information on the medicines that have actually been dispensed. The system also provides to the patient, educational material and adherence reminders to affect therapeutic outcomes.

Abstract: A drug delivery system for injecting a medicament is provided. The system includes a container configured to receive a medicament; a drive assembly which, upon actuation, is configured to expel the medicament from the container; a needle for injecting the medicament to a patient; a fluid path assembly comprising a tube in fluid communication with the container and the needle for conducting fluid from the container to the needle; and a tube crimping arrangement configured to engage the tube to block fluid flow through the tube. The drive assembly causes the tube crimping arrangement to engage the tube after a dose of the medicament has been delivered to the patient through the needle.

Abstract: An infusion device (1) for administering a medical fluid to a patient (P) comprises a pumping mechanism (11) for exerting a force onto a delivery set (2, 3) for delivering a medical fluid from the delivery set towards a patient (P), a sensor device (14) for measuring the force exerted on the delivery set (2, 3) by the pumping mechanism (11), the sensor device (14) being constituted to output a sensor signal indicative of the force exerted onto the delivery set (2, 3), and a processor device (15) for controlling operation of the infusion device (1). Herein, the processor device (15) is constituted to perform a diagnosis routine during which a sensor signal of the sensor device (14) is obtained and compared to an expected sensor signal, to allow for detecting a drift in the sensor signal of the sensor device (14).

Abstract: An infusion set includes a base (221) and a flexible catheter (242) movable from a first catheter position disposed substantially entirely within the base (221) to a second catheter position in which a free end of the catheter (242) is disposed externally of the base (221). An introducer needle (234) is located within the catheter (242) and is movable between a first introducer needle position disposed substantially entirely within the base (221) and a second introducer needle position in which a free end of the introducer needle (234) is disposed externally of the base (221). A spring (281) is activated to move the catheter (242) from the first to the second catheter position and the introducer needle (234) from the first to the second introducer needle position to facilitate insertion of the catheter (242).

Abstract: A tissue resecting device includes a handpiece assembly and an end effector assembly. The handpiece assembly includes a motor and a cooling assembly. The cooling assembly includes a housing, a fan assembly, and a fin pack. The fan assembly includes a tubular member configured to be received in the elongate cover, and a plurality of blades rotatably supported on the tubular member and operatively coupled with a drive rotor of the motor for concomitant rotation therewith. The fin pack includes a tubular base and a plurality of fins extending radially outward from the tubular base. The tubular base is disposed within the elongate cover and about the tubular member of the fan assembly. Actuation of the motor rotates the plurality of blades of the fan assembly to thereby advance air through a space between the fin pack and the elongate cover of the housing to facilitate cooling of the motor.

Abstract: Embodiments herein include systems and methods for detecting, predicting and/or assessing acute kidney injury. In an embodiment, a monitoring system to detect acute kidney injury is included. The monitoring system can include a sensor circuit configured to collect renal data including at least one of systemic renal data, direct renal data, urinary tract data, and renal-relevant extracorporeal data. The monitoring system can also include a memory circuit to store collected renal data, an evaluation circuit to assess renal status, and a telemetry circuit. The evaluation circuit can determine whether acute kidney injury has occurred or is likely to occur by comparing the renal data to at least one of threshold values, personal historical values, patient population values and patterns indicative of acute kidney injury. The evaluation circuit can initiate a warning notification if acute kidney injury has occurred or is likely to occur. Other embodiments are also included herein.

Abstract: A pneumatic vibrational injection apparatus suitable for use in a system for removal, delivery and/or transplantation of body tissues and other substances in medical procedures may include an apparatus housing having an air inlet chamber, an air outlet chamber, a connecting chamber connecting the air outlet chamber and the air inlet chamber and an injection chamber disposed between the air inlet chamber and the air outlet chamber. An injection nozzle may be disposed in fluid communication with the injection chamber. An injection cannula may be disposed in fluid communication with the injection nozzle. An inlet transducer wheel and an outlet transducer wheel may be mounted for rotation in the air inlet chamber and the air outlet chamber, respectively, of the apparatus housing. A vibration transducer may be disposed in physical contact with the inlet transducer wheel and the outlet transducer wheel. The injection nozzle may be disposed in physical contact with the vibration transducer.

Abstract: Apparatus configured to assist a user in correctly positioning the apparatus on a drug delivery device, the apparatus comprising: attachment means for attaching the apparatus to the drug delivery device; an imaging arrangement for capturing at least one image of a portion of a delivery device; a processor for processing the captured at least one image to determine a position of the apparatus relative to the drug delivery device and to determine a manner in which the apparatus should be moved in order to correctly position the apparatus on the drug delivery device; and a display for displaying an indication of the manner in which the apparatus should be moved in order to correctly position the apparatus on the drug delivery device.

Abstract: Aspects of the invention are related to a method and a system for administrating an infusion liquid pulse. The system includes a tubing system having an inlet connected to an external reservoir adapted to contain infusion fluids and an outlet connected to a catheter. The tubing system includes a check valve proximate to the inlet and an anti-siphon valve proximate to the outlet. The system further includes an automatic pulse flow generation device. The automatic pulse flow generation device includes an internal reservoir and a bidirectional pump configured to pump infusion fluid from the external reservoir to the internal reservoir and further pump an infusion fluid pulse from the internal reservoir to be injected by the catheter, the infusion liquid pulse has a volume of at least 2 ml and a velocity of at least 5 ml/min.

Abstract: An infusion pump apparatus including a pain controlled analgesic (“PCA”) input device is disclosed. The infusion pump apparatus includes a housing, a pump actuator supported by the housing, and a PCA input device. The infusion pump apparatus also includes electronics configured to control the pump actuator, provide a voltage to the PCA input device, and sense an electrical signal in response to the pain controlled analgesic input device being depressed. The infusion pump apparatus further includes a controller electrically coupled to the electronics and programmed to determine whether the sensed electrical signal is discontinuous, and if the sensed signal is discontinuous, transmit an output indicative of the pain controlled analgesic input device functioning improperly.

Abstract: A variety of location-based and/or proximity-based features related to diabetes management systems can be used to improve maintenance compliance and/or to provide important information to PWD designated assistance entities (e.g., family, friends, givers, HCPs, emergency medicine providers) under certain conditions. In some cases, a user's location can be tracked or determined to trigger and/or time alerts about upcoming maintenance tasks in a way that will increase the likelihood that the PWD will immediately perform the designated maintenance task. In some cases, methods, devices, and systems provided herein can use proximity to non-paired mobile computing devices to deliver data to PWD designated assistance entities.

Abstract: This disclosure refers to a dosing mechanism for use in a drug delivery device implementing a dialing mode and a dispensing mode, wherein the dosing mechanism comprises a dose button, a housing and a determination unit. The dose button is activatable by the user for dose dispense, causing displacement of an indicating element connected to the housing from a first position to a second position. The determination unit is adapted such that it detects the indicating element in its second position and thereby determines that the dosing mechanism is in the dispensing mode. With some embodiments, it is possible to distinguish between the dialing mode and the dispensing mode. Some embodiments further refer to a drug delivery device comprising the above dosing mechanism.

Abstract: A pneumatic vibrational injection apparatus suitable for use in a system for removal, delivery and/or transplantation of body tissues and other substances in medical procedures may include an apparatus housing having an air inlet chamber, an air outlet chamber, a connecting chamber connecting the air outlet chamber and the air inlet chamber and an injection chamber disposed between the air inlet chamber and the air outlet chamber. An injection nozzle may be disposed in fluid communication with the injection chamber. An injection cannula may be disposed in fluid communication with the injection nozzle. An inlet transducer wheel and an outlet transducer wheel may be mounted for rotation in the air inlet chamber and the air outlet chamber, respectively, of the apparatus housing. A vibration transducer may be disposed in physical contact with the inlet transducer wheel and the outlet transducer wheel. The injection nozzle may be disposed in physical contact with the vibration transducer.

Abstract: The present disclosure relates to a container for a liquid medicament that includes a wall structure with at least one flexible portion and confining an inner volume filled with the liquid medicament and an elongated extraction tube having at least a first portion and a second portion that are separated from each other along the tube and which are located inside the inner volume. The extraction tube is radially collapsible when exposed to a compressive force above a predefined threshold, and the first portion, which is located at a distal end of the extraction tube, is less resistive against radial collapsing than the second portion.

Abstract: This document discusses, among other things, an apparatus comprising a pump configured to deliver insulin, a processor, and a user interface including a bistable display. A display element of the bistable display is placed in one of two stable orientations upon application of a biasing voltage and stays in the stable orientation when the biasing voltage is removed. The processor includes a display module configured to display a non-blank reversion display screen on the bistable display when no input is received at the user interface after a specified time duration, and to recurrently change the reversion display screen until input is received at the user interface.

Abstract: A remote control device may be configured to be mounted over the toggle actuator of a light switch and to control a load control device. The remote control device may include a mounting assembly and a control unit that is removably attachable to the mounting assembly. The mounting assembly may include a release tab that is configured to be operated from a locking position in which the control unit is secured to the mounting assembly, to a release position in which the control unit may be detached from the mounting assembly. The mounting assembly may include a clamp that is configured to engage with the toggle actuator of a mechanical switch to which the remote control device is mounted.

Abstract: There is provided a fluid delivery system (100), comprising a pump (102) for pumping fluid from a cartridge (400) to an outlet. The pump comprises a housing (302), a cartridge which can be removably attached to the housing, and a switch (308) for activating the pump. The switch is arranged such that attaching the cartridge to the housing activates the switch to automatically activate the pump. The system may also include a control unit for wireless connection with the pump.

Abstract: A medication safety device and method can include an infusion pump and a drug library in communication with the infusion pump. The drug library can have upper hard and soft limits and lower hard and soft limits associated with at least one drug. A graphical user interface can display a bar chart showing upper and lower soft limit bars for the at least one drug. The upper and lower soft limit bars can be grabbed and dragged on the graphical user interface in touch screen fashion to new positions associated with new upper and lower soft limits. The graphical user interface and associated hardware and software can be configurable to responsively re analyze data and compare a particular infusion to the new upper and lower soft limits.

Abstract: The invention relates to a radially compressible and expandable rotor (13, 13a, 13b) for a pump having at least one impeller blade (20, 22, 36, 36a, 36b, 36c, 36d, 36e, 36f, 36g, 37, 37a, 37b, 37c, 37d, 37e, 37f, 74, 88, 89, 90), wherein the impeller blade has an impeller blade body whose material is elastically deformable as well as at least one stiffening strut (25, 26, 27, 30, 31, 32, 52, 53, 57, 58, 62, 63, 67, 95) which is at least partially embedded in the material of the impeller blade body. The struts are designed suitably in size, shape and arrangement and are integrated in suitable hollow spaces of the impeller blade body for stabilizing the impeller blade. Elements with tensile strength can additionally be provided.

Abstract: The present invention relates to medical pumping devices and more precisely to the detection of dysfunctions in such devices.

Abstract: Systems, components, and methods are disclosed for withdrawing drug from a liquid drug container and transferring drug to a medical device. One or more components may have keying features so that only the correct liquid drug container and medical device are accessed, making sure the medical device is filled with the correct drug. A syringe needle hub may have keying features corresponding to keying features on a cap on the liquid drug container and on the medical device. An alignment device facilitates easy-to-operate filling of a medical device. The alignment device aligns a liquid drug container over a fill port of the medical device and can include components for moving the liquid drug container into engagement with the medical device and for automatically initiating drug transfer to the medical device. A retractable skirt or needle cover protects the needle and is unlocked only when the skirt or needle cover is close to or touching the medical device.