A cardiac support system (20) is equipped with a retaining structure (30) for the cardiac support system, said retaining structure (30) being intended to fix the cardiac support system in place. The cardiac support system comprises a device for monitoring the integrity of the retaining structure (30).

A pump device (10) operable with a syringe (11) having a barrel (12) and a plunger (13). The pump device (10) is operable to cause relative movement between the syringe plunger (13) and the syringe barrel (12) for discharging fluid from the syringe (11). The pump device (10) comprises a portion (31) adapted to engage the syringe barrel (12), and a drive mechanism for moving the syringe plunger (13) relative to the syringe barrel (12) to discharge fluid from the syringe (11). The drive mechanism comprises an actuator (45) adapted to engage the syringe plunger (13) and a power mechanism (61) for moving the actuator (45) to effect movement of the syringe plunger (13) relative to the syringe barrel (12). The pump device (10) thus provides a syringe driving means. There is also provided an infusion system comprising a syringe driving means, the syringe driving means comprising the pump device (10). Further, there is provided an infusion system comprising a syringe driving means operable to maintain a constant pressure within a syringe and tubing with viscosity corrections for various antibiotic concentrations.

A servicing regime for a disposable set of a medical fluid therapy machine is disclosed. In an example, a medical fluid delivery system includes a medical fluid therapy machine operating with a disposable set over multiple treatments to mix for each treatment at least one concentrate with purified water to form a medical fluid. The medical fluid delivery system also includes a sensor configured to measure an accuracy of the medical fluid mixed by the medical fluid therapy machine. The sensor is configured to produce a mixing accuracy output. The medical fluid delivery system further includes a computer programmed to analyze the mixing accuracy output provided by the sensor to determine whether the disposable set needs to be replaced.

A method for determining predicted failure rates of drug injection devices includes receiving a set of parameters specifying physical properties of a syringe, a liquid drug, and a drug injection device configured to deliver the liquid drug to a patient via the syringe, the drug injection device including a mechanism that drives a plunger rod toward a plunger of the syringe encased in a syringe carrier. The method also includes receiving failure rate data specifying a measured rate of failure of the drug injection device in response to various peak pressures within the syringe, applying the set of parameters to a kinematic model of the drug injection device to determine a predicted peak pressure within the syringe, determining a probability of failure of the drug injection device using the failure rate data and predicted peak pressure, and providing an indication of the determined probability of failure to an output device.

An optical connector includes a first sub-assembly that is factory-installed to a first end of an optical fiber and a second sub-assembly that is field-installed to the first end of the optical fiber. The optical fiber and first sub-assembly can be routed through a structure (e.g., a building) prior to installation of the second sub-assembly. The second sub-assembly interlocks with the first sub-assembly to inhibit relative axial movement therebetween. Example first sub-assemblies include a ferrule, a hub, and a strain-relief sleeve that mount to an optical fiber. Example second sub-assemblies include a mounting block; and an outer connector housing forming a plug portion.

A peritoneal dialysis machine carries out of a peritoneal dialysis treatment having recurring cycles, the recurring cycles involving an inflow phase, a dwell period and a drainage phase for a dialysis fluid, wherein the peritoneal dialysis machine has a control unit and a measurement apparatus for determining the inflow rate and/or drainage rate of the dialysis fluid to and from a patient, wherein the control unit is configured to carry out a comparison between a time progression curve of the inflow rate and/or of the drainage rate determined by the measurement apparatus during the inflow phase and/or the drainage phase and a corresponding reference curve and to recognize on the basis of the comparison a disturbance in inflow and/or drainage of the dialysis fluid to and from the patient.

A fill adapter system for an infusion pump assembly. The system includes a reusable fill adapter base, the base including a volume control mechanism to adjust an available fill volume of a reservoir of the infusion pump assembly and a pump mechanism configured to pump air into a fluid vial. The system also includes a vial adapter assembly including a first needle configured to penetrate a septum of the fluid vial for fluidly coupling the pump mechanism to the fluid vial and a second needle having a first end configured to penetrate the septum of the fluid vial and a second end configured to penetrate a septum of the reservoir of the infusion pump assembly to allow transfer of fluid from the fluid vial to the reservoir of the infusion pump assembly in response to air being pumped into the fluid vial and a needle carriage adapted to carry the first needle and the second needle, wherein the needle carriage slidably attached to the interior of the vial adapter assembly, wherein the needle carriage adapted to slide from a vial end of the vial adapter to a receptacle end of the vial adapter.

Provided is an aerosol generation device that suppresses the effect that errors in the production of structural elements have on the accuracy with which shortage of an aerosol source is detected. An aerosol generation device that comprises: a power source; a load that has a temperature-variable electrical resistance value and atomizes an aerosol source by generating heat due to supply of power from the power source; a first circuit that is used for the load to atomize the aerosol source; a second circuit that is connected in parallel to the first circuit, has a higher electrical resistance value than the first circuit, and is used to detect voltage that changes as a result of changes in the temperature of the load; an acquisition part that acquires the value of voltage that is applied to the second circuit and the load; and sensors that output the value of the voltage that changes as a result of changes in the temperature of the load.

Systems and methods for performing Direct Sodium Removal (DSR) therapy are provided in which an implantable device includes a pump coupled to an inlet catheter designed for placement in a patient's peritoneal cavity, an outlet catheter designed to be coupled to the patient's bladder, and is operably coupled to an analyte sensor, the pump programmed to transfer and/or cease transfer of fluid from the patient's peritoneal cavity to the patient's bladder for voiding responsive to a level of analyte detected by the analyte sensor. In addition, the system may include a processor that computes an amount of analyte transferred per pumping session.

A processor associated with a respiratory therapy device (7040) applies acoustic techniques such as for airpath component identification. The device may include a pressure generator configured to generate a supply of pressurized air from an outlet along an air circuit to a patient interface. The device may include a sensor configured to generate a sound signal representing a sound in the air circuit. The device may include a dampening structure configured to reduce reflection of sound from the flow generator along the air circuit. The processor, such as of a controller, may be configured to process the sound signal so as to identify the patient interface and/or the air circuit. The processing may detect and combine acoustic signatures, such as by alignment and averaging, and/or may flatten a spectrum of the sound signal.