A flow sensor sub-assembly for sensing flow of a fluidic medicament is disclosed. The flow sensor sub-assembly includes a first spring contact and a second spring contact. The spring contacts are secured to a base that has a circuit for conducting an electrical signal to and from the spring contacts to a microprocessor. The first spring contact is in electrical communication with a first piezo element and the second spring contact is in electrical communication with a second piezo element. The first spring contact has a first contact force against the first piezo element and the second spring contact has a second contact force against the second piezo element, and the first and second contact forces are equivalent. A circuit board for interfacing to a flow sensor having a plurality of piezo elements for transmitting a flow signal indicative of flow of fluidic medicament is also disclosed.

A medication delivery monitoring device is disclosed. The device includes a user interface configured to receive input information, and a sensor configured to measure a plurality of fluid state parameters of a fluid delivery channel through which the medication is delivered by a vascular access device (VAD) to an infusion site region of the patient. The device also includes a processor configured to determine a state of the infusion site region based on the plurality of measured fluid state parameters and the input information, and an output device configured to provide a communication regarding the state of the infusion site region. Methods and computer-readable mediums for monitoring medication delivery are also disclosed.

A dispensing system includes a reservoir containing the product to be dispensed, a movable element slidably mounted in the reservoir in a sealed manner so as to move according to a level of product in the reservoir, an electric motor, a pump driven by the electric motor and connected to the reservoir to transfer the product from the reservoir to a dispensing device, a first detection member providing information on at least one parameter of the movable element, the first detection member comprising a signal transmitter and a signal receiver, a second detection member configured to determine at least one operating parameter of the pump or the electric motor, an electronic member cooperating with the first and second detection members to provide information relating to the dispensing of a predetermined dose of the product.

A method may include capturing, by a camera at an infusion pump, one or more images of the pump loaded with an infusion set. A machine learning model may be applied to the images to detect nonconformities that may be present in the images of the pump loaded with the infusion set. Examples of nonconformities include a misload of the intravenous set in which an upper fitment, a lower fitment, and/or a tubing of the intravenous set is misplaced within the pump. In response to an output of the machine learning model indicating a presence of a nonconformity in the one or more images of the pump loaded with the infusion set, a corrective action may be performed. For example, the pump may be prevented from performing an infusion and a message identifying the nonconformities may be generated. Related methods and articles of manufacture are also disclosed.

A pump for administering an agent to a patient includes a housing, a motor, a gearbox, a sensor, and a controller. The motor may be coupled to housing. The gearbox is operatively connected to the motor. The sensor senses a rotation of the motor. The controller acts to control operation of the motor and monitor the quantity of the agent delivered to the patient. The pump also includes a pump assembly such that the pump is configured such that the pump assembly may be interchangeable from a syringe pump assembly and a peristaltic pump assembly.

A digital syringe is used with conventional polymer disposable syringe construction to be practical in the medical environment. Errors associated with the larger volumes of the syringes (which exacerbate minor errors in plunger position) and the flexibility and dimensional variations of the polymer plungers are accommodated by direct measurement of the syringe plunger position rather than indirect measurement of motor position and inference of syringe plunger position. This direct measurement eliminates mechanical tolerances (“stack up”) in the motor, gear train, and lead screw on plunger movement, an effect exacerbated by flexibility of the plunger and changes in syringe resistance and medicament viscosity, for example, with different medicaments or when the syringe is refrigerated. The digital syringe may be combined with the motor unit to provide additional versatility.

A medical device system. The system includes a first medical device, a first remote interface, and a second remote interface in communication with the first remote interface and the first medical device, wherein the first medical device sends a command to the first medical device through the second remote interface, and wherein when the second remote interface receives the command, the command must be confirmed by the second remote interface before the command is send by the second remote interface to the first medical device.

An infusion apparatus and a method for testing extravasation are provided. The infusion apparatus includes a liquid driver, a detection unit, and a controller. The controller controls the liquid driver to be operated, so that an input liquid provided by a infusion supply unit is injected into a living body through a tube and a needle, and a blood return detecting procedure is performed. The blood return detecting procedure includes a stop driving step implemented by controlling the liquid driver to stop operating; and a determining step implemented by controlling the detection unit to test a state of a section of the tube adjacent to the needle to generate a detected signal, and determining whether or not the blood of the living body returns to the tube according to the detected signal.

Fluid delivery devices with occlusion management are described. For example, a fluid delivery system may include at least one force element, at least one moveable element configured to be moved in a dispensing direction by the at least one force element during a pump cycle to expel a fluid from the fluid delivery system, and an occlusion management system comprising at least one emergency element operably coupled to the at least one moveable element, the occlusion management system comprising logic operative to activate the at least one emergency element responsive to a determination of an occlusion to provide additional force to move the at least one moveable element in the dispensing direction. Other embodiments are described.

Systems and methods for controlling fluid delivery via a manually administrable medication container to a patient through a fluid delivery pathway are provided. The systems and methods described herein incorporate rules-based clinical decision support logic to drive a flow control valve within a flow pathway based on a determination of whether or not an IV fluid connected to an input port on the pathway is appropriate for patient administration by considering such factors as patient-specific clinical circumstances, current medical orders, and accepted delivery protocols. Related apparatus, systems, methods and articles are also described.