A syringe pump is disclosed that includes a pressure sensor assembly, a plunger, first and second pressure sensors, and a processor. The pressure sensor assembly senses a force and includes the plunger having a sensing surface configured to receive the force, the first pressure sensor operatively coupled to the plunger and configured to estimate the force applied to the sensing surface, and the second pressure sensor operatively coupled to the plunger and configured to estimate the force applied to the sensing surface. The processor is coupled to the first and second pressure sensors to estimate a magnitude of the force.

A pump for pumping fluid includes a tube platen, a plunger, a bias member, inlet and outlet valves, an actuator mechanism, a position sensor, and a processor. The plunger is configured for actuation toward and away from the infusion-tube when the tube platen is disposed opposite to the plunger. The tube platen can hold an intravenous infusion tube. The bias member is configured to urge the plunger toward the tube platen.

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.

Embodiments disclosed herein relate to detection systems for an infusion pump. An occlusion detector for an infusion pump includes a membrane that deforms in response to fluid pressure in a fluid flow path branching off of the main fluid flow path of the infusion pump. The membrane deforms in response to fluid pressure, applying an axial pressure to a piston, which in turn triggers a force sensor. A controller of the infusion pump triggers an alarm or alerts a user when a threshold is reached. A bubble detector for the infusion pump includes a light emitter and reflective surface. Light shines through the fluid flow path, refracting differently if there is air present in the flow path. A light sensor detects the light and conveys an output signal to the controller. If detected air surpasses a threshold, the controller sounds an alarm or otherwise alerts the user.

A system including a tube and a force sensor coupled to a wall of the tube via a restraining element and configured to obtain a value of a tubing force when the tube is deformed by the restraining element. The system includes a processor to determine parameters for fitting a curve including the value of the tubing force, to determine a fluid pressure value for a fluid in the tube based on the parameters for fitting the curve, and to activate an alarm responsive to the fluid pressure value and to the parameters for fitting the curve when an occlusion condition is identified in the tube. The parameters for fitting the curve comprise at least one time-decaying parameter(s) associated to the tubing force. A method for using the system and a non-transitory computer readable medium including instructions to perform the above method are also provided.

An infusion pump includes a housing with a door pivotally mounted to the housing, a tube channel on the housing configured to hold a tube in the infusion pump, a pumping mechanism including a shuttle, and a slide clamp ejection device.

A fluid flow sensing apparatus and method for detecting pressure and the presence of bubbles within a fluid tube. The flow sensor comprises a housing configured to receive a portion of the tube and to house the pressure sensor and the ultrasonic transmitter. The pressure sensor is positioned adjacent the tube and is configured to receive a pressure sensor signal, which correlates to a detected pressure differential within the tube. An internal controller transmits a drive signal to the ultrasonic transmitter, which emits ultrasonic waves through a portion of the tube and to the pressure sensor. The pressure sensor receives both the ultrasonic waves and a pressure sensor signal, and subsequently transmits an output signal to the internal controller. In the presence of a pressure differential or a bubble within the tube, the output signal will exhibit a DC shift or a distortion of its signal characteristics, respectively.

A system and method are provided for monitoring characteristics of a fluid being delivered from a fluid medication delivery device to an infusion site associated with a user. Model creation and development comprises, for each of one or more associated fluid delivery operations, collecting data streams from various sensors, assigning a fluid delivery state to the fluid delivery operation, and determining fluid delivery characteristics based on waveforms representing the time series data streams, and generating retrievable models correlating determined fluid delivery characteristics with the assigned fluid delivery state. Model implementation includes collecting time series data streams corresponding to a current fluid delivery operation, identifying models based on a selected fluid delivery state and determined fluid delivery characteristics from the data streams, and determining a correction factor to account for a difference between observed and predicted fluid delivery values. Alerts and/or automated control are further provided based on the correction factor.

A system including a tube and a force sensor coupled to a wall of the tube via a restraining element and configured to obtain a value of a tubing force when the tube is deformed by the restraining element. The system includes a processor to determine parameters for fitting a curve including the value of the tubing force, to determine a fluid pressure value for a fluid in the tube based on the parameters for fitting the curve, and to activate an alarm responsive to the fluid pressure value and to the parameters for fitting the curve when an occlusion condition is identified in the tube. The parameters for fitting the curve comprise at least one time-decaying parameter(s) associated to the tubing force. A method for using the system and a non-transitory computer readable medium including instructions to perform the above method are also provided.

The present invention concerns a medical pump comprising: a. A hard housing comprising a top (24) and bottom (1) hard shells, within which a rigid wall (3) and a movable membrane (2) create three distinct chambers; wherein i. said movable membrane tightly separates said second (29) and third (22) chambers ii. said first and third chambers have a watertight interface iii. said second chamber (29) is designed to contain a fluid iv. said first chamber (23) comprises a first venting mean (20) which is arranged to provide a fluidic communication between said first chamber (23) and the external environment; v. said third chamber (22) comprises a second venting mean which is arranged to provide a fluidic communication between said third chamber (22) and the external environment b. A pumping element (4) located in the first chamber (23) c. A least one pressure sensor which measure the pressure gradient between the first chamber (23) and the second chamber (29) d. A fluid pathway which permits: i. a first fluid connection (27) between said second chamber (29) and said pumping element ii. a second fluid connection (28) between said pumping element and a patient line (30).