A pump device includes a pump driver comprising a first diaphragm and a second diaphragm, the first and second diaphragms each comprising a middle portion bounded by an outer portion, the first and second diaphragms being spatially separated from each other at the respective outer portions, and coupled together at the respective middle portions. The pump also includes a fluid passageway and a pump chamber fluidly connected to the fluid passageway, wherein the pump chamber comprises a moveable wall coupled to the pump driver at the middle portions of the first and second diaphragms such that a fluid movement between the pump chamber and the fluid passageway is induced by movement of the middle portions. An input device is configured to obtain a target flow rate. A controller is configured to operate the pump driver and a flow regulator based on signals received from a flow detector.

A clamp includes a fixed portion on which a medical tube is placed, a movable portion that is provided above the fixed portion to face the fixed portion, and a closing portion that presses and closes the medical tube when the movable portion is pressed toward the fixed portion. The closing portion includes a presser that protrudes from the movable portion toward the fixed portion and presses the medical tube, a pair of sidewalls that extends, like a wall, from both sides of the fixed portion and prevents the medical tube from being shifted laterally, and a guide structure that allows the presser to be guided between the sidewalls.

A user-initiated fluid pathway connection includes: a connection hub, a piercing member, a sterile sleeve, and a drug container having a cap, a pierceable seal, a barrel, and a plunger seal, wherein the piercing member is initially retained within the sterile sleeve between the connection hub and the pierceable seal of the drug container. The connection hub may include an internal aperture within the connection hub which functions as a flow restrictor and wherein a piercing member is connected to one end of the internal aperture and a fluid conduit is connected to another end of the internal aperture. A drug delivery pump with integrated sterility maintenance features includes a housing, upon which an activation mechanism, an insertion mechanism, a fluid pathway connection as described above, a power and control system, and a drive mechanism connected to a drug container are mounted. Methods of assembly and operation are also provided.

A device, system and method are provided for controlling the rate of infusion of fluids during infusion therapy using non-electric infusion devices. Rotation of a flow regulator dial causes an orifice connected to the inlet to modify its position relative to a particular one or more orifices or groove portions, the characteristics of which provide a certain flow rate characteristic. The flow regulator allows for the infusion pump to infuse at a rate that may be varied during use by the user. Additionally, the flow regulator is made from a material selected to operate under a wide range of pressures, from 5-40 PSI, making the flow regulator compatible with pressurized devices, such as, a non-electric pump.

A pumping system comprising a pump comprising a door for access within a housing of the pump, a pump segment configured for conveying a fluid based on compression of the pump segment, a pump segment frame for preventing said pump segment from stretching, a visual placement indicator configured for facilitating in a proper placement of the pump segment frame in the housing, and a non-pinching valve configured to be disposed in the housing and to control a flow of the fluid without requiring pinching of a tube.

There is provided an infusion set capable of significantly reducing a period of time required for work of a worker during infusion. The infusion set includes a drip chamber, a tube which is connected to an outlet of the drip chamber, a roller clip which is provided in the tube, and an M clamp which is provided between the drip chamber and the roller clip in the tube and is used for storing liquid in the drip chamber. The tube has a first tube which can be mounted to an infusion pump device, a second tube which is connected to the outlet of the drip chamber and an inlet of the first tube, and a third tube which is connected to an outlet of the first tube. The M clamp is provided in the second tube, and the roller clip is provided in the third tube.

Disclosed is a tube connector for medical treatment including a housing including an internal channel configured to allow an inflow pipe disposed at the front end thereof and an outflow pipe disposed at the rear end thereof to fluidly communicate with each other, an insertion hole formed from the outer surface of the rear end of the housing to the internal channel, and at least one branch pipe disposed so as to fluidly communicate with the internal channel, a push button having a through hole, the push button being disposed in the insertion hole so as to be movable upwards and downwards, and an elastically deformable dome-shaped balloon configured to surround the insertion hole of the housing, the lower part of the balloon being open, wherein the internal channel of the housing is opened and closed through the upward and downward movement of the push button.

There is provided an IV infusion set comprising a patient access configured to connect to a vascular system of a patient, a source of medical fluid, an infusion line having one first end configured to connect to the source of medical fluid and one opposite second end configured to deliver the medical fluid towards the patient access, an infusion apparatus arranged on the infusion line, a sensor configured to emit a pressure signal indicative of a pressure of a medical fluid in the infusion line, and a control unit configured to receive the pressure signal and to determine a patient signal indicative of a vital signal of the patient based on the pressure signal. The IV infusion set further comprises a compliance element configured to attenuate pressure variations of medical fluid the infusion line, and a resistance element configured to reflect pressure waves moving along the infusion line. The sensor is arranged on the infusion line at a position downstream from the resistance element with respect to a direction of fluid flow along the infusion line from the medical fluid source towards the patient access. The infusion line may include a main infusion line and/or one or more auxiliary infusion lines connected to a main infusion line.

A sensor system for a volumetric pump operating according to the linear peristalsis principle includes at least one sensor unit; at least one sensor transmitter unit; and a sensor output signal processing unit. The sensor transmitter unit is arranged to apply a detection variable varying as a function of a travel position to the sensor unit along a predetermined travel along which a fixedly arranged sensor unit and a movably arranged sensor transmitter unit or a movably arranged sensor unit and a fixedly arranged sensor transmitter unit are moving relative to each other. The sensor unit is configured to output a detection signal corresponding to a travel position on the basis of the varying detection variable. The sensor output signal processing unit is arranged to receive the detection signal output by the sensor unit and discriminate at least three travel positions on the basis of the received detection signal.

A levered flow regulation clamp assembly for adjusting the fluid flow rate in a connector tube of an infusion set is provided. The levered flow regulation clamp assembly includes a housing to receive the connector tube and a slider rotatably engaged within the housing and configured to compress the connector tube to provide a fluid flow adjustment. Infusion sets and methods of adjusting fluid flow rates are also provided.