Abstract: A spiral wound membrane module including a specialized endcap assembly including a connecting conduit defining a passageway extending radially inward from its outer periphery, and a differential pressure sensor connected to the passageway of the connecting conduit.

Abstract: The invention relates to a system and an implementation method for pumping a fluid, the system comprising: a pump comprising a flexible membrane which has two opposing surfaces, the membrane comprising a spatially rotating permanent magnetization structure, a rigid support means to which at least a portion of the lower surface of the membrane is attached, a source of a magnetic field which is capable of generating a magnetic drive field at the location of the membrane, the magnetic drive field having a substantially homogeneous orientation.

Abstract: A transport device (100) comprises a housing (110), an actuator (130) and a drive (150). The housing has a fluid inlet (111, 113) and a fluid outlet (113, 111). The actuator (130) comprises a magnetic shape-memory alloy, and the actuator (130) is arranged at least in sections in the housing (110). The actuator (130) can be deformed by the drive (150) in such a way that at least one cavity (135, 135?) for the fluid is formed in the actuator (130), which cavity can be moved by the drive (150) in order to transport the fluid in the cavity (135, 135?) from the fluid inlet (111, 113) to the fluid outlet (113, 111). At least one section of the actuator (130) has a separation layer (1380) by which a direct contact between the fluid and the actuator (130) is prevented in said section of the actuator (130).

Abstract: A method includes receiving at an aspiration module of a pump assembly an input associated with a catheter parameter of a catheter coupled to the pump assembly. An aspiration profile associated with the catheter parameter is selected via the aspiration module from a list of preset aspiration profiles associated with different catheters and include upper and lower pressure limits, an aspiration speed, and an infusion speed. A first signal is sent to actuate the pump based on the aspiration profile to operate the pump in a first mode. A pressure signal is received at the aspiration module and a second signal is sent to actuate the pump based on the aspiration profile to operate the pump in a second mode, in which the pump is cycled between the aspiration speed and the infusion speed such that the catheter pressure cycles between the upper pressure limit and the lower pressure limit.

Abstract: The present specification describes a control mechanism to control fluid flow through one or more fluid channels that supply fluid to the distal tip of an endoscope. A pump is provided with an endoscope to control the flow of fluid from an external source to a combination of fluid channels within the endoscope, which supply fluid to front and side jets of a multi-jet endoscope assembly. The pump is preferably dual-direction pump that enables control of fluid to either the front jet or to the front and side jets of the endoscope.

Abstract: Disclosed and described is a hose for attachment to a dispensing cartridge for placement in a peristaltic pump, for stretching over a rotor of the peristaltic pump, and for conveying a medium by external mechanical deformation of the hose. The hose has a length of preferably 20 mm to 200 mm, an internal cross-sectional area of 0.07 to 7.07 mm2, and a wall thickness of 0.3 mm to 2.2 mm. Thickenings are formed at both ends of the hose and the distance between the thickenings is 40 mm to 100 mm. According to the invention, it is provided that the hose is manufactured by an injection molding process, the inner cross-sectional area has a tolerance of at most±33%, and the hose is suitable for closing completely when stretched over the rotor with a tension force of 1 to 10 N.

Abstract: Systems and methods are provided for a bodily fluid management system for pumping bodily fluid such as lymph. The bodily fluid management system may include an implantable pump with a rotor having a magnetic portion and inlet and outlet tubes that connect to a fluid chamber. The fluid chamber has a volume that can be selectively reduced or increased via the rotor. The rotor is designed to periodically open and close kinking valves at each of the inlet and outlet tube to permit bodily fluid to enter the fluid chamber during an intake cycle and exit the fluid chamber during a discharge cycle. The magnetic portion of the rotor may be caused to rotate by an external controller that is positioned outside of the body and adjacent to the pump. The external controller may have a magnet that magnetically interfaces with the rotor to cause the rotor to rotate.

Abstract: In some embodiments, apparatuses and methods are provided herein useful to provide fluid nutrition and hydration. In one illustrative example, a feeding set for use with a peristaltic enteral feeding pump has sections of flexible tubing or conduit, a dispensing control valve that is in fluid communication with the tubing, and a retention disk. In some configurations, the feeding set has as attachment mechanism, which may be formed by one clips or hooks extending from the dispensing control valve and coupling geometry of the retention disk. By some approaches, the clips or hooks and the coupling geometry are configured to attach the feeding set with the pump, such as by attaching the feeding set to an internal panel of the feeding pump. In operation, the feeding set and pump are used to move fluid nutrition and hydration from a container or bag to the patient in a controlled manner.

Abstract: An ambulatory medicament device can generate a dose control signal for delivery of medicament to a subject and secure at least some functionality of a user interface of the ambulatory medicament device. The ambulatory medicament device can have a locked state that restricts modification of at least one control parameter. The ambulatory medicament device can have an unlocked state that allows modification of at least one control parameter. The ambulatory medicament device can accept a user input of a security code that is validated against a passcode to enter from the locked state to the unlocked state.

Abstract: Peristaltic dosing pump including a pump housing, a dosing head, and a manual tool-less clamping arrangement for repeated detachable clamping of the dosing head on the pump housing. Reef aquarium LED array illumination units having a planar LED array for emitting illumination and a 3D stadium lens centrally mounted with respect thereto and underlying same for projecting a generally homogenous spectrum, diverging generally stadium shaped illumination beam.

Abstract: In general, arthroscopic medical implements and assemblies and methods of operating arthroscopic medical implements and assemblies are provided. Devices, systems, and methods are described herein in connection with accessing a surgical site using an arthroscopic medical implement. In an exemplary implementation, an optical sensor of the arthroscopic medical implement can gather and output image data, and an inertial sensor of the arthroscopic medical implement can gather and output orientation data. The orientation data can be used to modify the gathered optical image to maintain a display of the gathered optical image in a predetermined desired orientation before, during, and after any rotation of the arthroscopic medical implement. The arthroscopic medical implement can also include at least one sensor configured to gather and output pressure and/or temperature.

Abstract: A medical pumping system is provided. The medical pumping system includes a fluid pump having a fluid inlet connection, a fluid outlet connection, an actuator and a backing surface. A tube of an intravenous set is disposed between the fluid inlet connection and the fluid outlet connection of the fluid pump, and disposed between the actuator and the backing surface, and a binding contact interface. The tube and the actuator are coupled together by the binding contact interface. The actuator is configured to actively pull a portion of the tube into an open position during a pump cycle. A medical pump and an infusion set are also provided.

Abstract: A tubular pulsatile ventricular assist device (PVAD) system for providing forward flow of blood in a pulsatile, peristaltic, and non-hemolytic manner to help reduce the amount of blood clotting associated with current ventricular devices on the market. The system can encircle a portion of a blood vessel, and the system can sequentially apply a pressure through each port in a particular pre-determined patter so as to selectively occlude the lumen, thereby creating a pulsatile, peristaltic movement along a length of system. Said movement causes blood to flow through the portion of the blood vessel.

Abstract: A flow restrictor includes a flexible tube held in a housing and a linear actuator connected through an intermediate link to a distal link via a first revolute joint proximate the linear actuator and a second revolute joint connecting the intermediate and distal links. The distal link has a distal end adjacent the flexible tube and the intermediate and distal links are constrained to move such that when the linear actuator moves the first revolute joint toward the linear actuator, the distal end of the distal link is driven into the side of the tube thereby progressively occluding the flexible tube.

Abstract: Described is a method for regulating a volume of liquid delivered by a peristaltic pump and a peristaltic pump system that can be used to perform the method. The method includes sensing an ambient temperature of the peristaltic pump. The peristaltic pump includes a pump motor. At least one of a motor speed and a motor operation duration is determined from the sensed temperature, a selected volume of liquid to be delivered and a predetermined correspondence of the motor speed to ambient temperature. The pump motor is operated at the determined motor speed or for the determined motor operation duration to deliver the selected volume of liquid from the peristaltic pump.

Abstract: System for protecting and securing bags for bulk high pressure processing equipment including at least one tube provided with holes, covers for evacuating and connecting the ends of the tube or tubes, the tube or tubes being anchored to the covers, a protector for the bag adapted to lengthen the outlet path of the processed product once the depressurization of the equipment is produced, and a fitting for the protector for connecting the protector to the cover on the side from which the product in the bag comes out.

Abstract: A valve for a pneumatic system, has: a first enclosure defining a first chamber and a first connection port; a second enclosure defining a second chamber and a second connection port; a first shell subjected to a first pressure differential and movable from a default position to a reversed position via snap-through buckling upon the first pressure differential reaching a threshold; and a second shell having a shape different than a shape of the first shell, the second shell resiliently movable from an initial position to a deformed position when subjected to a second pressure differential, wherein a first flow rate of a fluid via the first connection port induces deformation of the second shell followed by a snapping of the first shell thereby generating a second flow rate greater than the first flow rate.

Abstract: In a blood transfusion system (a blood transfusion kit, a blood transfusion kit for emergency blood transfusion, or a method of using a blood transfusion kit), a flow path through which blood flows is formed using a tube having a channel therein. The flow path includes: a first path that connects an upstream path and a downstream path and has a leukocyte removal filter removing leukocytes at an intermediate position of the channel and a second path that connects the upstream path and the downstream path and bypasses the leukocyte removal filter.

Abstract: An LVP that provides peristaltic pumping to removably couplable administration set tubing assemblies supplying medical infusate. The LVP includes a housing, a drive-train assembly, and a controller. The housing includes an assembly receptacle configured to receive an administration set tubing assembly. The drive-train assembly provides mechanical peristaltic movement within the assembly receptacle. The drive-train assembly includes a stepper motor located within the housing and a camshaft assembly, driven by the stepper motor and at least partially extending into the assembly receptacle. The camshaft assembly includes a unitary camshaft and a plurality of tube engaging members that cooperatively move according to rotation of the unitary camshaft. Further, the controller is located within the housing that controls operation of the stepper motor and the camshaft assembly.

Abstract: An apparatus for delivering a fluid to a subject through infusion tubing (22). The apparatus includes a tube cassette (20) for receiving the infusion tubing. The tube cassette has an anti-free-flow valve (26) configured to (i) occlude the infusion tubing, and (ii) be actuated by a force external to the tube cassette to terminate the occlusion of the infusion tubing. The tube cassette is configured to be removably coupled to a pump (24). The pump is configured to, as part of a pumping cycle for delivering the fluid to the subject, repeatedly (a) actuate the anti-free-flow valve to terminate the occlusion of the infusion tubing, and subsequently (b) release the anti-free-flow valve to occlude the infusion tubing. Other applications are also described.

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

Abstract: Micropump (10) including a support structure (14), a pump tube (16), and an actuation system (18) comprising one or more pump chamber actuators (28), the pump tube comprising a pump chamber portion (24) defining therein a pump chamber (26), an inlet portion (20) for inflow of fluid into the pump chamber, and an outlet portion (22) for outflow of fluid from the pump chamber. The inlet, outlet and pump chamber portions form part of a continuous section of tube made of a supple material. The one or more pump chamber actuators are configured to bias against the pump chamber portion to expel liquid contained in the pump chamber via the outlet portion, respectively to bias away from the pump chamber portion to allow liquid to enter the pump chamber via the inlet portion. The pump chamber portion has a cross-sectional area Ap in an expanded state that is larger than a cross-sectional area Ai of the pump tube at the inlet and outlet portions.

Abstract: Peristaltic micropump assemblies configured to pump fluid from a patient and/or deliver pharmaceutical agents to the patient are provided. In some embodiments, a micropump assembly can include a rotor configured to rotate about an axis and comprising a compressing member configured to rotate along a circumference, and a fluid chamber positioned at least partially around the circumference. The fluid chamber includes a round outer ring and a membrane attached to the outer ring and opposing an inner face of the outer ring. The compressing member is configured to compress the fluid chamber and move a fluid through the fluid chamber. The assembly can fit within a housing that is sized and shaped to be implanted in the patient. For example, the micropump assembly can be inserted into the patient's ocular cavity and configured to displace fluid from the patient's eye.

Abstract: The present invention relates to breastmilk pumps imitating the suckling mechanism of a baby's mouth.

Abstract: A peristaltic pump having at least first, second, and third stages is provided. The peristaltic pump includes a plunger, inlet and outlet valves, a spring, and an actuator. The plunger actuates toward and away from a tube, the inlet valve is upstream of the plunger, the outlet valve is downstream of the plunger, the spring biases the plunger toward the tube, and the actuator mechanically engages and disengages from the plunger. In the first stage, the inlet valve is opened and the plunger is actuated from the tube, in the second stage, the inlet valve is closed, the plunger is actuated toward the tube, and the actuator is mechanically disengaged from the plunger, and in the third stage, the outlet valve is opened. In the third stage or in a fourth stage, the actuator actuates the plunger toward the tube to discharge fluid downstream past the outlet valve.

Abstract: A peristaltic pump includes a plunger-cam follower, a tube receiver, a spring-biased plunger, a spring, a position sensor, and a processor. The plunger-cam follower engages the plunger cam to follow the plunger cam and to disengage from the plunger cam. The spring-biased plunger is coupled to the plunger-cam follower and the spring biases the spring-biased plunger toward the tube receiver. The position sensor determines a position of the spring-biased plunger when the plunger-cam follower is disengaged from the plunger came. The processor estimates fluid flow utilizing at least the position of the spring-biased plunger as indicated by the position sensor when the plunger-cam follower is disengaged from the plunger cam and the spring biases the spring-biased plunger against the tube.

Abstract: An infusion pump, driven by a camshaft with one or two cams, controls two sets of angularly aligned fingers phased within a sleeve, compressing two parallel flexible tube-sections, drawing fluid from a fluid source, yielding a combined continuous flow of fluid output from the two tube-sections as a function of the camshaft rotation.

Abstract: A method produces a porous, arched aluminum fluidization element for a diaphragm pump for fluidizing, covering and delivering pulverized products, such as pulverized coal, using inert gas at pressures of up to 7 MPa. The fluidization element ensures that fluidizing gas is supplied and homogeneously distributed in the pump lower region, and the contour of the space for pulverized materials may be advantageously designed in the diaphragm deflection area and optionally adapted to the diaphragm guide rod. In this way, a homogeneous and reversible deformation of the diaphragm is obtained with minor wear as far as possible. At the end of the delivery process of the diaphragm pump, the diaphragm is applied to the arched, half-shell-shaped fluidization surface in an extensively flat manner, and a small dead volume can be obtained, which results in minimal space for pulverized materials with a high delivery rate and little high-pressure gas loss.

Abstract: A pumping segment having a low shut-off force is disclosed. The pumping segment includes a tube having an interior surface with at least two notches on opposite sides of the interior surface.

Abstract: An infusion pump apparatus includes a length of resilient tubing removably loadable in an infusion pump having a housing, a pumping mechanism, and a pump door. A latch member is pivotally mounted to the pump door and cooperates with a latch pin fixed on pump housing. A free-flow protection device is biased to pinch the tubing closed to stop fluid flow. The latch member has a first range of pivotal motion in a latching direction for causing the latch member to engage with the latch pin to secure the door in a closed position and a second range of pivotal motion in the latching direction for causing the latch member to actuate the free-flow protection device to unpinch the tubing and allow flow. The latch member pivots through at least a portion of the first range of pivotal motion before beginning to pivot through the second range of pivotal motion.

Abstract: An electronic assembly includes a casing to conduct electricity flowing between at least some electronic components disposed within the casing. The electronic components include an ultrasonic transducer coupled to emit ultrasonic signals, and a battery to provide the electricity. A controller is coupled to the ultrasonic transducer and the battery, and the controller includes logic that when executed by the controller causes the electronic assembly to perform operations, including: instructing the ultrasonic transducer to emit the ultrasonic signals.

Abstract: Pump systems with pinch valves for surgical procedures. At least some of the example embodiments are pump systems including a stationary housing defining a front face. A tube support extends outwardly from the front face for aligning and supporting a first tube and a second tube. At least one pinch member is movable relative to the tube support by a power actuator operably coupled to the at least one pinch member and configured to have three orientations that define: a first arrangement of the pinch member relative to the tube support configured to pinch closed the first tube, a second arrangement of the at least one pinch member relative to the tube support configured to pinch closed the second tube, and a third arrangement of the at least one pinch member relative to the tube support configured to pinch closed neither the first tube nor the second tube.

Abstract: The present invention relates to devices and methods of operating the devices that contribute to curbing appetite and/or reducing food intake. In some embodiments, the methods and devices of the present invention include as intestinal/duodenal insert comprising an elongated member with at least one flow reduction element that can cause the stimulation of one or more biological signals of satiety. Some embodiments of the inserted device are anchored at the duodenal site by an anchoring member residing in the stomach, other embodiments of the device are stabilized at a targeted site by appropriate dimensions of length as well as one or more angled portions of the device that correspond to angled portions of the targeted site in the dodenum. Embodiments of the device exert effects by virtue of physical presence, as well as by more active forms of intervention, including release of bioactive materials and electrical stimulation of neurons.

Abstract: A peristaltic pump and related-method are disclosed that includes a cam shaft having a plunger cam, a plunger-cam follower that engages the plunger cam of the cam shaft, a tube receiver, a spring, a plunger, a position sensor, and a processor. The tube receiver receives a tube. The spring provides a bias. The plunger is biased toward the tube by the spring and the plunger is to the plunger-cam follower, such that expansion of the plunger cam along a radial angle intersecting the plunger-cam follower as the cam shaft rotates actuates the plunger away from the tube. The position sensor determines a position of the plunger and the processor estimates fluid flow within the tube utilizing the position of the plunger.

Abstract: The invention relates to a blood treatment device having at least one metering line which opens into a fluid circuit, wherein a conveyor module is arranged in the metering line and comprises a membrane pump and a valve which is arranged at the pressure side thereof and which can act both as a blocking valve and as a restricting valve.

Abstract: A medicament delivery device and method of use thereof. The device includes a sensor module and an injector module. The injector module is adapted to (i) be coupled to the sensor module during injection of a cannula and a needle into subcutaneous tissue and during delivery of the medicament and (ii) be removed from the sensor module after the delivery of the medicament.

Abstract: A pumping finger subassembly for a peristaltic infusion pump has a housing, a pinch member, a block member, and at least one biasing spring. The housing includes a transverse slot, a first side wall, and an open second side through which the pinch member and biasing spring(s) are inserted into the transverse slot. The block member includes a foot portion and a side wall portion. The foot portion is insertable into the housing through the open second side such that the block member is constrained against movement relative to the housing and the side wall portion of the block member opposes the first side wall of the housing, whereby the pinch member is supported on both lateral sides to prevent tilting of the pinch member.

Abstract: A pump device for delivery of at least one delivery means, particularly at least one fluid, with at least one drive unit and with at least one delivery device, particularly a delivery membrane comprising at least one, particularly at least substantially annular base body which is elastically deformable and comprises at least one delivery surface arranged on a delivery side of the base body and comprising at least one activation element for connection to at least one drive element of the drive unit, which is arranged on an activation side of the base body, the activation element being designed as a positive or non-positive element that cooperates with the drive element at least for the transfer of a driving force acting in a direction facing away from the activation side, by means of a positive and/or non-positive connection, particularly by means of a positive and/or non-positive connection without adhesive force.

Abstract: A feeding set for use with a peristaltic enteral feeding pump to deliver nutritional liquid fluid to a patient includes a container having nutritional liquid. A conduit assembly includes tubing placeable in fluid communication with the container and adapted for mounting on the enteral feeding pump. The tubing provides a fluid pathway for delivering the nutritional liquid from the container to a patient when the tubing is mounted on the enteral feeding pump. An identification member is mounted on the conduit assembly and has at least one characteristic of a nutritional liquid associated with the feeding set represented by the identification member. The identification member is positioned on the conduit assembly so as to permit automatic identification by the enteral feeding pump of the at least one characteristic of the nutritional liquid upon mounting the conduit assembly on the enteral feeding pump.

Abstract: A fluid pump device includes an elastically deformable conduit, multiple volume displacement elements, and a controller. During operation, the controller controls movement of the multiple volume displacement elements (such as compensation volume displacement elements and occluding volume displacement elements) with respect to the elastically deformable conduit at different times to cause flow of fluid in the elastically deformable conduit downstream to a recipient. The controller controls movement of the multiple volume displacement elements to volumetrically balance: i) an input flow rate of input fluid conveyed from a fluid source downstream to an input of the elastically deformable conduit, and ii) an output flow rate of output fluid delivered from an output of the elastically deformable conduit downstream to a recipient.

Abstract: A fuel injection pump pressurizes and injects fuel. A cam rotates about a rotational axis of the cam. A housing includes a cam chamber that houses the cam and a sliding chamber communicated to the cam chamber. A roller rotates while being in contact with a surface of the cam. A shoe reciprocates in the sliding chamber by rotation of the cam and is in contact with and slides on a surface of the roller. A plunger reciprocates with the shoe. A cylinder houses the plunger and includes a pump chamber to pressurize and feed the fuel by reciprocation of the plunger. A deformed section is a groove or a protrusion which extends in a direction of a rotational axis of the cam, on a part of a surface of the cam, and has a shape different from a cam profile of the cam.

Abstract: A fluid quality sensor for measuring a quality of a fluid comprises a measurement section mounted to an output side of a pump for the fluid.

Abstract: A peristaltic pump having at least first, second, and third stages is provided. The peristaltic pump includes a plunger, inlet and outlet valves, a spring, and an actuator. The plunger actuates toward and away from a tube, the inlet valve is upstream of the plunger, the outlet valve is downstream of the plunger, the spring biases the plunger toward the tube, and the actuator mechanically engages and disengages from the plunger. In the first stage, the inlet valve is opened and the plunger is actuated from the tube, in the second stage, the inlet valve is closed, the plunger is actuated toward the tube, and the actuator is mechanically disengaged from the plunger, and in the third stage, the outlet valve is opened. In the third stage or in a fourth stage, the actuator actuates the plunger toward the tube to discharge fluid downstream past the outlet valve.

Abstract: The present invention relates to a device and method for transferring rotational, mechanical motion into sinusoidal wave-like motion.

Abstract: A peristaltic pump (200) is proposed which comprises a first housing component (210) and a second loading component (230), said second loading component being at least partially contained within said first housing component and being axially movable with respect to said first housing component inside thereto. The second loading component further comprises at least a couple of rollers (235) which engage and squeeze a delivery tube (146) for delivering a fluid passing there through when, in operation, the second loading component is fully snapped into said first housing component. Moreover the second loading component comprises a guiding path (240) for guiding the delivery tube around said at least a couple of rollers towards an exit port (244) which is provided at a distal end surface of the second loading component. The present invention also relates to a patient set and to an injection system comprising said peristaltic pump, as well as to a method of operating said injection system.

Abstract: Embodiments of the invention include methods and structures for controlling developer critical dimension (DCD) variations across a wafer surface. Aspects of the invention include an apparatus having developer tubing and an internal cam. The internal cam is coupled to a fixed axis. A flexible divider is positioned between the developer tubing and the internal cam. The flexible divider is coupled to the internal cam such that rotation of the internal cam about the fixed axis is operable to change an inner diameter of the developer tubing.

Abstract: An air-bag type inflating device includes an elastic bag body and a sealing member; the sealing member has a first membrane, a second membrane and a third membrane, the second membrane is connected to the first membrane, the third membrane is stacked and arranged at a connecting location of the first membrane and the second membrane and disposed at an inner side of the first membrane; a unidirectional nozzle passage is formed between the first membrane and the third membrane, and capable of being optionally operated for opening or closing the first chamber and the second chamber. Accordingly, an opening/closing status of the unidirectional nozzle passage can be stably and precisely controlled after the bag body is pressed.

Abstract: A one-time use plastic disposable lockbox enclosing an infusion system including the infusion device, method of delivery such as tubing, and source reservoir such as a fluid bag or syringe is provided. The lockbox includes first and second thermoplastic shells joinable along a separation plane to define a housing. The housing carries an IV bag volume abutting a periphery of a filled standard IV bag to restrain movement of that IV bag along the separation plane and a pump volume abutting a periphery of an IV pump to restrain movement of that IV pump along the separation plane. A channel extends between the pump volume and an exterior of the housing to allow egress of a standard IV line from the housing.

Abstract: A pumping finger subassembly for a peristaltic infusion pump has a housing, a pinch member, a block member, and at least one biasing spring. The housing includes a transverse slot, a first side wall, and an open second side through which the pinch member and biasing spring(s) are inserted into the transverse slot. The block member includes a foot portion and a side wall portion. The foot portion is insertable into the housing through the open second side such that the block member is constrained against movement relative to the housing and the side wall portion of the block member opposes the first side wall of the housing, whereby the pinch member is supported on both lateral sides to prevent tilting of the pinch member.

Abstract: A disposable cartridge (20) for a peristaltic micro pump is disclosed. The cartridge comprises a housing (21) with an inlet connector (25) and an outlet connector (26). A fluid channel (23) extends in the housing (21) between the inlet and the outlet with a channel section (22) of the fluid channel (23) provided by a flexible tube (24). One or more openings are provided adjacent to the channel section (22) in the housing (21) allowing one or more pump engaging elements of a pump drive to engage the flexible tube (24), compressing the flexible tube (24) to pump fluid through the fluid channel (23). Sealing elements (31, 32) with double flange extensions (31a, 31b) having a first inner flange (31a, 32a) and a second outer flange (31b, 32b) are provided to seal at the connectors (25, 26) and fix the tube (24) in the housing (21).