Abstract: Branching catheter systems with diagnostic components for detecting and isolating fluid flow problems (e.g., leaks, occlusions, etc.) and methods for detecting and isolating fluid flow problems are disclosed. Among the fluid flow problems that may potentially be detected are leaks in the branching catheter systems (e.g., cuts, disconnected components, etc.). Another fluid flow problem that may be detected using the diagnostic systems of the present invention is the presence of occlusions or other blockages that prevent fluid flow within the catheter systems. In addition to identifying that a problem exists, the diagnostic components may preferably also be used to identify the location of the fluid flow problem as discussed herein. Connectors for use in the branching catheter systems are also disclosed.

Abstract: The fluid delivery system generally includes a source of injection fluid, a pump device a fluid path set disposed between the source of injection fluid and the pump device, and a fluid control device. The fluid path set includes a multi-position valve. The fluid control device is operatively associated with the fluid path set and includes a valve actuator adapted to operate the multi-position valve. The valve actuator is adapted to close the multi-position valve to isolate the pump device from a patient and stop flow of the injection fluid to the patient at substantially any pressure or flow rate generated by the pump device for delivering a sharp bolus of the injection fluid to the patient. The valve actuator is generally adapted to selectively place the pump device in fluid communication with the source of injection fluid for supplying the injection fluid to the pump device and the patient.

Abstract: A fluid dispensing device includes a fluid bottle, a discharge tube, a pressurizing device coupled between the bottle and the discharge tube for forcing the fluid to flow through the discharge tube without gravity, the pressurizing device includes a container coupled between the bottle and the discharge tube, a piston is slidably received in the container, and a motor is coupled to the piston to move the piston in the reciprocating action within the container, and a speed reduction device is coupled between the motor and the piston for allowing the piston to be actuated by the motor with a reduced driving speed and an increased driving torque.

Abstract: A fluid dispensing device includes a bottle for receiving fluid, a discharge tube, and a pressurizing device coupled between the bottle and the discharge tube, for pressurizing the fluid and for forcing the fluid to flow through the discharge tube without gravity. The pressurizing device includes a container coupled between the bottle and the discharge tube, a piston slidably received in the container, and a moving device for moving the piston in a reciprocating action within the container. For example, a motor is coupled to the piston with a crank, to move the piston in the reciprocating action within the container.

Abstract: The present disclosure relates to an infusion control valve adapted to be actuated by a valve actuator. The present disclosure further relates to an infusion valve actuator adapted to actuate an infusion control valve upon being triggered by an authentication unit.

Abstract: An IV administration set identification kit includes identification elements for identifying an IV administration set having an IV solution container, a drip chamber, and an IV line including a Y-site or port. The identification elements are a first adhesive strip configured for attachment to the IV solution container, a second adhesive strip configured for attachment to the drip chamber, and a Y-site identification element configured for attachment to the Y-site, wherein the first and second adhesive strips and the Y-site identification element are marked with matching identification symbols. The first and second adhesive strips and the Y-site identification element are contained within a packet having an openable side. The packet may include a backing sheet to which the first and second adhesive strips are removably attached.

Abstract: A drop sensing device for monitoring intravenous (IV) fluid flow is provided. The device comprises a U-shaped clip mountable on a drip chamber of an IV infusion set. The clip has a light source provided at one side for emitting radiation and a hollow cylinder provided in a through hole on the side opposite the light source. The cylinder includes an aperture of a diameter smaller than an average diameter of fluid drops passing the drip chamber, and an optical sensor mounted on a rear end of the cylinder opposite the aperture, so as to substantially enhance sensitivity of light ray receiving.

Abstract: This invention relates to a device to monitor the administration of a fluid through a conduit, such as intravenous fluid, and detect the completion of fluid delivery by monitoring the fluid level inside a chamber. The device will monitor, through an optical fluid sensor comprising a radiation source, two sensors, a logic means, and an indicating means, the bottom half of any “user supplied” drip chamber that is normally full during the administration of fluids. When the fluid level in the chamber drops below a predetermined level, the indicating means will initiate an electromechanical device that releases a pinching device to occlude the conduit. The pinching device is a rotary pincher that derives its force from a torsion spring and is held in the open position by the electromechanical device.

Abstract: A portable medication delivery system enables a patient to elect slow continuous auto-administration or rapid bolus self-administration of a fluid medication. The medication delivery system has an infusion pump, which includes a fluid storage chamber and a spring-driven piston positioned in the fluid storage chamber. The fluid storage chamber is initially charged with the medication and the infusion pump automatically delivers a continuous dosage of the medication at a first flow rate over a long time from the fluid storage chamber to a treatment site in the patient. A bolus injector is positioned in series or in parallel with the infusion pump and is charged with a bolus dosage of the treatment fluid from the fluid storage chamber for alternate manual self-injection of the medication into the treatment site at a higher second flow rate for a short time.

Abstract: An apparatus for pumping fluid through tubing comprising a stop platen is disclosed. The stop platen is operatively arranged to depress a wall of the tubing along a section of a longitudinal axis of the tubing. The stop platen is narrower than the tubing along a transverse axis of the tubing. The invention further comprises a cabinet containing the stop platen, a door rotatably fixed to the cabinet, and locking means for preventing rotation of the door. The locking means are operatively arranged to be unlocked by a tubing occluder.

Abstract: The invention relates to a filter arrangement for the separation of blood into plasma and cellular components, comprising at least one filter element with an inlet line and an outlet chamber in a closed housing, separated by a fine pore membrane. The inlet chamber is connected to an inlet line for donor blood an dan outlet line for cellular components and the outlet chamber is connected to an outlet line for plasma. The arrangement further comprises a device for the production of a backpressure in the filter element, whereby the fine pore membrane is in the form of a U-shaped bundle of n=650 hollow fibers of the type Micro PES-TF 10 from Akzo Faser AG, the ends of which are fixed in an air-tight and germ-tight manner to an aperture plate which seals the open end region of the housing, which is open at just one end, in an air-tight and germ-tight manner.

Abstract: The object of this invention is to provide a device for regulating the flow rate of an intravenous medical solution during an injection using an intravenous drip unit. The device has a housing (10) mounted to a hose (300) to allow the flow of the solution from a solution container (200) into the vein, and a control member (20) rotatably assembled with the housing to regulate the flow rate of the solution. The housing has first and second seats (11, 12) communicating with inlet and outlet ports, and the control member has first and second bosses (21, 22) seated in the first and second seats. An arc-shaped solution path (23), a radial channel (24) and an annular groove (25) are formed on the control member to regulate the flow rate of the solution in accordance with an adjusted angle of the control member relative to the fixed housing.

Abstract: An infusion device includes an upstream pressure control device and a downstream flow control device. The device receives infusion liquid via an inlet and controls the level of liquid in a chamber by means of a float which can close both the inlet and an outlet. A filtered vent maintains atmospheric pressure in the chamber. The device receives infusion liquid at constant head via a flow pipe. A dripper delivers droplets into an airtight chamber. A taper needle renders an orifice adjustably open to a desired degree to deliver liquid at a selected rate. Screw threaded adjustment and calibration means allow calibrated adjustment. A flow pipe delivers a metered flow of infusion liquid for infusion into a human or animal body.

Abstract: A device for illuminating a drip chamber of an IV bag including a collar with an inner diameter suitable for affixing around the drip chamber and a chemiluminescent container affixed to the interior surface of the collar. The chemiluminescent container serves to emit light therefrom and into the drip chamber. A magnifying lens extends upwardly from the collar so as to magnify an interior of the drip chamber.

Abstract: A vent system for an infusion drip chamber is provided according to the invention. The vent system includes an automatic air eliminator communicating with an interior and an exterior of the infusion drip chamber. The automatic air eliminator is capable of automatically venting air from the infusion drip chamber in a substantially continuous manner. The vent system further includes a mechanical air eliminator communicating with the interior and the exterior of the infusion drip chamber. The manual air eliminator is capable of mechanically venting air from the infusion drip chamber at discrete time intervals.

Abstract: A method for administering intravenous fluids includes coupling a first fluid path in flow communication to a first fluid reservoir, coupling an inlet of a drip chamber in flow communication to the first fluid path, coupling an outlet of the drip chamber in flow communication to a patient supply path, and coupling a bypass fluid path in flow communication to the first fluid path. The method also includes directing fluid flow from the first fluid reservoir to the patient through the first fluid path and the drip chamber, and directing fluid flow from the first fluid reservoir to the patient through the bypass fluid path such that the drip chamber is bypassed.

Abstract: An apparatus and method for preventing the occurrence of free fluid in a fluid delivery system consists of a valve having a sealing element and elongate body disposed within the lumen of a flexible tube. The elongate body of the valve if further disposed within the inlet port of a connector. The perimeter of the sealing element and lumen of the flexible tube provide a tight seal preventing fluid flow when the flexible tube is in a relaxed state or when the longitudinal axis of the flexible tube is in alignment with the axis of the inlet port. The medical fluid is allowed to flow when the longitudinal axis of the flexible tube is not in alignment, e.g., when angularly stretched, with the axis of the inlet port.

Abstract: A portable medication delivery system enables a patient to elect slow continuous auto-administration or rapid bolus self-administration of a fluid medication. The medication delivery system has an infusion pump, which includes a fluid storage chamber and a spring-driven piston positioned in the fluid storage chamber. The fluid storage chamber is initially charged with the medication and the infusion pump automatically delivers a continuous dosage of the medication at a first flow rate over a long time from the fluid storage chamber to a treatment site in the patient. A bolus injector is positioned in series or in parallel with the infusion pump and is charged with a bolus dosage of the treatment fluid from the fluid storage chamber for alternate manual self-injection of the medication into the treatment site at a higher second flow rate for a short time.

Abstract: A contrast dispensing system (10) reduces cost by directly connecting a check valve (210) to and between the reservoir inlet port (220) and the mating luer connector (204) of a disposable set (200). A contrast dispensing system (10) includes as part of the reservoir (212) an integrally molded cap (280) having the inlet port (200) and a lateral pipe (300) to confine contrast media (14) therein and disperse it at separate locations (334, 336) within the chamber (260) of reservoir (212). The reservoir (212) may have a vent port (284) with a flip cap (294) for selectively opening or closing same.

Abstract: The present invention is an apparatus for intermittently providing oral medications to a patient being fed through a feeding tube, the apparatus having a dosage vessel, which preferably can be capped or sealed, and a secure fluid path to a tubing connector for connecting to the indwelling feeding tube.

Abstract: A pinch clip occluder system for infusion sets includes a housing and a clamp movably disposed within the housing to selectively occlude an infusion set. The pinch clip nests in an adapter placed on an enteral feeding pump such that when the pinch clip occluder is properly position, flow is allowed through the infusion set, but when the pinch clip occluder is not properly positioned in the adapter, flow through the infusion set is prevented.

Abstract: A method and apparatus for monitoring intravenous drips by the transmission and detection of a signal, for example a red light, through a fluid flow passage whereby detection of a signal of a given intensity activates an audible or visual indicator. A bracket is attached around a fluid flow passage of the intravenous drip and a signal is transmitted across the passage via optical fibers. The intensity of the signal is detected by a sensor contained within a remote housing.

Abstract: An infusion system is disclosed for delivering fluid wherein the system has a flow control element within a spike member (100). The spike member (100) is a fluid extraction spike member having a fluid passageway (110) and a micro-electromechanical system (MEMS) element (108) operatively connected to the fluid extraction spike member (100).

Abstract: An infusion system packaged in a light weight nylon portable mesh container, which is also the pump of the system, includes a removable therapy bag holding the Rx to be infused into the patient. A bladder within the pump is inflatable to provide pressure onto the therapy bag to aid in the discharge of the Rx. When filling the therapy bag, the pharmacist, using his computer to comply with standards, simultaneously programs an EPROM with data specifying the Rx as well as instructions for dispensing the Rx. In one embodiment of the invention, the EPROM fits into a docking receptacle in the pump, while in a second embodiment the EPROM is integral with the therapy bag. A microcomputer mounted in the pump is programmed to control the flow of the Rx to the patient, reading the data from the EPROM in generating the control signals. The microcomputer cyclically drives a fluid control module which outputs a fixed amount of Rx for each cycle of operation.

Abstract: A method enables fluids to be administered intravenously to a patient using an intravenous (IV) fluid supply system. The method comprises coupling a first fluid path in flow communication to a first fluid reservoir, coupling an inlet of a drip chamber in flow communication to the first fluid path, coupling an outlet of the drip chamber in flow communication to a patient supply path, and coupling a bypass fluid path in flow communication to the first fluid path. The method also comprises directing fluid flow from the first fluid reservoir to the patient through the first fluid path and the drip chamber, and directing fluid flow from the first fluid reservoir to the patient through the bypass fluid path such that the drip chamber is bypassed.

Abstract: A vent system for an infusion drip chamber is provided according to the invention. The vent system includes an automatic air eliminator communicating with an interior and an exterior of the infusion drip chamber. The automatic air eliminator is capable of automatically venting air from the infusion drip chamber in a substantially continuous manner. The vent system further includes a mechanical air eliminator communicating with the interior and the exterior of the infusion drip chamber. The manual air eliminator is capable of mechanically venting air from the infusion drip chamber at discrete time intervals.

Abstract: The present invention relates to a nonreturn warning device for an intravenous drip infusion which includes a top member and a bottom member both of which forms an accommodation which has an inlet pipe and an outlet pipe at the top and bottom thereof. The outlet pipe includes a flange around which a recess is provided. A conic valve with a middle hole is arranged onto the flange. A float with a cylindrical stopper is received in the accommodation formed after connection of the top member and the bottom member. The middle section of the float contains a magnetic element, and a warning device is fitted beside the top member. Besides, a magnetic reed switch is installed in the warning device. As the float sinks with the fluid surface in the accommodation, the magnetic element approaches the magnetic reed switch and the magnetic force of the float will activate a buzzer for giving out a warning sound which is transmitted through a headphone jack or a radio transmitter to the nurses' call station.

Abstract: An intravenous infusion flow indicator including a housing defining an infusion liquid inlet and an infusion liquid outlet, a hydrophilic membrane disposed in the housing and being operative, when wetted, for permitting liquid flow and preventing air flow therethrough to the liquid outlet, wherein the liquid flow may be observed as droplets, the housing defining at least one volume, whose size and configuration are selected such that irrespective of the orientation of the housing following priming, infusion liquid within the housing is always in touching relationship with the membrane, thereby permitting continued infusion liquid flow therethrough.

Abstract: A laser strikes and aseptically heats or sterilizes the end of two flexible tube ends for connection. Tube holders are pushed toward each other to bring the tube ends into contact. A weld detector checks the characteristics of the weld. A laser optics assembly may be used to change the direction of the laser and focus the laser at the tube ends. In addition, a crimping device is used to compress a single flexible tube for disconnection. The laser strikes the compressed area. The crimping device continues to pinch the area and forms a seal in the tube. The tube is separated into two tube segments, each segment has a sealed end.

Abstract: The present invention is a flow metering system for accurately metering and regulating the flow rate of fluid in a gravity fed intravenous fluid delivery system. The fluid flow is directed through a flow path guide that is suspended at an angle from one end. As the fluid flows through the flow path guide, the flow path guide bends due to the weight of the fluid. A drop of fluid forms at the end of the flow path guide then falls off, thereby releasing the flow path guide, which springs back it its original position. The sequence of drops and springing back continues throughout the fluid delivery procedure, and is monitored by sensors. The resultant data is used by a processor to determine the flow rate of the fluid. The flow rate may be adjusted as needed by a flow regulator that is responsive to an adjustment actuator that is controlled by the processor.

Abstract: A prewarning device for instillation of medical liquid includes a throttling cylinder having a tubular needle connected to an open top thereof. A pointed head portion of the tubular needle is inserted into a medical liquid bottle for the medical liquid to flow into the throttling cylinder via the tubular needle. A portion of the tubular needle between the head portion and the throttling cylinder is transparent for a clamp to clamp therearound. A sensor is provided on the clamp to connect to a warning unit via a wire. The tubular needle defines a downward tapered inner space to receive a float therein. When the medical liquid bottle becomes empty, the float lowers in the tubular needle and is sensed by the sensor for the latter to actuate the warning unit to sound. The lowered float also blocks up the tubular needle to stop air from passing therethrough.

Abstract: By interposing an adapter between the endotracheal or tracheal tube inserted to a patient and the ventilation and suction systems that are connected to the endotracheal tube, a catheter could be inserted via an input port built into the adapter so as to enable a medical personnel to provide localized treatments in the lungs of a patient without having to disconnect either one of the systems connected to the endotracheal tube. The adapter is configured to have a securing mechanism that allows the medical personnel to secure the medication catheter in place. A one way valve fitted to the apertured arm that forms the input port of the adapter prevents any back flow of fluid from the input port.

Abstract: A method and device for volumetric measurement of a drop of fluid administered in a gravity intravenous set. Radiation, preferably infrared light is passed through from the exterior of the drip chamber of the intravenous set and is detected and quantified by a receiver on the other exterior side of the chamber. The radiation passing through the chamber when a drop is not passing through the radiation path is taken as the background radiation level. When a drop passes through the chamber a loss in radiation passing through to the receiver occurs. This relative loss is converted into a volume with the aid of a lookup table. The lookup table is created by accumulating empirical data of drops passing through various infusion sets determining a relative loss of radiation during the passing of the drop through the radiation and then weighing the drops and determining the volume of each drop in proportion to its specific gravity. The device and method is suitable for use with any IV set and is non-invasive.

Abstract: A catheter system for fluid connection between a patient's vasculature and a fluid system that has a luer lock connector including a luer tip. The catheter system includes a catheter having a hub having an open end sealed with an elastomeric septum. The hub defines a female luer sized to be received into and locked to the connector of the fluid system when the luer tip is advanced into the septum. A needle extends through at least a portion of the septum, the needle having a tip projecting adjacent the catheter tip and a needle hub disposed adjacent the outer face of the septum. The needle is removable from the catheter and septum after the catheter is advanced into a blood vessel. The elastomeric septum seals subsequent to withdrawal of the hollow needle to provide a sealed outer face for engaging and receiving the luer tip.

Abstract: A tubing set includes a length of tubing having at least a section thereof that is fabricated to function with an infusion pump. The tubing set further preferably includes a first valve that is removably connected to the length of tubing on a first end thereof. The first valve is preferably in a closed state when disconnected from the length of tubing. The tubing set also preferably includes a second valve on a second end thereof. The second valve is preferably in a closed state until connected to another fluid path component. The tubing set is preferably suitable for use in an MR environment.

Abstract: A system is used for identifying IV administration set components, wherein the IV set includes an IV solution container, a drip chamber having a hollow spike for introduction into the container, and an IV line for delivering the IV solution to a patient. The system includes a first identification element that is removably attached to the drip chamber for subsequent attachment to the container; a second identification element permanently affixed to the drip chamber; and a third identification element that is either permanently or removable attached to a Y-site or port in the IV line. In a preferred embodiment, the first identification element is a strip or patch that is adhesively attached to the drip chamber in a manner that will allow it to be removed therefrom for subsequent attachment to the container. The second identification element is a marker, preferably a strip or a patch, that is permanently affixed to the drip chamber.

Abstract: Methods and apparatus are described for controlling the temperature and flow rate of fluids being delivered to patients. A control unit is disclosed that interfaces with specialized fluid administration set apparatus. The control unit provides power, user interface and integrated pumping and heat exchange apparatus that interfaces with a cartridge on the fluid administration set. The fluid administration set is a disposable apparatus while the control unit is a reusable device. The entire system, due to its portability and engineering features, is adapted for use either in-hospital or in the pre-hospital, emergency setting.

Abstract: An occlusion prevention apparatus for a gastrostomy button system is provided. The apparatus includes an occlusion prevention tube comprised of a corrugated tube. The occlusion prevention apparatus may be in surrounding relation about a gastrostomy extension tube comprised of a flexible tube connecting a feeding bag adapter and a gastrostomy button adapter. The occlusion prevention apparatus may include a slit through the wall of the corrugated tube, which is operative to enable the flexible tube portion of the gastrostomy extension tube to slide into and out of an interior portion of the occlusion prevention tube. The occlusion prevention tube is operative to reduce the occurrences of blockages of nutrition in the gastrostomy extension tube while an individual is sleeping, and thereby reduce the number of audible warnings output by an alarm device monitoring the feeding process.

Abstract: An in-line drug delivery pack that connects in-line with an intravenous (IV) line and allows for the mixing of diluent with a drug reagent to be delivered to the patient. An internal drug bed bypass mechanism is tailored to apportion diluent flow between the bypass and the drug bed. The apportionment is selected to achieve a solution concentration suitable for IV administration as the dried reagent is dissolved. Thus, both dissolution and precisely tailored dilution are performed in the same simple device.

Abstract: A disposable flow set for use with a pump includes a first administration tube, at least one tube-segment having a first end and a second end, the first end connected to the first administration tube, a second administration tube connected to the second end of the at least one tube-segment; and an identifying key member connected to the at least one tube-segment. The identifying key member includes a number of teeth that define a unique code, including a combination of location and width. The teeth fit into compatible niches located in the pump.

Abstract: Devices and kits for intracranial and other perfusions and methods of using the same including a container having a top and bottom including a flexible bag adapted to be suspended in top to bottom orientation and to hold, in a main chamber, a solution, suspension or emulsion filled up to a fill line, a first opening to the bag located below the fill line and adapted to be fitted to conduit, a second opening located below the fill line and adapted to be fitted to conduit, and a first fluid pathway incorporated into the bag adapted to conduct fluid pumped into the second opening from below the fill line to an outlet within the bag located above the fill line.

Abstract: An anesthetic metering system includes an anesthetic reservoir (1) having an anesthetic reserve (2), which is limited by a flexible material wall and to which pressure is admitted by means of a propellant (3) acting thereon via the wall material. The anesthetic reservoir (1) has a first valve (4), which is in flow connection with the liquid anesthetic reserve (2) and can be inserted into a mounting element (6) of an anesthesia apparatus. The metered release of anesthetic to the anesthesia apparatus takes place via a volumetric nozzle (8). The present invention provides an anesthetic metering device which avoids, on the one hand, the drawbacks of the anesthetic evaporators used previously, which are to be refilled with anesthetics at the workplace, and makes possible the refilling of the anesthetic reservoir (1) at the anesthetic manufacturer, on the other hand.

Abstract: This invention provides an apparatus and method for emergency administration or self-administration of thrombolytic therapy in early stage of a heart attack. The apparatus includes a needle injector for making a venipuncture, a battery operated micro cooler for maintaining low temperature environment for vials with lyophilized thrombolytic and adjuvant drugs, a container with a diluent for reconstitution of the lyophilized drugs, a programmable infusion pump, and a microprocessor for controlling the process of infusion and recording the data. As the system is activated, said container becomes fluidly communicable with the infusion pump and vials with drugs in the cooler. Designed for autonomous execution of several schedules of infusion, it also can be controlled remotely by a qualified operator via an Internet interface.

Abstract: A device (100) such as a drip chamber that can be filled to a predetermined level is disclosed. The device comprises a housing (14) and a porous medium (10), wherein the porous medium allows gas to pass therethrough.

Abstract: A fluid flow regulator of a type having a variable outlet defined by a spacing between an outlet aperture and a flexible diaphragm, and in which the position of the flexible diaphragm varies as a function of a pressure differential between a sensing chamber on a first side of the diaphragm and an outlet chamber on a second side of the diaphragm. The regulator includes an adjustable flow impedance configuration in the flow path from the sensing chamber to the outlet chamber has a two elements providing opposing cylindrical surfaces in sliding contact. One of the cylindrical surfaces has a groove configured to define a flow-attenuating passageway having a net flow vector substantially parallel to the axis of the cylindrical surfaces. Axial relative movement between the elements causes a variation in an extent of overlap between the cylindrical surfaces, thereby varying an operative length of the flow-attenuating passageway.

Abstract: Apparatus for providing control of infusion delivery using conventional infusion fluid bags includes an air bag which is pressurised by a pneumatic pump. A digital camera or imaging device is able to analyse drops passing through a drop chamber, by capturing an image of the drop as it passes through the drop chamber. The output of the imaging device is fed to an image processor which calculates the volume of the captured drop using the number of pixels in the image. An infra red detector detects each time a drops passes through the drop chamber, and the outputs of the both the image processor and the infra red detector are passed to a master controller. The master controller controls the fluid delivery process by counting the number of drops passing through the drop chamber and controlling a flow brake to achieve the required flow rate.

Abstract: A drip chamber including an inlet member, a transparent housing chamber and an outlet member wherein an impinging member connected to the inlet member breaks the flow of the intravenous fluid when the fluid forms a indiscernible fluid stream to cause the fluid to accumulate into droplets that are readily visible by medical personnel.

Abstract: A drip chamber for a medical fluid delivery system includes a housing having an inlet port and an outlet port, and defining a chamber between the inlet and outlet ports, the housing configured to channel medical fluid in a flow path from the inlet port through the chamber and to the outlet port. The inlet port includes a tubular member that extends into the chamber and redirects the path of the medical fluid against a side wall of the housing to reduce the velocity of the medical fluid and minimize formation of air bubbles in the medical fluid.

Abstract: A drip chamber for an intravenous fluid delivery system includes a housing having an inlet port and an outlet port, the inlet and outlet ports each having an inner diameter, and the housing defining a chamber between the inlet and outlet ports. The housing configured to channel intravenous fluid in a flow path from the inlet port through the chamber and to the outlet port. A member supported in the chamber between the inlet and outlet ports is positioned so that the intravenous fluid flowing through the chamber impinges against the member to reduce the velocity of the intravenous fluid and minimize formation of air bubbles in the intravenous fluid. The inner diameter of the inlet port being substantially equal to or greater than the inner diameter of the outlet port, such that a flow rate of the intravenous fluid exiting the outlet port is substantially equal to or less than a flow rate of the intravenous fluid entering the inlet port.

Abstract: A combined arterial-venous blood flow set comprises connected lengths of flexible tubing for receiving blood from a patient, for conveying the blood to a blood processing device such as a dialyzer or an LDL filter, and for returning the blood to the patient. An optional first bubble trap chamber is connected in series flow between two of the lengths of tubing at a flow position downstream from the patient and upstream from the blood processing device. A second bubble trap chamber is connected in series flow between two of the lengths of tubing at a flow position downstream from the blood processing device and upstream from the patient. A first portion of the tubing which is in a flow position upstream from the blood processing device extends by the second bubble trap chamber, and is physically, laterally connected to it without direct flow connection. This helps to stabilize the positioning of components of the flow set and to reduce confusion in set-up and priming.