Abstract: Embodiments are directed to portable infusion devices, systems, and methods of using the same for dispensing materials. In some cases, the devices, systems and methods may be used for infusing a material such as medicament, e.g., insulin, into a body in need thereof.

Abstract: Apparatus and methods for inhibiting the introduction of air into the body during a percutaneous procedure. The apparatus may include an instrument passage lumen defining a degassing region with a degassing region distal end and a degassing region proximal end, a fluid inlet port at the degassing region distal end, and a fluid outlet port at the degassing region proximal end. So configured, fluid will flow only from the degassing region distal end to the degassing region proximal end.

Abstract: For the administering of medicaments, an adapter is provided for connection to a haemodialysis tube set, which makes possible the direct connection of a standard injection vial to the extracorporeal circuit, avoiding the introduction of air into the circuit. The adapter has two conduit pathways. The conduit pathway for the application of medicament contains a gas-blocking element. The second conduit pathway serves for the aeration of the injection vial.

Abstract: The present disclosure provides for an airless intravenous (IV) bag which contains a specialized device, referred to herein as the airless intravasculature infusion device (AIVID). The AIVID allows one to view the amount of fluid in the IV bag but substantially decreases or completely prohibits the risk of an inadvertent air infusion into a patient.

Abstract: A repeater system may control a pump by using a repeater and a user interface. An adhesive patch system may be used for affixing a pump or other object to a human body. Such an adhesive patch system may include two sets of adhesive members, each member including an adhesive material on at least one side so as to attach to the body. The members of the first set are spaced to allow the members of the second set to attach to the body in spaces provided between the members of the first set, and the members of the second set are spaced to allow members of the first set to detach from the body without detaching the members of the second set. Also, fill stations and base stations are provided for personal pump systems.

Abstract: A bubble trap for separating and collecting air and bubbles from a high flow rate stream of infusate includes multiple flow chambers to collect air, a sensor support mounted to one of the chambers, an air vent disposed in one of the chambers, and a valve in fluid communication with the chambers to control the flow of infusate therethrough.

Abstract: A system for preventing air from entering a first catheter of a multi-catheter system. Air is prevented from entering the proximal end of the first catheter by an axially elongate chamber having an impeller, the chamber being affixed to the proximal end of the first catheter. The air is removed through a port near the centerline of the chamber. Liquid removed with the air is returned to the chamber to minimize liquid loss during the procedure. A second catheter inserted through the chamber and into the first catheter is unable to entrain gas into the first catheter because any gas that enters the chamber is routed to the centerline of the chamber where it is removed. Inflow of fluid from an external pump scrubs the second catheter shaft of air bubbles attached by surface tension.

Abstract: There is provided a venting system for enteral feeding. The system has a tube in fluid communication with an enteral feeding site on a patient. The tube receives gas and liquid from the patient as enteral pressure within the patient increases. The tube has a vent that relieves enteral gas pressure from the patient and the tube also returns any liquid to the patient. There is also provided an enteral feeding system having a nutrient source in fluid communication with a nutrient pump. The pump discharges to an enteral feeding site on a patient. The system has a vent bag also in fluid communication with the enteral feeding site and the bag receives gas and liquid from the site as enteral pressure increases within the patient. The bag has a vent that relieves enteral gas pressure and allows liquid to be returned to the patient via the pump.

Abstract: A laminar valve flow module is disclosed and may include a proximal chamber, a purge chamber, and a sheath chamber in fluid communication with each other and between an inlet opening and an exit opening. A guide chamber may be located within the proximal chamber and in fluid communication with the inlet opening, the proximal chamber, and the sheath chamber. The sheath chamber is in fluid communication with the exit opening.

Abstract: A needle assembly includes a transparent or translucent housing with a fluid inlet end, a fluid outlet end, a flashback chamber and a venting mechanism therebetween. Substantially axially aligned inlet and outlet cannulas extend from the housing and communicate with the chamber. A sealable sleeve covers the external end of the outlet cannula. Relative volumes of the cannulas, the chamber and the sleeve are selected to provide rapid reliable flashback indicative of venous entry with an internal vent plug over the outlet of the flashback chamber to inhibit leakage of blood from the needle on withdrawal from the patient.

Abstract: Methods and devices for filtering a fluid flowing through a medical device are disclosed. In one example, a medical device may include a catheter shaft including a proximal region having a coupling for coupling to a fluid source and a distal region including one or more irrigation apertures for expelling a fluid from the catheter. A fluid path can be defined by the catheter shaft between the coupling and the one or more irrigation apertures. A porous member can be positioned at a location in the fluid path such that the fluid being expelled from the catheter via the one or more irrigation apertures may flow through the porous member to filter, reduce, and/or break-up bubble formations in the fluid.

Abstract: A pump system simply and selectably controls the temperature, flow rate, flow volume, and flow pressure of a fluid being infused into a patient's body. The pump system a includes a central controller and user inputs that allow for simple selection and efficient operation of the pump system, which includes manually or automatically priming the pump system to remove air, selectably controlling and rapidly adjusting the flow rate over a wide range, selectably and safely controlling the pump system temperature controls, and selectably controlling the flow pressure during delivery. The pump system includes a pump housing with a central controller and a cartridge with infusion tubing removably coupled to the pump housing.

Abstract: A septum activator is disclosed herein. The septum activator has an outer tubular body and an inner tubular body. The outer tubular body and the inner tubular body each have a plurality of openings therein. The inner tubular body has a first position relative to the outer tubular body and a second position relative to outer tubular body. In the first position, the plurality of openings of the inner tubular body do not overlap with the plurality of openings in the outer tubular body. In the second position, the plurality of openings of the inner tubular body overlap with the plurality of openings of the inner tubular body.

Abstract: A pierced septum valve is disclosed herein. The pierced septum valve includes a septum that is located within a lumen of a body. A septum activator is positioned proximal the septum within the lumen of the body. A seal is disposed between an outer surface of the septum activator and the body to seal the portion of the septum activator distal the lumen from the portion of the septum activator proximal the lumen. One or more vents are disposed between the seal and the lumen of the body to permits the passage of air but not blood past the seal.

Abstract: An apparatus and a method for connecting medical tubing or any other type of fluidic circuit conduits (e.g., cannulae) to a ventricular assist device (“VAD”) or any other pumping device used for blood pumping during cardiac circulatory support for vascular surgery. The apparatus and the method prevent air bubbles from entering a cardiac circulatory support system when connecting cannulae to a VAD that may later enter the blood stream of a patient during cardiac surgery, and also provide for purging any air bubbles that may have entered the cardiac circulatory support system during a cannulae-VAD connection.

Abstract: An IV catheter introducer assembly including a catheter hub defining a chamber; a tubular member extending distally from the catheter hub having a length and defining a lumen, the lumen being in fluid communication with the chamber and configured to removably receive an introducer needle. The device also including a retention member disposed within the chamber having a body having a central lumen having a longitudinal length extending along a lengthwise direction to the length of the tubular member and sized to seal against an introducer needle. The retention member including a venting channel having at least a portion formed as a conic helix traversing a surface of the retention member along a radial path to the lengthwise direction.

Abstract: Various embodiments of the present invention are directed to limiting a presence of air bubbles in a fluidic medium expelled from a reservoir. In various embodiments, a plunger head within a reservoir is shaped so as to limit a presence of air bubbles in a fluidic medium expelled from the reservoir. Also, in various embodiments, a reservoir is shaped so as to limit a presence of air bubbles in a fluidic medium expelled from the reservoir. In some embodiments, both a reservoir and a plunger head within the reservoir are shaped so as to limit a presence of air bubbles in a fluidic medium expelled from the reservoir.

Abstract: A vascular access device incorporating a luer integrated air venting system, including a female luer fitting having a venting mechanism located within the female luer fitting and a fluid diverter located within the vent mechanism. The venting mechanism providing communication between said vascular access device and ambient surroundings until contact with a fluid.

Abstract: A Luer access device may include a housing, a septum, and a gas permeable vent in communication with at least a portion of the housing for venting gas from an extravascular system. A method of venting a medical device may include providing a gas permeable vent within a Luer access device as part of an extravascular system and venting gas from the extravascular system through the gas permeable vent of the Luer access device.

Abstract: A vascular access device may include a septum and a gas permeable vent in communication with at least a portion of the septum. The vent may be capable of venting gas from an extravascular system to which the vascular access device is capable of attaching. A method of venting a medical device may include providing a vascular access device having a septum and forming part of an extravascular system, providing a gas permeable vent in communication with at least a portion of the septum, and venting gas from the extravascular system through the gas permeable vent of the device.

Abstract: A device for priming and venting a hazardous drug within an intravenous administration set. The device includes various access ports and fluid channels to permit direct injection of a hazardous drug into the fluid reservoir, while eliminating the possibility of undesirable exposure to the hazardous drug. The device further includes priming and flushing ports to enable flushing of a hazardous drug from the system following an infusion procedure.

Abstract: A system for preventing air from entering a first catheter of a multi-catheter system. Air is prevented from entering the proximal end of the first catheter by an axially elongate chamber having an impeller, the chamber being affixed to the proximal end of the first catheter. The air is removed through a port near the centerline of the chamber. Liquid removed with the air is returned to the chamber to minimize liquid loss during the procedure. A second catheter inserted through the chamber and into the first catheter is unable to entrain gas into the first catheter because any gas that enters the chamber is routed to the centerline of the chamber where it is removed. Inflow of fluid from an external pump scrubs the second catheter shaft of air bubbles attached by surface tension.

Abstract: An infusion pump comprising a substance and pushing fluid inlet, a substance outlet, a central chamber communicating with said inlet and said outlet, and injecting means for injecting a substance into a biological object, wherein the infusion pump further includes a pushing fluid outlet in communication with the central chamber in such a way as to allow a pushing fluid to exhaust the pump. The outlet of the infusion pump is advantageously connected to the proximal end of a catheter, the distal end being inserted into the biological object. A sensor, e.g., an optical device, is preferably placed at the outlet of the infusion pump and checks that the outlet is free of gas. The infusion pump is preferably remotely controlled so that it can be placed in limited access locations. It is also preferably computer controlled.

Abstract: A method and pump that accurately senses air in a fluid delivery line pulses or activates and deactivates the air sensor(s) multiple times during the pumping phase of the fluid delivery cycle and can generate alarms based upon a single indication or a cumulative indication of air in the line. The pump can include multiple air sensors spaced along the delivery line so that the method can use the multiple signals therefrom to distinguish real moving air bubbles from false positives and/or air bubbles adhered to the inner wall of the line.

Abstract: A system for controlling fluid flow in a catheter assembly is disclosed herein. An intravenous catheter assembly has a catheter adapter and a needle hub, and the catheter adapter has an inner lumen. A septum is disposed within a portion of the inner lumen, and a slit is formed through the septum. A Parylene coating is disposed within the slit of the septum, the Parylene coating has a thickness of between approximately 0.00005 to 0.0005 millimeters. An introducer needle has a first end coupled to the needle hub and the second end extending through the inner lumen of the catheter adapter. A middle portion of the introducer needle is positioned within a portion of the septum.

Abstract: A flushable catheter assembly having features to enable selective activation of fluid flow through the catheter assembly is disclosed herein. A septum is placed within the catheter adapter of the catheter assembly and includes a pathway that is closed prior to being biased open via a septum activator also positioned within the catheter adapter. A plurality of air vent channels is interposed between the septum and the inner surface of the catheter adapter to permit “flashback” of blood during insertion of the catheter into a patient. The septum activator is advanced through the pathway of the septum as a coupler is attached to a proximal opening of the catheter adapter.

Abstract: The invention relates to a drug delivery device (1, 100), in particular for the delivery of drugs comprising molecules tending to spontaneously form nucleation seeds leading to fibrils, comprising a drug reservoir (2, 102) having a reservoir outlet (107) connected to a device outlet, adapted to deliver a drug fluid to a patient's body, through a pathway (5) including a fluid flow controlling system (4, 104). The pathway further includes a filtration module (6, 106) adapted to retain the nucleation seeds, preferably by forcing them through a filtering membrane pores and on the basis of hydrophobic interaction with the membrane.

Abstract: A medical fluid delivery system includes a fluid disposable configured to hold and transport a medical fluid and an air separation chamber in fluid communication with the fluid disposable. The air separation chamber includes at least one fluid baffle floating within the air separation chamber and configured to separate air from medical fluid traveling through the chamber.

Abstract: A fluid chamber having an inlet and an outlet at the top of the chamber. The inlet is arrange so that fluid entering the chamber at the inlet sweeps the top of the chamber so as to direct any air bubbles naturally collecting at the top of the chamber or which may be trapped in the entering fluid stream toward the outlet.

Abstract: A device, system and method deliver an agent to a soft mass, such as an area of the body, and more specifically the brain. One aspect includes creation of one or more channels, tunnels or grooves in tissue using a relatively small diameter, minimally-invasive stylet and then removing the stylet prior to infusion. The stylet-created channels become paths of increased hydraulic conductivity, through which the infusate will tend to flow and produce a predictable infusion pattern. Infusate will be carried into these channels with relatively low resistance, and then infuse outward from these channels into the surrounding tissue. By carefully positioning these channels, one can control and modify the preferred paths and duration of distribution.

Abstract: A system for preventing air from entering a first catheter of a multi-catheter system. Air is prevented from entering the proximal end of the first catheter by an axially elongate chamber having an impeller, the chamber being affixed to the proximal end of the first catheter. The air is removed through a port near the centerline of the chamber. Liquid removed with the air is returned to the chamber to minimize liquid loss during the procedure. A second catheter inserted through the chamber and into the first catheter is unable to entrain gas into the first catheter because any gas that enters the chamber is routed to the centerline of the chamber where it is removed. Inflow of fluid from an external pump scrubs the second catheter shaft of air bubbles attached by surface tension.

Abstract: A rotary medical manifold, for delivering various fluids through a patient delivery mechanism is described. The rotary manifold can include a manifold body and a valve stem. The manifold body can include a central cavity, an output port, a first fluid port, and a second fluid port. The valve stem can include an injector port, and a single central fluid passage. The valve stem can be adapted to slibably engage the central cavity of the manifold body and provide selective fluidic connectivity between the injector port and the output port, the first fluid port and the second fluid port.

Abstract: An improved surgical cassette for controlling intraocular pressure during ophthalmic surgery.

Abstract: A drip chamber for intravenous infusion including a support member having a longitudinal axis, two ends and at least one support face distanced from both ends, a membrane joined to the at least one support face, and a support member outlet formed in the support member and in fluid communication with the membrane, the support member outlet including a bore and being fluidly communicable with an outlet of the drip chamber.

Abstract: A kit for charging an infusion pump having a reservoir for holding a local anesthetic. The kit includes a first stopcock having an input port, a first input/output port and a second output port and a manual control for selectively coupling either the first input/output port or the second output port to the input port. The kit further includes a second stopcock having an input port, first and second output ports and a manual control for selectively coupling either the first output port or the second output port to the input port. The second output port of the first stopcock is adapted for coupling to the input port of the second stopcock. The kit further includes a syringe adapted to be coupled to the first input/output port of the first stopcock and tubing for coupling the input port of the first stopcock to a source of the liquid and for coupling the output port of the second stopcock to an input port of the pump.

Abstract: Disclosed is a drug delivery infusion pump assembly containing a drug delivery pump, a drug delivery cassette, a pump door, and a housing adapted to receive a drug vial. A drug vial centering mechanism ensures varieties of drug vial sizes are compatible with this device. The drug delivery cassette is capable of being positioned on the drug delivery infusion pump assembly so the drug delivery pump will interface with a drug delivery tube located on the drug delivery cassette.

Abstract: A bubble trap for separating and collecting air and bubbles from a high flow rate stream of infusate includes multiple flow chambers to collect air, a sensor support mounted to one of the chambers, an air vent disposed in one of the chambers, and a valve in fluid communication with the chambers to control the flow of infusate therethrough.

Abstract: A surgical cassette having a chamber for fluidly coupling to a source of vacuum in a surgical console and a bubble breaking structure disposed within the chamber. The cassette protects the source of vacuum from liquid.

Abstract: A flushable catheter assembly having features to enable selective activation of fluid flow through the catheter assembly is disclosed herein. A septum is placed within the catheter adapter of the catheter assembly and includes a pathway that is closed prior to being biased open via a septum activator also positioned within the catheter adapter. A plurality of air vent channels is interposed between the septum and the inner surface of the catheter adapter to permit “flashback” of blood during insertion of the catheter into a patient. The septum activator is advanced through the pathway of the septum as a coupler is attached to a proximal opening of the catheter adapter.

Abstract: Disclosed is a drug-delivery cassette for use with a drug delivery device. The cassette includes a main board and a luer site base portion connected to the main board for positioning a luer on the main board. A drip chamber is included on the main board to collect any drug that exits the luer when the luer is attached to the luer site portion. A deflectable sensor beam is positioned to detect the presence or absence of a luer in the luer site base portion. The drug-delivery cassette further includes a drug vial spike attachable to and detachable from the cassette main board that is connected to the luer by way of a drug delivery tube.

Abstract: A syringe device includes a syringe tube having a distal end with a passageway in fluid communication with a cavity thereof. A plunger rod slidingly and sealingly engages within the cavity of the syringe tube. The plunger rod includes at least one aperture in fluid communication with a hollow interior of the plunger rod. A plunger tip is engaged with a distal end of the plunger rod and interacts with an inner surface of the side wall of the syringe tube to separate the cavity into first and second areas. The at least one aperture fluidly connects the hollow interior of the plunger rod and the first area of the syringe tube cavity, such that the generally hollow plunger rod interior allows air to move between an outside of the syringe device and the first area of the cavity during sliding movement of the plunger rod within the syringe tube.

Abstract: A vented needle assembly is provided for sealably injecting biomaterial into an intradiscal space interiorly of the annulus of a spinal disc and for providing an exhaust for the intradiscal space. The vented needle assembly comprises a compressible seal body for pressing against an outer surface of the annulus, and a needle extending through the seal. The needle may be configured to connect to a syringe for pressure injection of the biomaterial. The seal includes a vent extending therethrough with an opening for communication with the intradiscal space and an opening for the discharge of excess biomaterial filling the intradiscal space. A kit of parts is also provided for use in the treatment of a spinal disc, the kit comprising the vented needle assembly and an inflatable trial device. The trial device is removably introduced into the intradiscal space and inflated to determine the available size of the intradiscal space.

Abstract: An improved surgical cassette for controlling intraocular pressure during ophthalmic surgery.

Abstract: The present invention relates to a system for increasing the temperature of a fluid being infused into a patient's body while the infusion is taking place. The present invention also provides for improved monitoring of air in the infusion system such to prevent the introduction of air into the patient's body receiving the fluid infusion. The present invention also provides for a system pump which provides a variable flow rate that serves a vast amount of infusion needs and purposes. A disposable cartridge in accordance with the present invention will allow for the efficient transfer of heat energy to the fluid being infused into the patient's body. The cartridge will further ensure that deleterious amounts of air will not be introduced into the patient's body.

Abstract: A sensor for sensing inclusions in a containerized medical fluid. In certain embodiments, the sensor may include an image capture device and an image processor communicatively interconnected to the image capture device. The image processor may include an inclusion identifier configured to detect data in an image indicative of inclusions in the medical fluid.

Abstract: A pre-filled syringe including a barrel 1, a base end gasket 4 which is fluid-tightly slidable in the barrel 1, a front end gasket 8 which is fluid-tightly slidable in the barrel 1, and a nozzle part 2 provided in a front end of the barrel 1, wherein the nozzle part 2 includes a front end gasket accommodation part 23 which is capable of accommodating the front end gasket 8, and liquid flow passages 21 extending in an axial direction in an inner periphery wall, through which a liquid medicine can pass when the front end gasket 23 is accommodated in the front end gasket accommodation part 23, and a sectional area of a front end of the liquid flow passages 21 is smaller than a sectional area of a base end.

Abstract: A priming indicator for a fluid infusion system includes a luer cap or other component of the infusion system having an indicator surface covered by a membrane. The membrane exhibits a first visual characteristic, such as being opaque, when dry and exhibits a second characteristic, such as becoming less opaque, when wet. Once the membrane becomes wet, indicia on the surface, which may be provided on a rod at least partially covered by the membrane, becomes visible, thereby indicating an intravenous tube to which the luer cap is secured has been primed or is nearly primed. The indicator may alternately be employed at an upstream end of an infusion set, such as at the port of a medical bag providing a supply of fluid, to indicate a low level of fluid in the medical bag.

Abstract: An extravascular system may include a fluid path and a gas vent in communication with the fluid path. A method of venting a medical device may include providing a closed extravascular system having a fluid path, providing a gas vent in communication with the fluid path, venting gas from the extravascular system through the gas vent, and maintaining closure of the extravascular system during and after venting.

Abstract: A vascular access device incorporating a luer integrated air venting system, including a female luer fitting having a venting mechanism located within the female luer fitting and a fluid diverter located within the vent mechanism. The venting mechanism providing communication between said vascular access device and ambient surroundings until contact with a fluid.

Abstract: Systems and methods handle air and rinsing fluid during fluid processing. The systems and methods eliminate air from a fluid processing system prior to, during, and after use. The systems and methods provide a connector assembly for establishing fluid flow from a fluid source. The connector assembly has discrete first and second passages that prevent communication between the fluid in first passage and the fluid in the second passage. Prior to system use, the connector assembly may be utilized in a priming function to remove residual air from a fluid circuit prior to use. The connector assembly may also be utilized after use to perform a rinse-back function.