Abstract: A flow control tip for a catheter comprises a partition dividing the catheter into first and second lumens, a first orifice fluidly connected to the first lumen and a second orifice fluidly connected to the second lumen, the first orifice being proximal to the second orifice, an elongate protrusion extending along a portion of the partition substantially along a centerline of the elongated body and a deflecting surface extending at an angle relative to the protrusion to direct flow from the first orifice away from the centerline.

Abstract: An implantable shunt that includes one or more catheters configured so that the implantable shunt has a resistance to flow greater than about 3 mm Hg/mL/minute. An implantable shunt system that includes one or more catheters and a fluid control device that utilizes the properties of the catheters to improve the expected function of the shunt by providing a higher or lower resistance to the flow through the shunt and reduces the effect of pulsations of cerebrospinal fluid on the shunt system.

Abstract: Multi-lumen catheters with improved tip configurations, including a triple-lumen catheter which may be useful for apheresis. In one variation, the catheter has three lumens with distal openings angularly spaced apart and staggered axially with respect to one another. In another variation, the catheter has two lumens exiting distally and one centrally positioned lumen exiting proximally. A third variation is a catheter with a single distal opening and two proximal openings. The staggered lumen openings along the axial length of the catheter may decrease recirculation while maximizing flow rates.

Abstract: A system for perfusing a localized site within a body includes a catheter assembly having a venous access line that is adapted to deliver perfusate to the localized site, a venous or arterial drainage line adapted to drain perfusate from the localized site, and an occlusion device adapted to prevent some or substantially all physiological blood flow between the localized site and the systemic circulation of the body during and in the course of perfusing and draining perfusate to and from the localized site. The system may include a blood circuit associated with the catheter assembly to facilitate blood conditioning for use as the perfusate, in the course of a controlled perfusion and/or drainage of untreated, treated, or inactivated treated blood to and from the localized site.

Abstract: The invention relates to a surgical system for controlling a fluid. The system includes an irrigation line, which is connected at one end to a first fluid container for holding irrigation fluid, and which is connected at another end to a surgical handpiece. The system also includes an aspiration inlet line, which is provided from the surgical handpiece to an inlet of a suction pump, such that fluid can be sucked through the handpiece by the suction pump. The system further includes a second fluid container for holding the irrigation fluid, and an aspiration ventilation line, which connects the second fluid container to the aspiration inlet line. In addition, the system includes a venting valve, which is provided in the aspiration ventilation line and which can be switched as a function of a fluid pressure in the aspiration inlet line. The second fluid container can be filled via a filling line.

Abstract: An ear medication delivery device for delivering a treatment liquid and retaining the treatment liquid within an ear canal of a patient including a unitary, one piece earplug formed of a soft resilient material including an ear canal engaging portion and an external portion and defining a single internal passage therethrough. The external portion includes a major disk and an annular medication applicator receiving portion in fluid communication with the internal passage. The ear canal engaging portion includes at least two minor disks of progressively different size extending outwardly in a generally radial direction. The ear canal engaging portion defines a molded resilient valve unitary with the earplug that is shiftable from a closed position to an open position in either direction under a preselected fluid pressure and that resiliently returns to the closed position below the preselected fluid pressure.

Abstract: Devices adapted to facilitate draining fluid from the abdominal/peritoneal cavity of a medical patient. The invention may be embodied in one or more element of an access port, insertion assist device, and/or abdominal catheter. A preferred abdominal catheter provides a drain field that can be inserted into the abdominal compartment, through an access opening having a small cross-section, in a stowed configuration and subsequently expanded to provide a large drain area through which to extract fluid from the compartment.

Abstract: An apparatus having a tube section and an expanded end. The tube section is flexible while the end section is rigid. The apparatus has a central bore, large enough to loosely receive an endoscope tube, and the end section has two peripheral bores which communicate with the central bore. There is a collar around the central bore which allows formation an air- and water-tight seal with the head of an endoscope. The tube may be fenestrated at its proximal end and may include medial pleats. This apparatus is mainly used by: sliding an endoscope into the central bore until the endoscope head forms an air- and water-tight seal with the central bore; connecting a lavage tube to one peripheral bore and a vacuum tube to the other peripheral bore; inserting the endoscope and the apparatus into a GI tract; and manually controlling the apparatus to apply lavage and vacuum.

Abstract: An ingestible capsule is provided for delivering medication to a subject. A capsule coating dissolves in a gastrointestinal tract of the subject. An inner core of the capsule has an outer surface associated therewith. The outer surface is disposed within the coating and expands when the coating dissolves. A medication is disposed on the outer surface, and the outer surface is configured such that the medication contacts an intestinal wall of the subject when the outer surface expands. Other embodiments are also provided.

Abstract: A bi-directional perfusion cannula is provided that includes an elongate tube for insertion into an artery. The elongate tube has a first aperture at a distal end of the tube which is forward during insertion and configured so that blood can flow into the artery in the direction of insertion, an elbow formed in the elongate tube, and a second aperture formed in or slightly rearward of the elbow and configured for supplying blood into the artery in a second direction which is generally opposite to the insertion direction.

Abstract: A dialysis catheter is provided which makes it possible to improve patency without reducing the ease of insertion, while also making it possible to effectively suppress the “clinging phenomenon”. The dialysis catheter has a first portion provided with a thickened part which increases the thickness of the peripheral wall of a blood feed lumen on the blood removal lumen side thereof, and the cross-sectional area of the first portion is smaller than the cross-sectional area of a second portion.

Abstract: Devices and methods are disclosed to conduct fluid away from or deliver fluid to an area of a treatment site of a patient's body. For example, a catheter is provided having a terminal end with a non-linear shape such that fluid is delivered to or drained from an area of a treatment site.

Abstract: A multi-path catheter includes an elongate tubular member and a withdrawal pathway along which unfiltered fluid is withdrawn in a distal to proximal direction. The withdrawal pathway originates at a distal point and is at least partially defined by the elongate tubular member. The elongate tubular member also defines, at least partially, at least one infusion pathway along which filtered fluid is returned in a proximal to distal direction. The at least one infusion pathway extends distally beyond the withdrawal pathway. First and second legs of the elongate tubular member are positioned on opposing sides of the withdrawal pathway at the distal point, and the at least one infusion pathway is at least partially defined by one of the first and second legs. The first and second legs have outer walls that are unattached to one another at distal ends thereof.

Abstract: A multilumen catheter with an inflow or an outflow lumen having at least two tube extensions extending from the distal end of the catheter that open into the inflow or outflow lumen. A device to selectively test each of the two tube extensions for occlusion.

Abstract: Devices and methods for the effective clearing of artificial tubes, especially in-situ clearing of artificial tubes in a living being are covered in this disclosure. The devices and methods provide an elongated clearing member having a first end that is coupled to a driving mechanism and having a second working end that is subjected to repetitive motion for clearing blockages within the artificial tube. The elongated clearing member includes either a fixed or an adjustable element that selectively defines the portion of the elongated clearing member that is insertable within the artificial tube. The proximal end of the clearing member is releasably secured to the driving mechanism and the driving mechanisms may comprise a wide variety of repetitive motion drivers such as voice coil motors, piezoelectric actuators, pneumatic actuators, DC motors, etc. These devices/methods may comprise a free-standing console for hands-free operation or may comprise hand-held versions.

Abstract: A dual lumen gastrointestinal feeding and aspirating device includes an aspiration channel which carries a feeding channel. The aspiration channel has a distal opening with a larger size than that of the feeding channel so it can operate more effectively as a stent and accommodate larger sized instruments. The distal end of the aspiration channel is repeatably moveable between open and closed conditions in response to the extension and retraction, respectively, of the instrument therethrough.

Abstract: A dual lumen gastrointestinal feeding and aspirating device includes an aspiration channel which carries a feeding channel. The aspiration channel has a distal opening with a larger size than that of the feeding channel so it can operate more effectively as a stent and accommodate larger sized instruments. The distal end of the aspiration channel is repeatably moveable between open and closed conditions in response to the extension and retraction, respectively, of the instrument therethrough.

Abstract: A multitube catheter is provided. The assembly includes two or more tubes fused together to form one catheter tube shaft. Each tube has at least one lumen extending longitudinally through the catheter from its distal end to its proximal end. The tubes are fused together by use of heat and pressure. A distal end of the united catheter tube can be split to form a split tip, stepped tip, or a tapered tip. The proximal segment (non-fused portion) forms catheter extension legs.

Abstract: A multiple catheter assembly including first and second catheters. The first catheter includes a first catheter outer surface defining a first lumen, a first distal end terminating in a first distal tip, and a first transition region. The second catheter includes a second catheter outer surface defining a second lumen, a second distal end terminating in a second distal tip, and a second transition region. At least a portion of each of the first and second catheters resides in a cannulating portion. The first and second transition regions of the first and second catheters transition cross sections of the first and second catheter outer surfaces at the first and second distal tips to cross sections of the first and second catheter outer surfaces in the cannulating portion. In exemplary embodiments, the portions of each of the first and second catheters in the cannulating portion are releasably bonded to one another.

Abstract: A multiple catheter assembly (100) including a first catheter (110) having a first proximal end region (112), a first distal end region (114) terminating in a first distal tip (116), and an outer surface (120) defining at least a first lumen (122) extending longitudinally therethrough between a first distal and a first proximal opening. The assembly (100) also includes a second catheter (130) having a second proximal end region (132), a second distal end region (134) terminating in a second distal tip (136), and a second outer surface (140) defining at least a second lumen (142) extending longitudinally therethrough between a second distal and a second proximal opening. The first (122) and second (142) lumens are independent from each other for facilitating simultaneous flow in opposite directions.

Abstract: A micro-dialysis probe extending longitudinally between a proximal probe opening and a distal probe tip and having a supply line and a drainage line for a drip-feed solution. A tube may be provided for supporting the drainage line. A dialysis section, wherein the flow channel for the drip-feed solution experiences an inversion, is formed generally between the supply line and the drainage line, in the vicinity of the distal probe tip. The supply line and the drainage line are respectively arranged substantially side by side and together form the probe shaft of the micro-dialysis probe.

Abstract: A combined surgical implement used in stomach reduction surgery and for serving as a template and testing integrity of a newly-formed gastric pouch is disclosed. A primary tube extending into a stomach of a patient carries a balloon inflatable to define a size and shape of a newly formed gastric pouch. Suction is applied through the tube to remove the stomach contents and deflate the stomach around the balloon, after which the gastric pouch is surgically formed. After surgical completion of the pouch, the pouch is tested by pressurizing and the pressure monitored. If a leak is present, the pressure falls and air bubbles in the saline solution surrounding the gastric pouch become evident, immediately indicating a leak in the newly-formed gastric pouch, which then may be repaired to seal the leak.

Abstract: A method for inserting a multiple catheter assembly into a patient. The assembly includes a first catheter which includes a first distal end region, a first outer surface defining a first lumen, and a first transition region transitioning cross sections of the first outer surface and the first lumen. A second catheter includes a second distal end region, a second outer surface defining a second lumen, and a second transition region transitioning cross sections of the second outer surface and the second lumen. The outer surfaces of the first and second catheters are releasably joined by a splittable bond for allowing first and second distal tips of the assembly to be at least partially longitudinally split from each other. The method includes steps of separating the first and second distal end regions, and inserting the first and second distal tips through an incision and into an area to be catheterized.

Abstract: A dual lumen guidewire support catheter for accurately crossing a chronic total occlusion in a vessel is disclosed. The dual lumen guidewire support catheter includes a first lumen portion and a second lumen portion sharing a common side and a common distal end. The first lumen portion can be a rapid exchange or over-the-wire portion, while the second lumen portion is an over the wire portion. One or both of the portions can include a discontinuity to enable removal of a guidewire following placement through or at an occlusion or lesion.

Abstract: A catheter is adapted to exchange heat with a body fluid, such as blood, flowing in a body conduit, such as a blood vessel. The catheter includes a shaft with a heat exchange region disposed at its distal end. This region may include hollow fibers which are adapted to receive a remotely cooled heat exchange fluid preferably flowing in a direction counter to that of the body fluid. The hollow fibers enhance the surface area of contact, as well as the mixing of both the heat exchange fluid and the body fluid. The catheter can be positioned to produce hypothermia in a selective area of the body or alternatively positioned to systemically cool the entire body system.

Abstract: An endoscope or other medical device includes a number of lumens positioned in an outer shaft. The lumens are formed as a multiple lumen assembly. In one embodiment, individual lumens are connected to each other with a sheet or webbing material. The lumen assembly is rolled or folded along its length for incorporation into the outer shaft of the medical device. The sheet or webbing material may be notched or perforated to facilitate folding the lumen assembly and/or separating individual lumens from the lumen assembly.

Abstract: The present disclosure relates to catheterization systems and components thereof. In one embodiment of the present disclosure, a catheterization system is disclosed that includes a catheter including a body with proximal and distal ends and defining first and second lumens extending therethrough, and a stylet. The stylet includes first and second stylet portions each having proximal and distal end regions, wherein the distal end regions of the first and second stylet portions together define a tapered penetrating portion. The first and second stylet portions are configured and dimensioned to be slidably positioned within the first and second lumens of the catheter, respectively. The first and second stylet portions extend from the proximal end of the catheter and beyond the distal end of the catheter, and are independently movable in relation to each other to facilitate selective removal of the first stylet portion and/or the second stylet portion from the catheter.

Abstract: A pumping system for use in medical applications where liquids must be infused and aspirated from a mammalian patient, and whose economics are such that it is cost effective to simply dispose of it after a single use. The system features positive displacement pump(s) such as reciprocating pump(s) containing a damping mechanism to dampen out the peaks and valleys in the fluid pressure that is pumped, which is important for preventing cavitation. The system furthermore features a shut-off valve on the extraction side so that certain injected fluids such as contrast medium, are not immediately pumped out of the patient. In a preferred embodiment, the system also features means for independently controlling the fluid pressure/volume on the infusion and extraction sides, self-priming capability, a continuous fluid path, and visual air bubble detection, with viewports located at important points in the fluid path, such as at pumps and valves.

Abstract: The present invention concerns a double-lumen catheter and a method for delivering or withdrawing fluids to/from a patient, in particular for use in hemodialysis. The double-lumen catheter comprises an elongated tubular body having a proximal end and distal end, with the distal end being positionable within a vessel of a patient, a divider wall extending along an interior of said tubular body and separating said interior into an intake lumen and a return lumen. The intake lumen and said return lumen each comprise an opening sloping toward the divider wall and toward the distal end of the tubular body, respectively, the openings.

Abstract: An anti-extravasation sheath includes a tube sized and dimensioned to permit fluid flow between the inner surface of the tube and an outer surface of an arthroscopic instrument when the arthroscopic instrument is disposed within the tube. A plurality of ribs extending inwardly from the inner surface of the tube and running longitudinally along the tube form a seal between the outer surface of the arthroscopic instrument, thus defining outer lumens between the outer surface of the arthroscopic instrument and the inner surface of the tube. At least one drainage lumen extending longitudinally along the tube and disposed within the ribs is in fluid communication with at least one drainage aperture disposed on the central portion of the tube.

Abstract: A catheter is adapted to exchange heat with a body fluid, such as blood, flowing in a body conduit, such as a blood vessel. The catheter includes a shaft with a heat exchange region disposed at its distal end. This region may include hollow fibers which are adapted to receive a remotely cooled heat exchange fluid preferably flowing in a direction counter to that of the body fluid. The hollow fibers enhance the surface area of contact, as well as the mixing of both the heat exchange fluid and the body fluid. The catheter can be positioned to produce hypothermia in a selective area of the body or alternatively positioned to systemically cool the entire body system.

Abstract: A catheter is adapted to exchange heat with a body fluid, such as blood, flowing in a body conduit, such as a blood vessel. The catheter includes a shaft with a heat exchange region disposed at its distal end. This region may include hollow fibers which are adapted to receive a remotely cooled heat exchange fluid preferably flowing in a direction counter to that of the body fluid. The hollow fibers enhance the surface area of contact, as well as the mixing of both the heat exchange fluid and the body fluid. The catheter can be positioned to produce hypothermia in a selective area of the body or alternatively positioned to systemically cool the entire body system.

Abstract: A catheter is adapted to exchange heat with a body fluid, such as blood, flowing in a body conduit, such as a blood vessel. The catheter includes a shaft with a heat exchange region disposed at its distal end. This region may include hollow fibers which are adapted to receive a remotely cooled heat exchange fluid preferably flowing in a direction counter to that of the body fluid. The hollow fibers enhance the surface area of contact, as well as the mixing of both the heat exchange fluid and the body fluid. The catheter can be positioned to produce hypothermia in a selective area of the body or alternatively positioned to systemically cool the entire body system.

Abstract: A catheter is adapted to exchange heat with a body fluid, such as blood, flowing in a body conduit, such as a blood vessel. The catheter includes a shaft with a heat exchange region disposed at its distal end. This region may include hollow fibers which are adapted to receive a remotely cooled heat exchange fluid preferably flowing in a direction counter to that of the body fluid. The hollow fibers enhance the surface area of contact, as well as the mixing of both the heat exchange fluid and the body fluid. The catheter can be positioned to produce hypothermia in a selective area of the body or alternatively positioned to systemically cool the entire body system.

Abstract: A peritoneal-based (“bloodless”) artificial kidney processes peritoneal fluid without need for additional fluids (“waterless”). Fluid is separated into a protein-rich stream and a protein-free stream. The protein-rich stream is regenerated using a sorbent assembly, and its protein composition can be modified by removal of selected protein(s) (“dialysate-pheresis”). It is then reconstituted with additives and returned into the peritoneal cavity, thereby reducing protein-loss and providing oncotic-pressure for ultrafiltration. The protein-free stream is used to produce free water, and an alkaline or acid fluid for optimization of the composition of the regenerated stream. The unused protein-free stream can be used to “reverse flush” the separator to maintain its patency and the excess discarded for fluid-balance regulation.

Abstract: A device for transferring fluids between an internal structure in a living body and an exterior thereof, comprises a housing including a pressure activated lumen extending to a distal end opening to a power injection lumen that extends to a distal port configured for connection to a fluid conduit extending to a target structure within the body and a pressure activated valve extending across the pressure activated lumen and controlling fluid flow therethrough, the pressure activated valve opening to permit fluid flow therethrough into the power injection lumen when a fluid pressure differential thereacross is at least a first predetermined threshold level and remaining sealed when the fluid pressure differential thereacross is less than the first threshold level in combination with a proximal port coupled to the housing for movement between a first position in which a proximal end of the power injection lumen opens to the proximal port and a second position in which a proximal end of the pressure activated lum

Abstract: A split-tip catheter for placement within the vasculature of a patient and for use in hemodialysis or other suitable procedures is disclosed. In one embodiment, the split-tip catheter includes a catheter body that defines a first lumen and a second lumen. The catheter body further comprises a split distal region, including a venous segment that defines a distal portion of the first lumen and an arterial segment that defines a distal portion of the second lumen. The venous segment includes a recess extending proximally of a nose portion; and a lateral opening in fluid communication with the first lumen. The arterial segment is separate from the venous segment and is removably seatable in the recess provided by the venous segment such that it “nests” therein. The arterial segment also includes a lateral opening in fluid communication with the second lumen.

Abstract: A triple lumen catheter comprises a transfusion lumen (4), a blood feeding lumen (2) and a blood removing lumen (3). The transfusion lumen (4) has a distal end and a leading end portion (12, 12A), the leading end portion progressively reducing in diameter to a proximal end. A transfusion port (4a) is formed in the proximal end of the transfusion lumen. The blood feeding lumen (2) has a blood feeding port (2a) in a region of the proximal end of the leading end portion, the blood feeding port opening at least partially in an axial direction of the leading end portion. The blood removing lumen (3) includes a pair of blood removing ports (3a, 3b) provided in opposite side walls of the catheter, the blood removing lumen extending from a distal end at least to the blood removing ports.

Abstract: The invention provides a variety of surgical instruments for forming a liquid jet, which are useful for performing a wide variety of surgical procedures. In some embodiments, the invention provides surgical liquid jet instruments having a pressure lumen and an evacuation lumen, where the pressure lumen includes at least one nozzle for forming a liquid jet and where the evacuation lumen includes a jet-receiving opening for receiving the liquid jet when the instrument is in operation. In some embodiments, the pressure lumen and the evacuation lumen of the surgical liquid jet instruments are constructed and positionable relative to each other so that the liquid comprising the liquid jet, and any tissue or material entrained by the liquid jet can be evacuated through the evacuation lumen without the need for an external source of suction.

Abstract: A multiple tube catheter, such as a hemo-dialysis catheter, has first and second tubes which are attached to each other over a zone by one or more longitudinally extending wires which joins the two tubes over that zone. When a catheter is implanted in the patient, the attached zone is within the patient so that the catheter cannot be removed or advanced. When the catheter is to be removed, the longitudinally extending wire or wires are pulled proximally out of the tubes involved so that the two tubes can be separated and individually removed. A flexible separating prong within the patient and proximal of the zone holds the tubes apart to further assure that the catheter cannot be moved.

Abstract: A hemodialysis catheter, including an elongate body with an outer wall enclosing an arterial lumen and a venous lumen, and a method of making same. A loop extends from a distal end of the body and defines an enclosed opening. An arterial inlet in fluid communication with the arterial lumen, and a venous outlet in fluid communication with the venous lumen, are positioned on the loop.

Abstract: Systems and methods for nasal irrigation are provided in which a nasal irrigation device includes a source of saline solution, an effluent receptacle, a nasal interface, a vacuum source, a fluid passageway to communicate the source of saline solution with the effluent receptacle through the nasal interface and a nasal cavity of the user, and a switch and valve assembly for selectively controlling the vacuum source and flow of the saline solution through the fluid passageway. The saline solution source is disposed relative to the device to provide gravitational inducement of saline solution to the nasal interface in engagement to the device user's nostrils. A combination of the gravitational inducement and the relative vacuum from the effluent receptacle generates a fluid flow for irrigating, cleansing and massaging the nasal cavity and ostia of a user. The entire device is assembled as a hand-held device for convenient lifting and disposal against the user's nostrils.

Abstract: A catheter (200) for insertion into a hollow viscus of a subject, comprising: a drainage opening (204) and an instillation opening at a distal end an inlet port (209) at a proximal end for instilling a fluid; an outlet port (205) at the proximal end for draining fluid from the viscus; a drainage channel (201) connecting the drainage opening to the outlet port; an instillation channel (211) connecting the inlet port to the instillation opening; a valve (223) proximate the drainage channel at the distal end for closing it against the entry of fluid from the viscus; a valve control port (220) at the proximal end for receiving a control fluid under pressure; and a control channel (222) connecting the valve control port to the valve such that the valve is responsive to admitted control fluid under pressure to close itself.

Abstract: A flow regulating implant is provided with one or more grooves for allowing fluid flow. One or more grooves may have a constant or varying cross-section along its length. One or more grooves may have in it biodegradable material, absorbable material, and/or threads or sutures. A resilient band or coating may be placed around the implant or one or more grooves, to act as a pressure regulator. The implant may have a side projection, such as a side pin, for engaging tissue. The implant may comprise two or more parts that are held at a distance from each other to allow fluid flow between the parts.

Abstract: A catheter for providing blood flow includes first and second lumen parts having a distal portion with at least one port for delivering and receiving flow from a patient and a non-linear profile along the distal portion.

Abstract: A split tip dialysis catheter having an outer tube and an inner tube, the two tubes which can be arranged over at least a portion of their length in a coaxial configuration. The inner tube may be connected to the outer tube at a proximal bifurcation, secured at a distal end of the outer tube or both, but generally the inner tube will remain free to move relative to the outer tube to optimize functionality. In addition, the inner tube can be arranged to be removable from the catheter for replacement thereof.

Abstract: A connector assembly for a heat exchanger has a fitting and a mount to which the fitting couples. The fitting has an elongate body having a proximal portion and a distal portion. At the proximal portion there is a crossbar, and at the distal portion there are an inlet and an outlet that protrude away from the body. Two wings extend from the body in a direction opposite to that of the inlet and outlet. There is formed on each of the wings a locking protrusion. The mount has a top portion where there is a groove dimensioned to accept the crossbar of the fitting. A longitudinal channel is formed orthogonal to the groove in the mount. Two sidewalls extend from the mount each for accepting a corresponding one of the wings, when the fitting is coupled to the mount. Apertures are provided at the sidewalls at the wings.

Abstract: A catheter includes an elongate body having first and second chambers extending within the elongate body from a proximal end to an intermediate section, the first chamber having a first opening and the second chamber having a second opening at the intermediate section. The catheter also includes a valve structure that may have first and second barrier elements to open or close the first and second openings, respectively. The first and the second barrier elements may be coupled by a connecting structure moving within an opening in a guide structure. Alternatively, the first and the second barrier elements may be coupled in a U-shaped structure that moves over the guide structure. To permit flushing of the chambers when the first and second openings are closed, the first and second chambers may also be connected by a connecting channel defined by an opening in a wall of the elongate body.

Abstract: A pumping system for use in medical applications where liquids must be infused and aspirated from a mammalian patient, and whose economics are such that it is cost effective to simply dispose of it after a single use. The system features positive displacement pump(s) such as reciprocating pump(s) containing a damping mechanism to dampen out the peaks and valleys in the fluid pressure that is pumped, which is important for preventing cavitation. The system furthermore features a shut-off valve on the extraction side so that certain injected fluids such as contrast medium, are not immediately pumped out of the patient. In a preferred embodiment, the system also features means for independently controlling the fluid pressure/volume on the infusion and extraction sides, self-priming capability, a continuous fluid path, and visual air bubble detection, with viewports located at important points in the fluid path, such as at pumps and valves.

Abstract: An enteral catheter provides access to both the stomach and the deep jejunum for feeding, aspiration and decompression. The catheter includes a triple lumen 16Fr tube that joins to a triple lumen “Y” connector at the proximal end of the tube. The connector serves the three lumens as a source for venting air, for fluid aspiration and for fluid infusion. The catheter includes a gastro/jejunal bolus which provides a large effective recessed port size opening varying from 172 degrees around the circumference of the bolus to a maximum recess circumference of 350 degrees. The gastric aspiration lumen, the jejunal feeding lumen, and the air vent lumen, all connect to the gastro/jejunal or midport connector bolus in the stomach at the distal end of the three lumen tube. The gastric lumen and the air vent lumen both open into the stomach through a common gastric port by the midport bolus. The jejunal lumen in the 16Fr tube communicates with jejunal lumen in the jejunal tube.