Abstract: The present invention describes a device for placement in the thoracic cavity of a patient. The device is a cannula, tube or catheter for chest drainage. The device serves as a conduit for drainage of excessive fluid or air buildup in the chest to a receptacle outside the body. The device also serves to prevent influx of fluid or air into the chest cavity, thus preventing pneumothorax or infection. The device incorporates systems for anchoring the chest drainage cannula to the chest and for steering the chest drainage cannula into the thoracic cavity.

Abstract: A medical apparatus flow restrictor includes a housing having an inlet and an outlet, and a fluid flow path defined through the housing between the inlet and outlet. At least one pair of opposed restriction surfaces are provided in contact with each other within the housing between the inlet and the outlet. The restriction surfaces are disposed in the flow path such that fluid delivered to the inlet passes between the opposed restriction surfaces prior to flowing from the outlet. At least one of the restriction surfaces comprises a pattern of fluid passages formed into the surface, the passages having a size and shape and cooperating with the opposed restriction surface such that a desired flow rate of fluid is achieved through the restrictor.

Abstract: A fluid control device is characterized in that the device is structured of a hollow first fluid path (21) and second fluid path (22), a housing portion (1) formed between the first fluid path and the second fluid path and having a hollow portion with a cross-sectional area larger than cross-sectional areas of both fluid paths, and a valve member (3) that has a main body (31) and a projection portion (32) that are installed in an opening portion where the first fluid path is connected to the hollow portion and that is formed of an elastic material. The fluid control device enables the circulation of liquid when the pressure of liquid flowing from the first fluid path toward the second fluid path is more than a predetermined level. The fluid control device enables accurate and safe measurement of pressure including blood pressure, and, when flushing operation of an infusion circuit etc.

Abstract: A method of preventing extravasation of contrast agent during a computed tomography injection. An automatic injector device facilitates ease of accomplishing the method. The method includes establishing the absence of extravasation using an absorbable injectate, such as saline, prior to injecting the contrast agent. The device includes a computerized injector head capable of switching between two injectates without physical human intervention. The device is controlled by a remote operating panel located in a control room that is protected from X-ray radiation. The device includes various software driven safety features that prevent the occurrence of unsafe conditions.

Abstract: A device for the metered administration of a fluid drug. The device has a container having a piston for administering the fluid drug through an outlet of the container, a catheter connected to the outlet of the container, the catheter having a front end facing away from the outlet and being connected to an injection needle, and a valve positioned between the outlet and the injection needle in a flow cross section of the fluid drug, the valve having an inlet end adjacent the outlet and an outlet end adjacent the injection needle, wherein the valve permits flow of the fluid drug through the valve from the outlet to the injection needle when a fluid pressure exerted on the inlet end of the valve exceeds a pressure on the inlet end caused by the dead weight of the fluid drug.

Abstract: A needleless connector for adding medication to a parenteral fluid is provided. The needleless connector comprises a connector adapted to receive a syringe and having a check valve to seal the port in place of a puncture pad. The check valve comprises a resilient disc held in place and biased closed by the tensile stress of the check valve material. When a syringe or other apparatus having a male luer connector is engaged with the connector and fluid pressure is applied to the check valve the resilient disc is deformed which allows the medication to flow through the connector into the tubing and thus to the patient.

Abstract: An apparatus for use in delivering pain medication to separate locations from a single source of pressurized medication includes a valve housing, a cap, and a flexible diaphragm. The valve housing includes a first end and a second end and an inlet passage. The first end includes first and second outlet orifices. The cap has a closed end and an open end and is removably coupled to the valve housing at the open end. The flexible diaphragm is coupled between the cap and the valve housing and is movable from a closed position to an open position. The flexible diaphragm seals a pressure chamber from the first and second outlet orifices when in the closed position and opens the first and second outlet orifices to the pressure chamber when in the open position.

Abstract: A pressure activated two-way slit valve assembly is designed to be used in combination with, but not limited to, a high flow rate catheter to prevent accidental ingestion of air or loss of blood if the closure cap comes off during non-use of the catheter. In addition, the potential for occlusion of the catheter due to blood clots in the catheter and catheter related infection is substantially reduced. The pressure activated two-way slit valve assembly includes a first end, a second end, a wall defining a dumbbell shaped channel, and a flexible, thin disk having a slit and positioned within the pressure activated two-way slit valve assembly to reside within the dumbbell shaped channel. The slit and the dumbbell shaped channel are sized to enable the slit to deform in response to a predetermined pressure differential across the slit to allow fluid to pass therethrough.

Abstract: A catheter body includes an exit port over which a pressure responsive sleeve is formed that allows material to exit a lumen of the catheter body at a given pressure. In one embodiment, a surface of the sleeve is approximately flush with a surface of the catheter body. In another embodiment the sleeve includes a tapered edge.

Abstract: A flow rate selection valve includes a gate cylinder having a gate cylinder rotational axis and having at least two flow rate determining passageways and passing laterally through the gate cylinder at orientations angularly displaced from each other and having cylinder rotation structure; and a valve housing containing a flow passageway and having a cylinder receiving bore intersecting the flow passageway into which the gate cylinder is rotatably and sealingly mounted, the gate cylinder dividing the flow passageway into a passageway inlet end and a passageway outlet end, the flow passageway containing a passageway registration barrier extending across the flow passageway and sealingly abutting the gate cylinder and having several flow ports with different minimum diameters, each flow port positioned to register with one of the flow rate determining passageway.

Abstract: A thrombectomy catheter device having an improved hemostasis valve which is self-sealing and which functions as a one-way valve. The self-sealing hemostasis valve can be factory preset to automatically seal with or without the inclusion of a guidewire at a certain desired pressure or allowable leakage. Such sealing is automatic without the need to manually manipulate a hemostasis nut to obtain hemostasis. The thrombectomy catheter device can, without hemostasis nut adjustment, be positioned along and about a guidewire while yet maintaining suitable pressure for sustaining hemostasis at a preferred level. Certain embodiments of the thrombectomy catheter device having a self-sealing hemostasis valve include an adjustable hemostasis nut which can be manually tightened to restrict flow or guidewire movement or loosened to reduce friction on the guidewire and allow fluid to flow out if desired.

Abstract: A valve arrangement for providing clinical nutrition is provided. The valve arrangement is suitable for use with a rotary peristaltic pump and is capable of allowing flow of fluid in a first direction and capable of preventing flow of fluid in a second direction, wherein the valve arrangement comprises a valve having a cracking pressure of about 0.10 to about 0.20 bar. Also described are a method of production of the valve arrangement, use of the valve arrangement in providing nutrition to a patient and a method of treatment of a patient that comprises administering an effective amount of a composition via the valve arrangement.

Abstract: An apparatus and method for preventing free flow through an infusion set utilizes an occluder disposed within the infusion set to selectively prevent flow therethrough. The occluder may be responsive to a pressure differential within the infusion set or may respond to compression of the infusion set. When a pair of occluders are used in sequence, an in-line pump may be formed.

Abstract: A device for delivering a substance into the skin of a patient includes a body and a skin penetrating device having at least one skin penetrating member, such as a microneedle. The body includes an internal cavity and a device for indicating the delivery of a sufficient amount of the substance to the patient and for producing a dispensing pressure to dispense and deliver the substance from the cavity. The indicating device is visible from the exterior of the delivery device. In some embodiments, the indicating device is an elastic expandable diaphragm which, when the cavity is filled with a substance, creates the dispensing pressure.

Abstract: An implantable fluid valve for the adjustable limitation of the fluid pressure in the brain of a patient, has all valve component parts composed of non-magnetic material, thereby making the valve MR-compatible.

Abstract: The invention concerns a syringe for administering medication to an animal. The syringe includes a handle that may be manually actuated to dispense medication to the animal. The syringe also includes a valve that controls the flow of medication both into and out of the syringe. A sensor device on the syringe monitors when the medication has been administered in order to inform any attached pump that the syringe may be refilled. An LED informs the user when the syringe has been filled with medication and is ready for the administration of medication to the animal.

Abstract: A flow control valve (22) such as for a catheter (10) allows discharge of urine from a bladder (12) by manual actuation. The valve (22) may be a double-duckbill valve (22) with a single slit (62) at one apex (60a) thereof. An elastomeric band (66) is positioned in a groove (68) of the valve member (22). An isolation member such as a stem (72) spaces the valve (22) from the walls (34, 36) of the valve housing (32). Crush limiting structure, such as a tube (76) or blade (82), is provided within valve member (22), or stop elements (86 or 92) are positioned external to valve member (22).

Abstract: The present invention is directed to a proximal catheter assembly configured to facilitate natural or suction-assisted aspiration through a catheter lumen. The proximal catheter assembly comprises a multi-function valve configured to perform functions associated with conventional check valves and relief valves. The valve is configured to regulate the direction of fluid flow, and further configured to regulate the rate of suction-assisted aspiration provided through the lumen of the catheter. When the rate of suction-assisted aspiration exceeds a predetermined threshold, the valve opens to allow fluid to be drawn from tubing coupled to the proximal catheter assembly, thereby mitigating excessively high rates of aspiration imposed upon the patient's vessel.

Abstract: A medical instrument for irrigation and/or suction has an instrument body in which at least one flow channel is present for the passage of a fluid, at least one shut-off member for alternately shutting off the at least one flow channel, and an actuating member for actuating the shut-off member. The at least one shut-off member is a ball which, in a closure position, lies sealingly on a sealing edge of the flow channel so that it closes off the internal cross section of the flow channel, the ball being movable, between the closure position for closing the flow channel and a release position for freeing the flow channel, substantially in a direction transverse to the longitudinal direction of the flow channel, and the actuating member for moving the ball between the closure position and the release position being movable in a direction transverse to the flow channel.

Abstract: The invention shows that conditions can be created in intravenous anaesthesia in which single-patient parts and accessories are separated from multi-patient parts and accessories by utilisation of a filter preventing contaminating particles from migrating from single-patient parts and accessories to multi-patient parts and accessories.

Abstract: A fluid delivery system for delivery of an injection fluid to a patient generally includes a first pump system, a second pump system, a patient interface in removable fluid connection with the first and second pump systems, and a fluid path in fluid connection between the first and second pump systems and the patient interface. The fluid path preferably includes a housing member defining a first inlet, a second inlet and an outlet. The first and second pump systems are placed in fluid connection with the respective first and second inlets of the housing member and the patient interface is placed in removable fluid connection with the outlet of the housing member. A first check valve is in fluid connection between an outlet of the first pump system and the first inlet of the housing member, and a second check valve is in fluid connection between an outlet of the second pump system and the second inlet of the housing member.

Abstract: A device cooperating with a pump for guiding a contrast medium from a source thereof to a catheter for delivery to a patient's vascular system. The device comprises a dual check valve, a tubular member, an in-line check valve and a three-port stopcock. The dual check valve has an inlet port connectable to the source of contrast medium, an inlet-outlet port connectable to the pump, and an outlet port coupled to the tubular member. The in-line check valve is connected to the tubular member at a point spaced from the dual check valve for preventing fluid flow towards the dual check valve. The stopcock connected at a first port to the in-line check valve, a second port of the stopcock being operatively connectable to the catheter. Using this device, medical personnel infuses contrast medium into the patient from the source without having to disconnect any element from the device during the infusion process.

Abstract: The invention relates to a unidirectional valve appliance, in particular a low pressure check valve for use for an infusion comprising a housing with an inlet and an outlet, and with at least one gasket in a pressure chamber. To prevent air entry into the infusion fluid circuit, the appliance includes an interruption of the flow by means of a static vacuum to the inlet and/or outlet or excess pressure at the outlet. This ensures in reliable manner that a flow of the infusion fluid in a reliable manner only when a static excess pressure differential is exposed to the inlet.

Abstract: Methods and apparatus for percutaneously accessing an implanted port using an access tube which is periodically introduced to the implanted port. The apparatus is preferably an implantable port having a pressure-responsive valve element. It has been found that repeated passage of the access tube through the same tissue tract to the implantable port reduces patient trauma, with minimized bleeding and reduction in sensitivity. The tract may be initially formed by percutaneously placing a penetrating element through intact skin to the port and leaving the element in place for a time sufficient to created the tract.

Abstract: An injector for liquid medicine comprises a cylindrical body 1, first and second gasket 2, 3 contained in a lumen of cylindrical body 1. The cylindrical body 1 is provided with a fluid inlet 13 and a fluid outlet 14 in opposite sides of the cylindrical body 1 with respect to the longitudinal axis thereof. Second gasket 3 is spaced from the first gasket 2 to form a fluid chamber 4 between them. The first gasket 2 is adapted to be moved by sliding along the inner wall of the cylindrical body 1 from a first position to the distal end 11 of cylindrical body 1 via a second position. The fluid inlet 13 is opened at a position closer to the distal end 11 of the cylindrical body 1 than the outlet 14 is. The first gasket 2 is stopped at a second position where the fluid chamber 4 is communicated with the fluid outlet 14 but prevented from fluid-communication with the fluid inlet 13.

Abstract: A tubular instrument including a hollow wall portion and a connector arranged to be used with a guide-wire. The guide-wire has a distal end portion and a proximal end portion, the distal end portion of the guide-wire is arranged to be extended to some interior position within the body of a living being, with the proximal end portion of the guide-wire being located outside the being's body. The connector is located at the distal end of the instrument and is arranged to be readily manipulated by a twisting action to connect the instrument onto the guide-wire for sliding movement therealong.

Abstract: A system for producing an image of a patient preferably includes a source of contrast medium, a pressurizing unit operably associated with the source of contrast medium for injecting the contrast medium into the patient, an imaging unit providing an internal image of the patient based upon a condition of the contrast medium in the patient, a control unit adapted to adjust the condition of the contrast medium injected into the patient, an electronic interface in communication with at least one of the pressurizing unit and the imaging unit, and a fluid path disposed between the pressurizing unit and the patient.

Abstract: A pressure isolation mechanism for use in a medical procedure includes a lumen, an isolation port in fluid connection with the lumen, and a valve having a first state and a second state. The first state occurs when the lumen and the isolation port are connected. The second state occurs when the lumen and the isolation port are disconnected. The lumen remains open for flow of fluid therethrough in the first state and in the second state. The valve is preferably spring-biased in the first state and is switchable to the second state when fluid pressure in the lumen reaches a predetermined pressure level. Alternately, an actuator can control the state of the valve. A pressure transducer can be in fluid connection with the isolation port of the pressure isolation mechanism. A fluid delivery system includes a syringe and a pressure isolation mechanism as described above.

Abstract: Indwelling catheter having an upper distal end having a portion that can expand within a bladder type spaces without having to be inflated. An embodiment allows for at least one slit on an upper side of the catheter tube and a head member that when pulled down by a stylette moving inside the catheter causes a bulge wing portion(s) that holds the catheter safely and painlessly within the bladder. Magnetic and electret valves can be included inside the tube of the catheter that can cycle between open and closed positions when activated by normal bladder pressure when urination is desired. The novel catheter tube can naturally conform to an opening and closing urethra during natural bladder drainage. The catheter tube surface can include an anti-microbial layer that is either or both coated and impregnated thereon with either an antibacterial and/or hydrophyllic materials. Sampling ports can be located on both inside catheter tube valves and on an externally attached magnetic valve.

Abstract: A gravity flow IV set up for administering fluids intravenously to a patient has a main, low-rate flow branch line and a shunt, high-rate flow branch line, and an auxiliary line above a junction of the main and shunt flow lines which can be used for a second or supplemental source of blood or an IV fluid. In order to ensure that there is no reflux of fluid from one of the main and shunt lines into the other, ball check valves are positioned in each line below the respective drip chamber and above the lower junction of the two lines. The ball check valves can withstand relatively high back pressures without danger of rupture or leakage.

Abstract: A debridement extension including a proximal end and a distal end, with the proximal end being adapted for connection to both an irrigation source and a suction source. The debridement extension includes a fitting adjacent the proximal end which includes both an irrigation port and a suction port. An inner cannula and an outer cannula are both attached to the fitting of the debridement extension and are, respectively, in fluid communication with the irrigation port and the suction port. A debridement tip is affixed to the distal end of the debridement extension and is independently in fluid communication with both the irrigation path and the suction path formed by the inner and outer cannulas, respectively.

Abstract: A catheter useful for non-surgical entry into a uterus to dispense a diagnostic fluid therein. The catheter includes a tubular body having a lumen extending from a first end thereof to a second end thereof. The lumen includes an external opening adjacent the first end for dispensing a diagnostic fluid into the interior of a subject uterus, and a balloon disposed marginally adjacent to the first end of the body for fluid sealing the interior of the subject uterus. The lumen further includes a second opening in fluid communication with the interior of the balloon for inflation thereof with the diagnostic fluid. In most applications, the catheter can be combined with a syringe to form a catheter apparatus.

Abstract: A method of selectively perfusing a non-preserved, non-heart beating cadaver with a perfusate to recreate vascular circulation in a cadaver as a mechanism for study of the vascular function, research and teaching of surgical procedures and general medical training. The arteries or veins of the cadaver are exposed, dissected, and flushed to remove clots and excess blood. A selected arterial tree of the cadaver is perfused with a solution via inflow through a point of access and outflow through at least one point of egress. The points of access and egress establish the limits of the circuit to be studied or used for testing.

Abstract: A multi-channel valve having a valve seat, a valve seal, and valve seal housing. The assembly of the apparatus creates a plurality of inlet, exit, and cross channels enclosed by elastomeric portions of a valve seal. The elastomeric portions of the valve seal create bounded distensible chambers. Pressure exerted by a fluid in excess of the cracking pressure of the seal tends to distend portions of the elastomeric seal and allow flow through and into the chambers. When inflow pressure falls, the elastic rebound of the elastomeric portions of the seal tends to expel fluid from the valve without backflow. Cross channel capacity allows mixing of the fluids. The plurality of, and differentials between, chambers allows one fluid to completely purge the valve of other fluids. The valve may be configured with additional backflow prevention capacities, such as channel variations, secondary elastomeric members, and variations in primary membrane properties.

Abstract: A manifold is disclosed which includes a manifold body that defines a main lumen, a primary injection line and a port. A check valve system is also provided which permits flow from the primary injection line to the main lumen while selectively preventing back flow from the main lumen to the primary injection line and, simultaneously, permitting flow from the port to the primary injection line while preventing back flow from the primary injection line to the port.

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: A valved catheter assembly is designed to be used to minimize patient discomfort and to prevent infection at an entry site. The valved catheter assembly includes a hub including a slit valve disposed therein and distal tubing extending in a distal direction from the hub when the valved catheter assembly is inserted into a body of a patient. The valved catheter assembly is free of proximal tubing extending in a proximal direction from the hub.

Abstract: A catheter port assembly is disclosed. The assembly includes an adapter having a body having a proximal end, a distal end, and a passageway extending therethrough between the proximal end and the distal end. The distal end is adapted to engage a catheter. The assembly further includes a tunneler releasably connectable to the proximal end of the adapter and a catheter port, having a valve disposed therein, releasably connectable to the proximal end of the adapter. In an alternative preferred embodiment, the valve may be disposed inside of the adapter, rather than the catheter port. Alternatively, the body of the port assembly may be one piece, having a valve disposed therein. A method of installing and operating the catheter port assembly is also provided.

Abstract: A syringe comprising a one-way filter which permits flow of fluid into the syringe unfiltered but which filters the fluid when expelled from the syringe.

Abstract: A device for storing and administering a medical fluid comprising a sealed flexible formed container with an opening part in its front end in which an insert is positioned. Over the insert, the container extends into a removable sealing cap. After removal of the sealing cap an injection means is attached to the insert and fluid administration through the insert is admitted in one direction by squeezing the container.

Abstract: A pressure responsive slit valve assembly is designed to be used in a variety of configurations of medical devices to manage contemporaneous and pressure responsive fluid communications between such devices and a plurality of fluid sources. The pressure responsive slit valve assembly of the present invention includes a valve housing adapted to receive fluids from at least two sources and a pressure responsive slit valve means corresponding to each fluid sources.

Abstract: A catheter body includes an exit port over which a pressure responsive sleeve is formed that allows material to exit a lumen of the catheter body at a given pressure. In one embodiment, a surface of the sleeve is approximately flush with a surface of the catheter body. In another embodiment the sleeve includes a tapered edge.

Abstract: An external surface of a catheter body includes a pressure responsive slit formed in an indentation wherein a wall thickness of the catheter body within the indentation is less than a wall thickness of a major portion of the catheter body. Material exits a lumen of the catheter body, via the pressure responsive slit, when a pressure inside the lumen exceeds an external pressure.

Abstract: A fluid delivery cannula which provides an interface between an access point or port in the body of a patient and a working channel which may receive tools or instruments used during minimally invasive surgery. The cannula allows introduction of fluid(s) at the port site, or another site within the body of the patient. The fluid delivery cannula can releasably attach to a hub associated with a trocar assembly or may be integrally formed with at least a portion of the hub. In one form, an inner cannula member includes a grooved outer surface to define multiple fluid passages and a perforated outer layer is placed over the inner cannula member. Another form provides an expandable sleeve that may itself comprise a cannula through which a trocar or trocar assembly is inserted or which may take the place of the perforated outer layer of the grooved cannula.

Abstract: A pressure isolation mechanism for use in a medical procedure includes a lumen, an isolation port in fluid connection with lumen, and a valve having a first state and a second state. The first state occurs when the lumen and the isolation port are connected. The second state occurs when the lumen and the isolation port are disconnected. The lumen remains open for flow of fluid therethrough in the first state and in the second state. The valve is normally in the first state and is switchable to the second state when fluid pressure in the lumen reaches a predetermined pressure level. A pressure transducer can be in fluid connection with the isolation port of the pressure isolation mechanism A fluid delivery system includes a manually operated syringe and a pressure isolation mechanism as described above.

Abstract: An autoinflating catheter and balloon assembly having an autoregulating structure to prevent overinflation of the balloon as a result of variable fluid flow rates through the catheter lumen. A tight-fitting elastomeric balloon is provided on the distal end of the catheter body, and the assembly is constructed so that at least a portion of the fluid flow through the lumen is directed to the balloon to inflate it. As the balloon is inflated, more and more of the fluid flow through the catheter is discharged from the catheter, thereby preventing overinflation of the balloon.

Abstract: A feeding set adaptor and related system for delivering solutions utilize a feeding set adaptor which engages a pump engaging portion of an infusion set and the feeding set adaptor structure to provide monitoring portions for detecting pressures within the infusion set, a sample cell for determining the presence of air within an infusion set, and an anti-freeflow device for selectively preventing freeflow through the infusion set. The feeding set adaptor is configured for mounting on an infusion pump which moves solution through the infusion set for delivery to a patient.

Abstract: An implantable device for administering a treatment solution has a first chamber for accommodating the active solution to be administered and a second chamber for accommodating a treatment solution bolus, each chamber having a port sealed with a septum. An infusion line leading to the infusion site is connected to the outlet of the first chamber. An inlet line branches off from the infusion line and is connected to the second chamber to accommodate the active solution bolus, and includes a flow device which releases the flow path to the infusion site only when the active solution bolus is supplied at a pressure above a predetermined minimum pressure. The occurrence of life-threatening situations due to sudden administration of a large quantity of active solution is prevented if the active solution is always supplied only at a pressure below the minimum pressure at which the flow path is released.

Abstract: In an embodiment, a slit valve catheter has a generally tubular catheter body with an exterior surface exposed to an environment and an interior surface defining a lumen. The catheter further includes a valve which has a protuberance projecting radially from the catheter body.

Abstract: A transdermal medication delivery device (20) for the remote controlled administration of medications (68, 70, 72) for absorption through the skin of a patient (22) includes a tubes (62) containing the medications (68, 70, 72). Tubes (62) are in fluid communication with valve inlets (76, 82, 88) of valves (74, 80, 86) formed on a micro-electro-mechanical-system-based (MEMS-based) valve chip (64, 162). A medication delivery component (26, 176) in fluid communication with valve outlets (78, 84, 90) of valves (74, 80, 86) has a surface (66, 178) adapted to be in contact with the skin of the patient (22) when in use. A controller (92) is configured to control a flow of the medications (68, 70, 72) through the valves (74, 80, 86), and a wireless communication interface (94), in communication with the controller (92), is configured to receive a medication control message (96) from a remote location (32).