Abstract: A limited backflow reflux valve for connection between a syringe, catheter, and bulk container of injection fluid. The reflux valve permits injection of fluid from the syringe through the catheter into the patient, and also permits refilling of the syringe from the bulk container, without disconnection of any tubing. The reflux valve also permits a limited volume of fluid to backflow from the catheter into the syringe, so that the catheter may be checked for patency, but prevents any further backflow along this path after this limited volume. Therefore, the limited backflow reflux valve not only permits injection through the catheter, but also permits both withdrawal of blood from the patient and refilling of the syringe from the bulk contrast media container, without requiring disconnection of the catheter or other tubing and without risk of contamination of the syringe or introduction of air, increasing the efficiency of the injection process, enhancing safety, and reducing waste of injection fluid.

Abstract: The invention relates to a suction catheter device usable with a respiratory support system which includes a catheter enveloped in a sleeve having a proximal end connector for connection to a suction source through a suction control device such as a suction control valve, and a distal end connector for attachment to a manifold of the respiratory support system. The proximal end connector includes a normally closed valve therein which prevents air flow through the catheter until a suction control device is attached thereto. The proximal end connector may also be adapted for use on a dual lumen catheter and thereby include a fluid injection passage having a one-way check valve therein. The distal end connector of the suction catheter device includes a magnifying window through which a portion of the catheter within the connector can be viewed.

Abstract: A partially disposable instrument for use in a medical procedure includes a rigid introducer assembly and a fiber-optic endoscope having a flexible shaft which may be removably inserted through the introducer assembly. The introducer assembly permits a fluid to be flushed therethrough and about the shaft such that the fluid exits through a terminal end of the introducer assembly. The instrument may be utilized in connection with a method for positioning a catheter within a body during a medical procedure, including the steps of placing the catheter over the introducer, inserting the shaft of the endoscope through the introducer, advancing the catheter, introducer and endoscope shaft into the body as a unit, positioning the catheter within the body utilizing the fiber-optic endoscope, and removing the endoscope shaft and the introducer from the body while leaving the catheter in place.

Abstract: A fluid manifold includes a housing having a first inlet and an outlet and a plurality of inlets intermediate the first inlet and the outlet which are provided with check valve action to prevent retrograde flow through the valved inlets, yet allow individual inlets to pass fluid when the fluid pressure in any individual inlet exceeds that of the interior of the chamber by a predetermined cracking pressure, and retrograde flow through the first inlet is controlled by a flapper portion which may be biased to an open position to allow unrestricted flow from the first inlet to the outlet or configured so as to be in sealing contact with a valve seat in order to preferentially inhibit flow.

Abstract: A fluid flow rate control device, especially adapted for controlling the flow of IV fluid to a patient, comprises a first vented fluid chamber having an upper fluid inlet end with a hollow spike which enables fluid connection with a conventional fluid container. A free floating float valve in the first chamber blocks the flow of fluid into the first chamber from the fluid container according to whether or not the fluid level in the first chamber is at a preestablished fluid level, thereby providing a constant pressure head regardless of fluid level in the fluid container. A lower end of the first chamber is connected, through a flow regulator, such as a screw-type valve, to an upper inlet end of a second, vented, drip chamber, the lower end of which is adapted for connection to a discharge tube, such as an IV tube.

Abstract: A low actuation pressure, unidirectional flow valve comprising a housing including a fluid flow passage extending therethrough which defines first and second sections. Disposed within the housing between the first and second sections is a valve member. The valve member comprises an annular ring portion having a disc portion disposed therewithin. Extending between the ring and disc portions are at least two spirally shaped connecting arm portions. The ring, disc and connecting arm portions define at least two side openings. The valve member is movable between a closed position wherein the disc portion covers and seals the first section of the flow passage, and an open position wherein the disc portion is separated from the first section and fluid flows from the first section to the second section via the side openings.

Abstract: A method and apparatus for removing fluid from the body of a patient, such as in paracentesis and thoracentesis, is provided. Fluid may be withdrawn via a needle assembly including a sharp introducing needle and a retractile blunt needle. The needle assembly may be withdrawn after the introduction of a drainage catheter, and a valve with multiple sealing points prevents body fluids from leaking from the device through the needle space and prevents communication between the atmosphere and the patient through the needle space. A second drainage port may be used after the needle is withdrawn.

Abstract: A coupler is adapted for inserted engagement with a dental ejector valve and serves to couple a vacuum hose to the valve. A passageway in the coupler is closed by a flexible disk which flexes open in response to a vacuum inducted ejector system flow from a source. The disk is confined in place across the passageway by a retainer which biases the disk into engagement with a valve seat surface. The flexible disk blocks any reverse flow through the coupler as when a reduced pressure occurs from interaction of the patient's mouth with a saliva ejector.

Abstract: Gastrostomy ports are disclosed for reliably providing enteral feeding to a patient over long periods of time. Gastrostomy ports shown herein provide one-way valves which include a resilient valve member which is compressively fitted within a receiving cavity defined by a rigid compression collar. The valve member has a diaphragm portion defining a slit. The compression collar presses inwardly against the outer peripheral edge of the diaphragm portion to apply laterally compressive forces which bias the slit toward a normally closed position. Gastrostomy ports are further shown for accessing the interior of a body cavity or organ which are self retaining and resist inadvertent pull-out but can be atraumatically implanted and removed.

Abstract: A gastrostomy feeding port is disclosed which incorporates a seal module which includes a valve housing and a resilient valve member contained therein. The valve housing defines an inner passageway to provide fluid communication into a long term indwelling catheter and includes a rigid compression collar portion which defines a valve member receiving cavity within the inner passageway. The resilient valve member has a diaphragm portion which has an "S" shaped slit therethrough, and an outer peripheral edge which generally conforms in shape to the valve member receiving cavity but is larger in dimension than the cavity when uncompressed. The resilient valve member also includes an outer wall portion which extends away from the outer peripheral edge of the diaphragm portion and which generally conforms in shape to the cavity.

Abstract: Gastrostomy feeding ports are disclosed which remain positively sealed after repeated and extensive use. In one embodiment, a valve housing defines an inner passageway to provide fluid communication into a long term indwelling catheter and includes a rigid compression collar portion which defines a valve member receiving cavity within the inner passageway. The resilient valve member has an outer peripheral edge which generally conforms in shape to the valve member receiving cavity but is larger in dimension than the cavity when uncompressed. The resilient valve member also includes an outer wall portion which extends away from the outer peripheral edge of the diaphragm portion and which generally conforms in shape to the cavity.

Abstract: An implantable device grafted directly to vascular structures for high volume blood and/or fluid infusion and/or removal for such purpose as hemodialysis, apheresis, exchange transfusion, or large volume fluid infusion. The device is also adaptable to intermittent access to the venous or arterial circulations for purpose of blood sampling or giving medications. The device is comprised of an implantable fluid chamber connected to a cannula or shunt segment which is then grafted directly to the vascular structure (e.g. artery or vein) using a sewable cuff located at the vascular end of the cannula or shunt segment. The vascular end of the device employs a valve which is directly adjacent to the vascular structure after grafting, in order to prevent reflux of blood and subsequent washout of anticoagulant during periods when the device is not in use. The device is accessed percutaneously with a needle or needle-introduced catheter and is filled with anti-coagulant prior to needle withdrawal to prevent thrombosis.

Abstract: An overpressure safety valve assembly for use during heart surgery is disclosed. The assembly comprises an elongated tubular body portion having an inlet end, and an outlet end and an unidirectional valve disposed therebetween. A relief valve portion is joined to and in flow communication with the tubular portion. The relief valve portion includes a first relief valve configured to open if the pressure within the overpressure safety valve diminishes below a predetermined level, and a second relief valve configured to open if the pressure adjacent the outlet end exceeds a predetermined level. The first and second relief valves are disposed in a side by side configuration in a common conduit.

Abstract: In general, the medical infusion device of the present invention includes at least one check valve chamber through which a primary intravenous stream is arranged to pass by way of a primary fluid inlet port and a primary outlet port. Each check valve chamber has at least one physically associated infusion port through which a medicational or nutritional fluid can be injected in any number of possible ways. Each check valve chamber has an interior volume, a check valve opening formed between its interior volume and its associated infusion port, a check valve chamber opening formed through the check valve chamber and axially aligned with the check valve opening, a flexible check valve element, and a check valve support element.

Abstract: Safety connector for infusion therapy for supplying several lines and having a casing (1) in which there is a chamber (4) that is bordered by an essentially cylindrical inside wall (5) of the casing into which several connecting channels (2) for joining infusion lines open and which has an outlet channel (9) for attaching an outlet line. The cylindrical outside wall of an elastic ring-shaped valve body is in contact with the inside wall (5) of casing (1) that surrounds chamber (4). The safety connector is simple and inexpensive and has an uncomplicated design. The cylindrical contact surfaces between the ring-shaped valve body and the cylindrical inside wall (5) surrounding chamber (4) result in a good seal for the non-return valves even at a low contact pressure. The sealing force can be determined even down to a very low pressure. Thus, for the first time a safety connector suitable for gravity infusion systems is available.

Abstract: A urine tube extends through a balloon which is inflatable in the neck of a bladder to form a seal around the urine tube. The balloon has a shape corresponding to the shape of the bladder chamber at the urethra orifice to facilitate establishing a seal. A valve is provided on the outlet end of the urine tube and an air tube extends along the substantial length of the urine tube into the balloon. A hypodermic syringe or the like may be inserted into the inlet end of the air tube for inflating the balloon. A hydrogel collar is positioned around the urine tube against the body at the outlet end of the urethra to hold the balloon in tight engagement with the bladder neck at the urethra orifice.

Abstract: An apparatus for infusion monitoring including a pressure transmission line branched from the infusion hose and a diaphragm connected with the infusion hose, the diaphragm being able to be connected with a pressure sensor for registering a change in curvature of the diaphragm. In order to achieve the aim of providing an apparatus of this type which renders possible on the one hand a reliable monitoring of infusion and on the other hand a way of preventing the production of a false alarm in a substantially reliable fashion, the apparatus of this type is so designed that in the infusion hose between the branch point of the pressure transmission line and the free end, adjacent to the patient, of the infusion hose a one-way valve is arranged, which permits a direction of flow to the patient.

Abstract: An irrigation syringe which is particularly adapted for injecting water into a human body cavity, such as for the cleansing of an ear, includes a pressure regulator unit which is connected to, and supported by, a faucet, and a handpiece including a manually operable valve. The regulator unit includes a supply chamber having an inlet which is connected to a pressure water supply such as a faucet, an outlet which supplies pressure regulated water to the handpiece, and a pressure relief outlet having a check valve which opens to allow water to drain, such as into a sink, when the water pressure inside the regulator unit exceeds a predetermined value. A flow limiting orifice at the inlet to the supply chamber helps smooth out pressure fluctuations from the water supply and provides a steady flow from the supply chamber outlet. Temperature and pressure readouts are provided on both the pressure regulator unit and the handpiece.

Abstract: A device for introducing an implantable appliance into a catheter including an attachment connected to said open end of catheter, the attachment being closed at its open end by a flexible check valve. A cartridge is removably attachable to the catheter attachment with the cartridge when attached having a front end portion communicating with the catheter and its other end closed by a second flexible check valve. This second check valve is open when the appliance to be implanted is introduced into the cartridge but thereafter is kept closed and the front end portion of the cartridge with the appliance now inside is inserted into to the first check valve of the attachment.

Abstract: An endoscopic portal for establishing communication with a body cavity for the introduction of instruments therethrough includes a sleeve for providing a passage through a cavity wall and a valve biased to a normal closed position preventing the passage of instruments and fluids through the sleeve. The sleeve includes a distal end for being disposed in a body cavity, a proximal end for being disposed externally of the body cavity and a lumen between the distal and proximal ends. The valve includes a cylindrical valve body extending in a transverse direction across the lumen and having a plurality of diametric valve passages therethrough of different cross sectional sizes. The valve body is biased to the normal closed position wherein the valve body blocks communication through the lumen and wherein the valve passages are not disposed within the lumen.

Abstract: A limited backflow reflux valve for connection between a syringe, catheter, and bulk container of injection fluid. The reflux valve permits injection of fluid from the syringe through the catheter into the patient, and also permits refilling of the syringe from the bulk container, without disconnection of any tubing. The reflux valve also permits a limited volume of fluid to backflow from the catheter into the syringe, so that the catheter may be checked for patency, but prevents any further backflow along this path after this limited volume. Therefore, the limited backflow reflux valve not only permits injection through the catheter, but also permits both withdrawal of blood from the patient and refilling of the syringe from the bulk contrast media container, without requiring disconnection of the catheter or other tubing and without risk of contamination of the syringe or introduction of air, increasing the efficiency of the injection process, enhancing safety, and reducing waste of injection fluid.

Abstract: The present invention relates to a double-valved variable pressure device for hydrocephaly having a vertical capsule with sloped ends ending in upper and lower coupling sectors appropriate for connection to a proximal catheter and a distal catheter that constitute the input and output for a cephalo-rachidian liquid through the body. The liquid or volume has its pressure controlled by means of two valves which maintain a constant drained volume along a wide range of pressures the device is submitted to.

Abstract: A method and apparatus is disclosed for supplying a fluid under pressure to a channel and for blocking a backflow of fluid from the channel to a catheter. The apparatus is a one-way valve assembly for use with a container supplying a fluid under pressure to a channel. The one-way valve assembly includes a first tube for communicating the fluid into a channel, a valve, and a second tube communicating with the container supplying the fluid and transmitting the fluid to the first tube via the valve. The valve comprises a base member with a hollow interior and a sealed distal end, which hollow interior is capable to communicate the fluid between the second tube and the first tube through at least one slit aperture which is positioned near the sealed distal end of the base member. The base member is engaged and covered by a flexible pressure-responsive surface which seals the slit aperture in order to prevent backflow of fluid from the first tube into the base.

Abstract: A self-sealing valve arrangement for use in a hemostasis cannula includes a distal wiping gasket and an outer proximal tricuspid gasket bonded on a peripheral interface therebetween. The distal wiping gasket strips clots and fibrotic tissue from a catheter or vessel dilator as it is extracted from the hemostasis cannula preventing a disruptive accumulation of clots in the tricuspid valve.

Abstract: A device for regulating the flow of an organic liquid between a production site and a resorption site of a patient in a drainage circuit that extends between the two sites, one of the sites being a site of small pressure variation and the other being a site of large pressure variation, particularly as a function of the position of the subject, the device comprising a valve for implanting beneath the skin and connected by a first duct to one of the sites and by a second cut to the other site, the valve comprising a body (1) defining an internal passage inter-connecting the two ducts, a member (14) for adjusting the section of said passage, and control means (7, 15) coupled to said adjustment member (14) to displace it between a first position in which the passage is closed and second positions in which the passage is opened to a controlled extent, the device being characterized in that the control means comprise a first chamber (12) formed in the body (1) and closed in sealed manner by a moving wall (7), a sec

Abstract: A nonreturn valve for use in controlling the flow of medical fluid. The valve has two mating valve shells which carry and communicate with first and second pipe connectors, respectively. A diaphragm with a protrusion on its periphery is held between the valve shells. Circumferentially disposed retaining formations on each of the valve shells causes pretension to occur in the diaphragm upon assembly of the valve shells. The axial location of the retaining formation on the valve shell which carries the valve seat is such that tension in the diaphragm lightly urges the diaphragm into sealing engagement with the valve seat, whereby a seal exists when there is no significant pressure on either side of the diaphragm.

Abstract: In general, the medical infusion device of the present invention includes at least one check valve chamber through which a primary intravenous stream is arranged to pass by way of a primary fluid inlet port and a primary outlet port. Each check valve chamber has at least one physically associated infusion port through which a medicational or nutritional fluid can be injected in any number of possible ways. Each check valve chamber has an interior volume, a check valve opening formed between its interior volume and its associated infusion port, a check valve chamber opening formed through the check valve chamber and axially aligned with the check valve opening, a flexible check valve element, and a check valve support element.

Abstract: An improved self-sealing gasket provides hemostasis while reducing the force required to move a catheter or guidewire positioned within the gasket. Slits formed on one surface of the gasket intersect with a central aperture formed on the opposite face of the gasket. An annular ring formed on the gasket assists in retaining the gasket within a catheter introducer. An annular shelf may be provided distally of the gasket to prevent dislodgement of the gasket if an instrument is inserted into the introducer off axially.

Abstract: A drinking aid device which is used for fluid intake, in particular for elderly people, patients and the like. The user receives the liquid from a valve assembly with the assistance of a mouthpiece member. The valve assembly includes an upper lid member, a lower housing member and a closure member which is disposed between the lid member and the housing member. The closure member has one or more apertures and is movable by suction between an open position and a closed position in a check valve fashion for allowing the liquid to flow therethrough.

Abstract: The invention provides a self-cleaning inlet head for a fluid, operable in a first, draining, mode and in a second, backflushing, mode, including a body having a front end and a rear end; a piston slidably mounted in the body and having having a front face and a rear face; a first space extending between the rear end of the body and the rear face of the piston and a second space extending between the front face of the piston and the front end of the body; a bore connecting the first space and the second space; a valve mounted in the first space for closing off the bore during the second mode of operation; an aperture for access of the fluid from outside the head into the second space in the first mode of operation, and for exit from the second space in the second mode of operation, wherein, at the onset of the second mode of operation, the valve closes off the bore and subsequently moves the piston, thereby initiating a mechanical shearing action loosening any occluding matter in the aperture.

Abstract: A method and apparatus is provided for high pressure one-way fluid valving in angiography. The method includes inhibiting the flow of a sterile saline solution through a catheter lumen using the pressure of an opaque dye injected therethrough. A one-way fluid valve connects a pressurized source of saline solution to an inlet fitting of a catheter Y adapter. A second inlet fitting of the Y adapter is connected to a high pressure opaque media source through a gate valve. The one-way fluid valve is sensitive to a pressure differential thereacross to selectively open and close in response to the pressure within the catheter lumen versus the pressure of the saline solution. The one-way fluid valve includes a stainless steel check ball, a stainless steel biasing spring and double sealing O-ring adapted for radial compression by the stainless steel biasing spring and the pressure differential across the valve.

Abstract: An angiographic injector includes a syringe which is connected to a fluid reservoir through a valve which permits radiographic contrast material to be drawn from the reservoir into the syringe during a fill operation. The valve permits air to be expelled from the syringe through the valve during a purge operation, but blocks flow of contrast material from the syringe back to the fluid reservoir. During an injection, the valve blocks flow of contrast material back to the fluid reservoir while the contrast fluid is being delivered under pressure from the syringe to a patient.

Abstract: An implantable device grafted directly to vascular structures for high volume blood and/or fluid infusion and/or removal for such purpose as hemodialysis, apheresis, exchange transfusion, or large volume fluid infusion. The device is also adaptable to intermittent access to the venous or arterial circulations for purpose of blood sampling or giving medications. The device is comprised of an implantable fluid chamber connected to a vascular shunt which is then grafted directly to the vascular structure (e.g. artery or vein). The vascular end of the device employs a valve to prevent reflux of blood and subsequent washout of anticoagulant during periods when the device is not in use. The device is accessed percutaneously with a needle or needle-introduced catheter and is filled with anti-coagulant prior to needle withdrawal to prevent thrombosis.

Abstract: An enteral fluid infusion system wherein fluid is pumped through a conduit from a fluid supply source to a patient by a rotary peristaltic pump operating in an intermittent duty cycle mode which includes a free flow detector. The free flow detector includes a sensor for the operation of the peristaltic pump, as for example by the rotation of the rotor and/or motor; a sensor for the flow of fluid in the conduit. The free flow detector compares the sensed operation of the pump with the sensed flow against predetermined criteria. During operation of the fluid infusion system, if flow is sensed when the pump is not operating, as determined by the fact that no rotation is occurring, an alarm will be initiated to indicate that a free flow condition exists.

Abstract: A device for percutaneous administration of fluid preparations into a body cavity, vessel or organ, the device including a tube having both a fluid lumen and an inflation lumen and defined by a proximal end lying outside of the body and a distal end lying within the body, the proximal end of the fluid lumen being in fluid communication with a fluid source and the distal end disposed within the body, the distal end of the inflation lumen in communication with an inflatable member disposed within the body. In one embodiment, one end of the tube is connected to a retention platform having a central portion with a recess to confront the patient's abdominal wall. The retention platform has a plurality of circumferentially-spaced fingers extending radially from said central portion where only the end portion of each finger rests on the abdominal wall of the patient. Preferably, the proximal end of the inflation lumen is remote from the fluid lumen.

Abstract: Pressure relief valve apparatus is disclosed for shunting fluids under conditions of overpressure, thereby preventing further increases in the pressure within a fluid delivery system. A presently preferred embodiment of the apparatus of the invention is formed of two components, a valve body member and a valve tube member. The valve body member is provided with first and second connector elements for use in connecting the pressure relief valve into a medical fluid delivery circuit. It is also provided with first and second bores passing through the first and second connector elements, respectively, and exiting at respective first and second exit ports on the side of the valve body member. A valve seat comprising a raised annular ridge around the circumference of the valve body member separates the first and second exit ports.

Abstract: A catheter having an elongate body has a first lumen extending therethrough. A concave wall is formed in the body proximate the distal end thereof such that the concave wall is a wall of the first lumen. A first slit is formed in the concave wall. The first slit opens in response to decreased fluid pressure within the lumen so as to facilitate aspiration via the first lumen. Optionally, a first convex wall is formed in the body such that the first convex wall is a wall of the first lumen. A second slit is formed in the first convex wall. The second slit opens in response to increased fluid pressure within the first lumen so as to facilitate infusion via the first lumen. Optionally, a second lumen extends through a substantial portion of the body. A second convex wall is formed in the body proximate the distal end thereof such that the second convex wall is a wall of the second lumen. A third slit is formed in the second convex wall.

Abstract: An improved self-lubricating catheter and guidewire introducer is provided with a reservoir containing lubrication fluid located proximally of a sealing gasket in a modified end cap. An improved self-sealing gasket provides hemostasis while reducing the force required to move a catheter or guidewire positioned within the gasket.

Abstract: A surgical trocar assembly includes a disposable valve assembly, a cannula assembly, and a trocar with a handle. The cannula assembly includes a cannula base having a valve assembly coupling device at its proximal end, and a cannula extending from its distal end. The disposable valve assembly has a coupling device for removably coupling it with the cannula base. The valve assembly also includes a valve body with a fluid passage communicating with the hollow cannula when it is coupled to the cannula base. A slit or flapper valve and a universal washer are mounted within the valve body and allow the insertion of the trocar or other endoscopic instruments therethrough while providing a fluid sealing of the fluid passage. The valve assembly may be provided with a side port which optionally contains an automatic valve actuated by a luer coupling. Several different valve assembly-cannula base couplings are disclosed as well as several different types of trocars.

Abstract: A method and apparatus for injecting radiographic dye during angiography are provided. A deformable holding chamber is interposed between a contrast dye bottle and a syringe manifold. A one-way valve and an integral disconnect/flow-stop are connected between the bottle and the holding chamber. A vent is provided in the holding chamber, with a second one-way valve. Squeezing and releasing the deformable chamber fills the chamber from the bottle. The holding chamber contains a floating baffle which acts as a shut off valve by plugging the chamber outlet if the chamber becomes empty. The syringe is used to withdraw dye from the holding chamber. If dye remains in the bottle after performance of the procedure, the disconnect/flow-stop fitting can be disconnected, and the dye can be saved.

Abstract: A relief valve for regulating the operation of a surgical suction device comprises a plunger adjustably screwable into a fluid escape channel. A conical tip at the end of the plunger is shaped and dimensioned to progressively obstruct an escape port. Longitudinal grooves along the threaded walls of the plunger provide a passage for the fluid from or toward the escape port.

Abstract: A fluidic infusion system introduces a select liquid chemical into the environment surrounding the functional end of an in vivo catheter or probe. The catheter/probe typically has a-sensor or electrode positioned near or at its closed distal end. A plurality of spaced radial openings are formed in an appropriate pattern adjacent to the end of the catheter/probe for introducing the select liquid chemical into the appropriate environment. The catheter/probe has at least one lumen extending through its length for directing the liquid chemical from a controlled pump to the radial openings. The openings are positioned within the catheter/probe so that when the catheter/probe is inserted into the appropriate environment, e.g.

Abstract: A medication infusion pump is provided of the type adapted for implantation into the body of a patient, and for programmable delivery of a selected medication through a catheter to the patient over an extended period of time. A side port assembly is mounted quickly and easily onto the pump and defines a flow path through which the medication is discharged to the catheter. The side port assembly includes an access port to permit transcutaneous needle access to the discharge flow path, in combination with a check valve to prevent backflow within the discharge flow path. The discharge side access port can be used to flush residue from the catheter, or in combination with a primary refill port on the pump to flush the pump and/or to determine actual pump stroke volume.

Abstract: An improved self-sealing gasket provides hemostasis while reducing the force required to move a catheter or guidewire positioned within the gasket. Slits formed on one surface of the gasket intersect with a central aperture formed on the opposite face of the gasket. An annular ring formed on the gasket assists in retaining the gasket within a catheter introducer. An annular shelf may be provided distally of the gasket to prevent dislodgement of the gasket if an instrument is inserted into the introducer off axially.

Abstract: An intravenous fluid flow control device includes a rigid casing having a fluid entrance and a fluid exit. A portion of the casing has a flow restrictor. A pin is disposed inside the casing and axially movable within the flow restrictor. The pin has an interior passageway and at least one upstream opening for a fluid to pass from the casing fluid entrance to the interior passageway of the pin. The upstream opening is elongated in a direction parallel to a pin longitudinal axis, the pin elongated opening being axially movable within the flow restrictor to variably restrict a flow of the fluid passing through the interior passageway of the pin. The pin has a downstream opening for fluid to pass from the interior passageway of the pin to exit the device. Biasing structure (preferably a spring) biases the pin against a fluid pressure of the fluid entering from the casing fluid entrance to cause the pin elongated opening to move with respect to the fluid restrictor.

Abstract: An injection site designed for use with a needleless syringe includes a housing placed in an infusion line and an inlet for engaging the syringe and conveying a fluid to be mixed with the infusate to the interior of the housing. A liner within the housing controls flow of fluid through the inlet by sealing the inlet when the pressure in the housing is equal to or exceeds the pressure in the syringe. The housing is made of two parts, each of which includes a flange. When assembled, the spaced flanges are on opposite ends of the liner, which is not directly attached to the housing, to limit movement of the liner to maintain its position in the housing.

Abstract: A system for controlling drainage of the female bladder comprising a valved catheter, a stylet for placing the catheter in the female urethra, and a spike for opening the valve in the catheter to allow voiding of the contents of the bladder. The system also includes a sizing device for determining the length of the urethra so that the proper fitting catheter is used. The catheter comprises a hollow shaft with a extendable holding portion on one end for placement through the urethra and a crown on the other end for placement external of the body. The valve nay integral with the shaft or insertable after the catheter is placed in the urethra.

Abstract: A tubing set for connecting a source of irrigating fluid to an intraoperative surgical instrument having a fluid delivery passage therein. The tubing set includes a first section having an inlet for connection to the source of irrigating fluid, a second section having an outlet for connection to the intraoperative medical instrument, and a pump connected between the first section and the second section. A valve is located between the inlet and the outlet and restricts flow so that flow is in a direction from the inlet toward the outlet. The tubing set can deliver a continuous flow or trickle of fluid from the source of irrigating fluid to the medical instrument and can deliver a bolus of fluid to the surgical instrument upon operation of the pump.

Abstract: A catheter introducing assembly is provided which includes a self-shielding needle while providing captured visual blood flowback. The catheter introducing assembly includes a clear Y-Connector which is used for contrast injection and has an additional port for medication. A V-Spring is placed unrestricted in a spring holder which is attached to the distal end of the Y-Connector. The spring acts as a guard, once the needle is withdrawn, to protect the needle from forward movement. An injection port is provided for high pressure introduction of medication or contrast media. A silicon ball is retained in the injection port which, when medication is required, will reseal after the needle is withdrawn. A luer/filter assembly is provided in fluid communication with the introducer needle to allow air to escape through the filter for visualization of blood flowback upon needle insertion.

Abstract: A system for controlling drainage of the female bladder comprising a valved catheter, a stylet for placing the catheter in the female urethra, and a spike for opening the valve in the catheter to allow voiding of the contents of the bladder which also includes sensing and transmission means incorporated therein. The valve which may be integral with the shaft or located in a cap on the shaft may be manually operated or opened electronically by a signal transmitted from an external source.