Abstract: A clamp apparatus for selectively occluding a resilient tube to prevent free flow of fluid in the tube. The device comprises a base member to which the resilient IV tube is attached or through which it passes, and a slide clamp that slides relative to the base member and relative to the tube. The aperture in the slide clamp has a relatively open hole at one end, through which the tube passes when the slide clamp is an open position, allowing fluid to flow through the tube. The aperture also has a relatively constricted slot at the other end, through which the tube passes when the slide clamp is in the occluding position, preventing fluid flow through the tube. The slide clamp includes a groove for receiving a cooperatively shaped rib on the base member. The groove and rib are configured to guide relative movement between the slide clamp and the base so as to prevent significant lateral movement.

Abstract: A valve comprising an inlet housing, an outlet housing, an elastomeric valve element having a generally dome-shaped configuration with a central integral stem positioned substantially concentrically therewith, the inlet housing and outlet housing being fastened together at a joint with the elastomeric valve element positioned therein and the valve element including a plurality of longitudinal ribs formed along an outer annular periphery of a lower end of the dome-shaped configuration that define flow channels that allow fluid flow from across an upper surface of the dome-shaped configuration through the flow channels.

Abstract: A needle-free medical connector includes a housing with a first port and a second port. The connector also includes a piston element defining a fluid passageway between the first and second ports. The piston element is movable between flow and non-flow positions. The piston element has an expandable section having a variable inner width and volume that forms a part of the flow path through the connector. As the piston is compressed to the flow position, the expandable section is expanded in width by movement over a flow post thereby maintaining or increasing the volume of the fluid passageway through the connector. The expandable section has a configuration permitting the continuous flow of fluid through its entirety.

Abstract: A catheter apparatus is provided that includes a tubular body having a distal end. The body defines first and second lumens. The first lumen has a first adapter that includes a first valve biased to seal the proximal end. The first lumen defines a first lateral port and the second lumen defines a second lateral port. A push rod is connected to the first valve for corresponding movement therewith and extends to a tip. The tip includes a first member extending into the first lumen and a second member extending into the second lumen such that the first member seals the first lateral port and the second member seals the second lateral port in a closed position of the tip. The first valve is engageable such that fluid communication is established between the proximal end of the first lumen and the first lumen, and the first and second members move to an open position whereby fluid communication is established.

Abstract: A medical valve includes a valve body having a central fluid passageway defined therein. A movable piston adapted in size and shape to be located within said central fluid passageway of said valve body. A sealing interface is defined between said movable piston and said central fluid passageway. An upper seal is located at an upper portion of said sealing interface. It is formed by a seal carried by said valve body. A lower seal is located at a lower portion of said sealing interface, and is formed by a seal carried by said movable piston. The lower seal remains intact until after said upper seal is broken.

Abstract: A self-sealing male Luer connector for connection with a female Luer connector. The male Luer connector includes a housing having a distally-projecting tubular male body and a surrounding cuff interconnected by a proximal wall in which is formed at least one activation opening. A valve plug is slidably installed within the housing and formed with a distal end configured to sealingly engage the distal end of the male body's interior flow passage and with at least one activation arm at its proximal end configured to extend through the activation opening into the cavity formed between the male body and the cuff. An elastomeric device is sealingly configured within the activation opening about the activation arm to secure the valve plug in position and bias it distally. The proximal end of the male Luer connector may be configured as a conventional female connector, a blood collection device, or other such device.

Abstract: Needleless access port valves are generally discussed herein with particular discussions extended to needleless access port valves comprising a resilient valve body. The resilient valve body includes a tapered set port that stretches when a plug is pushed by a medical implement which in turn pushes the set port. Pushing the plug against the set port opens fluid communication between the inlet port and the outlet port. Upon removal of the medical implement, the resilient valve body pushes the plug back to its closed position.

Abstract: A needle free medical connector includes a housing with a first port and a second port. The connector also includes a piston element defining a fluid passageway between the first and second ports. The piston element is movable between flow and non-flow positions. The piston element has a compressible section having a variable inner width that forms a part of the flow path through the connector. As the piston is compressed to the flow position, the compressible section self-expands in width thereby maintaining or increasing the volume of the fluid passageway through the connector. The compressible section has a configuration permitting the continuous flow of fluid through its entirety.

Abstract: A normally closed valve that may be opened upon insertion of a nozzle permits two-way flow when opened by a luer-taper nozzle. The valve also is able to resist large back pressures. The valve includes a substantially rigid housing that defines a passageway having an inlet section and an outlet section. The housing has an exterior inlet face to which the inlet section opens. The inlet section preferably has tapered and expanding zones. The tapered zone is adjacent to the exterior inlet face and is shaped to receive the nozzle. The expanding zone is adjacent to the tapered zone and has a larger inner diameter than the tapered zone's inner diameter. The exterior of the inlet section of the housing may have threads to accept luer-lock threads that may surround the nozzle.

Abstract: A method, system and apparatus for performing peritoneal dialysis are provided. To this end, in part, a cam arrangement for operating a series of valves in cooperation with a pump that pumps fluid to and from a patient, the valves including a supply valve, a drain valve, a from-patient valve and a to-patient valve is provided. The cam arrangement includes a camshaft and a series of cams connected to the camshaft. The cams are positioned and arranged to toggle back and forth between a first open position for the supply valve and a second open position for the drain valve, a third open position for the from-patient valve and the second open position, and the first open position and a fourth open position for the to-patient valve.

Abstract: A medical valve has a translating member that enlarges the volume of the interior of the valve when the valve is in an open mode (permitting fluid flow), and decreases the volume of the interior when the valve is in a closed mode (preventing fluid flow). This varying volume should substantially eliminate drawback into the valve. To that end, the valve includes a housing having an inlet and an outlet, and a fluid channel extending between the inlet and the outlet. The fluid channel includes a variable volume region. The valve further includes the above noted translating member, which is secured to the housing and at least partly bounds the variable volume region. The translating member has at least a portion that moves distally when the valve transitions from the closed mode to the open mode. The distal movement of the translating member enlarges the volume on the variable volume region.

Abstract: A flow control device includes a sealing component that can be positioned within a bronchial lumen. The sealing component can comprise two or more overlapping segments that are movable relative to one another such that the segments collectively form a seal that can expand and contract in size to fit within and seal bronchial lumens of various sizes.

Abstract: A needleless injection site comprising a housing defining proximal and distal ends and including a reseal member disposed therein. The reseal member has an elastically openable and closable aperture formed therein, and normally resides within the housing in a closed position wherein the aperture is in a closed configuration. The reseal member is deformable such that the application of distally directed pressure thereto will cause the reseal member to distally advance within the housing to an open position wherein the aperture assumes an open configuration. The removal of the distally directed pressure from the reseal member will cause it to resiliently return to the closed position wherein the aperture assumes the closed configuration.

Abstract: An improved needle-free intravenous injection port assembly is disclosed. Embodiments include a boot valve with a helical surface, a boot valve and septum which mate with mechanical interference, a spike with a rough outer surface coated with a lubricant, a septum having a shoulder and a single continuous swabbable surface, a septum and a boot valve which are pre-punctured with a solid core steel needle, a septum with a frustroconical extension and a combination single piece septum and boot valve. The injection port assembly provides neutral fluid displacement during coupling and uncoupling.

Abstract: A one-way valve assembly can be fitted to the end of a syringe to allow fluid to flow from the syringe and into a body cavity but to prevent backflow. The valve assembly is opened by insertion of the luer tip of the syringe into the assembly inlet. The valve has an internal elastic member that forms a variable volume internal chamber. This chamber expands upon insertion of the luer tip into the inlet and shrinks when the luer tip is removed from the assembly. The shrinking action creates a positive pressure in the valve assembly to prevent backflow.

Abstract: A device for delivery of a biocompatible polymer composition for treatment of urinary incontinence provides for delivery of biocompatible polymer material and a solidification agent through two lumens. The delivery device provides better control of the precipitation of the polymer in the periurethral tissue and detachment of the precipitated mass from the delivery device. The medical device includes a needle having a lumen and an inner cannula positioned within the needle lumen and movable longitudinally in the needle lumen from an extended position to a withdrawn position to sheer or cut the delivered mass of polymer material away from the needle tip.

Abstract: A needle free medical connector includes a housing with a first port and a second port. The connector also includes a piston element defining a fluid passageway between the first and second ports. The piston element is movable between flow and non-flow positions. The piston element has a compressible section having a variable inner width that forms a part of the flow path through the connector. As the piston is compressed to the flow position, the compressible section self-expands in width thereby maintaining or increasing the volume of the fluid passageway through the connector. The compressible section has a configuration permitting the continuous flow of fluid through its entirety.

Abstract: An over pressurization relief apparatus having a manual over pressurization selector which allows a user to manually select from at least a first and second over pressurization limit. The over pressurization relief apparatus includes a pressurization chamber, a pressure relief mechanism, a seal, and a manual over pressurization selector. The pressurization of the pressurization chamber corresponds with the pressurization of the pressure infusion bag. The pressure relief mechanism prevents additional pressurization of the pressure infusion bag once the over pressurization limit has been reached. The seal is positioned between the pressurization chamber and the pressure relief mechanism to prevent the loss of pressurization from the pressure infusion bag when the pressurization in the pressurization chamber is less than the over pressurization limit.

Abstract: A closed system, spikeless, positive-flow valve device includes a body defining an internal cavity. At the proximal end of the body is an opening which is preferably sufficiently large to receive an ANSI standard tip of a medical implement. The valve includes a plastic, resilient silicon seal which fills the upper cavity and opening with an oval seal cap having a slit. The opening presses the oval seal cap to keep the slit closed in the decompressed state. The slit opens as the nose of the medical implement compresses the seal into the cavity and the seal cap is free from the opening. The housing also includes a fluid space which facilitates fluid flow between the medical implement and a catheter tip.

Abstract: An intraluminally placeable tubular device includes an elongate hollow tubular member having a luminal surface and an exterior surface defining a wall portion therebetween. The hollow tubular member has an open proximal end and an opposed distal end. The wall portion has sufficient self-supporting rigidity to permit the device to be advanced through a body lumen during intraluminal placement. The tubular member includes yarns interconnected in a pattern defining opposed interior and exterior textile surfaces. At least one of the textile surfaces is the body fluid-contacting luminal surface or the body lumen-contacting exterior surface. A textile infusion and/or a textile aspiration valve is also provided. A percutaneously or orificially placeable catheter with such textile valves is provided.

Abstract: A low profile inflation valve located inside a balloon catheter that enables a user to inflate the balloon and exchange other medical apparatus over the catheter while the balloon remains inflated. The low profile inflation valve of the present invention includes a first tube having a lumen and at least one region of decreased inner diameter, and a structure movably located inside the lumen of said first tube, wherein said region of decreased inner diameter of said first tube forms a seal with a portion of said structure.

Abstract: A method and apparatus are provided for quickly connecting a handpiece to a pressurized fluid source. A hollow tube on the handpiece is inserted through an aperture in an annular gasket which is held in a chamber in a body. On application of pressurized fluid to the body, the gasket is pressed against the walls of the chamber, and against the tube, thereby channeling the pressurized fluid through the hollow tube. The handpiece is retained in connection with the body by a releasable connector, such as a latch. The handpiece can be removed and replaced by releasing and remaking the connection.

Abstract: A catheter with a distal end having a member formed from a hydrophilic composition is provided. The hydrophilic composition expands upon contact with an aqueous fluid to move the member from a quiescent state to an expanded state. The member may provide an open passageway in the quiescent state and be capable for forming a fluid tight seal by action of expansion of the hydrophilic composition. In such a case the member acts as a valve for permitting or preventing fluid flow through the catheter.

Abstract: A suction regulator valve adapted to be installed between a suction pump or other vacuum source and a suction tube or catheter, the valve comprising a hollow valve body having an outer surface with a generally transverse or circumferential opening therethrough, and a valve member slidably mounted on the valve body for generally transverse or circumferential movement thereon. The valve member is movable between an open position wherein the opening is uncovered and a closed position wherein the valve member covers and closes the opening. The valve member is positioned for engagement by the thumb or other finger of a user to enable the movement of the valve member to cover or uncover all or a portion of the opening. The suction regulator valve may be a separate member, may have a handle portion or may be formed integrally with a suction wand or other suction device.

Abstract: A needless valve is described which avoids the suctioning problems of the prior needleless devices upon deactivation and which preferably provides a positive self-purging effect. The valve is self-purging at the end of an administration cycle, avoiding clogging of attached catheters or other devices, and ensures that substantially all of liquid received into the valve is delivered to the receiver. The valve is also extremely simple in design and easy to construct and assemble, since it consists of only three pieces. The valve has a base with a connector for fluid communication attachment to tubing or other device, a solid elongated fluid channeling rod, and an internal fluid flow conduit; a flexible hollow expandable and contractible plug fitting over and moveable along the rod; and a tubular housing fitting over the plug and attached to the base.

Abstract: A slide clamp includes a slot formed in a plate though which a fluid tube is mounted. The tube may be moved to a flow section of the slot or to an occluding section of the slot. Interconnecting the flow and occluding sections is a pinch zone in which the slot is narrower than the occluding section. Because of this narrow slot, the pinch zone resists movement of the tube from either the occluding or the flow sections into another section. The pinch zone includes a pair of curved beams that are formed as a result of apertures formed in the plate at locations laterally outward from the slot of the pinch zone. As a tube is forced from the occluding section to the flow section the curved beams flex outwardly permitting the tube to pass. However, if enough force is not applied to the tube, it will not overcome the curved beams and they will stop movement of the tube. After the tube has passed, the curved beams resiliently return to their rest position once again providing a stop.

Abstract: A closed system, needleless valve device includes a generally tubular body defining an internal cavity. On the proximal end of the body there is an opening which is preferably sufficiently large to receive an ANSI standard tip of a medical implement. The distal end of the body has a generally tubular skirt. The valve also includes a hollow spike having a closed tip. The spike includes at least one longitudinal 18-gauge hole located distal the tip, and is seated inside the cavity such that the tip is below the proximal end of the body. An annular support cuff is connected to the spike which seals off a portion of the cavity of the body such that an upper cavity containing the tip is defined. The valve also includes a plastic, resilient silicone seal which fills the upper cavity and opening and covers the tip of the spike so as to present a flush surface. An adaptor enables the valve to be attached to a resealable container.

Abstract: A needle free medical connector includes a housing with a first port and a second port. The connector also includes a piston element defining a fluid passageway between the first and second ports. The piston element is movable between flow and non-flow positions. The piston element has a compressible section having a variable inner width that forms a part of the flow path through the connector. As the piston is compressed to the flow position, the compressible section self-expands in width thereby maintaining or increasing the volume of the fluid passageway through the connector. The compressible section has a configuration permitting the continuous flow of fluid through its entirety.

Abstract: A normally closed valve that may be opened upon insertion of a nozzle permits two-way flow when opened by a luer-taper nozzle. The valve also is able to resist large back pressures. The valve includes a substantially rigid housing that defines a passageway having an inlet section and an outlet section. The housing has an exterior inlet face to which the inlet section opens. The inlet section preferably has tapered and expanding zones. The tapered zone is adjacent to the exterior inlet face and is shaped to receive the nozzle. The expanding zone is adjacent to the tapered zone and has a larger inner diameter than the tapered zone's inner diameter. The exterior of the inlet section of the housing may have threads to accept luer-lock threads that may surround the nozzle.

Abstract: A closed system, needleless valve device includes a generally tubular body defining an internal cavity. On the proximal end of the body there is an opening which is preferably sufficiently large to receive an ANSI standard tip of a medical implement. The distal end of the body has a generally tubular skirt. The valve also includes a hollow spike having a closed tip. The spike includes at least one longitudinal 18-gauge hole located distal the tip, and is seated inside the cavity such that the tip is below the proximal end of the body. An annular support cuff is connected to the spike which seals off a portion of the cavity of the body such that an upper cavity containing the tip is defined. The valve also includes a plastic, resilient silicone seal which fills the upper cavity and opening and covers the tip of the spike so as to present a flush surface. An adaptor enables the valve to be attached to a resealable container.

Abstract: A medical valve has a translating member that enlarges the volume of the interior of the valve when the valve is in an open mode (permitting fluid flow), and decreases the volume of the interior when the valve is in a closed mode (preventing fluid flow). This varying volume should substantially eliminate drawback into the valve. To that end, the valve includes a housing having an inlet and an outlet, and a fluid channel extending between the inlet and the outlet. The fluid channel includes a variable volume region. The valve further includes the above noted translating member, which is secured to the housing and at least partly bounds the variable volume region. The translating member has at least a portion that moves distally when the valve transitions from the closed mode to the open mode. The distal movement of the translating member enlarges the volume on the variable volume region.

Abstract: A needleless injection site comprising a housing defining proximal and distal ends and including a reseal member disposed therein. The reseal member has an elastically openable and closable aperture formed therein, and normally resides within the housing in a closed position wherein the aperture is in a closed configuration. The reseal member is deformable such that the application of distally directed pressure thereto will cause the reseal member to distally advance within the housing to an open position wherein the aperture assumes an open configuration. The removal of the distally directed pressure from the reseal member will cause it to resiliently return to the closed position wherein the aperture assumes the closed configuration.

Abstract: A closed system, needleless valve device includes a generally tubular body defining an internal cavity. On the proximal end of the body there is an opening which is preferably sufficiently large to receive an ANSI standard tip of a medical implement. The distal end of the body has a generally tubular skirt. The valve also includes a hollow spike having a closed tip. The spike includes at least one longitudinal 18-gauge hole located distal the tip, and is seated inside the cavity such that the tip is below the proximal end of the body. An annular support cuff is connected to the spike which seals off a portion of the cavity of the body such that an upper cavity containing the tip is defined. The valve also includes a plastic, resilient silicone seal which fills the upper cavity and opening and covers the tip of the spike so as to present a flush surface. An adaptor enables the valve to be attached to a resealable container.

Abstract: A vial closure device, a sample vial incorporating such a vial closure device, and certain methods of using such a vial and closure device. The vial and closure device are intended to contain a gaseous sample or a headspace gas present above a liquid or solid material, so that the gaseous sample or headspace gas can be conveniently analysed, typically by means of an autosampler connected to an analytical instrument such as a mass spectrometer. Mass spectrometric methods of determining the isotopic composition of hydrogen and oxygen comprised in aqueous samples contained in vials fitted with such closure devices are disclosed. The vial closure device comprises a hollow body member locatable in the mouth of a vial, and a first seal for making a substantially gas-tight seal between the exterior of said hollow body member and said vial.

Abstract: A medical valve has a body and a flexible element. The body includes a wall structure defining an internal cavity having an inside and an outside. The body also has a proximal end and a distal end. The proximal end has an opening sufficiently large to receive a tip of a delivery end of a medical implement which transfers fluid through the delivery end. The body has a fluid escape space in its wall structure. The flexible element is adapted to be moved into a compressed state upon insertion of the tip of the medical implement into the opening. The flexible element is sufficiently resilient to return to a decompressed state upon removal of the tip of the medical implement from the opening. The fluid escape space is in fluid communication with the outside of the cavity when the seal is in its compressed state.

Abstract: A method of sterile needless vial access, utilized to transfer materials from one unit to another. The method utilizes a swab-able access port and a blunt cannula. The access port receives the blunt cannula to couple and aseptically transfer medical and body fluids. The swab-able access port permits disinfectant treatment before receipt of the blunt cannula to limit and prevent contamination of sterile fluids.

Abstract: An irrigator used in a celioscope surgery comprises a main casing, a water pumping stud and a water control stud which are engaged with the main casing. An interior of the main casing has a pumping opening and a suction opening, and a water outlet channel and a pumping flow channel which are vertical to the pumping opening and suction opening. Thereby, the water outlet channel and pumping flow channel are at an upper portion of the main casing. Thereby, dirty water accumulated in the affected part can be pumped out from a water outlet tube through the pumping flow channel. Since the water is pumped out along a straight way, it is prevented that dirty water is left in some bending portions. Therefore, dirty water can be pumped out completely. Furthermore, users may hold it by any hand conveniently.

Abstract: A closed system, needleless valve device includes a generally tubular body defining an internal cavity. On the proximal end of the body there is an opening which is preferably sufficiently large to receive an ANSI standard tip of a medical implement. The distal end of the body has a generally tubular skirt. The valve also includes a hollow spike having a closed tip. The spike includes at least one longitudinal 18-gauge hole located distal the tip, and is seated inside the cavity such that the tip is below the proximal end of the body. An annular support cuff is connected to the spike which seals off a portion of the cavity of the body such that an upper cavity containing the tip is defined. The valve also includes a plastic, resilient silicone seal which fills the upper cavity and opening and covers the tip of the spike so as to present a flush surface. An adaptor enables the valve to be attached to a resealable container.

Abstract: A closed system, needleless valve device includes a generally tubular body defining an internal cavity. On the proximal end of the body there is an opening which is preferably sufficiently large to receive an ANSI standard tip of a medical implement. The distal end of the body has a generally tubular skirt. The valve also includes a hollow spike having a closed tip. The spike includes at least one longitudinal 18-gauge hole located distal the tip, and is seated inside the cavity such that the tip is below the proximal end of the body. An annular support cuff is connected to the spike which seals off a portion of the cavity of the body such that an upper cavity containing the tip is defined. The valve also includes a plastic, resilient silicone seal which fills the upper cavity and opening and covers the tip of the spike so as to present a flush surface. An adaptor enables the valve to be attached to a resealable container.

Abstract: A valve which includes a stem having a slit at an end thereof. The valve stem is located in a valve body and is deformable. When a tip of an instrument is engaged with a slit in the stem, the stem shifts in the valve body, top portion folds inward, the slit seals against the instrument and allows liquid to flow through the stem, to or from the instrument. All components have circular cross sectional geometry.

Abstract: Embodiments of the present invention comprise one-part elastomeric valves which are manipulated after molding to preload the valve seal. The valves maintain positive seal until a fluidic pressure or mechanical force is applied to open the valve. The valves return to a closed state after the pressure or force is removed.

Abstract: A medical valve has a body which includes a wall structure defining an internal cavity having an inside and an outside. The body also has a proximal end and a distal end. The proximal end has an opening sufficiently large to receive a tip of a delivery end of a medical implement which transfers fluid through the delivery end. The body has a fluid escape space in its wall structure. The valve also has a spike with a tip and at least one hole located at or near the tip. The spike has a passageway in communication with the hole that allows fluid to flow through the spike. A resilient seal in the cavity surrounds the spike. This seal is adapted to be moved into a compressed state upon insertion of the tip of the medical implement into the opening. The seal is sufficiently resilient to return to a decompressed state upon removal of the tip of the medical implement from the opening. The fluid escape space is in fluid communication with the outside of the cavity when the seal is in its compressed state.

Abstract: A medical tubing and slide clamp set is disclosed for use with a medical infusion pump designed for operation with a preselected medical tubing set having predetermined size and functional characteristics. The medical tubing and slide clamp includes a preselected medical tubing set having predetermined size and function characteristics. An opaque slide clamp is provided with a grasping end and a longitudinal clamp plate extending from the grasping end. The longitudinal clamp plate defines a clamp slot with a wide open portion sized for receiving the preselected medical tubing without closing the tubing, a narrow open portion sized for closing the tubing and a transition portion interconnecting the narrow and wide portions. A plurality of orifices are formed along the longitudinal clamp plate at predetermined locations arranged according to the size and functional characteristics of the medical tubing set.

Abstract: A one way valve assembly has an inlet and an outlet, the inlet forming one end of a tubular passageway, a valve member which is slideable along the tubular passageway between a closed position where fluid is unable to flow through the valve assembly, and an open position, the valve member having an outer end and an inner end, and biasing means to bias the valve member to the closed position, characterized in that when the valve member is in the closed position, the outer end is substantially at the inlet of the valve assembly to close of the tubular passageway and to allow the inlet area to be sterilized.

Abstract: A surgical irrigation system is suitable for endoscopic and other surgical procedures. A hand held handpiece has a forward protruding hollow tip for supplying irrigation liquid to a surgical site, a hand actuable control for controlling irrigation liquid flow to the tip, and an irrigation liquid inlet. A self contained pumping unit is locatable adjacent a source of irrigation liquid and remote from the handpiece. The pumping unit comprises a housing containing an outlet for irrigation liquid, a pumping member for pumping irrigation liquid through the outlet, a motor for driving the pumping member, and an electric battery assembly for energizing the motor. An elongate tube connects the pumping outlet to the handpiece irrigation liquid inlet for supplying pumped irrigation liquid to the handpiece.

Abstract: A fluid transfer device comprising a hollow piercing element having a first end for receiving a standard syringe nose or other similar medical device and a second end having a tapered tip for accessing fluid inside a medication container is disclosed. In a preferred embodiment, the device has a disk-shaped stop for limiting entry of the piercing element into the vial. Preferably, the piercing element includes outwardly extending barbs which allow the device to be inserted into a vial but which prevent the device from being removed from the vial after insertion. After the syringe is disengaged from the device, the device and spent medication vial may be discarded as a unit. Alternatively, the device can remain attached to the vial, and a new syringe can be used to withdraw additional fluid from the vial when desired. In an alternate embodiment, a reusable, resealable valve is connected to the first end of the piercing element, which valve allows multiple syringes to be used with the piercing element.

Abstract: A fluid management system is disclosed which includes an injection device, a medical device, and a valve. The medical device is in fluid communication with the injection device. The valve is operatively associated with the medical device, and the valve includes a mechanism for slidably opening the valve.

Abstract: A medical coupling device manufactured from a device material provides an secure friction fit to a male nozzle device. To that end, the medical coupling device includes a fluid port (with an inner periphery) for receiving a male nozzle with a nozzle outer diameter, and a coupling material having a coupling material frictional value that is greater than the device material frictional value. The coupling material preferably is disposed about the inner periphery of the fluid port, while it and the inner periphery form an opening having an opening inner diameter. The opening inner diameter preferably is sized to receive and secure the male nozzle. The device material frictional value preferably is lower than the coupling material frictional value.

Abstract: A contrast fluid delivery method and system includes a multiple-reuse filling section for attachment by conduit to a contrast fluid supply container, and a delivery section that is removably attached to the filling section for delivering contrast fluid held in the filling section to a patient. The filling section includes a main body having a fluid chamber, a contrast fluid filling inlet with a gravity-operated valve, an opening for connecting an operable power syringe, and a contrast fluid outlet fed through a spring-loaded one-way check valve. The delivery section includes a first delivery conduit connected between the contrast fluid outlet of the main body and the fluid inlet of an inline aspirator syringe, and a second delivery conduit connected at one end to a fluid outlet of the aspirator syringe and at the other to a catheter for delivering the contrast fluid to a patient.

Abstract: A system and method for pressurizing bags of physiological fluids include a control valve for providing deflation of a bladder that compresses the bags. The toggle portion of the control valve is movable between a first and second position respectively for inflation and deflation of the bladder. When the toggle portion is in the first position, the control valve connects a source of pressurized air to the bladder, and when the toggle portion is in the second position, the control valve allows the bladder to exhaust directly to the atmosphere through an outlet port in the valve. The size of the outlet port is so large that it creates only very little resistance to the discharged air.