Abstract: Implanted catheters are locked with a solution comprising a lower alcohol, typically ethanol, propanol, or butanol, in a range from 1% to 99% by volume, and an additive in a range from 1% to 99% by volume, the additive comprising an anti-microbial, typically taurolidine or triclosan, or an anti-coagulant, typically riboflavin, sodium citrate, ethylene diamine tetraacetic acid, or citric acid. The use of an alcohol and additive solution can effectively reduce fouling of the catheter, particularly clotting and thrombus in intravascular catheters, as well as eradicate existing infections and/or reduce the risk of potential infections. Existing infections and/or potential infections can be further reduced by employing a catheter body which permits an anti-microbial solution to penetrate into the catheter body and preferably through the catheter into tissue surrounding the implanted catheter.

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 for selectively permitting a fluid flow between first and second medical implements is disclosed. The valve has a housing with an interface suitable for receiving a connector portion of a first medical device such as a catheter, and a seal made of a flexible material. The seal has a first end in fluid communication with the interface, a second end suitable for receiving the second medical device, and at least one slit in fluid communication with the first end and the second end. The slit defines a restricted fluid flow path and a relatively small interior volume when in an undisturbed state, defines an expanded fluid flow path and a larger interior volume upon the introduction of the second medical instrument into the slit, and retracts to define a restricted flow path and a small interior volume upon the withdrawal of the second medical device from the seal. The slit is constructed such that its upstream end initially is sealed as the second medical device is withdrawn.

Abstract: A needless connector is provided which utilizes a resealable preslit septum valve. The valve is resiliently restrained relative to a housing with the valve and housing configured to accept a standard male luer lock having a luer tip which penetrates the valve through the opening to extend within the housing and a luer locking flange of the luer lock extending about the housing. The valve includes a disk shaped upper portion covering the opening, a lower portion spaced from the housing and extending downward from the disk shaped portion into a passageway defined by the housing, and an annular skirt to attach the septum to the housing. The connector exhibits satisfactory leak pressure after multiple connections and disconnects to the luer lock fitting and long periods of indwell of the luer tip.

Abstract: A hemostasis cannula includes a housing having a passage therethrough sized to receive a catheter and a valve body mounted in the passage. The valve body includes an opening therethrough which forms a seal around a catheter enclosed within the cannula. In one embodiment, a ring of raised material surrounds the opening. In another embodiment, a ring of raised material surrounds the hole, and an internal ring of material lines at least a portion of the interior of the opening. The valve body is compressed within the cannula housing. When the catheter is removed, the valve body closes thus blocking air flow into the patient's blood vessel and also blocking blood flow out of the patient's blood vessel. The cannula housing also includes a side port for introducing fluids into the patient's blood vessel.

Abstract: A resealable barrier closure for a container with an open top and an annular snap ring below the open top. The closure includes a shell having an outer skirt dimensioned to telescope over the open top of the container. The outer skirt has a snap ring for engaging the snap ring on the container. The shell further includes an inner skirt to telescope into the open top of the container. An elastomeric diaphragm is sealingly engaged in the inner skirt. A barrier cup extends across the bottom face of the diaphragm and telescopes upwardly over the inner skin. The barrier cup initially is sealed hermetically to the container and to the plastic shell. The container may be opened by urging the plastic shell upwardly with sufficient force to break the seal between the barrier cup and the container. The container then may be resealed by merely urging the closure back over the open top of the container.

Abstract: A connector assembly and a fluid system or device comprise a connector assembly which includes first and second fittings, each fitting having an aperture, and a stem disposed in the aperture of the first fitting. In various embodiments of the invention, the connector assembly may further comprise a socket cooperatively arranged with one of the first and second fittings, at least one resilient sealing member, a sealing layer joined to the socket or covering the resilient sealing member, and/or a deformable locking device. A method for making a connection includes mating a first fitting having an aperture and a second fitting having an aperture without fluid within the first and second fittings, establishing a fluid flowpath through the first and second fittings by advancing a stem having a head through the aperture of the first fitting into the aperture of the second fitting, and establishing fluid flow through the first and second fittings by opening a fluid blocking mechanism.

Abstract: A septum penetrable by a member and which maintains a seal following member penetration in an axial direction and withdrawal. The septum includes a first layer of resilient material having first and second opposed surfaces, and a second layer extending across the first surface of the first layer and which is in radial tension. A third layer under tension may extend across the second surface. Septum assemblies and methods of fabricating the septa are also provided.

Abstract: A needleless luer access connector is disclosed having a septum disposed in a housing. The septum has a proximal portion with a cross section, a medial portion with a cross section smaller than the cross section of the proximal portion, and a distal portion. A longitudinal slit extends through the septum from the proximal portion to the distal portion. The septum and housing are designed so that septum will not be rotated or removed from the housing when the connector is accessed by a male luer taper. In addition, the septum and housing are designed to bias the slit at the distal portion closed and so a male luer connector does not have to extend completely through the distal portion to open the slit at the distal portion. Finally, the septum and housing are designed to minimize the amount of dead space in the connector when accessed with a male luer taper.

Abstract: A needleless connector for medical use, adapted to facilitate the flow of fluid therethrough, includes a housing having an inlet port and an outlet port. The connector also includes a flex-tube assembly defining a fluid path between the inlet port and the outlet port. The flex-tube assembly is movable between uncompressed and compressed states. The flex-tube assembly has a first internal volume when in the uncompressed state and a second internal volume, greater than or substantially equal to the first internal volume, when in the compressed state.

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 hemostasis cannula unit including a valve housing, a cap, and a hemostasis valve, wherein the hemostasis valve includes a proximal valve gasket and a distal valve gasket compressed against the valve gasket by the valve housing, wherein the proximal valve gasket is the same shape as the distal valve gasket.

Abstract: A partitioned hemostasis valve system for use with a splittable sheath, including a partitioned hemostasis valve housing which holds a partitioned hemostasis valve formed in at least two separate and distinct sections. Pivotable wing portions are secured to the partitioned valve housing such that upon pressure being placed on these wing portions, the separate sides of the partitioned hemostasis valve housing and the partitioned hemostasis valve are separated. The partitioned hemostasis valve system may also include a splittable adaptor system for securing to a splittable sheath.

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 valve assembly for the sealed reception of an elongated object is provided. The assembly includes a valve body defining at least one opening configured and dimensioned to permit entry of an elongated object and defining a central longitudinal axis, and an elongated seal member having a resilient sealing structure and defining an aperture in general alignment with the opening of the valve body whereby the aperture is configured and dimensioned such that upon insertion of the object into the aperture, the resilient sealing structure resiliently engages the outer surface of the object in a tight manner. The sealing structure includes a plurality of elongated bristle members attached to the seal member. The bristle members are positioned to engage the elongated object upon at least partial insertion of the elongated object into the valve body.

Abstract: Implanted catheters are locked with a solution comprising a lower alcohol, typically ethanol, propanol, or butanol, most preferably isopropanol. The use of an alcohol can both reduce fouling of the catheter, particularly clotting and thrombus in intravascular catheters, as well as reducing the risk of infection. The risk of infection can be further reduced by employing a catheter body which is sufficiently porous to permit the lower alcohol or other anti-microbial solution to penetrate into the catheter body and preferably through the catheter into tissue surrounding the implanted catheter.

Abstract: The positive flow needleless connector has a cannula slideably mounted within a tubular housing. A sleeve-like septum seals the cannula from an outside environment while also sealing an internal chamber of the cannula from a flow path in a male luer housing. Movement of the cannula from an extended position to a retracted position against the force of a spring exposes a second inlet of the cannula to the flow path of the male luer housing to permit flow therebetween. During disconnect, the inlet from the cannula is sealed prior to the cannula returning the extended position. This allows fluid to move from a reservoir between the cannula and septum to move into the passage of the male luer housing.

Abstract: The invention relates to a connector which has an inner displacement member. The flow is stopped by the connector, i.e. the connector is impervious, in a first position. In a second position of the displacement member, with a stop defining the position, flow apertures are released which release the flow into the flow carrying line.

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 valve apparatus comprising a tubular body having a lumen therethrough and which is adapted for accessing the cardiovascular or other intravenous system of a patient. The body includes a compression chamber communicating with the lumen and adapted to cooperate with a seal. The compressible seal being configured to selectively seal and unseal the lumen in response to a compressive force acting on the seal. The seal having a longitudinal passageway therethrough that communicates with the lumen and is selectively sealed and unsealed in response to changes in the compressive force generated by a plunger assembly. The plunger assembly is configured to apply a certain amount of compressive force on the seal via the engagement of a rotating member and an engagement member under the influence of a rotating end cap. A selecting mechanism comprising a selecting lever and a selecting assembly is movably coupled to the tubular body and communicates with the plunger assembly.

Abstract: A blood sampling/injecting valve includes a housing formed with a cavity extending along a longitudinal axis of the housing, the cavity is adapted for sealingly receiving a syringe Luer connector and the housing further is provided with an inlet port and an outlet port. The valve includes also a plunger formed with a through going communication conduit and with a flow path for a liquid. The flow path is configured as a recess, which is opened to a top face of the plunger and to a lateral surface of the plunger. The plunger is axially displaceable by the Luer connector between a flow position in which the communication conduit directly communicates between the inlet port and the outlet port and a sampling/injecting position in which the flow path directly communicates between the Luer connector and the outlet port, while the inlet port is disconnected from the outlet port. The plunger is normally biased into the flow position.

Abstract: A sealing rubber closure is provided for use with a syringe/container specified by ISO (the International Organization of Standardization) and having a Luer nozzle to be inserted into a Luer-nozzle-receiving part of the sealing rubber closure. The Luer-nozzle-receiving part is configured, on a side of an inner end portion thereof, in an untapered cylindrical form to assure tight-fitted insertion of a free end portion of the Luer nozzle and, on a side of a Luer-nozzle-receiving opening thereof, in a tapered, substantially cylindrical form to assure tight-fitted insertion of a basal end portion of the Luer nozzle. A plastic film is laminated on the sealing rubber closure at least in an area of the Luer-nozzle-receiving part, where a free end of the Luer nozzle is to be maintained in contact with the sealing rubber closure.

Abstract: Described is an accurate, an accurate, easy to use and inexpensive device and method for substantially immediate detection and indication of malfunction in an intravenous delivery system. The two piece device includes a disposable conduit body interconnected with the tubing of an intravenous delivery system and a reusable clamp apparatus that is deployed around the conduit body. The conduit body is highly sensitive to pressure changes inside the tubing. The clamp apparatus contains a sensing mechanism that discerns the responses of the conduit body to the change in line pressure from below to above atmospheric pressure. Also located in the clamp apparatus is an indication system that indicates if that change in pressure has occurred.

Abstract: A universal seal is shown with orbital movement of a center opening for use in endoscopic surgery. A two part seal housing encloses the universal seal in an annulus surrounding an insertion port. The outer periphery of the universal seal is clamped between the two parts at the outer edge of the annulus. An inner ring of the universal seal is free to move from side-to-side inside the annulus while maintaining rubbing contact with the upper and lower surfaces of the annuluses for vertical support. The seal housing and universal seal are mounted on a proximal end of a cannula which allows access therethrough for the endoscopic surgery. The center opening of the universal seal is in general alignment with the insertion port of the seal housing, but the center opening and inner ring may move from side to side when medical instruments are inserted through the insertion port, the center opening, and the cannula and moved from side to side.

Abstract: A device, system and method for improving delivery of hemostatic material, in which the device includes a vent cap body capable of removably engaging a cannula. The vent cap has a passage extending through the vent cap body from the cannula to an exterior of the vent cap body where a restricter for restricting the flow of fluid from the cannula to the exterior. In one embodiment, the vent cap has a valve which has an opened and closed position. In the closed position, the valve is designed to provide a back pressure or resistence. When a certain force is applied against the valve, the valve moves from the closed position to the opened position, where a gas or fluid may pass through the vent cap. The vent cap is designed to help maintain the continuity of the hemostatic material during delivery of the material from the adaptor to the trial staging chamber.

Abstract: A method of and system for providing vascular access in a patient for hemodialysis involves attaching the distal end of an access catheter to the abdominal aorta of the patient and the proximal end of the access catheter to a portion of the patient to allow selective access to an interior portion of the access catheter. A blood-withdrawal catheter and a blood-return catheter are placed into the access catheter until their distal ends are in the patients abdominal aorta and blood may be removed and return to the aorta. When finished, the blood catheters are removed. Selective access to the proximal end of the access catheter is provided, preferably, by a cutaneous port assembly that includes a screwable cap and anti-infection cuff.

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 drip chamber includes an elongated transparent container, and a cap. The container has open proximal and distal ends. The cap covers the distal end and further includes a drip forming tube, a cannula and an attachment element used to removably attach the chamber to a connector. The cannula extends distally away from the chamber and is surrounded by the attachment element. A pathway for fluid is established through the cannula and into the chamber.

Abstract: A check valve and, in particular, an anti-siphon valve, for medical infusion lines and the like, including an axial upstream passageway and an axial downstream passageway, staggered and parallel with respect to each other, and a diaphragm of elastic material cooperating with an annular valve seat for normally keeping communication between these passageways closed. The diaphragm is composed of the end wall of a cup-shaped element on which a plunger rests coaxially, the plunger being slidable between a retracted inoperative position and an advanced operative position. Valve opening occurs following flexion of the diaphragm, which can be spontaneous due to a predetermined fluid pressure developing in the upstream passageway, or positively operated via the plunger (9).

Abstract: An apparatus wherein the primary dye source is connected to a secondary dye source with sufficient safeguards, including at least one-way check valve and at least one stopcock between the primary dye source and the secondary dye source, to assure a sterile barrier between the primary and secondary dye sources so that less than the total amount of fluid can be transferred from the primary dye source in an amount sufficient to perform a cardiac catheterization procedure.

Abstract: A medical valve has a resilient member that is forcibly expanded to an expanded volume from a normal volume. Specifically, the valve operates in a closed mode that prevents fluid flow, and an open mode that permits fluid flow. To these ends, the valve has a housing having an inlet and an outlet, and the noted resilient member within the housing. The resilient member and housing form a fluid channel between the inlet and the outlet. The fluid channel at least in part extends through the resilient member. The fluid channel has a given portion formed by a variable volume portion of the resilient member. The variable volume portion has a normal volume when in the closed mode, and an expanded volume when the open mode. The expanded volume is greater than the normal volume.

Abstract: A gastrostomy feeding device having a bolster portion and a closure member. The bolster portion includes a feeding opening, a cap seat, and an anti-reflux valve and the closure member includes a secondary stop tab, which when received within the cap seat forms a seal against the anti-reflux valve.

Abstract: A vent system for an infusion drip chamber is provided according to the invention. The vent system includes an automatic air eliminator communicating with an interior and an exterior of the infusion drip chamber. The automatic air eliminator is capable of automatically venting air from the infusion drip chamber in a substantially continuous manner. The vent system further includes a mechanical air eliminator communicating with the interior and the exterior of the infusion drip chamber. The manual air eliminator is capable of mechanically venting air from the infusion drip chamber at discrete time intervals.

Abstract: A pressure activated valve for a three-way connection between a catheter, an injector and a pressure transducer is disclosed. The valve includes a body that has an inlet for connection to an injector, an outlet for connection to a catheter and a secondary connection for connection to a pressure transducer. The body also includes a seal seat disposed between the secondary connection in both the inlet and the outlet. The body is flexibly connected to a plug seal. The plug seal is disposed between the seal seat in both the inlet and the outlet. The plug seal is movable between an open position spaced apart from the seal seat and biased towards the inlet and the outlet and a closed position against the seal seat thereby isolating the secondary connection from both the inlet and the outlet.

Abstract: A catheter system for fluid connection between a patient's vasculature and a fluid system that has a luer lock connector including a luer tip. The catheter system includes a catheter having a hub having an open end sealed with an elastomeric septum. The hub defines a female luer sized to be received into and locked to the connector of the fluid system when the luer tip is advanced into the septum. A needle extends through at least a portion of the septum, the needle having a tip projecting adjacent the catheter tip and a needle hub disposed adjacent the outer face of the septum. The needle is removable from the catheter and septum after the catheter is advanced into a blood vessel. The elastomeric septum seals subsequent to withdrawal of the hollow needle to provide a sealed outer face for engaging and receiving the luer tip.

Abstract: A sealing rubber closure is provided for use with a syringe/container specified by ISO (the International Organization of Standardization) and having a Luer nozzle to be inserted into a Luer-nozzle-receiving part of the sealing rubber closure. The Luer-nozzle-receiving part is configured, on a side of an inner end portion thereof, in an untapered cylindrical form to assure tight-fitted insertion of a free end portion of the Luer nozzle and, on a side of a Luer-nozzle-receiving opening thereof, in a tapered, substantially cylindrical form to assure tight-fitted insertion of a basal end portion of the Luer nozzle. A plastic film is laminated on the sealing rubber closure at least in an area of the Luer-nozzle-receiving part, where a free end of the Luer nozzle is to be maintained in contact with the sealing rubber closure.

Abstract: An improved medication infusion set is provided of the type having a soft cannula for subcutaneous delivery of a selected medication to a patient. The infusion set comprises a cannula housing having a soft cannula protruding therefrom and a self-sealing septum mounted at an upstream end of the cannula. The cannula housing is initially assembled with an insertion hub having an elongated insertion needle extending through the septum and cannula for transcutaneously placing the cannula followed by separation of the insertion hub from the cannula housing. An infusion hub is then assembled with the cannula housing and includes a short infusion needle for coupling the cannula with the selected medication supplied from a source via a length of infusion tubing.

Abstract: A hemostasis valve which provides a fluid tight seal at all times to prevent back-bleeding, and offers relatively low friction when devices are inserted therein. The hemostasis valve may either be an integral part of a tubular device (e.g., sheath, catheter, or the like) or releasable from the tubular device (e.g., Y-adapter or the like). In one embodiment, the hemostasis valve is biased to a closed position in response to distal pressure to prevent back-bleeding. The hemostasis valve is also biased to an open position in response to proximal force or pressure to reduce friction when devices are inserted therein. For example, the hemostasis valve may comprise a plurality of leaflets or flaps. In another embodiment, the hemostasis valve is longitudinally actuated between an open position to reduce friction during device insertion and a closed position to prevent back-bleeding when no devices are inserted therein.

Abstract: A stopper for use in preventing any volume of gas from escaping from a drug container when used in connection therewith. The stopper has a body having a perimeter for slidable engagement with the interior of a drug receptacle; an outer surface; and an inner surface facing the bottom of the drug receptacle, the inner surface shaped so as to trap any volume of gas located within the drug receptacle when the body is slidably engaged therein. The invention is further directed to a drug container having a hollow body for holding a liquid. The body has an open end and a closed end. The container also has a stopper slidably received in the hollow body, and a feature for entrapping any volume of gas within the container.

Abstract: An apparatus for vascular access is disclosed which includes a vascular access port defining an elongated tubular body of predetermined length with a central lumen having opposed proximal and distal end portions, the distal end portion adapted and configured for introduction into a blood vessel, the apparatus further including an elongated cylindrical plug body dimensioned and configured for insertion into the central lumen of the vascular access port, the plug body having a length that is substantially equal to the length of the vascular access port so as to prevent blood flow into the lumen of the access port when the plug is engaged therein.

Abstract: A suction device system comprising a suction tip and a containing unit wherein the containing unit is configured to allow the suction tip to rest within the containing unit such that the suction tip does not contact the containing unit.

Abstract: A catheter system for fluid connection between a patient's vasculature and a fluid system that has a luer lock connector including a luer tip. The catheter system includes a catheter having a hub having an open end sealed with an elastomeric septum. The hub defines a female luer sized to be received into and locked to the connector of the fluid system when the luer tip is advanced into the septum. A needle extends through at least a portion of the septum, the needle having a tip projecting adjacent the catheter tip and a needle hub disposed adjacent the outer face of the septum. The needle is removable from the catheter and septum after the catheter is advanced into a blood vessel. The elastomeric septum seals subsequent to withdrawal of the hollow needle to provide a sealed outer face for engaging and receiving the luer tip.

Abstract: A prefilled syringe of cartridge barrel having a tamper evident closure. Tamper evidence is provided by: a frangible tip seal which is integral with the tapered tip of the barrel; a frangible tip cap covering the tip, the tip seal and a portion of the distal end of the barrel; and an overwrap covering the frangible tip cap and the distal end of the barrel sealed to the distal end of the barrel by a tamper evident seal. The tapered tip is optionally equipped with a luer collar to receive an external luer connector. Alternatively, the tapered tip can be provided with a bore therethrough which can be closed with an elastomeric plug and the external connector can be a tubing conduit.

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 inline pump may be formed.

Abstract: An anesthetic metering system includes an anesthetic reservoir (1) having an anesthetic reserve (2), which is limited by a flexible material wall and to which pressure is admitted by means of a propellant (3) acting thereon via the wall material. The anesthetic reservoir (1) has a first valve (4), which is in flow connection with the liquid anesthetic reserve (2) and can be inserted into a mounting element (6) of an anesthesia apparatus. The metered release of anesthetic to the anesthesia apparatus takes place via a volumetric nozzle (8). The present invention provides an anesthetic metering device which avoids, on the one hand, the drawbacks of the anesthetic evaporators used previously, which are to be refilled with anesthetics at the workplace, and makes possible the refilling of the anesthetic reservoir (1) at the anesthetic manufacturer, on the other hand.

Abstract: A fluid delivery system for delivery of an injection fluid to a patient generally includes a pump system to pressurize the injection fluid, a patient interface in removable fluid connection with the pump system, and a connector in fluid connection between the pump system and the patient interface. The pump system is connected to an inlet of the connector, and the patient interface is removably connected to an outlet of the connector. The connector includes a sealing member at least partly disposed within a housing of the connector that is biased to close the outlet when the patient interface is removed.

Abstract: A seal assembly for reception of an elongated surgical instrument is provided which includes a body having at least one opening configured and dimensioned to permit entry of an elongated surgical instrument and defining a central longitudinal axis; a seal member formed of a resilient material and defining an aperture therein, the aperture being configured and dimensioned such that insertion of the surgical instrument into the aperture causes the resilient material defining the aperture to resiliently contact the outer surface of the surgical instrument in a substantially fluid tight manner; and a fabric layer juxtaposed relative to the resilient material. A coating may be applied to the seal member to reduce friction between the seal member and surgical instrumentation inserted therein. The coating is preferably a hydrocyclosiloxane membrane prepared by plasma polymerization process.

Abstract: A mixing/charging port for medical treatment capable of reliably mixing/charging solutions or collecting the solutions in a medical instrument equipped with a solution feed passage, comprising a disc-like valve (1) having an insertion hole at the center, a cover (2) for restraining the valve (1) by covering at least the upper part of the periphery of the valve (1) with the center on the front surface side of the valve (1) left uncovered, and a round fitting hole (6) formed at the center of the cover (2) as anchor means for anchoring an insertion member to a mixing/charging port, the fitting hole (6) and the insertion member being so fitted to each other as to be capable of anchoring.

Abstract: A skin seal or trocar stabilizer with an inflatable balloon in the shape of a dumbbell, where the balloon may be stored within a cannula for easy placement in an incision and inflated to deploy the balloon inside the body, and a portion of the balloon expands inside the cannula, whereby medical instruments may be passed through the skin seal into a laparoscopic workspace while the balloon is inflated, thereby allowing the use of normal short surgical instruments during laparoscopic procedures and during insufflation.