Abstract: A connector is provided which has a fluid passage whose volume does not substantially vary with the opening/closing of a valve disc. The connector includes a substantially cylindrical connector main body, a valve disc made of elastic material and disposed at one of the opening ends of the connector main body, and a substantially cylindrical connecting member disposed on the outer periphery of the connector main body on the side of the valve disc and coaxially with the connector main body to be movable in an axial direction of the connector main body.

Abstract: A transfer needle safety apparatus including a guide port adapted to fit a variety of body fluid receptacle sizes. A sleeve substantially fills the cavity inside a needle shield. The sleeve includes a robust external lead-in structure for aligning/assembling and centering the sleeve in the shield and a robust internal lead-in structure for aligning and centering a narrow body receptacle onto a needle. The sleeve engages a long section of the outer surface of a receptacle thereby preventing rocking or lateral motion of a receptacle septum relative to a needle tip. Streamlined gripping features allow removal of the sleeve from the shield.

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 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 needle assembly for use with an injection device including a pair of housing members slidably coupled with one another. A needle is structurally attached to one of the housing members such that it is positioned within the two housing members. A first membrane is disposed on an opening of one housing member and a second membrane is disposed on an opening of the other housing member such that the needle is concealed from the view and access of a user thereof. The needle assembly may be contracted by sliding one housing member relative to the other causing the needle to penetrate one of the membranes and administer an injection into or below the skin of the user. Additionally, one or more locking mechanisms may be incorporated to prevent inadvertent needle sticks.

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

Abstract: A 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: 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 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 connector system for sterile connection includes a male type connector having a tube connecting portion at a rear end portion thereof, a protective cap for the patient side connector, an inner cap held in the protective cap and including a ring-shaped portion that supports a disinfectant-impregnated member therein, and a female type connector including an outer cylinder and an inner cylinder fixed at one end of the outer cylinder, where the inner cylinder includes an internal end portion located inside the outer cylinder and an external end portion exposed outside the outer cylinder. When the protective cap is fitted with the male type connector, the disinfectant-impregnated member contacts with the male type connector. When the protective cap is removed therefrom, the inner cap becomes retained in the male type connector.

Abstract: The invention concerns a device for the two-way transfer of a liquid (38) between a bottle (14) provided with a cap (44) capable of being perforated at a cartridge (12) comprising a cylindrical reservoir (26) wherein slides a piston (34) capable of being perforated. It comprises: a body (16) including means to be fixed on the bottle (14); a member (24) linking the piston (34) capable of being perforated to the body (16); a shuttle (20) relative to the body (16) and said linking member (24), the shuttle bearing a hollow needle (22) whereof one first end (112) is adapted to pierce the piston (34) and whereof the second end (114) is adapted to pierce the cap (44). The shuttle (20) is mobile between a piston wherein the needle ends (112, 114) are spaced apart from the piston (34) capable of being perforated and the cap (44) capable of being perforated and an end-of-stroke transferring position wherein the needle ends (112, 114) are received in the cartridge (12) and the bottle (14).

Abstract: A frangible hose connector that has a knit line at the intended point of fracture, as opposed to a circumferential groove or notch. The knit line provides a break zone which has a lower tensile strength than that of the parent material, thereby providing that the connector is relatively easy to fracture. The connector also includes finger grips which makes breaking the connector easier. The finger grips provide that the connector is configured to be fractured via a twisting or torsion force, as opposed to a bending force. As such, the connector tends to break in a manner wherein fluid does not fling or spray. The connector is formed of plastic, and the knit line is created during the plastic injection molded process, wherein two mold fronts are “squared-up” and meet in the mold cavity to form the knit line.

Abstract: An intravenous drug access system. In one embodiment of the invention, the drug access system includes an IV bag having an inlet port and an outlet port, whereby the inlet port is a female luer integral therewith. The integral female luer fitting may be fitted with a sealed end cap including a male luer insert with a closed end. An alternative embodiment of the present invention comprises a discrete pre-molded connector made with a spike at one end and a female luer fitting at the opposing end. The spike is used to penetrate a standard IV bag through a conventional inlet port.

Abstract: A vial access transfer set for use with a bottle containing a medicinal fluid that provides a mechanism for securely attaching an administration set to the bottle and also provides a universal spike port to which any primary IV line can be readily attached. The vial access transfer set includes a novel, vented vial access adapter to which a length of tubing can be connected, the adapter comprising a top wall, a cannula connected to the top wall and a uniquely configured, resiliently deformable slitted skirt connected to the top wall and extending therefrom. With this construction, during the interconnection of the vial access transfer set with the bottle, the rubber septum of the bottle can readily be pierced by the cannula and the resiliently deformable skirt positively snapped into place over the neck portion of the drug vial or bottle to maintain the adapter in secure connection with the bottle.

Abstract: The present invention relates to antimicrobial compositions, methods for the production of these compositions, and use of these compositions with medical devices, such as catheters, and implants. The compositions of the present invention advantageously provide varying release kinetics for the active ions in the compositions due to the different water solubilities of the ions, allowing antimicrobial release profiles to be tailored for a given application and providing for sustained antimicrobial activity over time. More particularly, the invention relates to polymer compositions containing colloids comprised of salts of one or more oligodynamic metal, such as silver. The process of the invention includes mixing a solution of one or more oligodynamic metal salts with a polymer solution or dispersion and precipitating a colloid of the salts by addition of other salts to the solution which react with some or all of the first metal salts.

Abstract: A needleless access system adapted to be mounted on a vial comprising a generally elongated tubular housing having an interior dividing wall, flexible hooks projecting upwardly from the dividing wall which are diametrically opposed, a pair of confronting splines projecting upwardly from the interior dividing wall, a hub insert having a piercing tip normally supported in an armed position by hook elements, a series of outwardly projecting teeth which engage and are guided in the splines during axial displacement of the hub insert relative to the splined housing, and said hub insert having means for mounting a syringe assembly whereby the hub insert maybe activated axially guided by the splines so that the piercing tip engages the stopper in a vial aligned therewith.

Abstract: A container closure system for delivering a fluid. The system includes a stopper constructed to seal fluidly a container. A closure member is mounted on an upper surface of the stopper. The closure member includes a base having an upper surface and a lower surface. The closure member further includes an outer wall and an inner wall extending from the upper surface of the base with the inner wall spaced from the outer wall. The base defines therethrough a needle access port between the inner and outer walls. The inner wall defines a chamber therein. The base further defines therethrough an aperture adjacent the chamber defined by the inner wall. A piercing member is movably disposed within the chamber defined by the inner wall. The piercing member has a first end portion and a second end portion, the first end portion being positioned proximally to the stopper. A piercing tip is mounted on the first end portion and is constructed to pierce the stopper.

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: 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.

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 connecting a fluid sampling device to a fluid source is provided that includes a body adapted to be secured to the fluid source and a valve member moveably disposed within the body. The body includes a coupling interface configured to sealingly mate with the sampling device. The valve member is actuated by the sampling device during attachment of the sampling device to the valve body. The sampling device actuated valve member is moveable between a first position in which a flow path between the fluid source and the sampling device is closed and a second position in which the flow path between the fluid source and the sampling device is open. When the fluid flow path is open, the sampling device can withdraw a fluid sample for inspection and return the fluid sample to the fluid source without exposing the fluid to the surrounding environment.

Abstract: An apparatus for establishing aseptic/sterile connections including a substantially flexible, substantially transparent sterile barrier enclosing a terminal end of a conduit and a resilient, deformable support card which further includes an adhesive perimeter covered by a release paper and a rolling membrane with a continuous, removable, yieldable, flexible strip material. A portion of the rolling membrane is removably adhered to the support card and overlies the end of the conduit. A force applied to the free end of the rolling membrane withdraws the entire rolling membrane to expose the end of the conduit so that an aseptic/sterile connection is achieved by adhering opposing support cards together, removing the rolling membrane to create a sterile corridor between a first sterile barrier and a second sterile barrier, and mating the terminal end of a first conduit and a second conduit together.

Abstract: In a ureter drainage device comprising a ureteral catheter (10), a sliding hose (12) to be coupled to the proximal end of the ureteral catheter (10), and a control hose (18) to be mounted over the sliding hose (12), it is provided that the ureteral catheter (10) and the sliding hose (12) comprise mutually engaging coupling elements (33,38). At least one coupling element (38), provided on the sliding hose (12), is radially outwardly biased in the release direction and retained in the engagement position by the control hose (18) covering this coupling element (38).

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: Blood lines for hemodialysis and other blood handling procedures may be reused by placing connectors intermediately along the length of the blood lines so that the lines can be disconnected to separate out reusable portions thereof. Specifically, the bulk of the blood lines used may comprise branchless lengths of tubing which are easily reusable, and may be cleaned and stored along with a dialyzer or similar device by connection to a conventional reuse machine. Also, the connectors on the blood lines which are reused may have first and second sealing surfaces. The first sealing surfaces are used in the connections made to form the blood line in its normal form for use. Then, during cleaning and sterilization for reuse, the reusable connectors can connect first and second lengths of blood lines together making use of a second sealing surface, in which the first sealing surfaces are exposed to cleaning/storing solution to cause cleaning and antibacterial action on the first sealing surfaces.

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 housing that can be used to form and maintain a fluid-tight connection between a container and a medical device. The housing comprises an internal receiving surface circumscribing a cavity into which a fitting of the medical device can be inserted. The internal receiving surface comprises a first wall portion having a first contact annulus and a second wall portion having a second contact annulus. Upon insertion of the fitting into an opening in the cavity of the housing, the fitting forms a primary seal with the first contact annulus and a secondary seal with the second contact annulus. The primary seal is formed as the surface of the fitting contacts the first contact annulus of the internal receiving surface of the housing. The secondary seal is formed as the surface of the fitting contacts the second contact annulus of the internal receiving surface of the housing.

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 cap assembly for a container has a hollow housing with an upper end that receives a fluid transfer device and a lower end that engages a stopper on the container. The housing has an internal cavity open at the upper and lower ends and a radially outwardly extending portion at the lower end. A penetrator is received in the internal cavity. The penetrator has a pointed distal end opposite the stopper and an upper end constructed to be engaged by a fluid transfer device. A cap is constructed the hollow housing. The cap has a closed upper end, an open lower end, a radially outwardly extending portion at the open end, and a circumferential line of weakness connecting the upper and lower ends. A ferrule is over the radially outwardly extending portion of the hollow housing and the radially outwardly extending portion of the cap.

Abstract: Blood lines for hemodialysis and other blood handling procedures may be reused by placing connectors intermediately along the length of the blood lines so that the lines can be disconnected to separate out reusable portions thereof. Specifically, the bulk of the blood lines used may comprise branchless lengths of tubing which are easily reusable, and may be cleaned and stored along with a dialyzer or similar device by connection to a conventional reuse machine. Also, the connectors on the blood lines which are reused may have first and second sealing surfaces. The first sealing surfaces are used in the connections made to form the blood line in its normal form for use. Then, during cleaning and sterilization for reuse, the reusable connectors can connect first and second lengths of blood lines together making use of a second sealing surface, in which the first sealing surfaces are exposed to cleaning/storing solution to cause cleaning and antibacterial action on the first sealing surfaces.

Abstract: A connector system for sterile connection includes a male type patient side connector having a tube connecting portion at a rear end portion thereof, a protective cap for the patient side connector, an inner cap held in the protective cap and including a ring-shaped portion that supports a disinfectant-impregnated member therein, and a female type circuit side connector including an outer cylinder and an inner cylinder fixed at one end of the outer cylinder, where the inner cylinder includes an internal end portion located inside the outer cylinder and an external end portion exposed outside the outer cylinder. When the protective cap is fitted with the patient side connector, the disinfectant-impregnated member contacts with the patient side connector. When the protective cap is removed therefrom, the inner cap becomes retained in the patient side connector.

Abstract: A method and a needleless injection system for administering a medication. In order to simplify as far as possible the handling necessary for loading the injector with medication and thereby eliminate risks caused by a complex handling the method and system according to the invention provide loading of medication into a needleless injector device by means of a syringe prefilled with a medication, this loading step preferably including connecting the syringe to the injector device by means of a suitable coupling member or adapter and operating the syringe for transferring medication prefilled therein into the injector device. After this transfer the syringe and/or the coupling member or adapter are detached from the injector device, which is then ready to be operated for ejecting the loaded dosage of said medication from the injector device and thereby pass the selected dosage through the skin of an injection receiver.

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 coupler for receiving a threaded male luer fitting in sealed relationship includes a housing having an attachment end, a conduit end opposite the attachment end and defining a central passageway for providing fluid communication between the luer fitting and a conduit. An arrangement is attached to the housing for establishing a sealed connection between a luer tip and the central passageway. The conduit end has a relatively larger diameter than the attachment end and defines a shoulder at a junction of the attachment end and the conduit end. A resilient member is disposed on the attachment end adjacent the shoulder for exerting an axially directed compressive force upon the male luer fitting as it is threadably engaged upon the attachment end.

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: 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 thermoformed PVC, modified PVC, CPVC, metal or coated metal cover, covering system and method is provided for covering assemblies of pipe and pipe insulation, hangers, support rods and mechanical assemblies wherein the assembly is biocide treated, covered by and completely enclosed by the cover, the cover is sealed in order to prevent bacteria growth within the cover while allowing a smooth outside surface for biocide application. The cover can be modified to facilitate the application of biocide after the assembly is covered by providing resealable openings in said cover.

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 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 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 pre-slit injection site (34) includes a housing (40) with a flow path therethrough. A first end (42) of the housing (40) carries a pre-slit septum (52). One form of a blunt cannula (98), usable with the injection site (34), carries a locking member (100). When the pre-slit injection site (34) slidably receives the blunt cannula (98), the locking member (100) latches to the injection site (34) and creates a mechanically coupled unit. Another form of the cannula (280) includes a tube having a tapered distal end region (298) and having elongate discharge slots (294) for reducing contact surface area and for directing the flow laterally out of the cannula. The cannula may also include a rounded lead post (330), an annular barb (394), and axially oriented grooves (268).

Abstract: A medical valve has a first housing portion and a second housing portion capable of mating with the first housing portion to form an interior. The medical valve also has a valving element within the interior. The first and second housing portions have mating longitudinal snap-fit structures for longitudinally mating the first housing portion to the second housing portion. The first and second housing portions also have mating rotational snap-fit structures for substantially preventing the first housing portion from rotating relative to the second housing portion when the longitudinal snap fit structures are mated.

Abstract: A connector is provided which has a fluid passage whose volume does not substantially vary with the opening/closing of a valve disc. The connector includes a substantially cylindrical connector main body, a valve disc made of elastic material and disposed at one of the opening ends of the connector main body, and a substantially cylindrical connecting member disposed on the outer periphery of the connector main body on the side of the valve disc and coaxially with the connector main body to be movable in an axial direction of the connector main body.

Abstract: A valve that has at least one internal port on a valve core and at least one an internal slot in a valve body. The valve core is biased into a position wherein the port of the valve core is aligned with a sealing surface of the valve body thereby prohibiting fluid flow through the valve. The valve core is slidable such that the port of the valve core becomes aligned with the internal slot of the valve body thereby allowing fluid flow through the valve. Another valve includes a self-aligning valve seat carrier which is pivotably engaged with a valve core member. The self-aligning valve seat carrier engages a sealing surface in a valve body to prohibit fluid flow through the valve, but the valve core is slidable such that the self-aligning valve seat carrier disengages from the sealing surface in order to allow fluid flow through the valve.

Abstract: The invention relates to an apparatus for combining under sterile conditions a liquid component held in a first container and a solid or liquid component held in a second container.

Abstract: A fluid delivery system includes a connector assembly and a container for holding fluids. The connector assembly includes a first fitting defining a first aperture and a second fitting that is couplable to the first fitting and defines a second aperture. The container for holding fluids including a fitment, wherein one of the first and second fittings is directly coupled to the fitment.