Abstract: A stylet instrument is positionable within a catheter to facilitate placement of the catheter during a surgical procedure. The stylet instrument has application in a hemodialysis procedure where the catheter is positioned via a subcutaneous tunneling technique. The stylet instrument includes a hub, first and second stylet members extending from the hub and operatively connected to permit positioning within corresponding lumens of a catheter, and securing means associated with the hub to releasably secure the catheter to the hub. The securing means includes at least one locking detent.

Abstract: A steerable medical device is used to controllably introduce a guidewire or other medical instrument into a body of a patient and direct placement of the guidewire or other medical instrument in the body of the patient. The steerable medical device can include an elongated member, a steering mechanism, and an attachment member. The elongated member extends along a longitudinal axis and comprises a deflectable distal portion that is deflectable off of the longitudinal axis. The steering mechanism is adapted to control longitudinal and rotational movement of the elongated member and to control off-axis deflection of its deflectable portion. The attachment member is removably couplable to another medical device. The attachment member is moveably coupled to the steering mechanism and the elongated member.

Abstract: Connectors and methods for connecting medical tubing (e.g., catheters) to an implantable infusion pump are described herein. In some embodiments, the connectors may include a housing having an internal guide surface that assists in guiding the connector onto a stem port received by the connector when the connector is misaligned with the stem port.

Abstract: A method of placing a catheter into a patient while preventing disadvantageous escape of fluid from the patient comprises providing a catheter secured to a valve housing. The catheter has a proximal end, a distal end and an interior lumen. The valve housing has a first port, a second port, and a fluid path running between the first and second ports. The catheter and the valve housing have a hollow needle extending therethrough.

Abstract: A male adaptor is provided with a nose for penetrating into a housing of the female connector. A septum is disposed over the nose of the male adaptor to maintain a seal with the female connector during coupling and uncoupling. Upon coupling, the septum dilates to allow the nose to pass through. The female connector may have a septum that also dilates to allow penetration of the nose of the male adaptor. Alternatively, the septum of the female connector may be retractable under the force of the nose of the male adaptor.

Abstract: The invention relates to a catheter device, having a catheter (1), an actuation device (8) at a first end of the catheter and also a mechanical transmission element (9, 10) for transmitting a movement along the catheter to the actuation device, the actuation device having a coupling element (14) which is connected to the transmission element (9, 10) and can be actuated by the latter relative to the longitudinal direction of the catheter in a first degree of freedom, and also a conversion element (15) which can be actuated by the coupling element and which converts the actuation movement at least partially into a movement in a second degree of freedom. As a result, a combined movement at the distal end of the catheter can be produced particularly simply for compression and release of a functional element.

Abstract: Fluid communication to an end of a catheter is afforded through a connection hub selectively attachable thereto. The connection hub includes a catheter receiving element and a fluid coupling element that are relatively rotatable coaxially between a catheter receiving condition and a catheter capture condition of the connection hub. The catheter capture condition, a compressible sealing sleeve disposed interior of the connection hub between a pair of clamping jaws projecting from the catheter receiving element is urged into sealing engagement with the exterior of the catheter, catheter is gripped mechanically through the sealing sleeve by the clamping jaws. The exteriors of each of the catheter receiving element and the fluid coupling element are formed into planar actuation handles that facilitate relative rotation of the catheter receiving element and the fluid coupling element into coplanar alignment in the catheter capture condition of the connection hub.

Abstract: A latching female tubing coupler comprises an opening, a collet finger, and an actuation member. The opening is adapted to guide a male connector along a first line of action as the male connector passes into the opening to be received within the latching female tubing coupler. The collet finger includes an engagement feature adapted to engage a coupling feature of the male connector and displace along a second line of action generally normal to the first line of action. The actuator member is adapted to displace along a third line of action generally normal to the first and second lines of action in order to disengage the engagement feature from the coupling feature of the male connector. When the engagement feature is engaged with the coupling feature on a male connector, a fluid conduit of the male connector is held in fluid communication with a fluid conduit of the latching female tubing coupler.

Abstract: Drug delivery devices having non-luer connections and adapters and adaption connectors for providing non-luer connections to drug delivery devices are provided. An exemplary drug delivery device for use with a catheter connection includes a blunt needle component with a non-luer connection and a filter component with a non-luer connection, wherein the non-luer connections of the blunt needle component and filter component are incompatible with standard luer fitting and intravenous route-accessing devices. In one or more embodiments, an adapter having a non-luer connection at one end and a luer connector is provided for use with blunt needle components and filter components wherein one of the blunt needle component and the filter component includes a luer connection and the other of the blunt needle component and the filter component includes a non-luer connection. Methods of delivering liquid medication to a catheter are also provided.

Abstract: A modular catheter includes an elongate tubular member having a proximal end and a closed, distal end. A lumen extends from the proximal end to the distal end and a plurality of electrodes are arranged at, or adjacent, the distal end, conductors for the electrodes being contained within a wall of the tubular member. An elongate shape-imparting mechanism is removably received within the lumen of the tubular member such that a distal end of the shape-imparting mechanism is substantially in register with the distal end of the tubular member. A control device has a proximal end and a distal end, the proximal end of the tubular member and a proximal end of the shape-imparting mechanism being releasably connectable to the distal end of the control device.

Abstract: A proximal terminal end of a proximal section of a catheter, preferably tapered, defines a perimeter of an opening into a lumen of the catheter and includes an exposed sealing area. A sealing assembly, that may be removed from the catheter, includes a relatively soft part and a relatively rigid part, wherein the exposed sealing area is formed by the soft part, and the relatively rigid part may include an attachment feature for removable connection of the assembly to the catheter. The lumen of the catheter, within the proximal section, may include a seal zone portion, which preferably includes a slit segment intersecting a funnel-like segment of a bore. The catheter proximal section may further include a feature for interlocking engagement with an accessory tool.

Abstract: The invention relates to a connection piece (4) for the tube (3) of an enteral feeding tube (1), having a proximal fitting piece (4A) for fitting the tube of an enteral feeding tube, and a distal fitting piece (4B) for fitting a connection piece (8) of an enteral transfer system (2). The connection piece (4) according to the invention of the feeding tube (1) comprises two rigidly connected sections (9), (10), of which the first section (9) is made of a material which has a higher hardness than the material which the second section (10) of the connection piece is made of. The two-piece structure of the connection piece made of the two materials of different hardness has the advantage that the material properties of the two sections (9), (10) can be adapted to the different requirements for the respective connections.

Abstract: A multiple-line connective device for use in a medication infusing system includes a connective device body forming a main flow passage from an inlet to an outlet along a longitudinal axis, the main flow passage including an interior surface having a raised surface feature configured to induce turbulent liquid flow through the main flow passage. One or more branches extend from the connective device body, each defining at least one branch passage in communication with the main flow passage. Each branch passage enters the main flow passage at an angle with respect to the longitudinal axis that imparts a flow through the branch passage that has a directional component that is parallel to the longitudinal axis and in the direction from the inlet to the outlet.

Abstract: A catheter proximal section is preferably formed from a relatively soft part and a relatively rigid part, and includes a proximal terminal end that defines a perimeter of an opening into a lumen of the catheter. The proximal section may further include a feature for interlocking engagement with an accessory tool. An inner surface of each of the relatively soft and rigid parts may be located opposite one another, on either side of the catheter lumen. The relatively soft and rigid parts may be included in a sealing assembly that further includes an attachment feature for removable connection of the assembly to the proximal section catheter.

Abstract: The present invention aims at offering: a syringe connectable to a port in a fixed manner as well as capable of demonstrating high operational performance even in the case of direct connection where a connector is not used; a connector used for the syringe; and a syringe able to attach the connector thereto. For the attainment of the above objectives, the medical syringe of the present invention is a medical syringe including a cyrindrical connection supporting member which enhances the holding force of a luer part inserted into a port when the medical syringe is connected to the port. The connection supporting member is set by sliding along the luer or a syringe body in a state of being movable between a first position near a tip of the luer and a second position away from the tip of the luer. The medical syringe is characterized in that, when the connection supporting member is moved to the second position, the tip of the luer part is exposed.

Abstract: A medical connector for use with one or more medical implements. In some embodiments, the connector minimizes or eliminates the retrograde flow of fluid into the connector from one end or port upon the disconnection of a medical implement from the other end or port. In some embodiments, the connector generates a positive flow of fluid out of the connector from one end or port when a medical implement is disconnected from the other end or port.

Abstract: An adapter assembly (120) for connecting a catheter assembly (50,52) to a tunneler (110) having a generally tubular body (122) having a first end (124), a second end (126) and a longitudinal axis (128) extending therethrough between the first end and the second end. The first end (124) of the adapter is constructed to engage the proximal end (114) of a trocar (110). The second end (126) of the adapter is constructed to releasably engage at least one catheter lumen (50,52). A slider (140) is disposed about the adapter (120) and is longitudinally slidable along the adapter. When the slider (140) is slid towards the second end (126) of the adapter, the slider engages a plurality of legs (134a-134d) on the adapter and biases the plurality of legs toward each other and the longitudinal axis of the adapter.

Abstract: Improved anastomosis devices having structural upgrades to increase ease of use while simultaneously increasing patent safety. The anastomosis device can include an introducer member having an introducer rod and an introducer cap to provide additional support to a catheter portion of the anastomosis device such that damage associated with installation of the catheter, deployment of tissue approximating structures and/or removal of the catheter can be minimized. The anastomosis device can further include a valve cap designed to constrain and reinforce a thin-walled section of a proximal funnel portion of the anastomosis device such that ballooning of the thin-walled section under the influence of a pressurized inflation fluid can be avoided during inflation as well as a time of tissue approximation and tissue healing.

Abstract: A breakaway hemostasis hub for a catheter or introducer sheath includes a splittable or separable housing, a seal within the housing, an actuator partially slidably disposed within the housing, a pair of spring retainer members in the housing each adapted to receive at least one spring, and a pair of actuator retainer members adapted to retain the seal, the actuator, and the spring retainer members in the housing. The actuator is operable to assume a closed position and an open position and includes a dilator member configured to dilate the seal when the actuator is in the open position. The hub is splittable or separable into two generally symmetrical sub-assemblies to facilitate cutting the catheter for retraction from the patient's body without displacing its payload.

Abstract: Methods and apparatus for securing a medical or surgical line with respect to a patient are described. In particular, a fastener is described comprising an elongate braided tubular sleeve (110) for receiving the line therethrough, the sleeve having a first end for fixing adjacent to the patient, in use, and a second end for arranging, in use, proximal to medical equipment coupled to the line. The fastener also includes a first substantially rigid collar (112) coupled to the sleeve at the first end of the sleeve and a second substantially rigid collar (114) coupled to the sleeve at the second end of the sleeve. An enlarged flange (116) is provided, secured to the first collar (112) at the first end of the sleeve and an adhesive plaster (118) for securing the fastener with respect to a patient is provided, the adhesive plaster being secured to the enlarged flange (116).

Abstract: A disinfecting and pre-opening device is disclosed for use with a female needleless connector. The disinfecting and pre-opening device includes a housing comprising a chamber having a distal opening and configured to fit over the female needleless connector, and an elongated finger attached to the housing and disposed within the chamber such that the elongated finger opens the fluid path through the female needleless connector when the distal opening of the disinfecting and pre-opening device is placed proximally adjacent to the septum and the disinfecting and pre-opening device is advanced in the distal direction.

Abstract: An adapter assembly (120) for connecting a catheter assembly (50,52) to a tunneler (110) having a generally tubular body (122) having a first end (124), a second end (126) and a longitudinal axis ( )128 extending therethrough between the first end and the second end. The first end (124) of the adapter is constructed to engage the proximal end (114) of a trocar (110). The second end (126) of the adapter is constructed to releasably engage at least one catheter lumen (50,52). A slider (140) is disposed about the adapter (120) and is longitudinally slidable along the adapter. When the slider (140) is slid towards the second end (126) of the adapter, the slider engages a plurality of legs (134a-134d) on the adapter and biases the plurality of legs toward each other and the longitudinal axis of the adapter.

Abstract: A cap assembly is disclosed for use with a lock solution delivery device. The cap assembly includes a housing defining a receptacle and having an inlet end and an outlet end. A plunger is movable axially within the receptacle from a retracted position to an advanced position and is rotatably supported within the receptacle from a first position to a second position. The plunger includes an axial extension configured to non-rotatably engage a syringe connected to the inlet end of the housing. The plunger is positioned to move from the first position to the second position in response to rotatable detachment of a syringe from the inlet end of the housing.

Abstract: A luer lock connector is disclosed. The luer lock connector includes a connector body having a distal end, a proximal end, and a gripping portion between the distal end and the proximal end. A substantially flexible material is disposed on at least the outer surface of the gripping portion of the connector body. An intravenous line is coupled to the distal end of the connector body. A luer connector fitting is disposed on the proximal end of the body, the luer connector having an outer diameter less than a maximum exterior thickness of the gripping portion of the connector body.

Abstract: A catheter for use in accessing the vasculature of a patient and for optionally transferring a volume of blood from a patient to a hemodialysis machine. The catheter includes one or more connectors, which are secured to a transition member of the catheter. The one or more connectors have a threaded securement component for facilitating the securement of a secondary apparatus, such as an extension tube member to the one or more connectors.

Abstract: The invention relates to a fluid connection device and to a continuous automated system and method for taking fluid microsamples using this device. A device (20) according to the invention, which is intended to be connected to a first line (21) via a first opening and includes a second opening through which a second line (28) passes, comprises: a female fluid connector (22) that defines the first opening and has an internal fitting surface (23) terminating in a female end (24) into which this first line opens; and a male fluid connector (25) that defines the second opening, which is fitted into the female connector via its external surface (26) and terminates via its male radial end (27) inside the female connector.

Abstract: A needle shroud assembly (10) comprises a barrel (16), a needle shroud (18) captively telescoped relative to the forward end of the barrel for movement between retracted and extended positions and is biased towards said extended position by a spring (25). A separate locking element (42) is mounted within the barrel moveable between a safe position (as seen in FIG. 5) in which it prevents or limits retraction movement of said needle shroud (18), and a live position in which it is clear of the rearward path of the needle shroud (18). The locking member is moved from its safe position to its live position by means of an externally operable actuating member (54), having a cam (52) which cooperates with a cam surface (46) on the locking element (42). The cam (52) is driven back to its original position by the rearward end of the shroud (18) as it moves to the fully retracted position.

Abstract: Certain embodiments of the present invention include a male luer connector having a valve arrangement for keeping a passage that extends through the male luer connector closed when the male luer connector is not attached to a corresponding female luer connector. This passage of the male luer connector may be opened by connecting the male luer connector to a female luer connector. The valve arrangement of the male luer connector may include a movable sealing element arranged around a central fluid conduit. In some embodiments, the male luer connector may include a filter that is permeable to gas, but substantially impermeable to liquid, thus allowing gas to be purged from the male luer connector while substantially preventing liquid from leaking from the connector at least when the male luer connector is not connected to a female luer connector.

Abstract: A catheter assembly includes a catheter hub defining an interior cavity and a catheter tube extending distally thereof. A rigid actuator extends proximally in the interior cavity and supports a seal member thereon. The seal member includes a central membrane, a distal portion, and a proximal portion. An hourglass shaped actuator cavity is formed in the distal portion and receives a barbed end of the actuator. The outer surface of the seal member is in partial circumferential engagement with the catheter hub to define an air path that allows fluid communication between areas of the interior cavity distal and proximal of the seal member. A punch tool is provided to form a tri-slit in the membrane of the seal member.

Abstract: A method for connecting a plurality of solution line connectors to a plurality of supply line connectors of a dialysis system includes: translating a tip protector remover in a first direction towards the plurality of supply line connectors to remove a plurality of solution line tip protectors from the plurality of solution line connectors; locking the tip protector remover to each of a plurality of supply line tip protectors connected to the plurality of supply line connectors; translating the tip protector remover in a second direction towards the plurality of solution line connectors to remove the plurality of supply line tip protectors from the supply line connectors; translating the tip protector remover in a third direction different from the first and second directions; translating one of the plurality of solution line connectors and the plurality of supply line connectors the other of the solution line connectors and the supply line connectors to connect each of the solution line connectors to one of

Abstract: A docking station for male medical line connectors, including a base housing securable to a stationary surface and having a plurality of docking bays, each of which is dimensioned and contoured for respectively receiving and temporarily retaining ampules containing sterilization fluid. Each of the ampules has a chamber therein containing the sterilization fluid and an access mouth exteriorly exposed when the ampule is secured in one of the bays, and each mouth has a female medical line connection dimensioned and contoured for temporarily receiving and securing a male medical line connector thereto with the tubular tip of the male connector immersed in sterilization fluid during the period of time that the infusion tubing is disconnected from the patient.

Abstract: A multifunction adaptor for an open-ended catheter that allows placement of the catheter without risk of air embolism or blood loss through the open (proximal) end of the catheter body. The present design allows passage of a standard guidewire for “over the guidewire” placement techniques and a connection for catheter flushing using a standard syringe.

Abstract: An infusion set, patch pump, or elements thereof, having an exemplary catheter (14) provided with one or more channels, grooves and coatings (24, 34, 44), configured and arranged to provide a degree of strength and flexibility. The catheter (14) can also have an exemplary flexible union with the hub (12) having at least one of a ball-and-socket joint (66, 68), a sliding plate (86), and a flexible bushing (106), and which is sealed to allow even further movement of the catheter (14) while preventing leakage of medication through the junction. In doing so, a number of benefits associated with the use of rigid materials in catheter construction can be provided while at the same time, benefits associated with the use of flexible materials in catheter construction and/or flexible engagement with the hub can also be provided.

Abstract: In general, this disclosure relates to techniques for implementation and use of a fluid connection assembly, having a locking mechanism, which may be connected to a medical fluid injection device. An example fluid connection assembly includes at least one fluid connector, a mating mechanism coupled to the at least one fluid connector and configured to connect the at least one fluid connector to a medical fluid injection device, and a locking mechanism coupled to the mating mechanism and movable into a locked position or an unlocked position. In this example, the fluid connection assembly becomes affirmatively coupled with the medical fluid injection device when the locking mechanism is in the locked position, and the fluid connection assembly becomes removably decoupled from the medical fluid injection device when the locking mechanism is in the unlocked position.

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

Abstract: Methods of manufacturing septa for use with vascular access devices include forming a septum body and forming a slit within the septum body.

Abstract: The present invention relates to a piercing member protection device (9) which comprises a first, a second and a third cylindrical member (100, 200, 300). The first cylindrical member (100) is at least partly encompassed by the second cylindrical member (200), and the second cylindrical member (200) is at least partly encompassed by the third cylindrical member (300). The third cylindrical member (300) comprises a piercing member (400) having a piercing tip (401). A first locking arrangement (250) is arranged to enable or prevent the turning of the first and third cylindrical member, with respect to the second cylindrical member, while a second locking arrangement (350) is arranged to enable or prevent movement of the piercing member (400) along the longitudinal center axis A, so as to expose the piercing tip (401) of the piercing member (400). The piercing member protection device (9) provides a safe device which reduces the risk of accidental exposure of the piercing tip (401) and contamination for a user.

Abstract: The present invention is a modular implantable medical device that is used deliver materials or energy into a patient's physiology, or from one region of a patient's physiology to another. The device includes a port element with a passageway therethrough for directing and anchoring a conduit element in a desired location. Both elements can be adjusted during placement to maximize the safety, comfort, and efficacy of use. In one embodiment, the port element is comprised of two components such that the passage way is formed after the components are assembled. This modularity enables a large diameter section of the conduit to be advanced past the port location, and the port to be assembled about a smaller proximal section of the conduit, thereby establishing full contact between the port and conduit elements to anchor the device in an optimal position.

Abstract: A coupling wire guide structured to be slidably coupled to a previously introduced wire guide during intracorporeal procedures. The coupling wire guide includes a main body and a tip portion, the tip portion having first, second and third sections. The first section is connected to the main body, while the second section interconnects the first and third sections. The third section defines an axial passageway having a distal opening and a proximal opening. The axial passageway is sized to receive the previously introduced wire guide therein. The second section includes a strip sized to leave an open area in communication with the proximal opening.

Abstract: A safety catheter includes a catheter hub, a catheter tube, a needle hub, a needle cannula having a tip, and a tip protector. The tip protector includes an outer member having a flexible tab configured to releasably engage with the catheter hub and release therefrom upon inward flexing of the tab. An inner member is positioned entirely within the outer member and has a portion that impedes inward flexing of the tab when disposed adjacent the tab. The inner member is axially shiftable relative to the outer member between a first position wherein the needle tip is distal of the tip protector and the inner member portion is disposed adjacent the tab to impede release from the catheter hub, and a second position wherein the tip is within the outer member and the inner member portion is no longer adjacent the tab and no longer impedes release from the catheter hub.

Abstract: A soft grip medical connector comprises a housing with an upstream end, a downstream end and a lumen extending through a central portion thereof. A flexible member comprises a valve portion integrally formed with a sleeve portion. The valve portion is positioned within a section of the housing and is configured to control a flow of fluid through the housing lumen. The sleeve is inverted to envelope at least a portion of the outer surface of the housing. In some embodiments the gripping portion is integrally formed with the valve portion. In some embodiments, the connector is also generally configured to create a positive pressure in a catheter lumen upon removal of a syringe or other medical device from the upstream end of the connector. Methods of making a medical fluid connector generally comprise forming a valve member with a sleeve extending there from, and assembling the valve, sleeve and housing.

Abstract: A monitor-driven intracranial catheter assembly including dual lumen catheter for monitoring intracranial pressure via a pressure sensor located in one lumen while simultaneously draining cerebrospinal fluid through another lumen. A third lumen can also be provided with a side port for receiving a stylet. The stylet is used as a stiffening agent to aid in advancing the catheter into the patient's brain. The pressure sensor is preferably a spectral modulation sensor that communicates with a photodetector apparatus by means of a single optical fiber, thus minimizing the diameter of the catheter. The photodetector is self-correcting for signal errors caused by temperature change, changes in intensity of the input light, and transmission losses within the optical apparatus.

Abstract: A vascular access device may include a body, a single-disk septum in communication with the body, and a rigid member supporting the septum. A method of manufacturing a vascular access device may include providing a body, providing a single-disk septum in communication with the body, and supporting the septum with a rigid member.

Abstract: Catheter connectors, systems, and methods of use in which a catheter is attached to a connector such that the catheter is retained on the connector by inward radial compression between an outer surface of a hollow pin located within the catheter and a collet fitted over the portion of the catheter containing the pin. The collet may be moved from an unlocked position to a locked position by axial displacement of the collet along a longitudinal axis of the connector.

Abstract: A contact sensing assembly including a catheter and an electrode including a tip portion and a base portion, and a generally central axis, with the electrode being connected to a distal end of the catheter. Optical sensor(s) may be provided for emitting and/or receiving an optical signal, with a part of the optical signal being transverse to the central axis. Optical interference member(s) may be provided for interfering with the optical signal. A method for sensing contact force exerted by an electrode on a tissue includes directing an optical signal along a portion of a catheter, emitting and/or receiving an optical signal, with a part of the optical signal being at a predetermined angle relative to the central axis, and sensing changes in intensity of the optical signal based on displacement associated with the electrode tip portion based on the contact force exerted by the electrode on the tissue.

Abstract: A catheter assembly and method for internally anchoring a catheter in a patient. According to one embodiment, the catheter assembly includes a catheter, a tubular fitting coupled to one end of the catheter, and an internal bolster coaxially mounted around the tubular fitting. The tubular fitting has a waist portion, and the internal bolster is secured thereto by a snap-fit. To internally anchor the catheter in a patient, one inserts the end of the catheter to which the fitting is coupled into the patient and then, while the fitting and its coupled end of the catheter are within the patient, inserts the internal bolster over the fitting until it snap-fits into place over the waist portion, thereby internally anchoring the catheter within the patient.

Abstract: An adapter for an introducer comprises a medical device having a tubular port on a proximal end such as a splittable hemostatic valve. A tubular fitting is provided on a proximal end of the introducer. An elastomeric member is disposed between the port of the medical device and the tubular fitting of the introducer for providing a fluid tight and mechanically secure connection therebetween. The introducer and valve are manually connectable and reconnectable with each other while maintaining the fluid tight connection between them. A side port may communicate with the hemostatic valve, the side port having a controllable valve ending. In the preferred embodiment the introducer comprises a splittable introducer. In the illustrated embodiment the elastomeric member provides a slip fit between the medical device and the tubular fitting of the introducer. A tab extends from the tubular fitting of the introducer to facilitate manual manipulation of the tubular fitting.

Abstract: A releasable medical device connector comprises a connector fitting with a spin nut which connects to an adaptor. The connector fitting has at least one radially extending member with a variable radius cross section. The spin nut is disposed upon the connector fitting proximal of the radially extending member and is both axially slidable and rotatable upon the elongated body of the connector fitting. A screw thread within a proximal portion of the spin nut is used to secure the tapering portion of the connector fitting to an external thread disposed upon the adaptor. To release the connector, the spin nut is unscrewed from the adaptor and slid so that a distal receptacle of the spin nut engages the radially extending member of the connector fitting. With the spin nut and connector fitting engaged, the medical line can be released from the adaptor by twisting and pulling upon the spin nut.

Abstract: The invention relates to a device for loading a patient connector for peritoneal dialysis with a closure plug. To permit an arbitrary number of disconnection/connection procedures with patient connectors that insert a sterile closure plug into the patient's abdominal connector during disconnection, a device for loading a patient connector for peritoneal dialysis with a closure plug is suggested, said device consisting of a housing containing a closure plug and of means for transferring the closure plug out of the device and into a patient connector. This permits loading, under sterile conditions, of a patient connector whose closure plug has already been used with a new closure plug. By loading a new closure plug, the push-button with which the closure plug is inserted is returned to its starting position, so that the patient connector is again available for a connection/disconnection procedure.

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.