Abstract: An infusion pump system is described that increases patient comfort and convenience. The infusion pump system includes an infusion site interface that is releasably connected to an infusion pump body, and has no tubing associated between the infusion site interface and the pump body. The infusion pump body may include a carrier frame that may be adhered to the skin of a user.

Abstract: An infusion pump system is described that increases patient comfort and convenience. The infusion pump system includes an infusion site interface that is releasably connected to an infusion pump body, and has no tubing associated between the infusion site interface and the pump body. The infusion pump body may include a carrier frame that may be adhered to the skin of a user.

Abstract: An infusion pump system is described that increases patient comfort and convenience. The infusion pump system includes an infusion site interface that is releasably connected to an infusion pump body, and has no tubing associated between the infusion site interface and the pump body. The infusion pump body may include a carrier frame that may be adhered to the skin of a user.

Abstract: A rail-guided epidural-spinal needle, which includes an epidural needle including a base and a needle shaft connected to the base, the needle shaft having a groove that is formed on an outer surface of the needle shaft and extends along an axis of the needle shaft, the base having an elevated spinal needle inlet disposed thereon, the spinal needle inlet having a conduit formed therein, the conduit being of an acute angle with the groove in a side view of the epidural needle, and being in alignment with the groove in a top view of the epidural needle. The rail-guided epidural-spinal needle also includes a spinal needle having a tip with a unilaterally curved conformation down one side, such that, when the spinal needle is inserted into the conduit of the spinal needle inlet, and pushed forward, the tip thereof reaches the groove and slides along the groove.

Abstract: An infusion pump system is described that increases patient comfort and convenience. The infusion pump system includes an infusion site interface that is releasably connected to an infusion pump body, and has no tubing associated between the infusion site interface and the pump body. The infusion pump body may include a carrier frame that may be adhered to the skin of a user.

Abstract: Catheter assembly (100) having at least one lumen (150 or 160) and joined to hub (106). While the lumen inner diameter(s) remain constant from distal end (144) of the catheter (140) to proximal end (142), the outer catheter diameter increases proximate the hub (106) providing increased resistance to kinking during connection and disconnection from medical apparatus. The increased proximal catheter diameter preferably is sufficiently large to plug the proximal end of an introducer sheath through which the catheter is inserted during patient placement, to plug the proximal sheath end and minimize blood aspiration therethrough, and later serves to fill the vascular insertion upon complete catheter insertion after removal of the introducer sheath again to minimize blood aspiration through the vascular incision. The catheter may have two lumens (150,160) or more, joined to respective extension tubes in hub (106). The two lumens may each have a respective inner diameter of between about 0.020 in and 0.025 in.

Abstract: The present invention generally provides methods and devices for removing fluid from a surgical instrument. Surgical access devices and seal systems are generally provided having one or more valves or seal assemblies to create a closed system between the outside environment and the environment in which the surgical access device is being inserted. In one embodiment, a seal assembly is provided and can include a seal having an opening configured to receive a surgical instrument therethrough and a fluid remover in the form of an absorbent element, a scraper element, a wicking element, or any combination thereof can be associated with the seal and configured to remove fluid from the opening and/or a surgical instrument.

Abstract: A catheter for introduction and removal of fluids from a body and tunneling device therefor, the catheter has a body having a first conduit for removing fluid from the body and a second conduit for delivering fluid to the body wherein at least a part of each of the conduits is integrally formed within a first end of the body of the catheter and extends along side one another. The first conduit extends beyond the second conduit and forms a terminal point of the first end and defines a first opening thereat and the second conduit extends to a point short of the terminal point defining a second opening. A bumper portion is adjacent the second opening extending toward the terminal point. Another part of each the first and the second conduits are disjoined and form part of a second Y-shaped end. The tunneling device has a channel to removably receive the catheter.

Abstract: A catheter insertion apparatus with visual indication of needle penetration of a blood vessel and placement of the catheter cannula within the blood vessel, using blood vessel pressure to indicate needle penetration by the presence of blood within a transparent chamber within the apparatus and the displacement of a plunger to create a negative pressure on the cannula and thus allowing blood to be visible within the catheter hub thereby indicating the introduction of the cannula into the blood vessel.

Abstract: A tearaway introducer sheath assembly (10) for use in implantation of a catheter into a patient, having an elongated polytetrafluoroethylene sheath tube (12) and a proximal polyethylene hub component (16). The hub comprises two halves (22) insert molded about the sheath tube proximal end and joined to each other by frangible webs (28) enabling manual splitting. At least one pair of opposed holes (42) is formed through the tube proximal end portion 44, and a polyethylene liner (46) is inserted into the tube's proximal end portion. The polyethylene flows into the at least one pair of holes (42) to fuse with the liner, establishing a pair of physical joints (50?) integrally joining the liner (46) to a respective hub half (22). Upon manual splitting of the hub halves, the sheath tube easily splits along its length as a result of a property of the polytetrafluoroethylene material.

Abstract: Drainage belongs to medical equipment, particularly to medical tools and is specified for drainage of cavities. Drainage comprises a first tube, an additional tube, which is fixed upon it, a unit of the clot's splitter and the splitter's fixing element. The additional tube has a smaller diameter with an opening, inside which the conductor is mounted, a unit of clots splitter is installed on the working end of the drainage, it comprises a cylinder, a tube with an opening, placed on it, which is the continuation of the additional tube of the drainage and a spring with a cutter inside the cylinder. A cutter is located diametrically inside the working head, while in the end of the wall of the first tube and the splitter's unit comprises a channel, inside which splitter's fixing element was led, its working end is inside the unit's cylinder and fixes the splitter.

Abstract: A sheath shaped and dimensioned for reducing trauma and easing insertion thereof includes an inner sheath member shaped and dimensioned to fit around a guidewire in a manner permitting relative movement, the inner sheath member including an inner sheath tip having a primary bevel and a circumferential conical surface. The sheath also includes an outer sheath member shaped and dimensioned to fit around the inner sheath member in a manner permitting relative movement. The outer sheath member includes an outer sheath tip having a primary bevel and a circumferential conical surface.

Abstract: An assembly for the delivery of a cardiac surgical device is disclosed herein. In one embodiment, the assembly includes a slittable delivery device and a bypass assembly. The slittable delivery device may include a hub, a shaft integrated into the hub and forming at least a segment of the circumferential surface of the hub, and a hemostasis valve contained substantially within the hub. The bypass assembly may include a cap and a valve bypass tool. The cap may be on a proximal end of the hub and may include an opening in the cap extending radially outward from a point near a radial center of the cap through a circumferential edge of the cap. The valve bypass tool may be operably coupled to the cap and may include a longitudinally extending open channel.

Abstract: A sheath shaped and dimensioned for reducing trauma and easing insertion thereof includes an inner sheath member, the inner sheath member including an inner sheath tip having a primary bevel and a circumferential conical surface. The sheath also includes an outer sheath member shaped and dimensioned to fit around the inner sheath member in a manner permitting relative movement. The outer sheath member includes an outer sheath tip having a primary bevel and a circumferential conical surface.

Abstract: A device for facilitating the use or application of skin penetrators, the device including a puncturing part for piercing the skin, an indwelling part which can be introduced into the skin through an opening generated by the puncturing part and remains there, wherein the puncturing part and indwelling part are operably associated with the device, and a guide operably associated with the device, wherein, in use, the indwelling part is moved, via the guide, into a position of use after the puncturing part has pierced the skin. In some embodiments, the puncturing and indwelling parts are separate from each other prior to use. A method of using skin penetrators is encompassed and includes sequentially introducing the puncturing part and the indwelling part into the skin.

Abstract: Systems for gaining access into a body of a patient around an implanted body of an elongate medical device include a sheath having a deformable wall that allows insertion of the device body into a lumen surrounded by the sheath wall. The sheath wall may include first and second edges that extend from a proximal end to a distal end of the lumen, or just extend along a distal portion of the lumen. A tool, which includes a groove sized to grasp about a circumference of the device body, may facilitate insertion of the device body into the lumen of those sheath embodiments that include the first and second edges, by spreading at least one of the first and second edges of the wall apart from the other of the first and second edges while the device body is grasped within the tool.

Abstract: A catheter system for positioning an instrument within a body that includes a hub defining a lumen therethrough for passage of the instrument toward the body. The catheter system also includes an elongate tubular member defining a lumen therethrough. The lumen of the elongate tubular member is in communication with the lumen of the hub for further passage of the instrument toward the body. The system also includes a slitter member that is coupled to the hub. The slitter member is disposed to slit the elongate tubular member as the elongate tubular member moves relative to the hub.

Abstract: A safety IV catheter includes a unitary, resilient needle guard received in a catheter hub. The needle guard includes a proximal arm or wall that includes an opening through which a needle passes for axial movement. When the needle is retracted from the catheter, it releases the force that had previously prevented movement of the needle guard within the catheter hub. This in turn causes the needle guard to snap into a position in which it is clamped onto the needle shaft and in which its distal wall blocks access to the needle tip. In this condition, the spring needle guard and needle can be removed from the catheter hub. A slot or crimp may be formed in the needle shaft that engages with the needle guard after the protected needle and needle guard are removed from the catheter hub, thereby to prevent removal of the protected needle from the needle guard.

Abstract: Indwelling needle includes a cylindrical body, a needle having a sharp edge at a tip thereof, a cylindrical hub retaining proximal end of needle and moveable along main body, a protective cover moveable along main body and projecting from main body, and a spring elastically installed between hub and protective cover. First engaging portion of actuating lever is provided on body engaged with first projection of protective cover and second through-hole in hub to allow first retention mechanism to retain indwelling needle in a use state. First engaging portion is moved upward to release first retention mechanism. This separates protective cover and hub from each other under elastic force of spring. Protective cover and hub are thus retained in a housed state by second retention mechanism and third retention mechanism, respectively. This configuration reduces length of member contacting patient in the use state.

Abstract: A percutaneous peel-away vascular introducer that includes an elongated tubular sheath having opposed proximal and distal ends, and a pair of diametrically opposed peel lines that extend along the length of the sheath from the proximal end thereof to the distal end thereof, wherein the diametrically opposed peel lines have an axially extending pitch. The introducer further includes a pair of spreadable handles associated with the proximal end of the sheath for splitting the sheath along the peel lines.

Abstract: A cannula insertion device includes a housing defining an opening for receiving therethrough a cannula and further defining a channel, and a cannula forming a lumen, the cannula adapted for sliding movement within the housing from a retracted position to an extended position. When the cannula is in the retracted position, the lumen is located remotely from the channel and the channel is in fluidic communication with the opening. When the cannula is in the extended position, the lumen is in fluidic communication with the channel.

Abstract: A detachable introducer and method of using such introducer is disclosed for inserting an embolic coil deployment system into the tortuous vasculature of the human brain for placing an embolic coil within an aneurysm. The introducer includes a sheath having a lumen, a side opening and a longitudinal slit. A deployment catheter with a conical expander member is slideably disposed through the side opening of the sheath and through the lumen of the sheath. The conical expander member detaches the introducer from the deployment catheter through the longitudinal slit of the sheath.

Abstract: An adjustable length catheter device, a kit and a method of providing the adjustable length catheter device to a patient are provided. The catheter device includes an elongate shaft having a proximal portion, a distal portion, a first lumen and a second lumen extending at least partially therethrough. The catheter device further includes a manifold operably connected to the shaft. The manifold is configured to longitudinally move along the shaft towards the distal portion for separating the proximal portion of the shaft into a first proximal shaft portion including the first lumen and a second proximal shaft portion including the second lumen.

Abstract: A catheter head for medical and therapeutic applications including a catheter head housing, a cannula which protrudes from the catheter head and is to be introduced into organic tissue, a container connection for connecting a container containing a fluid to be administered, a fluid channel through which the fluid flows during the administration thereof, an injection needle connection for connecting an injection needle, a connection chamber which is adjacent to the cannula, the injection needle connection, and the fluid channel, and a connector that is arranged in a first position such that the injection needle can be guided from the injection needle connection into the connection chamber and then into the cannula, and in a second position such that it closes the connection chamber from the injection needle connection in a sealing manner after the injection needle has been removed.

Abstract: Disclosed is an apparatus for deploying a bronchial isolation device in a bronchial passageway in a lung of a patient. In one embodiment, the apparatus includes an outer shaft having a distal end. A housing is coupled to the distal end of the outer shaft and configured to receive the bronchial device. An inner shaft is slidably disposed within the outer shaft. A handle is adapted to move the outer shaft relative to both the inner shaft and the handle while the inner shaft remains fixed relative to the handle so as to eject the bronchial isolation device from the housing.

Abstract: A catheter system for positioning an instrument within a body that includes a hub defining a lumen therethrough for passage of the instrument toward the body. The catheter system also includes an elongate tubular member defining a lumen therethrough. The lumen of the elongate tubular member is in communication with the lumen of the hub for further passage of the instrument toward the body. The system also includes a slitter member that is coupled to the hub. The slitter member is disposed to slit the elongate tubular member as the elongate tubular member moves relative to the hub.

Abstract: Valves for medical devices and methods for making them are provided. In one embodiment, a valve is injection molded as a single piece that includes a tubular body and a flap. The tubular body includes an open first end, a closed second end, and a passage extending between the first and second ends defining a central longitudinal axis. The second end includes an end wall including a hole therein communicating with the passage. The flap is formed in the end wall over the hole and is movable away from the second end when an elongate device is introduced through the passage and the hole. Apparatus are also provided for delivering a medical device into a patient's body that includes an elongate tubular member including proximal and distal ends, a lumen extending between the proximal and distal ends; and a valve attached to the proximal end.

Abstract: Systems and methods for integrating a continuous glucose sensor, including a receiver, a medicament delivery device, and optionally a single point glucose monitor are provided. Manual integrations provide for a physical association between the devices wherein a user (for example, patient or doctor) manually selects the amount, type, and/or time of delivery. Semi-automated integration of the devices includes integrations wherein an operable connection between the integrated components aids the user (for example, patient or doctor) in selecting, inputting, calculating, or validating the amount, type, or time of medicament delivery of glucose values, for example, by transmitting data to another component and thereby reducing the amount of user input required. Automated integration between the devices includes integrations wherein an operable connection between the integrated components provides for full control of the system without required user interaction.

Abstract: A penetrating instrument and method for piercing a desired tough or elastic tissue to a controlled and predetermined depth so as to avert any danger of damaging organs or tissues more deeply disposed. The instrument may comprise an introducer needle capable of independently penetrating bodily tissue and having a central hollow channel wherein a piercing needle is axially movable therein. The piercing needle may comprise a distal tip that is preferably fully disposed within the central hollow channel when the piercing needle is in a retracted position, but the piercing needle is capable of being deployed a predetermined distance beyond the distal end of the central hollow channel when disposed in an extended/piercing position. The introducer needle may be advanced through tissue until selected, problematic, or tough tissue is encountered. Subsequently, the piercing needle may be deployed and retracted, as necessary, to facilitate advancement of the instrument through the specific tissue.

Abstract: A method comprises the steps of inserting a microneedle or micropuncture device into a body cavity to achieve a micropuncture into the cavity while reducing tissue trauma at a puncture site. A stepped or tapered guidewire having a reduced diameter distal portion is telescopically disposed through the inner diameter of the microneedle or Micropuncture device. A proximal portion of the guidewire has a diameter larger than the inner diameter of the microneedle or Micropuncture device and extends to a proximal end of the guidewire. The proximal portion is adapted for guiding a larger diameter instrument into and through the vascular system. The microneedle or micropuncture device is withdrawn from the micropuncture while leaving the distal portion of the guidewire extending through the micropuncture. The microneedle or micropuncture device is removed from the guidewire without removing the microneedle or Micropuncture device over the proximal end of the guidewire.

Abstract: A slitter for slitting a guide catheter is assembled from a handle, a blade assembly coupled to the handle, and a holding mechanism coupled to the handle. The blade assembly includes a shroud for receiving an elongated body of a medical device and a slitting blade having an exposed cutting edge to slit the guide catheter.

Abstract: A device for facilitating the use or application of skin penetrators, the device including a puncturing part for piercing the skin, an indwelling part which can be introduced into the skin through an opening generated by the puncturing part and remains there, wherein the puncturing part and indwelling part are operably associated with the device, and a guide operably associated with the device, wherein, in use, the indwelling part is moved, via the guide, into a position of use after the puncturing part has pierced the skin. In some embodiments, the puncturing and indwelling parts are separate from each other prior to use. A method of using skin penetrators is encompassed and includes sequentially introducing the puncturing part and the indwelling part into the skin.

Abstract: A catheter insertion sheath assembly (100) including a tubular sheath body (106) having a proximal end (102), a distal end (104), and a hollow passage (107) extending between the proximal end and the distal end. A handle portion (110,114) is disposed at the proximal end of the tubular sheath. A clamp (120;300;400) extends from the handle portion for releasably closing the sheath prior to insertion of a catheter thereinto and includes a relatively movable portion (130) or portions (310,310?;410,410?) that is or are movable between an open position and a closed position, wherein, when the clamp is in the open position, fluid may flow through the hollow passage between the proximal end and the distal end and when the clamp is in the closed position, fluid flow is restricted through the hollow passage between the proximal end and the distal end.

Abstract: What is described here is a trocar sleeve for endoscopic applications, comprising an elongate part including at least one passage for insertion of an instrument such as an endoscopic, scissors or the like, and pivotable parts mobile on the distal end. The inventive trocar sleeve is characterized by the provision that the distal section is formed by several longitudinal sections articulated on the proximal section of the trocar sleeve, and that a mechanism is provided for pivoting the individual longitudinal sections about an axis orthogonal on the longitudinal axis of the trocar sleeve.

Abstract: A device for implanting catheters has a tube with a wall and a wire. The tube is intended to be introduced into a body so that at least one catheter can be inserted for implantation through the tube. The wall of the tube has an inside surface and an outside surface. The wire is preferably fixed at its first end in the region of the proximal end of the tube to the inside surface or the outside surface of the wall and the wire is guided in the proximity of that surface along the longitudinal direction of the tube from the proximal end of the tube to the distal end thereof and is then returned in the proximity of the respective other surface of the wall along the longitudinal direction from the distal end of the tube to the proximal end thereof. The wire is used to cut the tube open after insertion of the catheter.

Abstract: A surgical trocar device having an obturator and cannula that requires less force to insert and remove from tissue. The cannula includes a head assembly and the obturator includes a cap assembly that have cooperating surfaces that bear against each other so that when the obturator is rotated about its axis the obturator is axially deflected within the cannula and thus more easily removed from the tissue into which the obturator is inserted. The tip of the obturator and the end of the cannula are designed to minimize tissue damage and insertion effort by providing a smooth, unencumbered surface transition. In one aspect of the invention, the tip of the cannula is smooth, continuous, and flexible and can radially deflect when the larger-diameter obturator is inserted or withdrawn though the cannula.

Abstract: A multi-well assembly according to one embodiment comprises a multi-well block and a guide plate. The multi-well block defines a plurality of wells, with each well having a fluid-impermeable bottom surface. The guide plate defines a plurality of fluid passageways corresponding to the wells of the multi-well block. The guide plate is configured such that, whenever the guide plate is registered with the multi-well block, fluid communication is established between each well and an associated fluid passageway.

Abstract: A connection system for connecting a hemostasis valve to a splittable sheath is disclosed. The connection system includes an adapter fitting having a shaft defining a lumen. The shaft has a proximal end and a distal end. On an external surface of the proximal end of the shaft, threading is provided for engagement with the hemostasis valve. A cannula portion defines the distal end of the shaft for interfacing with a splittable sheath. A wedge is disposed on an external surface of the cannula portion for interfacing with a weakened portion of the splittable sheath. A sliding connector is disposed about the shaft for engagement with the splittable sheath. Upon a first level of engagement between the sliding connector and the splittable sheath, a fluid-tight seal is created. Upon a second level of engagement between the sliding connector and the splittable sheath, the wedge initiates separation of the splittable sheath.

Abstract: An intravascular catheter system, such as a dilatation catheter system for angioplasty procedures, which provides for the replacement of the catheter or the guidewire during the procedure. The intravascular catheter has a guidewire-receiving inner lumen extending along its length. A first guidewire port is provided in the catheter body at or near the proximal end of the catheter. A second guidewire port is provided in the catheter body at a location spaced distally from the first guidewire port and proximally from a diagnostic or therapeutic tool, such as a dilatation balloon, on a distal portion of the catheter. A third guidewire port is provided in the distal end of the catheter. The guidewire ports are in communication with the guidewire-receiving inner lumen.

Abstract: An assembly for delivering a stent to an intraluminal location comprising a catheter having an inner member and an outer member, a stent positioned between the inner member and the outer member at the catheter distal end, and a cutter/slider/deployment mechanism slidable secured to the catheter proximal end. A user may vary the length of the catheter by slidably advancing the cutter/slider/deployment mechanism along the catheter, whereby excess portions of the catheter are cut away. When the desired length is achieved, the user can secure the cutter/slider/deployment mechanism to the catheter to prevent further slidable advancement. The user may also vary the configuration of the catheter handle by adding or removing a removable platform from the handle. Upon stent deployment, the stent is released from the outer member, and the stent will expand as desired.

Abstract: The present invention provides improved medical introducer devices which incorporate a single or multi-layer PTFE peelable sheath. Devices of the present invention are suitable for use in inserting an ancilliary medical device, e.g., a catheter, guide wire and the like, into a patient. Methods of the present invention also are disclosed which employ a precision sintering process in order to produce sheaths having excellent tear properties and optimal peelability.

Abstract: The present invention relates to a multi-size catheter for use in biliary endoscopic procedures. The multi-size catheter comprises an outer diameter defined by a plurality of superimposed peelable layers. The peelable layers allow the multi-size catheter to function as a single operator exchange catheter without the need, and additional expense, of an endoscope sheath. Before positioning the multi-size catheter within the working channel of an endoscope, the peelable layers may be selectively removed in order to obtain an outer diameter for the catheter that is less than, but approximate to, the inner diameter of the working channel of the endoscope. The resulting fit eliminates the potential for a guidewire to slip out of the guidewire channel and become pinched between the catheter and the endoscope working channel. With an incorrect fit, a pinched guidewire would restrict the desired movements of both the guidewire and the catheter.

Abstract: System for the subcutaneous delivery into the body of a patient of a fluid from a remote vessel. The system includes a main assembly and placement member with a needle. A delivery tube for carrying the fluid is attached at a near end to the remote reservoir or vessel. At removed end, the delivery tube has a needle for engagement with the main assembly. The main assembly includes a rotating member that when the rotating is perpendicular to the main assembly, it will accept the handle and needle for emplacement of the body onto a patient. After the handle and needle are removed, the delivery tube can be attached to the rotating member which can then be rotated down to a position along to and adjacent the skin of the patient. This provides for a flush mounted infusion device.

Abstract: Devices for the controlled release of one or more drugs are provided. The devices include an implantable stent, at least two reservoirs in the stent, and a release system contained in each of the at least two reservoirs, wherein the release system comprises one or more drugs for release.

Abstract: The present invention is directed toward an improved spinal needle. A needle hub is disposed about a proximate end of a hollow needle. The needle hub side port indicators provide visual and tactual verification by a user of the orientation of the side port on the needle. The needle hub also includes a window with a magnified view. The invention provides a stylet cap disposed about a proximate end of a stylet that freely slides inside the hollow needle and needle hub. The stylet cap forms a pressure fit with the needle hub, and can be engaged in the pressure fit from any axial orientation.

Abstract: An introducer system for introducing a lead or catheter and a method of use. The introducer system includes an elongated introducer sheath which has a luer hub mounted to its proximal end through which a lead or catheter is introduced and a slitter for slitting the luer hub and the introducer sheath. The slittable luer hub takes the form of a conical or cylindrical member carrying a laterally extending tab adapted to engage internal threading on a female luer lock fitting and has a slittable portion angularly displaced from the tab. The slitter includes a blade, a handle carrying the blade, a mechanism for engaging the lead or catheter in the vicinity of the blade and a mechanism for engaging the lead or catheter proximal to the blade, configured such that the lead or catheter body when engaged by the slitter is angled proximal to the blade of the slitter.

Abstract: A surgical trocar device having an obturator and cannula that requires less force to insert and remove from tissue. The cannula includes a head assembly and the obturator includes a cap assembly that have cooperating surfaces that bear against each other so that when the obturator is rotated about its axis the obturator is axially deflected within the cannula and thus more easily removed from the tissue into which the obturator is inserted. The tip of the obturator and the end of the cannula are designed to minimize tissue damage and insertion effort by providing a smooth, unencumbered surface transition. In one aspect of the invention, the tip of the cannula is smooth, continuous, and flexible and can radially deflect when the larger-diameter obturator is inserted or withdrawn though the cannula.

Abstract: A holding device and method of use with a peelable or otherwise splittable introducer sheath or catheter through which a cardiac pacing lead or other elongated flexible instrument extends into the body of a living being. The introducer is arranged to be grasped by a user to pull the introducer in the proximal direction so that can be withdrawn out of the being's body. The holding device comprises a first or “gripper” portion and a second or “splitter” portion. The gripper portion includes at least one gripping member, e.g., a pair of jaws or at least one recessed engagement surface, to grasp or frictionally engage a portion of the periphery of the elongated flexible member to enable the user to hold the pacing lead at a desired position within the being's body. The splitter portion of the holding device is arranged to cause the introducer to separate longitudinally, e.g.

Abstract: A vascular introducer is disclosed which includes an elongated primary sheath defining an interior lumen and having opposed proximal and distal end portions, and at least an elongated secondary sheath disposed within the interior lumen of the primary sheath and adapted for movement from a collapsed condition to an open condition in response to insertion of a dilator through an interior lumen thereof.

Abstract: A body cavity access assembly is disclosed. The body cavity access assembly includes a conduit having an exterior surface, a dispensing mechanism, and a reservoir for receiving a biologically active compound. The exterior surface of the conduit has first exit port and a second exit port defined therein which are in fluid communication with the reservoir. The first exit port and the second exit port are selectively positionable between an open mode of operation and a closed mode of operation with the dispensing mechanism. An associated medical procedure for dispensing a biologically active compound is also disclosed.