Abstract: A contrast dispensing system (10) reduces cost by directly connecting a check valve (210) to and between the reservoir inlet port (220) and the mating luer connector (204) of a disposable set (200). A contrast dispensing system (10) includes as part of the reservoir (212) an integrally molded cap (280) having the inlet port (200) and a lateral pipe (300) to confine contrast media (14) therein and disperse it at separate locations (334, 336) within the chamber (260) of reservoir (212). The reservoir (212) may have a vent port (284) with a flip cap (294) for selectively opening or closing same.

Abstract: Medical devices that are configured for insertion into a body lumen, such as the male urethra, are provided with one or more inflatable balloons having elastic sleeves, wherein each elastic sleeve is adapted to inflate in response to inflation of a respective balloon, and to deflate in response to deflation of the respective balloon. When a balloon is in a deflated condition, a respective elastic sleeve exerts a circumferentially compressive force against the balloon to cause a smooth, reduced cross-sectional profile of the balloon along an axial extent thereof. This smooth, reduced cross-sectional profile can facilitate passage of the medical device through a body lumen during both insertion and extraction of the medical device. A thin layer of fluid may be disposed between a treatment balloon and a respective elastic sleeve to facilitate heat transfer from a treatment balloon to a surrounding elastic sleeve or to administer a therapeutic agent to localized tissue.

Abstract: The invention tissue injection catheters are designed to facilitate injection of a therapeutic or diagnostic agent to an interior body cavity, especially the myocardium or epicardium of the heart with precisely controlled depth penetration. The invention injection catheters, which include mechanisms for precisely controlling the length of needle tip exposed for tissue penetration, are designed to be used in an assemblage with a sterile container and delivery actuator for reinjection of autologous cell-containing fluids, such as autologous bone marrow aspirate. In preferred embodiments, the assemblage is designed to be hand-held. When used in such an assemblage, the invention catheters are particularly useful as a gene delivery device to effect angiogenesis of ischemic areas of the heart.

Abstract: A device for delivering oxygenated blood and occluding the ascending aorta is provided. The device has a blood flow lumen with a movable portion. The movable portion is movable from a position contained within a body of the device to a position which extends outwardly from the device. The movable portion is made of a tube of flexible material and everts when moving to the extended position.

Abstract: Disclosed is a check valve for placement near the distal end of a catheter. A continuously smooth outer surface for the catheter with check valve system assures that there is no propensity for a blood clot to form in cracks on the system's outer surface. The check valve is a formed from a low durometer, highly elastic, elastomer cylindrical tube that is shrunk into a cylindrical groove that would typically be located near the catheter's distal end. When pressurized fluid is injected through the catheter, the cylinder that is placed over one or more holes in the cylindrical groove in the catheter is forced to expand radially outward which allows the fluid to be injected into the blood vessel. When the pressure is removed, the elastomer tube retracts to its normal position which position tightly covers the holes thereby preventing any blood from entering the catheter.

Abstract: A 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.

Abstract: A drug and drug delivery system may be utilized in the treatment of vascular disease. A local delivery system is coated with rapamycin or other suitable drug, agent or compound and delivered intraluminally for the treatment and prevention of neointimal hyperplasia following percutaneous transluminal coronary angiography. The local delivery of the drugs or agents provides for increased effectiveness and lower systemic toxicity.

Abstract: Methods and devices are provided for enhancing corrosion of an electrode in a biocompatible fluid. The method comprises (1) placing a primary electrode and a counter electrode in an electroconductive biocompatible fluid to form an electrochemical cell; and (2) applying a time-varying potential, through the electrochemical cell, to the primary electrode. In a preferred embodiment, the primary electrode is metal and comprises a reservoir cap of a microchip device for the release of molecules or exposure of device reservoir contents. The potential preferably is characterized by a waveform having a maximum potential effectively anodic to meet or exceed the corrosion potential of the primary electrode. Also, the minimum potential preferably is effectively cathodic to be below the value where re-deposition of metal ions on the metal electrode can substantially occur, thereby corroding the metal electrode.

Abstract: The technical field of the invention is that of pre-filled and disposable needleless syringes, used for intradermal, subcutaneous and intramuscular injections of liquid active principle for therapeutic use in human and veterinary medicine. The inventive syringes (1) are mainly characterised in that they function with a pyrotechnic charge (6) consisting of a mixture of powder with high burning rate and a powder with low burning rate. Indeed, the combustion of the powder with a high burning rate enables to communicate instantly, through a piston (3), a very high speed to the active principle (4), whereas the combustion of the powder with a low burning rate enables to maintain a threshold pressure level to proceed with the injection, so as to ensure that the active principle (4) penetrates through the skin. Thus, the injection is properly and homogeneously without any loss of active liquid (4).

Abstract: A split tip dialysis catheter having an outer tube and an inner tube, the two tubes which can be arranged over at least a portion of their length in a coaxial configuration. The inner tube may be connected to the outer tube at a proximal bifurcation, secured at a distal end of the outer tube or both, but generally the inner tube will remain free to move relative to the outer tube to optimize functionality. In addition, the inner tube can be arranged to be removable from the catheter for replacement thereof.

Abstract: A micro-injection molded disposable needle assembly having more than one passageway formed therein to permit the simultaneous drawing and administering of fluids through separate passageways is disclosed. The micro-injection molded disposable assembly includes one or more sensors disposed therein for measuring and monitoring one or more desired body or surrounding environmental conditions. A method of forming the disposable needle from an elastomeric material using micro-injection molding is also disclosed.

Abstract: A medical device, such as a Huber-type device, includes a structure that enhances operator safety by reducing the likelihood that a needle will accidentally injure an operator. In one embodiment, the device includes a collapsible structure that can move from a use position to a non-use position. The device includes first and second wing portions and a channel for covering the needle as it is extracted from the patient. The structure enables the operator to leverage applied pressure for a smooth removal of the needle into the device for safe disposal.

Abstract: A protector sleeve is disclosed for protecting an expandable member disposed on a catheter during pre-deployment handling. In one embodiment, the protector sleeve includes a tubular member with proximal and distal portions and preferably an elastomer seal therebetween, wherein the proximal portion of the tubular member is designed to slidably engage the expandable member in its collapsed state, while the distal portion permits fluid access to a catheter lumen, e.g., a guidewire lumen, without exposing the protected expandable member to the fluid.

Abstract: Microneedle devices and methods of use thereof are provided for the enhanced transport of molecules, including drugs and biological molecules, across tissue by improving the interaction of microneedles and a deformable, elastic biological barrier, such as human skin. The devices and methods act to (1) limit the elasticity, (2) adapt to the elasticity, (3) utilize alternate ways of creating the holes for the microneedles to penetrate the biological barrier, other than the simply direct pressure of the microneedle substrate to the barrier surface, or (4) any combination of these methods. In preferred embodiments for limiting the elasticity of skin, the microneedle device includes features suitable for stretching, pulling, or pinching the skin to present a more rigid, less deformable, surface in the area to which the microneedles are applied (i.e. penetrate).

Abstract: A disposable syringe includes a tubular barrier member retained in a rear passageway of a barrel. A tubular needle seat for fixing a needle cannula is retained on the barrier member, and abuts against an abutment wall in the front passageway of the barrel while the needle cannula is disposed outwardly of the barrel. A plunger is slidable in the rear passageway, and has a seal member to seal a cavity confined in a plunger body and containing a fluid at a reduced pressure. When a pushing force applied to the plunger body moves the barrier member against the first and second frictional forces, the needle seat is released, and the seal member is ruptured, so that the needle seat and the needle cannula are suctioned into the cavity due to the pressure difference between the ambient atmosphere and the reduced pressure.

Abstract: A catheter having a mandrel secured to the catheter or constrained within a dedicated lumen. In one embodiment, the catheter has an inner tubular member and an outer tubular member with a sidewall configured to define a mandrel lumen longitudinally along an inner surface of the outer tubular member or along an outer surface of the inner tubular member. The mandrel lumen may be configured to allow the mandrel to be exchanged to adjust the handling characteristics of the catheter. The mandrel may occupy an intermediate portion of the catheter shaft, or may extend from the proximal end to within proximal or distal shaft sections of the catheter. In coronary artery applications, the mandrel is configured to support the catheter as it bends through the aortic arch and enters the coronary artery.

Abstract: An apparatus for delivering aerosolized fibrin endoscopically to a wound is disclosed. The apparatus has a pair of syringes for holding fibrin precursors, a mixing chamber for mixing the fibrin precursors separately with pressurized gas to form individual aerosol solutions, and a delivery tube for delivery of the aerosol solutions to a remote surgical site for formation of an aerosolized fibrin seal.

Abstract: A new and improved anesthetic delivery tool and method of using the tool in transmucosal absorption applications of a gel topical anesthetic agent and in subdermal injections of a liquid anesthetic agent is disclosed. The anesthetic delivery tool comprises a housing unit having a hollow central cavity with a slip plate containing a plurality of needles directed towards the front end of the housing unit. The slip plate and the front portion of the hollow central cavity defining a front-end cavity for affixing a therapeutically effective aliquot of gel topical anesthetic agent. The anesthetic delivery tool also comprises a thin membrane positioned directly behind the slip plane and a push plate positioned at the rear end of the housing unit. The push plate, the thin membrane and the rear portion of the hollow central cavity defining a rear-end cavity for affixing a therapeutically effective amount of liquid anesthetic agent.

Abstract: The present invention relates to a system for delivering and injecting an agent into a target site within the body without penetrating the tissue of the target site with anything other than the agent. The system comprises a nozzle assembly and a propulsion mechanism. The nozzle assembly comprises an ampule with a reservoir, having a reservoir orifice, for containing the agent; a dispersion fixture that has a dispersion orifice; and a channel in fluid communication between the reservoir orifice and the dispersion orifice. The propulsion mechanism is operatively coupled to the reservoir for propelling the agent from within the reservoir, through the reservoir orifice and the channel and the dispersion orifice, at a pressure sufficient to cause the agent to penetrate the target site without penetration of the target site with the dispersion fixture. Methods of using and making the system are also disclosed.

Abstract: An automatic needle retracting mechanism (1) for a hypodermic syringe (2) comprises a body (3) which slidingly supports a needle (27). A retainer (9) for an actuator (8) and the needle (27) is kept in a retaining position by a spacer (11), which after some time in contact with an injectant loses its mechanical strength. A filing of the needle with an injectant causes a deformation of the spacer (11), a release of the actuator (8) and a retracting of the retainer (9) and needle (27) into a needle retraction chamber (4). The needle retracting mechanism may also include an inner sleeve (20) which is manually movable towards the retainer (9) for a manual release of the actuator (8). The needle retracting mechanism may be included in a needle holder (33) or integrated in a syringe (2′).