Abstract: This invention relates to an improvement in a process for forming a carton from paperboard stock comprising the steps: applying an aqueous based adhesive to select parts of a paperboard carton blank obtained from a paperboard feedstock; drying the aqueous based adhesive; folding the select parts of the adhesive coated carton blank onto cooperating parts of the paperboard blank; and, heat sealing the select and cooperating parts thereby forming the carton; wherein the aqueous based adhesive is comprised of a vinyl acetate/ethylene polymer formed by emulsion polymerization and having (a) a crystalline melting point (Tm) ranging from 35 to 110° C., preferably 50 to 90° C.; measured at a heat rate of 20° C./minute and, (b) a tensile storage modulus of at least 1×104 dynes/cm2 at 115° C. measured at 6.28 rad/sec.

Abstract: A method for modeling the effect of turbulence on the cut point function of a decanting centrifuge includes inputting data related to the centrifuge including the bowl radius, r2, the pond top radius, r1, the bowl length, LB, the angular velocity, ?, of the centrifuge into an analyzer, measuring data related to the feed fluid including a fluid density, ?f, a particle density ?s, a fluid viscosity, ?, and the flow rate, Q, and inputting the measured data into the analyzer, calculating a d100 cut point as a function of the flow rate, modeling a first cut functions for laminar flow as a function of a particle diameter, di, using the calculated d100 cut point function, calculating a maximum point within the pond, Ib, Ip, at which a particle having particle diameter, di, must reach a laminar boundary layer within the pond to be captured within the bowl, wherein Ib is defined as the distance from the inlet at which the particle having particle diameter, di encounters the laminar boundary layer and Ip is defined as

Abstract: A heart assist system includes an axial-flow blood pump capable of being implanted in the descending thoracic aorta; a pressure-feedback controller connected to the pump, for controlling the pump, the controller capable of being implanted in the body; and a rechargeable battery pack connected to the pump and to the controller, for providing power to the pump, the battery pack capable of being implanted in the body. A method for assisting a failing heart comprises the steps of a) in response to when a measured dP/dT signal increases during systole, signaling an implanted aortic blood pump to go into a systolic mode and pump blood at a first flow rate; and b) in response to when the dP/dT signal peaks in the negative region, signaling the pump to go into a diastolic mode and pump blood at a second flow rate.

Abstract: A cardiac harness for treating congestive heart failure is disclosed. The harness applies elastic, compressive reinforcement on the left ventricle to reduce deleterious wall tension and to resist shape change of the ventricle during the mechanical cardiac cycle. Rather than imposing a dimension beyond which the heart cannot expand, the harness provides no hard limit over the range of diastolic expansion of the ventricle. Instead, the harness follows the contour of the heart throughout diastole and continuously exerts gentle resistance to stretch. Also disclosed is a method of delivering the cardiac harness to the heart minimally invasively.

Abstract: An endoscope hood has a protrusion portion which protrudes in an observation visual field direction of an endoscope at an end of a cylindrical press fitting fixing portion attached by press fitting in a state that an attachment position in a circumferential direction is positioned at a distal end portion of an endoscope insertion portion in an appropriate direction. Further, there is provided attachment state confirming device which increases an area of the protrusion portion displayed in an endoscope observation image when the press fitting fixing portion is attached to a distal end portion of a second endoscope insertion portion having a size different from that of a first endoscope insertion portion to which the press fitting fixing portion can be appropriately attached, and gives a warning about an inappropriate attachment state.

Abstract: A surgical wound retractor is adapted to dilate a wound to a desired diameter. The retractor includes first and second rings, each having a diameter greater than that desired for the wound. The first and second rings are adapted for disposition interiorly and exteriorly of the wound, respectively. A plurality of retraction elements is disposed in a generally cylindrical relationship between the first and second rings and extends through the wound to exert a radial retraction force on the wound that is dependent on the distance separating the first and second rings. Retraction elements, both distensible and non-distensible, are contemplated with appropriate attachment elements at the rings to provide for variations in the retraction force. With a suitable retraction sleeve, a third ring can be provided to form a circumferential retainer to vary the retraction force. Rings can also be made inflatable or self-expanding to vary the retraction force.

Abstract: In accordance with the present invention, there is disclosed surgical methods and apparatus for accessing and stabilizing the heart. The methods and apparatus facilitate access to an anastomosis site, allows various instruments or devices to be maneuvered and secured in place, and provide stabilization of the heart. In particular, the apparatus involves a retractor assembly having a pair of opposing blades having a channel adapted to engage an incision in a patient. The retractor blades may have features to cooperatively engage an instrument mount. The instrument mount may hold an instrument, such as a tissue stabilizer, and allows the instrument to be easily maneuvered. The retractor blades may have a number of suture locks for securing sutures used during surgery. The retractor system is particularly useful in accessing, positioning and stabilizing the beating heart for coronary artery bypass graft surgery.

Abstract: A health monitoring system is disclosed. According to one embodiment, the health monitoring system includes a first server configured to receive a first set of information from a monitoring device, wherein the first set of information includes a health condition reading of a subscriber, and wherein the first server is configured to process the first set of information and transmit a second set of information to the monitoring device and/or a telecommunications device, wherein the second set of information includes medical treatment information and/or medical advice concerning the subscriber. The health monitoring system also includes a database in communication with the first server and configured to store a third set of information therein, wherein the third set of information includes emergency contact information, one or more health conditions of the subscriber, monitoring time intervals, and/or numerical ranges defining acceptable health conditions and medical alert conditions.

Abstract: Methods of probing a material under investigation using an ultrasound beam. Echolocation data is generated using a multi-dimensional transform capable of using phase and magnitude information to distinguish echoes resulting from ultrasound beam components produced using different ultrasound transducers. Since the multi-dimensional transform does not depend on using receive or transmit beam lines, a multi-dimensional area can be imaged using a single ultrasound transmission. In some embodiments, this ability increases image frame rate and reduces the amount of ultrasound energy required to generate an image.

Abstract: Ultrasonic acoustic imaging finds many uses, particularly in the field of non-invasive medical testing. Detection of Doppler shifted acoustic frequencies permits observation of flow of a particle-containing liquid, for example, blood flow. In order to see slower moving blood by Doppler ultrasound investigation, as the blood moves from major blood vessels into arterioles and capillaries, it is necessary to lower the pulse repetition frequency. The herein disclosed invention is an interleaving technique that lowers the effective pulse repetition frequency at each probe position without exacting these system penalties.

Abstract: A monitoring device, method and system are disclosed herein. The monitoring device is capable of determine when a user's wrist is at rest using a motion sensor disposed within a wrist module that is attached to the user's wrist. When at rest, the monitoring device utilizes a vital sign monitor to determine a plurality of vital signs of the user. The vital sign monitor preferably comprises a light source and photodetector in communication with a pulse-oximetry circuit. The motion sensor is preferably an accelerometer.

Abstract: The present invention relates to a biological component measurement apparatus set, in which a puncture mechanism for puncturing skin of a subject to collect a sample blood is integrated with a biosensor measurement apparatus. The puncture mechanism includes a puncture needle, and a cap which is detachably engaged with a body of the apparatus, wherein the cap has a skin contact surface which is brought into contact with the skin for puncturing. The skin contact surface having an opening through which the puncture needle moves to puncture the skin, and is shaped so as to fit a surface shape of the skin to be punctured. The set includes a plurality of different caps each corresponding to a different sample collection site so that a plurality of different sample collection sites can be selected.

Abstract: A therapy apparatus includes a container having an interior volume and having an opening providing access to the interior volume and massaging elements freely located in the interior volume of the container. Each massaging element has a generally spherical exterior and has multiple protrusions projecting from its generally spherical exterior. A patient's hand may be inserted into the container through the opening and be moved among the massaging elements to be stimulated by massaging elements contacting the fingers and both the front and the back of the hand.

Abstract: A warm air massager for heating and massaging a body part includes a massage node which includes openings for directing streams of heated air to the body part being massaged. The body part is massaged by the reciprocating motion of the massage node produced by an internal massage motor. The massage motor may rotate to cause an eccentric connector to impart reciprocating motion to a shaft coupled to the massage node. The massage motor may be located within the housing, within the massage node, or there may be multiple massage motors located in each of the housing and the massage node. Intake ambient air enters the massage housing by means of a fan which withdraws ambient air from outside, directs the ambient air through a heater element and directs streams of the heated air through the massage node to the body part being massaged. Each of the fan, the heater element and the massage motor or motors may include multiple settings. The fan and massage motor are preferably separately controlled.

Abstract: A treatment device for a user's hand and/or wrist. The treatment device includes a housing having an outer surface defined at least partially by a membrane adapted for placement against the user's hand and/or wrist. The treatment device creates localized outwardly deformations in the membrane adapted to create a massaging effect in the user's hand and/or wrist.

Abstract: The present invention provides systems, methods and apparatuses for medical fluid delivery systems that employ a pumping cassette. In particular, the present invention provides systems, methods and apparatuses for cassette-based dialysis therapies including hemodialysis, hemofiltration, APD (including tidal modalities) and CFPD. The embodiments described include a combined pump/valve housing, a fail safe pump/valve arrangement, a cassette auto-alignment feature, a pumping membrane material, a multiplexing valve arrangement, an expert fluid pumping management system, an integral port vent and an in-line air separation chamber and combinations of each of these.

Abstract: A pumping system 10 provides a physiological pulsatile flow and includes controller 121, a pump drive head 50 coupled to a motor 12 and a fluid housing 52 having at least one port 60. The port 60 includes a ball valve retainer region 69, a valve seat 73, and an occluder ball 71 disposed in the ball valve retainer region 69. During operation, the motor 12 forces the fluid in and out the fluid housing 52 and causes the occluder ball 71 to move from a first position whereby the fluid cannot pass through the port 60, to a second position whereby the fluid moves annular to and generally around the occluder ball 71. This movement creates a slight flow reversal that “breaks up” any blood clots that may form. The pumping system may be used as part of a cardiopulmonary bypass system, a ventricular assist device (VAD) and/or a heart pump.

Abstract: A catheter system for controlling the body temperature of a patient by modifying the temperature of blood flowing within a blood vessel of the patient. The catheter system comprises a catheter body having a heat exchange region in contact with the blood; and a mechanism for moving the heat exchange surface, thereby increasing heat exchange between the heat exchange surface and blood flowing past the heat exchange surface. Various methods of moving the heat exchange surface are disclosed.

Abstract: A needle-free injection device is described. The injection device includes a user-grippable housing and a syringe assembly movably secured to the housing. The syringe assembly is configured to expel injectable fluid out of a nozzle upon application of pressurized gas to the syringe assembly. The injection device also includes a pressurized gas delivery mechanism disposed within the housing and configured to selectively apply pressurized gas to the syringe assembly. The pressurized gas delivery mechanism is at least partly actuated by pressing the nozzle onto an injection site so that the syringe assembly moves relative to the housing.

Abstract: An intravascular balloon catheter includes a tubular catheter body having a balloon structure removably mounted over the catheter body. The catheter body has a guidewire lumen, and the catheter body may be left in place within a patient's vasculature while the balloon structure is withdrawn and optionally a second balloon structure introduced over the catheter body. The catheter and methods of the present invention are particularly suitable for performing angioplasty and subsequent procedures, such as stent placement, which are best performed using successive interventional balloon structures.

Abstract: A safety indwelling needle including an inner needle unit 1 having an inner needle 8, an inner needle hub 14 and a housing member 13 disposed at a distal side of the inner needle hub 14, and an outer needle unit 2 having an outer needle 4, an outer needle hub 5 and an outer needle cap 9, characterized in that the housing member 13 includes openings for allowing penetration of the inner needle 8 at a distal end and a proximal end thereof, an internal space for storing only a distal end portion of the inner needle 8 including a needlepoint 3 thereof when the inner needle 8 is drawn out from the outer needle 4, and a shielding member which automatically closes the opening at the proximal end of the housing member 13 by a magnetic force.

Abstract: This invention prevents the danger of falling of body temperature by making the blood temperature similar to the body temperature in the injection of Ringer's solution fluid or blood transfusion, and also alleviates the patient's pain and improves the speed at which Ringer's solution fluid or blood enters the body. The warming device is much cheaper than previously released products, and small and light in weight, and allows blood or solution fluids to flow most effectively by allowing sufficient time for heat transfer as a pack type. The operation is convenient and sanitary in its single usage only. The inventive purpose has the methods of utilizing the temperature sensor in adjusting temperature by utilizing them PTC heating element's resistance specialty against the temperature as well as temperature sensor.

Abstract: A system for controlling pressurized infusion and temperature of intravenous fluids according to the present invention includes a housing, a heating assembly and a flexible cover. The heating assembly is recessed within the housing and includes a generally U-shaped configuration to surround and uniformly heat fluid within a fluid container placed thereon. The cover wraps around a portion of the fluid container to secure the fluid container against the heating assembly. The cover includes a pressurization member to apply a desired pressure to the fluid container to achieve a desired flow rate of intravenous fluid from the fluid container to an infusion site on a patient. The system further includes a controller to control the heating assembly and pressure within the pressurization member in accordance with desired temperature and pressure information entered into the controller for system operation.

Abstract: The invention concerns a medical device comprising an inflatable sheath (2), a tubing (3) integral with a non-return valve (4), a rigid disc (5) forming a horizontal platform above the chamber (2) and means for receiving (6, 7, 18) the cannula (13, 20).

Abstract: A tampon disposal system for efficiently and sanitarily removing and disposing of a soiled tampon. The tampon disposal system includes a housing having at least one wall, an inner cavity, a plurality of perforated edges and a cleansing wipe that is enclosed within the housing. Removal of the perforated edges from the housing creates an opening along each perforation thereby exposing the inner cavity of the housing and the cleansing wipe positioned therein. Upon removal of the cleansing wipe, the string attached to a soiled tampon is insertable through the openings of the housing whereby removal and disposal of the tampon can be achieved in a relatively sanitary and efficient manner.

Abstract: A vaginal cleaning device is disclosed, which includes an axial support post having a head disposed at the front end and a circular disk around the rear end, a tubular applicator body disposed around the post between the head and the disk, an applicator extension and a handle. Further disclosed is a vaginal cleaning device which includes a hollow axial support post having a head disposed at the front end, a circular disk around the rear end, a plurality of apertures around the body of the hollow axial support post, a tubular applicator body disposed around the post between the head and the disk, a hollow applicator extension and a fluid supply means connected to the applicator extension. A fluid can be delivered through the hollow applicator extension and the hollow axial support post into the tubular applicator body for cleaning the vagina.

Abstract: A disposable diaper includes a basic absorbent batt structure and a supplementary absorbent batt structure placed thereon. An elastic member is provided between the two batt structures so as to transversely cross them. Contraction of the elastic member causes opposite side edge regions of the two batt structures to be pulled nearer to a longitudinal center line thereof. This results in a zone of the former batt structure underlying a distal end portion of the latter batt structure to curving downward with respect to a lower surface of the latter batt structure while the distal end portion of the latter batt structure curves upward with respect to a body facing surface of the basic absorbent batt structure. The curving of the batt structures forms a pocket opening from a front waist region toward a crotch region of the disposable diaper.

Abstract: A method is disclosed for photodisrupting a surface in the stroma of an eye at a substantially constant distance from the anterior surface of the eye. A frame of reference is established for the eye that includes an axis of rotation. Next, the focal point of a laser beam is positioned in the stroma at a radial distance from the axis. At least one laser pulse is delivered to the stromal tissue at the focal point, photodisrupting the tissue there and creating a photodisruption bubble having a diameter “d”. The focal point is then rotated about the axis through an arc length substantially equal to “d” and the photodisruption step is repeated. During rotation, the distance between the focal point and the axis is decreased at a rate substantially equal to the distance “d” per revolution. The method can be used to create a flap for a LASIK type procedure.

Abstract: The present invention provides methods, systems, and apparatus for calibrating a laser ablation system, such as an excimer laser system for selectively ablating a cornea of a patient's eye. The invention also facilitates alignment of eye tracking cameras that measure a position of the eye during laser eye surgery. A calibration and alignment fixture for a scanning laser beam delivery system having eye tracking cameras may include a structure positionable in a treatment plane. The structure having a feature directing laser energy incident thereon to a calibration energy sensor, at least one reference-edge to determine a characteristic of the laser beam (shape, dimensions, etc.), and an artificial pupil to determine alignment of the eye tracking cameras with the laser system.

Abstract: Device for performing laser angioplasty, in which laser light is beamed via a laser radiation device in the area of a catheter tip, with simultaneous OCT monitoring, for the ablation of plaque. The feed lines for the laser radiation device and the rotating OCT signal lines are disposed in a common catheter sheath, said feed lines leading to an OCT sensor disposed within a ring-shaped window running around the circumference of the catheter sheath, said OCT sensor being disposed at a distance from the laser radiation device.

Abstract: A method and apparatus for forming a lesion in tissue along a desired ablation path with treating a body tissue in situ (e.g., an atrial tissue of a heart to treat) atrial fibrillation include a lesion formation tool including is positioned against the heart surface. The lesion formation tool includes a guide member having a tissue-opposing surface for placement against a heart surface. An ablation member is coupled to the guide member to move in a longitudinal path relative to the guide member. The guide member includes a track. A carriage is slidably received with the track. The ablation member is secured to the carriage for movement therewith. The guide member includes a visualization component.

Abstract: A method and apparatus for treating a body tissue in situ (e.g., an atrial tissue of a heart to treat atrial fibrillation) include a lesion formation tool is positioned against the heart surface. The apparatus includes a guide member having a tissue-opposing surface for placement against a heart surface. The guide member also has interior surfaces and a longitudinal axis. A guide carriage is sized to be received with the guide member and moveable therein along the longitudinal axis. An optical fiber is positioned within the guide carriage with the carriage retaining the fiber. The carriage receives the fiber with an axis substantially parallel to the longitudinal axis and bends the fiber to a distal tip with an axis of said fiber at said distal tip at least 45 degrees to the longitudinal axis and aligned for discharge of laser energy through the tissue opposing surface.

Abstract: A high-frequency generator for high-frequency surgery comprises a power generator for supplying high frequency energy at a base frequency. A standardizing factor is determined, with which an output variable from the power generator must be scaled in order to attain a given desired value. Furthermore, harmonics of the base frequency are determined from the output variable and scaled using this factor. By means of an input, the thus obtained signal now controls the output power of the generator. With this arrangement, a reliable first cut may be performed on various kinds of tissue without occurrence of any coagulation.

Abstract: The invention provides a transurethral ablation device comprising a catheter sized for insertion into a urethra of a male patient. A distal end of the catheter defines a lateral cavity. A vacuum line applies vacuum pressure to the cavity to capture a portion of the urethra and a portion of the prostate into the cavity. An ablation probe has a distal tip mounted within the catheter adjacent the cavity, and is movable for insertion into the captured portion of the prostate. The ablation probe can be inserted with an orientation substantially parallel to the urethral wall. Alternatively, multiple ablation probes can be provided for simultaneous use in ablating tissue with a target site in the prostate. A suction cannula may be used to remove ablated tissue from the target site.

Abstract: System and method for treating a skin target. A temperature effector creates a temperature difference between the target and the skin tissue surrounding the target such that the target is at a higher temperature than the surrounding tissue by at least 5° C. One or more RF electrodes are attached to the skin and RF energy is applied.

Abstract: A tissue ablation probe, system, and method are provided. The ablation probe comprises an elongated member, an ablative element mounted on the distal end of the elongated member, and at least one thermoelectric device mounted to the member in thermal communication with the ablative element. The system may include the ablation probe, thermal control circuitry for controlling the thermal effect of the thermoelectric device, and an ablation source for suppying ablation energy to the ablative element. A plurality of circumferentially distributed thermoelectric devices can be provided, so that radial tissue sectors can be selectively affected by independently controlling the thermal effect of the thermoelectric devices. In one embodiment, the thermoelectric device(s) can be used to cool a heat ablative element. In another embodiment, the thermoelectric device(s) can be used to heat an ablative element, thereby forming a heat ablative element.

Abstract: An apparatus and method for cutting a material including conducting and non-conducting materials such as biological tissue, cellulose or plastic while the material is submerged in a conductive liquid medium. The apparatus has a cutting electrode with an elongate cutting portion having an aspect ratio (length to width) of 1 or more and a return electrode. The two electrodes are immersed in the conductive medium and a voltage is applied between them to heat the medium, thus producing a vapor cavity around the elongate cutting portion and ionizing a gas inside the vapor cavity to produce a plasma. The voltage applied between the electrodes is modulated in pulses having a modulation format selected to minimize the size of the vapor cavity, its rate of formation and heat diffusion into the material while the latter is cut with an edge of the elongate cutting portion. The modulation format includes pulses ranging in duration from 10 ?s to 10 ms, as well as minipulses and micropulses, as necessary.

Abstract: An interbody fusion device in one embodiment includes a tapered body defining a hollow interior for receiving bone graft or bone substitute material. The body defines exterior threads which are interrupted over portions of the outer surface of the device. The fusion device defines truncated side walls so that on end view the body takes on a cylindrical form. The side walls are provided with vascularization openings, and the body wall device includes opposite bone ingrowth slots extending through the interrupted thread portion of the body. In another embodiment, the tapered body is solid and formed of a porous biocompatible material having sufficient structural integrity to maintain the intradiscal space and normal curvature. The material is preferably a porous tantalum having fully interconnected pores to facilitate complete bone tissue ingrowth into the implant.

Abstract: In an implant for fixing neighboring bone plates of the cranial bone comprising an inner bearing element which covers a spacing gap between the bone plates, an outer bearing element which covers the spacing gap and a connecting device which penetrates the spacing gap and which, when said bearing elements approach one another, connects the bearing elements together by means of a latching or a clamping connection in such a manner that they are no longer able to be moved apart, it is proposed that the two bearing elements be additionally connected by a thread-like tensioning element which is passed through the outer bearing element in displaceable manner and, when tensioned, moves the inner bearing element towards the outer bearing element in order to simplify the process of applying the implant and to ensure a secure connection of the bearing elements.

Abstract: Methods and apparatus for arthroscopic tenodesis using sockets in bone created by retrograde cutting. A cannulated pin is drilled through bone and into a joint space in the normal, antegrade direction, guided by a drill guide. A strand provided through the cannulated pin is used to draw a retrodrill cutter into the joint space. The retrodrill cutter is threaded onto the cannulated pin, which is turned for retrograde cutting of a socket into the bone. The method is used to form a pair of sockets in the joint, which accept the respective ends of a replacement graft. The graft is brought into position in the joint space using loops formed in the strands, in a manner similar to introduction of the retrodrill cutter. The reconstruction is completed by securing suture attached to the graft ends with a button implant installed at the bone surface.

Abstract: A surgical apparatus that makes possible the replacement of ankle tissue between the bottom of the tibia and the adjoining top of the talus bone comprises: (a) a base having primary and secondary anchoring holes that extend through the base and through which anchoring pins may be extended for anchoring withh the tibia, anchoring holes having adjoining and cooperating, threaded, set screw holes and set screws that cooperate to assist in fixing the position of the base relative to the anchoring pins and the tibia, (b) a surgical blade positioning shelf, the front surface of the shelf configured to approximate the curvature observable in the top portion of the talus and the rear surface of the shelf having attached to it a shaft which may slide in and out from an opening in the front surface of the base, and (c) indicia attached to the shaft which allows one to record the position of the front surface of the surgical blade positioning shelf relative to the base.

Abstract: A surgical ring, designed to be implanted around biological organs comprising a pouch or a duct, so as, on the one hand, to form a closed loop between these two extremities (1, 2), thus forming a first (1) and a second (2) extremity and, on the other hand, to reduce the diameter of the opening of the organ when it is tightened by the ring, the ring including a system for reversibly controlling the variation in its diameter. The system also includes a flexible filiform element (4), inserted longitudinally with possibility of sliding into the material constituting the body of the ring between the first (1) and second (2) extremities, so as to define a fixed portion (5) connected to the first extremity (1) and a free portion (7) associated with an actuator (8) mounted on the ring near the second extremity (2).

Abstract: A blood withdrawal system for withdrawing blood for diagnostic purposes including a lancing device having a housing with an opening and a support surface, and a lancet holder movably mounted in the opening including a lancet and a bearing member that rests on the support surface. The device further includes a trigger unit which, when moved linearly, causes a rotational movement to initiate a lancing process.

Abstract: Non-fluidized tissue expanders, tissue expander systems, and methods of expanding tissue are disclosed. The tissue expanders, systems, methods of the present invention incorporate an expandable encapsulated body mass implantable within the patient and operative to selectively expand to promote growth of an enlarged area of skin and subcutaneous tissue. Such tissue expansion is accomplished utilizing internal one or more distraction mechanisms disposed within the tissue expanders that are operative to expand by mechanical or electromechanical means. The present invention omits any type of inflatable body requiring the injection of fluids to effectuate expansion of the tissue expander.

Abstract: Device for implanting occlusion spirals in body cavities or blood vessels with a catheter, an occlusion spiral that can be moved within the catheter in the longitudinal direction, and at least one securing means attached in the occlusion spiral, structured as a flexible lengthwise element, which passes through the length of the occlusion spiral at least in a partial region, which is characterized in that the securing means contains a material with shape memory properties.

Abstract: A surgical stapling apparatus includes a staple anvil and a staple cartridge having a working surface, one or more rows of individual staple slots formed in the working surface, a knife track formed along a length of the working surface, and a plurality of surgical staples individually disposed within the individual staple slots. The apparatus further includes an actuation sled having a knife and being configured and adapted to movably position the knife axially within the knife track. The apparatus also includes a wound closure material applicator assembly having a needle secured to the knife to dispense a quantity of wound closure material along a length of the knife track as the actuation sled and knife are moved therealong.

Abstract: A skin-contacting heatable dressing including a pressure-sensitive adhesive layer having a first skin-contacting side and a second side; heat generating conductive carbon fibers contained within the skin-contacting pressure sensitive adhesive layer; and a source of electrical energy electrically connected to the carbon fibers. In one embodiment, the pressure-sensitive adhesive layer may include a transdermally absorbable medicament. In one embodiment, the dressing may include a backing layer. In one embodiment, the source of electrical energy may be a thin film battery, which may supplement or take the place of the backing layer.

Abstract: A device and method for treating pathological narrowing of fluid-carrying conduits of the human body (such as blood vessels) in an area of a bifurcation is disclosed. In particular, a stent system comprising a pair of dissimilar stents, one of which is particularly suited for treating a widened portion of a blood vessel immediately proximal to a bifurcation. A stent delivery system including a handpiece adapted to selectively deliver the stents is also disclosed.

Abstract: A fastening for fixing an exposed stent (2) to a graft material (1). At least two spaced apart fastenings (7, 8) are used, each fastening has at least one turn and preferably two turns of an elongate flexible fiber through the graft material and around a portion of the stent. Each fastening has a knot (9) which is at least two thumb knots and preferably four thumb knots.

Abstract: A stent for use in animals including humans is disclosed which includes unprotected and protected regions, each protected regions including a bioactive or biopenetrating agent containing therein where the protected regions are protected by the unprotected regions when the stent is in its undeployed state which has a smaller cross-sectional dimension than the stent in its deployed state. And when the stent is in its deployed state the bioactive or biopenetrating agent(s) are brought into direct and intimate contact with a tissue or interior of a blood vessel of an animal including a human.