Abstract: An implantable medical device including an expandable stent with an amorphous fluoropolymer coating, and methods of coating the stent. The amorphous fluoropolymer coating may be optically transparent and resistant to chemical corrosion.

Abstract: A method of making a multi-lumen catheter includes forming a catheter body including a first lumen and a second lumen, and forming a catheter tip having a first channel terminating distally in a first opening on a first side of the catheter tip, and a second channel terminating distally in a second opening on a second side of the catheter tip opposite of the first side. The first and second openings of the catheter tip extend through an outer wall of the catheter tip to a dividing section. The catheter tip is affixed to the catheter body such that the first channel is aligned with the first lumen and the second channel is aligned with the second lumen.

Abstract: A delivery system for deploying a medical device, such as a stent, at increasing deployment speed is described. The system comprises a catheter comprising a catheter shaft, a retractable sheath slidably mounted on the catheter shaft, and the device in a compressed state sandwiched between the shaft and sheath. A control handle is included with a housing and knobs for a user to apply a rotary or other force to retract the sheath. The sheath is attached to a slider that is mounted on a slide rod and attached to a drive belt. A take up pulley is provided in the housing and connected to the belt input knob, so that the pulley turns when the knob is turned. The belt is attached to the pulley so that the drive is wound onto the rotating pulley. As the belt winds upon the pulley, the overall outside diameter of the pulley increases, thereby increasing the deployment speed.

Abstract: A catheter assembly including a coaxial catheter and insert, and method of making. The catheter assembly includes a coaxial catheter, an insert, and a hub. The coaxial catheter includes an inner lumen and an outer lumen. The insert includes first and second passageways, the first passageway defined from a first opening on a distal end of the insert to a second opening on a proximal end of the insert, the second passageway branching from the first passageway to a third opening. A portion of the insert distal end is received in a proximal opening of the outer lumen, and a proximal section of the inner lumen extends through the first passageway. The hub is molded over the insert and a proximal section of the outer lumen.

Abstract: A catheter connector system for a subcutaneously placed catheter and method of attaching a catheter to extracorporeal medical equipment. The catheter connector system and method enables proximal trimming of the placed catheter and facilitates precise positioning of both distal and proximal ends of a catheter. The method includes sliding a boot and dilator combination over a portion of a catheter extending from a venipuncture site until a distal end of the boot is positioned in the venipuncture site, removing the dilator from the boot, and trimming a portion of the catheter extending from a proximal end of the boot. A bifurcation assembly may be attached to the proximal end of the boot following trimming of the catheter.

Abstract: A helical stent having bio-resorbable connecting members connecting sections of the stent. The connecting members provide various spring rates or spring constants to the stent, and permit a change in the flexibility of the stent subsequent to implantation while maintaining the unitary design of the stent.

Abstract: A catheter connection system and a method of connecting the catheter connection system to a catheter. The catheter connection system includes a hub assembly and a collar. The hub assembly includes a cannula extending from a distal end thereof, and a collet defining an inner surface spaced apart from the cannula to permit passage of a catheter wall between the body and the cannula. The collet includes a proximal barb on an outer surface and the collar includes an attachment barb on an inner surface, engagement of the respective barbs acting to provide a permanent connection between the collar on the collet, while permitting free rotation of the collar about the collet.

Abstract: A power injection catheter for high flow rate delivery of fluids. The power injection catheter may include a pressure relief mechanism for preventing overpressurizing within the lumen of the catheter. The pressure relief mechanism may be configured to prevent sudden pressure build-up inside the catheter lumen by absorbing, buffering or releasing pressure inside the lumen during pressure spikes. The power injection catheter may also take the form of a multi-lumen catheter capable of simultaneous infusions of a single fluid through two or more of the lumens in the catheter.

Abstract: A vascular filter guide wire including a collapsible filter that deploys radially in response to axial movement of a core wire relative to a shaft to trap particulate matter arising from treatment of a lesion.

Abstract: Multi-functional urine collection devices, embodiments of which can include a self-expanding container having a receptacle for receiving urine from the tubing, a pump for moving urine through the tubing and into a receptacle, extendable tubing that may be shortened and/or lengthened, and/or one or more meters for monitoring, measuring, transmitting or storing a characteristic from the urine.

Abstract: The present invention provides tissue capture devices configured to hold tissue in a distorted configuration. The devices may hold precaptured tissue in a distorted configuration or it may change their shape to cause the tissue to become deformed. Some embodiments of the device alter the configuration in areas that remain external to the tissue, while other embodiments change their configuration in areas that are implanted in the tissue. Other embodiments may be mechanically altered to hold the tissue in a distorted shape.

Abstract: An endoscope tool coupling that facilitates the placement and positioning of a surgical tool within an endoscope. The tool coupling may be configured to accommodate differences in lengths between the surgical tool and the endoscope, which may allow a user to precisely position and maintain the distal end of a surgical tool in a desired location relative to the distal end of the endoscope despite differences and variations in lengths. The tool coupling may have an adjustable configuration to accommodate variations in tool and/or endoscope lengths. The tool coupling employ an arrangement that allows a user to easily increase or decrease the length of the coupling, such as by using a telescoping arrangement. A locking arrangement or mechanism may be provided to secure the coupling in a selected configuration for maintaining the surgical tool in a desired location relative to the endoscope.

Abstract: A probe cap for use with an ultrasound probe including a head portion and an acoustic surface is disclosed. In one embodiment, the probe cap includes a body that defines a cavity sized for releasably receiving the head portion of the probe therein. The probe cap body further defines a hole that is proximate the acoustic surface of the head portion. A compliant spacer component is disposed in the hole. The spacer component can include a hydrogel and provides an acoustic path between the acoustic surface and a tissue surface of a patient. The spacer component includes a skin contact surface that defines a concavity and is deformable against the tissue surface.

Abstract: Methods of selecting operating parameter values for tissue ablation procedures are disclosed. Energy supply parameters may be selected based on inputs such as fluid flow rate, impedance, and the distance from an ablation electrode surface to a target tissue surface. The distance to place an ablation electrode surface from a target tissue surface may be selected based on various operating parameter values and/or operating condition values. Operating curves, lookup tables, or processors may be used to select operating parameter values.

Abstract: The present application discusses techniques and structures that incorporate calcium salts in the luminal surface of grafts. In an embodiment, a graft, stent-graft or TIPS may incorporate bio-compatible calcium salt, which is essentially non-osteoinductive in nature, on the surfaces of the implantable device.

Abstract: A surgical fastener system includes a plurality of fasteners having a throughbore with a non-circular cross section portion. The fasteners may engage with a splined mandrel that passes through the throughbore of the fasteners and rotates the fasteners relative to the mandrel to move at least one of the fasteners along the mandrel, e.g., along the mandrel's longitudinal axis. A distal end of the mandrel may be inserted into a material, such as a tissue, prosthetic or other, and a fastener may be deployed from the distal end of the mandrel while the distal end is positioned in the material.

Abstract: An implantable port with an integral attachment mechanism. The implantable port includes one or more suture needles enclosed within a port body, the suture needle(s) coupled to a movable member such that movement of the movable member results in movement of the suture needle(s) out of the port body and into the tissue of a body into which it is implanted. The movable member can be a cam or tensioning member that rotates about a central port axis. The movable member can be coupled to a gear to permit movement of the movable member following implantation of the port within a subcutaneous pocket.

Abstract: Lesion size or volume prediction shortly after the onset of an ablation procedure can inform or control the ablation procedure. The prediction and/or control is made without regard to an actual detected temperature in the vicinity of the ablation electrodes. As a consequence, the system has utility with irrigated catheter constructions and other situations in which local irrigation in the vicinity of an ablation site would otherwise interfere with a prediction or control scheme that solely relies upon temperature measurements.

Abstract: Systems and methods for marking a body cavity. In one embodiment, a system includes means for inspecting a body cavity, and means for visibly marking the body cavity so as to convey visual information regarding the body cavity. In one embodiment, a method includes inspecting a body cavity and marking the body cavity with a marking material to provide a visual indication regarding the cavity. In one embodiment, a marking material for marking a body cavity includes a radiopaque contrast agent that is viewable through fluoroscopy and a colored dye that is viewable using an internal viewing device.

Abstract: There is disclosed herein a method of loading a self-expanding stent (10) into a delivery sheath (12) that is by itself strong enough to preserve the stent in a radially compressed pre-deployment configuration, comprising the steps of: (i) compressing the stent (10) to a relatively small diameter; (ii) providing a loading sheath (18) with an inner diameter d1; (iii) with the stent (10) exhibiting an outside diameter of d2, where d2<d1, providing relative translational movement between the stent (10) and the loading sheath (18), whereby the stent is accommodated within the lumen of the loading sheath (18); (iv) advancing the loading sheath (18), containing the stent (10), into the lumen (16) of the delivery sheath (12); and {v} deploying the stent into the lumen (16) of the delivery sheath (12), by withdrawing the loading sheath (18) while restraining the stent (10) from axial movement out of the lumen (16) of the delivery sheath (12).