Abstract: A catheter connector for a subcutaneously placed catheter. The catheter connector can be configured for a single lumen catheter or a multiple lumen catheter. The connector facilitates precise positioning of both distal and proximal ends of a catheter, providing enhanced functionability and patient comfort.

Abstract: An annular mesh expandable radially from a compact diameter to a radially-expanded deployed disposition in which the mesh is capable of sustaining a radially outwardly directed resistive force even when flexing its longitudinal axis out of a straight line, the mesh being composed of stenting struts, the stenting struts being arranged in a plurality of zig-zag strings around the circumference of the lumen, with occasional connector struts joining adjacent strings to create a closed circumference unit cell between two such connector struts and two adjacent connected strings there being a plurality of such unit cells arranged in sequence around the circumference between said two adjacent strings; and characterised in that there is a non-constant increment of strut length, serving to displace along the longitudinal axis each unit cell relative to the circumferentially next adjacent unit cell.

Abstract: A stent-graft, including a generally tubular vascular graft of biocompatible material, and a plurality of bio-resorbable discrete annular members spaced apart along a longitudinal axis of the vascular graft and attached thereto.

Abstract: An implantable prosthesis, including a generally tubular substrate and a continuous shape memory member disposed over the outer surface of the substrate. The shape memory member may include a series of zig-zag struts alternating between a first strut with a first length and a second strut with a second length different from the first length. A graft member may be positioned over the substrate and shape memory member.

Abstract: In one embodiment, an introducer includes a handle, a needle extending from the handle, the needle having a distal end and defining an inner lumen, the needle further having an opening that provides access to the inner lumen, a snare having an implant coupling element, the snare being positioned within the inner lumen of the needle, the snare being extendable from the needle opening to an extended position in which the implant coupling element is positioned outside of the inner lumen and retractable to a retracted position in which at least a portion of the implant coupling element is positioned within the inner lumen, and a snare extension mechanism provided on the handle, the extension mechanism being configured to alternately extend and retract the snare.

Abstract: A catheter connector system for a subcutaneously placed catheter. The catheter connector system permits proximal trimming of the placed catheter, which is a procedure that provides numerous advantages over traditional methods of trimming catheter distal ends prior to implantation. The catheter connector system can be configured for a single lumen catheter or a multiple lumen catheter. The catheter connector system facilitates precise positioning of both distal and proximal ends of a catheter, providing enhanced functionability and patient comfort.

Abstract: A covered radially-expansible stent (50), capable of being advanced along a bodily lumen, and capable of performing as an arteriovenous shunt, and with a covering that stops short of one end of the stent at a line that slants to the longitudinal axis of the stent at an angle intermediate between 0° and 90°.

Abstract: A coaxial cannula for extracting samples from tissue having a biopsy needle unit provided with a space for sample extraction and a sample separation unit that coaxially encompasses the biopsy needle on an external wall and that is longitudinally movable. The coaxial cannula includes a sealing element that is arranged on the proximal end thereof and closes the space between the internal wall of the coaxial cannula and the external wall of the sample separation unit. The sealing element opens an air outlet when the biopsy needle unit is inserted, and prevents air intake when the biopsy needle unit is positioned and vacuum is produced in the internal chamber of the biopsy needle.

Abstract: Preferred embodiments of an implantable medical device with a high degree of flexibility is shown and described. One aspect includes an implantable stent having an intermediate portion with a helical winding and first and second end portions. The implantable stent further includes a coupling portion with a helical winding, and bridges joining struts of defining the helical windings. The stent also includes a paddle providing a bridge joining the ends or the helical windings. Another aspect relates to a radially self-expansible stent with a plurality of radiopaque markers attached to it. The markers are shaped and located at the stent end such that the compressive stress exerted on the end annulus of the stent during release of the stent is shared between the markers and the inflection zones that do not carry a marker.

Abstract: A substantially flexible implant holder for holding a substantially tubular implant structure during fatigue testing of the implant structure, the implant holder having a substantially elongate cavity for occupation by the tubular implant structure and a cavity-surrounding part which extends from at least a first longitudinal end of the cavity to at least a second longitudinal end of the cavity, the cavity-surrounding part having a stiffness which gradually changes from a relatively high stiffness adjacent each of the longitudinal ends of the cavity to a relatively low stiffness adjacent a middle portion which is situated between the two longitudinal ends of the cavity.

Abstract: A medical retrieval device may include an elongated member having first and second end portions and a middle portion, The elongated member may be configured such that the first and second end portions are proximal one another and extend substantially parallel to one another along a longitudinal axis The middle portion may have an unconstrained basket configuration A first sheath may be configured to receive at least a portion of the first end portion, and a second sheath may be configured to receive at least a portion of the second end portion At least one of the first and second sheaths may be movable relative to the middle portion so as to constrain the middle portion in an elongated configuration.

Abstract: A valved sheath introducer for venous cannulation, including a valve, sheath, handle and cap. The valve is configured to permit safe introduction and removal of medical instruments through the sheath introducer. The valve may have one or more anchoring members and a thickened central portion through which a slit is formed. The central portion may have one or more concave surfaces and the slit can be angled with respect to the top surface of the valve. The cap is attached to the handle, compressing a portion of the valve therebetween.

Abstract: Described herein are coatings containing water-soluble oligodynamic metal salts that are formulated and applied from hydrophobic solvents. In particular, articles of manufacture comprising polymer coatings containing oligodynamic metal salts can include hydrophobic polymer coatings made from water-reactive monomers and hydrophilic polymers compounded in hydrophobic solvents which contain a small amount of water that aids in the solubilization and suspension of the oligodynamic metal salts. Methods of preparing these antimicrobial polymer coatings, and methods of coating a substrate to produce an article of manufacture having an antimicrobial polymer coating are also described.

Abstract: An implant for repairing pelvic floor disorders, such as urinary incontinence or prolapse, by lifting the prolapsed tissue or organ into a more anatomically correct position is provided. The prosthesis is shaped with a central support section and one or more lateral anchoring sections or arms extending outwardly from the central section. The support section lifts the prolapsed organ to a more anatomically correct position, whereas the anchoring secton(s) are positioned through soft tissue away from the organ being supported to hold the implant in place by allowing tissue ingrowth into the anchoring sections. The implant may be formed of both synthetic and more natural materials.

Abstract: A blood filter delivery system for delivering a blood filter into a vein includes a push rod for pushing the blood filter through and out of a catheter, the push rod having a filter positioning assembly on one end. The filter positioning assembly includes positioner members, which retain anchor members of the filter. The filter positioning assembly can position the end of the delivery catheter near the blood vessel centerline before releasing the filter's anchor members, thereby helping to align the blood filter along the centerline of the blood vessel.

Abstract: A system and method providing a catheter assembly for engaging a stenosis. The assembly includes a catheter defining a first lumen and a second lumen spaced apart and disposed about a longitudinal axis. The catheter includes an opening in communication with the first lumen to define a flow path having an angle incident to the longitudinal axis. A first marker; and a second marker disposed on the catheter are spaced equidistantly from the opening. The assembly includes a balloon having a first end and a second end each sealed about the catheter and equidistantly from the opening to define a holding volume therebetween. The opening is disposed within the holding volume thereby placing the first lumen in sealed fluid communication with the holding volume. In a preferred embodiment, the catheter assembly includes a stent disposed about the balloon, and the balloon is configured to engage the stent with a stenosis.

Abstract: A catheter delivery device for a self-expanding stent is described. The delivery device includes a distal catheter component and a distal sheath that releases the stent by moving proximally relative to the distal catheter component and the stent. A proximal catheter shaft including a tube and a pull wire within a lumen of the tube may be provided, the pull wire being attached to the distal sheath such that pulling the pull wire proximally relative to the tube pulls the distal sheath proximally to release the stent progressively. A casing tube may be provided to surround the catheter shaft, the casing tube having a distal end that receives telescopically a proximal end of the distal sheath.

Abstract: A method for forming a self-expanding stent-graft, including coupling a shape memory member to a polymer cladding to form a polymer clad member, winding a length of the polymer clad member about a mandrel so that adjacent windings include regions of polymer cladding that overlap, heating the wound polymer clad member to join and seal the overlapping regions to one another, manipulating the stent-graft from a first diameter to a second diameter smaller than the first diameter, and loading the stent-graft into a restraining sheath, wherein the restraining sheath prevents the stent-graft from reverting to the first diameter.

Abstract: A surgical irrigation system comprises a reusable console and a disposable pump unit. The disposable pump unit includes a pump/motor module which includes a pump and a motor for driving the pump. The module is adapted to be mechanically supported within a seat in the console. The console produces a direct voltage at a pair of terminals within the seat. When the pump/motor is placed within the seat, the console terminals are connected to contacts on the module to provide a source of direct voltage for the pump motor. In the preferred embodiment, the disposable unit includes a handpiece and an irrigation valve. A flow sensing device within the outlet tube if the pump/motor module is actuated when the valve is open to turn the motor on and drive the pump. When the valve is closed, the flow sensing device turns the motor off.

Abstract: A helical stent having bioresorbable 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. A method of making the helical stent includes forming a tube with a section made of a bioresorbable material prior to forming the stent.