Abstract: A device for performing a remote ischemic conditioning treatment. The device includes an inflatable cuff and a cartridge which is a source of gas for inflating the cuff. A first valve controls the flow of gas from the cartridge to the cuff so as to maintain a predetermined pressure in the cuff during an ischemic period. A second valve allows gas to escape from the cuff during a reperfusion period of the remote ischemic conditioning treatment. A controller which may be battery-powered is used to control the opening and closing of the valves. The cartridge may contain a gas, or materials which, under certain conditions, react to produce a gas. The chemical reaction may be initiated by an electrical pulse or signal from the controller.

Abstract: Intraocular lens insertion apparatus includes a cylindrical body member configured to retain an intraocular lens, a fore-end opening provided for a tip of the body member, and a planate protrusion provided for a tip of the fore-end opening. Further, an end surface of the fore-end opening is an oblique surface which is oblique to a plane perpendicular to a central axis of the body member, and a fore-end area including a pair of lateral walls which are parallel to each other across the central axis is formed on a side of the tip of the fore-end opening.

Abstract: A device for moving an elongate member relative to an elongate body through which it extends, the device including a housing, a mover, and a pre-mover. The housing is connectable to the elongate body. The mover is associated with the housing and is connectable to the elongate member for moving the elongate member relative to the housing. The pre-mover is associated with the housing and is connectable to the elongate member for adjusting the elongate member in preparation for moving the elongate member with the mover.

Abstract: An inflation device includes a syringe body containing a bore. The bore holds a fluid that is used to inflate a separate device such as a dilation balloon. A plunger assembly slides within the syringe bore and contains a sealing member that forms a fluid tight seal with the syringe body. A shut-off valve is disposed within the distal end of the syringe body. The distal end of the syringe body has a fluid bypass channel fluidically coupled to the aperture of a connector. The shut-off valve has a spring-biased moveable piston with a bypass lumen contained therein, wherein the bypass lumen forms a fluid path between the bore and the fluid bypass channel when the pressure of the fluid is below a threshold value. The fluid path between the bore and the fluid bypass channel is interrupted when the pressure of the fluid is above the threshold value.

Abstract: Methods for assembling a stent delivery system are provided, as well as the stent delivery assemblies and devices formed by such methods. Also provided is a method for loading a stent into a delivery system.

Abstract: A clip for use during the loading of a prosthetic heart valve into a delivery device having an operating handle, a catheter assembly having a compartment for receiving the prosthetic heart valve, and an outer shaft joining the catheter assembly to the operating handle. The clip includes a first receiver coupleable to the operating handle of the delivery device and a second receiver coupleable to the outer shaft of the delivery device. The first and second receivers may be arranged orthogonally to one another so that in use the clip orients the catheter assembly substantially orthogonally to the operating handle.

Abstract: An endoscopic surgical clip applier is provided, wherein a distal end of the surgical clip applier is introduced to a target surgical site through a cannula having a fixed diameter lumen. The surgical clip applier comprises an endoscopic portion supported by and extending from a handle assembly, and a pair of jaws supported at a distal end of an outer tube, wherein the pair of jaws are movable between a fully open condition and approximated conditions. When the pair of jaws are in the fully open condition the pair of jaws extend radially beyond an outer diameter of the outer tube to a dimension greater than the fixed diameter of the lumen of the cannula; and when the pair of jaws are in at least one approximated condition the pair of jaws have a transverse dimension permitting passage through the lumen of the cannula.

Abstract: A braided stent having an integral retrieval and/or repositioning loop includes a plurality of wires having first and second ends interbraided in a braided pattern to form a tubular stent having opposed atraumatic first and second open ends with each open end having a circumference; wherein said first and second wires ends are disposed at said second stent open end and said wires are looped at said second stent open end so that none of the first or second wires ends are exposed at the circumference of second stent open end; wherein at least of two of said wires are formed into a repositioning and/or retrieval loop having an elongated portion circumferentially disposed at said first opposed open end; and wherein said reposition and/or retrieval loop comprises two sections which run adjacent to each other prior to crossing to permit grabbing of both sections simultaneously by a practitioner.

Abstract: A vessel access and closure device places a running suture in the wall of a blood vessel using a rotating helical suture needle that carries the suture along a helical path passing through the vessel wall, then reverses rotation to release a suture anchor attached to the distal end of the suture. A loose helical coil of suture is left behind as the helical suture needle withdraws. The device is withdrawn and replaced with a vessel dilator and an introducer sheath that opens up a larger access opening into the blood vessel and creates a pathway that passes though the helical coil of suture for introducing an interventional device into the blood vessel. After the interventional procedure is completed, the interventional device and the introducer sheath are withdrawn and the running suture is tightened and secured with a suture lock to close the access opening into the vessel.

Abstract: A router device is a intraluminal prosthesis which is used in the repair of aneurysms and other diseases of the aorta. The device also has applications in other vascular beds. The device incorporates an inflatable cuff or sequence of cuffs at one end for fixation and sealing. This cuff may be placed proximal to branch vessels of the aorta. Attached to the cuff is a tubular graft consisting of a generally cylindrical graft material. The graft material may contain one or more fenestrations, intended to align with branch vessels as they emerge from the parent vessel, the aorta in the preferred embodiment. The device features a deliberate taper of its diameter as the device crosses the area of branch vessels. This taper brings the diameter of the graft material to a lesser diameter than that of the parent vessel, leaving a deliberate and distinct space between the device and the wall of the vessel.

Abstract: A braided stent having an integral retrieval and/or repositioning loop includes a plurality of wires having first and second ends interbraided in a braided pattern to form a tubular stent having opposed atraumatic first and second open ends with each open end having a circumference; wherein said first and second wires ends are disposed at said second stent open end and said wires are looped at said second stent open end so that none of the first or second wires ends are exposed at the circumference of second stent open end; wherein at least of two of said wires are formed into a repositioning and/or retrieval loop having an elongated portion circumferentially disposed at said first opposed open end; and wherein said reposition and/or retrieval loop comprises two sections which run adjacent to each other prior to crossing to permit grabbing of both sections simultaneously by a practitioner.

Abstract: A surgical apparatus for guiding the movement of a surgical tool in relation to the surrounding anatomy of a patient includes a surgical tool having an articulation member. The apparatus also has an image capturing device, a monitor, a control member, and at least one marker on the surgical tool for determining an orientation and attitude of the surgical tool in relation to the visual image on the monitor. The image capturing device takes visual images of the articulating member. The monitor displays the visual images taken by the image capturing device. The control member operates and guides movement of the articulating member. The marker can be colors, symbols, letters, number, or in any combination thereof. An endoscope and a display may also be included.

Abstract: A method involves introducing a gathering part into a lumen in an ureteral access sheath in which is located calculus, wherein at least a part of the ureteral access sheath is located in an ureter in a living body. The gathering part is moved along the lumen in the ureteral access sheath in a forward direction toward the calculus, and then movement of the gathering part in the forward direction is stopped to position the gathering part adjacent the calculus so that the calculus is positioned between the distal end of the ureteral access sheath and the gathering part. The gathering part is expanded while the gathering part is positioned adjacent the calculus, and the calculus is then introduced into the gathering part.

Abstract: A dilation device including a dilation instrument which includes a distal radially expandable section which is coupled via an elongate shank to a handling section, and an expandable covering with a closed distal end and an open proximal end, for the expansion section of the dilation instrument. The covering has a shank section extending along the shank of the dilation instrument. The open proximal end of the covering is detachably coupled to the distal end of the handling section of the dilation instrument. Furthermore, the covering is disclosed per se, which consists of a mesh material and has a shank section, which is connected to a coupling sleeve at the open proximal end.

Abstract: Mechanical thrombectomy apparatuses that may be configured to prevent or reduce jamming (e.g., “anti-jamming” thrombectomy devices), grab clot, and/or macerate the thrombus, e.g., clot, being removed. These mechanical thrombectomy apparatuses may include a tractor comprising a flexible tube of material that inverts as it rolls over itself while being drawn into a catheter in a conveyor-like motion. In particular, described herein are mechanical thrombectomy apparatuses having tractors selectably extendable projections that may aid in grabbing and/or macerating a clot. Also described herein are seesawing tractors for mechanical thrombectomy apparatuses.

Abstract: Described herein is a suture for connecting a human or animal tissue comprising a suture strand, wherein at least two protrusions are provided on the suture strand, the protrusions are provided spaced apart from each other along the suture strand. Also described herein is a soft anchor, the soft anchor having a proximal end and a distal end in an insertion direction. At the proximal end and the distal end the soft anchor includes respectively at least one opening for a suture. The proximal end and the distal end of the soft anchor are connected with at least one, in particular two, connecting portions. The soft anchor has a first state, in which it is adapted to be inserted into a bore in the insertion direction, and a second state, in which it is locked in a bore. In the first state, the distal end and the proximal end defines the extension of the soft anchor in insertion direction.

Abstract: A surgical suturing device comprises an arced needle comprises a length of suture. An elongate shaft comprises a proximal end and a distal end. A needle driver is on the distal end of the elongate shaft operable to engage and rotate the needle in a circular path. The needle driver reciprocates between a drive stroke wherein the needle is rotated and a return stroke. A trigger is on the proximal end of the elongate shaft. A drive rod in the elongate shaft operably connects the trigger and the needle driver. Moving the trigger in a first direction actuates the needle driver through its drive stroke, and moving the trigger in a second direction actuates the needle driver through its return stroke. A spring is operably connected to the drive rod limiting a load transmitted through the drive rod. The spring may limit the load transmitted through the drive rod when the trigger is moved in a first direction.

Abstract: Surgical instruments are disclosed that are couplable to or have an end effector or a disposable loading unit with an end effector, and at least one micro-electromechanical system (MEMS) device operatively connected to the surgical instrument for at least one of sensing a condition, measuring a parameter and controlling the condition and/or parameter.

Abstract: A pusher guide wire and a delivery system can smoothly pass through the inside of even a curved blood vessel without causing excessive burden to a stent, a catheter, and the like. A pusher guide wire has a tubular member capable of moving in a radial direction relative to a core shaft of the pusher guide wire. When the pusher guide wire is used together with a stent in a delivery system, the tubular member makes contact with the stent in an appropriate manner when passing through the inside of a curved blood vessel. The stent may include a proximal end engagement portion provided at a proximal end of the stent. When the stent is placed so that the proximal end engagement portion engages with the pusher guide wire, the stent can be pulled back inside the catheter by pulling the pusher guide wire in the proximal direction.

Abstract: A balloon catheter can evenly transmit a pushing force applied to a reinforcing member to an outer shaft and an inner shaft by fixing the distal end of the reinforcing member to an adhesion part of the outer shaft and the inner shaft. In a balloon catheter, the distal end of a reinforcing member is fixed by an adhesion part of an outer shaft and an inner shaft. Thus, a pushing force of an operator is evenly transmitted to the outer shaft and the inner shaft from the distal end of the reinforcing member through the adhesion part, reducing a relative displacement of the outer shaft and the inner shaft. Moreover, the adhesion part can reduce the detachment of the distal end of the reinforcing member from the outer shaft or the inner shaft.