Abstract: A delivery device for implanting a prosthetic heart valve. The device includes an inner shaft assembly, an outer sheath and a connector assembly. The inner shaft assembly defines a guide wire lumen. The outer sheath is slidably received over the inner shaft assembly, and forms an exit port proximate a distal end thereof. The connector assembly establishes a guide wire passageway between the guide wire lumen and the exit port. The connector assembly is configured to permit sliding movement of the outer sheath relative to the inner shaft assembly when deploying the prosthetic heart valve. The connector assembly can include first and second tubes that are slidable relative to one another in facilitating movement of the outer sheath relative to the inner shaft assembly.

Abstract: An occlusion device comprises a distal end, a proximal end and an elastic braided body which is provided between the proximal end and the distal end and made of wires. The elastic braided body is composed of a multi-stage braided net, which comprises at least a first-stage braided net that is closest to the distal end and made of a plurality of first-stage wires, and a second-stage braided net which is braided by a plurality of first-stage wires and second-stage wires all together. The minimum cross-section area of the first-stage braided net after being compressed toward the direction perpendicular to an axis of the elastic braided body is less than the minimum cross-section area of any other-stage braided net after being compressed toward the axis. A method for manufacturing the occlusion device is also provided.

Abstract: The apparatus includes a ureter occlusion apparatus, which comprises, in combination: at least one longitudinally extending plug body (26) of flexible, physiologically acceptable material which obstructs the passage of all particulate matter great than 5 microns in diameter, is laterally compressible to a compressed diameter of not more that 2 millimeters and is laterally expandable in the presence of liquid to an external diameter of at least 1.

Abstract: A micro-catheter delivery system that includes radio-opaque marker bands optimized for the purpose of length reference to assist the operating physician to estimate the length of a tortuous lesion and to anticipate foreshortening of stents with multiple sizes. The radio-opaque maker bands are positioned at the distal end of a stent delivery catheter at a certain intervals acts like a ruler. In another embodiment, a stent delivery system includes a stent delivery wire with one or more radio-opaque markers distanced from the stent distal end for indicating the non-restrained length of the stent when discharged from the delivery catheter.

Abstract: A ligator system for applying an expanded ligator ring to an anatomical region of a living being to be ligatured by the ring in its relaxed state, which comprises a ligator with a holding tube, which receives inside it the anatomical region to be ligatured in each case and with its outer surface keeps a number of ligator rings arranged one behind the other expanded, wherein the ligator system comprises at least one intermediate ring, which is arranged on the holding tube between two ligator rings and keeps the two ligator rings at a distance from one another in the direction of the longitudinal axis of the holding tube.

Abstract: An endoscopic treatment instrument includes a pressing tube with an insertion lumen; a clip main body that has a first arm being inserted into the insertion lumen; a second arm fixed to the pressing tube; and an operation wire connected to the clip main body to move it with respect to the pressing tube, wherein the first arm approaches the second arm while being moved to a proximal end side of the pressing tube, in an initial state before the clip main body is pulled by the operation wire, a position of a distal end of the first arm is more distal than a position of a distal end of the second arm, and the distal end of the first arm is approaches the distal end portion of the second arm when the clip main body is pulled to the proximal end side of the pressing tube.

Abstract: A pre-fabricated tourniquet that is easy to apply, that ensures consistent and even circumferential pressure, that is light weight, that provides standard life saving operation, and that can be utilized in any setting or situation, and related methods are provided. Mechanically constricting tourniquet apparatus and related methods are provided that are comprised of a tourniquet body, a carriage, a torsion bar, a receiver and a slider. The tourniquet is long enough to encircle a human limb, for example, an arm or leg.

Abstract: A tattooing device is designed for ingraining a design on the skin. The tattooing device includes an electric drive motor with a rotatable motor pin. The motor pin defines an axis of rotation. A rotatable actuator cam is operatively connected to the motor pin, and comprises a cam post axially offset from the motor pin and the axis of rotation. An elongated drive shaft is operatively connected to the cam post, such that rotation of the actuator cam effects simultaneous substantially linear reciprocating movement of the drive shaft. A needle assembly is operatively connected to the drive shaft, and adapted for carrying a pointed tattooing needle for penetrating the skin.

Abstract: The disclosure provides an IVC filter device and method to filter. The device has a first bar and a first slider. The first slider has a first bore formed therethrough slidably disposed on the first bar. The device further comprises a second bar and a second slider. The second slider has a second bore formed therethrough and slidably disposed on the second bar. The device further has a first set of filter struts with a first filter strut being arcuate and attached to the first bar. The first filter strut may extend to the second slider. In addition, a second set of filter struts has a second filter strut being arcuate and attached to the second bar, extending to the first slider. When disposed in the vena cava, the device may receive a force through its filter struts and slide one of the sliders to accommodate the force.

Abstract: A clot retrieval system includes a delivery catheter defining a lumen and having proximal and distal ends. An elongate shaft has proximal and distal ends and is configured for receipt within the delivery catheter. An inverted sleeve has a closed end attached to a distal segment of the elongate shaft and an open end. An outer section of the inverted sleeve that includes the open end is folded over onto an inner section of the inverted sleeve that includes the closed end at a rolling fold. An expansion device is supported on the elongate shaft at an axial location proximally spaced from the closed end and aligned with or distally spaced from the open end. The expansion device is configured for radially expanding the open end of the inverted sleeve.

Abstract: Apparatus, systems, and methods are provided for percutaneous transcatheter delivery and fixation of annuloplasty rings to heart valves. An annuloplasty ring includes an outer tube, an inner body member, and an anchor deployment system. The outer tube includes a plurality of windows and has an axis along its length. The internal body member includes a plurality of anchors formed perpendicular to the axis. The anchor deployment system selectively rotates the internal body member with respect to the axis of the outer tube. The rotation deploys the plurality of anchors through the plurality of windows.

Abstract: The present invention relates to a Left atrial appendage occluder comprising an elastic closure disc. The left atrial appendage occluder also comprises an elastic fixing frame connected with the closure disc and located on one side of the closure disc. The fixing frame comprises a central end connected with the closure disc and a plurality of interconnected and bent struts, wherein at least one anchor is set near the end of at least one strut with the anchor pointing toward the closure disc. The left atrial appendage occluder has a stable structure, a good positioning and sealing effect on the cavity wall in the left atrial appendage, and it is easy to position repeatedly; it can also be recycled before separating from a conveyor. When in surgical operation, the left atrial appendage occluder can select the position area based on the actual shape and size of the patient's left atrial appendage, so the surgical risk is lowered.

Abstract: A selective aortic balloon device includes a catheter comprising an open distal end configured to be inserted into a body cavity or vessel, and a plurality of adjustable port regions with inflatable balloons between adjacent adjustable port regions. Each adjustable port region is configured to move between a closed position and an open position to selectively allow fluid flow to enter the catheter through the open distal end and to exit the catheter through one or more of the plurality of adjustable port regions depending on an inflation pattern of the inflatable balloons.

Abstract: A collapsible device, such as an annuloplasty ring or prosthetic heart valve, is configured to be collapsed prior to being introduced into a patient via minimally-invasive access points such as port holes or intercostal incisions. A holder is configured to hold the collapsible device, and to selectively collapse the device for introduction into the patient and then re-enlarge the device at the desired deployment site. Collapsible devices include devices that can hingedly fold about hinge lines, and devices that can elongate to form substantially spiral forms with reduced diameters.

Abstract: A catheter system with a proximal end and a distal end element at the proximal end to actuate a device at the distal end of the system, and an actuator element (32) that runs the length of the system, from the actuator element to the device and actuates the device by transmitting a physical force from the proximal end to the distal end and characterized by a pre-tensioner (40) near the distal end of the system, that can be set in a pre-tensioning disposition prior to actuation of the device, the pre-tensioner thereby reducing the magnitude of the physical force that must be transmitted from the proximal end when actuation of the device is required.

Abstract: An abdominal aortic tourniquet having one-piece member for the bladder and cover portions and whose bladder has a triangular cross-sectional shape when inflated that significantly increases the amount of point pressure such that the intended artery is properly occluded. The one-piece bladder/cover design provides for a reduction in cost of materials and provides for a more compact piece as compared to prior designs. The abdominal aortic tourniquet uses a single piece of weldable and gas impermeable fabric that is configured in a novel manner to create a three-dimensional, pneumatic piston while also serving as storage/transport cover, attachment structure, and major component of the belt member.

Abstract: An implant delivery system including a catheter having a delivery lumen; a pusher member slidably disposed in the catheter delivery lumen; a retaining member coupled to a distal end portion of the pusher member, the retaining member configured to retain an expandable implant in a collapsed configuration on the pusher member for delivery of the implant through the catheter delivery lumen; and an expandable actuator coupled to the distal end portion of the pusher member and operatively associated with the retaining member, wherein expansion of the actuator causes the retaining member to disengage from an implant carried on the pusher member, to thereby allow the implant to expand from the collapsed configuration.

Abstract: A hydrodynamic catheter includes a catheter body with a catheter lumen and an infusion tube extending within the catheter body, the infusion tube configured for coupling with a fluid source near the catheter proximal portion. An inflow orifice and an outflow orifice are positioned at locations along a catheter body perimeter. A fluid jet emanator is in fluid communication with the infusion tube, where the fluid jet emanator includes one or more jet orifices configured to direct one or more fluid jets through the catheter lumen from near the inflow orifice toward the outflow orifice. A pivot cylinder located along the catheter body perimeter is positioned distal relative to one or more of the fluid jet emanator, the inflow orifice, or the outflow orifice.

Abstract: Described herein is an apparatus for treatment of an ocular condition of a patient, comprising a hollow elongate member sized to penetrate an eye of the patient and including a body portion, a distal tip, and a lumen extending though both. The body portion includes a proximal end, a distal end, and a first diameter, and defines longitudinal axis. The distal tip extends from the distal end of the body portion and is arranged to treat tissue in the eye. The distal tip includes an inner tube defining the lumen in part, an outer sheath surrounding the inner tube, and a second diameter. The distal tip is configured to transition between a first rigid orientation and a second less rigid orientation.

Abstract: A dual-purpose surgical bougie is disclosed for vertical sleeve gastrectomy (VSG) procedures, and other related operations, that can serve the purpose of both operating as a guide or dilator for stapling and resecting a stomach and also securing, containing, and trans-orally extracting the resected stomach, thereby promoting faster patient recovery, minimizing and reducing the size and number of incisions, and further minimizing VSG procedure related complications, among other advantages. In one aspect of the disclosure described herein, the dual-purpose medical device can include a surgical bougie having a distal end and a proximal end, wherein the bougie can be made of at least one of rubber, silicone, plastic, and metal. In addition, the bougie can include a channel or passage disposed within its central axis extending from its distal end to the proximal end, and a securement member coupled to the bougie.