Devices for delivering and deploying a prosthesis are disclosed and comprise a sheath, a prosthesis disposed within a distal end portion of the sheath, and a wire having a first end coupled to the prosthesis and a second end coupled to the sheath. A body portion of the wire comprises a slack in the wire, and the sheath, prosthesis, and wire are configured so that a proximal movement of the sheath relative to the prosthesis reduces the slack in the wire, and a subsequent proximal movement of the sheath relative to the prosthesis decouples the wire from the prosthesis. Additional devices, systems, and methods are disclosed.

A bile duct tube has a first portion which has a first end portion of the bile duct tube and is formed to have a diameter that allows insertion into a bile duct, a second portion which has a second end portion of the bile duct tube and is formed to have a diameter that allows insertion into an intestinal tract, and a first expansion member placed at the first portion. The first expansion member expands in a radial direction of the bile duct tube when a gas or liquid is injected into a void inside the first expansion member.

A bile duct stent and a method of manufacturing the same are disclosed. The bile duct stent having a backflow preventing means according to an embodiment of the present invention includes: a cylindrical body having a mesh structure formed by zigzagging metal wires of a shape memory alloy on a plurality of pins each disposed in a circumferential direction X and a longitudinal direction Y of a cylindrical jig; a film portion coated on cells of the metal wires of the mesh structure; and a backflow-preventing pattern film in which a hole is formed in the film portion of each cell formed at an outlet end of the cylindrical body and threads (Lasso) fixed by zigzagging to the cells of the metal wires in the circumferential direction by passing through any one hole (h) cross the outlet end one time or more to form a network structure.

The invention discloses a Zn—Ga series alloy and a preparation method and application thereof, belonging to the technical field of medical alloys. The Zn—Ga series alloy includes Zn and Ga, and Ga accounts for 0-30 wt % but not including 0. The preparation method is to mix Zn and Ga or Zn, Ga and trace elements, then to obtain a Zn—Ga series alloy by coating paint after smelting or sintering. The mechanical properties of the prepared Zn—Ga series alloy meet the requirements of the strength and toughness of medical implant materials, and it can be degraded in vivo. It has the dual characteristics of biological corrosion degradation and suitable corrosion rate to provide long-term effective mechanical support.

The present invention relates to a stent delivery device having: a first support rod into which a first movable body is inserted; a fixed magnet; and a second support rod into which a second movable body is inserted, wherein a first driving magnet included in the first movable body and a second driving magnet included in the second movable body rotate relative to each other by means of the control of an external magnetic field at a predetermined angle around an axis in a first direction with respect to the fixed magnet, thereby separating a first coupling piece and a second coupling piece from a first coupling groove and a second coupling groove and enabling a stent to unfold.

Provided is a stent which is not easily displaced from a dwell site in a biological lumen and which has an excellent ability to follow a biological lumen. This stent (bile duct stent 100) is to dwell inside a biological lumen (bile duct B) and is provided with a stent main body section (110) having a cylindrical shape. The stent main body section is configured to be capable of expanding and contracting in the radial direction that is approximately orthogonal to an axial direction, has a relatively large expanding force in one portion (center portion) corresponding to the predetermined position at the indwelling site in the biological lumen, and a relatively small expanding force at other portions (both end portions) which have different positions in the axial direction from that of the one portion.

Medical devices and methods for making and using the same. An example medical device may include an elongate tubular member, an endosurgery stent disposed on the outer surface of the tubular member, a push tube slidably disposed along the outer surface of the tubular member, and a push member slidably disposed in a lumen formed in the tubular member. The push member may be coupled to the push tube.

A stent includes a tubular body possessing a plurality of gaps. The tubular body includes a plurality of circumferentially extending linear struts. The stent includes a plurality of links connecting the linear struts. At least one of the links has first and second connection portions. The first connection portion is integrally formed with one strut, and the second connection portion is integrally formed with an adjacent strut. The stent includes a biodegradable material between the first connection portion and the second connection portion to connect the first and second connection portions to each other. The biodegradable material restrains the one strut and the adjacent strut from moving to their original shapes. The first and second connection portions move relative to one another in a separation direction when a connection by the biodegradable material is released so that the original shapes of the struts are restored.

This document provides implantable intraluminal stent graft medical devices. In some embodiments, the stent graft devices provided herein are implantable in bodily conduits that have side branches, and the stent graft devices are operable to allow the flow of fluids between the conduit and the side branches. In some embodiments, the walls of the stent graft devices provided herein include compliant channels which allow for fluid communication between the interior and the exterior of the stent graft devices. In some embodiments, the compliant channels are configured to inhibit or reduce tissue ingrowth, tissue bridging, and/or endothelialization.

In a method for inserting an endoscopic device, a guide wire is punctured into a subject from outside the body. A tip portion of the wire is inserted into a first hollow organ. A tip-side portion of the inserted wire is projected into a lumen of a second hollow organ that communicates with the first via an opening, from the opening. An endoscopic device is inserted through a flexible endoscope and pushed into the second hollow organ. A tip portion of the device is locked onto the tip-side portion of the wire projecting into the second hollow organ. A portion of the wire outside the body of the subject is held and is tugged outside of the body. The tip portion of the device is thus pulled into the first hollow organ from the second, via the opening. Therefore, the endoscopic device can be led to the first hollow organ.