A stent graft configured to facilitate the placement of a secondary stent is provided and a method thereof. The stent graft can include an elongated body with a frame structure, a lumen, and apertures at both ends of the elongated body. The frame structure can be covered by a graft material. At least one station can be located in the graft material. The at least one station has a perimeter defined by a ring structure connected to the graft material and an aperture bounded by the perimeter. The aperture can be covered by graft material. The at least one station can be fenestrated to facilitate placement of a secondary stent.

The disclosure relates to a medical kit for the treatment of vascular malformations, in particular aneurysms and/or fistulas, having a permanently implantable covering device, in particular a stent, for covering the vascular malformation, the covering device having a tubular, self-expandable lattice structure and a covering made of an electrospun fabric, the covering being connected to the lattice structure and overlapping the lattice structure at least in part such that, when implanted, the covering is placed over the vascular malformation; and an embolisation means, which can be applied by a feed means in the implanted state for treatment of the vascular malformation, the covering forming a porous membrane which can be penetrated by the feed means for application of the embolisation means and which is designed to lie against the outer periphery of the feed means in the penetrated state.

A small diameter vascular prosthesis includes an outer textile graft, an intermediate self-supporting coil or stent and an inner microporous layer. The outer textile graft allows for tissue ingrowth. The inner microporous layer provides blood impermeability without preclotting the prosthesis. The coil or stent provides kink resistance and resistance again collapsing of the outer textile graft and the inner microporous layer.

The present invention relates to an implantable endoluminal graft comprised of a microporous thin-film metal covering having a plurality of openings and a structural support element underlying and physically attached to the microporous thin-film metal covering, the microporous thin-film metal covering having shape memory properties.

A personalized prosthesis for implantation at a treatment site of a patient includes a self-expanding mesh or membrane having collapsed and expanded configurations. The collapsed configuration is adapted to be delivered to the treatment site, and the expanded configuration engages the personalized prosthesis with the treatment site. The mesh or membrane is personalized to match the treatment site in the expanded configuration, and has an outer surface that substantially matches the treatment site shape and size. The self-expanding mesh or membrane forms a central lumen configured to allow blood or other body fluids to flow therethrough. Methods of manufacturing and delivery of the personalized prosthesis are also disclosed.

An endograft (102) includes a stent structure. An optical shape sensing (OSS) system (104) is associated with the endograft and is configured to measure shape, position and/or orientation of the stent structure. The OSS system (104) is connected to the stent structure and removable in a plurality of ways. Methods for deployment and removal of the OSS system are also provided.

Provided are a silicone stent (100), an implantation system, and a manufacturing method. The silicone stent (100) includes a stent body (110). The stent body (110) includes a mesh frame (112) and a silicone body (111) molded on the mesh frame (112). A circumferentially sealed space (116) is defined within the silicone body (111). A distal end and a proximal end of the silicone body (111) respectively have a distal-end opening (115) and a proximal-end opening (114) that communicate with the space (116). The mesh frame (112) circumferentially covers the silicone body (111), and runs in an axial direction of the silicone body (111). The mesh frame (112) extends from the proximal end of the silicone body (111) to the distal end of the silicone body (111).

Vascular endografts and methods of making and using the same are provided. The vascular endograft includes an elongated body defining a lumen configured to allow blood to flow therethrough and further defining an exterior surface, and a plurality of bristles extending outwardly from the exterior surface of the elongated body. In an instance in which the endograft is positioned within a blood vessel at a location corresponding to a blood vessel pathology, the bristles encourage positive remodeling of the blood vessel.

The present invention belongs to the field of medical devices, and specifically relates to a stent-graft. The stent-graft has a proximal greater curvature side and a proximal lesser curvature side. The stent-graft includes a stent body, an inner cover membrane disposed on the inner side of the stent body, and an outer cover membrane disposed on the outer side of the stent body. The stent body includes a plurality of wave rings axially arranged at intervals. Alternatively arranged crests and troughs are formed on the wave rings. The outer cover membrane is provided with a first opening, and the first opening exposes at least one trough located at or nearer to the proximal greater curvature side. According to the stent-graft of the embodiments of the present invention, the exposed trough can easily hang on a vessel wall, and thereby achieving the function of preventing the stent-graft from shifting. The crests and troughs located at the proximal lesser curvature side of the stent-graft remain covered by the outer cover membrane. Therefore, the stack state of the cover membrane and the wave ring in a stent lumen is in the blood flow direction, thereby reducing the risk of thrombosis.

A method of manufacturing a covered stent is disclosed. The method includes winding a first PTFE tape around a cylinder body of a jig, winding a second PTFE tape around a stent including the jig fitted therein, heating the stent in an oven, fitting the stent into upper and lower elastic members, fitting the elastic members into a mold, pressing the upper elastic member to bond the PTFE tapes to each other and to thus form a first film at a cylindrical body of the stent, taking the elastic members out of the mold, taking the stent out of the elastic members, removing the jig from the stent, forming a silicone coating layer at an expansion portion of the stent, and sewing the spaces in the expansion portion, the second PTFE tape, and the silicone coating layer to form a second film at the expansion portion.