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.

A method of detecting the presence or absence of a sealant applied to a textile graft includes the steps of: providing a textile graft having a first surface and an opposed second surface; providing a water soluble masking agent; applying the water soluble masking agent to at least a portion of the first surface of the textile graft; providing a sealant solution; providing a visual indicator; applying the water insoluble sealing agent and the visual indicator to the second surface of the textile graft; and removing the water soluble masking agent after the step of applying sealing solution. The second surface has visual indication of the visual indicator and the first surface is substantially free of visual indication of the visual indicator. An implantable textile graft includes the selectively applied visual indicator.

It is an object to provide a woven fabric which can stably form a folding shape superior in shape retention and followability and which can be sewn while maintaining the folding structure, and also to provide a method for manufacturing the same. There is provided a woven fabric having pleats, wherein the height of the pleats is 2 to 10 times the average diameter of yarns arranged in the same direction as the pleats.

It is an object to provide a woven fabric which can stably form a folding shape superior in shape retention and followability and which can be sewn while maintaining the folding structure, and also to provide a method for manufacturing the same. There is provided a woven fabric having pleats, wherein the height of the pleats is 2 to 10 times the average diameter of yarns arranged in the same direction as the pleats.

A stent graft, including multiple wavy rings. The stent graft includes, in a circumferential direction, a region A and a region B connected to the region A. Each wavy ring includes a first wavy section located in the region A, and a second wavy section located in the region B. The wave included angle of the first wavy section is about 70°-120°; the ratio of the wave height of the first wavy section to the spacing between adjacent first wavy sections is 1/4-3; the wave included angle of the second wavy section is 30°-60°, the ratio of the wave height of the second wavy section to the spacing between adjacent second wavy sections is 1/4-3/2, and the ratio of the wave height of the first wavy section to the wave height of the second wavy section is greater than or equal to 1/3 and less than 1.

An implant (in particular a stent) includes a main structure and a sensor assembly for measuring a body parameter. The sensor assembly includes at least one electrical conductor and at least one capacitor which are connected in such a way that the conductor and the capacitor form at least one electrical resonant circuit. The electrical conductor is surrounded by an electrical insulation. The electrical conductor is in the form of a coil having at least one turn. The capacitor is in contact at least on one side with the surrounding environment and its capacitance changes depending on the body parameter that is to be determined.

An implant (in particular a stent) includes a main structure and a sensor assembly for measuring a body parameter. The sensor assembly includes at least one electrical conductor and at least one capacitor which are connected in such a way that the conductor and the capacitor form at least one electrical resonant circuit. The electrical conductor is surrounded by an electrical insulation. The electrical conductor is in the form of a coil having at least one turn. The capacitor is in contact at least on one side with the surrounding environment and its capacitance changes depending on the body parameter that is to be determined.

Devices and methods for protecting the neurovascular structures about the vertebral column are provided. One embodiment of the invention comprises a neuroprotective stent or device adapted for placement in an intervertebral foramen of a vertebral column and configured to resist compression or impingement from surrounding structures or forces. The stent or device may further comprise a flange or hinge region to facilitate attachment of the device to the vertebrae or to facilitate insertion of the device in the foramen, respectively.

Devices and methods for protecting the neurovascular structures about the vertebral column are provided. One embodiment of the invention comprises a neuroprotective stent or device adapted for placement in an intervertebral foramen of a vertebral column and configured to resist compression or impingement from surrounding structures or forces. The stent or device may further comprise a flange or hinge region to facilitate attachment of the device to the vertebrae or to facilitate insertion of the device in the foramen, respectively.

Some embodiments are directed to methods and systems for percutaneously treating dissections in a patient's vasculature, such as, without limitation, the aorta. The method can include deploying a catheter containing a collapsed anchoring element, frame, and cover through a first vessel to an entry point of the dissection. The anchoring element can be secured to the second branch vessel. The frame can be expanded in the first branch vessel. The cover can be unfolded over at least a portion of the entry point. The cover then reduces blood flow into the entry point.