Expandable docking stations for docking an expandable valve can include a valve seat, one or more sealing portions, and one or more retaining portions. The valve seat can be unexpandable or substantially unexpandable beyond a deployed size. The one or more sealing portions are connected to the valve seat and extend radially outward of the valve seat. The one or more sealing portions are constructed to expand outward of the valve seat and provide a seal over a range of sizes. The one or more retaining portions are connected to the one or more sealing portions. The one or more retaining portions are configured to retain the docking station at a deployed position.

Described here are wireless monitoring devices, systems, and methods for estimating one or more physiological parameters of a patient. These devices and systems may measure or receive a signal waveform transmitted through one or more of fluid and a physiological structure of a patient. This measured signal waveform may be processed to generate waveform parameter data used to estimate a physiological parameter such as blood velocity, heart wall thickness, and the like.

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.

Methods and systems for improving the competency of a venous valve wherein one or more compressor(s) (e.g., space occupying material(s) or implantable device(s)) is/are delivered to one or more location(s) adjacent to a venous valve to compress the venous valve in a manner that causes one or both leaflets of the valve to move toward the other, thereby improving closure or coaptation of the valve leaflets. The compressor(s) may be delivered by an open surgical approach, by a direct percutaneous approach or by a transluminal catheter-based approach.

Methods are provided to make a prosthetic valve having a thin, biocompatible, high-strength, composite material. In one aspect, the composite material maintains flexibility in high-cycle flexural applications, making it particularly applicable to high-flex implants such as a heart valve leaflet. The composite material includes a porous expanded fluoropolymer membrane and an elastomer, wherein the elastomer is present in the pores of the porous expanded fluoropolymer.

An intravascular cuff acts as a lining between a native vessel and an intravascular prosthetic device. During deployment, the ends of the cuff curl back upon themselves and are capable of trapping native tissue, such as valve leaflet tissue, between the ends. The cuff creates a seal between the vessel and the prosthetic, thereby preventing leakage around the prosthetic. The cuff also traps any embolic material dislodged from the vessel during expansion of the prosthetic.

A venous valve with a frame and a cover on the frame for unidirectional flow of a liquid through the valve.

An implantable device for regulating blood flow through a blood vessel comprising an elongated support dimensioned and configured to be implanted in a blood vessel. The support includes a linking member linking axially spaced apart portions to one another. A valve membrane extends between the axially spaced apart support portions and includes first region folded over the first linking member and attached thereto and a second region adjacent the first region and unattached to the first linking member. The second region is movable between a first position to enable blood flow and a second position to inhibit blood flow.

Implantable devices including conduits that have markings along the length of the conduit are described herein.

A prosthetic valve, solving the technical problem of an existing prosthetic valve, when implanted in a certain valve site, not being adaptive to the physiological anatomy condition of the heart, being difficult to mount and fix properly and being easy to become displaced, and consequently affecting the function of the valve. The prosthetic valve comprises an annular frame (2) which has a mesh structure and can radially expand to deform; a connection line (10) is provided on the frame (2); the prosthetic valve is connected and fixed to an anatomical structure of a mounting position of a human body by means of the connection line (10); the connection line (10) surrounds the outside of the frame (2) to form several connection portions which extend out along the radial direction of the frame (2); the space surrounded by the connection portions can receive the thickness of the anatomical structure. The prosthetic valve is connected and fixed by means of the connection line (10) to an anatomical structure of a mounting position in a human body, e.g. a vessel wall, being mounted stably and being applicable to a patient on whom a valve replacement surgery is difficult to perform, e.g. a pulmonary artery stenosis patient.