A penile prosthesis includes a first penile implant implantable into a first corpora cavernosum and a second penile implant implantable into a second corpora cavernosum, and a pump assembly coupled to the implants by tubing. Each implant includes a tubular film sealed in a liquid-tight arrangement between a proximal tip implantable into a crus penis and a distal tip implantable into a glans penis, a scaffold nested inside of the tubular film, and a first liquid volume contained inside of the tubular film.

The present invention relates to a stent graft, comprising: a base stent having a first and a second longitudinal end, a lumen extending longitudinally through the base stent, a covering material provided so as to line the base stent, the base stent having a roughened surface that is at least partially penetrated by the covering material so as to form a positive fit.

A system and method for the installation and operation of a cardiac assist device. Flexible guides are advanced into a prepared space using minimally invasive techniques. A heart pump construct is advanced into position in the pericardial area along the flexible guides. Once in position, the heart pump construct is activated while still engaged with the flexible guides. The flexible guides provide structural integrity to the heart pump construct needed in order for the heart pump construct to function properly. The forces supplied to the heart by the heart pump construct are affected by the presence of the flexible guides. The structure of the flexible guides, the position of the flexible guides and the structure of the heart pump construct are customized to supply the forces needed by a particular heart in order to assist the heart in pumping more efficiently.

According to an aspect, an implant, includes an inflatable member, a pump assembly, a tubular member and a coupling member. The pump assembly is configured to facilitate a transfer of fluid to and from the inflatable member. The coupling member is configured to facilitate a coupling of the tubular member to the pump assembly.

The invention relates to an implant for arranging and expanding in the human gastrointestinal tract for the purpose of lining a section of the gastrointestinal tract in order to prevent the resorption of supplied nourishment in said section, having a first end section (1) which, as a securing section, allows the fixation of the implant in the human stomach/gastrointestinal tract and/or to an applicator (10); a tubular section which adjoins the first end section (1), comprising a longitudinal section (2) which extends in the provided expansion direction, a transition section (3) which adjoins the longitudinal section (2), and an inverted section (4) which runs within the longitudinal section opposite the provided expansion direction; and a second end section (8). According to the invention, a region of the inverted section (4) and a region of the longitudinal section delimit a flow channel (5), via which a fluid (15) blown into the tubular section can penetrate the transition section (3) in order to exert pressure thereon, wherein the inverted section (4) radially delimits a cavity (6) and has a closure section (7) which forms the second end section (8) and axially delimits the cavity (6).

Devices and methods for joining a first and second tissue in a patient are disclosed that include a base with a plurality of recurved tines oriented to a tine axis and extending from a first surface of the base. The tines provide unidirectional traction of the first tissue along the tine axis toward the first surface. The first tissue is secured to the first surface of the device at the plurality of recurved tines and the second tissue is secured to the device at a second surface opposite the first surface to join the first and second tissues.

A fluid controlled system for a cardiac assist device and its method of operation. The cardiac assist device has a cup assembly with a receptacle area. The cup assembly has at least one inflatable membrane that expands into the receptacle area. A single pressure tube connects the cup assembly to a fluid pump. A valve assembly is incorporated into the cardiac assist device. The valve assembly includes at least one valve that controls fluid flow between the inflatable membranes and the pressure tube and/or fluid flow between the receptacle area and the pressure tube. The valve assembly controls fluid flow to advance the cup assembly onto the heart, to maintain the cup assembly in an operable position, to operate the cup assembly, and to remove the cup assembly.

Intraocular implants and methods of making intraocular implants are provided. The intraocular implants can improve the vision of a patient, such as by increasing the depth of focus of an eye of a patient. In particular, the intraocular implants can include a mask having an annular portion with a relatively low visible light transmission surrounding a relatively high transmission central portion such as a clear lens or aperture. This construct is adapted to provide an annular mask with a small aperture for light to pass through to the retina to increase depth of focus. The intraocular implant may have an optical power for refractive correction. The intraocular implant may be implanted in any location along the optical pathway in the eye, e.g., as an implant in the anterior or posterior chamber.

The invention relates to a device (4) in the form of a medical prosthesis (9, 17), medical osteosynthesis device, hearing aid or hearing aid housing, essentially made of metal, wherein the device (4, 9, 17) comprises at least one optical diffractive element with a grating (6) which is directly embossed in an exposed metal surface in the form of a security and/or identification element. The invention furthermore relates to methods for making such devices and to uses of such devices.

A sensing valve repair system includes a delivery system and a heart valve repair device. The delivery system is configured to deploy the heart valve repair device. The sensing valve repair system has a first sensor associated with one or more of the delivery system and the valve repair device. The first sensor is attached to one or more of an inner paddle and a fixed arm of a clasp.