A medical device for narrowing or closing an anatomical channel includes a band part (1) which can be placed around the body tissue (2) surrounding the anatomical channel and which can be closed to form a ring that encloses a through-opening (6) for the body tissue, wherein the band part (1) has a hollow chamber (3), and wherein the through-opening (6) can be made smaller by introducing a fluid into the hollow chamber (3). The medical device moreover includes a pump unit (10) which serves to convey the fluid and which has an electric drive (15) controllable by an electronic control system of the device, wherein a pressure value corresponding to the pressure of the fluid in the hollow chamber (3) or dependent on this pressure can be detected by the electronic control system. The device moreover has an air pressure sensor (23) for detecting the atmospheric pressure.

An eye-implantable electrowetting lens can be operated to control an overall optical power of an eye in which the device is implanted. A lens chamber of the electrowetting lens contains first and second fluids that are immiscible with each other and have different refractive indexes. By applying a voltage to electrodes of the lens, the optical power of the lens can be controlled by affecting the geometry of the interface between the fluids. To prevent fouling the surface due to folding or other manipulation of the lens during the insertion process, one or more surfaces within the lens chamber is highly underwater oleophobic.

An apparatus for treating a urinary retention of a patient by discharging urine from a mammal urinary bladder through a mammal urethra. The apparatus comprises an expandable member adapted to be implanted inside the urinary bladder of the patient, a control device adapted to control the volume of the expandable member for emptying the mammal urinary bladder, and an implantable restriction devices adapted to close each ureter of a patient when discharging urine from the urinary bladder.

A needle guiding arrangement, for guiding a surgical needle when applying sutures joining two skin surfaces inside an opening of a transformer core to implant the transformer core under the skin of a patient, the needle guiding arrangement comprising: a first needle guiding member; a second needle guiding member; and an alignment arrangement configured to align the first needle guiding member and the second needle guiding member on opposite sides of the opening of the transformer core along an alignment axis passing through the first needle guiding member, the opening of the transformer core and the second needle guiding member.

Techniques and mechanisms for the wireless transmission of power or control signals between two components of an implantable ophthalmic system are disclosed herein. An example device includes an accommodating intraocular lens (aIOL) and separate auxiliary electronics, both enclosed in biocompatible materials. The aIOL includes a dynamic optic, control logic, a battery and an antenna. The auxiliary electronics include an antenna, an energy storage cell, and a sensor. The auxiliary electronics may be wirelessly coupled to the aIOL for the wireless transmission of power or control signals.

An operable implant adapted to be implanted in the body of a patient, the operable implant comprising an operation device and a body engaging portion, wherein the operation device comprises a first unit comprising a receiving unit for receiving wireless energy and a first gear system adapted to receive mechanical work having a first force and first velocity, and output mechanical work having a different second force and a different second velocity. The operation device further comprises a second unit comprising an electrical motor adapted to transform electrical energy to the mechanical work, and a distance element adapted to separate the first and second units such that the receiving unit, when receiving wireless energy, is not substantially affected by the second unit.

This prosthesis is likely to be implanted surgically in males for the treatment of erectile disfunction, higher degree of female satisfaction, erection improvement, greater erection management, cosmetic enhancement, and or premature ejaculation concerns and it has at least one flexible semi-rigid inflatable computerized remote controlled software driven sleeve bladder that can be inflated to create an erection or deflated on demand, implanted inside the inner wall and encompassing the circumference of the penis, and can incorporate at least one rechargeable vibrator device, at least one flexible inflatable computerized remote controlled cylindrical bladder, implanted inside the penis body, that can be inflated to create an erection, a computerized remote controlled fluid-filled reservoir implanted under the abdominal wall, a wirelessly rechargeable computerized remote controlled pump and release valve placed under the abdominal wall with a subcutaneous wireless recharging system. Each device is controlled by an erection management system (EMS) and corresponding software.

The present disclosure relates to implantable neuromodulation devices, and in particular to a wireless power coil for a neuromodulation device that is to be implanted in a minimally invasive manner, for example, through a trocar or cannula. Particularly, aspects of the present disclosure are directed to a medical device that includes a lossy housing surrounding a power supply, and a receiving coil configured to exchange power wirelessly via a wireless power transfer signal and deliver the power to the power supply. The receiving coil is spaced a predetermined distance from the lossy housing. The medical device further includes a gap provided between the lossy housing and the receiving coil on a vertical plane, and a spacer that fills in at least a portion of the gap to maintain the lossy housing a predetermined distance from the receiving coil.

Adjustable flow glaucoma shunts are disclosed herein. In one embodiment, for example, an adjustable flow shunt can include an outflow drainage tube having a proximal inflow region and a distal outflow region. The proximal inflow region can include aperture(s) defining a fluid inlet area positioned to allow fluid to flow therethrough. The shunt further comprises an inflow control assembly at the proximal inflow region. The inflow control assembly can include a control element configured to slidably engage the proximal inflow region and a spring element. The spring element is configured to be activated by non-invasive energy and, upon activation, slidably move the control element along the proximal inflow region such that (a) the one or more apertures are accessible and have a first fluid flow cross-section or (b) the one or more apertures are at least partially covered by the control element and have a second, different fluid-flow cross-section.

“An artificial stomach for replacing the normal stomach of a patient comprises a food reservoir adapted to collect food, an inlet connected to a first opening of the food reservoir and further being adapted to upstream connect to the patient's gastrointestinal tract, and an outlet connected to a second opening of the food reservoir and further being adapted to downstream connect to the patient's gastrointestinal tract”.