The present invention relates to a medical chamber system (700) for implantation in the chest of a patient to support the heart activity, preferably by displacing the heart apex (105), comprising at least a first chamber (702) for arrangement inside the heart sac (300) and a second chamber (701) for arrangement outside the heart sac (300), wherein the chambers (701, 702) comprise at least one connection portion or connection channel (703) which connects the two chambers (701, 702) to each other, the chambers (701, 702) and the connection channel (703) are further embodied to be filled with fluid (705) and, preferably in the implanted state, to be arranged such that the heart activity acts on the first chamber (702) and that the second chamber (701) acts as a volume storage and/or energy storage for the fluid (705). Furthermore, the present invention relates to an introduction system for a medical chamber system (700) and to a kit, encompassing a medical chamber system (700) and an introduction system.

Embodiments of the present invention include a portable medical device with an integrated web server. The portable medical device is configured to establish a communication session with a user device. The integrated web server is configured to load software onto the user computing device for exchanging data with the portable medical device.

A medical device includes an artificial contractile structure which may be advantageously used to assist the functioning of a hollow organ, an artificial contractile structure including at least one contractile element (100) adapted to contract an organ, in such way that the contractile element (100) is in a resting or in an activated position, at least one actuator designed to activate the contractile structure, and at least one source of energy for powering the actuator. The ratio “current which is needed to maintain the contractile element in its activated position and in its resting position/current which is needed to change the position of the contractile element” is less than 1/500, preferably less than 1/800, and more preferably less than 1/1000. The medical device further includes elements for reducing corrosion of the medical device.

There is provided a method for controlling a flow of fluid and/or other bodily matter in a lumen formed by a tissue wall of a patient's organ. The method comprises gently constricting (i.e., without substantially hampering the blood circulation in the tissue wall) at least one portion of the tissue wall to influence the flow in the lumen, and stimulating the constricted wall portion to cause contraction of the wall portion to further influence the flow in the lumen. The method can be used for restricting or stopping the flow in the lumen, or for actively moving the fluid in the lumen, with a low risk of injuring the organ. Such an organ may be the esophagus, stomach, intestines, urine bladder, urethra, ureter, renal pelvis, aorta, corpus cavernosum, exit veins of erectile tissue, uterine tube, vas deferens or bile duct, or a blood vessel.

A device for assisting the operation of a natural heart is provided. A supporting jacket shaped to surround at least a portion of a heart has an expandable membrane attached to the inside wall of the jacket so that the membrane faces the heart. An inflatable cavity is formed between the jacket and the membrane. The cavity is connected to an expandable fluid reservoir via a length of flexible tubing. Pumps are used to pump fluid back and forth between the cavity and the reservoir. The cavity if inflated as the heart contract to aid the heart in pumping blood. The cavity is deflated as the heart relaxes to allow the heart to refill with blood. The cycle of pumping fluid is synchronized with the cardiac cycle.

A device, a kit and a method is presented for permanently augmenting the pump function of the left heart. The mitral valve plane is assisted in a movement along the left ventricular long axis during each heart cycle. The very close relationship between the coronary sinus and the mitral valve is used by various embodiments of a medical device providing this assisted movement. By means of catheter technique an implant is inserted into the coronary sinus, the device is augmenting the up and down movement of the mitral valve and thereby increasing the left ventricular diastolic filling when moving upwards and the piston effect of the closed mitral valve when moving downwards.

The present invention relates to an apparatus (500) for supporting the heart action, preferably by displacing the heart base (110) and/or the aortic root (201), comprising at least a first anchor (501) and a pulling device or guiding device (502, 503, 732, 732a, 732b) for moving the first anchor (501), wherein the first anchor (501) is provided and designed for implantation in or on the heart base (110), the heart skeleton (120), the aortic root (201) and/or a structure in local proximity to the aortic root (210), and/or comprising at least one lifting drive (502, 503). The present invention further relates to a control device (901), an insertion system, a kit and a method for supporting the heart action.

The present invention relates to an apparatus (500) for supporting the heart action, preferably by displacing the heart base (110) and/or the aortic root (201), comprising at least a first anchor (501) and a pulling device or guiding device (502, 503, 732, 732a, 732b) for moving the first anchor (501), wherein the first anchor (501) is provided and designed for implantation in or on the heart base (110), the heart skeleton (120), the aortic root (201) and/or a structure in local proximity to the aortic root (210), and/or comprising at least one lifting drive (502, 503). The present invention further relates to a control device (901), an insertion system, a kit and a method for supporting the heart action.

A cardiac assist system includes a pneumatic effector which is implanted beneath a pericardial sac and over a myocardial surface overlying the patient's left ventricle. A port is implanted and receives a percutaneously introduced cannula. The port is connected to supply a driving gas received from the cannula to the pneumatic effector. An external drive unit includes a pump assembly and control circuitry which operate the pump to actuate the pneumatic effector in response to the patient's sensed heart rhythm. A connecting tube has a pump end connected to the pump and a percutaneous port-connecting end attached to the implantable port.

The present invention provides a direct cardiac compression device for individualized support at different locations around the heart, the device comprising: a housing shaped to conform to the shape of the heart and to surround the heart; two or more active chambers positioned adjacent to the housing, wherein the two or more active comprise one or more right active chambers positioned on the right ventricle side of the heart and one or more left active chambers positioned on the left ventricle side of the heart, wherein the two or more active chambers are designed to conform to the shape of the heart, each active chamber comprising an inner membrane sealingly attached along its periphery to the housing and an active fluid individually supplied thereto; a right input connection in fluid communication with the one or more right active chambers to ingress the active fluid into each of the one or more right active chambers; a left input connection in fluid communication with the one or more left active chambers to ingress the active fluid into each of the one or more left active chambers, and a driver in fluid communication with each of the right input connection and the left input connection to individually and periodically ingress and egress the active fluid therefrom, wherein the active fluid individually inflates the one or more right active chambers and the one or more left active chambers to compress the heart.