Device for a dynamically sealing occlusion or a space-filling tamponade of a hollow organ
AssigneeCreative Balloons GmbH
InventorFred Göbel
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AssigneeCreative Balloons GmbH
InventorFred Göbel
Estimating the term…
The invention is directed to a device for the sealing occlusion and/or for the space-filling tamponade of hollow organs or other cavities in the human body, comprising a preferably fully and residually formed balloon (2) which applies a sealing pressure that is as constant as possible to the wall of the organ to be occluded or tamponaded. The device comprises an isobarically acting regulator (3) for the filling pressure within the interior of the balloon, the regulator having a volume reservoir (3) situated extracorporeally outside of the body, and a feed line (6) for communicatively connecting the extracorporeal volume reservoir of the regulator to the interior of the balloon. The connecting feed line between the balloon and the regulator has a flow-directing one-way valve (26) that prevents backflow from the balloon to the volume reservoir of the regulator, while a nonflow-directing throttle element (27) is provided which allows a slow volume compensation between the balloon and the volume reservoir.
A device for the sealing occlusion and/or for the space-filling tamponade of a hollow organ or a cavity in a human body, comprising a fully and residually formed balloon (2) which is configured to apply an appreciably constant sealing pressure to a wall of the hollow organ or cavity to be occluded or tamponaded in use, characterized by an appreciably isobarically acting regulator for a filling pressure within the interior of the balloon (2), the regulator having an extracorporeal volume reservoir which is configured to be situated extracorporeally outside of the human body in use and a feed line (6) for communicatively connecting the extracorporeal volume reservoir of the regulator to the interior of the balloon (2), wherein the connecting feed line (6) between the balloon (2) and the regulator comprises:
A device for the sealing occlusion and/or for the space-filling tamponade of a hollow organ or a cavity in a human body, comprising a prcfcrably fully and residually formed balloon (2) which is intended to be configured to apply an appreciably constant sealing pressure to a wall of the hollow organ or cavity to be occluded or tamponaded in use, comprising a regulating unit for a filling pressure within the interior of the balloon (2), which regulating unit is intended to be configured to be situated extracorporeally outside of the human body during use and comprises an extracorporeal volume reservoir (9) which is intended to be configured to be situated extracorporeally outside of the human body in use, and a feed line (6) for communicatively connecting the extracorporeal volume reservoir (9) to the interior of the balloon (2), wherein the connecting feed line (6) between the balloon (2) and the extracorporeal volume reservoir (9) comprises (i) a supply channel with a cross-sectional area corresponding to a circular cross-sectional area with a diameter of at least 2 mm, (ii) a flow-directing one-way valve (26) that prevents backflow from the balloon (2) to the extracorporeal volume reservoir (9), and (iii) a nonflow-directing bypass throttle element (27) which allows a slow volume compensation between the balloon (2) and the extracorporeal volume reservoir (9), wherein the nonflow-directing throttle element (27) is arranged in parallel to the flow-directing one-way valve (26) as a bypass thereto, and wherein the regulating unit is implemented
A device for the sealing occlusion and/or for the space-filling tamponade of a hollow organ or a cavity in a human body, comprising a preferably fully and residually formed balloon (2) which is intended to be configured to apply an appreciably constant sealing pressure to a wall of the hollow organ or cavity to be occluded or tamponaded in use, comprising a regulating unit for a filling pressure within the interior of the balloon (2), which regulating unit is intended to be configured to be situated extracorporeally outside of the human body in use and comprises an extracorporeal volume reservoir (9) which is intended to be configured to be situated extracorporeally outside of the human body in use, and a feed line (6) for communicatively connecting the extracorporeal regulating unit to the interior of the balloon (2), wherein the connecting feed line (6) between the balloon (2) and the extracorporeal volume reservoir (9) comprises:
Dependencies are inferred from the claim text.