A method of testing the rotor engagement of a peristaltic pump rotor. The method comprising steps of providing a pump system comprising a peristaltic pump rotor; a tube; a valve; a pressure sensor; a comparator; and a processor. The pressure sensor is configured to monitor the pressure in a fluid in the tube downstream of the peristaltic pump rotor and upstream of the valve. The comparator is configured to continuously monitor the pressure sensor and compare the measured fluid pressure data with a predetermined parameter. The processor is configured to receive a signal from the comparator and generate an alert signal when the measured pressure data falls outside the predetermined parameters.

The invention relates to a medical treatment apparatus comprising a tube set 20, a peristaltic pump 6 for conveying fluid, and a monitoring apparatus 15 for monitoring the occlusion of the positive displacement elements 13A, 13B of the peristaltic pump. In addition, the invention relates to a tube set 20 for a medical treatment apparatus, and to a method for monitoring the occlusion of the occlusion elements of a peristaltic pump for conveying a fluid for a medical treatment apparatus. The invention is based on the fact that the occlusion of the positive displacement elements 13A, 13B of the peristaltic pump 6 is monitored in order to monitor the fluid flow in the hose line 5. For this purpose, the electrical resistance or a variable which correlates with the electrical resistance is measured between a first and a second electrode 16A, 16B, the first electrode 16A being arranged on the hose line 5 upstream of the occlusion elements 12 of the peristaltic pump 6 and the second electrode 16b being arranged on the hose line downstream of the occlusion elements such that an electrical contact is produced between the first and second electrode 16A, 16B and the fluid flowing in the hose line 5. The electrodes 16A, 16B are preferably integral component parts of a connecting piece 10, by means of which the hose segment 5A to be inserted into the peristaltic pump 6 is fixed in the form of a loop.

The invention relates to a medical treatment apparatus comprising a tube set 20, a peristaltic pump 6 for conveying fluid, and a monitoring apparatus 15 for monitoring the occlusion of the positive displacement elements 13A, 13B of the peristaltic pump. In addition, the invention relates to a tube set 20 for a medical treatment apparatus, and to a method for monitoring the occlusion of the occlusion elements of a peristaltic pump for conveying a fluid for a medical treatment apparatus. The invention is based on the fact that the occlusion of the positive displacement elements 13A, 13B of the peristaltic pump 6 is monitored in order to monitor the fluid flow in the hose line 5. For this purpose, the electrical resistance or a variable which correlates with the electrical resistance is measured between a first and a second electrode 16A, 16B, the first electrode 16A being arranged on the hose line 5 upstream of the occlusion elements 12 of the peristaltic pump 6 and the second electrode 16b being arranged on the hose line downstream of the occlusion elements such that an electrical contact is produced between the first and second electrode 16A, 16B and the fluid flowing in the hose line 5. The electrodes 16A, 16B are preferably integral component parts of a connecting piece 10, by means of which the hose segment 5A to be inserted into the peristaltic pump 6 is fixed in the form of a loop.

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.

A dual lumen drainage cannula configured for use in a veno-arterial extracorporeal membrane oxygenation (VA ECMO) system includes a first drainage tube having a proximal end, a distal end, and at least one aperture defined in the distal end. The dual lumen drainage cannula further includes a second drainage tube having a proximal end, a distal end, and at least one aperture defined in the distal end. The dual lumen drainage cannula further includes an outlet fitting in fluid communication with the first drainage tube and the second drainage tube. The distal end of the second drainage tube is joined to a portion of the first drainage tube between the proximal and distal ends of the first drainage tube.

The present invention relates to various methods of treatment using a novel blood perfusion device. The blood perfusion device comprises a perfusion chamber comprising at least one compartment A and at least one compartment B, compartment A comprising a first opening which is in direct fluid communication to a second opening, wherein the first opening of compartment A is in direct fluid communication to a first port of the perfusion chamber and the second opening of compartment A is in direct fluid communication to a second port of the perfusion chamber; and compartment B comprising a first opening which is in direct fluid communication to a second opening, wherein the first opening of compartment B is in direct fluid communication to a third port of the perfusion chamber and the second opening of compartment B is in direct fluid communication to a fourth port of the perfusion chamber, wherein compartment A is separated from compartment B by at least one membrane, said membrane being configured to prevent cells from crossing the membrane.

The present invention relates to various methods of treatment using a novel blood perfusion device. The blood perfusion device comprises a perfusion chamber comprising at least one compartment A and at least one compartment B, compartment A comprising a first opening which is in direct fluid communication to a second opening, wherein the first opening of compartment A is in direct fluid communication to a first port of the perfusion chamber and the second opening of compartment A is in direct fluid communication to a second port of the perfusion chamber; and compartment B comprising a first opening which is in direct fluid communication to a second opening, wherein the first opening of compartment B is in direct fluid communication to a third port of the perfusion chamber and the second opening of compartment B is in direct fluid communication to a fourth port of the perfusion chamber, wherein compartment A is separated from compartment B by at least one membrane, said membrane being configured to prevent cells from crossing the membrane.

An arterial cannula connects to a heart-lung machine for supplying a patient with oxygen-rich blood and includes a tubular body having a front end region for positioning at the aortic arch, a main region, and a rear end region for connection to the supply side. The length of the tubular body is dimensioned so that the cannula can be placed at the femoral artery and extends to the aortic arch. The tubular body is flexible and includes a lumen, and perforations in the front end region. The front end region is pre-curved, following the shape of the aortic arch. An insertion aid is located inside the tubular body for placing the cannula and is slidable into or withdrawable from the tubular body after the cannula has been placed. The curvature of the front end region adjusts automatically after the cannula is placed and the insertion aid withdrawn.

Provided is a blood dialyzing apparatus having multiple fluid chambers each having an internal space, a chamber pressurizing member compressing or expanding the internal spaces of the chambers, a chamber pressurizing member driver driving the chamber pressurizing member, and a flow control unit. The chambers are each connected with a first flow tube through which a fluid is provided to the chamber and a second flow tube through which a fluid of the chamber is discharged therefrom. The flow control unit controls a flow through the flow tubes connected to the multiple fluid chambers.

A dialysis apparatus has a connection channel that communicatively connects a dialysate circuit and a blood circuit, and circulates dialysate from the dialysate circuit to the blood circuit via the connection channel during a priming operation. A blood pump has a tube attachment device that switches from an unattached state in which a tube is positioned outside a housing and permits liquid to circulate thereinside, to an attached state in which the tube is in the housing and a rotor compresses the tube. At the time of priming, the liquid feeding pump feeds dialysate from the dialysate circuit to the blood circuit via the connection channel. With the blood pump being in the unattached state, the dialysate is circulated past the blood pump, and then, with the blood pump in the attached state, the dialysate is circulated in a direction opposite to the blood pump.