A rotation unit includes a drive shaft and rotor of a peristaltic pump. The drive shaft attaches a rotor of the blood pump, extends along a central axis, and has a head delimited by a groove. A sliding section is arranged on the head. The rotation unit includes the drive shaft and the rotor with tube rollers which is attachable to the drive shaft. The groove has a flank arranged perpendicularly to the central axis. A locking element is movable transversely to the central axis. An abutment section is biased in the direction of the central axis and in the direction of the groove bottom by a spring arranged in the rotor. The abutment section is movable away from the central axis and groove bottom by an actuating section mounted on or formed integrally with the locking element. An abutment surface is arranged perpendicularly to the central axis.

A drive unit for a diaphragm pump may be provided, wherein the drive unit comprises a hollow body and a piston which is arranged so as to be movable in the first hollow body along an axis of the hollow body, wherein the piston divides the hollow body into a first chamber, which is connectable to the diaphragm pump, and a second chamber, which is coupleable to a gas reservoir. The second chamber comprises an inlet valve and an outlet valve, such that a gas flow is drawn into the chamber via the inlet valve and is forced out of the chamber via the outlet valve.

A drive unit for a diaphragm pump may be provided, wherein the drive unit comprises a hollow body and a piston which is arranged so as to be movable in the first hollow body along an axis of the hollow body, wherein the piston divides the hollow body into a first chamber, which is connectable to the diaphragm pump, and a second chamber, which is coupleable to a gas reservoir. The second chamber comprises an inlet valve and an outlet valve, such that a gas flow is drawn into the chamber via the inlet valve and is forced out of the chamber via the outlet valve.

A circulatory support system may include a blood pump, one or more sensors, and a controller. The blood pump may include a driven component and a motor in communication with the driven component and the controller to drive the driven component to pump a blood flow through the blood pump. The controller may be configured to determine a command signal based on a value related to a speed of the motor, provide the command signal to the motor to drive the driven component, determine a value of a parameter related to operation of the blood pump based on the command signal and the value related to the speed of the motor, and output an indication a blood pump transition is recommended based on one or more determined values of one or more parameters related to operation of the blood pump.

A circulatory support system may include a blood pump, one or more sensors, and a controller. The blood pump may include a driven component and a motor in communication with the driven component and the controller to drive the driven component to pump a blood flow through the blood pump. The controller may be configured to determine a command signal based on a value related to a speed of the motor, provide the command signal to the motor to drive the driven component, determine a value of a parameter related to operation of the blood pump based on the command signal and the value related to the speed of the motor, and output an indication a blood pump transition is recommended based on one or more determined values of one or more parameters related to operation of the blood pump.

Provided is a slide device which includes a fixed-side slide member having an annular-shaped first slide surface, and a rotary-side slide member having an annular-shaped second slide surface, with the slide device being configured such that the first slide surface and the second slide surface are positioned opposite to each other, and an outer peripheral side of the fixed-side slide member and an outer peripheral side of the rotary-side slide member are brought into contact with a liquid containing a blood component, and a region where the first slide surface and the second slide surface face each other along the rotary-side slide member, the first slide surface and the second slide surface are brought into contact with each other on an outermost periphery of the opposite-facing region of the first and second slide surfaces.

The invention relates to a temporary circulatory assistance or support device for the heart (13) of a patient (12), a first pressure sensor (50) being disposed in the admission portion (19) and this pressure sensor (50) having a measurement time constant of less than 20 milliseconds so that the control means (40) modulate or stop the pumping of the extracted blood when the pressure detected by the sensor (50) attains a threshold pressure value and/or the pressure increases/decreases above or below a threshold pressure acceleration/deceleration slope.

The invention relates to a temporary circulatory assistance or support device for the heart (13) of a patient (12), a first pressure sensor (50) being disposed in the admission portion (19) and this pressure sensor (50) having a measurement time constant of less than 20 milliseconds so that the control means (40) modulate or stop the pumping of the extracted blood when the pressure detected by the sensor (50) attains a threshold pressure value and/or the pressure increases/decreases above or below a threshold pressure acceleration/deceleration slope.

An implant device having a biointerface. The implant device comprises a cavity and a structure enabling a flow path between the cavity and an environment of the implant device. An actuatable membrane is interposed in the flow path. The device includes a power-generating unit and a control unit, where the latter is connected to the power-generating unit. An electromechanical is connected to both the control unit and the power-generating unit. The electromechanical system includes at least one actuator configured to mechanically contact the membrane. This actuator is permanently attached to the membrane. The control unit and the electromechanical system are jointly configured to cause the electromechanical system to controllably actuate the membrane via at least one actuator to control a transfer of substances between the cavity and the environment through the flow path. The invention is further directed to related operation and fabrication methods.

An implant device having a biointerface. The implant device comprises a cavity and a structure enabling a flow path between the cavity and an environment of the implant device. An actuatable membrane is interposed in the flow path. The device includes a power-generating unit and a control unit, where the latter is connected to the power-generating unit. An electromechanical is connected to both the control unit and the power-generating unit. The electromechanical system includes at least one actuator configured to mechanically contact the membrane. This actuator is permanently attached to the membrane. The control unit and the electromechanical system are jointly configured to cause the electromechanical system to controllably actuate the membrane via at least one actuator to control a transfer of substances between the cavity and the environment through the flow path. The invention is further directed to related operation and fabrication methods.