The holder for a curved duct portion of a tube pump comprises: a supply-side connector comprising a first cavity and a first plate connected together, the first cavity being adapted for receiving an end of the curved duct portion, and a discharge-side connector comprising a second cavity and a second plate connected together, the second cavity being adapted for receiving another end of the curved duct portion, where said connectors are movable the one with respect to the other between a storage configuration, in which the supply-side connector is positioned away to the discharge-side connector, and an operating configuration, in which the supply-side connector is close to the discharge-side connector and in which the first and second plate are engaged together substantially on a same plane.

The invention relates to an apparatus for extracorporeal blood treatment, comprising a blood treatment unit 1 that comprises at least one compartment 3. The invention further relates to an apparatus 15A, 15B for collecting blood clots for a blood line 5, 7 for supplying blood to or removing blood from a blood treatment unit 1 of an extracorporeal blood treatment apparatus, and to a method for determining a hemodynamic parameter during extracorporeal blood treatment using an extracorporeal blood treatment apparatus. In order to determine the hemodynamic parameter, the conveying direction of the blood pump 10 is reversed from a normal blood flow to a reversed blood flow. It has been found in practice that, in the event of a reversal in the conveying direction of the blood pump in order to carry out a measurement for determining a hemodynamic parameter, there is a risk of blood clots reaching the patients, although the dialyser traps blood clots. The apparatus according to the invention provides an apparatus 15A for catching blood clots, at least in the blood line of the extracorporeal blood circuit I that leads to the blood treatment unit 1 during a normal blood flow. The blood treatment unit traps blood clots during blood treatment having a normal blood flow. In the case of a reversed blood flow, the apparatus for catching blood clots in the blood line that leads to the blood treatment unit 1 during a normal blood flow traps blood clots that may have previously accumulated at the inlet of the blood treatment unit.

A medical fluid pumping system includes (i) a medical fluid pump including a pump chamber, inlet and outlet valve chambers in fluid communication with the pump chamber, the pump chamber associated with a pumping chamber motive fluid connection, the inlet valve chamber associated with an inlet valve motive fluid connection, and the outlet valve chamber associated with an outlet valve motive fluid connection; and (ii) a medical fluid chassis including a motive fluid source, and a first motive fluid connecting structure, a second motive fluid connecting structure, a third motive fluid connecting structure. The pumping chamber motive fluid connection, the inlet valve motive fluid connection, and the outlet valve motive fluid connection are translated simultaneously to mate respectively with the first motive fluid connecting structure, the second motive fluid connecting structure, and the third motive fluid connecting structure for fluid communication with the motive fluid source.

A medical fluid delivery device includes a process fluid body including first and second sides defining a first process fluid inlet valve seat and a first process fluid outlet valve seat and a second process fluid inlet valve seat and a second process fluid outlet valve seat; a first motive fluid plate defining a first aligned motive fluid inlet valve actuation area and a first aligned motive fluid outlet valve actuation area; and a second motive fluid plate defining a second aligned motive fluid inlet valve actuation area and a second aligned motive fluid outlet valve actuation area. The device further includes a first inlet valve diaphragm disposed between the first motive fluid inlet valve actuation area and the first process fluid inlet valve seat; and a first outlet valve diaphragm disposed between the first motive fluid outlet valve actuation area and the first process fluid outlet valve seat.

A blood pump system for persistently increasing the overall diameter and lumen diameter of peripheral veins and arteries by persistently increasing the speed of blood and the wall shear stress in a peripheral vein or artery for a period of time sufficient to result in a persistent increase in the overall diameter and lumen diameter of the vessel is provided. The blood pump system includes a blood pump, blood conduit(s), a control system with optional sensors, and a power source. The pump system is configured to connect to the vascular system in a patient and pump blood at a desired rate and pulsatility. The pumping of blood is monitored and adjusted, as necessary, to maintain the desired elevated blood speed, wall shear stress, and desired pulsatility in the target vessel to optimize the rate and extent of persistent increase in the overall diameter and lumen diameter of the target vessel.

A blood processing system includes a collection line for carrying blood, a blood separation device for separating the blood into first and second fractions, a plasma delivery line for delivering the first blood fraction to an adsorption device, and a peristaltic pump. The adsorption device adsorbs plasma of the first blood fraction. Portions of the collection and plasma delivery lines are positioned in a channel of the peristaltic pump, and the peristaltic pump causes the blood to flow through the collection line at a first flow rate and causes the first blood fraction to flow through the plasma delivery line at a second flow rate that is less than the first flow rate. In some implementations, the collection and plasma delivery lines are tubes having different internal diameters facilitating such differential flow rates. In some implementations, the peristaltic pump is the only pump in the blood processing system.

A blood processing system includes a collection line for carrying blood, a blood separation device for separating the blood into first and second fractions, a plasma delivery line for delivering the first blood fraction to an adsorption device, and a peristaltic pump. The adsorption device adsorbs plasma of the first blood fraction. Portions of the collection and plasma delivery lines are positioned in a channel of the peristaltic pump, and the peristaltic pump causes the blood to flow through the collection line at a first flow rate and causes the first blood fraction to flow through the plasma delivery line at a second flow rate that is less than the first flow rate. In some implementations, the collection and plasma delivery lines are tubes having different internal diameters facilitating such differential flow rates. In some implementations, the peristaltic pump is the only pump in the blood processing system.

A system for generating a blood circulation in at least part of an organ of a vertebrate, including a first artificial cavity and a second artificial cavity. The cavities each include a flexible membrane capable of beating under the action of a gas. Each of the membranes separate in a sealed manner a blood circulation chamber and a chamber containing the gas. The system also includes: a first low pressure gas buffer reservoir; a second high-pressure gas buffer reservoir; a gas distribution; and a pneumatic pump.

A microfluidic photoreactor for treating excess bilirubin in blood, having: a microfluidic channel module; an illumination module comprising one or more illumination sources disposed about the microfluidic channel module and configured to illuminate blood passing through at least one microfluidic channel of the microfluidic channel module; and a heat exchanger module coupled to the at least one microfluidic channel module, wherein the heat exchanger module is configured to extract heat from the at least one microfluidic channel. A system including a microfluidic photoreactor and a method of treating excess bilirubin in blood.

A mechanical circulatory support device includes an inner housing having an inlet end, an outlet end, and a flow path there between. The flow path defines a longitudinal axis. A volute downstream of the outlet end has an outlet port. A rotor mounted within the inner housing upstream of the volute and configured to rotate about the longitudinal axis is included. The volute includes an inner surface having a minimum radius immediately adjacent the rotor and a maximum radius at the outlet port that is larger than the minimum radius.