A blood filtering device comprises a casing defining a containment volume and provided with at least a first inlet for the venous blood, at least a second inlet for the intracavitary blood, at least a third inlet for the extra cavitary blood and at least an outlet mouth for the blood; blood filtering means which are housed inside the containment volume and delimiting at least one filtering volume communicating with the blood inlets and at least one collecting volume communicating with the outlet mouth; where filtering means comprise: at least a first filtering element defining a closed profile and delimiting a first filtering volume communicating with the first inlet; at least a second filtering element defining a closed profile and delimiting a second filtering volume communicating with the second inlet; at least a third filtering element defining a closed profile and delimiting a third filtering volume communicating with the third inlet.

Described are embodiments that include methods and devices for separating components from multi-component fluids. Embodiments may involve use of separation vessels and movement of components into and out of separation vessels through ports. Embodiments may involve the separation of plasma from whole blood. Also described are embodiments that include methods and devices for positioning portions, e.g., loops, of disposables in medical devices. Embodiments may involve use of surfaces for automatically guiding loops to position them into a predetermined position.

Described are embodiments that include methods and devices for separating components from multi-component fluids. Embodiments may involve use of separation vessels and movement of components into and out of separation vessels through ports. Embodiments may involve the separation of plasma from whole blood. Also described are embodiments that include methods and devices for positioning portions, e.g., loops, of disposables in medical devices. Embodiments may involve use of surfaces for automatically guiding loops to position them into a predetermined position.

A process includes removing air bubbles from extracorporeal blood via chemical entrapment of nitrogen (N.sub.2) gas.

The present disclosure relates to a pressure measuring line, with a connector to connect the pressure measuring line to a blood treatment apparatus, and to a membrane. In some embodiments, the pressure measuring line comprises at least two consecutive lumen sections, namely the first lumen section and the second lumen section. The first lumen section comprises a first lumen geometry and the second lumen section comprises a second lumen geometry, whereby the first lumen geometry and the second lumen geometry differ from each other in at least their diameters. Further, a monitoring method and devices are described.

The introduction pipe is extend from an inlet port to the inside of the chamber body, and has, as an end opening thereof, a discharge port provided in the inner circumferential surface of the chamber body so as to be directed toward the circumferential direction. The inner circumferential surface of the chamber body is provided so as to spirally extend, along the circumferential direction, from a discharge point at which the discharge port is disposed, to a connection point at which the outer circumferential surface of the introduction pipe is connected to the inner circumferential surface of the chamber body. The inner circumferential surface is formed such that a second radius connecting the connection point to the center axis of the chamber body is shorter than a first radius connecting the discharge point to the center axis of the chamber body.

Described are embodiments that include methods and devices for separating components from multi-component fluids. Embodiments may involve use of separation vessels and movement of components into and out of separation vessels through ports. Embodiments may involve the separation of plasma from whole blood. Also described are embodiments that include methods and devices for positioning portions, e.g., loops, of disposables in medical devices. Embodiments may involve use of surfaces for automatically guiding loops to position them into a predetermined position.

The disclosed arterial chambers for hemodialysis may include a cap with a blood inlet port for conveying an intended patient's blood into the arterial chamber, an auxiliary port configured to provide fluid access to the arterial chamber, and a needleless access port configured to couple to a needleless syringe. The needleless access port may be configured for administering a substance to an interior of the arterial chamber from the needleless syringe and/or for withdrawing blood from the interior of the arterial chamber into the needleless syringe. Various tubing sets, hemodialysis systems, and other components, systems, and methods are also disclosed.

A dialysis machine has a balancing system with a balancing chamber for a volumetrically exact supply and removal of dialysis solution to and from a dialyzer fluidically connected to the balancing system in operation; a water inlet system connected to the balancing system for the supply of fresh dialysis liquid, with the water inlet system having an apparatus for degassing water that is connected to an air separator of the dialysis machine, with a first subsection of the air separator serving as a mixing chamber and being connectable to at least one concentrate source via at least one concentrate line and being in fluid communication with the balancing system via at least one dialysate line, wherein the filling volume of a balancing chamber corresponds to or exceeds the sum of the volume of the mixing chamber and the inner volume of the dialysate line.

A primer may be used with IV catheter systems. The primer may be positioned along the tubing of an extension set such that the primer divides the IV catheter system into a downstream portion and an upstream portion. The primer may vent air from both the upstream and downstream portions to allow blood to flow up to the primer while also allowing priming solution to flow down to the primer. As a result, the catheter may be inserted into the patient's vasculature without first priming the catheter. Once the air has been vented from the upstream and downstream portions of the IV catheter system, the primer may be actuated to open a fluid pathway through the primer. With the fluid pathway opened, the priming solution may commence flowing towards the patient's vasculature thereby flushing the blood from the IV catheter system.