A manual clot aspiration and filtration system enables a method of removing a clot without general anesthesia and the expense of an operating room. An aspiration and filtration system for bodily fluid utilizes a syringe coupled with a filter unit to draw bodily fluid through the filter unit to collect debris on the filter. A flow valve may then be turned and the plunger depressed to force the filtered fluid back into the body. The filter may be configured to capture particles such as blood clots and plaque. The filter unit has a cover that can be removed for inspection and/or removal of the collected debris. When the cover is replaced, trapped air may be removed by turning the flow-valve to a purge direction and pressing the plunger into the syringe to force fluid back toward the filter unit to purge the trapped air through the purge valve.

A catheter device having a catheter (24) in which a rotating shaft (25) which is made at least partially from a magnetic material is arranged, and a separating device which contains an annular body (27) surrounding the rotating shaft and having a cavity containing a magnetic body (13′), the magnetic body being arranged downstream from a point at which the shaft (25) exits the catheter (24) which it surrounds with respect to the direction of flow of the fluid through the catheter.

The invention relates to a catheter device (100) comprising a catheter (68) for insertion into a living being and at least one lumen (69, 70, 74, 79) for guiding a fluid flow within a section of the catheter device, and comprising a valve for controlling a fluid flow, in particular through a catheter, having a valve control chamber (12, 12a), into which an inlet opening (1a) of an inlet channel (1) and an outlet opening (2a) of an outlet channel (2) open, and further having a closure element (5, 13, 17) which can be moved in the valve control chamber (12, 12a) in a controlled manner and which, in at least a first position (I), closes the outlet opening (2a), in at least a second position (II) closes the inlet opening (1a), and which, in at least a third position (III), keeps open a connecting channel between the inlet opening (1a) and the outlet opening (2a), a valve train (A, A′, B, B′, 3, 14, 18) being provided and optionally moving the closure element (5, 13, 17) to at least the first, second or third position, and the at least one lumen (68, 70, 74, 79) being fluidically connected to the inlet channel or the outlet channel.

A manual clot aspiration and filtration system enables a method of removing a clot without general anesthesia and the expense of an operating room. An aspiration and filtration system for bodily fluid utilizes a syringe coupled with a filter unit to draw bodily fluid through the filter unit to collect debris on the filter. A flow valve may then be turned and the plunger depressed to force the filtered fluid back into the body. The filter may be configured to capture particles such as blood clots and plaque. The filter unit has a cover that can be removed for inspection and/or removal of the collected debris. When the cover is replaced, trapped air may be removed by turning the flow-valve to a purge direction and pressing the plunger into the syringe to force fluid back toward the filter unit to purge the trapped air through the purge valve.

Apparatus and methods are described, including apparatus (20) for implanting in a heart of a human subject. The apparatus includes an interatrial anchor (22) shaped to define an opening (26) having a diameter of 4-8 mm, and a bag (24) in fluid communication with the opening of the anchor. The apparatus is shaped to fit within a right atrium of the heart of the subject, and has a capacity of between 4 and 20 cm3. Other applications are also described.

Disclosed are example embodiments of a dialysis machine having a frame, a cartridge cassette, one or more alignment-locking features, and an actuation mechanism. The frame is fixedly coupled to the dialysis machine, and the cassette is slidably coupled to the frame. The cassette can have one or more track structures, with each of the one or more track structures having a rotor and one or more rollers. The one or more alignment-locking features extend from the frame and are configured to be inserted into one or more alignment features of a disposable cartridge that functions to secure or release the disposable cartridge. The actuation mechanism is made to slide the cassette with respect to the one or more track structures.

Catheter blood pumps with an inlet cage, cannula, impeller assembly and a multiple lumen shaft that is coupled to a that provides connectors that connect to external components. First and second fiberoptic pressure sensors extend inside and along a length of the multi-lumen catheter. The first fiberoptic pressure sensor is longer than the second fiberoptic pressure sensor and extends longitudinally distal to the multi-lumen catheter to terminate at a distal end portion of the cannula, proximal to the inlet cage. The sensor heads of the first fiberoptic pressure sensor and the second fiberoptic pressure sensor are exposed to local environmental conditions. The sensor head of the second fiberoptic pressure sensor can terminate proximal to the impeller cage windows. A pressure differential identified by a difference in pressure provided by the first and second fiberoptic pressure sensors can be used to confirm proper placement during intravascular placement into the heart.

Catheter blood pumps with an inlet cage, cannula, impeller assembly and a multiple lumen shaft that is coupled to a that provides connectors that connect to external components. First and second fiberoptic pressure sensors extend inside and along a length of the multi-lumen catheter. The first fiberoptic pressure sensor is longer than the second fiberoptic pressure sensor and extends longitudinally distal to the multi-lumen catheter to terminate at a distal end portion of the cannula, proximal to the inlet cage. The sensor heads of the first fiberoptic pressure sensor and the second fiberoptic pressure sensor are exposed to local environmental conditions. The sensor head of the second fiberoptic pressure sensor can terminate proximal to the impeller cage windows. A pressure differential identified by a difference in pressure provided by the first and second fiberoptic pressure sensors can be used to confirm proper placement during intravascular placement into the heart.

A catheter device having a catheter (24) in which a rotating shaft (25) which is made at least partially from a magnetic material is arranged, and a separating device which contains an annular body (27) surrounding the rotating shaft and having a cavity containing a magnetic body (13), the magnetic body being arranged downstream from a point at which the shaft (25) exits the catheter (24) which it surrounds with respect to the direction of flow of the fluid through the catheter.

A disposable fluid pump is provided with a housing including first and second faces, with a sidewall extending between the first and second faces. The housing defines a chamber, with an inlet and an outlet in fluid communication with the chamber. An impeller is rotatably mounted within the chamber and includes a plurality of flexible vanes. Such a pump may be incorporated into a disposable fluid flow circuit that is adapted to be mounted on a durable hardware for processing a fluid. In such a fluid flow circuit, the fluid pump may be integrated into a cassette of the circuit or, alternatively, the inlet and outlet of the fluid pump may be directly connected to fluid flow conduits of the circuit.