A system and methods of using a multi-lumen catheter and a blood pump to increase cardiac output and blood oxygenation are described. The system diverts deoxygenated blood from the right atrium to the left atrium, through the atrial septum. The catheter is adapted for simultaneously pumping blood to and from a patient's heart. A gas exchanger may be used as part of the system to remove CO.sub.2 and add o.sub.2 to the blood that is pumped via the system. Components or portions of the system may be implantable in the patient.

A medical fluid management assembly includes: a pneumatic manifold including a plurality of pneumatic passageways and a plurality of pneumatic connectors; a pump and valve engine including a plurality of valve chambers and at least one pump chamber, the pump and valve engine including a plurality of pneumatic connectors mated sealingly and releaseably with the pneumatic connectors of the pneumatic manifold, the pump and valve engine further including a plurality of fluid connectors; and a fluid manifold including a plurality of fluid pathways and a plurality of fluid connectors mated sealingly and releaseably with the fluid connectors of the pump and valve engine.

Described are systems for performing a medical procedure at a treatment site in a cerebral vessel of a patient. The system includes a catheter and an inner member sized to slide within the catheter lumen. The inner member defines a single lumen and has a distal portion and a distal-most end having a distal opening, the distal portion having a first outer diameter that tapers distally to a second outer diameter that is smaller than the first outer diameter. A flexibility of the distal portion decreases smoothly from a flexibility at the second outer diameter to a flexibility at the first outer diameter when the system is in an advancement configuration. The system is sufficiently flexible that, when in the advancement configuration, the system is configured to be advanced distal to a petrous portion of an internal carotid artery.

Medical fluid management assembly includes: a pneumatic manifold including multiple plates forming pneumatic passageways, a pneumatic valve chamber and a pneumatic pump chamber, the valve chamber in pneumatic communication with at least one passageway, the pump chamber in pneumatic communication with at least one passageway; and a fluid manifold including multiple fluid pathways, a fluid valve chamber in selective fluid communication with a fluid pump chamber and at least one fluid pathway, wherein (a) the pneumatic valve chamber and the fluid valve chamber are mated together to compress a membrane and (b) the pneumatic pump chamber and the fluid pump chamber are mated together to compress a membrane, wherein at least one of the pneumatic valve chamber or the pneumatic pump chamber extends from the at least one plate, or the fluid valve chamber or the fluid pump chamber extends from the fluid manifold to aid in compressing the membranes.

Provided is a tube set which is capable of easily determining whether a holder has been mounted when the holder is mounted on a housing. The tube set, which is provided in a tube pump that feeds a liquid, includes a pump tube and a holder. The holder has a flexible flat plate and includes first engagement portion and second engagement portions that arc located away from each other in a first direction. The first engagement portion and second engagement portions are configured to be fitted into first engagement groove and second engagement grooves formed in the housing, respectively, when the holder is pushed into the housing in a state of being bent in a thickness direction. The holder is elastically restored to be attached to the housing when the first engagement portion and the second engagement portions are fitted into the respective first engagement groove and the second engagement grooves, respectively. The holder has a flexural modulus of 500 MPa or more and 3500 MPa or less.

The present disclosure relates to an effluent bag for collecting accumulated blood treatment effluent. The effluent bag comprises a closeable effluent opening or connection to an exterior of the effluent bag. The disclosure further relates to methods, a blood treatment apparatus, and a discharge hose system.

A processor of a medical device configured to communicate with a remote server can be programmed to protect the medical device from exposure to unauthorized or malicious software. A system or method to implement this form of protection can include, for example, at least one processor on the medical device, a control software module that controls the operation of the medical device and is executable on the processor, a data management module that manages data flow to and from the control software module from sources external to the medical device, and an agent module that has access to a limited number of designated memory locations in the medical device. In addition, a hemodialysis apparatus can be configured to operate in conjunction with an apparatus for providing purified water from a source such as a municipal water supply or a well. A system for controlling delivery of purified water to the hemodialysis apparatus can comprise a therapy controller of the hemodialysis apparatus configured to communicate with a controller of a water purification device, and a user interface controller of the hemodialysis apparatus configured to communicate with the therapy controller, and to send data to and receive data from a user interface.

A blood magnetic stimulation device includes a magnetic stimulation unit that has a stimulating coil for being connected to a blood delivering unit or directly worn by a user. The stimulating coil is further connected to a pulse-generating unit that outputs a pulse current to excite the stimulating coil, so as to use electromagnetic pulses to apply strong yet transient magnetic stimulation to blood passing through the magnetic stimulation unit or to blood in the user's subcutaneous vessels, thereby providing magnetic treatment for viremian and related diseases. As compared to the existing blood treating devices, the magnetic stimulation provided by the blood magnetic stimulation device incurs no sharp pain and uncomfortableness, and is safer and more acceptable to patients.

The invention relates to a medical fluid cassette and a medical hose set having a medical fluid cassette for receiving and/or carrying a medical fluid. The invention relates in particular to a blood hose set having a medical fluid cassette for the extracorporeal blood treatment. An easily manufactured insert having a clot filter is proposed, this insert being inserted or pushed into a receptacle, for example, a groove, in the interior of a chamber of the housing body of the medical fluid cassette.

A negative-balanced isolated pelvic perfusion method, in which a drug is administered into the closed pelvis while keeping the volume of suction from the vein larger than that of injection into the artery, does not require allogeneic blood transfusion. A perfusion device is for recovering a liquid containing a drug and/or blood from a tube connecting to the inferior vena cava and for injecting the liquid obtained into a tube connecting to the artery, provided with a unit for closing the inside of the pelvis by including a unit for blocking the artery from the heart to the pelvis, a unit for blocking the inferior vena cava from the pelvis to the heart, and a unit for blocking a blood flow from the pelvis to the lower limbs. The perfusion device is provided with a pelvic perfusion unit equipped with a reservoir, an autotransfusion unit, and a dialysis unit.