A blood treatment device includes an extracorporeal blood circuit, a dialyzer and a dialysis fluid circuit. The extracorporeal blood circuit has an arterial portion, a venous portion, an air detector configured to monitor whether air is present in the venous portion, at least one blood pump configured to pump blood through the extracorporeal blood circuit, a venous hose clamp configured to selectively clamp or release the venous portion, a user interface, and a control unit. When the control unit receives information from the air detector that there is air in the venous portion, the control unit is configured to stop the blood pump, close the venous hose clamp, raise an alarm, and display on the user interface instructions for removing air in the venous portion and displaying status reports about the removal of air, and carry out automatic removal of air from the venous portion on a user-initiated basis.

An air trap chamber is provided with a chamber body and a filter. An introduction pipe of the chamber body is provided so as to extend to the inside of the chamber body , and an inlet port which is an end opening of the introduction pipe is provided, on the inner circumferential surface of the chamber body, so as to be directed toward the circumferential direction. The filter is provided inside the chamber body, and covers an outlet port of the chamber body. Openings are formed, at multiple stages along the center axis direction, in the cylindrical portion of the filter. An opening at an upper stage on the ceiling portion side of the filter has a circumferential width greater than that of an opening at a lower stage on the outlet port side.

A blood purification apparatus that accurately calculates the colloid osmotic pressure of a patient's blood. A dialyzer included in the blood purification apparatus has thereinside blood flow routes and dialysate flow routes that are separated from each other by hollow fibers. An ultrafiltration pump draws out water from the blood in the blood flow routes through the hollow fibers into the dialysate flow routes. Four detecting units measure the pressures of liquid flowing into the blood flow routes, the liquid discharged from the blood flow routes, dialysate flowing into the dialysate flow routes, and the dialysate discharged from the dialysate flow routes. The pressures at the four positions, the transmembrane pressure difference can be calculated. The blood flow routes are filled with a priming solution, and the transmembrane pressure difference (TMPa) is measured. Subsequently, the blood flow routes are filled with the patient's blood, and the transmembrane pressure difference (TMPb) is measured. Referencing TMPa and TMPb, the colloid osmotic pressure of the patient's blood can be calculated. Referencing colloid osmotic pressure, the plasma total protein can be calculated. Referencing plasma total protein, the patient's state of nutrition can be estimated.

A blood purification apparatus capable of performing pre-substitution and post-substitution simultaneously is provided. A patient's blood flows through an arterial blood circuit and reaches a dialyzer. The blood purified by the dialyzer flows through a venous blood circuit and returns into the patient. A first substitution pump delivers substitution fluid through a substitution line to a branching point. A pre-substitution line connects the branching point and the arterial blood circuit to each other and is provided with a second substitution pump at a halfway position thereof. A post-substitution line connects the branching point and the venous blood circuit to each other and is provided with a check valve at a halfway position thereof. When the two pumps are activated simultaneously, the substitution fluid is supplied to the arterial blood circuit (pre-substitution). When only the first substitution pump is activated, the substitution fluid is supplied to the venous blood circuit (post-substitution). When the flow rate of the second substitution pump is set higher than the flow rate of the first substitution pump, pre-substitution and post-substitution are performed simultaneously.

A blood purification apparatus that includes a blood circuit including an arterial blood circuit and a venous blood circuit and having a flow route that allows a patient's blood to extracorporeally circulate from a distal end of the arterial blood circuit to a distal end of the venous blood circuit; a blood purifier connected to a proximal end of the arterial blood circuit and to a proximal end of the venous blood circuit and that purifies the blood flowing through the blood circuit; an air-trap chamber connected to the blood circuit and that traps bubbles contained in liquid flowing in the flow route of the blood circuit; and a blood pump provided to the arterial blood circuit and being capable of delivering the liquid within the blood circuit. An upstream bubble-detecting unit attached to a position of the blood circuit on an upstream side with respect to the air-trap chamber and that detects bubbles contained in the liquid flowing in the blood circuit; and a control unit that reduces, at the detection of any bubbles by the upstream bubble-detecting unit, a flow rate of the liquid flowing into the air-trap chamber.

A dry disconnect device including a first portion defining an outlet and an outlet portion of a fluid pathway and a female valve disposed within the first portion having an extended position, including the female valve being configured to seal the outlet portion, and a retracted position. A second portion defining an inlet and an inlet portion of the fluid pathway is lockingly engageable with the first portion. A male valve is disposed within the second portion including a male valve transition member configured to translate the male valve from an extended position to a retracted position including the male valve being configured to seal the inlet portion. The extended position of the male valve causes the female valve to transition from the extended position to the retracted position and causes the outlet portion and the inlet portion of the fluid pathway to be in fluid communication with each other.

An occlusion assembly for compressing a pair of collapsible tubes comprises a frame comprising a tubing guide configured for positioning the collapsible tube. The occlusion assembly also comprises a tubing occluder mounted to the frame with an occluding member constructed and positioned to controllably occlude or release occlusion of the collapsible tube. A door mounted to the frame is positioned to cover at least a portion of the collapsible tube and tubing occluder when closed and provide user access when open. The assembly includes a retainer mechanism engaged by the door when the door is closed to permit operation of the tubing occluder when the door is closed and retain the tubing occluder in a non-occluding configuration when the door is opened.

A dry disconnect device including a first portion defining an outlet and an outlet portion of a fluid pathway and a female valve disposed within the first portion having an extended position, including the female valve being configured to seal the outlet portion, and a retracted position. A second portion defining an inlet and an inlet portion of the fluid pathway is lockingly engageable with the first portion. A male valve is disposed within the second portion including a male valve transition member configured to translate the male valve from an extended position to a retracted position including the male valve being configured to seal the inlet portion. The extended position of the male valve causes the female valve to transition from the extended position to the retracted position and causes the outlet portion and the inlet portion of the fluid pathway to be in fluid communication with each other.

A medical fluid management assembly includes a pneumatic manifold, a pump and valve engine, and a fluid manifold. The pneumatic manifold includes a plurality of pneumatic passageways and a plurality of pneumatic connectors. The pump and valve engine includes a plurality of valve chambers, at least one pump chamber, and a plurality of pneumatic connectors mated sealingly and releasably with the pneumatic connectors of the pneumatic manifold. The pump and valve engine also includes a plurality of fluid connectors. The fluid manifold includes a plurality of fluid pathways and a plurality of fluid connectors mated sealingly and releasably with the fluid connectors of the pump and valve engine.

A method and system for infusing medical liquid with gasses, the system comprising a gas source, a vacuum pump, a temperature-controlled container including a fluid reservoir coupled to the gas source and the vacuum pump, a heating and cooling system, and a sonicator, and a controller configured to de-gas a liquid in the fluid reservoir by activating the vacuum pump, re-gas the liquid in the fluid reservoir by releasing gas from the gas source to the fluid reservoir via a first fluid line, and deliver the re-gassed liquid from the fluid reservoir to a catheter via a second fluid line.