Abstract: A plug body for chemical container capable of preventing the contact thereof with chemical and preventing ruptured film from failing into the chemical, comprising a valve (1) having an insert hole (3) formed at the center thereof a cover (2) for holding the valve (1) by covering at least the upper peripheral edge of the valve (1), and a locking means for locking an insert body to the cover (2) by using the edge part of the cover (2) having a fitting hole formed therein when the insert body is inserted into the insert hole (3), wherein the rear surface peripheral part of the valve (1) is held by a pedestal part (5), and a film (4) covering the rear surface of the valve is disposed on the upper surface of the pedestal part (5).

Abstract: A septum (1) is held in the cavity of a cover (6) and mounted on a pedestal (7) forming part of a flow channel, and comprises a main body having a through passageway and compression ribs formed in the sides thereof. In the main body, the vertical diameter of the cross section orthogonal to the through passageway is longer than the transverse diameter, and the through passageway includes a vertical diameter direction slit (4) formed in the vicinity of the outer end surface of the main body, and a hole (5) that is formed in a region extending from the slit to the inner end surface of the main body and whose cross section is spindle-shaped having a longer axis extending in the vertical diameter direction. The compression ribs are formed in the opposite sides of the main body in the transverse diameter direction, and the cavity of the cover is of circular cross section whose diameter is shorter than the outer surface spacing between the compression ribs.

Abstract: The peritoneal function of a peritoneal dialysis patient is examined to evaluate the condition of the patient. An examining method comprises a step of alternately repeating introduction/drainage of a predetermined quantity of a peritoneal dialyzing fluid of an osmotic pressure and introduction/drainage of a predetermined quantity of another peritoneal dialyzing fluid of an osmotic pressure different from the former one, a step of examining the drain to determine the quantity of peritoneal dialyzing fluid staying in the abdominal cavity of the patient and the concentration of a solute of interest, a step of conducting a peritoneal equilibrium test, and a step of conducting a blood test to grasp the change of the state of the blood caused by the introduction and drainage. The blood test step is executed only once.

Abstract: An apparatus for blood dialysis composed at least of a hemodialyzer (a) whereby blood is brought into contact with a dialysate via a semipermeable membrane and thus purified; a blood circulation system (b) composed of a blood circuit in the arterial side whereby blood is taken out from a patient and flown into the hemodialyzer and another blood circuit in the venous side whereby the blood flown out from the hemodialyzer is returned to the patient; a dialysate supplying/discharging system (c) for supplying and discharging the dialysate composed of a dialysate-supply line for supplying the dialysate to the hemodialyzer and a dialysate-discharge line for discharging the dialysate flown out from the hemodialyzer, and a means (d) of controlling the back-filtration speed. Owing to this constitution, individual steps from the preparation of the dialysis (treatment) to the completion of the treatment and the change from a specific step to the next step can be safely, surely and quickly carried out in most cases.

Abstract: A plug body for chemical container capable of preventing the contact thereof with chemical and preventing ruptured film from falling into the chemical, comprising a valve (1) having an insert hole (3) formed at the center thereof, a cover (2) for holding the valve (1) by covering at least the upper peripheral edge of the valve (1), and a locking means for locking an insert body to the cover (2) by using the edge part of the cover (2) having a fitting hole formed therein when the insert body is inserted into the insert hole (3), wherein the rear surface peripheral part of the valve (1) is held by a pedestal part (5), and a film (4) covering the rear surface of the valve is disposed on the upper surface of the pedestal part (5).

Abstract: A connector system for sterile connection includes a male type connector having a tube connecting portion at a rear end portion thereof, a protective cap for the patient side connector, an inner cap held in the protective cap and including a ring-shaped portion that supports a disinfectant-impregnated member therein, and a female type connector including an outer cylinder and an inner cylinder fixed at one end of the outer cylinder, where the inner cylinder includes an internal end portion located inside the outer cylinder and an external end portion exposed outside the outer cylinder. When the protective cap is fitted with the male type connector, the disinfectant-impregnated member contacts with the male type connector. When the protective cap is removed therefrom, the inner cap becomes retained in the male type connector.

Abstract: In a method of configuring a blood circuit for medical application, one unit component is selected for each of the divided unit sections and the selected unit components are combined to configure a blood circuit component. A blood circuit system database in which data with respect to the unit sections and unit components are stored is used. On the basis of the database, the selected unit component input to the computer. An assembly drawing of the blood circuit obtained by combining the selected unit components, a full length and an amount of filled blood are displayed on a display by using the database. When the displayed assembly drawing etc. is not fit for the desired specification, the selection of the unit component is changed, so as to display again the assembly drawing etc. of the blood circuit.

Abstract: A rotary connector with valve, comprising first and second connector members (1, 2) having connector terminal parts (5, 6) and fitting parts (7, 8) with hollows (3, 4) as fluid passages formed therein and a valve member (12), wherein the first and second connector members are rotably connected to each other by fitting the fitting parts thereof to each other and the valve member is stored in a valve storage part (11) formed in the fitting part, valve pressing parts (14, 15) are provided on the first and second connectors (1, 2) on the side of the valve storage part, and at least a part of the valve member is pressingly held between the both valve pressing parts to hold a sealability, and a frictional force acting between the both valve pressing parts and the valve member is set so as to come within such a range that the first and second connector members can be rotated each other, whereby a structure allowing an easy assembly and an absorption of the twist of a line can be provided.

Abstract: A mixing/charging port for medical treatment in which no air bubble is retained inside thereof even at the time of priming, and which is capable of infusing a drug solution or transfusing blood into a patient safely.

Abstract: A turbo blood pump having a small size, that is, a small amount of blood to be filled and capable of adjusting and maintaining the slight amount of flow, and a turbo blood pump in which hemolysis is not likely to occur even if it is used at a practically high rotational speed necessary to obtain a predetermined discharging ability. The turbo blood pump to be used includes a housing having an inlet port and an outlet port; and an impeller disposed rotatably in the housing; wherein the impeller includes at least a rotation shaft and an annular connection portion to which the plural vanes are attached. The vane is manufactured so that an inlet side part is in the skew position with respect to an outlet side part.

Abstract: A hemodialyzing unit includes a dialytic fluid supply line for feeding a dialytic fluid from a dialytic fluid supply/discharge unit to a dialyzer, a dialytic fluid discharge line for feeding a dialytic fluid discharged from the dialyzer to the dialytic fluid supply/discharge unit, and a bypass line for connecting both lines at an intermediate portion of each. A flow rate adjusting member is provided to a downstream supply line between a coupling portion for coupling the dialytic fluid supply line to the bypass line and the dialyzer. A wider range of treatments such as CHD (or CHDF), SHD (or SHDF), and HD (or HDF) can be conducted without employing a device for the exclusive use of the CHD or CHDF.

Abstract: A first sensor (13-1), the mounting position of the first sensor (13-1) being recognized as a counting number of instruction pulses to a pulse motor (3), is arranged along a plate (11) with slits of an encoder at a portion between a position where a pushing holder (7) is connected to a plunger (9) for the liquid infusion, and a start position where the pushing holder (7) is separated from the plunger (9). A counting means (16) for counting encoder pulses from the encoder, is reset when a first sensor (13-1) is detected by a position detecting device (14) moved together with the pushing holder (7), and started to count the encoder pulses according to the movement of the pushing holder (7). A time to complete the liquid infusion is calculated by using a distance between the position where the plunger (9) is connected to the holder (7) and a liquid infusion finish position proper to the syringe, and a predetermined liquid infusion speed.

Abstract: A mixing/charging port for medical treatment capable of reliably absorbing air bubbles. The mixing/charging port for medical treatment includes a disc-like valve having an insertion hole at the center, a seating for supporting the lower part of the periphery of the valve with the center of the rear surface side of the valve not supported, and a cover for restraining the valve by covering at least the upper part of the periphery of the valve with the center on the front side surface of the valve left uncovered, wherein a fitting hole defined by an inner periphery of the cover works as an anchor for anchoring an insertion body to the mixing/charging port by fitting the insertion body to the fitting hole when the insertion body is inserted into the insertion hole; and the tip of the depressed part of the valve is brought into contact against the inner bottom surface of the seating when the valve is depressed by the insertion member.

Abstract: A connector system for sterile connection includes a male type connector having a tube connecting portion at a rear end portion thereof, a protective cap for the patient side connector, an inner cap held in the protective cap and including a ring-shaped portion that supports a disinfectant-impregnated member therein, and a female type connector including an outer cylinder and an inner cylinder fixed at one end of the outer cylinder, where the inner cylinder includes an internal end portion located inside the outer cylinder and an external end portion exposed outside the outer cylinder. When the protective cap is fitted with the male type connector, the disinfectant-impregnated member contacts with the male type connector. When the protective cap is removed therefrom, the inner cap becomes retained in the male type connector.

Abstract: A turbo blood pump having a small size, that is, a small amount of blood to be filled and capable of adjusting and maintaining the slight amount of flow, and a turbo blood pump in which hemolysis is not likely to occur even if it is used at a practically high rotational speed necessary to obtain a predetermined discharging ability. The turbo blood pump to be used includes a housing having an inlet port and an outlet port; and an impeller disposed rotatably in the housing; wherein the impeller includes at least a rotation shaft and an annular connection portion to which the plural vanes are attached. The vane is manufactured so that an inlet side part is in the skew position with respect to an outlet side part.

Abstract: A turbo blood pump includes a housing 1 having a pump chamber 2, an inlet port 3, and an outlet port 4, an impeller 5 disposed rotatably in the pump chamber, an upper bearing 9 and a lower bearing 10 supporting the impeller rotatably, and a driving force transmitting unit for driving the impeller to rotate. The upper bearing is supported at a position in the pump chamber below the inlet port, so that a cross-sectional area of the pump chamber in a plane including an upper end of the upper bearing and being orthogonal to a shaft of the impeller is larger than a cross-sectional area of a flow path of the inlet port at a portion where the inlet port is coupled to the pump chamber, and thus obstruction with respect to blood flow by the upper bearing is of such a degree as to be permissible from a practical viewpoint, while an impeller is supported by upper and lower bearings. Thereby, the pump is less likely to cause problems of blood stagnation and thrombus formation.

Abstract: In a method of configuring a blood circuit for medical application, one unit component is selected for each of the divided unit sections and the selected unit components are combined to configure a blood circuit component. A blood circuit system database in which data with respect to the unit sections and unit components are stored is used. On the basis of the database, the selected unit component input to the computer. An assembly drawing of the blood circuit obtained by combining the selected unit components, a full length and an amount of filled blood are displayed on a display by using the database. When the displayed assembly drawing etc. is not fit for the desired specification, the selection of the unit component is changed, so as to display again the assembly drawing etc. of the blood circuit.

Abstract: A mixing/charging port for medical treatment capable of reliably absorbing air bubbles. The mixing/charging port for medical treatment includes a disc-like valve having an insertion hole at the center, a seating for supporting the lower part of the periphery of the valve with the center of the rear surface side of the valve not supported, and a cover for restraining the valve by covering at least the upper part of the periphery of the valve with the center on the front side surface of the valve left uncovered, wherein a fitting hole defined by an inner periphery of the cover works as an anchor for anchoring an insertion body to the mixing/charging port by fitting the insertion body to the fitting hole when the insertion body is inserted into the insertion hole; and the tip of the depressed part of the valve is brought into contact against the inner bottom surface of the seating when the valve is depressed by the insertion member.

Abstract: A mixing/charging port for medical treatment capable of cleanly wiping out a residual liquid, residual blood, or the like. The mixing/charging port includes a disk-like valve having an insertion hole at the center, a seating for supporting a lower part of the periphery of the valve, and a cover for restraining the valve. A fitting hole defined by an inner edge portion of the cover works as an anchor for anchoring an insertion member to the mixing/charging port, the thickness of the center of the valve is larger than the thickness of the periphery of the valve, and the thickness of the edge portion of the cover provided with the fitting hole substantially corresponds to the difference between the thickness of the center of the valve and the thickness of the periphery of the valve.

Abstract: An infusion filter comprising a bundle of hydrophilic porous hollow fibers with the outside of both ends fixed with a potting material and a housing that has a liquid inlet port and a liquid outlet port and that is packed with the hollow fibers, wherein a filtration portion is provided between the liquid inlet port and the liquid outlet port, and wherein a packing rate of the hollow fibers packed in the housing is set in the range from 15 to 40%. With such a structure, the infusion filter having the great filtration capacity can be provided at low cost.