Abstract: An adhesion-preventive film is provided that is excellent in flexibility and can prevent cracks from occurring. The adhesion-preventive film contains a copolymer of lactide and caprolactone. The lactide and the caprolactone of the copolymer has a mole ratio in the range of 65:35 to 80:20. Even when this adhesion-preventive film is used in a curved state in vivo or is wound around an affected part such as a tendon, for example, it can provide an adhesion-preventive function for a sufficiently long period without cracking.

Abstract: A rotator 2 is supported rotatably on a base 1, and a roller 7 is supported rotatably at the outer periphery of the rotator 2. A pressing member 4 has a circular arc pressing surface 4a and can be located selectively in a retracted position where a groove-shaped space 8 is formed between the pressing surface and the rotator and in a proximity position where the pressing surface is closer to the rotator. When the pressing member is in the retracted position, a pump tube can be inserted in the groove-shaped space. The pressing member is moved to the proximity position with the pump tube being held, and then the rotator is rotated, so that the pump tube is pressure-driven by the roller. The injection device with a simple structure easily can extract almost the entire semi-solidified nutritional supplement from a nutritional supplement container and inject it into a patient.

Abstract: An example of the closed-type blood reservoir of the invention is furnished with an outer shell in which a space is formed within its interior, a flexible septum that is interposed between a blood storage chamber shell and a volume adjustment chamber shell and that divides the space into a blood storage chamber for storing blood and a volume adjustment chamber for storing volume adjustment liquid, a blood inlet port, a blood outlet port, and a blood storage chamber air discharge port that are provided in the blood storage chamber shell such that they are in communication with the blood storage chamber, and a volume adjustment liquid port that is provided in the volume adjustment chamber shell such that it is in communication with the volume adjustment chamber, for injecting and ejecting the volume adjustment liquid into and away from the volume adjustment chamber, wherein the blood inlet port and the blood outlet port each are provided tangentially to the inner surface of the blood storage chamber shell such

Abstract: An automatic priming method in which an arterial-side chamber is maintained in a normal position during priming, as in a case of dialysis treatment, and in which forward and backward rotations of a blood pump are employed, and a speed of rotation, in particular, backward rotation, is adjusted to be low, so that air or the like is reliably prevented from entering a dialyzer. The priming method for use in a blood purification circuit in which priming is conducted by supplying physiological saline into a circulation circuit formed by connecting an arterial blood circuit with a venous blood circuit includes filling the venous blood circuit with a priming solution (physiological saline), discharging the priming solution for cleaning the arterial blood circuit, conducting a treatment in a direction opposite to the overflow step, which may be followed by a forward direction re-circulation step, and re-circulating in a forward direction.

Abstract: The present invention provides a communication member for a medical container capable of allowing communication between the inside and the outside of a container body containing a liquid in a state of being fixed to the container body. The communication member includes: a valve 2 having an insertion hole 2a; a tubular body 3 supporting the valve 2; and a closing film 4 for closing a bore of the tubular body 3 in the bore and in the vicinity of the valve 2. The tubular body 3 and the closing film 4 are molded integrally. A groove 4a that passes through the center of the closing film 4 is formed on either a surface of the closing film 4 on the valve 2 side or a surface opposite to the valve side.

Abstract: A medical heat exchanger includes a thin tube bundle 2 in which a plurality of heat transfer thin tubes 1 for letting heat medium liquid flow therethrough are arranged and stacked, seal members 3a to 3c sealing the thin tube bundle while allowing both ends of the heat transfer thin tubes to be exposed and forming a blood channel 5 which allows blood to flow therethrough so that the blood comes into contact with each outer surface of the heat transfer thin tubes; a housing 4 containing the seal members and the thin tube bundle and provided with an inlet port 8 and an outlet port 9 of the blood positioned respectively at both ends of the blood channel; and a pair of heat transfer thin tube headers 6, 7 forming flow chambers 14a, 14b, 15a, 15b that respectively surround both ends of the thin tube bundle and having an inlet port 6a and an outlet port 7a of the heat medium liquid.

Abstract: In a heat exchanger including a plurality of tubes 1 through which a first fluid passes, a housing 2 in which the tubes 1 are installed, and sealing members for sealing a second fluid that flows over surfaces of the tubes 1, the housing 2 includes an inlet 4 for introducing the second fluid therein and a first outlet 5 and second outlets 6 for discharging the second fluid, and the sealing members include a first sealing member 3a positioned on one of end sides of the tubes 1, a second sealing member 3b positioned on the other end side of the tubes 1, and a third sealing member 3c positioned between the first and second sealing members 3a and 3b. The third sealing member 3c is provided so that a gap 7 is provided between the first sealing member 3a and the third sealing member 3c while another gap 7 is provided between the second sealing member 3b and the third sealing member 3c, and that a flow path for the second fluid is formed therein. The second outlets 6 are provided so as to be connected to the gaps 7.

Abstract: A medical container (1) includes a bag-like container body (10) made up of two flexible sheets (12a, 12b). At least one of a pair of long-side sealed areas (11La, 11Lb) formed by the two sheets being bonded together is provided with a sealed protruding portion (20a, 21a, 20b, 21b) protruding toward the other long-side sealed area such that the spacing between the pair of long-side sealed areas is locally narrowed. A crease (30a, 31a, 30b, 31b) passing through the sealed protruding portion is formed in the sheets when a liquid substance has been injected into the container body in a volume greater than or equal to 10% of a defined volume of the container body and the medical container is hung. Accordingly, it is possible to know the exact amount of a liquid substance in the container by using a scale provided on the sheets constituting the container even if a crease is formed in the sheets due to the liquid substance being in the container.

Abstract: Provided is a hemodialyzer for preventing beforehand any medical accident such as air inclusion or blood loss during a medical treatment by detecting even a minute connection failure, if any.

Abstract: Provided is a roller pump that can easily install/remove an elastic tube and appropriately control a discharge flow rate. The roller pump includes a pump slide that is connected to a pump block cover via two slider links and restricts an arrangement of the elastic tube by an inner peripheral surface; a pump block cover that operates an opened state and a closed state of the pump slide; a first slider link that has a substantially circular contact surface in contact with the second slider link, having one end rotatably connected to the pump slide using a support pin and the other end rotatably connected to the pump block cover using a support pin; and a second slider link that has a substantially circular contact surface in contact with the first slider link and is rotatably connected to a fixed part of a base using a support pin.

Abstract: A probe for measuring oral pressure according to the present invention includes: a balloon 1; a hollow tube 3 that has a first opening portion 3b and a second opening portion 3c and is connected to the balloon so that the first opening potion 3b communicates with an inside of the balloon 1; and a port member 20 with a valve 13 connected to the hollow tube 3 so as to block the second opening portion 3c. The probe for measuring oral pressure according to the present invention preferably further includes a hard ring 8 mounted on a portion between an inflated portion and an attaching portion of the balloon 1. The valve 13 may be a disk-shaped valve with an insertion hole 13a, for example.

Abstract: A separation container that can prevent the contamination with unnecessary components is provided. A separation container 1 for separating a separation subject from a sample by causing the separation subject to gather on the bottom thereof by centrifugation includes a container main body 11 and a dividing portion. The container main body 11 is a tubular container elongated in the axial direction with an upper end thereof being open and a lower end thereof being the bottom. The dividing portion has a partition 12 formed along the axial direction of the container main body, and an inner space of the container main body 11 is divided into a sample supply chamber 14 and a separation subject discharge chamber 15 by the partition 12. The sample supply chamber 14 and the separation subject discharge chamber 15 communicate with each other via a through hole 13 formed in a lower portion of the partition 12.

Abstract: An upper limb restraint device 1 comprises a base 2 placed on the top surface of an upper limb rest 51, an upper limb rest engagement part 3 provided at an end of the base 2 close to the wrist joint 104 of an upper limb 100, an elbow joint supporting part 4 provided at the other end of the base 2 close to the elbow joint 102, and two strings 5 and 6. The upper limb rest engagement part 3 is formed in the shape of a pocket capable of receiving an end of the upper limb rest 51. The elbow joint supporting part 4 is formed to cover the elbow joint 102 of the upper limb 100 laid on the upper limb rest 51. The root ends of the strings 5 and 6 are attached to the elbow joint supporting part 4. The strings 5 and 6 are bound around the upper limb rest 51 with the elbow joint supporting part 4 covering the elbow joint 102.

Abstract: Teeth 31 and 32 are formed on opposite sides of a strip portion 2 of a band 1 in the width direction. Protruding portions 51-54 are formed in a proximal portion 20 of the strip portion 2 so as to respectively engage the teeth 31 and 32 on the opposite sides of the strip portion 2 in the width direction. A release portion is provided between the protruding portions 51-54 for allowing a portion of the distal portion 22 and the intermediate portion 21 of the strip portion 2 where the teeth 31 and 32 are formed to be moved into and out of a space between the protruding portions 51-54.

Abstract: A single needle hemodiafiltration apparatus is provided. The single needle hemodiafiltration apparatus includes circuits for blood supply from a patient and blood return to a patient, a dialysis fluid supply system for supplying a dialysis fluid, and a system for controlling the blood flow and dialysis fluid flow in a separation device which is equipped to perform filtration and back-filtration operations. A controller is provided that controls, in a series of coordinated operations, the flow of blood from the patient into the separation device, the flow of filtration fluid and back filtration fluid, and the return of blood to the patient.

Abstract: A blood filter device has a housing that includes: a head portion (2) provided with a blood inlet (5) and forming an upper structure of the housing, a filtration portion (3) positioned below the head portion and forming a middle structure of the housing, and a bottom portion (4) disposed below the filtration portion and provided with a blood outlet (7); and a filter (8) mounted in a cavity of the filtration portion and partitioning a cavity of the housing into a head portion side and a bottom portion side. The filter is formed of a filter sheet folded to have a plurality of pleats, and disposed so that ridgelines of the plurality of pleats traverse respectively the cavity of the filtration portion in parallel. The bottom portion has a conical portion (4a) on the inner bottom face protruding downward to form a conical face.