Abstract: The medical needle device includes: a shield 4 including a substantially cylindrical portion 4a; a tube 13; a first hub 2 that is inserted into an inner bore of the shield movably in an axial direction. The rear end of the first hub 2 is connected with the tube 3. A rigid needle 1 is fixed to a front end portion of the first hub; and a hub movement controlling member 14 that is attached to the shield detachably. The hub movement controlling member 14 includes: a stopper portion 14a that can be inserted from the rear end side of the shield into an inner bore of the shield exsertably.

Abstract: A vial shield (1) has a shield main body (10) and a valve element (20). The shield main body (10) includes an annular top plate (11) that is to be laid on top of an upper surface of a stopper (86) that seals a mouth (83) of the vial bottle (80), a plurality of legs (15) extending downward from the top plate (11), and a plurality of claws (16) provided in the plurality of legs (15), the claws being engageable with the mouth (83) of the vial bottle (80). The valve element (20) blocks an opening at the center (12) of the top plate (11). A cut (22) passing through the valve element (20) in a vertical direction is formed in the valve element (20).

Abstract: A medical needle device includes a hub having an injection needle fixed at a top end thereof, and a substantially cylindrical sheath which is fit on the hub and having a pair of wings mounted on both sides thereof. The pair of wings are bent along the both sides of the sheath, overlapped and held together at a time of puncturing so that an inner peripheral surface of the sheath strongly presses an outer peripheral surface of the hub, thereby preventing movement of the hub caused by transfer of the hub relative to the sheath both in a rotational direction and a longitudinal direction. sheath has a plurality of protrusions provided on the inner peripheral surface thereof in a circumferential direction, the protrusions being spaced out from each other; and the outer peripheral surface of the hub abuts the protrusions.

Abstract: The present invention provides a blood purification apparatus and a blood purification circuit, by which a circuit can be shared by different modes for performing respective continuous blood purification methods, a structure of the apparatus performing the continuous blood purification methods can be simplified, and CHF, CHD, CHDF, and ECUM can be performed.

Abstract: A blood storage container suitable for quick and efficient production of a large amount of serum while ensuring high safety, and a method of separating blood and a regenerative medical process using the same are provided. A blood component separation storage apparatus is provided for separating a plurality of blood components of blood so as to be stored therein. The blood component separation storage apparatus includes a blood reservoir for holding the blood and a component storage part connected to the blood reservoir aseptically and in an air-tight manner. The blood reservoir contains an anticoagulant which suppresses coagulation of the blood. The blood reservoir has a serum producing function to remove coagulation factors from the blood to an extent enabling use in practical applications as a serum, and the component storage part stores each blood component generated by separation of the blood in the blood reservoir.

Abstract: A male member (1) includes a tubular member (10) and a cover (20) covering at least a tip (11) of the tubular member. A lateral hole (14) that communicates with a flow path (13) is formed in an outer peripheral surface of the tubular member. The cover includes an outer peripheral wall (21) that can be deformed elastically by compression and a head part (23) that is provided at one end of the outer peripheral wall. The head part includes an interior cavity (24) into which the tubular member is inserted, and a slit (25) is formed in an innermost part (24a) of the interior cavity. In a state where the outer peripheral wall is not deformed by compression, an inner peripheral surface of the interior cavity contacts closely with the outer peripheral surface of the tubular member so as to block the lateral hole, and the tip of the tubular member and the innermost part of the interior cavity are spaced apart from each other.

Abstract: When a hub (40) is in an initial position at which it is located on the front end side of an inner cavity of a shield (20), an inner needle (50) penetrates an outer needle (30) and protrudes from a leading end of the outer needle to the outside, and when the hub is in a retracted position at which it is located on the rear end side of the inner cavity of the shield, the inner needle is housed within the inner cavity of the shield. A first side hole (31) is formed in an outer circumferential face of the outer needle, and a second side hole (51) is formed in an outer circumferential face of the inner needle.

Abstract: An inner hub (9) with a needle attached to a tip thereof is housed in a cylindrical body (2). The inner hub (9) includes a through-hole (22) penetrating the inner hub (9) in a radial direction of the inner hub (9), and a recessed portion (23a) formed in an outer circumferential surface (23) of the inner hub (9). An opening of the through-hole (22) and the recessed portion (23a) are connected together in a circumferential direction of the inner hub (9). A liquid flowing out from the opening of the through-hole (22) is limited so that the liquid flows along the recessed portion (23a), and the flow of the liquid moving in the circumferential direction of the inner hub (9) is promoted. As a result, the removal of air bubbles in the circumferential direction of the inner hub (9) is promoted, whereby air bubbles can be prevented from remaining on the outer circumferential surface (23) of the inner hub (9).

Abstract: A blood circuit capable of automatically performing priming for safe treatments. The blood circuit includes: a hemofilter (56) purifying blood; a blood removal line that has an end connected to an inlet of the hemofilter (56) and that includes a first blood removal line (84), a second blood removal line (88), and a third blood removal line (89); a blood return line that has an end connected to an outlet of the hemofilter (56) and that includes the first blood return line (92) and the second blood return line (94); and an anticoagulant (bypass) line (90) reducing a difference between (a) a pressure of a priming fluid flowing in the blood removal line and (b) a pressure of the priming fluid flowing in the blood return line.

Abstract: A medical connector structure configured in such a manner that a first member body which constitutes a connector base and a second member body which consists of a different material from the first member body are formed by two-color injection molding. The first member body is a tube body which has a connector-side section having a structure connected to a mating section, and also has a tube-side section having on the surface thereof projections and recesses. The second member body is a tube body which allows a raw material to be filled into the portion in which the projections and recesses are provided and into which a raw material is filled so as to allow a tube body to be inserted. The tube-side section and the tube body are adhered together.

Abstract: An impeller is provided with a rotating shaft rotatably supported at the upper and lower ends thereof by an upper bearing and a lower bearing, a plurality of vanes connected to the rotating shaft on the inner circumferential edge side thereof, an annular coupling portion connecting outer circumferential edges of the vanes, and driven magnet portions provided in a lower portion of the annular coupling portion. The rotation of a rotor is transmitted to the impeller through magnetic coupling between the driven magnets and drive magnets provided to the rotor. The upper edge of each of the vanes has a bend point, and an angle ? formed by a peripheral upper vane edge and an angle ? formed by a central upper vane edge relative to the downward direction of the rotating shaft are both acute angles and have a relationship of ?<?. An inner wall surface of a housing in a region opposed to the upper edge of the vane has a shape following the upper edge of the vane.

Abstract: A weight measuring apparatus can ensure safety even if a trouble or deterioration of measurement accuracy occurs. The weight measuring apparatus (10) measures a weight of fluids and includes the followings. A first arm (110) has a first fitting (111) to fit a supply fluid container (20). A second arm (120) is connected to the first arm (110) and has a second fitting (121) to fit a filtrate container (30). A third arm (130) is connected to the second arm (120). A first measuring device (220) measures, as a first total weight, a total weight of the supply fluid container (20) and the filtrate container (30) based on a change of the second arm (120). A second measuring device (230) measures, as a second total weight, the total weight based on a change of the third arm (130). An alarm (300) alarms, when the first and second total weights have different values having a difference equal to or greater than a predetermined value.

Abstract: A blood storage container suitable for quick and efficient production of a large amount of serum while ensuring high safety, and a method of separating blood and a regenerative medical process using the same are provided. In a blood component separator 1 for separating collected blood into a plurality of blood components and preserving them, the separator 1 including a blood reservoir 10 for reserving the blood and a component storage part 20 aseptically connected in an air-tight manner to this blood reservoir 10, to the aforementioned blood reservoir 10 being imparted a serum producing function to remove coagulation factors from the blood to an extent enabling use in practical applications as a serum, and the aforementioned component storage part 20 storing each blood component generated by separation of the blood in the blood reservoir 10.

Abstract: Provided is a cell cryopreservation container which is provided with a plurality of storage chambers and enables efficient storage of cells in a definite capacity. The cell cryopreservation container (1) comprises a plurality of storage chambers (2), dividing areas (3), and communicating parts (4), wherein a front face part (11) is formed in one side in a third direction (TD) while a back face part (12) is formed in the other side in the third direction (TD). In the cell cryopreservation container (1), the front face part (11) has a convex and concave shape configured of the storage chambers (2) projecting toward one side in the third direction (TD) while the back face part (12) has a planar shape, and the length in a first direction (WD) of the dividing areas (3) exceeds the length in the first direction (WD) of the storage chambers (2).

Abstract: A liquid component collecting device capable of more easily collecting a liquid component. A liquid component collecting device (100) is provided with: a flexible cylindrical liquid component storage container (21) having an opening at one end thereof; a cylindrical first housing container (22) for housing the liquid component storage container (21) and having an opening at one end thereof; and a first cap (23) connected to the opening in the liquid component storage container (21) and fitted to the opening in the first housing container (22). A pressure regulating space (26) independent of the internal space of the liquid component storage container (21) is formed between the outer side of the liquid component storage container (21) and the inner side of the first housing container (22).

Abstract: A male member (1) includes a tubular member (10) and a cover (20) covering at least a tip (11) of the tubular member. A lateral hole (14) that communicates with a flow path (13) is formed in an outer peripheral surface of the tubular member. The cover includes an outer peripheral wall (21) that can be deformed elastically by compression and a head part (23) that is provided at one end of the outer peripheral wall. The head part includes an interior cavity (24) into which the tubular member is inserted, and a slit (25) is formed in an innermost part (24a) of the interior cavity. In a state where the outer peripheral wall is not deformed by compression, an inner peripheral surface of the interior cavity contacts closely with the outer peripheral surface of the tubular member so as to block the lateral hole, and the tip of the tubular member and the innermost part of the interior cavity are spaced apart from each other.

Abstract: An antiadhesive material that is excellent in biocompatibility and bioabsorbability, as well as excellent strength in suturing and bonding, is provided. A reinforcing material 12 made of a biodegradable polymer is placed in a gelatin solution so that the reinforcing material 12 is impregnated with the solution, and the gelatin is caused to gelate and dried. By so doing, an antiadhesive material in which a gelatin film 11 and the reinforcing material 12 are integrated is obtained. The reinforcing material 12 preferably is arranged in a portion of the gelatin film 11 to be subjected to suturing, and preferably is arranged along a periphery of the gelatin film 11. The gelatin film 11 preferably is a cross-linked gelatin film, and the reinforcing material 12 preferably is a nonwoven fabric.

Abstract: A catheter lock solution which is a catheter lock preparation having a bacteriostatic property at physiological osmotic pressure without practically containing a bacteriostatic component such as a preservative, an antimicrobial agent, or an antibiotic and having high safety, characterized in that the preparation contains a weak acid having an acid dissociation constant (pKa) of 3.0 to 6.5 as a buffer, a pH of the solution is less than 6.0, preferably from 3.0 to about 5.5, an osmotic pressure ratio is from 0.5 to 3.0, and a pH change (variation) can be suppressed to less than the 6.0 with the weak acid, and a container containing the catheter lock solution.

Abstract: A hub (40) can be displaced between an initial position at which the hub is located on a front end side of an inner cavity of a shield (20) and an inner needle (50) penetrates an outer needle (30) and a retracted position at which the hub is located on a rear end side of the inner cavity of the shield and the inner needle is housed within the inner cavity of the shield. A stopper (170) includes an insertion portion (172) that is inserted into the inner cavity of the shield and a base portion (180) that is located on a rear end of the insertion portion. The base portion includes a roof portion (183) that exposes part of an outer circumferential face of a tube (60) connected to the hub and covers the remainder thereof, and a pair of grasping portions (185) that are arranged to sandwich the tube and can be elastically displaced so as to grip the tube.

Abstract: It is intended to provide a serum which contains a large amount of growth factors capable of efficiently promoting the growth of stem cells. A human serum for cell culture which shows a residual ratio of platelets remaining within 20 minutes after blood collection in relation to the whole amount of the platelets is 0% to 20%, and a release ratio of cell growth factors is 20% to 100%.