Abstract: A medical connector includes: a male connector portion that is connectable to a closed female connector portion of another medical connector, the closed female connector portion comprising an opening formed on a top wall, and a valve body blocking the opening and having a slit, an outer peripheral edge portion of the valve body being secured to the top wall; wherein the male connector portion includes: a tubular body having an outer diameter equal to or less than a length that is twice a distance between a center of a top surface of the valve body and an end of the slit that is radially furthest from the center, the tubular body being insertable into the slit, a limiting portion configured to limit an insertion depth of the tubular body, a sealing portion configured to surround the slit, and a locking portion.

Abstract: A biological information detection device includes: a needle body configured to pierce the living body; and a sensor that has an elongated shape and is configured to detect biological information using a distal end portion of the sensor that is configured to indwell inside a living body. The distal end portion of the sensor is insertable into the living body by moving along the needle body after the needle body has pierced the living body.

Abstract: An imaging apparatus is disclosed for diagnosis generating a first tomographic image and a second tomographic image inside a lumen of a measurement subject body by using an ultrasound signal which is transmitted and received by a first transmitting and receiving unit and an optical signal which is transmitted and received by a second transmitting and receiving unit in a case where a transmitting and receiving unit in which the first transmitting and receiving unit performing transmission and reception of the ultrasound signal and the second transmitting and receiving unit performing transmission and reception of the optical signal are disposed moves in an axial direction while rotating in the lumen of the measurement subject body.

Abstract: A blood component collection system, which is one form of a biological component collection system, is equipped with a centrifugal separation device and a biological component collection device. The biological component collection device comprises a pressed soft portion pressed by a load detecting unit. The centrifugal separation device includes a collection and returning pump, and a control unit having an internal pressure computation unit which calculates a circuit internal pressure of the biological component collection device on the basis of a detection value of the load detecting unit. The internal pressure computation unit performs a zero reset process of setting a pressure value corresponding to the detection value of the load detecting unit, so as to become zero at each instance of a predetermined timing at which the collection and returning pump is stopped.

Abstract: A syringe body for a prefilled syringe includes: a hollow body portion; a proximal-end opening portion provided at a proximal end portion of the body portion; and a distal-end nozzle provided at a distal end portion of the body portion. The body portion is made of a cyclic olefin polymer or a cyclic olefin copolymer. The body portion has a thick body portion accounting for 80% or more of the body portion along an axial direction. A wall thickness of the thick body portion is 2.23 to 2.40 mm.

Abstract: A catheter assembly includes a catheter, a catheter hub fixed to the proximal end portion of the catheter, a hollow inner needle removably located in the catheter and including a distal end portion at which is located a needlepoint to puncture skin of a patient, and a guide wire slidably positioned in the inner needle. The guide wire is longer than both the inner needle and the catheter. A wire operating member is connected to the guide wire and is displaceable in the forward direction relative to the inner needle and the catheter. A main body is detachably connected to the catheter hub and includes a finger-engaging projection at a distal portion of the main body that is engageable by a user's finger to advance the main body and the catheter in the forward direction. The wire operating member is superimposed on the main body.

Abstract: The present invention is a sterile peritoneal dialysis fluid, including an acidic first liquid containing only icodextrin and 0 to 2.34 g/L of sodium chloride, and an alkaline second liquid containing an alkaline pH regulator, in which the first liquid after sterilization has a pH of 5.0 to 5.5, the second liquid after sterilization has a pH of 6.5 to 7.5, and a mixture of the first liquid and the second liquid after sterilization has a pH of 6.0 to 7.5. The present invention can provide a peritoneal dialysis fluid containing icodextrin, in which the stability of icodextrin during the heat sterilization and the subsequent storage can be improved to the maximum, and the pH of the peritoneal dialysis fluid is close to the physiological range.

Abstract: A biocompatible peritoneal dialysate according to the present invention is a sterilized biocompatible peritoneal dialysate composed of an acidic first solution containing icodextrin and a second solution containing a pH adjuster, wherein the pH after mixing of the sterilized first solution with the sterilized second solution is 6.0 to 7.5.

Abstract: A catheter assembly is disclosed, which includes a catheter; a catheter hub fixed to a proximal end portion of the catheter; a needle having a needlepoint, and inserted into the catheter so as to be separable; an elongated member coupled to the needle; a protector displaceable in an axial direction in a range regulated with respect to the elongated member, and configured to cover at least the needlepoint of the needle in accordance with evulsion of the needle from the catheter; and wherein, in an initial state, the catheter and the needle are exposed from a distal end of the elongated member, and the elongated member overlaps the catheter hub and the protector.

Abstract: A medical elongated body includes a tube shaped body provided with a spiral slit. The tube shaped body has a pair of opposing surfaces, on both sides of the slit, opposing surfaces have a first side and a second side, a first convex portion protrudes from the first side and a second convex portion protrudes from the second side, the first convex portion and the second convex portion are adjacent to each other in the circumferential direction of the tube shaped body, and base portions of the first convex portion and the second convex portion are located on a common first spiral.

Abstract: A hemostatic device is comprised of a covering member that includes a main body to which an inflatable member is connected, a first arm portion extending away from the main body, and a second arm portion extending away from the main body while forming an obtuse angle with a longitudinal direction of the first arm portion. The first arm portion includes an enlarged portion protruding in a width direction of the first arm portion at an end portion of the first arm portion. The second arm portion is longer than the first arm portion and is configured to be secured to the enlarged portion and to be secured to the second arm portion by passing between fingers of the patient in a state in which the second arm portion is wrapped around a limb of a patient.

Abstract: A hemostatic device includes a covering member having a main body connected to an inflatable member, a first arm portion extending from the main body, and a second arm portion extending from the main body in a direction different from a longitudinal direction of extent of the first arm portion. The first arm portion is configured to be secured to the second arm portion by virtue of a part of the first arm portion passing between fingers of a patient while the second arm portion is wrapped around a limb of the patient. The second arm portion has a belt portion for wrapping around the patient's limb and a support portion connecting the main body and the belt portion and located on a straight line connecting the first arm portion and the inflatable member. The belt portion is securable to the support portion while wrapped around the patient's limb.

Abstract: According to the present invention, there is provided a complex in which a carrier and a physiologically active substance are integrated, the complex being conveniently obtainable, having excellent efficiency for the integration of a physiologically active substance, and having a satisfactory membrane disruptive function promoting effect. The complex according to the present invention is formed by supporting a physiologically active substance on an aggregate of a pH sensitive carrier, wherein the aggregate is formed by aggregating under acidic conditions.

Abstract: A hemostatic device includes a flexible band configured to be wrapped around a part of an arm to be subjected to hemostasis in which a radial artery and an ulnar artery are disposed, a securing portion that secures the band in a state of being wrapped around the arm, a first inflatable portion connected to the band to press a part to be subjected to hemostasis located in the radial artery by being inflated in response to injection of a fluid, a second inflatable portion disposed at a different position from the position of the first inflatable portion in the longitudinal direction of the band to press the ulnar artery by being inflated in response to injection of a fluid, and an auxiliary balloon disposed between the band and the second inflatable portion such that at least a portion overlaps the second inflatable portion and presses the second inflatable portion.

Abstract: An information selection device includes a pulsation input unit capable of inputting a pulsation cycle of a heart of a subject, a respiration input unit capable of inputting a respiration cycle of the subject, an information input unit capable of inputting inner wall surface information on the heart at different times, and a control unit that selects, as selection information, the inner wall surface information input at a timing at which a predetermined pulsation phase range included in the pulsation cycle and a predetermined respiration phase range included in the respiration cycle overlap each other, out of a plurality of the input inner wall surface information.

Abstract: A treatment method is disclosed, which includes preparing a catheter assembly by inserting an inner catheter into an outer catheter and screwing a protrusion of the outer catheter into a helical groove of the inner catheter; introducing the catheter assembly into the radial artery along a guide wire; pushing the catheter assembly along the guide wire to a target site in front of a stenosis of a blood vessel; releasing the screwing between the helical groove of the inner catheter and the protrusion of the outer catheter after a distal end of the catheter assembly reaches the target site; and causing the outer catheter to abut on at least a part of wall surfaces of a thoracic aorta and an abdominal aorta while drawing a helix and causing the treatment device to protrude from a distal end of the outer catheter at the stenosis.

Abstract: An adjuvant composition includes a pH-sensitive carrier and a substance with stimulus to activate innate immune system. The adjuvant composition serves as a carrier which is highly safe and capable of efficient induction of CTL.

Abstract: A medical device has a rotatable drive shaft, a rotary body that includes a cutting edge for applying a cutting force to a stenosed site, and that is disposed on a distal side of the drive shaft so as to be rotated in conjunction with rotation of the drive shaft, a switching portion whose distal end is disposed at a position protruding from the cutting edge, and a holding portion that holds the switching portion so as to move the switching portion on the same plane as the cutting edge or to a position away from the stenosed site beyond the cutting edge in accordance with a pushing force, when the switching portion is pushed against the stenosed site.

Abstract: An imaging apparatus is disclosed for diagnosis including a plurality of transmitting and receiving units, an error of a scale of a tomographic image to be generated is reduced. The imaging apparatus includes a transmitting and receiving unit comprising a first transmitting and receiving unit configured to perform transmission and reception of an ultrasound signal and a second transmitting and receiving unit configured to perform transmission and reception of an optical signal when rotating in the lumen of the measurement subject body; and a processor configured to: convert positional information of each position outside the range in which the flushing liquid flows regarding the ultrasound line data generated by the processor based on a ratio between the ultrasound propagation velocity in the flushing liquid and the ultrasound propagation velocity in the blood vessel; and construct the first tomographic image using the ultrasound line data which is converted by the processor.