Abstract: There is provided a medicinal liquid injection port to be implanted subcutaneously. A housing main body is provided with a medicinal liquid storage portion therein, an opening portion that opens the medicinal liquid storage portion, and a discharge hole that communicates with the medicinal liquid storage portion and configured to be connected with a tube. A septum attached to the opening portion of the housing main body and provided with a puncturable region that can be punctured with a puncture needle. A contrast portion is disposed in the septum over a thickness direction of the septum so as to detect the puncturable region of the septum with the ultrasonic wave. The contrast portion is provided in the septum within a thickness region of the septum and all of the contrast portion is positioned at an inner side of the septum in the thickness direction of the septum.

Abstract: A light emitting type capsule treatment tool for irradiating light with a specific wavelength required for photoimmunotherapy, includes a power receiving coil, a magnetic member, a light emitting member and a capsule. The power receiving coil is formed by winding a conductive wire and configured to receive electric power supplied from an external transmission antenna via a magnetic flux. The magnetic member is placed on an inner circumference of the power receiving coil. The light emitting member is configured to be supplied with electric power from the power receiving coil and to emit the light with the specific wavelength. The capsule houses the power receiving coil, the magnetic member and the light emitting member.

Abstract: There is provided a medicinal liquid injection port to be implanted subcutaneously. A housing main body is provided with a medicinal liquid storage portion therein, an opening portion that opens the medicinal liquid storage portion, and a discharge hole that communicates with the medicinal liquid storage portion and configured to be connected with a tube. A septum attached to the opening portion of the housing main body and provided with a puncturable region that can be punctured with a puncture needle. A contrast portion is disposed in the septum over a thickness direction of the septum so as to detect the puncturable region of the septum with the ultrasonic wave. The contrast portion is provided in the septum within a thickness region of the septum and all of the contrast portion is positioned at an inner side of the septum in the thickness direction of the septum.

Abstract: A stent has strut parts bent in a zigzag shape, connected at both ends thereof, and formed in a ring shape, and bridge parts for connecting the strut parts in an axial direction, peak parts of strut parts excluding a strut part at the lead toward one end are all connected by bridge parts and clustered a plurality thereof at a time by the bridge parts, and connected to valley parts of struts adjacent toward the one end of the stent, and each strut part includes valley parts which are not connected to a bridge part.

Abstract: Provided are a stent to be placed in the bile duct and a process for producing the stent, the stent hollow being less apt to be blocked even when the stent is placed in the bile duct for a long period. The inner peripheral surface of the stent is coated with a resin layer with resistance to sludge formation that includes a polymer obtained by polymerizing 2-methoxyethyl acrylate. This stent is produced by applying a coating fluid that contains 0.1-0.5 mass % polymer obtained by polymerizing 2-methoxyethyl acrylate, to the inner peripheral surface of a stent.

Abstract: The foreign matter capture instrument includes: a first manipulation wire; framework wire materials, the base end parts being coupled to a leading end part of the first manipulation wire, and the leading end parts being respectively bundled together; and a second manipulation wire which is coupled to the leading end parts of the framework wire materials, separates from the first manipulation wire extending toward the base end side of the first manipulation wire. By moving the first manipulation wire toward the leading end side relative to the second manipulation wire, the framework wire materials expand and configure a basket, and by further relatively moving the first manipulation wire toward the leading end side, the basket becomes shallower.

Abstract: A stent has strut parts bent in a zigzag shape, connected at both ends thereof; and formed in a ring shape, and bridge parts for connecting the strut parts in an axial direction, peak parts of strut parts excluding a strut part at the lead toward one end are all connected by bridge parts and clustered a plurality thereof at a time by the bridge parts, and connected to valley parts of struts adjacent toward the one end of the stent, and each strut part includes valley parts which are not connected to a bridge part.

Abstract: One embodiment provides a balloon catheter which has an inner tube having a main lumen and an outer tube which forms an expansion lumen. A part of the inner tube is connected to the outer tube at a position closer to the proximal end than a balloon, a side hole is open at the connection section, and a weak section is provided to the inner tube a position closer to the distal end than the side hole. The weak section has lower rigidity than the remaining portion of the inner tube. When the balloon is expanded by fluid supplied to the expansion lumen, the weak section is pressed by the fluid pressure to thereby close the main lumen of the inner tube.

Abstract: A medical tube, which is inserted into a tubular organ and discharges and suctions fluid, is provided with a tube-shape main body which extends a prescribed length and with a valve which is disposed in a portion of the main body that is inserted into the tubular organ and can discharge or suction a fluid, wherein the valve includes multiple slits which are formed so as to extend axially of the body a prescribed length, reaching from the outer periphery to the inner periphery of the main body, and which are provided spaced in the circumferential direction of the main body. Each slit is formed tilted in the same direction with respect to a radially-extending line which passes through the axial center of the main body.

Abstract: A highly elastic stent is made of an alloy that exhibits superelasticity at body temperature. At least a part of the highly elastic stent has such a property that load increases with displacement without exhibiting a distinct yield on a load-displacement curve obtained by a compression test and a bending test.

Abstract: An abdominal cavity-vein shunt stent provided for transporting ascites accumulated in the abdominal cavity of a patient to a vascular system, includes: a stent body which extends cylindrically long and which has one end disposed in the intrahepatic vein, and the other end piercing the liver parenchyma and disposed in the abdominal cavity; and a one-way valve which is disposed in the stent body, which is opened to drain ascites into the intrahepatic vein when a differential pressure obtained by subtracting the pressure of the intrahepatic vein from the pressure in the abdominal cavity is not lower than a predetermined value, and which is closed when the differential pressure is lower than the predetermined value.

Abstract: In a background-art medical gripping device, when a wall surface of an in vivo tissue has a large tear, a side portion of the tear can be gripped by the gripping device, but the other side portion opposed to the side portion cannot be gripped simultaneously. Therefore, to close the tear, complicated operation is required to be performed using plural gripping devices. A medical gripping device according to the present invention includes a fixed clip, a pair of movable clips made from an elastic material and provided to face the fixed clip, the movable clips having lower ends fixed to the fixed clip and the other ends opened, and a control mechanism which shifts from each other a timing at which a gripping target is gripped between one of the movable clips and the fixed clip and a timing at which the target is gripped between the other movable clip and the fixed clip.

Abstract: An abdominal cavity-vein shunt stent provided for transporting ascites accumulated in the abdominal cavity of a patient to a vascular system, includes: a stent body which extends cylindrically long and which has one end disposed in the intrahepatic vein, and the other end piercing the liver parenchyma and disposed in the abdominal cavity; and a one-way valve which is disposed in the stent body, which is opened to drain ascites into the intrahepatic vein when a differential pressure obtained by subtracting the pressure of the intrahepatic vein from the pressure in the abdominal cavity is not lower than a predetermined value, and which is closed when the differential pressure is lower than the predetermined value.

Abstract: Provided is an endoscopic duct cleaning tool which uses elastic porous members to prevent the inside of a duct of an endoscope from being damaged, and which can firmly fix the elastic porous members to a core wire and secure a sufficient thickness in each of the elastic porous members. This endoscopic duct cleaning tool 1 is inserted into a duct 53 of an endoscope 50 to clean the duct 53. The endoscopic duct device 1 includes a core wire 10 consisting of a stranded wire, plural cylindrical elastic porous members 20 disposed at certain intervals and at certain places in an axial direction of the core wire 10 so as to cover an outer circumference of the core wire 10 directly, and resin tubes 30 covering outer circumferences of portions of the core wire 10 which are not covered with the elastic porous members 20. An outer diameter of each of the resin tubes 30 is formed to be larger than an inner diameter of each of the elastic porous members 20.

Abstract: A drug solution infusion catheter includes a distal end wall made of an elastic material. The distal end wall closes a distal end surface of the catheter. A center portion of the distal end wall is thinner than a peripheral edge portion of the distal end wall. The center portion of the distal end wall defines a hole or an incision. The hole or the incision closes normally. When a guide wire is pressed against the hole or the incision from an inner side of the catheter or an outer side of the catheter, the hole or the incision elastically opens to allow the guide wire to pass therethrough. An outside of the peripheral edge portion of the distal end wall makes up the distal end surface of the catheter.

Abstract: A stent includes a plurality of annular units each made of a linear portion which extends circumferentially while folding in a zigzag manner and which is connected annularly, and connection portions which connect axially adjacent ones of the annular units with each other. Predetermined annular units have radiopaque markers each fixedly attached midway between one folded portion and a next folded portion in the linear portion located in a predetermined circumferential position.

Abstract: A drug solution infusion catheter includes a distal end wall made of an elastic material. The distal end wall closes a distal end surface of the catheter. A center portion of the distal end wall is thinner than a peripheral edge portion of the distal end wall. The center portion of the distal end wall defines a hole or an incision. The hole or the incision closes normally. When a guide wire is pressed against the hole or the incision from an inner side of the catheter or an outer side of the catheter, the hole or the incision elastically opens to allow the guide wire to pass therethrough. An outside of the peripheral edge portion of the distal end wall makes up the distal end surface of the catheter.

Abstract: It is a catheter for a peritoneovenous shunt, which has a tapered distal inlet at an end of a catheter body constituted by a polyurethane tube that is 90 cm in length, 3 mm in outside diameter, and 2.8 mm in inside diameter. Further, a side inlet consisting of a plurality of through holes is provided in a side wall at a distance of 15 cm from this end. Moreover, an outlet consisting of a plurality of parallel linear slits is provided at a distance of 37 cm from the distal inlet of the catheter body.

Abstract: In a catheter guide wire 1 formed of an identical material, since the catheter guide wire 1 consists of a portion 7 having a transformation point and portions 3, 5 not having a transformation point, the body portion 3 will not be excessively flexible and has appropriate rigidity while the connect portion 7 maintains flexibility, so that the power of pressing the catheter guide wire 1 is sufficiently transmitted to the connect portion 7 side from the body portion 3 side, whereby insertion operability of the guide wire 1 is improved.

Abstract: The catheter of the present invention includes a tube-shaped catheter main body, a shaping member provided at least at the front end portion of the catheter main body such that the shaping member can impart a winding shape to the front end portion of the catheter, and a cavity portion formed at the inner side of the shaping member.