Abstract: A stent graft includes a tubular member, a plurality of stent rings, and an uncovered section. The tubular member extends between a proximal end and a distal end. The plurality of stent rings extend in a ring shape while alternatingly bending toward the proximal end side and toward the distal end side. The plurality of stent rings include a plurality of fluctuating rings and a small fixed ring. The plurality of fluctuating rings have a first region in which the amplitude is a first value and a second region in which the amplitude is a second value smaller than the first value. The small fixed ring exhibits a maximum amplitude which is a third value which is smaller than the first value. The uncovered section extends while alternatingly bending toward a base end side and toward a tip end side.

Abstract: A stent graft includes a tubular member and a plurality of stent rings. The plurality of stent rings are alternately bent toward a central end side and toward a peripheral end side. The plurality of stent rings include a plurality of fluctuating rings and a small fixed ring. The plurality of fluctuating rings are arranged in order of a first fluctuating ring, a second fluctuating ring . . . , from the proximal end side toward the distal end side. A first distance that is a maximum value of a distance between a center position of the first fluctuating ring and a center position of the second fluctuating ring is greater than any nth distance that is a maximum value of a distance between a center position of an nth fluctuating ring and a center position of an n+1th fluctuating ring.

Abstract: The stent graft (10) comprises a cylinder comprising a graft material in the form of a film and a stent that supports the cylinder. Further, the stent graft (10) is inserted within a region from the ascending aorta to the sinus of valsalva, and the stent graft comprises cylindrical body section (11) arranged in the ascending aorta and the sinus of valsalva section (12) arranged in the sinus of valsalva and having an inner diameter larger than that of the body section (11).

Abstract: The stent graft (10) comprises a cylinder comprising a graft material in the form of a film and a stent that supports the cylinder. Further, the stent graft (10) is inserted within a region from the ascending aorta to the sinus of valsalva, and the stent graft comprises cylindrical body section (11) arranged in the ascending aorta and the sinus of valsalva section (12) arranged in the sinus of valsalva and having an inner diameter larger than that of the body section (11).

Abstract: A blood supply flow rate controlling device (2), which is a device for controlling the blood supply flow rate in an extracorporeal circulation device connected to a living body (10), includes rotational frequency detecting means that detects the rotational frequency of the centrifugal pump (40) of the extracorporeal circulation device, inlet pressure detecting means and outlet pressure detecting means that detect the inlet pressure and the outlet pressure of the centrifugal pump (40), respectively, flow rate regulating means that regulates a flow rate of blood supplied to the living body by adjusting a flow path cross section area of the blood circulation circuit (20), and controlling means that controls the flow rate regulating means.

Abstract: The stent graft (10) comprises a cylinder comprising a graft material in the form of a film and a stent that supports the cylinder. Further, the stent graft (10) is inserted within a region from the ascending aorta to the sinus of valsalva, and the stent graft comprises cylindrical body section (11) arranged in the ascending aorta and the sinus of valsalva section (12) arranged in the sinus of valsalva and having an inner diameter larger than that of the body section (11).

Abstract: A blood supply flow rate controlling device (2), which is a device for controlling the blood supply flow rate in an extracorporeal circulation device connected to a living body (10), includes rotational frequency detecting means that detects the rotational frequency of the centrifugal pump (40) of the extracorporeal circulation device, inlet pressure detecting means and outlet pressure detecting means that detect the inlet pressure and the outlet pressure of the centrifugal pump (40), respectively, flow rate regulating means that regulates a flow rate of blood supplied to the living body by adjusting a flow path cross section area of the blood circulation circuit (20), and controlling means that controls the flow rate regulating means.

Abstract: The evoked spinal cord potential monitoring apparatus of the present invention includes: a pair of electrodes 14; and a holding section 12 for holding the pair of electrodes 14, a tip section of each of the electrodes 14 being extended outwards from an end of the holding section 12, and the electrodes 14 being movable relative to the holding section 12. A hook section 15 engageable to an intercostal nerve is provided at the tip section of each of the electrodes 14, and the electrodes 14 or the holding section 12 is moved while the hook section 15 is coupled to the intercostal nerve such that the hook section 15 and the holding section 12 are able to hold the intercostal nerve therebetween. The apparatus requires no preoperative preparation, is capable of coping with an emergency case, and further, is unsusceptible to the influence of anesthetics.

Abstract: The evoked spinal cord potential monitoring apparatus of the present invention includes: a pair of electrodes 14; and a holding section 12 for holding the pair of electrodes 14, a tip section of each of the electrodes 14 being extended outwards from an end of the holding section 12, and the electrodes 14 being movable relative to the holding section 12. A hook section 15 engageable to an intercostal nerve is provided at the tip section of each of the electrodes 14, and the electrodes 14 or the holding section 12 is moved while the hook section 15 is coupled to the intercostal nerve such that the hook section 15 and the holding section 12 are able to hold the intercostal nerve therebetween. The apparatus requires no preoperative preparation, is capable of coping with an emergency case, and further, is unsusceptible to the influence of anesthetics.

Abstract: A check valve includes a casing member, a tear-drop shaped ball member installed in the casing member, a latching member which is formed at an inner wall of the casing member and an airtight valve which is formed at an inner wall of the casing member. When forward flux occurs, the ball member is fixed at the latching members absolutely to circulate the forward flux stably. When backward flux occurs, the ball member is latched at the airtight member to close the casing member and thus, to suppress the backward flux.

Abstract: A check valve includes a casing member, a tear-drop shaped ball member installed in the casing member, a latching member which is formed at an inner wall of the casing member and an airtight valve which is formed at an inner wall of the casing member. When forward flux occurs, the ball member is fixed at the latching members absolutely to circulate the forward flux stably. When backward flux occurs, the ball member is latched at the airtight member to close the casing member and thus, to suppress the backward flux.

Abstract: When both the IABP and the PCPS are used, they exhibit an excellent circulation assisting effect. In this case, however, sequela such as hypoxic encephalopathy may well occur after the heart failure is remedied. The invention provides an intraaortic balloon catheter capable of preventing such sequela. The balloon catheter of the invention includes a catheter main body part which is to be inserted into an aorta, and a balloon section formed on an outer peripheral portion of the catheter main body, to be inserted into the aorta together with the main body, and to be expandable and contractible in the aorta under the control of the IABP. An end portion of the catheter main body functions as an introductory portion of the catheter, and has a blood feed hole formed therein for introducing, into an artery such as the aortic arch, arterial blood of high oxygen concentration fed from a circulation assisting unit such as the PCPS.

Abstract: A cardiopulmonary function assisting device includes a gas guide tube of which peripheral wall does not transmit gas or liquid such as blood and has a suitable rigidity and a suitable flexibility. A header is coaxially attached to an opening at the distal end of the gas guide tube. A plurality of balloons are attached to the distal end of the header. The balloons are formed of a gas permeable film and left in a blood vessel. Oxygen is supplied to the balloons through the gas guide tube, thereby expanding the balloons; oxygen is discharged from the balloons, thereby contracting the balloons. The expanding and contracting operations are repeated. As a result, when the balloons are expanded, oxygen is transmitted through the balloons and added to blood on the periphery of the balloons and the expanded balloons remove the blood away from the periphery. When the balloons are contracted, the periphery of the balloons is filled with blood.