Abstract: A nitric oxide administration device 1 includes a first flow path 101 including a first intake port 101a and an oxygen supply port 101b, an oxygen generation unit 100 which is arranged in the first flow path 101 and which generates concentrated oxygen from air introduced via the first intake port 101a, the generated concentrated oxygen being supplied via the oxygen supply port 101b, a second flow path 201 which is branched from the first flow path 101 and which includes an NO supply port 201b, and an NO generation unit 200 which is arranged in the second flow path 201 and which generates NO from gas distributed from the first flow path 101, the generated NO being supplied via the NO supply port 201b.

Abstract: A phototherapy device including: an irradiation probe for radiating irradiation light toward a living body; a probe fixing unit into which the irradiation probe is inserted and at the same time fixed on a living body; an observation module placed on the probe fixing unit and provided with an observation means for observing an irradiation site irradiated with irradiation light which is radiated to the living body; and a moving means capable of moving the observation module to a space where the irradiation probe is to be placed in the probe fixing unit during observation of the irradiation site.

Abstract: A nitric oxide administration device 14 includes a second flow path 201 including an intake port 201a and an NO supply port 201b, a discharge unit 205 which is arranged in the second flow path 201 and which generates NO from air introduced via the intake port 201a, generated NO being supplied via the NO supply port 201b, an NO2 adsorption unit 206 which is arranged downstream of the discharge unit 205 and removes NO2, a bypass flow path 217 for reflux from downstream of the NO2 adsorption unit 206 to upstream of the NO2 adsorption unit 206, and a three-way valve 216 for switching the opening and closing of a flow path from downstream of the NO2 adsorption unit 206 to the NO supply port 201b.

Abstract: A nitric oxide administration device 1 includes a first flow path 101 including a first intake port 101a and an oxygen supply port 101b, an oxygen generation unit 100 which is arranged in the first flow path 101 and which generates concentrated oxygen from air introduced via the first intake port 101a, the generated concentrated oxygen being supplied via the oxygen supply port 101b, a second flow path 201 which is branched from the first flow path 101 and which includes an NO supply port 201b, and an NO generation unit 200 which is arranged in the second flow path 201 and which generates NO from gas distributed from the first flow path 101, the generated NO being supplied via the NO supply port 201b.

Abstract: A relay administration device 50 for use in connection to a nitric oxide administration device 20 which supplies NO generated from air, includes an NO densitometer 506, a flowmeter 507 or pressure gauge 504, a control unit 600 which calculates a dosage of NO to be administered to a patient based on an NO concentration measured by the NO densitometer 506 and a value of the flowmeter 507 or the pressure gauge 504, and a two-way valve 505 which is configured to increase a flow rate when the calculated dosage is less than a predetermined value and to decrease the flow rate when the calculated dosage is greater than a predetermined value.

Abstract: A nitric oxide administration device 25 includes a second flow path 201 including an intake port 201a and an NO supply port 201b, a discharge unit 205 which is arranged in the second flow path 201 and which generates NO from air introduced via the intake port 201a, generated NO being supplied via the NO supply port 201b, an NO2 adsorption unit 206 which is arranged downstream of the discharge unit 205 and which removes NO2, an NO densitometer 208 which is arranged downstream of the discharge unit 205 or which is arranged in a flow path for reflux from downstream of the NO2 adsorption unit 206 to upstream of the NO2 adsorption unit 206, and a concentration estimation unit 301 which estimates an NO concentration and an NO2 concentration in a predetermined position based on an oxygen concentration in the atmosphere or the second flow path 201, an NO concentration measured by the NO densitometer 208, and a residence time of gas containing NO in the second flow path 201 between the NO2 adsorption unit 206 and the

Abstract: The purpose of the invention is to provide a transcranial magnetic stimulation system capable of guiding a patient into an optimum posture for treatment. The system 1 of the invention includes an optical device 502 for projecting a light spot 805 to a head of a patient and detecting a reflection light of the light spot; a memory means 71 for memorizing information included in the reflection light detected by the optical device as a reference information when the projected light spot on the patient overlaps a marking (800) provided on the patient; a calculation means 72 for using the reference information memorized in the memory means and a comparison information included in the reflection light of the light spot to calculate an overlap ratio between the marking and the light spot corresponding to the comparison information; and a display means 504 for displaying the overlap ratio.

Abstract: Provided is a magnetic stimulation device, which does not feel hot to the user. The magnetic stimulation device (1) comprises: a contact plate (2) to be disposed near the user's head; an exciting coil (3) to be held above the contact plate (2); a casing (4), which covers at least the upper side of the exciting coil (3), in which openings (17, 18) are provided above the center of the exciting coil (3) winding, and in which a gap that is open on the outside of the exciting coil (3) is formed between the casing and the contact plate (2); and a suction fan (5) for drawing out air between the contact plate (2) and the casing (4) from the openings (17, 18) of the casing (4).

Abstract: An electrical surgical system 1 for cutting or cauterizing tissue comprises a guide needle 11 having at least one open part 13 and a front end part able to pierce the skin and at least one electrode 12 able to cut or able to cauterize tissue configured to be able to project to the outside of the guide needle 11 and able to be retracted to the inside of the guide needle 11 through the at least one open part 13, in the state where the at least one electrode 12 projects out, the distal end of the at least one electrode 12 being arranged at a position separated from the axis of the guide needle 11.

Abstract: The purpose of the invention is to provide a transcranial magnetic stimulation system capable of guiding a patient into an optimum posture for treatment. The system 1 of the invention includes an optical device 502 for projecting a light spot 805 to a head of a patient and detecting a reflection light of the light spot; a memory means 71 for memorizing information included in the reflection light detected by the optical device as a reference information when the projected light spot on the patient overlaps a marking (800) provided on the patient; a calculation means 72 for using the reference information memorized in the memory means and a comparison information included in the reflection light of the light spot to calculate an overlap ratio between the marking and the light spot corresponding to the comparison information; and a display means 504 for displaying the overlap ratio.

Abstract: The purpose of the invention is to provide a transcranial magnetic stimulation system capable of being readily set into an optimum position for treatment. The system 1 of the invention includes a support mechanism 30 configured to support a patient, a first mechanism 200 configured to move the coil in a left and right direction of the patient about a first axis 220 extending in a back and forth direction of the patient relative to a head of patient supported by the support mechanism, and a second mechanism 300 configured to move the coil in the back and forth direction about a second axis 320 extending in the left and right direction relative to the head of the patient.

Abstract: Provided is a magnetic stimulation device, which does not feel hot to the user. The magnetic stimulation device (1) comprises: a contact plate (2) to be disposed near the user's head; an exciting coil (3) to be held above the contact plate (2); a casing (4), which covers at least the upper side of the exciting coil (3), in which openings (17, 18) are provided above the center of the exciting coil (3) winding, and in which a gap that is open on the outside of the exciting coil (3) is formed between the casing and the contact plate (2); and a suction fan (5) for drawing out air between the contact plate (2) and the casing (4) from the openings (17, 18) of the casing (4).

Abstract: Provided is an inexpensive device capable of accurately positioning a medical instrument relative to the head of a user. A head positioning device (7) is used. The head positioning device (7) is provided with: a pair of holding members (11, 12) which holds the face of a user from both sides by elasticity and prevents both the forward tilting of the user's head and the rotation of the neck; a neck rest (13) which comes into contact with the back side of the user's neck and determines the position of the neck in the front-rear direction; and a head-back rest (14) which comes into contact with the back of the head and which prevents the head from tilting backward.