Abstract: A compression patch configured to achieve hemostasis in a living body, the compression patch including a compression feature extruding out towards a patient contact surface; a base configured to provide support to the compression feature, the base including an opening within a perimeter of the base; and a patch feature configured to provide stability to the compression patch by adhering to the patient contact surface.

Abstract: A medical device and methods for hemostasis in a living body are disclosed. The medical device including a base configured to arranged on an upper surface of the tissue in the living body; a plurality of levers, each of the plurality of levers having a needle arranged on a lower surface thereof and configured to puncture the tissue in the living body, and wherein the plurality of lever are configured to be received with a slot or track of the base; and at least one tie, the at least one tie configured to hold together the plurality levers and needles upon compressing the tissue in the living body upon moving the plurality of levers inward in the slot or track of the base.

Abstract: This display device is provided with: a gate driver that drives a display panel; and a control circuit that controls driving of the gate driver. The control circuit is provided with: a Voltage supply circuit that supplies a Voltage to the gate driver; and a current detection circuit that detects a current to be supplied to the gate driver. The display device reduces, in stages, the voltage to be supplied to the gate driver, and detects the current to be supplied to the gate driver, and in the cases where the detected current is equal to or lower than a predetermined value or a current increase is detected, the display device acquires a first voltage being supplied to the gate driver, and sets a second voltage as a drive voltage for driving the gate driver, said second voltage being obtained by adding a predetermined voltage to the acquired first voltage.

Abstract: A compression device according to the present disclosure includes a main body portion that is fixable to a biological surface; a compression portion configured to compress the biological surface; a hinge portion that supports the compression portion so as to be rotatable around a rotational axis with respect to the main body portion; and a pressing portion configured to press the compression portion in one rotational direction around the rotational axis. The compression portion rotates around the rotational axis to be configured to compress the biological surface.

Abstract: An adhesion device includes an adhesion sheet including an adhesion surface that is adherable to a biological surface, and a mounting surface located on a side opposite the adhesion surface; a device main body mounted to the mounting surface of the adhesion sheet; and a release sheet releasably adhered to the adhesion surface. The adhesion sheet includes a first portion to which the device main body is mounted, and a second portion to which the device main body is not mounted. The release sheet includes a release layer adhered to the adhesion surface of the adhesion sheet, and a folded layer formed of at least one layer and folded to a side, which is opposite to the adhesion surface with respect to the release layer, to be layered. The folded layer is layered on the release layer at least at a position of the second portion of the adhesion sheet.

Abstract: This display device is provided with: a gate driver that drives a display panel; and a control circuit that controls driving of the gate driver. The control circuit is provided with: a Voltage supply circuit that supplies a Voltage to the gate driver; and a current detection circuit that detects a current to be supplied to the gate driver. The display device reduces, in stages, the voltage to be supplied to the gate driver, and detects the current to be supplied to the gate driver, and in the cases where the detected current is equal to or lower than a predetermined value or a current increase is detected, the display device acquires a first voltage being supplied to the gate driver, and sets a second voltage as a drive voltage for driving the gate driver, said second voltage being obtained by adding a predetermined voltage to the acquired first voltage.

Abstract: A compression device includes an adhesion sheet including an adhesion surface; and a compression member mounted on the adhesion sheet and configured to compress a biological surface. The compression member includes a fixing portion fixed to the adhesion sheet on a side of the sheet opposite the adhesion surface in a thickness direction, and a compression main body portion provided in a portion of the compression member, in a plan view seen along the thickness direction, that does not overlap the adhesion sheet. The compression main body is configured to protrude or be protrusible further toward one side in the thickness direction than the adhesion surface. The adhesion sheet includes a first portion to which the fixing portion is fixed and a second portion to which the fixing portion is not fixed. The second portion is provided on at least a compression main body portion side of the adhesion sheet.

Abstract: A system for deploying a prosthesis over a Carina between an ipsilateral lumen and a contralateral lumen includes a guidewire, a guidewire capture catheter, a self-expanding tubular prosthesis, and a delivery catheter. The guidewire is first placed in the ipsilateral lumen. The guidewire capture catheter is then advanced from the contralateral lumen to a position at or above the ipsilateral lumen. The guidewire is typically advanced through an occlusion, which may be a total occlusion, and captured by a capture element on the guidewire capture catheter. The guidewire capture catheter pulls the guidewire out through the contralateral side, and the guidewire is used to advance a delivery catheter from the ipsilateral side. The delivery catheter delivers a first segment of the tubular prosthesis in the ipsilateral lumen and a second segment of the prosthesis in the contralateral lumen.

Abstract: A vaginal insertion portion is disclosed, the vaginal insertion portion including a base portion, a proximal holding portion located on a proximal side of the base portion, and a suction portion located on distal side of the proximal holding portion.

Abstract: A system for deploying a prosthesis over a Carina between an ipsilateral lumen and a contralateral lumen includes a guidewire, a guidewire capture catheter, a self-expanding tubular prosthesis, and a delivery catheter. The guidewire is first placed in the ipsilateral lumen. The guidewire capture catheter is then advanced from the contralateral lumen to a position at or above the ipsilateral lumen. The guidewire is typically advanced through an occlusion, which may be a total occlusion, and captured by a capture element on the guidewire capture catheter. The guidewire capture catheter pulls the guidewire out through the contralateral side, and the guidewire is used to advance a delivery catheter from the ipsilateral side. The delivery catheter delivers a first segment of the tubular prosthesis in the ipsilateral lumen and a second segment of the prosthesis in the contralateral lumen.

Abstract: A medical device and methods for hemostasis in a living body are disclosed. The medical device including a base configured to arranged on an upper surface of the tissue in the living body; a plurality of levers, each of the plurality of levers having a needle arranged on a lower surface thereof and configured to puncture the tissue in the living body, and wherein the plurality of lever are configured to be received with a slot or track of the base; and at least one tie, the at least one tie configured to hold together the plurality levers and needles upon compressing the tissue in the living body upon moving the plurality of levers inward in the slot or track of the base.

Abstract: A line-compression patch and method are disclosed configured to achieve hemostasis in a living body. The line-compression patch includes a line-compression feature extruding out towards a patient contact surface; a base providing the support to the line-compression feature; and a patch feature that provides stability to the line-compression patch by adhering to the patient contact surface.

Abstract: A vaginal insertion portion is disclosed, the vaginal insertion portion including a base portion, a proximal holding portion located on a proximal side of the base portion, and a suction portion located on distal side of the proximal holding portion.

Abstract: A puncture apparatus is disclosed, which can include an insertion portion that is insertable into a living body, the insertion portion including an urethral insertion portion and a vaginal insertion portion, the urethral insertion portion and the vaginal insertion portion each having at least two sensors; a puncture needle that punctures living body tissues near the insertion portion in a state in which the insertion portion is inserted into the living body, the puncture needle having at least one sensor on a distal portion of the puncture needle; and a monitor configured to receive information relating to a positional relationship between a distal portion of the puncture needle and the insertion portion.

Abstract: The present application describes an implant system useable for positioning an implant device such as a device useful for restricting passage of ingested food into the stomach. In one embodiment, the disclosed system includes a plurality of anchors that may be coupled to tissue within the stomach, or to a tissue tunnel formed by plicating stomach wall tissue. The anchor includes a loop. During use, the implant device is inserted through the loop and expanded such that it retains its position within the loop until removed. Instruments for implanting and explanting the implant device are also described.

Abstract: A system for deploying a prosthesis over a Carina between an ipsilateral lumen and a contralateral lumen includes a guidewire, a guidewire capture catheter, a self-expanding tubular prosthesis, and a delivery catheter. The guidewire is first placed in the ipsilateral lumen. The guidewire capture catheter is then advanced from the contralateral lumen to a position at or above the ipsilateral lumen. The guidewire is typically advanced through an occlusion, which may be a total occlusion, and captured by a capture element on the guidewire capture catheter. The guidewire capture catheter pulls the guidewire out through the contralateral side, and the guidewire is used to advance a delivery catheter from the ipsilateral side. The delivery catheter delivers a first segment of the tubular prosthesis in the ipsilateral lumen and a second segment of the prosthesis in the contralateral lumen.

Abstract: A system for deploying a prosthesis over a Carina between an ipsilateral lumen and a contralateral lumen includes a guidewire, a guidewire capture catheter, a self-expanding tubular prosthesis, and a delivery catheter. The guidewire is first placed in the ipsilateral lumen. The guidewire capture catheter is then advanced from the contralateral lumen to a position at or above the ipsilateral lumen. The guidewire is typically advanced through an occlusion, which may be a total occlusion, and captured by a capture element on the guidewire capture catheter. The guidewire capture catheter pulls the guidewire out through the contralateral side, and the guidewire is used to advance a delivery catheter from the ipsilateral side. The delivery catheter delivers a first segment of the tubular prosthesis in the ipsilateral lumen and a second segment of the prosthesis in the contralateral lumen.

Abstract: The present application describes an implant system useable for positioning an implant device such as a device useful for restricting passage of ingested food into the stomach. In one embodiment, the disclosed system includes a plurality of anchors that may be coupled to tissue within the stomach, or to a tissue tunnel formed by plicating stomach wall tissue. The anchor includes a loop. During use, the implant device is inserted through the loop and expanded such that it retains its position within the loop until removed. Instruments for implanting and explanting the implant device are also described.

Abstract: A puncture apparatus is disclosed, which can include an insertion portion that is insertable into a living body, the insertion portion including an urethral insertion portion and a vaginal insertion portion, the urethral insertion portion and the vaginal insertion portion each having at least two sensors; a puncture needle that punctures living body tissues near the insertion portion in a state in which the insertion portion is inserted into the living body, the puncture needle having at least one sensor on a distal portion of the puncture needle; and a monitor configured to receive information relating to a positional relationship between a distal portion of the puncture needle and the insertion portion.

Abstract: A vaginal insertion portion is disclosed, the vaginal insertion portion including a base portion, a proximal holding portion located on a proximal side of the base portion, and a suction portion located on distal side of the proximal holding portion.