Abstract: According to one embodiment, a magnetic memory device includes a lower insulating layer, first and second conductive portions provided in the lower insulating layer, first and second memory cells provided on the lower insulating layer and on the respective first and second conductive portions, and each including a magnetoresistance effect element, a switching element and a bottom electrode connected to corresponding one of the first and second conductive portions. As viewed from a third direction, a width of each of the first and second conductive portions is less than a width of a corresponding bottom electrode. The lower insulating layer has a void under a region between the first and second memory cells.

Abstract: According to one embodiment, a magnetic memory device includes a first wiring line extending in a first direction, a second wiring line provided on an upper layer side of the first wiring line and extending in a second direction intersecting the first direction, and a memory cell provided between the first wiring line and the second wiring line and including a magnetoresistance effect element and a switching element which are stacked in a third direction intersecting the first direction and the second direction. The first wiring line includes a first conductive layer and a second conductive layer provided on the first conductive layer and formed of a material containing carbon (C).

Abstract: According to one embodiment, a magnetic memory device includes an electrode, and a magnetoresistance effect element provided on the electrode. The electrode includes a first electrode portion and a second electrode portion provided between the magnetoresistance effect element and the first electrode portion and containing a metal element selected from molybdenum (Mo) and ruthenium (Ru).

Abstract: A medical connector includes: a first connection section that defines a first passage, the first connection section comprising a first tubular portion; a second connection section that defines a second passage communicating with the first passage, the second connection section comprising a second tubular portion inserted into the first tubular portion; and a rotation control section that controls relative rotation of the first connection section and the second connection section in a connection state.

Abstract: A medical connector includes: a housing comprising a male connector attachment/detachment part, the housing defining a liquid flow path; and a valve that is vertically movable with respect to the housing between a closed position for closing the male connector attachment/detachment part, and an open position in which a flow path in a male connector communicates with the liquid flow path, by the valve being pressed down from the closed position by the male connector against a biasing force. The valve comprises a head portion that closes the male connector attachment/detachment part when the valve is at the closed position, and a body portion that is connected to a bottom end of the head portion and receives the biasing force. A Young's modulus of the body portion is larger than a Young's modulus of the head portion.

Abstract: A medical connector includes: a first connection section that defines a first passage; a second connection section that defines a second passage communicating with the first passage; and a rotation control section that controls relative rotation of the first and second connection sections. The second connection section includes a first wall face configured to abut on the first connection section to restrict the first connection section from moving in a direction to be separated from the second connection section. In a state in which the first wall face abuts on the first connection section, the rotation control section allows the second connection section to rotate relative to the first connection section in a first circumferential direction about the axis and restricts the second connection section from rotating relative to the first connection section in a second circumferential direction opposite to the first circumferential direction.

Abstract: Medical devices are provided comprising a spike including proximal and distal ends, and a central axis extending from the proximal to the distal end; a valve body; a biasing body which biases the valve body; a distal tube that moves integrally with the valve body to both sides in the axial direction relative to the spike; a proximal tube fixed in the axial direction relative to the spike, the distal tube comprising a guided portion guided toward the proximal tube, and an engagement control unit which moves the guided portion toward one side in the radial direction by connection of the different medical device to the distal tube allowing the guided portion to engage with the proximal tube, and moves the guided portion toward the other side in the radial direction releasing engagement with the proximal tube when the different medical device is detached from the distal tube.

Abstract: A medical connector includes: a body member that partitions a flow path between a proximal side opening and a distal side opening; and a male connector connection portion including: a valve body facing the flow path, and a male connector connection port openable and closable by the valve body. The body member comprises a male connector housing portion configured to house a distal end portion of a male connector connected to the male connector connection portion. The male connector housing portion is configured to cause the male connector to communicate with the distal side opening and to prevent inflow of a fluid from the proximal side opening to the male connector housing portion by connection of the male connector to the male connector connection portion.

Abstract: Medical devices are provided comprising a spike including proximal and distal ends, and a central axis extending from the proximal to the distal end; a valve body; a biasing body which biases the valve body; a distal tube that moves integrally with the valve body to both sides in the axial direction relative to the spike; a proximal tube fixed in the axial direction relative to the spike, the distal tube comprising a guided portion guided toward the proximal tube, and an engagement control unit which moves the guided portion toward one side in the radial direction by connection of the different medical device to the distal tube allowing the guided portion to engage with the proximal tube, and moves the guided portion toward the other side in the radial direction releasing engagement with the proximal tube when the different medical device is detached from the distal tube.

Abstract: A medical connector includes: a first connection section that defines a first passage; a second connection section that defines a second passage communicating with the first passage; and a rotation control section that controls relative rotation of the first and second connection sections. The second connection section includes a first wall face configured to abut on the first connection section to restrict the first connection section from moving in a direction to be separated from the second connection section. In a state in which the first wall face abuts on the first connection section, the rotation control section allows the second connection section to rotate relative to the first connection section in a first circumferential direction about the axis and restricts the second connection section from rotating relative to the first connection section in a second circumferential direction opposite to the first circumferential direction.

Abstract: An infusion set includes a first infusion line set that forms a first infusion line with an injection port; and a connector including a male connector end that is insertable into the injection port, a female connector end to which a second infusion line can be connected, a flow channel, and a partition. The injection port and the connector are configured such that, when the male connector end of the connector is inserted into the injection port, the flow channel of the connector is divided by the partition into an in-flow channel configured to let in a liquid from the injection port in the first infusion line and an out-flow channel configured to let out the liquid that has entered the in-flow channel to the injection port.

Abstract: A connector includes a housing including: an insertion section into which a male connector is insertable from an outside of the housing, and a flow path communicating with the insertion section; and an elastic valve body having a slit and configured to block the insertion section. An inner wall of the housing defining the flow path is integrally formed with a liquid barrier face. The housing is configured such that, when the male connector is inserted in the insertion section, the liquid barrier face faces a tip opening of the male connector in an insertion direction of the male connector such that liquid flowing out from the tip opening collides with the liquid barrier face.

Abstract: A medical connector includes: a body member that partitions a flow path between a proximal side opening and a distal side opening; and a male connector connection portion including: a valve body facing the flow path, and a male connector connection port openable and closable by the valve body. The body member comprises a male connector housing portion configured to house a distal end portion of a male connector connected to the male connector connection portion. The male connector housing portion is configured to cause the male connector to communicate with the distal side opening and to prevent inflow of a fluid from the proximal side opening to the male connector housing portion by connection of the male connector to the male connector connection portion.

Abstract: An infusion set includes a first infusion line set that forms a first infusion line with an injection port; and a connector including a male connector end that is insertable into the injection port, a female connector end to which a second infusion line can be connected, a flow channel, and a partition. The injection port and the connector are configured such that, when the male connector end of the connector is inserted into the injection port, the flow channel of the connector is divided by the partition into an in-flow channel configured to let in a liquid from the injection port in the first infusion line and an out-flow channel configured to let out the liquid that has entered the in-flow channel to the injection port.

Abstract: A connector includes a housing including: an insertion section into which a male connector is insertable from an outside of the housing, and a flow path communicating with the insertion section; and an elastic valve body having a slit and configured to block the insertion section. An inner wall of the housing defining the flow path is integrally formed with a liquid barrier face. The housing is configured such that, when the male connector is inserted in the insertion section, the liquid barrier face faces a tip opening of the male connector in an insertion direction of the male connector such that liquid flowing out from the tip opening collides with the liquid barrier face.

Abstract: An edge exposure unit includes a projector, a projector holding unit, a substrate rotating unit, an outer edge detecting unit and a surface inspection processing unit. Each component of the projector holding unit operates to move the projector in an X direction and a Y direction. The projector irradiates a peripheral portion of a substrate with light transmitted from a light source for exposure through a light guide. Edge sampling processing is performed based on distribution of an amount of light received in a CCD line sensor of the outer edge detecting unit. Surface inspection processing is performed based on distribution of an amount of light received in a CCD line sensor of the surface inspection processing unit.

Abstract: An edge exposure unit includes a projector, a projector holding unit, a substrate rotating unit, an outer edge detecting unit and a surface inspection processing unit. Each component of the projector holding unit operates to move the projector in an X direction and a Y direction. The projector irradiates a peripheral portion of a substrate with light transmitted from a light source for exposure through a light guide. Edge sampling processing is performed based on distribution of an amount of light received in a CCD line sensor of the outer edge detecting unit. Surface inspection processing is performed based on distribution of an amount of light received in a CCD line sensor of the surface inspection processing unit.

Abstract: A booster circuit generates a boosted output by boosting a low voltage output supplied as a target to be boosted and feeds back a part of the boosted output, an output by the booster circuit itself, to the booster circuit as operation energy. An auxiliary booster circuit outputs start-up energy generated based on a low voltage output to the booster circuit as start-up energy that is necessary for starting up the booster circuit.

Abstract: A booster circuit generates a boosted output by boosting a low voltage output supplied as a target to be boosted and feeds back a part of the boosted output, an output by the booster circuit itself, to the booster circuit as operation energy. An auxiliary booster circuit outputs start-up energy generated based on a low voltage output to the booster circuit as start-up energy that is necessary for starting up the booster circuit.

Abstract: A booster circuit generates a boosted output by boosting a low voltage output supplied as a target to be boosted and feeds back a part of the boosted output, an output by the booster circuit itself, to the booster circuit as operation energy. An auxiliary booster circuit outputs start-up energy generated based on a low voltage output to the booster circuit as start-up energy that is necessary for starting up the booster circuit.