Abstract: A biological information measuring device includes a buckle including a first plate having a plate shape and being fixed to the other end of a second plate frame member and a second plate having a plate shape being rotatable. The second plate has a part that extends beyond the first plate when the second plate overlaps an outer surface of the first plate. A first fixing element is on a side of the extended part that becomes an inner surface when the second plate overlaps the outer surface of the first plate. A second fixing element is engageable with the first fixing element on the outer surface of the front end of the belt. An first engagement protrusion is on the first plate, and a second engagement protrusion overlaps the first engagement protrusion in a direction with the first engagement protrusion is on the second plate.

Abstract: A blood pressure monitor cuff is formed by stacking an outer circumferential layer arranged on a side opposite to that of a measurement site and a fluid bladder arranged on the measurement site side. The outer circumferential layer and the fluid bladder are formed of an elastomer material. Two edge portions in a lengthwise direction of the outer circumferential layer protrude in a thickness direction toward the measurement site. The fluid bladder includes a base layer that opposes the outer circumferential layer and a top layer overlapping with the base layer, and the edge portions of the base layer and the top layer are welded together forming a bladder shape. Additional sheets are welded in the thickness direction to the welded edge portions of the top layer and the base layer. The fluid bladder is arranged between the two edge portions of the outer circumferential layer in the width direction.

Abstract: A bodily information measurement apparatus includes: a belt for wrapping around a measurement site; a main body arranged at a base end portion in a lengthwise direction of the belt and on which an element that measures bodily information is mounted; and a buckle for joining the base end portion and a leading end portion of the belt such that the belt forms a loop shape. The buckle includes first and second plate frame members, which include, respectively, first and second opening portions that penetrate through the respective members with respect to a plate surface. In a state in which the inner surface of the main body and the first and second plate frame members of the buckle are folded in so as to overlap, the first and second opening portions of the first and second plate frame members, respectively, are continuous in a thickness direction of the main body.

Abstract: A biological information measuring device includes a buckle including a first plate having a plate shape and being fixed to the other end of a second plate frame member and a second plate having a plate shape being rotatable. The second plate has a part that extends beyond the first plate when the second plate overlaps an outer surface of the first plate. A first fixing element is on a side of the extended part that becomes an inner surface when the second plate overlaps the outer surface of the first plate. A second fixing element is engageable with the first fixing element on the outer surface of the front end of the belt. An first engagement protrusion is on the first plate, and a second engagement protrusion overlaps the first engagement protrusion in a direction with the first engagement protrusion is on the second plate.

Abstract: An appliance includes a belt that is worn by being wound around a wrist. The appliance includes: at least a first display region that is positioned in an area of the belt that corresponds to a volar-side surface or a radius-side surface of the wrist; and a second display region that is positioned in an area of the belt that corresponds to a back-side surface of the wrist. During a blood pressure measurement period, first control for displaying ongoing blood pressure measurement information only on the first display region is performed, and during a period other than the blood pressure measurement period, second control for displaying information that needs to be displayed on the first or second display region is performed.

Abstract: A blood pressure meter includes a pump and a first fluid path provided inside a main body. The first fluid path feeds a fluid from the pump to a fluid bladder or discharges the fluid from the fluid bladder. A pressure sensor is mounted on a first substrate disposed inside the main body. A second fluid path that introduces the fluid from the fluid bladder to the pressure sensor is provided. The second fluid path includes an inlet pipe that is integrally formed with a sensor package that incorporates the pressure sensor, and extends straight between the fluid bladder and the pressure sensor. A second substrate on which a blood pressure measurement element is mounted is disposed in a space that is located between the first substrate and the fluid bladder in a thickness direction and is adjacent to the second fluid path in a planar direction.

Abstract: A bodily information measurement apparatus includes a band-shaped belt to be wrapped around a measurement site; a main body that is connected to a base end portion in the lengthwise direction of the belt and on which a pressure detection unit and a fluid supply unit are mounted; and a fastening unit for fastening the base end portion and the leading end portion of the belt. The belt is formed by stacking an outer circumferential layer and a fluid bladder for compressing the measurement site. The bodily information measurement apparatus is attached to the measurement site due to the base end portion and the leading end portion being fastened by the fastening portion in a state in which the fluid bladder and the leading end portion of the belt overlap.

Abstract: An appliance includes a belt that is worn by being wound around a wrist. The appliance includes: at least a first display region that is positioned in an area of the belt that corresponds to a volar-side surface or a radius-side surface of the wrist; and a second display region that is positioned in an area of the belt that corresponds to a back-side surface of the wrist. During a blood pressure measurement period, first control for displaying ongoing blood pressure measurement information only on the first display region is performed, and during a period other than the blood pressure measurement period, second control for displaying information that needs to be displayed on the first or second display region is performed.

Abstract: A bodily information measurement apparatus includes: a belt for wrapping around a measurement site; a main body arranged at a base end portion in a lengthwise direction of the belt and on which an element that measures bodily information is mounted; and a buckle for joining the base end portion and a leading end portion of the belt such that the belt forms a loop shape. The buckle includes first and second plate frame members, which include, respectively, first and second opening portions that penetrate through the respective members with respect to a plate surface. In a state in which the inner surface of the main body and the first and second plate frame members of the buckle are folded in so as to overlap, the first and second opening portions of the first and second plate frame members, respectively, are continuous in a thickness direction of the main body.

Abstract: A bodily information measurement apparatus includes a band-shaped belt to be wrapped around a measurement site; a main body that is connected to a base end portion in the lengthwise direction of the belt and on which a pressure detection unit and a fluid supply unit are mounted; and a fastening unit for fastening the base end portion and the leading end portion of the belt. The belt is formed by stacking an outer circumferential layer and a fluid bladder for compressing the measurement site. The bodily information measurement apparatus is attached to the measurement site due to the base end portion and the leading end portion being fastened by the fastening portion in a state in which the fluid bladder and the leading end portion of the belt overlap.

Abstract: A blood pressure monitor cuff is formed by stacking an outer circumferential layer arranged on a side opposite to that of a measurement site and a fluid bladder arranged on the measurement site side. The outer circumferential layer and the fluid bladder are formed of an elastomer material. Two edge portions in a lengthwise direction of the outer circumferential layer protrude in a thickness direction toward the measurement site. The fluid bladder includes a base layer that opposes the outer circumferential layer and a top layer overlapping with the base layer, and the edge portions of the base layer and the top layer are welded together forming a bladder shape. Additional sheets are welded in the thickness direction to the welded edge portions of the top layer and the base layer. The fluid bladder is arranged between the two edge portions of the outer circumferential layer in the width direction.

Abstract: A blood pressure meter includes a pump and a first fluid path provided inside a main body. The first fluid path feeds a fluid from the pump to a fluid bladder or discharges the fluid from the fluid bladder. A pressure sensor is mounted on a first substrate disposed inside the main body. A second fluid path that introduces the fluid from the fluid bladder to the pressure sensor is provided. The second fluid path includes an inlet pipe that is integrally formed with a sensor package that incorporates the pressure sensor, and extends straight between the fluid bladder and the pressure sensor. A second substrate on which a blood pressure measurement element is mounted is disposed in a space that is located between the first substrate and the fluid bladder in a thickness direction and is adjacent to the second fluid path in a planar direction.

Abstract: An oral care apparatus includes: a care member; an orientation detection unit; an area estimation unit; a light source that emits light having a predetermined wavelength to which plaque reacts; a photoelectric conversion unit that receives light and converts the received light into an electric signal; an image capture unit that causes the light source to irradiate the care area with light, and that obtains image data, based on the electric signal of light reflected from the care area that is converted by the photoelectric conversion unit; a plaque detection unit for detecting an amount of plaque in the care area, based on the image data obtained by the image capture unit; and a storage unit for storing, in a memory, the care area estimated by the area estimation unit and the amount of plaque in the care area detected by the plaque detection unit in association with each other.

Abstract: An oral care apparatus includes: a care member; an orientation detection unit; an area estimation unit; a light source that emits light having a predetermined wavelength to which plaque reacts; a photoelectric conversion unit that receives light and converts the received light into an electric signal; an image capture unit that causes the light source to irradiate the care area with light, and that obtains image data, based on the electric signal of light reflected from the care area that is converted by the photoelectric conversion unit; a plaque detection unit for detecting an amount of plaque in the care area, based on the image data obtained by the image capture unit; and a storage unit for storing, in a memory, the care area estimated by the area estimation unit and the amount of plaque in the care area detected by the plaque detection unit in association with each other.

Abstract: In a radiation image recording system wherein a stimulable phosphor carrying a radiation image stored therein is scanned by stimulating rays to emit light in proportion to the radiation energy stored, and the emitted light is converted to an electric signal which is processed and used to reproduce a visible image in a light-sensitive material, a value within the range of 0.2 to 0.5 and two values at least 0.5 different from each other within the range of 0.4 to 2.6 are selected as the reference optical density values of the reproduced image. An image is once recorded in the light-sensitive material by using reference signals representing the reference values, and the optical densities at the image portions corresponding to the reference values are measured. Differences between the measured values and values on a reference gradation curve are corrected so that the sensitivity is equal to the sensitivity on the reference curve at the portion corresponding to the value selected within the range of 0.2 to 0.