Abstract: An analyzing device mixes a sample liquid with a reagent by rotation of the analyzing device about a rotation center to generate a centrifugal force. A measurement cell is formed so as to extend in a direction along which the centrifugal force is applied, and a capillary area to which the sample liquid is sucked by a capillary force is formed on one of the side walls of the measurement cell, the side walls being arranged in a rotational direction. The capillary area extends from the outer periphery position to the inner periphery of the measurement cell, thereby reducing the size of the analyzing device. Further, the sample liquid in the measurement cell is sucked to the capillary area by slowing or stopping a rotation, and then the rotation is accelerated to return the sample liquid in the capillary area to the measurement cell.

Abstract: A control apparatus, which controls a refrigerating apparatus including a compressor and a first circuit breaker that interrupts a current flowing through the compressor when the current, flowing from a power supply through the compressor to cause the compressor to work, becomes greater than a predetermined current and that is closed according to an operation by a user, includes: a voltage-measuring unit to measure a power-supply voltage a control unit to trip a second circuit breaker disposed in series with the first circuit breaker so that the current from the power supply flowing through the compressor is interrupted, when the measured power-supply voltage becomes lower than a predetermined voltage, and close the second circuit breaker after the power-supply voltage becomes higher than the predetermined voltage, the predetermined current corresponding to a current greater than the current flowing through the compressor when the power-supply voltage is equal to the predetermined voltage.

Abstract: A sensor chip is configured to measure the temperature of a blood sample and includes a capillary section and an electrode unit. The capillary section allows the blood sample to be introduced therein. The electrode unit is configured to measure the temperature of the blood sample and includes a working electrode and a counter electrode. The working electrode and the counter electrode respectively include a reaction reagent layer containing an electrolyte. Further, the electrode unit is configured to receive a predetermined voltage to be applied in measuring the temperature of the blood sample for allowing a result of the measurement to be less affected by increase and reduction in a glucose concentration and the like.

Abstract: Disclosed is an analyzing apparatus including a first drive part (71) for rotating a turntable (101) on which an analyzing device is set, a second drive part (72) selectively engaged with the first drive part (71) to reciprocate the analyzing device, and a third drive part (73) for relatively moving the first drive part (71) and the second drive part (72) a position where the first and second drive parts are engaged with each other and a position where the first and second drive parts are not engaged with each other. Thus in the mixing and agitation of a small amount of fluid, necessary acceleration can be obtained even in a short time.

Abstract: A refrigerating apparatus includes first and second refrigerant circuits including respective first and second compressors, condensers, pressure reducers, and evaporators, connected circularly with first and second refrigerant pipes, respectively, refrigerants discharged from the first and second compressors being respectively condensed at the first and second condensers and thereafter respectively evaporated at the first and second evaporators to acquire a cooling effect; a temperature sensor that detects a temperature of an internal portion of a cold storage cabinet, the first and second evaporators being disposed to cool the internal portion simultaneously; and a first control device that controls the first and second compressors such that the first compressor and the second compressor start being alternately operated each time a temperature detected by the temperature sensor reaches a first temperature, and are continuously operated until the detected temperature reaches a second temperature lower than th

Abstract: The objective of the invention is to enhance measurement accuracy in a device for measuring a biological sample. To attain this objective, the invention is provided with a main case (2) having a sensor insertion section (1), a measurement section (7) connected to the sensor insertion section (1), a controller (8) connected to the measurement section (7), and a display (3) connected to the controller (8). An acceleration sensor (5) is furnished for detecting a shock applied to the sensor insertion section (1).

Abstract: There is disclosed a refrigeration apparatus including a cascade heat exchanger and capable of reducing the depth dimension of the apparatus itself without being influenced by the thickness dimension of an insulating material for covering the cascade heat exchanger, so that the apparatus can easily be carried indoors through a usual carrying entrance. In a refrigeration apparatus 1 including a high-temperature-side refrigerant circuit 25 and a low-temperature-side refrigerant-circuit 38, an evaporator 34 of the high-temperature-side refrigerant circuit 25 and a condensing pipe 42 of the low-temperature-side refrigerant circuit 25 constitute a cascade heat exchanger 43, and an evaporation pipe 62 of the low-temperature-side refrigerant circuit 38 is configured to cool a storage chamber 4 constituted in an insulating box body 2 to an extremely low temperature.

Abstract: Provided are a nitric oxide detection element capable of detecting NO gas contained in a mixed gas at a high speed even when the amount thereof is a super trace amount of ten and several parts per billion; and a process for producing the element. In a nitric oxide detection element having a substrate 12 and a sensing film 11 formed on a surface of the substrate, the sensing film is composed of nitric oxide sensing particles and a polymer adhesive. The nitric oxide sensing particles are produced by adsorbing a dye having a porphyrin skeleton and having, as a central metal, divalent cobalt onto surfaces of inorganic particles.

Abstract: A first recess (102) of a lower substrate (100) is coated with conductive ink to form a first auxiliary electrode layer (104), a lower electrode pattern (105) is formed thereon by vacuum deposition, a second recess (202) of an upper substrate (200) is coated with the conductive ink to form a second auxiliary electrode layer (204), an upper electrode pattern (205) is formed thereon by vacuum deposition, the upper and lower substrates are bonded to each other with an electric element (300) interposed between the lower substrate (100) and the upper substrate (100), and the upper and lower substrates are cut at positions on the overlap portion of the first auxiliary electrode layer (104) and the lower electrode pattern (105) and the overlap portion of the second auxiliary electrode layer (204) and the upper electrode pattern (205) so as to expose the cut surfaces of the substrates.

Abstract: In a chromatography quantitative measuring apparatus according to the present invention, a beam applied from a light source to a chromatography test strip is formed into an elliptical shape by an optical means such as a cylindrical lens, a variation in absorbance that accompanies elution of a marker regent is detected while the elliptical beam is applied between a marker reagent hold part and a detection part, and a measurement is automatically started in a prescribed period of time since the detection of variation. According to the chromatography quantitative measuring apparatus so configured, non-uniform coloration is reduced by shaping the beam elliptically with the optical means, whereby the accuracy of quantitative analysis is enhanced, and the apparatus can be operated easily.

Abstract: A pharmaceutical injection device comprises a main body case (2); a pharmaceutical syringe mounting component (3) that is provided inside the main body case (2) and onto which a pharmaceutical syringe (4) is mounted; a piston (5) provided movably with respect to the pharmaceutical syringe (4) mounted onto the pharmaceutical syringe mounting component (3); a drive mechanism (6) for driving the piston (5); a memory (46) that stores a preset pharmaceutical injection schedule; and a controller (7) that resets a current pharmaceutical dose by comparing a planned cumulative pharmaceutical dose, which is a planned cumulative amount of pharmaceutical injected up to the last time on the basis of the pharmaceutical injection schedule stored in the memory, and an actual cumulative pharmaceutical dose, which is a cumulative amount of pharmaceutical actually injected up to the last time.

Abstract: A culture apparatus includes a heat insulating box main body having an inner box; a culture vessel; a duct and a circulation blower forcing convection of a gas in the culture vessel; a humidifying pan disposed on the bottom of the culture vessel and positioned inside the duct; a heat pipe having a heat insulating section, a heat input section disposed at one end of the heat insulating section and a heat dissipation section disposed at the other end of the heat insulating section. The heat pipe is attached to the culture apparatus with the heat dissipation section being disposed outside the culture apparatus, the heat insulating section passing through the heat insulating box main body and the inner box, and the heat input section being disposed in a gas passage in the duct.

Abstract: A method for manufacturing a semi-finished blank for a varifocal liquid crystal lens includes coating the front of a first substrate and/or the rear of a second substrate with an adhesive agent, leaving an adhesive agent-free region that surrounds a liquid crystal holder; after said coating operation, reducing the pressure inside a sealed vessel that holds the first substrate and the second substrate, with respect to atmospheric pressure; affixing the second substrate over the front of the first substrate in the reduced pressure environment produced in said reducing the pressure operation; performing a standby operation including continuing the affixed state between the first substrate and the second substrate for a specific length of time in the reduced pressure environment produced in said reducing the pressure operation after the substrates have been affixed; and after said standby operation, restoring the pressure of the sealed vessel.

Abstract: This pharmaceutical injection system is provided with a pharmaceutical injection device, a charging device, a detector, and an alarm section. The pharmaceutical injection device has a main body case and a pharmaceutical syringe mounting portion provided within the main body case and to which a pharmaceutical syringe is removably mounted. The pharmaceutical injection device is placed in the charging device, and the charging device has a charger for charging the pharmaceutical injection device. The detector is provided to the pharmaceutical injection device and/or the charging device and detects whether or not the pharmaceutical syringe has been mounted to the pharmaceutical syringe mounting portion. The alarm section is connected to the detector and emits an alarm when it is detected that the pharmaceutical syringe has been mounted onto the pharmaceutical syringe mounting portion.

Abstract: This pharmaceutical injection device comprises a main body case (2) that has an injection needle insertion and retraction opening (1); pharmaceutical syringe mounting portion (3) that is provided within the main body case (2); a piston (5) that is provided movably with respect to a pharmaceutical syringe (4) that is mounted to the pharmaceutical syringe mounting portion (3); a drive mechanism (6) that drives the piston (5); a controller (7) that is electrically connected to the drive mechanism (6); and a display section (35) that is electrically connected to the controller (7). The controller (7) updates the display content that is displayed on the display section (35) according to the number of times the drive mechanism (6) has been driven, and saves this updated display content in a memory (51), so that when the drive mechanism (6) has been driven a specific number of times, the display contents during the various instances of drive that were saved in the memory (51) are combined.

Abstract: A medication administering device has mounted thereto a preparation syringe containing a preparation and comprises a substantially cylindrical syringe cover that supports the preparation syringe on the inner peripheral face side, a piston that presses on the rear end of the preparation syringe, and a piston case that surrounds the piston, that guides the outer peripheral face of the syringe cover in the direction of the piston on the substantially cylindrical inner peripheral face side, and that is mounted in a state in which the syringe cover is removable. The medication administering device comprises a syringe holder that guides the outer peripheral face of the preparation syringe in the direction of the piston on the cylindrical inner peripheral face side, and whose outer peripheral face is removably fitted together with the inner peripheral face of the syringe cover.

Abstract: The pharmaceutical injection device includes a pharmaceutical syringe mounting portion (3) provided within a main body case (2) and to which a pharmaceutical syringe (4) is removably mounted, a piston (5) provided movably with respect to the pharmaceutical syringe (4) mounted to the pharmaceutical syringe mounting portion (3), a drive mechanism (6) for driving the piston (5), a controller (7) that is electrically connected to the drive mechanism (6), a display section (35) that is connected to the controller (7), and an encoder (26) that is connected to the controller (7) and detects the amount of the pharmaceutical remaining inside the pharmaceutical syringe (4). The controller (7) displays a warning on the display section (35) recommending removal of the pharmaceutical syringe (4) from the pharmaceutical syringe mounting portion (3) when the presence of a pharmaceutical is detected by the encoder (26).

Abstract: A puncturing apparatus includes a housing having a first case and a second case, the housing configured to move at least one of the first case and the second case so that the cases are in an overlapping state in which the first case and the second case overlap one another or a non-overlapping state. A puncturer is housed in the housing and a puncture starting mechanism, having a puncturing button, is configured to activate the puncturer. A first safety section is configured to prevent at least one of the puncturing opening and the puncturing button from being exposed, by placing the first case and the second case in the overlapping state, and a second safety section is configured to disable operation of the puncture starting mechanism in the non-overlapping state of the first case and the second case.

Abstract: An isolator for cultivating cells including a working chamber having a plurality of gloves arranged side by side into which operator's hands are inserted to operate cells, the working chamber being sectioned into at least an operation area for operating the cells, and an auxiliary working area for opening a packaged auxiliary instrument used to operate the cells, a gas supply unit that supplies gas into the working chamber so that the gas flows downwardly from an upper side in the working chamber, and a gas flow control unit for controlling the flow of the downwardly flowing gas so that the gas flows from the operation area to the auxiliary working area around the gloves, wherein the gas flow control unit has an exhaust hole portion that has an opened area for passing the gas therethrough and is provided at a lower portion of at least the auxiliary working area, and through which the gas in the auxiliary working area is exhausted.

Abstract: The method includes: acquiring data a related to a temperature of a blood sample on a sensor chip, based on a dimension of a current flowing in the blood sample by applying a first voltage to the pair of electrodes in contact with the blood sample, the first voltage being set so as to reduce an effect of hematocrit on a temperature measurement result; acquiring data b related to the concentration of an analyte in the blood sample, based on a dimension of a current flowing in the blood sample by applying a second voltage that is equal to or less than the first voltage, utilizing a reaction mediated by an oxidoreductase that uses the analyte in the blood sample as a substrate; and measuring a concentration that determines the analyte concentration in the blood sample based on the data a and the data b.