Abstract: The present invention relates to an administration instrument for medical use that can perform injection of a drug solution with stability and with great reliability. For example, at the administration, it is possible to prevent a force that presses the injection button from acting in a direction of inserting the needle that is inserted into the skin deeper, and enables the administration under a stable state where the needle does not wobble, thereby alleviating physical and mental pain of the administration patient. With a structure in which an injection button (3) is pressed at an angle that is not parallel to the needle with respect to a direction in which the needle (4) is inserted into the skin, it is possible to prevent the force of pressing the injection button from being transmitted in a direction of inserting the needle into the skin deeper than the initial insertion of the needle, thereby achieving an administration under a stable state.

Abstract: A personal computer (1) of a surgery assistance system (100) performs navigation during surgery while combining and displaying an image of the distal end (surgical instrument image (33a)) of a surgical instrument (33) and a distance from the surgical instrument distal end to the resection site, in a three-dimensional image produced by a volume rendering computer (13).

Abstract: An analysis device includes: a separation cavity 18 for separating a test liquid into a solution component and a solid component by using a centrifugal force; a higher specific gravity component quantitative cavity 23 for holding a portion of the separated solid component which has been transferred; a sample solution overflow cavity 22 arranged between the higher specific gravity component quantitative cavity 23 and the separation cavity 18 and connected to a connecting channel 21 for transporting the sample liquid from the separation cavity 18; and a capillary cavity 19 formed in the separation cavity 18 for temporarily holding a separated solution component (blood plasma) in the separation cavity 18. A blood plasma component 57a remaining in the separation cavity 18 is trapped by the capillary cavity 19.

Abstract: An injection device with a puncture function includes, in a single casing, a cylindrical cartridge in which insulin is enclosed, a cartridge holder to which the cartridge is inserted, a needle inserted at a front end of the cartridge, a reciprocation unit for reciprocating the cartridge toward the needle, and an extrusion member for extruding the insulin from a rear end of the cartridge toward the needle, and the motion speed and the motion amount of the reciprocation unit are made variable.

Abstract: There is provided a biosensor measurement system which can output a highly-precise measurement result even when an impact such as falling of the sensor occurs or the biosensor is an exposed sensor. An abnormal waveform detection electrode is provided in addition to electrodes for quantitative determination of a target substance. Therefore, when an impact is caused by such as falling of the sensor in a halt period where no voltage is applied in a voltage application algorithm, the abnormal waveform detection electrode can detect the impact. Further, also an exposed sensor can be detected by the abnormal waveform which is detected by the abnormal waveform detection electrode.

Abstract: An isolator includes: a working chamber in which work is conducted; an atomizer configured to atomize air or a decontamination material in the working chamber: a pump configured to supply the decontamination material to the atomizer; a compressor configured to supply air to the atomizer; a pressure sensor configured to measure an internal pressure of the working chamber; and a control unit configured to perform a leak test, in which the compressor is driven to supply air from the atomizer into the working chamber thereby pressuring the working chamber, and airtightness of the working chamber is tested based on the internal pressure of the working chamber measured by the pressure sensor.

Abstract: An engagement component that engages with the rear part of a sensor mounted to a sensor connector, and a manipulation body that moves this engagement component to a sensor insertion opening side are provided. In addition, there are provided a manipulation rod that is engaged at one end with the manipulation body and whose other end is pulled out of a main body case through a through-hole provided to the main body case, and a manipulation component that is linked to the other end side of this manipulation rod. The device further comprises an annular wall that is provided outside the main body case and around a through-hole, and a metal slide bearing that covers this annular wall, and a resin sliding member that is slid with respect to a metal slide bearing is provided on the metal slide bearing side of the manipulation component.

Abstract: A sample solution including blood components is processed with a denaturalization reagent comprising a nonionic surface-activating agent and an oxidizing agent to denaturalize a hemoglobin derivative in the sample solution, and thereafter, an immunoassay is performing utilizing an antibody that is specific to a denaturalized site of the hemoglobin derivative to measure the amount of the hemoglobin derivative in the sample. Therefore, when performing assay of hemoglobin derivative, denaturalization of hemoglobin can be performed speedily and reliably while minimizing adverse effects of the denaturalization reagent on immune reaction.

Abstract: A puncture needle cartridge including a puncture needle, a lancet body adapted to cover part or all of a tip of the puncture needle, a cylindrical puncture needle holder disposed on an outer surface of the lancet body to permit the lancet body to move in an axial direction of the puncture needle; and a protective cap that is separable from the puncture needle holder. The protective cap includes a base adapted to cover an opening in the puncture needle holder, a shaft protruding from the base, and arms mounted on the shaft and configured to abut an inner circumferential surface of the opening in the puncture needle holder by spreading in the opening. A space between tips of the arms is larger than an inside diameter of the opening in the puncture needle holder, and is reduced by elastic deformation when the arms are housed in the opening.

Abstract: A storage case (100) for storing a pharmaceutical syringe unit (4) that is mounted to a pharmaceutical administering device (8) comprises a base body (1) that is open at its upper face, and a cover (2) for covering the opening in the base body (1). The base body (1) has in its interior a concave portion (5) that holds the cylindrical pharmaceutical syringe unit (4). The concave portion (5) has holders (6) that hold two ends of the pharmaceutical syringe unit (4), and a center concave portion (7) for attaching and removing the pharmaceutical syringe unit (4) and being provided in a position that corresponds to the main body portion of a stored pharmaceutical syringe unit (4). The center concave portion (7) further has a bottom part positioned lower than the holders (6), and is formed such that the pharmaceutical administering device (8) can be disposed in an upright position.

Abstract: The protrusion relates to a device comprising a main body case having a sensor mounting component, a measurement component that is connected to the sensor mounting component, a controller that is connected to this measurement component, and a display component that is connected to this controller. A communication component that is connected to the controller communicates pharmaceutical injection information and non-pharmaceutical-injection information to a specific pump.

Abstract: In a read label as an information recording medium and a method for recording information thereon according to the present invention, the read label includes: an adhesive layer 3; a metal film layer 4 disposed on the surface of the adhesive layer 3; and a light-transmissive protective film layer 5 disposed on the surface of the metal film layer 4. The adhesive layer 3 and the light-transmissive protective film layer 5 are larger in thickness than the metal film layer 4, and an evaporated and removed portion is formed in a part of the metal film layer 4 by radiating a laser beam from the side of the light-transmissive protective film layer 5.

Abstract: A vibrating dental device vibrates a specific tooth in a dentition attached with a bracket, a wire or a mouthpiece as an orthodontic appliance. The vibrating dental device includes a vibration source, a connector connected to the orthodontic appliance, and a vibration transmitter, which transmits vibration generated by the vibration source to the connector. The connector is detachably attached to the orthodontic appliance.

Abstract: A biological sample measurement apparatus includes container (10) having an opening in a top surface thereof and right and left accommodation chambers (12) and (13) formed by separating an inner space and the opening in container (10) by partition wall (11a), measurement device (1) accommodated in accommodation chamber (12) of container (10), and a holder accommodated in accommodation chamber (13) of container (10) and holding measurement device (1). Provided are recesses (15, 16) configuring holding means holding measurement device (1) on an outer peripheral wall configuring accommodation chamber (12) or in accommodation chamber (12) in a state where sensor mounting section (4) of measurement device (1) is projected to an outside of accommodation chamber (12).

Abstract: An isolator includes: a chamber to be decontaminated including an inlet provided with an intake filter and an outlet provided with a discharge filter; a first flow path through which outside air is taken into the chamber via the intake filter; a second flow path through which gas in the chamber is discharged via the discharge filter; a blower configured to take in the outside air to the chamber through the first flow path, as well as produce an air current to discharge the gas in the chamber through the second flow path; a decontaminating gas supply unit configured to supply decontaminating gas into the chamber without flowing through the intake filter and the discharge filter; and a third flow path through which the gas in the chamber is discharged via the intake filter when the decontaminating gas is supplied into the chamber.

Abstract: A biosensor measurement system and a method for detecting abnormal measurement in a biosensor, which can significantly enhance the measurement precision without depending on the user's operation manner or the like, can be provided. A voltage application pattern for applying a voltage to a working electrode, a counter electrode, and a detection electrode has a halt period between a first application period and a second application period, and a reduction current measurement value obtained in the first application period is compared with a reduction current measurement value obtained in the second application period, and the measurement values are not outputted when a difference between the measurement values is outside a predetermined range.

Abstract: The pharmaceutical syringe unit includes a cylindrical syringe cover having at one end side thereof a needle mount for an injection needle and a piston-inserting portion at the other end side, and a pharmaceutical syringe configured to be loaded in the syringe cover. The syringe cover includes, on an outer surface thereof, a discrimination mark that is detectable by the pharmaceutical injection device and indicates a type of a drug. The syringe cover includes, on an outer surface thereof, a rotation marker that indicates a rotation direction of the pharmaceutical syringe unit with respect to the main body when the pharmaceutical syringe unit is mounted on the main body.

Abstract: A partition wall is provided between a display section and a sensor mount inside a main case. A control board housing chamber is disposed on the display unit side of the partition wall, and a measurement board housing chamber is disposed on the sensor mount side of the partition wall. A control board is housed in the control board housing chamber, and a measurement board and a temperature sensor are housed in the measurement board housing chamber.

Abstract: Provided are a method for increasing an amount of glucose oxidase to be immobilized on the self-assembled monolayer and a sensor which comprises glucose oxidase immobilized with the method. The method of the disclosed technology is characterized by that one molecule of an amino acid is interposed between the self-assembled monolayer and the molecule of the glucose oxidase.

Abstract: A sensor storage container includes: a lid configured to cover in an openable and closable manner an opening of an open-topped main body case that stores an elongated plate-like sensor lying flat; and a sensor ejecting tool configured to take the sensor out of the main body case. The sensor ejecting tool is elongated, and includes two ends, one end being linked to one of end sides of an opening portion of the main body case, and the other end being rotatable in a vertical direction between a bottom portion of the main body case and a position above the opening portion. A sensor adhesive portion at the other end of the sensor ejecting tool is provided with an adhesive face on a side of the sensor adhesive portion facing a bottom face of the main body case.