This pathological diagnosis support system comprises an image diagnosis server and a pathologist's personal computer. The image diagnosis server uses an image analysis unit to set confirmation frames in which the abnormality score exceeds a threshold value, assigns a frame number of “1,” “2,” or “3” to each of the confirmation frames, and sends setting information about the pathological diagnosis image and the confirmation frames and the frame number “1,” “2,” or “3” of the confirmation frames to the pathologist's personal computer. When the pathological diagnosis image is displayed on a display unit, the personal computer controls the display unit so that the confirmation frames and the frame number “1,” “2,” or “3” are displayed within the pathological diagnosis image, and the frame number “1,” “2,” or “3” is displayed on the outside of the pathological diagnosis image.
G16H 50/20 - ICT specially adapted for medical diagnosis, medical simulation or medical data mining; ICT specially adapted for detecting, monitoring or modelling epidemics or pandemics for computer-aided diagnosis, e.g. based on medical expert systems
A cold storage includes a box including a cold storage chamber, a sliding door that opens and closes the cold storage chamber, and a machine chamber; a compressor disposed in the machine chamber and constituting a refrigeration circuit that cools the inside of the cold storage chamber; a fan that generates an airflow passing around the compressor and blown to the sliding door through an air outlet opened to the machine chamber; a heater disposed in the cold storage chamber; and a control apparatus that operates the heater when a condition of a set temperature for the cold storage chamber being equal to or lower than a specified temperature and a condition of the compressor being in an operating state are satisfied.
A cold storage includes a box with an opening at front, a frame bordering the opening, a sliding door attached to the frame and including, in at least one of a left-side end portion and a right-side end portion, a drain channel extending vertically, and a porous body with water permeability, the porous body being attached to an upper surface of the sliding door to establish fluid communication with the drain channel.
F28D 20/00 - Heat storage plants or apparatus in general; Regenerative heat-exchange apparatus not covered by groups or
4.
PHARMACEUTICAL REFRIGERATOR OPERATION SUPPORT SYSTEM, PHARMACEUTICAL REFRIGERATOR OPERATION SUPPORT METHOD, AND NON-TRANSITORY COMPUTER-READABLE MEDIUM
A pharmaceutical refrigerator operation support system includes a server, a pharmaceutical refrigerator, a first computer that sends to the server information about a first medicine, information about a first RFID tag attached to the first medicine, and information about a first pharmaceutical distribution institution, and a second computer that sends to the server information about a second medicine, information about a second RFID tag attached to the second medicine, and information about a second pharmaceutical distribution institution. The server manages a status of medicine in the pharmaceutical refrigerator by identifying the first medicine as a medicine delivered by the first pharmaceutical distribution institution and identifying the second medicine as a medicine delivered by the second pharmaceutical distribution institution, based on information received from the pharmaceutical refrigerator, the first computer, and the second computer.
G16H 20/10 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
G06Q 10/087 - Inventory or stock management, e.g. order filling, procurement or balancing against orders
A cold storage includes a box with a cold storage chamber, a compressor constituting a refrigeration circuit that cools the inside of the cold storage chamber, a defrost heater that heats an evaporator constituting the refrigeration circuit, and a control apparatus that controls the compressor and the defrost heater. The control apparatus operates the defrost heater when the compressor is not operated. When an outside air temperature is equal to or higher than a chamber temperature in the cold storage chamber, the control apparatus operates the compressor upon the chamber temperature rising up to a first threshold and stops the compressor upon the chamber temperature dropping down to a second threshold lower than the first threshold. When the outside air temperature is lower than the chamber temperature, the control apparatus does not operate the compressor even when the chamber temperature rises up to the first threshold.
An insulin infusion device includes a cannula for infusing insulin under the skin and an insulin infusion section for storing therein insulin to be delivered to the cannula. The insulin infusion device also includes a motion measurement section that measures the tilt angle or rotation angle of a center axis of the insulin infusion section from a neutral position thereof, or vibration applied to the insulin infusion section, to output a measured value as motion information of living activity. The insulin infusion device also includes a controlling section that controls, based on the motion information, a process of notifying a user of the timing or recommended direction of priming of the insulin infusion section.
A drug cartridge includes: a cylinder 11 having a cylindrical cylinder columnar space extending in a longitudinal direction; a gasket 13 supported in the space so that the gasket is movable in the longitudinal direction; a drug 14 held in the space and at least including a liquid first component; and a first temperature sensor and an RF tag 16 arranged on a side surface of the cylinder. The RF tag 16 stores drug information that includes at least information indicating a type of the drug, and wirelessly transmits at least the information indicating the type of the drug and first temperature information indicating a temperature detected by the first temperature sensor in response to an instruction from outside.
A locking device includes a lever configured to sway around a rotation axis and including a restriction part restricting an operation of a handle, a hole, and an attaching portion where a moving member configured to move in accordance with an operation of an actuator is attached; and a pressure member disposed in the hole and configured to make a first back-and-forth movement in accordance with an unlocking operation of a key. The pressure member moves the restriction part from a position for restricting the operation of the handle to a position for allowing the operation of the handle by swaying the lever around the rotation axis by pressing a first portion which is a portion of the hole in a forward movement of the first back-and-forth movement, and moves away from the first portion without swaying the lever in a backward movement of the first back-and-forth movement.
A drug supply device includes: a plurality of cassettes configured to eject a drug one by one; and a control device configured to set a plurality of groups including a plurality of cassettes selected from among the plurality of cassettes. The control device selects a cassette that performs a drug ejection operation from each of the plurality of groups such that a number of tablets of a drug to be ejected from the plurality of cassettes that perform the drug ejection operation is each levelled in one of the plurality of group and among the plurality of groups.
A61J 7/00 - Devices for administering medicines orally, e.g. spoons; Pill counting devices; Arrangements for time indication or reminder for taking medicine
B65B 1/30 - Devices or methods for controlling or determining the quantity or quality of the material fed or filled
B65B 61/02 - Auxiliary devices, not otherwise provided for, for operating on sheets, blanks, webs, binding material, containers or packages for perforating, scoring, or applying code or date marks on material prior to packaging
A drainage cap includes: a body part configured to be inserted to a drainage outlet; and a flange part provided at the body part, and including a notch and an opposing part at a peripheral portion of the flange part, the opposing part being configured to face a peripheral portion of the drainage outlet.
A refrigeration circuit includes: a gas-liquid separator into which a gas-liquid two-phase refrigerant flowed out from a condenser flows, the gas-liquid separator being configured to separate the gas-liquid two-phase refrigerant into a vapor phase refrigerant and a liquid phase refrigerant; and a plate heat exchanger including a first heat exchanging part and a second heat exchanging part, the first heat exchanging part being a part where the vapor phase refrigerant flowed out from the gas-liquid separator and the liquid phase refrigerant flowed out from the gas-liquid separator exchange heat, the second heat exchanging part being a part where the vapor phase refrigerant flowed out from the first heat exchanging part and a returning refrigerant flowed out from an evaporator exchange heat.
F25B 43/04 - Arrangements for separating or purifying gases or liquids; Arrangements for vaporising the residuum of liquid refrigerant, e.g. by heat for withdrawing non-condensible gases
F28D 9/00 - Heat-exchange apparatus having stationary plate-like or laminated conduit assemblies for both heat-exchange media, the media being in contact with different sides of a conduit wall
12.
CELL CULTURE CONTROL DEVICE, CELL CULTURE DEVICE PROVIDED WITH SAME, CELL CULTURE CONTROL METHOD, AND CELL CULTURE CONTROL PROGRAM
A PC comprises a measurement unit, a consumption rate calculation unit, a culture medium replacement detection unit, and a next step transition determination unit. The measurement unit acquires the amount of consumed glucose from the result of continuously measuring the concentration of glucose contained in a culture medium (X) of a culture vessel. The consumption rate calculation unit calculates the consumption rate at which glucose is consumed by differentiating the amount of glucose consumed. The culture medium replacement detection unit detects that the culture medium (X) in the culture vessel has been replaced or added. When the culture medium (X) is replaced or added, the next step transition determination unit determines whether or not to proceed to the next step according to whether or not the consumption rate after the replacement or addition of the culture medium (X) calculated by the consumption rate calculation unit satisfies a specific condition.
A sensor unit has sensors for measuring the components of a culture medium in a culture vessel, and comprises a plurality of sensors and a linking portion. The plurality of sensors each have a main body and a sensing unit disposed on the lower end side of the main body and immersed in the culture medium to measure the components of the culture medium. The linking portion links the plurality of sensors on the upper end side of the main body.
This sensor has a probe inserted into a living body, and measures an analyte, wherein the probe has a substrate, an electrode formed on the substrate, a reagent layer formed on the electrode, a first protective film formed on the reagent layer, and a second protective film which is thinner than the first protective film and formed on the first protective film.
Provided is a binary refrigeration apparatus including: a low-temperature side refrigeration circuit including a spiral heat exchanger including a main tube and a spiral tube wound around the main tube in a spiral form, the main tube being a tube where a low-temperature side refrigerant that flows into a low-temperature side compressor enters, the spiral tube being a tube where the low-temperature side refrigerant flown out from the low-temperature side compressor enters; and a high-temperature side refrigeration circuit where a high-temperature side refrigerant that exchanges heat with the low-temperature side refrigerant through a plate heat exchanger circulates.
F25B 7/00 - Compression machines, plants or systems, with cascade operation, i.e. with two or more circuits, the heat from the condenser of one circuit being absorbed by the evaporator of the next circuit
F28D 9/00 - Heat-exchange apparatus having stationary plate-like or laminated conduit assemblies for both heat-exchange media, the media being in contact with different sides of a conduit wall
F25B 6/02 - Compression machines, plants or systems, with several condenser circuits arranged in parallel
This sensor is for measuring an analyte and has a probe to be inserted inside a living body. The probe of the sensor includes a substrate, an electrode formed on the substrate, and a reagent layer that contains an oxidoreductase and that is formed on the electrode. At at least one end of the probe in the width direction, the reagent layer and the electrode are trimmed along the insertion direction of the probe toward the inside of the living body.
A61B 5/1473 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value using chemical or electrochemical methods, e.g. by polarographic means invasive, e.g. introduced into the body by a catheter
A61B 5/1486 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value using enzyme electrodes, e.g. with immobilised oxidase
17.
CASSETTE, MEDICINE INJECTION DEVICE, AND MEDICINE INJECTION SYSTEM
A cassette including: a cartridge holder including a first end, a second end having a holder opening, and a holder columnar space located between the first end and the second end and capable of accommodating a drug cartridge, drug cartridge including: a cylinder including a first end at which an injection needle is insertable/extractable, a second end at which a cylinder opening is located, and a cylinder columnar space located between the first end and the second end; a drug placed in the cylinder columnar space; and a gasket being placed in the cylinder columnar space; a cassette cap capable of opening and closing the holder opening, the cassette cap including a first end having a cap opening that is opposed to the holder opening, a second end having a piston insertion opening, and a cap columnar space located between the first end and the second end.
This sensor has a probe to be inserted into a living body and measures an analyte. The probe has a substrate, an electrode formed on the substrate, and a reference layer formed on the electrode. The upper surface of the reference layer is covered with a film, and the side surfaces thereof are exposed.
A61B 5/1473 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value using chemical or electrochemical methods, e.g. by polarographic means invasive, e.g. introduced into the body by a catheter
A61B 5/145 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value
A61B 5/00 - Measuring for diagnostic purposes ; Identification of persons
A sample analysis substrate mountable and detachable to a sample analysis device and includes: a plate-shaped base substrate; and a chamber, the chamber being a space in which to cause a binding reaction, The sample analysis device includes: a motor to rotate the sample analysis substrate; a first magnet unit to attract the magnetic particles; a first actuator to move the first magnet unit to change relative positions of the first magnet unit and the sample analysis substrate; and a control circuit to control the motor, the drive circuit, and the first actuator. The first magnet unit shaped as a whole shape or a partial shape of a circle or a ring. During a B/F separation for separating reacted substance from unreacted substance, the first actuator moves the first magnet unit to a position where the magnetic particles in the chamber are attracted by the first magnet unit.
G01N 33/543 - Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
G01N 35/02 - Automatic analysis not limited to methods or materials provided for in any single one of groups ; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations
B01L 3/00 - Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
20.
CELL CULTURE ANALYZER AND CELL CULTURE ANALYSIS METHOD USING SAME, ADDITIVE SUPPLY UNIT AND CELL CULTURE ANALYZER PROVIDED THEREWITH, AND SENSOR UNIT AND CELL CULTURE ANALYZER PROVIDED THEREWITH
A cell culture analyzer comprises a stirring member and an air discharge and intake unit. The stirring member is used in a state of being immersed in a medium, and has a liquid discharge and intake port for discharging or drawing in the medium, and an air discharge and intake port for discharging or drawing in air in order to discharge or draw in the medium from the liquid discharge and intake port. The air discharge and intake unit is linked to the air discharge and intake port of the stirring member, and discharges or draws in the air discharged or drawn in from the air discharge and intake port.
A pharmaceutical management system includes: at least one pharmaceutical storage box to store at least one pharmaceutical having corresponding at least one IC tag attached thereto; a reading device to read information stored in the IC tag, the information representing the pharmaceutical; a controller to obtain the information of the IC tag from the reading device, to manage the pharmaceutical; and a pharmaceutical refrigerator to store the pharmaceutical storage box to refrigerate the pharmaceutical, the controller including a first and second entry/exit monitoring unit to monitor entry/exit of the pharmaceutical into/from the pharmaceutical storage box; and after monitoring by the first entry/exit monitoring unit, a state of entry of the pharmaceutical into the pharmaceutical storage box is determined based on a result of monitoring by the second entry/exit monitoring unit.
A61J 7/04 - Arrangements for time indication or reminder for taking medicine, e.g. programmed dispensers
G16H 20/13 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered from dispensers
A pharmaceutical storage box to be stored in a pharmaceutical refrigerator so as to be freely movable in and out of the pharmaceutical refrigerator, the pharmaceutical storage box including: a bottom plate on which a pharmaceutical is placed, the pharmaceutical having an attached IC tag; a first side plate having an attached first antenna, the first side plate removably connected to a first end surface of the bottom plate; a second side plate removably connected to a second end surface of the bottom plate; and a back plate removably connected to a third end surface of the bottom plate, wherein the first side plate has a first connection structure connectable to the second end surface, wherein the second side plate has a second connection structure that is connectable to the first end surface.
A61J 1/00 - Containers specially adapted for medical or pharmaceutical purposes
B65D 6/00 - Containers having bodies formed by interconnecting or uniting two or more rigid, or substantially rigid, components made wholly or mainly of metal, plastics, wood or substitutes therefor
F25D 25/00 - Charging, supporting, or discharging the articles to be cooled
G06K 19/077 - Constructional details, e.g. mounting of circuits in the carrier
23.
NUCLEIC ACID TESTING DEVICE AND NUCLEIC ACID TESTING METHOD
A nucleic acid testing device includes: a stage on which is placed a tissue section to which a solution has been added, in which the solution contains a labeling substance of a target nucleic acid and an amplification reagent for the target nucleic acid; a temperature adjuster that adjusts the temperature of the tissue section on the stage; a temperature controller that controls the temperature adjuster to advance nucleic acid amplification reaction in the tissue section; an intensity detector that detects label intensity in the tissue section over time; and a storage unit that stores detection information generated by the intensity detector.
A culture apparatus includes an inner box for housing a culture, an outer box surrounding the inner box, and a first vibration prevention mechanism that is disposed between the inner box and the outer box, and is configured to prevent the inner box from vibrating due to the vibration of the outer box.
F16F 15/02 - Suppression of vibrations of non-rotating, e.g. reciprocating, systems; Suppression of vibrations of rotating systems by use of members not moving with the rotating system
F16F 15/00 - Suppression of vibrations in systems; Means or arrangements for avoiding or reducing out-of-balance forces, e.g. due to motion
25.
SENSOR, MEASUREMENT DEVICE PROVIDED THEREWITH, SENSOR UNIT, CELL CULTURE ANALYSIS DEVICE, AND LIQUID SAMPLE MEASUREMENT METHOD
A sensor performs measurement of a culture medium and is used in a state of being immersed in a medium placed in a well, the sensor comprising a main body having a first surface and a second surface that is on the opposite side from the first surface; an electrode unit that is provided on the first surface in the main body and to which a specific voltage is applied in the course of performing measurement in a state of being immersed in the medium; and a liquid holding portion that is provided around the electrode unit on the first surface, and that is disposed near the inner wall surface of the well and holds the medium up to above the electrode unit, in between the inner wall surfaces.
G01N 33/487 - Physical analysis of biological material of liquid biological material
G01N 27/22 - Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating capacitance
A sensor unit (9) comprises a substrate (13) having a sensor (16), wiring (19) connected to the sensor (16), connection portions (20a, 20b) connected to the sensor (16) via the wiring (19), and a bent portion (17) where the sensor (16) is bent downward. The sensor (16) is formed so as to be cut out from the substrate (13) in a state in which the bent portion (17) remains on the substrate (13).
The present disclosure provides an electrode substrate including an insulating substrate having, on a surface thereof, a region where at least one fine uneven structure is formed and a plurality of smooth regions separated by the fine uneven structure; and a conductive thin film formed on the entire of at least one surface of the insulating substrate where the fine uneven structure is formed. According to the present disclosure, the conductive region and the insulating region can be simultaneously formed on the insulating substrate only by forming the conductive thin film in a single step on the entire surface of the single insulating substrate on which the fine uneven structure is formed.
The present disclosure provides a means for preventing or suppressing the leaching of a redox mediator constituting a reagent layer in a probe of an embedded biosensor, in particular, a means capable of improving preservation stability (durability) while maintaining glucose measurement sensitivity. The high molecular weight redox polymer according to the present disclosure is represented by general formula (A1), wherein X− represents an anionic species; L represents a linker; Poly represents a high molecular weight polymer; and R1 to R8 each independently represent a hydrogen atom or a substituent. The biosensor according to the present disclosure has a working electrode, a counter electrode, a reagent layer disposed on the working electrode, and a protective film covering at least the reagent layer, and the reagent layer contains an oxidoreductase that oxidizes or dehydrogenates the analyte and at least one high molecular weight redox polymer represented by general formula (A1).
The present disclosure provides a means for preventing or suppressing the leaching of a redox mediator constituting a reagent layer in a probe of an embedded biosensor, in particular, a means capable of improving preservation stability (durability) while maintaining glucose measurement sensitivity. The high molecular weight redox polymer according to the present disclosure is represented by general formula (A1), wherein X− represents an anionic species; L represents a linker; Poly represents a high molecular weight polymer; and R1 to R8 each independently represent a hydrogen atom or a substituent. The biosensor according to the present disclosure has a working electrode, a counter electrode, a reagent layer disposed on the working electrode, and a protective film covering at least the reagent layer, and the reagent layer contains an oxidoreductase that oxidizes or dehydrogenates the analyte and at least one high molecular weight redox polymer represented by general formula (A1).
A refrigeration apparatus performs refrigeration by freezing circuitry using refrigerant. The refrigeration apparatus includes: an inner door that is provided with a thermal insulation material inside; a case section that includes a peripheral edge section facing a perimeter section of the inner door while the inner door is closed, and that is refrigerated inside by the refrigerant; a packing that is pressed between the perimeter section of the inner door and the peripheral edge section while the inner door is closed; a pipe that is placed along the peripheral edge section, and that circulates the refrigerant warmed by a compression effect of a compressor; and an outer door that covers the inner door while the inner door is closed.
A refrigeration apparatus includes: a housing that surrounds an internal space (refrigeration chamber) where a refrigeration target is stored; and a negative pressure release port that includes a pipe (cylindrical body) attached to the housing so as to protrude into the internal space, a heating element provided in the pipe, and a rib joining the pipe and the heating element.
F25D 17/04 - Arrangements for circulating cooling fluids; Arrangements for circulating gas, e.g. air, within refrigerated spaces for circulating gas, e.g. by natural convection
A medicine dispensing apparatus includes: a hopper that receives a medicine and causes the medicine to proceed to a guiding port; a holding section that is provided to the hopper and holds the medicine; and a delivering section that is provided to the hopper and delivers the medicine held by the holding section to the guiding port.
A61J 7/00 - Devices for administering medicines orally, e.g. spoons; Pill counting devices; Arrangements for time indication or reminder for taking medicine
B65B 1/02 - Machines characterised by the incorporation of means for making the containers or receptacles
B65B 1/06 - Methods of, or means for, filling the material into the containers or receptacles by gravity flow
32.
PHARMACEUTICAL INJECTION ASSESSMENT SYSTEM AND PHARMACEUTICAL INJECTION ASSESSMENT PROGRAM
A pharmaceutical injection assessment system comprises a blood glucose level measurement device, a smartphone, and a terminal device. The blood glucose level measurement device measures the blood glucose level and acquires a dose of insulin on the basis of the measured blood glucose level. The smartphone captures a confirmation image showing the type and dose of insulin. The terminal device has a communication unit for receiving a confirmation image, and a display for prompting the administrator to confirm the type and dose of insulin.
G16H 20/17 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
A61M 5/172 - Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters electrical or electronic
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
33.
LIQUID SURFACE DETECTION DEVICE, ATOMIZATION DEVICE, AND CULTURE DEVICE
This liquid surface detection device comprises: a liquid retention part in which hydrogen peroxide water is retained, the hydrogen peroxide water to be atomized by a vibrating plate in which a through-hole is provided; a float positioned inside the liquid retention part; and a sensor that detects, via the float, the arrival of the liquid surface of the hydrogen peroxide water retained in the liquid retention device at a prescribed position.
G01F 23/30 - Indicating or measuring liquid level or level of fluent solid material, e.g. indicating in terms of volume or indicating by means of an alarm by floats
C12M 3/00 - Tissue, human, animal or plant cell, or virus culture apparatus
B05B 17/06 - Apparatus for spraying or atomising liquids or other fluent materials, not covered by any other group of this subclass operating with special methods using ultrasonic vibrations
This refrigeration apparatus comprises: an inner box having a top surface and side surfaces; and an evaporator constituted by bent pipes comprising a top surface portion in contact with the top surface, an upper side-surface portion in contact with the side surfaces, and a lower side-surface portion in contact with the side surfaces below the upper-side surface portion. The pipes constituting the upper side-surface portion are more densely arranged than the pipes constituting the lower side-surface portion. The total length of the pipes constituting the top surface portion and the upper side-surface portion is 62.5% or more of the lengths of the pipes in contact with the inner box.
F25D 11/02 - Self-contained movable devices associated with refrigerating machinery, e.g. domestic refrigerators with cooling compartments at different temperatures
35.
BIOLOGICAL INFORMATION MEASUREMENT DEVICE AND BIOLOGICAL INFORMATION MEASUREMENT METHOD
A biological information measurement device comprises a sensor insertion port, a measurement unit, a communication unit, and a control unit. In the sensor insertion port is mounted a sensor for measuring biological information about a patient. The measurement unit is connected to the sensor mounted in sensor insertion port and measures the blood glucose level. The communication unit acquires information about the patient whose biological information is being measured. The control unit determines the risk status of the patient on the basis of the information about the patient acquired by the communication unit, and issues a warning about the measurement of the biological information of the patient with the measurement unit on the basis of the determination result.
G01N 33/66 - Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving blood sugars, e.g. galactose
G16H 10/40 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for data related to laboratory analysis, e.g. patient specimen analysis
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
This refrigeration device comprises: a high temperature side refrigerant circuit in which a high temperature side refrigerant circulates; a low temperature side refrigerant circuit in which a low temperature side refrigerant circulates; and a cascade heat exchanger that cools the low temperature side refrigerant with the high temperature side refrigerant. In the low temperature side refrigerant circuit, a low temperature side decompressor is disposed downstream of the cascade heat exchanger and a temperature sensor is installed in a piping portion between the cascade heat exchanger and the low temperature side decompressor.
F25B 49/02 - Arrangement or mounting of control or safety devices for compression type machines, plants or systems
F25B 7/00 - Compression machines, plants or systems, with cascade operation, i.e. with two or more circuits, the heat from the condenser of one circuit being absorbed by the evaporator of the next circuit
A biosensor includes: a base plate; an electrode layer located on a major surface of the base plate and including a first electrode pair; a spacer plate provided on the electrode layer, the spacer plate having a first opening and at least one partition located in the first opening and connected with a periphery of the first opening at one end so as to divide part of the first opening into two or more portions; a first reagent layer provided in each of the two or more portions of the first opening; and a cover plate having an entrance section including at least one entrance opening and provided on the spacer plate, the entrance section overlapping at least part of the first opening, wherein part of the first electrode pair is located in the two or more portions of the first opening of the spacer plate.
A sample storage device may include: a storage chamber; paired rail sections separated in separating direction and extending in an extending direction; an antenna array substrate extending between the rail sections and having antennas; paired slide sections separated from each other in the separating direction and disposed at a position opposite to the antenna array substrate with respect to the rail sections and, so as to be slidable in the extending direction relative to the rail sections, respectively; a support plate transparent to radio waves, extending between the slide sections; and a storage box containable a plurality of containers each holding a sample and a radio tag, the storage box to be set on the support plate such that radio waves can be transmitted between the radio tag and corresponding one of the plurality of antennas.
A sensor insertion device comprises a lower case and an upper case. A base holder and a needle holder are disposed in the lower case. A needle holder raising mechanism is disposed above the needle holder. A sensor base having a sensor unit is held by the base holder. When the upper case is pushed down, the base holder and the needle holder move toward an opening on the lower surface side of the lower case, and the needle holder is raised by the needle holder raising mechanism. A protrusion that holds the upper case on the lower case is provided to the upper case in a state in which the upper case has been pushed down until the opening on the lower surface side comes into contact with the skin.
A61B 5/1473 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value using chemical or electrochemical methods, e.g. by polarographic means invasive, e.g. introduced into the body by a catheter
A61B 5/1486 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value using enzyme electrodes, e.g. with immobilised oxidase
A sample analysis substrate capable of holding a plurality of liquids. The sample analysis substrate has a microchannel structure for transferring a liquid through rotary motion, the sample analysis substrate including: a substrate body having a rotation axis; a first and a second container holding a first and a second liquid therein; a first and a second accommodating section accommodating the first and the second container; and a cap having a first and second projection and movably supported on the substrate body. As the cap moves, the first drive projection and the second drive projection move the first container and the second container with staggered timing, thereby releasing the first and the second liquid accommodated therein.
G01N 1/36 - Embedding or analogous mounting of samples
G01N 35/08 - Automatic analysis not limited to methods or materials provided for in any single one of groups ; Handling materials therefor using a stream of discrete samples flowing along a tube system, e.g. flow injection analysis
A culture medium replacement device includes: multiple reservoirs that are mounted on a well plate including multiple wells, which each contain a culture and a culture medium, and are provided respectively for the multiple wells and that each contain a culture medium to be supplied to a corresponding well; a gas supply pump that discharges a gas supplied to the multiple reservoirs; a gas supply passage unit that connects the gas supply pump and the multiple reservoirs and that transmits the gas from the gas supply pump to the multiple reservoirs; and multiple liquid supply passages that each connect a reservoir and a corresponding well and transmit, to the corresponding well, the culture medium pushed out from the reservoir by the gas flowing into the reservoir.
This medicine case comprises: a case body for accommodating a medicine, the case body being such that a discharge opening for the medicine is provided in a bottom part thereof; and a rotating member disposed inside the case body, the rotating member rotating about a rotating shaft. The rotating member has a first side wall member and a second side wall member that are parallel to each other and that constitute a passage through which the medicine is guided to the discharge opening. The first side wall member and the second side wall member approach and separate from each other while remaining parallel to each other, adjusting the width of the passage.
A61J 7/00 - Devices for administering medicines orally, e.g. spoons; Pill counting devices; Arrangements for time indication or reminder for taking medicine
A61J 1/03 - Containers specially adapted for medical or pharmaceutical purposes for pills or tablets
B65B 1/30 - Devices or methods for controlling or determining the quantity or quality of the material fed or filled
A culture device comprising: an adjusting gas supplier which supplies to a culture space an adjusting gas for adjusting the concentration of a definite gas component in the culture space; an adjuster which adjusts the moisture in the culture space; and a controller which controls the adjuster, wherein the controller controls the adjuster depending on the supply amount of the adjusting gas or a parameter correlated to the supply amount.
A sample collection device includes a grip portion and a collection portion connected to the grip portion, wherein the collection portion includes a first surface and a capillary having a groove shape provided on the first surface and formed with openings at opposite ends thereof.
This substrate for sample analysis, which transfers a sample-containing liquid by means of rotation and analyzes a specific substance in a sample, is provided with: a space which holds the sample-containing liquid in a substrate having a rotary shaft; a reaction chamber having an inlet and an outlet connected to the space; and a dried reagent disposed in the space of the reaction chamber. The space has a first end and a second end spaced apart from each other in a circumferential direction. The inlet and the outlet are arranged at the first end and the second end, respectively. The space has a capillary portion, and a first non-capillary portion which is connected to the capillary portion, is located at the second end, has an opening, and extends in a radial direction. The outlet is connected to the outer peripheral side of the first non-capillary portion.
G01N 35/04 - Automatic analysis not limited to methods or materials provided for in any single one of groups ; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations - Details of the conveyor system
G01N 35/00 - Automatic analysis not limited to methods or materials provided for in any single one of groups ; Handling materials therefor
To estimate concentration of a cellular metabolite contained in a culture medium where certain cells are cultured, using a simple method, etc., spectroscopy. The number of the certain cells is estimatable by applying previously obtained information regarding relationship between a cellular metabolite concentration and the number of the certain cells.
To estimate concentration of a cellular metabolite contained in a culture medium where certain cells are cultured, using a simple method, etc., spectroscopy. The number of the certain cells is estimatable by applying previously obtained information regarding relationship between a cellular metabolite concentration and the number of the certain cells.
In spectroscopy, the higher the cellular metabolite concentration, the more accurately the actual concentration of the cell consumed-substance can be estimated. Accordingly, the concentration of a cell-consumed substance, decreasing as cells are cultured, are estimated in the early to middle stages of culture, and the concentrations of a cell-produced substance, increasing as cells are cultured, are estimated in the middle to late stage of the culture. This enables estimation of the number of cells in the entire range from beginning to end of cell culture.
Provided is a method for measuring a component of a biological sample with a biosensor provided with: a capillary for introducing the biological sample; an electrode part including a first electrode system that includes a first working electrode and a first counter electrode in the capillary; and a reagent part disposed so as to be in contact with the electrode part, the reagent part containing an enzyme and a mediator, and the method including a step of starting voltage application for a duration longer than 0 second and up to 0.7 second to the first electrode system within 0 second to 0.5 second after detection of the introduction of the biological sample to obtain a hematocrit value based on a current value obtained thereby.
C12Q 1/00 - Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
G01N 27/30 - Electrodes, e.g. test electrodes; Half-cells
This culturing apparatus is provided with a humidifying pan which is disposed in a culturing space and in which a liquid for humidification is retained, a first heater for heating the humidifying pan; and a second heater for controlling the temperature of the culturing space, the first heater and the second heater being separately provided.
A wearable sensor device comprises a sensor at least part of which is inserted into a human body and which has a first connection terminal; a mount unit on which at least part of the first connection terminal is disposed and which is mounted on a skin of the human body; and an electronic unit that is mounted to the mount unit and has a second connection terminal connected to the first connection terminal via a mounting mechanism, and a control unit for acquiring signals from the sensor. The mounting mechanism forms a first state where the mount unit and the electronic unit are mounted such that the first connection terminal and the second connection terminal have yet to be connected, and a second state where the mount unit and the electronic unit are mounted such that the first connection terminal and the second connection terminal have been connected.
The biological information measurement device comprises: an adhesive tape having on its bottom side an adhesive surface to be affixed to the skin of a user; a mounting substrate disposed on the top side of the adhesive tape; a guide needle insertion cylinder provided on the top side of the adhesive tape, on which the mounting substrate is held; a sensor electrically connected to the mounting substrate for measuring biological information; and a cover covering the top side of the mounting substrate. The bottom side of the mounting substrate is in a state of not being affixed to the top side of the adhesive tape, and the adhesive tape and the cover are more stretchable than the mounting substrate.
A cooling device comprises a storehouse having an opening, a door to open and close the opening, and a cooling unit to cool the interior of the storehouse. The cooling unit has a compressor, a condenser, a blower device to blow air to the condenser and the compressor, and a frame pipe. The frame pipe is disposed near the opening and refrigerant, that has been discharged from the compressor but has not reached the condenser, flows therein. The amount of air flow from the blower device is reduced as the interior temperature, which is the temperature inside the storehouse, gets lower or as the elapsed time, which is the time from when the compressor starts operation, becomes longer. The reduction of air flow from the blower device includes stopping the air flow from the blower device.
F25B 13/00 - Compression machines, plants or systems, with reversible cycle
F25D 17/06 - Arrangements for circulating cooling fluids; Arrangements for circulating gas, e.g. air, within refrigerated spaces for circulating gas, e.g. by natural convection by forced circulation
An evaporation unit includes a first and second pipe conduits. The first and second pipe conduits each include a near-end part, a long circumference part, a junction part, a short circumference part, and a far-end part. Around a storage chamber, the first long circumference part extends in a first direction, the first junction part turns, and the first short circumference part extends in the first or second direction. The second short circumference part extends in the first direction, the second junction part turns, and the second long circumference part extends in the first or second direction. The first and second turning part located at the same position counted from the respective near-end part sides are disposed respectively on wall surfaces facing each other.
F28D 15/02 - Heat-exchange apparatus with the intermediate heat-transfer medium in closed tubes passing into or through the conduit walls in which the medium condenses and evaporates, e.g. heat-pipes
F25D 11/02 - Self-contained movable devices associated with refrigerating machinery, e.g. domestic refrigerators with cooling compartments at different temperatures
F25D 17/02 - Arrangements for circulating cooling fluids; Arrangements for circulating gas, e.g. air, within refrigerated spaces for circulating liquids, e.g. brine
A pharmaceutical management system includes: an IC tag attached to a pharmaceutical; a pharmaceutical storage box to store the pharmaceutical and read information of the IC tag; a controller to acquire the information of the IC tag from the pharmaceutical storage box and manage the pharmaceutical; and a pharmaceutical refrigerator to store the pharmaceutical storage box to refrigerate the pharmaceutical.
A pharmaceutical storage box to be stored in a pharmaceutical refrigerator and managed by a controller, the pharmaceutical storage box includes: a storage portion to store a pharmaceutical, the pharmaceutical having an IC tag attached thereto; and an antenna configured to receive information of the IC tag.
G16H 40/40 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management of medical equipment or devices, e.g. scheduling maintenance or upgrades
F25D 25/02 - Charging, supporting, or discharging the articles to be cooled by shelves
F25D 29/00 - Arrangement or mounting of control or safety devices
G06K 7/10 - Methods or arrangements for sensing record carriers by corpuscular radiation
B65D 25/06 - Partitions adapted to be fitted in two or more alternative positions
A transmitter comprises a main body case, a controller that is provided inside the main body case, a communication unit that is connected to the controller, and an elongated antenna unit that is connected to the communication unit. The antenna unit is disposed along an inner wall surface of the main body case.
A drug supplying device provided with: a first drug discharging section that discharges a first drug from a first tablet case; a first temporary storage section that is arranged downstream of the first drug discharging section in a path, and that temporarily stores the first drug; a second drug discharging section that is arranged downstream of the first temporary storage section in the path, and that discharges a second drug from a second tablet case; a second temporary storage section that is arranged downstream of the second drug discharging section in the path, and that temporarily stores the first drug and the second drug; and a third drug discharging section that is arranged downstream of the second temporary storage section in the path, and that discharges a third drug from a third tablet case.
B65B 57/14 - Automatic control, checking, warning or safety devices responsive to absence, presence, abnormal feed, or misplacement of articles or materials to be packaged and operating to control, or stop, the feed of articles or material to be packaged
B65B 1/30 - Devices or methods for controlling or determining the quantity or quality of the material fed or filled
B65B 37/02 - Supplying or feeding fluent-solid, plastic, or liquid material, or loose masses of small articles, to be packaged by gravity flow
A cartridge adapter includes: a cartridge holder having a space that can accommodate therein a drug cartridge, the drug cartridge including a cylinder having a tubular internal space extending in a longitudinal direction, a gasket supported in the internal space so as to be movable in the longitudinal direction, and a drug held in the internal space; a piston that moves the gasket in the longitudinal direction in the internal space of the cylinder; a piston guide that movably supports the piston and connected to the cartridge holder; and a piston driving mechanism that drives the piston in the longitudinal direction.
The invention is provided with a housing which has an inner space open in a first direction, a partition body which divides the inlet of the inner space into a plurality of openings arranged next to each other in a second direction perpendicular to the first direction, a door which is provided to each of the openings and which closes the opening from the first direction side, a first vacuum heat insulating material which is disposed inside the partition body, and a second vacuum heat insulating material which is disposed inside the door. The first vacuum heat insulating material and the second vacuum heat insulating material are arranged so as to overlap each other when viewed from the first direction side or from the second direction side.
A sample analysis substrate in which transfer of a liquid is effected through rotational motions, including: a substrate having a rotation axis; a first retention chamber being located in the substrate and retaining a diluent; a measurement chamber being located in the substrate; at least one reagent; a reagent chamber being located in the substrate and having the at least one reagent disposed therein, the reagent chamber being connected to the measurement chamber; and a first diluent path being located in the substrate, and connecting the first retention chamber and the measurement chamber or reagent chamber.
The present disclosure provides, as a film structure useful for a probe of a biosensor, a film structure comprising a detection layer including an analyte-responsive enzyme; and a protection film formed on the detection layer, in which the protection film includes alone poly(styrene-ran-4-vinylpyridine-ran-propyleneglycol methacrylate); or the protection film includes a copolymer mixture including poly(styrene-ran-4-vinylpyridine-ran-propyleneglycol methacrylate); and poly(4-vinylpyridine)-block-poly(C1-15 alkyl methacrylate), or poly(4-vinylpyridine-ran-2-hydroxyethyl methacrylate).
C12Q 1/00 - Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
C08F 226/06 - Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a heterocyclic ring containing nitrogen
C08F 220/28 - Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
A61B 5/1486 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value using enzyme electrodes, e.g. with immobilised oxidase
Provided is a biological substance detection sensor used in an electrochemical measurement method and allowing high-precision measurement by reducing a blank current. A biological substance detection sensor of the present invention for analyzing a component in a testing solution using a mediator includes at least: an insulating substrate; a conductive part formed on a surface of the insulating substrate and including at least one pair of a working electrode and a counter electrode; and a reagent part disposed in contact with or in a vicinity of the conductive part and including at least one of protein and the mediator. The reagent part further includes at least one additive selected from the group consisting of a halide and/or a pseudo halide.
A sensor insertion device includes a cylindrical main body case that has a lower end opening and an upper end opening; a needle insertion button that is disposed slidably in and out of the upper end opening of the cylindrical main body case; a carrier that is provided inside the cylindrical main body case and linked to the needle insertion button; a guide needle holder that is provided at a lower end portion of the carrier and configured to detachably hold a guide needle for guiding a sensor in an insertion direction; a cylindrical needle extraction sleeve that is provided slidably around an outer periphery of the cylindrical main body case; and a grip portion that is provided along a lengthwise direction of the cylindrical main body case on an outer periphery of the cylindrical needle extraction sleeve.
The present invention forms a detection layer in an embedded biosensor probe by using a phenazine derivative as a redox mediator in which a phenazine group is covalently bonded to a high molecular weight polymer having a carboxyl group or an amino group, such as polyamino acid, polyimine, or polyallylamine; and the distance between the phenazine group and the high molecular weight polymer main chain is increased by using a polyethylene glycol chain.
A61B 5/1486 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value using enzyme electrodes, e.g. with immobilised oxidase
C12Q 1/00 - Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
73.
Method for measuring amount of blood component in blood
The present invention provides a method for accurately measuring a blood component despite uneven distribution of blood introduced into a capillary. The measurement method according to the present invention is characterized in that a plurality of electrode systems for measuring the hematocrit are provided in a capillary of a biosensor to measure the hematocrit at different positions in the capillary. By measuring the hematocrit at the plurality of positions in the capillary as described above, the hematocrit can be measured mom accurately despite uneven distribution of blood introduced into the capillary.
The present disclosure provides, as a film structure useful for a probe of a biosensor, a film structure comprising a detection layer including an analyte-responsive enzyme; and a protection film formed on the detection layer, in which the protection film includes a copolymer mixture including poly(styrene-ran-4-vinylpyridine-ran-propyleneglycol methacrylate); and poly(4-vinylpyridine)-block-poly(C1-15 alkyl methacrylate), or poly(4-vinylpyridine-ran-2-hydroxyethyl methacrylate).
A61B 5/1486 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value using enzyme electrodes, e.g. with immobilised oxidase
C08L 53/00 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
A61B 5/145 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value
A sensor insertion device comprises a sheath, a handle, an operating body provided in the handle, a carrier provided below the operating body, a guide needle unit holder that provided at the lower end of the carrier and detachably holds a guide needle that guides a sensor in the insertion direction, and an arm that is rotatably supported by the cylindrical portion of the sheath. The arm has an outer end portion disposed outside the sheath and an inner end portion disposed inside the sheath. The handle has an arm operation surface that abuts on the outer end portion of the arm. The carrier has a ceiling that abuts on the inner end portion of the arm.
A61B 5/145 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value
A61B 5/00 - Measuring for diagnostic purposes ; Identification of persons
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
Provided is a cooling device capable of surely stopping the operation of a compressor when stopping the operation of the compressor is required. A cooling device comprises: a motor for driving a compressor that constitutes a refrigerant circuit for cooling a cooling room (R); and a first relay and a second relay that are arranged in series on an electric circuit for supplying electric power to the motor.
This cold storage device comprises a compressor, a condenser, a throttling device, and an evaporator, which form a cooling medium circuit through which a mixture of a cooling medium, a lubricating oil, and an oil carrier circulates. The oil carrier molecular structure includes a carbon double bond and a chlorine atom bonded to one carbon atom forming the carbon double bond.
The present invention provides a method for accurately measuring a blood component despite uneven distribution of blood introduced into a capillary. The measurement method according to the present invention is characterized in that a plurality of electrode systems for measuring the hematocrit are provided in a capillary of a biosensor to measure the hematocrit at different positions in the capillary. By measuring the hematocrit at the plurality of positions in the capillary as described above, the hematocrit can be measured more accurately despite uneven distribution of blood introduced into the capillary.
A reagent layer of a sensor contains as a mediator a quinone compound having a hydrophilic functional group, phenanthrenequinone, and/or a phenanthrenequinone derivative. The quinone compound has a lower redox potential than a conventional mediator, so interfering substances have less effect on detection results with this sensor.
C12Q 1/00 - Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
C12Q 1/32 - Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase involving dehydrogenase
G01N 21/84 - Systems specially adapted for particular applications
Provided is a living organism information measurement device which users can easily and reliably operate. A living organism information measurement device for acquiring living organism information and generating measurement data relating to the information is provided with a device body, and a panel detachably attached to the device body. The device body comprises a control unit which executes a plurality of functions of the device body, a living organism information measurement unit which is connected to the control unit and generates the measurement data, and a first communication unit connected to the control unit. The panel comprises a second communication unit including a memory storing predetermined information. When the panel is attached to the device body, the first communication unit receives the predetermined information from the second communication unit. The control unit selects and executes a function corresponding to the received predetermined information among the plurality of functions.
A61B 5/00 - Measuring for diagnostic purposes ; Identification of persons
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
G01N 33/487 - Physical analysis of biological material of liquid biological material
A61B 5/145 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value
A measurement method includes a first measurement in which a characteristic amount of a specific analyte in a biological fluid is measured with a biosensor. The method also includes a second measurement in which motion information of living activity is measured. Additionally, the method may include recording the motion information and the characteristic amount measured in the first measurement with the motion information and characteristic amount associated with each other.
A pharmaceutical syringe unit is configured to be mounted to a pharmaceutical injection device main body and hold a pharmaceutical-filled pharmaceutical syringe, in order to mount the pharmaceutical syringe to a pharmaceutical injection device, wherein a syringe cover is configured to slide forward and backward with respect to a distal end cap by operation of the pharmaceutical injection device main body, thereby allowing movement between a needle insertion position at which insertion of an injection needle into a target is to be completed, and a needle withdrawal position at which withdrawal of the injection needle from the target is to be completed, and a guide component is configured to guide the syringe cover over a range that is greater than a distance between the needle insertion position and the needle withdrawal position.
A61M 5/32 - Syringes - Details - Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
A61M 5/00 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests
A61M 5/20 - Automatic syringes, e.g. with automatically actuated piston rod, with automatic needle injection, filling automatically
A61M 5/24 - Ampoule syringes, i.e. syringes with needle for use in combination with replaceable ampoules or cartridges, e.g. automatic
A61M 5/145 - Pressure infusion, e.g. using pumps using pressurised reservoirs, e.g. by means of pistons
A61M 5/315 - Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod; Appliances on the rod for facilitating dosing
A61M 5/34 - Constructions for connecting the needle
A61M 5/36 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests with means for eliminating or preventing injection or infusion of air into body
A refrigeration device includes: a refrigerator; a heat pipe that includes a condensation unit connected to the refrigerator and adapted to condense a refrigerant, includes an evaporation unit connected to a storage chamber and adapted to evaporate the refrigerant, and includes a piping for circulating the refrigerant between the condensation unit and the evaporation unit; a heat pipe temperature sensor that detects a temperature of the heat pipe; and a control unit that controls driving of the refrigerator based on a result of detection by the heat pipe temperature sensor. The control unit controls the refrigerator so that the temperature of the heat pipe does not fall below a standard boiling temperature of the refrigerant.
An analyzing device has one end of a supplying capillary channel opened at a spot application section formed so as to protrude from an analyzing device main body. The supplying capillary channel is connected to a microchannel structure formed inside the analyzing device main body. A sample liquid is applied to the spot application section and is suctioned by a capillary force of the supplying capillary channel. The analyzing device is used for reading in which a suctioned solution is accessed. The analyzing device includes a leading end of the spot application section that has an inclined face. The end of the supplying capillary channel is opened on the inclined face.
A61B 5/151 - Devices for taking samples of blood specially adapted for taking samples of capillary blood, e.g. by lancets
A61B 5/145 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value
A61B 5/1455 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value using optical sensors, e.g. spectral photometrical oximeters
G01N 35/00 - Automatic analysis not limited to methods or materials provided for in any single one of groups ; Handling materials therefor
G01N 35/04 - Automatic analysis not limited to methods or materials provided for in any single one of groups ; Handling materials therefor using a plurality of sample containers moved by a conveyor system past one or more treatment or analysis stations - Details of the conveyor system
85.
Sample analysis device, sample analysis system, and method of measuring luminescence of a sample
A sample analysis device includes: a motor to rotate a sample analysis substrate with a sample introduced thereon around a rotation axis of the sample analysis substrate; a drive circuit to drive the motor; a photodetector to measure a number of photons associated with a luminescence from the sample being transmitted through a window of a measurement chamber of the sample analysis substrate; and a control circuit to calculate a measurement value of the luminescence of the sample by using a number of photons measured by the photodetector while the motor rotates the sample analysis substrate.
G01N 21/66 - Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light electrically excited, e.g. electroluminescence
This refrigeration device, which cools by means of a refrigeration cycle using a refrigerant, is provided with: a door; a box which has a peripheral edge that is opposite of the outer peripheral portion of the door when the door is in a closed state, and which is internally cooled by the refrigerant; and multiple pipes which are arranged along the surface of the peripheral edge and which circulate a refrigerant warmed by the compression action of a compressor.
F25D 21/04 - Preventing the formation of frost or condensate
F25D 11/02 - Self-contained movable devices associated with refrigerating machinery, e.g. domestic refrigerators with cooling compartments at different temperatures
The present invention provides: a reagent composition having higher storage stability; a sensor involving the reagent composition; and others. According to the present invention, a specific heterocyclic compound is added to a reagent composition to improve the storage stability of the reagent composition and reduce the degree of fluctuation in current values in a sensor that utilizes reagent composition.
C12Q 1/00 - Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
C12Q 1/26 - Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase
C12Q 1/32 - Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase involving dehydrogenase
88.
Method for measuring components of biological sample
Provided is a method for measuring a component of a biological sample with a biosensor provided with: a capillary for introducing the biological sample; an electrode part including a first electrode system that includes a first working electrode and a first counter electrode in the capillary; and a reagent part disposed so as to be in contact with the electrode part, the reagent part containing an enzyme and a mediator, and the method including a step of starting voltage application for a duration longer than 0 second and up to 0.7 second to the first electrode system within 0 second to 0.5 second after detection of the introduction of the biological sample to obtain a hematocrit value based on a current value obtained thereby.
C12Q 1/00 - Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
G01N 27/30 - Electrodes, e.g. test electrodes; Half-cells
This refrigeration device is provided with: an evaporator configuring a refrigeration circuit; a cascade condenser configuring the refrigeration circuit; and a thermal insulation board arranged between the evaporator and the cascade condenser.
F25B 6/02 - Compression machines, plants or systems, with several condenser circuits arranged in parallel
F25B 7/00 - Compression machines, plants or systems, with cascade operation, i.e. with two or more circuits, the heat from the condenser of one circuit being absorbed by the evaporator of the next circuit
This accommodation device is for performing sterilization through irradiation with ultraviolet light. The device is provided with an ultraviolet light lamp for emitting ultraviolet light, electric wires for supplying power to the ultraviolet light lamp, socket parts for supporting the ultraviolet light lamp, and a housing in which the ultraviolet light lamp is disposed, wherein: the socket parts have formed therein first opening portions which are open to the inside of the housing, and second opening portions which are in fluid connection with the first opening portions and through which the electric wires pass; and the housing has formed therein third opening portions which guide the electric wires to the outside and which are in fluid connection with the second opening portions.
G01N 21/78 - Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
92.
Liquid sample measurement device, liquid sample measurement method, and biosensor
It is intended to provide, for example, a liquid sample measurement device capable of measuring the amounts of components of a liquid with a high accuracy. A first voltage is applied to an electrode pair 21, 22, which composes a biosensor 1, to obtain a first response value, a second voltage is applied to an electrode pair 23, 24, which composes the biosensor 1, to obtain a second response value, and a current that is generated when a third voltage is applied to an electrode pair 23, 27, which composes the biosensor 1, is detected to obtain a third response value. A liquid sample measurement device 6 uses the first response value, the second response value, and the third response value to obtain the concentration of glucose and the amount of blood cells of blood as well as the value equivalent to the temperature of the biosensor 1.
An incubator includes: an insulated box including an incubation space surrounded by multiple inner faces; a humidifying unit that humidifies an incubation space; a first heating unit that heats a first inner face among the multiple inner faces, with electric power supplied; a second heating unit that heats a second inner face, different from the first inner face, with electric power supplied; and a control unit that controls the magnitude of electric power supplied to each of the first heating unit and the second heating unit. The control unit repeatedly changes the magnitude of electric power supplied to the first heating unit at first timing, and also repeatedly changes the magnitude of electric power supplied to the second heating unit at second timing different from the first timing.
Provided is a negative pressure release port that can prevent freezing in a channel. This negative pressure release port comprises: a cylindrical member made of a pipe in which a fluid can pass through and a base; a heating element disposed on one end inside the pipe; a retaining member that retains the heating element; a rib that connects an inner wall face of the pipe and the retaining member; and a check valve that is provided inside the base provided more toward the other end than the heating element, that allows air passing through the interior of the base to flow from the other end to the one end, and prevents flow from the one end to the other end.
F25D 17/04 - Arrangements for circulating cooling fluids; Arrangements for circulating gas, e.g. air, within refrigerated spaces for circulating gas, e.g. by natural convection
F16K 17/04 - Safety valves; Equalising valves closing on insufficient pressure on one side spring-loaded
95.
Heat insulation box manufacturing method and heat insulation box
A method for manufacturing a heat insulation box, wherein said method involves disposing an outer box over the outside of an inner box such that there is space therebetween, covering an opening with an elastic sheet from the outside of the outer box, inserting a jig into the opening from the outside of the outer box to force the elastic sheet into the space between the inner box and the outer box, and injecting the urethane foam heat insulating material into the space between the inner box and the outer box so as to foam therein to form a recess with the elastic sheet tightly adhering to the surface thereof.
F25B 7/00 - Compression machines, plants or systems, with cascade operation, i.e. with two or more circuits, the heat from the condenser of one circuit being absorbed by the evaporator of the next circuit
A sensor insertion device comprises a main body, needle slider, disposal slider, spring, puncture knob, and opening mechanism (window member and handle). The needle slider grips a needle and a sensor on a first end side, and is slidable inside the main body. The disposal slider is slidable inside the main body. The puncture knob has an insertion hole into which the rear end portion of the needle slider can be inserted. The opening mechanism puts the insertion hole into a closed state when the needle slider is being slid in the sensor insertion direction, and, puts the insertion hole in an open state in which the second end side of the needle slider has been inserted into the insertion hole by opening up the contact portion between the puncture knob and the second end side of the needle slider when the puncture operation is complete.
A61B 5/1473 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value using chemical or electrochemical methods, e.g. by polarographic means invasive, e.g. introduced into the body by a catheter
A61B 5/00 - Measuring for diagnostic purposes ; Identification of persons
The present invention relates to a pharmaceutical injection device, and it is an object thereof to prompt the user to replace the injection needle as needed. To achieve this object, the present invention is configured such that a needle detector switch 8 that directly or indirectly detects the mounting of an injection needle to a pharmaceutical syringe 5 is provided to a main case 2, this needle detector switch 8 is connected to a controller 21, and the controller 21 displays on a display component 19 an injection needle removal message that directly or indirectly prompts the user to remove an injection needle 6 from the pharmaceutical syringe 5 when the mounting of the injection needle 6 to the pharmaceutical syringe 5 has been detected by the needle detector switch 8 in the switching off the a power switch 16.
A61M 5/50 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests having means for preventing re-use, or for indicating if defective, used, tampered with or unsterile
A61M 5/20 - Automatic syringes, e.g. with automatically actuated piston rod, with automatic needle injection, filling automatically
A61M 5/34 - Constructions for connecting the needle
A61M 5/00 - Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests
A61M 5/24 - Ampoule syringes, i.e. syringes with needle for use in combination with replaceable ampoules or cartridges, e.g. automatic
98.
Drug injection device, cartridge adapter, and drug injection system
A drug injection system includes a cartridge adapter and a drug injection device. The cartridge adapter includes: a main body case; an attachment portion provided on the main body case used for attachment to the drug injection device; an accommodating portion that accommodates therein a drug cartridge; a piston; a piston gear that allows the piston to slide therethrough; a stopper that stops movement of the piston gear; and a release lever that releases a locked state of the piston gear. The drug injection device includes: a casing that accommodates therein a portion of the cartridge adapter; an engagement portion that engages with the cartridge adapter; a drive gear to which the piston gear of the cartridge adapter is connected; a motor connected to the drive gear; and a release bar that drives the release lever of the cartridge adapter.
A61M 5/24 - Ampoule syringes, i.e. syringes with needle for use in combination with replaceable ampoules or cartridges, e.g. automatic
A61M 5/145 - Pressure infusion, e.g. using pumps using pressurised reservoirs, e.g. by means of pistons
A61M 5/20 - Automatic syringes, e.g. with automatically actuated piston rod, with automatic needle injection, filling automatically
A61M 5/315 - Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod; Appliances on the rod for facilitating dosing
A61M 5/32 - Syringes - Details - Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
A61M 5/34 - Constructions for connecting the needle
A blood glucose measurement device comprises a sensor connector, a blood glucose value calculator, a barcode reader, a liquid crystal display, a data storage component, a report storage area, a central controller, and a touch sensor. The central controller causes the liquid crystal display to activate an input screen for inputting a comment for each measurement by the blood glucose value calculator. When a comment is inputted to the touch sensor, the central controller associates the comment with identification information in correspondence with each measurement by the blood glucose value calculator and stores the result in the report storage area. When a patient ID is read by the barcode reader, the central controller checks whether there is a comment on the basis of the information stored in the report storage area, and if there is a comment, the comment is displayed on the liquid crystal display.
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
A61B 5/00 - Measuring for diagnostic purposes ; Identification of persons
A61B 5/145 - Measuring characteristics of blood in vivo, e.g. gas concentration, pH-value
G16H 10/65 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records stored on portable record carriers, e.g. on smartcards, RFID tags or CD
G16H 15/00 - ICT specially adapted for medical reports, e.g. generation or transmission thereof
G16H 10/60 - ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
G01N 15/06 - Investigating concentration of particle suspensions
G01N 33/49 - Physical analysis of biological material of liquid biological material blood
This pharmaceutical injection device may be provided with a main body case, a pharmaceutical syringe mounting portion, a piston, a piston feed screw or the like, and a cover. At a first end, the main body case may have an injection needle mounting portion to which an injection needle is mounted. The pharmaceutical syringe mounting portion may be provided inside the main body case, and a pharmaceutical syringe may be mounted thereto. The piston may be provided movably with respect to the pharmaceutical syringe that is mounted to the pharmaceutical syringe mounting portion. The piston feed screw or the like drives the piston. The cover may be provided on the first end side of the main body case and operates to open and close the injection needle mounting portion.
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