To clean a reagent probe 7a, 8a or a sample probe 11a, 12a with a heated cleaning solution, after a first cleaning solution is caused to overflow from a first cleaning container 23 or a second cleaning container 24, the first cleaning solution is temporarily drawn back into the cleaning-solution heating passage 125 to be heated by the heating mechanism 123. After the heating, the first cleaning solution thus heated is re-supplied to the first cleaning container 23 or the second cleaning container 24. As a result, the cleaning solution heated to clean a dispensing probe can be supplied to a cleaning bath with efficiency.

An automated analysis device includes: a first measurement unit having a reaction disc for retaining a plurality of reaction cells containing a mixed solution of sample and reagent on a circumference, a light source for irradiating the mixed solution contained in the reaction cells with light, and a light-receiving unit for detecting the irradiated light; a cleaning mechanism for cleaning the reaction cells having undergone measurement; disposable reaction containers for containing the mixed solution of sample and reagent; a second measurement unit that has a plurality of measurement channels for retaining the disposable reaction containers, and includes a light source for irradiating the disposable reaction containers retained in each of the plurality of measurement channels with light; a read unit for reading identification information; and a control unit for controlling an analysis condition for the sample on the basis of the information that has been read.

To provide a preprocessing apparatus with a function of stirring and sucking a sample in a sample container carried on a conveyor line outside the preprocessing apparatus.

The preprocessing apparatus includes a sampling unit, a unit that stirs a sample before suction, and a stirring operation control unit. The sampling unit includes a sample probe that sucks a sample in the sample container, and is configured to move the sample probe to the sample container set in the sample container setting part and to an external suction location set on a conveyor line located outside the preprocessing apparatus. The unit that stirs a sample before suction includes a stirring probe which stirs a sample in the sample container, and moves the stirring probe at least to the external suction location or a location upstream of the external suction location on the conveyor line. The stirring operation control unit is configured to control operation of the sampling unit and the unit that stirs a sample before suction so that a sample in the sample container is stirred by the stirring probe before the sample is sucked by the sample probe.

An automatic analysis device has a plurality of types of photometers having different quantitative ranges, and an analysis control unit for quantifying the desired component in specimens based on measurement values of one or more photometers selected from among the plurality of types of photometers. The analysis control unit: sets a switching region in an overlap region of respective quantitative ranges of the plurality of types of photometers, said switching region having a greater width than does the variation in quantitative values of the desired component based on the measurement values of photometers having the same specimen; compares the quantitative value of a quantitative range portion that corresponds to the switching region and the quantitative values of the desired component based on the measurement values of the photometers; and selects a photometer to be used in quantitative output of the desired component from among the plurality of types of photometers.

A high-throughput automatic analyzer integrates a biochemical analysis section and a blood coagulation analysis section. The analyzer is capable of achieving a reduction in size, system cost, and lifecycle cost. The automatic analyzer includes: a reaction disk; a first reagent dispensing mechanism that dispenses a reagent to reaction cells on the reaction disk; a photometer that irradiates a reaction solution in the reaction cell with light; a reaction cell cleaning mechanism; a reaction vessel supply unit that supplies a disposable reaction vessel for mixing and reacting a sample and a reagent with each other; a second reagent dispensing mechanism that dispenses a reagent to the disposable reaction vessel; a blood coagulation time measuring section that irradiates a reaction solution in the disposable reaction vessel with light to detect transmitted or scattered light; and a sample dispensing mechanism that dispenses a sample to the reaction cell and the disposable reaction vessel.

An analyzer system for in vitro diagnostics includes a sample handler module having a robot arm that delivers samples from drawers into carriers on a linear synchronous motor automation track. Samples are delivered via the automation track to individual track sections associated with individual analyzer modules. Analyzer modules aspirate sample portions directly from the sample carriers and perform analysis thereon.

A sample handling device for a laboratory automation system comprising a first carousel with a disc supported on a first axis, a second carousel with a disc supported on a second axis parallel to the first axis, and a transfer element between the first and second carousels is presented. Each disc has recesses distributed radially about the disc perimeter. Each recess receives a tube carrier. The first carousel and the second carousel connect via a passage for transferring sample tube carriers between the first and second carousels. The transfer element is a track switch which when in a rest position partly closes the passage to separate the first carousel from the second carousel. The track switch is swiveled and/or rotated about a third axis parallel to the first axis out of the rest position for transferring a tube carrier from the first carousel to the second carousel via the passage.

To be adapted to various types of latex reagents for detecting scattered light and thereby measuring agglutination reactions with high sensitivity while sufficiently ensuring integration time. To be adapted to various types of latex particles of different particle sizes, a plurality of light receivers are arranged in a plane perpendicular to the direction of cell movement by rotation of a cell disk. To ensure sufficient integration time, the angle between the optical axis of the irradiation light and each of a plurality of optical axes of scattered light viewed from above the cell is made equal to or less than 17.7? including a mounting error.

A method and automated apparatus for rapid non-invasive detection of a microbial agent in a test sample is described herein. The apparatus may include one or more means for automated loading, automated transfer and/or automated unloading of a specimen container. The apparatus also includes a detection system for receiving a detection container, e.g., container or vial, containing a biological sample and culture media. The detection system may also include one or more heated sources, holding structures or racks, and/or a detection unit for monitoring and/or interrogating the specimen container to detect whether the container is positive for the presence of a microbial agent therein. In other embodiment, the automated instrument may include one or more, bar code readers, scanners, cameras, and/or weighing stations to aid in scanning, reading, imaging and weighing of specimen containers within the system.

An automatic biochemical analyzer, comprises a reaction wheel comprising an inner ring and an outer ring, wherein the reaction wheel is equally divided into multiple cuvette positions; the inner ring and the outer ring have a photoelectric detection position, a sample injecting position, a reagent injecting position, a sample stirring position, a reagent stirring position and a cuvette cleaning position; the photoelectric detection position of the inner ring is offset relative to that of the outer ring by a first cuvette position along a counterclockwise or clockwise direction; and the sample injecting positions, the reagent injecting positions, the sample stirring positions, and the reagent stirring positions of the inner ring are offset relative to those of the outer ring by a second cuvette position along the same direction, the first cuvette position is equal to the second cuvette position, or a difference between those two is one cuvette position.