Abstract: In order to improve the reliability of the measurement by judging the precision of a measured value and judging the effectiveness of the measurement based on a result of the precision judgment, the optical characteristic of a reagent solution is previously measured in measuring the concentration of a specific component in a sample solution. Consequently, the precision of the concentration measurement is ensured based on the degree of degradation of the reagent solution.

Abstract: A method of and apparatus for flow injection analysis using a reaction chamber having a continuously variable volume, where the volume of the reaction chamber may be varied before, during or after introduction of an analyte solution and reagent solution into the reaction chamber. A microprocessor may be incorporated to control the volume of the reaction chamber and other components, either in a preprogrammed manner or in response to particular data measured by a detection device.

Abstract: A film-type vaporizer in a vaporization enclosure, for example the upper column of a double air-distillation column, is associated with a measurement and analysis box where a polished surface and a spillway reconstruct the flow of liquid in the vaporizer in order to check for the absence of the deposition of impurities in the liquid that is to be evaporated. If deposition occurs, the impurities involved are quantified and analyzed and appropriate action taken on the settings of the machine.

Abstract: The present invention relates to conducting a plurality of chemical reactions in a system including an apparatus which provides energy for the chemical reactions, such as chemical reactions in organic synthesis, where a particular advantage is the use of predetermined reaction parameters corresponding to similar chemical reactions. The present invention also relates to a system for performing said method and to corresponding kits and software. The system comprises an apparatus which can provide energy for the chemical reactions, said apparatus comprising a reaction cavity and a liquid handler, and a parameter selecting unit having a user interface means, a search unit means, apparatus control unit means, and storage means for carrying a database.

Abstract: An apparatus for performing a assays includes an axially rotatable substrate including a plurality of layers of a semiconductor material and numerous radially-arrayed reaction sites. The apparatus further includes a rotary stepper motor which rotates the substrate at an adjustable and substantially continuous speed and controls the rotation of the substrate by adjusting the speed and a direction of rotation. In addition, the apparatus includes a dual function head which has a fluid dispenser that has a fluid dispenser outlet and delivers a fluid to a reaction site and also has a readout device that has a sensor which receives an identifying signal from the reaction site on the substrate or scans the substrate to read identifying marks at the reaction site. Moreover, the apparatus may be aligned by a computer having a memory for storing a start location for the dispenser outlet on the substrate and additional electronics.

Abstract: Devices, methods, and systems for processing sample materials are disclosed. The present invention may provide a bridge between standard microtiter plate systems, methods, protocols, etc. (that include wells arranged in rectangular arrays) and rotating sample processing devices and systems that allow users to obtain the rapid processing advantages of the more advanced sample processing devices. The sample processing devices preferably include a rectangular body to improve compatibility of the sample processing devices of the present invention with equipment designed for use with more conventional microtiter plates (which are typically rectangular in shape). The sample processing devices also include at least one set of process chambers arranged in one or more circular arcs and may include input and/or output chambers arranged in a rectilinear grid array.

Abstract: The invention relates generally to methods, systems, and devices for measuring the concentration of target analytes present in a biological system using a series of measurements obtained from a monitoring system and a Mixtures of Experts (MOE) algorithm. In one embodiment, the present invention describes a method for measuring blood glucose in a subject.

Abstract: An apparatus for producing blood component products. In one embodiment, a plurality of a predetermined type of blood component is harvested from a source of whole blood. At least two on-line yield determination techniques are utilized to determine the yield of the harvested blood components. One is a predetermined yield prediction technique and the second is a predetermined yield monitoring technique, each of which are individually calibrated in relation to a predetermined off-line yield determination technique. The predetermined yield prediction and monitoring techniques each provide the yield of the harvested blood components and each is then utilized to provide a determined yield. Consequently, when the harvested blood components are packaged the determined yield may be associated therewith, thereby providing a blood component product.

Abstract: The invention provides methods for preparing a reaction substrate for use as assay devices comprising parallel printing of arrays of biosites on reaction substrates, wherein each biosite comprises a single type of capture probe bound to the reaction substrate and the array of biosites is deposited on the reaction substrate by a capillary bundle printer device.

Abstract: A sample handling system comprising: a transportation line including a combination of plural partitive line units; and a plurality of handling units, wherein each of the plural partitive line units and each of the plurality of handling units form a pair, and each handling unit is installed removably from its corresponding partitive line unit. Each handling unit transmits inoperative information to the transportation line when it becomes inoperative. The transportation line transmits this inoperative information to the central controller. The central controller monitors handling units at which the sample rack can stop over. The sample rack avoids stopover at the inoperative handling unit, but is allowed to advance to the subsequent handling unit passing through the partitive line unit which makes a pair with the inoperative handling unit.

Abstract: Calibrating an immunoassay by generating two reaction rate measuring curves, from samples having higher and lower relative levels of antigen, extrapolating a combination of the curves to cover sample concentrations known to contain an excess of antigen relative to an amount of capture reagent and combining the low end linear potion of the higher reaction rate measuring curve with the higher end portion of the extrapolated reaction rate measuring curve, thereby eliminating measuring inaccuracies otherwise arising from the hook effect. For antigen concentrations higher than the assay range, a high antigen signal utilizing the two rates avoids reporting false results.

Abstract: A system setup for a sample analysis system having a plurality of analysis units placed along a main conveyor line prior to its analysis operation. The system setup includes setup of analysis units in combination with different types of reagent supply units, setup of analysis routes as to whether it is a stationary type or an automatic type, and setup of analysis items for each analysis unit as to which analysis item should be assigned to which analysis unit having which reagent supply type. These settings are executed through monitoring of setup screens displayed on a screen display unit, and the contents of such a setting are stored and registered in a memory of the controller.

Abstract: Apparatus and processes for water impurity analysis and for impurity analysis of various other liquids as well. Apparatus and processes are provided for physical characterization of liquid drops as a liquid sample builds up and then drops from a sample needle or other source. Liquid drop characterization is through utilization of infrared liquid drop measuring and computer modeling to measure a liquid drop as it builds up and then measures the falling liquid drop. By optically measuring an infrared radiated falling drop, and/or by characterizing the manner by which a sample drop is formed, a very precise way of determining the exact volume of a liquid sample is accomplished. Sample volume is typically directly proportional to concentration levels of the chemical constituent to be measured. By computer modeling, a falling drop can be quantified as to volume, rather than depending on the otherwise standard way of injecting a “known” volume.

Abstract: Apparatus for producing a plurality of arrays of reagent regions is disclosed. A dispensing assembly in the apparatus has a plurality of heads which are spaced for depositing reagents at selected positions in different array areas in a substrate. As the heads in the assembly are advanced along array area, the regions in a row in that array are successively filled, allowing parallel deposition in several array areas at reagent regions which are closely spaced relative to the spacing between deposition heads in the assembly. Also disclosed is a method for producing a plurality of arrays using the apparatus.

Abstract: A method for detecting an analyte of interest present in a mixture at an ultralow concentration includes selecting a radioactive derivatizing agent comprising a multiphoton-emitting radioisotope moiety and a moiety reactive with the analyte of interest, the radioisotope moeity being bound to the derivatizing agent by a bond that is stable under the conditions employed in the other steps of the method, derivatizing the analyte of interest with the derivatizing agent, separating the analyte of interest from other components of the mixture by chromatography, and detecting the analyte of interest using multiphoton detection. The derivatizing step may be performed before or after fractionation. A radiophore for multiphoton emission enhanced chromatography has a first moeity bound to a multiphoton-emitting radioisotope, and a second moiety that is reactive with a functional group of an analyte of interest.

Abstract: An electrostatic deceleration system is provided for use with a flow cytometer to decelerate the movement of electrically charged droplets formed by the flow cytometer in order to minimize damage to the cells contained in the droplets when the droplets are collected in corresponding collection vessels. The deceleration system includes a plurality of deceleration devices which are each used to decelerate droplets charged to a particular magnitude and polarity. Each deceleration device includes a steering plate arrangement and a deceleration ring arrangement. The steering plate arrangement directs the droplets having a particular magnitude and polarity of charge into the corresponding deceleration ring arrangement. The deceleration ring arrangement includes a plurality of deceleration rings to which are applied electrical potentials of a polarity the same as the polarity of the charged droplet.

Abstract: The wetting-agent solution proposed contains of water and at least one organic solvent miscible with water. The speed of sound in the solution is measured and, from the value obtained, a control signal is generated to keep the composition of the solution constant.

Abstract: A device for detecting chemiluminescence from a sample. The device may include a stage for supporting a sample and one or more of the following elements: (1) an optics head, (2) an optical relay structure for transmitting chemiluminescence from the sample to a detector, (3) a drive mechanism, (4) a sensor for detecting proximity of the optical relay structure to the sample, (5) a mask structure for selecting an effective diameter of the optical relay structure, and (6) a baffle for blocking extraneous light from entering the optical relay structure.

Abstract: An automatic sample processing system containing:a) a sample vessel,b) a sample vessel carrier having a chamber to receive the sample vessel, andc) a sample identification component which carries a readable identification of a sample. The sample identification component is removably attachable to the sample vessel and to the sample vessel carrier.

Abstract: The invention relates to an automated device for determining or identifying and measuring a random number of different molecular classes, molecular parts or molecular groups in liquid or solid objects, in particular in cells and tissue specimen, said device comprising a combination of a pipetting system, a 3D handling system and an optical measuring system, preferably a microscope stand including an imaging device.The invention further relates to an automated method for determining or identifying and mapping a random number of molecular classes, molecular parts and molecular groups in objects, with which a random number of different reagent solutions may be applied simultaneously or sequentially to a liquid or solid object, in particular a cell, cells or a tissue specimen, and measured. An important field of application of the invention is cancer research as well as research into the immune system.

Abstract: There is disclosed an automatic biochemical analyzer having a sample turntable and a reaction turntable. Plural sample containers for holding samples are arrayed on the sample turntable. Plural reaction containers are arrayed on the reaction turntable. A sampling pipette draws in a sample from some sampling container and injects the sample into some reaction container. A reagent pipette draws in some reagent from some reagent container and injects the reagent into the same reaction container. The resulting mixture is stirred by a stirring device. Produced reaction products are detected by a detector. Let N be the number of the reaction containers on the reaction turntable. The reaction turntable is rotated in M pitches in one step. Note that M and N do not have any common factor. First and second injecting positions adjacent to each other are established as positions where the reagent pipette can inject a reagent into the reaction container in position.

Abstract: An apparatus is used to determine whether a container moving along a conveyor is suitable for storing water. The apparatus includes a sampler that obtains a sample from the interior of the container as the container moves along the conveyor. A PID is connected to the sampler to receive the sample and produce a signal corresponding to contents of the sample. A controller is connected to the PID and receives and analyzes the signal to determine whether the container is suitable for storing water. The apparatus may include a vacuum source connected to the PID that produces a reduced pressure for drawing the sample through the PID. A flow restrictor may be positioned between the sampler and PID. The flow restrictor may provide variable resistance to set a desired clearance time through the PID and sensitivity of the PID.

Abstract: Formed constituents of a quiescent anticoagulated whole blood or other biologic fluid sample are optically analyzed by an optical scanning instrument. The sample is contained in a sample chamber that has a varying through plane thickness. The thickness of any fields of view in the blood sample which contain plasma lacunae can be calculated by the instrument as a function of signal emission strength emanating from the colored plasma in the lacunae. The signal emissions can be the result of sample fluorescence or can be the result of signal density emanating from the sample. Particle volumes can be measured as a function of signal emission suppression which is caused by formed particles in the blood sample.

Abstract: A method of verifying sample volume quantifies the fluid volume aspirated and verifies sample uniformity by detecting the presence of foam or clots in the sample. After aspiration, a pressure sensor is used to measure the vacuum needed to hold up the column of fluid in the probe tip. By knowing the geometry of the probe tip, the vacuum can be converted to a sample weight and volume, based on sample densities. Non-ideal conditions, such as foam on the surface of the fluid or a clot in the fluid, result in a sample volume much lighter, in the case of foam, or much greater, in the case of a clot, than anticipated. The method also determines the elapsed time of the aspiration. Foamy samples result in aspiration times shorter than normal. Clotted samples result in aspiration times longer than normal. Additionally, a determination can be made as to whether an error condition occurred.

Abstract: A sample of a sample rack is sampled at analyzing units in the middle of a transfer line. A standby unit and a rack collecting unit are arranged near an exit of the transfer line. After sampling, sample racks are sorted out to the standby unit or the rack collecting unit at a first switching unit. The racks contained in the standby unit are sorted out to a returning line or the rack collecting unit in a second switching unit corresponding to a judged result of whether or not reexamination is required.

Abstract: Apparatus and method for simultaneously performing at least two assays using certain reagents for a plurality of liquid samples on a continuous analytical system is disclosed. The method comprising the steps of combining an aliquot of each liquid sample with at least one reagent in a first reaction container to form a first assay reaction for each liquid sample, and combining an aliquot of each liquid sample with at least one of the other reagents in a second reaction container to form a second assay reaction for each liquid sample. The method further comprises the steps of incubating the assay reactions of each assay being conducted at least one time, and performing other activities associated with each assay and using the first and second assay reactions to complete each assay, including analyzing the incubated assay reactions.

Abstract: A method and apparatus for an automated biological reaction system is provided. In the processing of a biological reaction system, there is a need for consistently placing an amount of liquid on a slide. In order to accomplish this, several methods are used including a consistency pulse and a volume adjust means. Moreover, in order to reliably operate an automated biological reaction system, the dispenser must be reliable, easy to assemble and accurate. Among other things, in order to accomplish this, the dispense chamber is substantially in line with the reservoir chamber, the reservoir chamber piston is removed, and the flow of liquid through the dispenser is simplified. Further, in order to operate the automated biological reaction system more reliably, the system is designed in modular pieces with higher functions performed by a host device and the execution of the staining operations performed by remote devices.

Abstract: When an operator touches a reagent interruption key during a continuous analyzing operation of samples in an operation state, the succeeding sampling operation is temporarily suspended and a reagent interruption screen is displayed on a screen of a CRT. A reagent delivery operation as to pipetted samples and a light-measurement operation as to the reaction solution are continued. A waiting time period until an operation for exchanging a reagent bottle can be started is displayed on the screen. When the waiting time period becomes zero minutes, an operator touches an execution key. Then, a screen representing readiness for exchanging a reagent bottle is displayed and an analyzing apparatus is placed in a reagent exchange waiting state for waiting for exchanging the reagent bottle. When an operator touches the execution key after exchanging the reagent bottle, the analysis apparatus reads bar codes o the reagent bottles on the reagent disks and registers the reagent information.

Abstract: A method and apparatus for analyzing molecular structures within a sample substance using an array having a plurality of test sites upon which the sample substance is applied. The invention is also directed to a method and apparatus for constructing molecular arrays having a plurality of test sites. The invention allows for definitive high throughput analysis of multiple analytes in complex mixtures of sample substances. A combinatorial analysis process is described that results in the creation of an array of integrated chemical devices. These devices operate in parallel, each unit providing specific sets of data that, when taken as a whole, give a complete answer for a defined experiment. This approach is uniquely capable of rapidly providing a high density of information from limited amounts of sample in a cost-effective manner.

Abstract: An automatic analyzer has a plurality of analytical units to which analysis items are allocated. When necessity of execution of calibration or accuracy management occurs, a display block relating to an occurrence cause on a state inspection screen flickers. When a receiving button corresponding to the flickering display block is instructed, the related analysis item name and analytical unit name are displayed in the display area and calibration or accuracy management is executed.

Abstract: A vial carrier having plural reagent compartments disposed linearly along the length of the carrier. Each compartment is adapted for receiving one of plural reagent vials. The carrier is provided with indicia uniquely identifying it to an automated assay device. Similarly, each compartment of the carrier has associated with it indicia which are at least unique to the particular carrier. Lastly, each vial installable within a carrier compartment has indicia unique to the contents of the vial. A film seal is applied to the vial opening prior to an integrated cap/seal assembly for the purpose of ensuring that the assembly is liquid-tight. The carrier is configured to be disposed on a slide of an inclining tray within an enclosure. Data reflecting which vial is located in which compartment of a given carrier is collected and provided to the automated instrument prior to installation of the carrier into the enclosure.

Abstract: A dispensing apparatus and method is provided for accurately and precisely dispensing various desired patterns of reagent onto a substrate or other receptive surface or receptacle. The invention provides high-speed on-the-fly dispensing of various desired reagent patterns as provided by the operator in the form of a graphic bit map file. In one embodiment the dispensing apparatus comprises a dispensing head having an inlet end and an outlet end. The dispensing head is responsive to a first signal to dispense droplets of liquid reagent onto a substrate. The substrate or dispensing head are secured in association with a table or carriage. The table is responsive to a second signal for providing for relative X, X-Y or X-Y-Z motion between the substrate and the dispensing head.

Abstract: A diluent is discharged by a dispensing device into a dilution bath 11 containing a sample, and a given amount of a diluted sample 12 is sucked from the upper face by the dispensing device and discarded by discharging it into a waste fluid cup to remove many small bubbles 13 generated during the preparation of the diluted sample used for determination. The diluted sample 12 remaining in the dilution bath 11 is used for determination to improve the precision and reproducibility of determination and to prevent failure of the dispensing device due to inclusion of bubbles.

Abstract: A fluid assembly and a method are provided. In one embodiment, the fluid assembly is insertable into a container holding a first fluid to be supplied to a diagnostic instrument and comprises a first element, a second element, and a first conduit fluidly connected between the first element and the second element such that the first fluid in the container moves through the first conduit towards the diagnostic instrument. A second conduit containing a second fluid is fluidly connected between the first element and the second element. A pressure transducer is fluidly connected with the second conduit such that the second fluid is bounded within the second conduit by the first fluid and the pressure transducer. The pressure transducer monitors pressure of the second fluid to indicate a volume of the first fluid in the container.

Abstract: A nethod of verifying sample volume quantifies the fluid volume aspirated and verifies sample uniformity by detecting the presence of foam or clots in the sample. After aspiration, a pressure sensor is used to measure the vacuum needed to hold up the column of fluid in the probe tip. By knowing the geometry of the probe tip, the vacuum can be converted to a sample weight and volume, based on sample densities. Non-ideal conditions, such as foam on the surface of the fluid or a clot in the fluid, result in a sample volume much lighter in the case if foam, or much greater, in the case of a clot, than anticipated. The method also determines the elapsed time of the aspiration. Foamy samples result in aspiration times shorter than normal. Clotted samples result in aspiration times longer than normal.

Abstract: A system for a clinical lab that is capable of automatically processing, including sorting, of multiple specimen containers. The system comprises a central controller, a workstation, one or more analyzers, and an automated centrifuge. The workstation has automatic detectors for detecting the presence of a holder holding specimen containers. The workstation has a bar code reader for reading bar codes on the containers. The system has a transport subsystem, preferably a workstation robotic arm and an analyzer robotic arm for transporting the specimen containers, moving them to and from the workstation, to and from the analyzers, and to and from the centrifuge. The centrifuge is loaded with buckets containing specimen containers. The workstation can be provided with a balance system for balancing the weight of the buckets used. The workstation can also have a decapper for automatically removing caps from the specimen containers.

Abstract: Quality control of an analyzing system that includes a portable analyzer with insertable single-use cartridges whose sample chamber contains optical and/or electrochemical sensors is accomplished by bringing the sensors in the single-use cartridge into contact, or are in contact with, a calibrating and/or conditioning medium, the calibrating and/or conditioning medium exhibiting chemical and/or physical parameters which influence the characteristic of at least one of the sensors. Just before a sample is measured, the sensors are contacted with a quality control liquid which is identical with the calibrating and/or conditioning medium within a predetermined desired range of accuracy for the sample components to be measured, as regards the chemical and/or physical parameters influencing the characteristic of at least one sensor during calibration and/or conditioning. The instantaneous control values obtained on the basis of the calibration values are subsequently compared to known target control values.

Abstract: Test sample cards containing biological samples are moved through an analytical instrument past a card detection device and detected by the device. The card detection device has an actuator that reciprocates relative to a housing between first and second positions. The actuator has a surface that comes into contact with the card as the card is moved past the device. The actuator carries an optical interrupt flag which is used in conjunction with an optical sensor placed in proximity to the actuator. When the card comes into contact with the actuator, the actuator is moved from the first position to the second, or retracted position. This action moves the flag relative to the optical sensor, triggering the optical sensor and a detection of the card. In one possible embodiment, multiple cards are placed in a cassette for movement around the instrument. The cassette has a number of slots for the cards, one card per slot.

Abstract: Methods of allocating resources in a system comprising at least two instruments are provided. In one such method, a list of tests to be performed by the system within a reaction vessel is generated. The list includes a number of reaction vessels used in performing each test to be performed by the system in a given time period. The list of tests is sorted according to the number of reaction vessels used in performing each test to be performed by the system in a given time period. A duplication percentage for the tests is determined. The duplication percentage is compared with the sorted list of tests. Resources associated with the tests are duplicated across the at least two instruments based on the comparison of the duplication percentage with the sorted list of tests such that at least one of the tests is performed by at least two of the at least two instruments.

Abstract: A test meter of the type which receives a disposable test strip and a sample of bodily fluid from a patient and performs an electrochemical analysis of the amount of an analyte such as glucose in the sample includes a receptacle for receiving a container in which disposable test strips are provided, and a mechanism for reading information about the disposable test strips that is affixed to the container. For example, calibration values can be applied to the container in the form of a machine readable bar-code, a magnetic stripe, a memory chip or as a resonant wire loop. By automatically obtaining calibration values from the container in which the strips are provided, the chances of using the wrong calibration information are greatly reduced. The container may also contain information readable by the meter including the expiration date, and the number of test strips in the container.

Abstract: A method for automatic testing of a laboratory specimen includes the initial step of obtaining a specimen to be tested and placing the specimen in a specimen container. The container is removably mounted in an independent carrier designed to carry an individual specimen through a laboratory to one or more of a plurality of work stations, where a predetermined test will be performed on the specimen. Once the test has been performed, the carrier is moved to another work station based on the result of the first test and then to an archiving station for storage of the specimen.

Abstract: A pre-processor for use in performing heterogeneous immunoassays on samples for analytes in the sample employing concentrically positioned incubating and processing carousels. A single transfer station permits reaction vessels containing sample and reagents to be moved between the carousels. The samples are separated, washed and mixed on the processing carousel and incubated on the incubating carousel thus speeding up processing throughput.

Abstract: In an analyzing apparatus of the present invention, sample racks, in each of which a plurality of sample containers are held, are transferred from a rack feeding unit to a discrimination unit for discriminating a type of each sample container. After the discrimination unit, a plurality of analyzing units are installed along a transfer line, and pipetters of different types are provided in the respective analyzing units. The discrimination unit detects information on the length and the width of each sample container held in each sample rack by using an optical detector. A control part selects one of the analyzing units, suitable for analyzing the sample container of which type was discriminated, based on the information detected by the discrimination unit, and transfers the sample container of which type was discriminated, to a sample pipetting position in the selected analyzing unit.

Abstract: A hydrogen sulfide analyzer that continuously samples waste water from a waste stream or reservoir and measures the concentration of purgeable H.sub.2 S present (H.sub.2 SP) This information, when combined with the volume of water present, provides a control quality signal that regulates the feed rate of the destructor chemical into the waste stream. This results in chemical savings for the user. A second result is the reduction in odor complaints and the corrosion problems associated with H.sub.2 S emissions. The analyzer measures only the purgeable H.sub.2 S contained in the liquid sample. The analyzer violently agitates the sample containing dissolved H.sub.2 S in solution to simulate actual conditions at points of agitation in the waste water stream. It also provides nearly optimal partial pressure conditions for the H.sub.2 S to exit the solution as a free gas. Any H.sub.

Abstract: An installation for monitoring an apparatus for generating atmospheres. The installation includes a measuring device for measuring at least one parameter representing the actual operation of the apparatus, an evaluator for evaluating the drift of each representative parameter over time and a trigger for triggering an intervention on the apparatus as a function of the drift before values of each representative parameter reach predetermined critical values.

Abstract: A sample of a sample rack is sampled at analyzing units in the middle of a transfer line. A standby unit and a rack collecting unit are arranged near an exit of the transfer line. After sample, sampleracks are sorted out to the standby unit or the rack collecting unit at a first switching unit. The racks contained in the standby unit are sorted out to a returning line or the rack collecting unit in a second switching unit corresponding to a judged result of whether or not reexamination is required.

Abstract: An automatic sample testing machine for testing samples stored in test cards. The machine has a test sample positioning system for moving a tray containing a plurality of test sample cards and fluid receptacles among various stations in the machine. The machine has a diluting station for adding a predetermined quantity of diluent to the receptacles as needed. A pipetting station transfers fluid from one receptacle to another. A vacuum station is provided having a vacuum chamber moveable relative to the tray between upper and lower positions. The chamber cooperates with the tray to make a sealing engagement with the top surface of the tray when it is lowered to the lower position. A vacuum generator supplies vacuum to the chamber. When the vacuum is released from the chamber, the fluid samples are loaded into the cards from the receptacles.

Abstract: A filling process for filling an analytic liquid in a container is optically accurately and automatically carried out using a laser beam. An automatic filling system is capable of automatically and continuously cleaning and drying the container in pretreating processes prior to an analysis.

Abstract: A method and a device for dispensing microdoses of aqueous solutions are provided, whereby the substance is transferred by the free surface end of a rodlike transferring element; the temperature of the transferring element is maintained at essentially the dew point of the ambient air during the transfer. The device may comprise a plate-like base to which are affixed a plurality of rods; the unfixed butt ends of the rods are coplanar. The device further comprises a means for maintaining the temperature of the unfixed butt ends of the rods essentially equal to the dew point of the ambient air during transfer of the aqueous substance.

Abstract: Disclosed is an automated method for reading a test strip for the analysis of one or more analyte in a liquid test sample. The method involves the spectrophotometric reading of a test strip which bears at least two marker fields on its surface which are capable of reflecting light at different spectral regions from each other. The reading means of the spectrophotometer is programmed to discern information concerning the strip, such as what analyte the strip is designed to detect, from the sequences of spectral classifications by spectral reflectancy measurements of the strip's marker fields.