Abstract: The invention relates to a method and device for measuring blood gas parameters, preferably pH, pCO2, and pO2, in a blood sample, where the blood sample of a patient is fed into at least one measuring cell of an analyzer. In order to obtain accurate values for the blood gas parameters even in cases where the temperature of the patient deviates from normal temperature, the temperature of the patient or blood sample is measured upon sample withdrawal, and the measured temperature is transmitted to the analyzer or is recorded by the analyzer, and the temperature of the measuring cell of the analyzer is adjusted to the measured temperature by cooling or heating.

Abstract: An oximeter for spectro-photometric in-vitro determination of hemoglobin derivatives in a sample, typically a hemolyzed blood sample, is provided comprising a single measurement light source emitting measurement radiation, a sample chamber, for instance a measurement cuvette containing the sample, a detector device, which records a spectrum of the measurement radiation after its interaction with the sample, and an evaluation unit following the detector device, which determines the hemoglobin derivatives and at least one further analyte from the spectrum recorded by the detector device.

Abstract: The invention relates to a method and device for the monitoring of a medical microsample in the flow measuring cell of an analyzer with regard to position and absence of bubbles by means of an alternating voltage applied to the measuring cell, the measuring cell being provided with a multitude of electrode systems placed one behind the other, each system comprising a number of single electrodes for measuring a substance contained in the microsample by means of a measurement voltage which essentially is a DC voltage. To monitor the exact position of the microsample and/or to detect air bubbles in the area of each electrode system, the alternating voltage and the measurement voltage are simultaneously and directly applied to the single electrodes of the corresponding electrode system, and the measured AC component respectively the measured impedance gives a measure for the position of the microsample and the absence of bubbles.

Abstract: The invention relates to a method and device for the monitoring of a medical microsample (P) in the flow measuring cell (1) of an analyzer with regard to position and absence of bubbles by means of an alternating voltage applied to the measuring cell (1), said measuring cell (1) being provided with a multitude of electrode systems (2, 3) placed one behind the other, each system comprising a number of single electrodes (WE, RE, CE) for measuring a substance contained in the microsample (P) by means of a measurement voltage which essentially is a DC voltage. To monitor the exact position of the microsample (P) and/or to detect air bubbles in the area of each electrode system, the alternating voltage and the measurement voltage are simultaneously and directly applied to the single electrodes (WE, RE, CE) of the corresponding electrode system (2, 3), and the measured AC component respectively the measured impedance gives a measure for the position of the microsample (P) and the absence of bubbles.

Abstract: The invention relates to a method for determining the current filling level of a liquid, preferably a calibrating, quality control, or cleaning fluid, or waste water, in a container, for example of an analyzer, where an immersion pipe is dipped into the liquid in the container to be filled or drained. The immersion pipe is connected to a pumping device via a tube system. The pressure p in the tube system is measured and increased, starting from the ambient pressure p0, until a first discontinuous pressure change occurs at pressure p1 due to the liquid column in the immersion pipe being forced out of the pipe, and/or the pressure p in the tube system is decreased until the liquid column in the immersion pipe reaches a change in cross-section of the immersion pipe, which change is situated above the maximum filling level of the liquid, such that a second discontinuous pressure change occurs at pressure p2 due to the liquid column reaching the change in cross-section.

Abstract: The invention relates to a method for determining the current filling level of a liquid, preferably a calibrating, quality control, or cleaning fluid, or waste water, in a container, for example of an analyzer, where an immersion pipe is dipped into the liquid in the container to be filled or drained. The immersion pipe is connected to a pumping device via a tube system. The pressure p in the tube system is measured and increased, starting from the ambient pressure p0, until a first discontinuous pressure change occurs at pressure p1 due to the liquid column in the immersion pipe being forced out of the pipe, and/or the pressure p in the tube system is decreased until the liquid column in the immersion pipe reaches a change in cross-section of the immersion pipe, which change is situated above the maximum filling level of the liquid, such that a second discontinuous pressure change occurs at pressure p2 due to the liquid column reaching the change in cross-section.

Abstract: The invention relates to a method and device for measuring blood gas parameters, preferably pH, pCO2, and pO2, in a blood sample, where the blood sample of a patient is fed into at least one measuring cell of an analyzer. In order to obtain accurate values for the blood gas parameters even in cases where the temperature of the patient deviates from normal temperature, the temperature of the patient or blood sample is measured upon sample withdrawal, and the measured temperature is transmitted to the analyzer or is recorded by the analyzer, and the temperature of the measuring cell of the analyzer is adjusted to the measured temperature by cooling or heating.

Abstract: In a process for mixing two initial solutions to produce a working solution with an accurately defined mixing ratio, the two initial solutions are coarsely mixed in a first step, having a mixing ratio lying within a given range, and the value of an internal parameter of the working solution is determined in a second step. The values of this internal parameter are known and differ significantly for the two initial solutions. Then the accurate mixing ratio of the working solution is determined from the measured value of the internal parameter in a third step.