Abstract: A biosensor system determines an analyte concentration using one or more calibrated correlation equations for an optical and/or electrochemical analysis of a biological fluid. The biosensor system may be implemented using a measurement device and a sensor strip. The measurement device applies test signals to a sequential conductive pattern on a sensor strip. The measurement device selectively and sequentially connects test contacts with conductive and non-conductive areas on the sequential conductive pattern, which generates code signals in response to the test signals. The measurement device uses the code signals to calibrate one or more of the correlation equations. The measurement device uses the calibrated correlation equations to determine the analyte concentration.

Abstract: An auto-calibration circuit or label is adapted to be used with different instruments. The auto-calibration circuit comprises a first plurality of electrical connections and at least one electrical connection. The first plurality of electrical connections is utilized by the different instruments to auto-calibrate. The first plurality of electrical connections includes a first plurality of contact areas. At least one electrical connection is utilized solely by the second instrument to auto-calibrate and includes at least one contact area. This electrical connection is distinct from the first plurality of electrical connections. The first plurality of electrical connections is routed directly from each of the first plurality of contact areas to a respective first or second common connection. The at least one electrical connection is routed directly from the at least one contact area to the respective first common connection, the second common connection or a no-contact area.

Abstract: An auto-calibration circuit or label (20) being adapted to be used with different first and second instruments. The first instrument being different from the second instrument. The auto-calibration label comprising first and second plurality of electrical connections. The first electrical connections conveys first instrument encoded-calibration information (82) corresponding to a sensor The first instrument information is adapted to be utilized by the first instrument to auto-calibrate for the first sensor The first plurality of electrical connections includes contact areas. The second electrical connections conveys second encoded-calibration information (84) corresponding to the first sensor The second information is adapted to be utilized by the second instrument to auto-calibrate for the sensor The second electrical connections includes a second plurality of contact areas, which are distinct from the first contact areas.

Abstract: A biosensor system determines an analyte concentration using one or more calibrated correlation equations for an optical and/or electrochemical analysis of a biological fluid. The biosensor system may be implemented using a measurement device and a sensor strip. The measurement device senses circuit patterns on an encoding pattern of the sensor strip. The measurement device determines calibration information in response to the circuit patterns, and uses the calibration information to calibrate one or more of the correlation equations. The measurement device uses the calibrated correlation equations to determine the analyte concentration.

Abstract: A method for controlling a test sequence for performing an analysis of an analyte in a fluid sample includes providing a hard-coded software application adapted to process a plurality of blocks to perform the test sequence. The blocks include a wait block, a read block, and a threshold block. A test-sequence table having a plurality of attributes defined therein for each of the blocks is provided. The attributes are utilized by the software application to process the blocks. The test sequence is determined through the attributes defined within the test-sequence table.

Abstract: A system, method and biosensor apparatus are provided for data communications with a personal data assistant. The biosensor apparatus includes a sensor for receiving a user sample to be measured and a microcontroller for performing a predefined test sequence for measuring a predefined parameter value. An interface logic block is coupled to the microcontroller for communicating the predefined parameter data value to the personal data assistant. The personal data assistant provides an operator interface, data management and analysis of biosensor results.

Abstract: A system, method and biosensor apparatus are provided for data communications with a personal data assistant. The biosensor apparatus includes a sensor for receiving a user sample to be measured and a microcontroller for performing a predefined test sequence for measuring a predefined parameter value. An interface logic block is coupled to the microcontroller for communicating the predefined parameter data value to the personal data assistant. The personal data assistant provides an operator interface, data management and analysis of biosensor results.

Abstract: A method and apparatus are provided for data management authentication in a clinical analyzer. The clinical analyzer includes a sensor for receiving a user sample to be measured and a processor for performing a predefined test sequence for measuring a predefined parameter value. A memory is coupled to the processor for storing predefined parameter data values. An authentication password is associated with each data transmission by the clinical analyzer and read by an associated computer system to validate each data transmission. The authentication password is generated by the clinical analyzer utilizing predetermined information in each data transfer.

Abstract: A method and apparatus are provided for calibrating a sensor for determination of analyte concentration. The meter includes a sensor for receiving a user sample to be measured and a processor for performing a predefined test sequence for measuring a predefined parameter value. A memory can be coupled to the processor for storing predefined parameter data values. A calibration code is associated with the sensor and read by the processor before the user sample to be measured is received. The calibration code is used in measuring the predefined parameter data value to compensate for different sensor characteristics.

Abstract: A fluid sensing pipette includes an outer conductive tube forming a first electrode and an inner conductive tube forming a second electrode. The inner conductive tube is disposed concentrically within the outer conductive tube. To insulate the inner conductive tube from the outer conductive tube, the inner conductive tube is coated with a thin, uniform, and consistent Parylene coating. A hydrophobic polymeric tube is disposed concentrically within the inner conductive tube to prevent cross-contamination between different biological samples aspirated into the pipette. The inner and outer conductive tubes are separately coupled to a level detection circuit which permits the pipette to detect entry of the pipette into a conductive fluid. The level detection circuit determines the impedance between the first and second electrodes and produces a control signal in response to the impedance falling below a predetermined threshold.

Abstract: A position sensing and motion verification assembly for a motor-driven mechanism includes a base member on which a sensor pattern is fabricated. The sensor pattern includes a predetermined orientation of tabs and notches of varying widths. A home position is defined in the sensor pattern and the polarity of the pattern is inverted on opposite sides of the home position. A single sensor such as an optical interrupter is mounted in the assembly in a position relative to the sensor pattern to sense the tabs and notches.

Abstract: A slow start motor control circuit for applications wherein extremely accurate speed control is required, such as, in a centrifugal blood separator application is disclosed. In a blood separator, the degree of separation of cellular components, such as red blood cells and platelets, from the blood plasma is a function of the rotational speed of the centrifuge and the spin time. The control circuit controls the spin time and the rotational speed of the drive motor by controlling the voltage applied to the motor. The control circuit allows the drive motor to start relatively slowly to avoid cell breakage which can contaminate the plasma. After the centrifuge attains its desired operational speed, the speed of the motor is regulated and is relatively uninfluenced by ambient temperature variations.