Abstract: An immunodiagnostic test card includes a flat planar member and at least one dilution chamber that is supported by the flat planar member. The at least one dilution chamber can be disposed adjacent chambers used for testing a patient sample that are provided on the immunodiagnostic test card or can be provided separately.

Abstract: An immunodiagnostic test card includes a flat planar member and at least one dilution chamber that is supported by the flat planar member. The at least one dilution chamber can be disposed adjacent chambers used for testing a patient sample that are provided on the immunodiagnostic test card or can be provided separately.

Abstract: An immunodiagnostic test card includes a flat planar member and at least one dilution chamber that is supported by the flat planar member. The at least one dilution chamber can be disposed adjacent chambers used for testing a patient sample that are provided on the immunodiagnostic test card or can be provided separately.

Abstract: An analyzer, preferably a desktop analyzer, includes: a component transport system; a liquid dispense or aspirating station; a member removably located on the transport system. The removable holder includes: a probe tip dispenser; a fluid supply section for holding a sample; a test element recess for holding one or more test elements or test element holders, wherein the removable holder is configured to contain the test element recess such that a test element can be acted upon by the liquid dispense or aspirating station, while the test element is in the recess; and a measurement device to analyze a sample. Another aspect provides a removable centrifuge model on the transport system, which separates samples, such as whole blood before analysis.

Abstract: A clinical analyzer for determining the presence or amount of an analyte in a sample includes at least one reagent supply and at least one reaction containment device for containing a volume of sample and a volume of said at least one reagent from said at least one reagent supply. A wash-free delivery system introduces reagent into at least one reaction containment device without requiring washing of delivery components.

Abstract: An analyzer, preferably a desktop analyzer, includes: a stationary probe capable of dispensing or aspirating a liquid; one or more of a movable test element or movable liquid source; and a conveyor for moving the movable test element or liquid source with respect to the stationary probe. In a preferred embodiment, the conveyor includes a dual rotor conveyor. A method of dispensing or aspirating a liquid into a test element includes: providing a movable test element having identifying marks, such as a barcode, thereon and a movable sample liquid supply; providing a stationary probe; reading the identifying marks to determine which test is to be performed and the dimensions of the test element; moving the movable sample liquid supply into registration with the probe; aspirating sample into the stationary probe; and moving the movable test element into registration with the probe, wherein the registration of the test element with the probe is controlled by the test to be performed.

Abstract: An immunodiagnostic test card includes a flat planar member and at least one dilution chamber that is supported by the flat planar member. The at least one dilution chamber can be disposed adjacent chambers used for testing a patient sample that are provided on the immunodiagnostic test card or can be provided separately.

Abstract: A clinical analyzer for determining the presence or amount of an analyte in a sample includes at least one reagent supply and at least one reaction containment device for containing a volume of sample and a volume of said at least one reagent from said at least one reagent supply. A wash-free delivery system introduces reagent into at least one reaction containment device without requiring washing of delivery components.

Abstract: An incubator includes an incubator ring assembly having at least two concentric rings supported for rotation about a common axle defining an axis of rotation. Each concentric ring includes a plurality of circumferentially defined load positions, each load position being sized for accommodating a test sample. At least one test station is arranged in relation to the plurality of load positions to selectively test a test sample, the test samples being are sequentially shuttled into and out of load positions of at least one of the concentric rings to increase the overall throughput of the analyzer.

Abstract: A clinical analyzer for determining the presence or amount of an analyte in a sample includes at least one reagent supply and at least one reaction containment device for containing a volume of sample and a volume of said at least one reagent from said at least one reagent supply. A wash-free delivery system introduces reagent into at least one reaction containment device without requiring washing of delivery components.

Abstract: An analyzer, preferably a desktop analyzer, includes: a first rotor for holding a test element and at least one of a sample reservoir for a sample to be analyzed, a wash reservoir, and a probe tip dispenser; a second rotor arranged concentrically with the first rotor and adapted to receive the test element from the first rotor; an incubator arranged in cooperation with the second rotor to incubate a sample disposed in the second rotor; and a measurement device to analyze a sample located in the second ring.

Abstract: An analyzer, preferably a desktop analyzer, includes: a stationary probe capable of dispensing or aspirating a liquid; one or more of a movable test element or movable liquid source; and a conveyor for moving the movable test element or liquid source with respect to the stationary probe. In a preferred embodiment, the conveyor includes a dual rotor conveyor. A method of dispensing or aspirating a liquid into a test element includes: providing a movable test element having identifying marks, such as a barcode, thereon and a movable sample liquid supply; providing a stationary probe; reading the identifying marks to determine which test is to be performed and the dimensions of the test element; moving the movable sample liquid supply into registration with the probe; aspirating sample into the stationary probe; and moving the movable test element into registration with the probe, wherein the registration of the test element with the probe is controlled by the test to be performed.

Abstract: A test element holder for an automated analyzer includes: a body portion for holding at least one test element; and a guide adapted to receive a probe, such as an aspirating or dispense nozzle to position the probe in a desired registration with a test element. In a preferred embodiment, the test element holder further includes a cover disposed over at least a portion of the body portion and test element and the guide comprises at least one opening in said cover. In a preferred embodiment, the analyzer is a desktop analyzer and/or a veterinary analyzer.

Abstract: A clinical analyzer for determining the presence or amount of an analyte in a sample includes at least one reagent supply and at least one reaction containment device for containing a volume of sample and a volume of said at least one reagent from said at least one reagent supply. A wash-free delivery system introduces reagent into at least one reaction containment device without requiring washing of delivery components.

Abstract: An incubator includes an incubator ring assembly having at least two concentric rings supported for rotation about a common axle defining an axis of rotation. Each concentric ring includes a plurality of circumferentially defined load positions, each load position being sized for accommodating a test sample. At least one test station is arranged in relation to the plurality of load positions to selectively test a test sample, the test samples being are sequentially shuttled into and out of load positions of at least one of the concentric rings to increase the overall throughput of the analyzer.