Abstract:
An in-vitro medical diagnostic system includes a host (1), a removable test card (2) and a removable reagent pack (3). The reagent pack (3) includes a calibrating liquid needed in a process for calibrating the test card (2); the reagent pack (3) is clamped to the host (1), with only first power drive and valve control transmission being provided between the host (1) and the reagent pack (3); and the test card (2) is mounted on the host (1) during the entire test process, with only second power drive and an optical conduction path being provided between the host (1) and the test card (2). No liquid path is present in the host (1) of the in-vitro diagnostic system, thus eliminating hidden medical dangers. Tests for blood gas, hemoglobin and derivatives thereof can be achieved in a single test card.
Abstract:
A detection assembly for a medical detection device and a medical detection device are disclosed. The detection assembly includes a housing and a detection electrode. The housing includes a top surface, a bottom surface, at least one side surface, a fluid inlet, and a fluid outlet. The at least one side surface is connected to each of the top surface and the bottom surface. A cavity is defined within the housing. Each of the fluid inlet and the fluid outlet is communicated with the cavity. A groove is recessed from an area of the top surface that is adjacent to the at least one side surface. The detection electrode is disposed in the groove.
Abstract:
The present invention relates to a recognition and calibration method for the blood gas chemistry analytic system, which comprises the following steps: getting reagent information recorded in the two-dimension code glued to or printed on the test card or reagent package; extracting the basic information of the test card from the reagent information, examining the correctness of the usage of the test card and feeding back the error messages and exiting the test if the usage is incorrect; if the usage is correct, extracting the feature information of the test card from the reagent information, obtaining the feature parameters of the test card and setting them as the feature parameters of the present test; collecting the present test signals and processing the operation of computation and adjustment for the signals according to the feature parameters of the present test and thus, obtaining the test results.
Abstract:
A control method and a non-transitory computer-readable storage medium are provided. The control method includes: obtaining the number of detection cards; determining a strategy for rotating a card holder of a multi-flux centrifugal platform, wherein the strategy corresponds to the number of the detection cards; controlling the card holder to rotate according to the strategy, and exposing a card position of the card holder at a card placement port.
Abstract:
A molecular diagnostic device and a detection card conveying seat for the same. The detection card conveying seat includes: a pressure plate, arranged with a first slide rail component, where the pressure plate is slidable along a sliding direction of the first slide rail component; and a transporting assembly, configured to place a detection card. The transporting assembly includes: a sliding frame, where the sliding frame is slidable together with the pressure plate along the sliding direction under an action of an abutting force; and a card tray, connected to the sliding frame and configured to place the detection card, where the pressure plate is configured to move toward the detection card and movable to a position abutting against the detection card, in condition of the sliding frame being subjected to a force that overcomes the abutting force.
Abstract:
The present invention relates to a detection system for improving accuracy of hematocrit measurement and an operation control method. The detection system for hematocrit measurement comprises a central processing unit, an excitation source unit, a blood sample unit, a precise measurement circuit unit and a signal collecting unit. The present invention has the beneficial effects that the HCT measurement precision is improved by generating a sine wave by the excitation source unit and performing control by the central processing unit; the detection system of the present invention is simple and reliable, and implements precise measurement; and the measurement precision in the present invention is far greater than that of a conventional measurement technology and can be within 0.2%. Furthermore, due to a self-detection function, the measurement is quite reliable without the risk of resulting incorrect measurement data from a circuit failure.
Abstract:
A detection assembly, including a first liquid path, a second liquid path, a liquid inlet, a liquid outlet, and a valve assembly. An end of the first liquid path is in communication with the liquid inlet, and another end is in communication with the liquid outlet; an end of the second liquid path is in communication with the liquid inlet, and another end is in communication with the liquid outlet. The valve assembly can be switched between a first turn-on state and a second turn-on state. In the first turn-on state, a first external liquid flows into the first liquid path from the liquid inlet and out of the first liquid path from the liquid outlet. In the second turn-on state, a second external liquid flows into the second liquid path from the liquid inlet and out of the second liquid path from the liquid outlet.
Abstract:
A medical tested object auto-ejection structure comprises a detection instrument and a tested object (1). An insertion port is formed in the detection instrument. When the tested object (1) is inserted in the instrument through the insertion port, the bottom end of the tested object (1) presses a bulge (21) used for rebounding, and a raised step (11) arranged on the surface of one side of the tested object (1) is locked on a clamping buckle (31) arranged at a position corresponding to the step on the instrument simultaneously, and after a test is finished, the instrument releases the locking of the clamping buckle (31) for the tested object (1) by a transmission device, and the tested object (1) is ejected from the instrument in time under the action of the bulge (21) used for rebounding, thus solving the problem of forgetting to pull the tested object out or inability to pull it out in time, and improving the reliability of the product.