CN111273567A - Device on-off control method, in-vitro diagnosis device, assembly line and storage medium - Google Patents

Device on-off control method, in-vitro diagnosis device, assembly line and storage medium Download PDF

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Publication number
CN111273567A
CN111273567A CN201811473889.XA CN201811473889A CN111273567A CN 111273567 A CN111273567 A CN 111273567A CN 201811473889 A CN201811473889 A CN 201811473889A CN 111273567 A CN111273567 A CN 111273567A
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time
preset
vitro diagnostic
vitro
shutdown
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CN201811473889.XA
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CN111273567B (en
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曾凡顺
李奔
刘建超
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Shenzhen Mindray Bio Medical Electronics Co Ltd
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Shenzhen Mindray Bio Medical Electronics Co Ltd
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Priority to CN202211395988.7A priority patent/CN115718199A/en
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    • GPHYSICS
    • G05CONTROLLING; REGULATING
    • G05BCONTROL OR REGULATING SYSTEMS IN GENERAL; FUNCTIONAL ELEMENTS OF SUCH SYSTEMS; MONITORING OR TESTING ARRANGEMENTS FOR SUCH SYSTEMS OR ELEMENTS
    • G05B19/00Programme-control systems
    • G05B19/02Programme-control systems electric
    • G05B19/04Programme control other than numerical control, i.e. in sequence controllers or logic controllers
    • G05B19/042Programme control other than numerical control, i.e. in sequence controllers or logic controllers using digital processors
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P90/00Enabling technologies with a potential contribution to greenhouse gas [GHG] emissions mitigation
    • Y02P90/02Total factory control, e.g. smart factories, flexible manufacturing systems [FMS] or integrated manufacturing systems [IMS]

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  • General Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Automation & Control Theory (AREA)
  • External Artificial Organs (AREA)
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  • Testing And Monitoring For Control Systems (AREA)

Abstract

The embodiment of the application discloses a device startup and shutdown control method, an in-vitro diagnosis device, a production line and a storage medium, which comprise the following steps: acquiring the current time of in-vitro diagnostic equipment in a production line and the current state of the in-vitro diagnostic equipment; if the current time reaches a preset time, determining a preset mode corresponding to the current time; if the current state of the in-vitro diagnosis equipment meets the preset switching condition, controlling the in-vitro diagnosis equipment to enter the preset mode; the preset switching condition comprises that if the preset mode corresponding to the preset moment is shutdown, the in-vitro diagnostic equipment is in an idle state at the current moment.

Description

Device on-off control method, in-vitro diagnosis device, assembly line and storage medium
Technical Field
The present application relates to the medical and testing arts, and relates to, but is not limited to, device power on and off control methods, in vitro diagnostic devices, pipelines, and storage media.
Background
In an in vitro diagnosis equipment assembly line, an actual operator end and a clinical laboratory operator need to close the in vitro diagnosis equipment assembly line when going off work and need to manually execute a starting-up process when going on work in the morning. When an operator goes off duty, the flow line needs to be manually closed, and even the operator needs to walk to each In Vitro Diagnostic device (IVD) to close each device one by one before waiting for the shutdown process to be completed. During work, the assembly line and each IVD device need to be started manually, the whole starting process needs about 30 minutes, then the work of the day can be carried out, and the samples are analyzed. Therefore, the waiting time is too long for the operator to start or close the production line each time, the time of the operator is delayed, and particularly, the operator needs to wait for nearly half an hour when the machine is started, which is equivalent to submitting the operator to work for half an hour every day.
Disclosure of Invention
In view of the above, embodiments of the present application provide an apparatus power on/off control method, an in-vitro diagnostic apparatus, a pipeline, and a storage medium to solve at least one problem in the related art.
The technical scheme of the embodiment of the application is realized as follows:
in a first aspect, an embodiment of the present application provides an apparatus power on/off control method, which is applied to an in vitro diagnosis assembly line, and includes:
acquiring the current time of in-vitro diagnostic equipment in a production line and the current state of the in-vitro diagnostic equipment;
if the current time reaches a preset time, determining a preset mode corresponding to the current time; if the current state of the in-vitro diagnostic equipment meets a preset switching condition, controlling the in-vitro diagnostic equipment to enter the preset mode;
the preset switching condition comprises that if the preset mode corresponding to the preset moment is shutdown, the in-vitro diagnostic equipment is in an idle state at the current moment.
In a second aspect, an embodiment of the present application provides an in-vitro diagnostic apparatus, which includes a processor configured to:
acquiring the current time of the in-vitro diagnostic equipment and the current state of the in-vitro diagnostic equipment;
if the current time reaches a preset time, determining a preset mode corresponding to the current time; if the current state of the in-vitro diagnostic equipment meets a preset switching condition, controlling the in-vitro diagnostic equipment to enter the preset mode;
the preset switching condition comprises that if the preset mode corresponding to the preset moment is shutdown, the in-vitro diagnostic equipment is in an idle state at the current moment.
In a third aspect, an external diagnosis pipeline is provided in an embodiment of the present application, where the external diagnosis pipeline includes a plurality of external diagnosis devices and a host, and the host is configured to receive a test result returned by each of the external diagnosis devices;
the host is also used for uniformly controlling the plurality of in-vitro diagnostic devices to be turned on and turned off;
each in-vitro diagnosis device also comprises a processor for realizing the startup and shutdown control method of the device.
An embodiment of the present application provides a storage medium, where a program is stored in the storage medium, and the program, when executed by a processor, implements the steps of the method for controlling on/off of a device as described above.
The embodiment of the application provides an equipment startup and shutdown control method, an in-vitro diagnosis device, a production line and a storage medium, wherein the current time of the in-vitro diagnosis device in the production line and the current state of the in-vitro diagnosis device are obtained firstly; if the current time reaches a preset time, determining a preset mode corresponding to the current time; if the current state of the in-vitro diagnostic equipment meets a preset switching condition, controlling the in-vitro diagnostic equipment to enter the preset mode; the preset switching condition comprises that if the preset mode corresponding to the preset moment is shutdown, the external diagnostic equipment is in an idle state at the current moment, and the startup and shutdown time of the external diagnostic equipment is set in advance, so that the external diagnostic equipment can reach the preset moment, namely, the external diagnostic equipment is automatically started and shutdown, and a large amount of waiting time is saved for an operator operating the external diagnostic equipment.
Drawings
FIG. 1 is a schematic structural diagram of a flow line of an in-vitro diagnostic apparatus according to an embodiment of the present application;
fig. 2A is a schematic flow chart illustrating an implementation of a device power on/off control method according to an embodiment of the present application;
fig. 2B is a schematic flow chart illustrating an implementation of a device power on/off control method according to an embodiment of the present application;
fig. 2C is a schematic flow chart illustrating an implementation of a device power on/off control method according to an embodiment of the present application;
fig. 2D is a schematic flow chart illustrating an implementation of a device power on/off control method according to an embodiment of the present application;
fig. 2E is a schematic flow chart illustrating an implementation of a device power on/off control method according to an embodiment of the present application;
fig. 2F is a schematic flow chart illustrating an implementation of a device power on/off control method according to an embodiment of the present application;
fig. 2G is a schematic flowchart of an implementation process of the device power on/off control method according to the embodiment of the present application;
FIG. 3 is a schematic flow chart illustrating an implementation of a device power on/off control method according to an embodiment of the present application;
fig. 4A is a schematic flowchart illustrating a process of implementing a scheduled shutdown by using an apparatus power on/off control method according to an embodiment of the present application;
fig. 4B is a schematic flowchart of a process of implementing a scheduled shutdown by using an apparatus power on/off control method according to an embodiment of the present application;
FIG. 5 is a schematic diagram of the in-vitro diagnostic apparatus according to the embodiment of the present application.
Detailed Description
The technical solutions in the embodiments of the present application will be clearly and completely described below with reference to the drawings in the embodiments of the present application.
For better understanding of the embodiments of the present invention, the flow of sample analysis in the related art will be described first.
Fig. 1 is a schematic structural diagram of an in-vitro diagnostic apparatus assembly line according to an embodiment of the present application, and as shown in fig. 1, the in-vitro diagnostic apparatus assembly line at least includes: an unloading platform 101, an in-vitro diagnosis device 1, an in-vitro diagnosis device 2, an in-vitro diagnosis device n, a host machine 102 and a loading platform 103; the in-vitro diagnostic apparatuses 1 to n are sequentially transported from the loading platform 103 to the unloading platform 101, and finally unloaded on the unloading platform 101. The host computer 104 is used for receiving the test results fed back after the in-vitro diagnostic devices 1 to n analyze the samples in the sample test tube racks; the host 102 may collectively manage the on and off of the in-vitro diagnostic apparatuses 1 to n, or may individually manage the on and off of each in-vitro diagnostic apparatus, and receive and display the test results of the in-vitro diagnostic apparatuses 1 to n. The in-vitro diagnostic apparatus 1, the in-vitro diagnostic apparatus 2, and the in-vitro diagnostic apparatus n may be used for testing the same sample, or may be used for testing different samples, for example, the in-vitro diagnostic apparatus 1 is a blood analyzer, and the in-vitro diagnostic apparatus 2 is a slide pusher. Wherein each in vitro diagnosis device also comprises a processor which can be independently controlled to carry out tests and the like. In the related art, an operator needs to manually close an in-vitro diagnostic equipment production line every off duty, and when the in-vitro diagnostic equipment is closed, a series of operations need to be performed on the in-vitro diagnostic equipment, for example, the operations are performed on the in-vitro diagnostic equipment, probe liquid maintenance, liquid path cleaning, air source closing, screen closing and the like, and a large amount of time is consumed for completing the series of operations; similarly, the startup process needs to be manually executed when the user is on duty in the morning; the start-up of the in-vitro diagnostic device also requires a series of operations, such as starting up an air source, initializing each component, cleaning a liquid path, and the like, and also consumes a lot of time, so that the operator needs to take up normal work time or delay off-work time to start up and shut down the in-vitro diagnostic device every day.
An embodiment of the present application provides a method for controlling power on and power off of a device, and fig. 2A is a schematic flow chart of an implementation of the method for controlling power on and power off of the device according to the embodiment of the present application, and as shown in fig. 2A, the method includes the following steps:
step S201, obtaining the current time of the in-vitro diagnosis equipment in the production line and the current state of the in-vitro diagnosis equipment.
Here, the extracorporeal diagnostic apparatus may be various extracorporeal diagnostic apparatuses such as a hematology analyzer, (C-reactionprotein, CRP) C-reactive protein meter, a push plate machine, and the like. The assembly line is an in-vitro diagnostic device assembly line shown in figure 1; the current status of the in vitro diagnostic device includes: an idle state and a test state.
Step S202, if the current time reaches a preset time, determining a preset mode corresponding to the current time; and controlling the in-vitro diagnosis equipment to enter the preset mode if the current state of the in-vitro diagnosis equipment meets the preset switching condition.
Here, the preset time may be a preset startup time, or a preset shutdown time, or the like; the preset mode corresponding to the current time can be understood as a start-up mode corresponding to the preset start-up time and a shutdown mode corresponding to the preset shutdown time. The condition that the preset switching condition is met may be understood as that, if the preset mode corresponding to the preset time is the shutdown time and the in-vitro diagnostic device is in the idle state, it is determined that the preset mode meets the switching condition, and the in-vitro diagnostic device is switched to the shutdown mode. The condition that the preset switching condition is met may also be understood as that, if the preset mode corresponding to the preset time is the power-on time and the in-vitro diagnostic device is in the power-off state, it is determined that the preset switching condition is also met in this case, and the in-vitro diagnostic device is switched to the power-on mode.
In this embodiment, when the current time of the in vitro diagnosis in the assembly line reaches the preset on-off time, if the current state of the device meets the switching condition, the device is controlled to enter the corresponding preset mode, so that the on-off time of the in vitro diagnosis device is set in advance, the in vitro diagnosis device can reach the preset time, namely, the in vitro diagnosis device is automatically turned on and off, and a large amount of waiting time is saved for an operator operating the device.
An embodiment of the present application provides a method for controlling power on and power off of a device, and fig. 2B is a schematic flow chart of an implementation of the method for controlling power on and power off of the device according to the embodiment of the present application, and as shown in fig. 2B, the method includes the following steps:
step S221, obtaining a time when the in-vitro diagnostic device first enters the test state in each preset time period of I preset time periods, to obtain a first time set including I times.
Wherein I is an integer of 1 or more; and determining a preset starting-up time of the in-vitro diagnostic equipment according to the first time set. The I preset time periods may be I days before the current time, for example, 7 days before the current time, and the time at which the test state is first performed every day in the 7 days is counted to obtain a first time set including 7 times.
Step S222, determining a preset startup time of the in vitro diagnostic apparatus according to the first time set.
Here, since it takes a while for the in-vitro diagnostic apparatus to enter the test state from the start-up, the preset start-up time needs to be properly earlier than the time in the first time set, for example, the first time set to enter the test state is 9 o 'clock, and since a series of operations need to be performed before the in-vitro diagnostic apparatus is started up, the preset start-up time needs to be set to 9 o' clock, that is, 8 o 'clock is needed to be prepared for start-up, that is, the preset start-up time is set to 8 o' clock.
In the above step S221 and step S222, a manner of "determining the preset starting time" is provided, in which, firstly, the time when the in-vitro diagnostic device enters the test state for the first time in the preset time period in the historical data is counted, and the preset starting time is determined according to the times, so that the preset starting time can be accurately set for the in-vitro diagnostic device, thereby starting the in-vitro diagnostic device in advance at regular time.
Step S223, obtaining a time when the in-vitro diagnostic device finally exits from the test state in each preset time period of the I preset time periods, to obtain a second time set including I times.
Here, I is an integer of 1 or more.
Step S224, determining a preset shutdown time of the in vitro diagnostic apparatus according to the second time set.
Here, the time when the test state is last exited in the second time set is 4 o 'clock and half afternoon, and the off-duty time of the operator who operates the in-vitro diagnostic apparatus is 5 o' clock, then 5 o 'clock may be set as the preset shutdown time, and four o' clock and half clock may be set as the preset shutdown time.
In the above step S223 and step S224, a manner of "determining the preset shutdown time" is provided, in which, firstly, the time when the external diagnostic apparatus exits the test state for the last time in a preset time period in the historical data is counted, and the preset shutdown time is determined according to the times, so that the preset shutdown time can be accurately set for the external diagnostic apparatus, thereby performing the shutdown in advance at regular time, and saving the waiting time for the operator.
Step S225, the current time of the in-vitro diagnosis device in the production line and the current state of the in-vitro diagnosis device are obtained.
Step S226, if the current time reaches a preset time, determining a preset mode corresponding to the current time; and controlling the in vitro diagnosis equipment to enter the preset mode if the current state of the in vitro diagnosis equipment meets the preset switching condition.
Here, the pipeline may be an in-vitro diagnosis device in a unified management pipeline, and receives and displays the test results of each device; the software for controlling the on-off of the in-vitro diagnostic device, which is provided by the embodiment and is provided with the corresponding program, can be installed at the host end of the assembly line, and when the preset starting time or the preset shutdown time arrives, the host sends an instruction to control the on-off of the in-vitro diagnostic device; as shown in fig. 1, the host 102 is installed with a power on/off control software for controlling each extracorporeal diagnosis device, so that the host 102 can control the power on/off time of each extracorporeal diagnosis device, or set the power on/off time of all the extracorporeal diagnosis devices to be the same time, or set the power on/off time of each extracorporeal diagnosis device individually according to the test condition of each extracorporeal diagnosis device, for example, the wafer pushing machine is not commonly used, so that the wafer pushing machine can be set to be powered off as soon as possible, and for a blood analyzer to be commonly used, the last group of tests is set to be completed and then powered off; in this way, the on-off control software for controlling each in-vitro diagnostic device is arranged on the host 102, which is convenient for arrangement and management of the in-vitro diagnostic device; in this embodiment, each in vitro diagnostic apparatus is separately equipped with the power on/off control software, and the in vitro diagnostic apparatus independently controls the power on/off of the in vitro diagnostic apparatus;
the in-vitro diagnostic equipment in the assembly line also comprises some unusual instruments, such as a chip pushing machine, which can be started later than other in-vitro diagnostic equipment or less used in-vitro diagnostic equipment, and the in-vitro diagnostic equipment is manually controlled to be started and stopped, and the in-vitro diagnostic equipment which is frequently used (or necessary) is started and stopped on time every day; therefore, the starting time and the shutdown time of each in-vitro diagnosis device in the assembly line are flexibly set, and the user experience is improved.
An embodiment of the present application provides a method for controlling power on and power off of a device, and fig. 2C is a schematic flow chart of an implementation of the method for controlling power on and power off of the device according to the embodiment of the present application, and as shown in fig. 2C, the method includes the following steps:
step S231, obtaining the current time of the in-vitro diagnostic device in the pipeline and the current state of the in-vitro diagnostic device.
Step S232, if the current time reaches a preset shutdown time and the current state of the in vitro diagnostic apparatus is an idle state, and it is determined that a preset switching condition is met, controlling the in vitro diagnostic apparatus to enter a shutdown mode.
Step S233, if the current time reaches the preset startup time and the current state of the in vitro diagnostic apparatus is the shutdown state, and it is determined that the preset switching condition is met, controlling the in vitro diagnostic apparatus to enter the startup mode.
The above steps S232 and S233 provide a method for implementing that "if the current time reaches a preset time, a preset mode corresponding to the current time is determined; if the current state of the in-vitro diagnostic equipment meets a preset switching condition, controlling the in-vitro diagnostic equipment to enter a mode of a preset mode, wherein the current time reaches the shutdown time, and if the in-vitro diagnostic equipment is in an idle state, the in-vitro diagnostic equipment is shut down; when the power-on time is reached, the external diagnostic equipment is powered on when the current state is the power-off state, so that the external diagnostic equipment is controlled to be powered on and off in advance, and the waiting time is saved for operators.
An embodiment of the present application provides a method for controlling power on and power off of a device, and fig. 2D is a schematic flow chart of an implementation of the method for controlling power on and power off of the device according to the embodiment of the present application, and as shown in fig. 2D, the method includes the following steps:
step S241, obtaining the current time of the in-vitro diagnostic device in the pipeline and the current state of the in-vitro diagnostic device.
Step S242, if the time that the in-vitro diagnostic apparatus is in the idle state is longer than a preset idle time and the preset shutdown time is not reached, adjusting the working mode of the in-vitro diagnostic apparatus to a sleep mode.
Here, if it is monitored that the in-vitro diagnostic apparatus is in an idle state for a long time before the preset shutdown time is not reached, the in-vitro diagnostic apparatus is controlled to enter a sleep mode in order to save resources.
Step S243, if the time for the in vitro diagnostic apparatus to enter the sleep mode is longer than a preset sleep time period and the preset shutdown time is not reached, adjusting the in vitro diagnostic apparatus from the sleep mode to exit the sleep mode.
Here, if it is monitored that the preset shutdown time is not reached after the in-vitro diagnostic device enters the sleep mode for a period of time, the device is not in the sleep mode when testing is required, and therefore the in-vitro diagnostic device is controlled to enter and exit the sleep mode.
The above steps S242 and S243 provide a way to avoid being in an idle state for a long time and save resources, in which, if the device is in an idle state for a long time and does not reach the time of shutdown, the device is controlled to enter a sleep mode; when the sleep time reaches the preset sleep time period, the sleep mode is exited, so that resources can be saved, and the normal use of the equipment cannot be influenced.
An embodiment of the present application provides a method for controlling power on and power off of a device, and fig. 2E is a schematic flow chart of an implementation of the method for controlling power on and power off of the device according to the embodiment of the present application, and as shown in fig. 2E, the method includes the following steps:
step S251, obtaining the current time of the in-vitro diagnostic device in the pipeline and the current state of the in-vitro diagnostic device.
Step S252, if the current time of the in vitro diagnostic apparatus reaches a preset shutdown time and the in vitro diagnostic apparatus is in a test state, acquiring a time when the test of the in vitro diagnostic apparatus is completed.
Step S253, updating the preset shutdown time according to the time when the in vitro diagnostic device completes the test, or performing shutdown within a preset time (for example, after 1 hour after the test is completed) after the in vitro diagnostic device completes the test.
The steps S252 and S253 described above implement that if the preset shutdown time is reached, but the test state is still in the test state, the shutdown is not performed first, and the shutdown is performed after the test is completed, thereby avoiding the test interruption caused by the sudden shutdown during the test process.
In this embodiment, if the shutdown time is up, but the in-vitro diagnostic device is still testing, a small window "test in progress, please delay shutdown" may be popped up on the host 102, or a period of time may be automatically delayed, or an automatic shutdown may be completed by waiting for the current test; therefore, the test interruption caused by sudden shutdown in the test process is avoided.
An embodiment of the present application provides a method for controlling power on and power off of a device, and fig. 2F is a schematic flow chart of an implementation of the method for controlling power on and power off of the device according to the embodiment of the present application, and as shown in fig. 2F, the method includes the following steps:
step S261, acquiring a current time of the in-vitro diagnostic apparatus in the pipeline and a current state of the in-vitro diagnostic apparatus.
Step S262, if the current time reaches a preset time, determining a preset mode corresponding to the current time; and controlling the in-vitro diagnosis equipment to enter the preset mode if the current state of the in-vitro diagnosis equipment meets the preset switching condition.
Step S263, if the in-vitro diagnostic apparatus is in the shutdown mode or the sleep mode, turning off the backlight indicator and the buzzer of the in-vitro diagnostic apparatus.
Step S264, if the in-vitro diagnostic device is in the power-on mode or exits the sleep mode, turning on the backlight indicator and the buzzer of the in-vitro diagnostic device.
In the above steps S263 and S264, if the in vitro diagnostic apparatus is turned off, the backlight and the buzzer of the apparatus are turned off at the same time, so as to save resources; if the in-vitro diagnosis equipment is started, the backlight lamp and the buzzer of the equipment are started at the same time, so that the use by an operator is facilitated.
An embodiment of the present application provides a method for controlling power on and power off of a device, and fig. 2G is a schematic flow chart of an implementation of the method for controlling power on and power off of the device according to the embodiment of the present application, and as shown in fig. 2G, the method includes the following steps:
step S271, obtaining N times respectively corresponding to the first N in-vitro diagnostic apparatuses entering the test state in the assembly line within a preset historical time period, and obtaining a third time set including the N times.
Here, M, N are each an integer greater than 0, and N is equal to or less than M. In step S171, it can be understood that the time corresponding to the first time that the N external diagnostic devices in the pipeline enter the test state every day is counted, where the N times are the first N times of the times that all the devices in the pipeline enter the test state.
And step S272, determining a preset starting time for starting all the in-vitro diagnostic equipment in the assembly line according to the third time set.
Here, since these N times, the time at which most of the in vitro diagnostic apparatuses in the pipeline first enter the test state every day is indicated; based on this, a uniform boot time is determined for all devices. Therefore, the hosts in the pipeline can uniformly manage the startup of the devices.
Step S273, obtaining Q times corresponding to the last Q in-vitro diagnostic devices exiting from the test state in the pipeline within the preset historical time period, and obtaining a fourth time set including the Q times.
Here, Q is an integer greater than 0, and Q is equal to or less than M.
Step S274, determining a preset shutdown time for closing all the in-vitro diagnostic apparatuses in the pipeline according to the fourth time set.
Here, since these Q times, the time at which most of the in vitro diagnostic apparatuses in the pipeline last exited the test state per day is indicated; based on this, a uniform shutdown time is determined for all devices. Thus, the hosts in the pipeline can uniformly manage the shutdown of the devices.
In this embodiment, the time when most of the devices first enter the test state and the time when most of the devices last exit the test state are obtained, so that the unified startup time and shutdown time are determined, and the in-vitro diagnosis devices in the assembly line can be conveniently and uniformly managed by the assembly line.
An embodiment of the present application provides a method for controlling power on and power off of a device, fig. 3 is a schematic flow chart of an implementation of the method for controlling power on and power off of the device according to the embodiment of the present application, and as shown in fig. 3, the method includes the following steps:
step S301, determining the preset starting-up time.
Here, the time when the in-vitro diagnostic device first enters the test state within each preset time period of I preset time periods is obtained, and a first time set including I times is obtained; wherein I is an integer greater than or equal to 1; and determining a preset starting-up time of the in-vitro diagnostic equipment according to the first time set.
Step S302, determining the preset shutdown time.
Here, the time when the in-vitro diagnostic device exits the test state for the last time in each of the I preset time periods is obtained, so as to obtain a second time set including I times; and determining the preset shutdown time of the in-vitro diagnostic equipment according to the second time set.
Step S303, obtaining the current time of the in-vitro diagnosis equipment in the production line and the current state of the in-vitro diagnosis equipment.
Step S304, if the current time reaches a preset shutdown time and the current state of the in vitro diagnostic apparatus is an idle state, and it is determined that a preset switching condition is met, controlling the in vitro diagnostic apparatus to enter a shutdown mode.
Step S305, turning off a backlight indicator lamp and a buzzer of the in-vitro diagnosis device.
Step S306, if the current time reaches a preset startup time and the current state of the in vitro diagnostic apparatus is a shutdown state, and it is determined that a preset switching condition is met, controlling the in vitro diagnostic apparatus to enter a startup mode.
Step S307, turning on a backlight indicator and a buzzer of the in vitro diagnostic equipment.
In this embodiment, when the current time of the in-vitro diagnosis in the assembly line reaches the preset on-off time, if the current state of the device meets the switching condition, the device is controlled to enter a corresponding preset mode, and the backlight and the buzzer are timely turned on and off, so that the on-off time of the in-vitro diagnosis device is set in advance, the in-vitro diagnosis device can reach the preset time, namely, the in-vitro diagnosis device is automatically turned on and off, and a large amount of waiting time is saved for a person operating the device.
The embodiment of the present application provides a method for controlling on/off of a device, in this embodiment, according to actual working needs of an operator, a time point for starting up and shutting down each device is set in advance, when the time point arrives, the device is automatically turned on or shut down, when the operator is on duty, a whole assembly line is ready to start up, work can be carried out immediately, when the operator is off duty, the operator can leave an office at the point on time, assembly line devices can be automatically shut down, fig. 4A is a schematic flow diagram illustrating that the reserved shutdown is realized by using the device on/off control method in the embodiment of the present application, as shown in fig. 4A, if on/off control software is installed at a host end of the assembly line, the method includes the following steps:
in step S401, the host of the pipeline detects that the current time reaches a preset shutdown time, and then the process goes to step S402.
In step S402, if the host computer of the pipeline detects that the current status of the in-vitro diagnostic apparatus is in an idle status, the process goes to step S403 or step S404.
Here, if the current state of the extracorporeal diagnostic apparatus is the test state, the process does not proceed to step S403 or to step S404 until the test is completed.
In step S403, the host computer of the pipeline turns off the in-vitro diagnostic apparatus.
Here, after the extracorporeal diagnostic apparatus is turned off, the flow proceeds to step S405.
In step S404, the host of the pipeline controls the in-vitro diagnostic apparatus to go to sleep.
Here, after the in-vitro diagnostic apparatus goes to sleep, the process proceeds to step S405.
Step S405, the host computer of the assembly line closes the backlight indicator light and the buzzer of the in vitro diagnosis equipment.
In this embodiment, the power on/off control software may also be installed in each extracorporeal diagnosis apparatus, i.e., step S401 to step S405, and may also be executed by a processor of each extracorporeal diagnosis apparatus.
In this embodiment, when the preset shutdown time is reached, if the device is in an idle state, the device is controlled to be turned off or to enter a sleep mode.
Fig. 4B is a schematic flowchart of a process of implementing a scheduled shutdown by using an apparatus startup and shutdown control method according to an embodiment of the present application, where as shown in fig. 4B, if startup and shutdown control software is installed at a host end of a pipeline, the method includes the following steps:
in step S421, the host of the pipeline detects that the current time reaches a preset startup time or receives a touch operation to start the device, and then the process goes to step S422.
Step S422, the host of the assembly line starts a backlight indicator lamp and a buzzer.
In step S423, if the in-vitro diagnostic apparatus is currently in the power-off mode, the host of the pipeline controls the in-vitro diagnostic apparatus to switch to the power-on mode.
In step S424, if the in-vitro diagnostic apparatus is currently in the sleep mode, the host of the pipeline controls the in-vitro diagnostic apparatus to switch to exit the sleep mode.
In this embodiment, the power on/off control software may also be installed in each of the in-vitro diagnostic apparatuses, i.e., step S421 to step S424, and may also be executed by a processor of each of the in-vitro diagnostic apparatuses.
In this embodiment, when a preset startup time is reached or a user manually touches the screen to start up, the control device switches to the startup mode or exits from the sleep mode; thereby saving a lot of waiting time for the personnel operating the device.
An extracorporeal diagnosis apparatus is provided in an embodiment of the present application, fig. 5 is a schematic composition diagram of the extracorporeal diagnosis apparatus in the embodiment of the present application, and as shown in fig. 5, the extracorporeal diagnosis apparatus 500 includes a processor 501, and the processor 501 is configured to:
acquiring the current time of the in-vitro diagnostic equipment and the current state of the in-vitro diagnostic equipment;
if the current time reaches a preset time, determining a preset mode corresponding to the current time; if the current state of the in-vitro diagnosis equipment meets the preset switching condition, controlling the in-vitro diagnosis equipment to enter the preset mode;
the preset switching condition comprises that if the preset mode corresponding to the preset moment is shutdown, the in-vitro diagnostic equipment is in an idle state at the current moment.
In other embodiments, the processor 501, configured to determine the preset boot time, includes: acquiring the moment when the in-vitro diagnostic equipment firstly enters the test state in each preset time period of I preset time periods to obtain a first time set containing I moments; wherein I is an integer greater than or equal to 1; determining a preset starting time of the in-vitro diagnostic equipment according to the first time set;
determining the preset shutdown time includes: acquiring the moment when the in-vitro diagnostic equipment exits the test state for the last time in each preset time period in the I preset time periods to obtain a second moment set containing I moments; and determining the preset shutdown time of the in-vitro diagnostic equipment according to the second time set.
In other embodiments, the processor 501 is configured to control the in-vitro diagnostic apparatus to enter a shutdown mode if the current time reaches a preset shutdown time and the current state of the in-vitro diagnostic apparatus is an idle state, and it is determined that a preset switching condition is met; alternatively, the first and second electrodes may be,
and if the current time reaches the preset starting-up time and the current state of the in-vitro diagnosis equipment is the shutdown state, and the preset switching condition is determined to be met, controlling the in-vitro diagnosis equipment to enter a starting-up mode.
In other embodiments, the processor 501 is further configured to:
if the time that the in-vitro diagnostic equipment is in the idle state is longer than the preset idle time and the preset shutdown time is not reached, adjusting the working mode of the in-vitro diagnostic equipment to be a sleep mode;
and if the time for the in-vitro diagnostic equipment to enter the sleep mode is longer than the preset sleep time period and the preset shutdown time is not reached, adjusting the in-vitro diagnostic equipment from the sleep mode to exit the sleep mode.
In other embodiments, the processor 501 is further configured to obtain a time when the test of the in-vitro diagnostic apparatus is completed if the current time of the in-vitro diagnostic apparatus reaches a preset shutdown time and the in-vitro diagnostic apparatus is in a test state;
updating the preset shutdown time according to the test completion time of the in-vitro diagnostic equipment; or shutting down the in-vitro diagnostic equipment at a preset time after the in-vitro diagnostic equipment completes the test.
In other embodiments, the processor 501 is further configured to adjust the extracorporeal diagnostic apparatus from a shutdown mode to a startup mode, or adjust the extracorporeal diagnostic apparatus from a sleep mode to an exit sleep mode according to a user operation instruction;
if the in-vitro diagnosis equipment is in a shutdown mode or a sleep mode, turning off a backlight indicator lamp and a buzzer of the in-vitro diagnosis equipment;
and if the in-vitro diagnosis equipment is in a starting mode or exits from a sleep mode, turning on a backlight indicator lamp and a buzzer of the in-vitro diagnosis equipment.
In other embodiments, the processor 501 is further configured to obtain N times corresponding to the first N in-vitro diagnostic apparatuses entering the test state in the pipeline within a preset historical time period, to obtain a third time set including the N times; m, N are all integers greater than 0, and N is less than or equal to M;
determining a preset starting time for starting all in-vitro diagnostic equipment in the assembly line according to the third time set;
acquiring Q moments respectively corresponding to the last Q in-vitro diagnostic devices which exit the test state in the assembly line within the preset historical time period to obtain a fourth moment set containing the Q moments; wherein Q is an integer greater than 0 and Q is less than or equal to M;
and determining the preset shutdown time for closing all the in-vitro diagnostic equipment in the assembly line according to the fourth time set.
It should be noted that, if the determination method of the substance concentration is implemented in the form of a software functional module and sold or used as a separate product, it may also be stored in a computer readable storage medium. Based on such understanding, the technical solutions of the embodiments of the present invention may be essentially implemented or a part contributing to the prior art may be embodied in the form of a software product, which is stored in a storage medium and includes several instructions for causing a computer device (which may be a personal computer, a server, or a network device) to execute all or part of the methods described in the embodiments of the present invention. And the aforementioned storage medium includes: various media capable of storing program codes, such as a usb disk, a removable hard disk, a Read Only Memory (ROM), a magnetic disk, or an optical disk. Thus, embodiments of the invention are not limited to any specific combination of hardware and software.
The embodiment of the application provides an in-vitro diagnosis assembly line, which at least comprises a plurality of in-vitro diagnosis devices and a host, wherein the host is used for receiving a test result returned by each in-vitro diagnosis device; the host is also used for uniformly controlling the plurality of in-vitro diagnostic devices to be turned on and turned off; each in-vitro diagnostic device further comprises a processor for implementing the device power-on and power-off control method provided by the above embodiment.
Accordingly, an embodiment of the present invention further provides a computer storage medium, where computer-executable instructions are stored on the computer storage medium, and when the computer-executable instructions are executed by a processor, the steps of the device power on/off control method provided in the foregoing embodiment are implemented.
The above description of the sample analysis system and computer storage medium embodiments is similar to the description of the method embodiments above, with similar beneficial results as the method embodiments. For technical details not disclosed in embodiments of the sample analysis system and computer storage medium of the present invention, reference is made to the description of embodiments of the method of the present invention for understanding.
It should be appreciated that reference throughout this specification to "one embodiment" or "an embodiment" means that a particular feature, structure or characteristic described in connection with the embodiment is included in at least one embodiment of the present application. Thus, the appearances of the phrases "in one embodiment" or "in an embodiment" in various places throughout this specification are not necessarily all referring to the same embodiment. Furthermore, the particular features, structures, or characteristics may be combined in any suitable manner in one or more embodiments. It should be understood that, in the various embodiments of the present application, the sequence numbers of the above-mentioned processes do not mean the execution sequence, and the execution sequence of each process should be determined by its function and inherent logic, and should not constitute any limitation to the implementation process of the embodiments of the present application. The above-mentioned serial numbers of the embodiments of the present application are merely for description and do not represent the merits of the embodiments.
It should be noted that, in this document, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus. Without further limitation, an element defined by the phrase "comprising an … …" does not exclude the presence of other like elements in a process, method, article, or apparatus that comprises the element.
In the several embodiments provided in the present application, it should be understood that the disclosed apparatus and method may be implemented in other ways. The above-described device embodiments are merely illustrative, for example, the division of the unit is only a logical functional division, and there may be other division ways in actual implementation, such as: multiple units or components may be combined, or may be integrated into another system, or some features may be omitted, or not implemented. In addition, the coupling, direct coupling or communication connection between the components shown or discussed may be through some interfaces, and the indirect coupling or communication connection between the devices or units may be electrical, mechanical or other forms.
The units described as separate parts may or may not be physically separate, and parts displayed as units may or may not be physical units; can be located in one place or distributed on a plurality of network units; some or all of the units can be selected according to actual needs to achieve the purpose of the solution of the embodiments of the present application.
In addition, all functional units in the embodiments of the present application may be integrated into one processing unit, or each unit may be separately regarded as one unit, or two or more units may be integrated into one unit; the integrated unit can be realized in a form of hardware, or in a form of hardware plus a software functional unit.
Those of ordinary skill in the art will understand that: all or part of the steps for realizing the method embodiments can be completed by hardware related to program instructions, the program can be stored in a computer readable storage medium, and the program executes the steps comprising the method embodiments when executed; and the aforementioned storage medium includes: various media that can store program codes, such as a removable Memory device, a Read Only Memory (ROM), a magnetic disk, or an optical disk.
Alternatively, the integrated units described above in the present application may be stored in a computer-readable storage medium if they are implemented in the form of software functional modules and sold or used as independent products. Based on such understanding, the technical solutions of the embodiments of the present application may be embodied in the form of a software product, which is stored in a storage medium and includes several instructions for causing a terminal to execute all or part of the methods described in the embodiments of the present application. And the aforementioned storage medium includes: a removable storage device, a ROM, a magnetic or optical disk, or other various media that can store program code.
The above description is only for the embodiments of the present application, but the scope of the present application is not limited thereto, and any person skilled in the art can easily conceive of changes or substitutions within the technical scope of the present application, and all such changes or substitutions should be covered by the present application.

Claims (10)

1. A device startup and shutdown control method is applied to an in-vitro diagnosis assembly line and is characterized by comprising the following steps:
acquiring the current time of in-vitro diagnostic equipment in a production line and the current state of the in-vitro diagnostic equipment;
if the current time reaches a preset time, determining a preset mode corresponding to the current time; if the current state of the in-vitro diagnostic equipment meets a preset switching condition, controlling the in-vitro diagnostic equipment to enter the preset formula;
the preset switching condition comprises that if the preset mode corresponding to the preset moment is shutdown, the in-vitro diagnostic equipment is in an idle state at the current moment.
2. The method according to claim 1, wherein the current operating state further comprises a test state, and the preset time comprises a preset power-on time and a preset power-off time, wherein:
determining the preset starting-up time comprises the following steps: acquiring the moment when the in-vitro diagnostic equipment firstly enters the test state in each preset time period of I preset time periods to obtain a first time set containing I moments; wherein I is an integer greater than or equal to 1; determining a preset starting time of the in-vitro diagnostic equipment according to the first time set;
determining the preset shutdown time includes: acquiring the moment when the in-vitro diagnostic equipment exits the test state for the last time in each preset time period in the I preset time periods to obtain a second moment set containing I moments; and determining the preset shutdown time of the in-vitro diagnostic equipment according to the second time set.
3. The method according to claim 2, wherein if the current time reaches a preset time, determining a preset mode corresponding to the current time; and if the current state of the in vitro diagnostic equipment meets a preset switching condition, controlling the in vitro diagnostic equipment to enter the preset mode, wherein the preset mode comprises the following steps:
if the current time reaches the preset shutdown time and the current state of the in vitro diagnostic equipment is an idle state, and the preset switching condition is determined to be met, controlling the in vitro diagnostic equipment to enter a shutdown mode; alternatively, the first and second electrodes may be,
and if the current time reaches the preset starting-up time and the current state of the in-vitro diagnosis equipment is the shutdown state, and the preset switching condition is determined to be met, controlling the in-vitro diagnosis equipment to enter a starting-up mode.
4. The method of any of claims 1 to 3, wherein the predetermined time comprises a predetermined shutdown time, the method further comprising:
if the time that the in-vitro diagnostic equipment is in the idle state is longer than the preset idle time and the preset shutdown time is not reached, adjusting the working mode of the in-vitro diagnostic equipment to be a sleep mode;
and if the time for the in-vitro diagnostic equipment to enter the sleep mode is longer than the preset sleep time period and the preset shutdown time is not reached, adjusting the in-vitro diagnostic equipment from the sleep mode to exit the sleep mode.
5. The method of any of claims 1 to 3, wherein the predetermined time comprises a predetermined shutdown time, the method further comprising:
if the current time of the in-vitro diagnosis equipment reaches the preset shutdown time and the in-vitro diagnosis equipment is in a test state, acquiring the time when the test of the in-vitro diagnosis equipment is finished;
updating the preset shutdown time according to the test completion time of the in-vitro diagnostic equipment; or shutting down the in-vitro diagnostic equipment at a preset time after the in-vitro diagnostic equipment completes the test.
6. The method according to any one of claims 1 to 3, further comprising:
according to a user operation instruction, adjusting the in-vitro diagnosis equipment from a shutdown mode to a startup mode, or adjusting the in-vitro diagnosis equipment from a sleep mode to an exit sleep mode;
if the in-vitro diagnosis equipment is in a shutdown mode or a sleep mode, turning off a backlight indicator lamp and a buzzer of the in-vitro diagnosis equipment;
and if the in-vitro diagnosis equipment is in a starting mode or exits from a sleep mode, turning on a backlight indicator lamp and a buzzer of the in-vitro diagnosis equipment.
7. The method of any one of claims 1 to 3, wherein the in-vitro diagnostic apparatus is included in a flow line, and wherein the flow line includes M in-vitro diagnostic apparatuses, the method further comprising:
acquiring N moments respectively corresponding to the first N in-vitro diagnostic devices entering the test state in the assembly line within a preset historical time period to obtain a third moment set containing the N moments; m, N are all integers greater than 0, and N is less than or equal to M;
determining a preset starting time for starting all in-vitro diagnostic equipment in the assembly line according to the third time set;
acquiring Q moments respectively corresponding to the last Q in-vitro diagnostic devices which exit the test state in the assembly line within the preset historical time period to obtain a fourth moment set containing the Q moments; wherein Q is an integer greater than 0 and Q is less than or equal to M;
and determining the preset shutdown time for closing all the in-vitro diagnostic equipment in the assembly line according to the fourth time set.
8. An in vitro diagnostic apparatus comprising a processor configured to:
acquiring the current time of the in-vitro diagnostic equipment and the current state of the in-vitro diagnostic equipment;
if the current time reaches a preset time, determining a preset mode corresponding to the current time; if the current state of the in-vitro diagnostic equipment meets a preset switching condition, controlling the in-vitro diagnostic equipment to enter the preset mode;
the preset switching condition comprises that if the preset mode corresponding to the preset moment is shutdown, the in-vitro diagnostic equipment is in an idle state at the current moment.
9. An in-vitro diagnosis assembly line is characterized by at least comprising a plurality of in-vitro diagnosis devices and a host computer, wherein the host computer is used for receiving a test result returned by each in-vitro diagnosis device;
the host is also used for uniformly controlling the plurality of in-vitro diagnostic devices to be turned on and turned off;
each in vitro diagnostic device further comprises a processor for implementing the method of any one of claims 1 to 7.
10. A computer storage medium, characterized in that a program is stored in the computer storage medium, which program, when being executed by a processor, carries out the method of any one of claims 1 to 7.
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