Abstract: A detection probe, a transmission apparatus, and a detection device are provided. The detection probe includes a housing, a detection mechanism, a driving mechanism, and a rope transmission mechanism. The housing defines an accommodation space. The detection mechanism is arranged on one end of the housing, and is configured to perform a detection function. The driving mechanism is arranged in the accommodation space, and is configured to output a force. The rope transmission mechanism is arranged in the accommodation space, and includes a rope set and a tension member. One end of the rope set is connected to the driving mechanism, and other end of the rope set is connected to the detection mechanism. The tension member is connected to the rope set, and is configured to apply a force to one end of the rope set away from the detection mechanism.

Abstract: A detection probe, a transmission device, and a detection instrument. The detection probe includes a housing defining a receiving space, a detection mechanism disposed on an end of the housing and configured to perform a detection function, a drive mechanism disposed in the receiving space and configured to output power, a rope transmission mechanism disposed in the receiving space and including a rope connected to the driving mechanism and the detection mechanism respectively and a reversing assembly including at least two reversing pulley groups arranged along an extension path of the rope, and a gear transmission mechanism disposed in the receiving space and connected to the driving mechanism and the rope transmission mechanism respectively, so as to receive the power output by the driving mechanism and transmit the power to the rope transmission mechanism.

Abstract: A sample test card and a blood gas analyzer are provided. The sample test card includes a first channel, a second channel, a first electrode located in the first channel, and a second electrode located in the second channel. The first electrode is configured to obtain an electrochemical parameter of a sample in the first channel, and the second electrode is configured to obtain an electrochemical parameter of a reference solution in the second channel. The sample test card further includes a salt bridge. An end of the salt bridge is exposed in the first channel, and the other end of the salt bridge is exposed in the second channel.

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 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 application relates to the technical field of medical monitoring. Specifically disclosed are a method for managing monitoring data, a probe assembly, and a system for managing monitoring data. The method for managing monitoring data based on the probe assembly comprises the following steps: establishing a communication connection with a first monitor; in response to a data roll-out instruction, receiving first monitoring data from the first monitor, and after the transmission of the first monitoring data is completed, breaking the communication connection with the first monitor; establishing a communication connection with a second monitor; and sending at least the first monitoring data to the second monitor, and cooperating with the second monitor to execute a monitoring task.

Abstract: A monitoring equipment, a monitoring system and a monitoring method. The monitoring equipment includes a measurement unit that acquires monitoring parameters and a control unit connected with the measurement unit to determine current stage-of-labor progress based on types of acquired monitoring parameters, to thereby determine a monitoring object that includes a mother and a fetus and/or a newborn. A display unit is connected with the control unit to display corresponding monitoring parameters in areas corresponding to each monitoring object on a monitoring interface. The monitoring interface includes one or a plurality of a mother monitoring area, a fetus monitoring area and a newborn monitoring area. The measurement unit is provided in the monitoring equipment. The control unit determines the current stage-of-labor progress to determine a monitoring object.

Abstract: A molecular diagnosis device and a control method based on the molecular diagnosis device are provided, relating to the technical field of molecular testing. The control method includes: controlling preheating of a first heating component (55, 832) for a sample loading cavity (9411) on a test card (93); controlling the first heating component (55, 832) to heat the sample loading cavity (9411); controlling preheating of a second heating component (54, 8211) for a testing cavity (9461) on the test card (93); and controlling the second heating component (54, 8211) to heat the testing cavity (9461).

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: An ultrasound probe and an ultrasound imaging device are provided. In the ultrasound probe, a sound head assembly is accommodated in a housing, a base is accommodated in the housing, and a traction line is accommodated in the housing and connected to the sound head assembly. A traction mechanism is accommodated in the housing. In the traction mechanism, a traction wheel is disposed on the base and rotatable relative to the base for winding the traction line, so that the sound head assembly is driven to swing by the traction line. An elastic member is disposed on the traction wheel and fixedly connected to the traction line, so as to adjust the tension of the traction line when the elastic member elastically deforms.

Abstract: Disclosed is a three dimensional mechanical ultrasound probe, which includes a transducer, a driving motor and a transmission mechanism configured to drive the transducer to reciprocatingly oscillate within a predetermined angle. The transmission mechanism includes a transducer base fixed and connected with the transducer, a face gear arranged on the transducer base, and a cylindrical gear meshed with the face gear. A rotating shaft of the face gear is positioned on the transducer base, and the face gear drives the transducer base to reciprocatingly oscillate. A transmission shaft is arranged on the axis of the cylindrical gear, and the transmission shaft is connected with the driving motor. The three dimensional mechanical ultrasound probe provided by the present application aims at simplifying the internal structure of the three dimensional mechanical ultrasound probe, reducing the internal installation complexity and improving motion stability.

Abstract: Provided are a method and device for detecting an excessive antigen concentration, and a storage medium. The method includes: subjecting a sample containing antigens to an immune reaction, obtaining a photovoltage value of the sample after subjected to the immune reaction; and determining whether an antigen concentration of the sample is excessive according to the photovoltage value of the sample.

Abstract: An ultrasonic transducer (200) includes: a piezoelectric vibrator assembly (10), an acoustic matching layer (20), a heat sink (30), and an acoustic absorption layer (40). The heat sink (30) comprises a body (31), and a head portion (32) and a tail portion (33). The body (31) has a central axis extending in a direction from the head portion (32) to the tail portion (33). A surface of the tail portion (33) of the heat sink (30) disposed away from the head portion (32) is a first surface (331). The first surface (331) is an oblique surface or a tapered surface. The angle between the first surface (331) and the central axis is an acute angle. The acoustic absorption layer (40) at least covers the first surface (331).

Abstract: A detection probe and a fetal monitor. The detection probe comprises a probe body (2) and a mounting structure (1), detachably mounted on the probe body (2) and having a heart rate sensor for heart rate detection, a socket (4) for data transmission, and a lead line (5) for connecting the heart rate sensor and the socket (4) arranged thereon. A variety of functions can be achieved by means of a single detection device and thus the degree of integration is high; moreover, when the heart rate sensor is failed or aged, because the mounting structure (1) can be separated from the probe body (2), it is only necessary to repair and replace a corresponding part, so that the maintenance is convenient and the cost is reduced. Furthermore, the mounting structure (1) can also product the probe body (2) to some extent, and thus the anti-dropping capability of the detection probe is improved.

Abstract: An ultrasound system (100) includes an ultrasound transducer, a processing circuit (210, 300), and a display. The ultrasound transducer is configured to detect ultrasound information regarding a patient and output the ultrasound information as an ultrasound data sample. The processing circuit (210, 300) is configured to segment the ultrasound data sample into a binary image including at least one first region and at least one second region, obtain a first location of a first vascular feature of the binary image based on a boundary between the at least one first region and the at least one second region, and modify the binary image based on the first location of the first vascular feature. The first vascular feature is associated with an intima media thickness. The display is configured to display the modified image.

Abstract: An ultrasound processing system includes an ultrasound interface and processing electronics. The ultrasound interface receives imaging information. The processing electronics are coupled to the ultrasound interface and are configured to utilize the ultrasound imaging information to use time-varying frame selection to estimate strain so that the processing electronics perform the time-varying frame selection by comparing a single frame to a plurality of previous frames and selecting a single comparison set for each frame for strain estimation.

Abstract: An ultrasound processing system includes an ultrasound interface and processing electronics. The ultrasound interface receives imaging information. The processing electronics are coupled to the ultrasound interface and are configured to perform processing across a plurality of ultrasound channels by combining channel data for adaptively reducing the common mode noise prior to beamforming for a transmit event. The combination of the channel data may be computing an arithmetic mean, which is then multiplied to a weighting coefficient. This value may then be removed from the individual channel data. The modified channel data is then transmitted to a beamformer, which processes the channel data for directional signal transmission and reception.

Abstract: The present disclosure relates to a method, device and system for amending a heartbeat type. The method includes: displaying an interface for presenting heartbeat waveforms; based on a user interface provided on the interface for presenting the heartbeat waveforms, detecting a currently triggered heartbeat type; and when detecting that at least one electrocardiogram waveform on the interface for presenting the heartbeat waveforms is selected, amending a heartbeat type of the selected at least one electrocardiogram waveform as the currently triggered heartbeat type. The technical solutions provided by the present disclosure can simplify operations for amending heartbeat types and thereby improve working efficiency.

Abstract: A computing system includes a memory configured to store instructions, and one or more processors configured to execute the instructions to receive data relating to an image or a user, determine a feature from the data, identify a user preference from a user profile, obtain a model, and segment the image based on the feature, the user preference, and the model. The model is generated by determining a historical feature from historical data as an input, determining a desired output, obtaining a preliminary model based on the input and the desired output, determining an actual output of the preliminary model, determining error criteria between the actual output and the desired output, and generating the model by updating the preliminary model based on the error criteria.