A panel kit for a blood purification apparatus

Abstract

This application discloses a panel kit for a blood purification device, including a power assembly and a monitoring assembly. The power assembly includes a power panel and at least two pump tubing segments mounted on the power panel. The power panel is detachably mounted to the main unit. When the power panel is mounted to a first target position on the main unit, the pump tubing segments respectively cooperate with the pump assembly to drive the flow of corresponding blood and medical fluids. The monitoring assembly includes a monitoring panel and at least two monitoring tubing segments mounted on the monitoring panel. The monitoring panel is detachably mounted to the main unit, and the monitoring panel and power panel can be independently installed and removed. The at least two monitoring tubing segments are used to monitor parameter information of blood and / or medical fluids. At least one monitoring tubing segment is provided with a second interface. The monitoring assembly can be manually installed so that the monitoring panel is mounted to a second target position on the main unit and the second interface is simultaneously connected to the first interface of the main unit. This application has the advantage of convenient installation.

Description

[0001] This application claims priority to Chinese Patent Application No. 202510180720.9, filed on February 18, 2025, entitled "A Panel Kit for a Blood Purification Device", the entire contents of which are incorporated herein by reference. Technical Field

[0002] This application belongs to the field of medical devices, and in particular relates to a panel kit for a blood purification device. Background Technology

[0003] Blood purification therapy is a treatment method that involves drawing the patient's blood outside the body and then using a filtration unit to remove pathogenic substances from the blood in order to purify the blood. The main treatment methods include hemodialysis, hemofiltration, hemodiafiltration, hemoperfusion, and plasma exchange.

[0004] In related technologies, blood purification therapy is typically achieved by connecting a blood purification device to the patient's blood vessels. Therefore, the blood purification device requires numerous tubing segments to deliver the patient's blood, replacement fluid, anticoagulants, etc. Furthermore, to ensure the safety of the blood returning to the patient, the tubing segments must be replaced after each use, and the large number of tubing segments makes installation quite challenging. Summary of the Invention

[0005] In a first aspect, embodiments of this application provide a panel kit for a blood purification device, the blood purification device including a main unit, the main unit having a pump assembly and a first interface, and the panel kit including: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least another pump tubing segment cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and A monitoring component includes a monitoring panel and at least two monitoring tube segments. The monitoring panel is detachably mounted to the host computer and is separately disposed from the power panel, making them independent panels that can be independently installed and removed. The at least two monitoring tube segments are mounted on the monitoring panel and are used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. The monitoring component can be manually installed so that the monitoring panel is mounted to a second target position on the host computer and the second interface is simultaneously connected to the first interface. When the second interface is connected to the first interface, the monitoring tube segments are used by the host computer to monitor the parameter information.

[0006] Secondly, embodiments of this application also provide a panel kit for a blood purification device, the blood purification device including a main unit, the main unit having a pump assembly and a retractable first interface, the panel kit including: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least another pump tubing segment cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and A monitoring component includes a monitoring panel and at least two monitoring tube segments. The monitoring panel is detachably mounted to the host unit and is separately disposed from the power panel, making them independent panels that can be independently installed and removed. The at least two monitoring tube segments are mounted on the monitoring panel and are used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. When the monitoring panel is mounted at a second target position on the host unit, the first interface can extend to connect with the second interface. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information.

[0007] Thirdly, embodiments of this application also provide a panel kit for a blood purification device, the blood purification device including a main unit, the main unit having a pump assembly and a first interface, and the panel kit including: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least another pump tubing segment cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and A monitoring component includes a monitoring panel and at least two monitoring tube segments. The monitoring panel is detachably mounted to the host unit and is separately disposed from the power panel, making them independent panels that can be independently installed and removed. The at least two monitoring tube segments are mounted on the monitoring panel and are used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. When the monitoring panel is mounted in a second preset position on the host unit, the host unit can drive the monitoring panel to a second target position, so that the second interface connects to the first interface. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information.

[0008] Fourthly, embodiments of this application also provide a panel kit for a blood purification device, the blood purification device including a main unit, the main unit having a pump assembly and a first interface, and the panel kit including: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least another pump tubing segment cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and A monitoring component includes a monitoring panel and at least two monitoring tube segments. The monitoring panel is detachably mounted to the host unit and is separately disposed from the power panel, making them independent panels that can be independently installed and removed. The at least two monitoring tube segments are mounted on the monitoring panel and are used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. The second interface is movably disposed relative to the monitoring panel. When the monitoring panel is mounted at a second target position on the host unit, the second interface can be manually operated to connect the first interface and the second interface. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information.

[0009] Fifthly, embodiments of this application also provide a panel kit for a blood purification device, the blood purification device including a main unit, the main unit having a pump assembly, a conductive component and a first interface, the panel kit including: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least one of the pump tubing segments cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and... A monitoring component includes a monitoring panel, a monitoring tube segment, and an electrostatic discharge unit. The monitoring panel is detachably mounted to the host unit and is separate from the power panel, making them independent panels that can be independently installed and removed. The monitoring tube segment and the electrostatic discharge unit are both mounted on the monitoring panel. The monitoring tube segment is used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. The monitoring component allows the monitoring panel to be manually installed to a second target position on the host unit, simultaneously connecting the second interface to the first interface and the electrostatic discharge unit to the conductive element. When the second interface is connected to the first interface, the monitoring tube segment allows the host unit to monitor the parameter information. When the electrostatic discharge unit is connected to the conductive element, it can release static electricity from the panel assembly.

[0010] Sixthly, embodiments of this application also provide a panel kit for a blood purification device, the blood purification device including a main unit, the main unit having a pump assembly, a conductive element and a retractable first interface, the panel kit including: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least one of the pump tubing segments cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and... A monitoring component includes a monitoring panel, a monitoring tube segment, and an electrostatic discharge unit. The monitoring panel is detachably mounted to the host unit and is separately disposed from the power panel, making them independent panels that can be independently installed and removed. The monitoring tube segment and the electrostatic discharge unit are both mounted on the monitoring panel. The monitoring tube segment is used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. When the monitoring panel is mounted at a second target position on the host unit, the first interface can extend to connect with the second interface. The electrostatic discharge unit is electrically connected to a conductive element fixed on the host unit, or the electrostatic discharge unit is connected to a conductive element extending outward from the host unit. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information. When the electrostatic discharge unit is connected to the conductive element, it can release static electricity from the tube segment of the panel assembly.

[0011] In a seventh aspect, embodiments of this application also provide a panel kit for a blood purification device, the blood purification device including a main unit, the main unit having a pump assembly, a conductive component and a first interface, the panel kit including: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least one of the pump tubing segments cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and... A monitoring component includes a monitoring panel, a monitoring tube segment, and an electrostatic discharge unit. The monitoring panel is detachably mounted to the host unit and is separately configured from the power panel, making them independent panels that can be independently installed and removed. The monitoring tube segment and the electrostatic discharge unit are both mounted on the monitoring panel. The monitoring tube segment is used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. When the monitoring panel is mounted in a second preset position on the host unit, the host unit can drive the monitoring panel to a second target position, so that the second interface is connected and fixed to the first interface, and the electrostatic discharge unit is connected to the conductive element. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information. When the electrostatic discharge unit is connected to the conductive element, it can release static electricity from the panel assembly. Eighthly, embodiments of this application provide a panel kit for a blood purification device, the blood purification device including a main unit, the main unit having a pump assembly, a conductive element and a first interface, the panel kit including: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least one of the pump tubing segments cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and... A monitoring component includes a monitoring panel, a monitoring tube segment, and an electrostatic discharge unit. The monitoring panel is detachably mounted to the host unit and is separately configured from the power panel, making them independent panels that can be independently installed and removed. The monitoring tube segment and the electrostatic discharge unit are both mounted on the monitoring panel. The monitoring tube segment is used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one monitoring tube segment has a second interface. The second interface is movably configured relative to the monitoring panel. When the monitoring panel is mounted at a second target position on the host unit, the second interface can be manually operated to connect the first interface and the second interface. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information. The electrostatic discharge unit, when connected to a conductive element, can release static electricity from the panel assembly.

[0012] In this embodiment, on the one hand, by setting at least two pump tubing segments on the power panel, the user can assist in the installation of at least two pump tubing segments through the installation action of the power panel, thereby reducing the installation difficulty and the probability of incorrect installation of at least two pump tubing segments; on the other hand, in this embodiment, the connection between the first interface and the second interface can be achieved through the installation of the monitoring panel, thereby reducing the installation steps of the panel kit to the blood purification equipment, or after the monitoring panel is installed in place, the second interface can be further connected to the first interface by manual operation, thereby avoiding the difficulty of installing the first interface of the panel kit in one go, and thus reducing the installation difficulty of the panel kit. Attached Figure Description

[0013] The technical solution and its beneficial effects will become apparent from the following detailed description of specific embodiments of this application, in conjunction with the accompanying drawings.

[0014] Figure 1 This is a schematic diagram of the main unit of the blood purification device provided in an embodiment of this application.

[0015] Figure 2 for Figure 1 The diagram shows the installation structure of the main unit and the panel kit.

[0016] Figure 3 for Figure 2 The diagram shows a second structural schematic of the power assembly of the panel kit shown.

[0017] Figure 4 for Figure 2 The diagram shows a second structural representation of the monitoring panel of the panel kit shown.

[0018] Figure 5 for Figure 2 The diagram shows a structural schematic of a monitoring pipe section of the panel kit shown.

[0019] Figure 6 This is a schematic diagram of a second structure of the panel kit according to an embodiment of this application.

[0020] Figure 7 for Figure 6 A schematic diagram of the blood flow path in the panel kit shown.

[0021] Figure 8 for Figure 6 The diagram shows the flow path of the TCM liquid from the first filter unit in the panel kit shown.

[0022] Figure 9 This is a schematic diagram of the secondary membrane pressure monitoring tube section of the panel kit in this embodiment.

[0023] Figure 10 for Figure 6 The diagram shows the flow path of anticoagulant drugs in the panel kit.

[0024] Figure 11 for Figure 6 The diagram shows the flow paths of the replacement fluid and dialysate in the panel kit shown.

[0025] Figure 12 This is a schematic diagram of a third structure of the panel kit in the embodiments of this application.

[0026] Figure 13 for Figure 2 The diagram shows a third structural design of the monitoring panel of the panel kit shown.

[0027] The labels in the diagram are as follows: 100. Panel kit; 11. Power assembly; 111. Power panel; 1111. First connection; 1112. First region; 1113. Second region; 112. Pump tubing section; 1121. Blood pump tubing section; 1122. Waste hydraulic fluid pump tubing section; 1123. Pre-pump tubing section; 1124. Dialysis fluid pump tubing section; 1125. Replacement fluid pump tubing section; 1126. Medical fluid pump tubing section; 12. Monitoring assembly; 121. Monitoring panel; 1211. Second connection; 122. Monitoring tubing section; 122a. Blood pressure monitoring tubing section; 122b. Pre-filter pressure monitoring tubing section; 122c. Waste hydraulic fluid monitoring tubing section; 122d. Blood leakage monitoring tubing section; 122e. Secondary membrane pressure monitoring tubing section; 1221. Second interface; 1222. Pressure monitoring module; 1222a. Fluid section; 1222b. Gas section; 12 22c. Diaphragm; 1301. Blood drainage path; 1302. Blood pumping path; 1303. Waste fluid path; 1304. Connecting path; 1305. Blood return path; 1306. Injection path; 1307. First inlet path; 1308. Second inlet path; 1309. Third inlet path; 1310. Fourth inlet path; 1311. Fifth inlet path; 1312. Sixth inlet path ; 1313, Degassing vessel; 1314, Degassing vessel monitoring unit; 1315, Collection flow path; 14, Electrostatic discharge unit; 15, Heating assembly; 151, Heating panel; 152, Heating container; 1521, First heating container; 1522, Second heating container; 153, Liquid outlet flow path; 1531, First liquid outlet flow path; 1532, Second liquid outlet flow path; 1533, Third liquid outlet flow path; 200. Host computer; 21. Pump assembly; 22. First interface; 23. First drive mechanism; 231. First gripper; 24. First position detection mechanism; 25. Second drive mechanism; 251. Second gripper; 26. Second position detection mechanism; 27. First pipeline switching device; 28. Second pipeline switching device; 300. First filtration unit; 400. Second filtration unit. Detailed Implementation

[0028] The technical solutions of the embodiments of this application will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only a part of the embodiments of this application, and not all of them. All other embodiments obtained by those skilled in the art based on the embodiments of this application without creative effort are within the scope of protection of this application.

[0029] Please refer to Figure 1 and Figure 2In a first aspect, embodiments of this application provide a panel kit 100 for a blood purification device. The blood purification device may include a hemodialysis machine and a continuous renal replacement therapy device, etc., and embodiments of this application are not limited thereto. The blood purification device may also include a main unit 200. The main unit 200 is provided with a pump assembly 21 and a first interface 22.

[0030] The panel kit 100 may include a power component 11 and a monitoring component 12.

[0031] The power assembly 11 includes a power panel 111 and at least two pump tubing segments 112. The power panel 111 is detachably mounted to the main unit 200. At least two pump tubing segments 112 are mounted on the power panel 111. At least one pump tubing segment 112 cooperates with the pump assembly 21 to drive blood flow along the pump tubing segment 112, and at least another pump tubing segment 112 cooperates with the pump assembly 21 to drive medical fluid flow along the pump tubing segment 112. When the power panel 111 is mounted to the first target position on the main unit 200, the pump tubing segments 112 are adapted to the pump assembly 21. When the pump tubing segments 112 are adapted to the pump assembly 21, the pump tubing segments 112 can be driven by the pump assembly 21 to drive the corresponding blood or medical fluid flow. Furthermore, after the power panel 111 is mounted to the first target position, the user does not need to manually install and fix the pump tubing segments 112 to the pump assembly 21, making the installation of the power panel 111 simpler and reducing the risk of incorrect installation of the at least two pump tubing segments 112.

[0032] The monitoring component 12 includes a monitoring panel 121 and at least two monitoring tube segments 122. The monitoring panel 121 is detachably mounted to the main unit 200. The monitoring panel 121 is separate from the power panel 111, allowing independent installation and removal of the two panels. The at least two monitoring tube segments 122 are mounted on the monitoring panel 121 and are used to monitor parameters of blood and / or medical fluids, including at least pressure parameters. At least one monitoring tube segment 122 has a second interface 1221. The monitoring component 12 can be manually installed so that the monitoring panel 121 is mounted to a second target position on the main unit 200, simultaneously connecting the second interface 1221 to the first interface 22. This reduces the steps required to independently install the second interface 1221 and improves the accuracy of its installation. Furthermore, since at least two monitoring pipe segments 122 are installed on the monitoring panel 121, the installation of the monitoring panel 121 can also assist in the installation of at least one other monitoring pipe segment 122. For example, at least one other monitoring pipe segment 122 can be moved to the vicinity of the corresponding position on the host 200 or directly moved to the corresponding position connected to the host 200. Therefore, the panel kit 100 of this embodiment can reduce the difficulty of installing the pipes in the panel kit 100 and reduce the probability of incorrect pipe installation.

[0033] It should be noted that the monitoring component 12 can be manually installed so that the monitoring panel 121 is installed at the second target position of the host 200, and simultaneously the second interface 1221 is connected to the first interface 22. This can be understood as the operation of installing the monitoring panel 121 at the second target position causing the second interface 1221 to connect to the first interface 22, thus achieving the installation and fixation of both the monitoring panel 121 and the second interface 1221 in a single action. During this process, the installation of the monitoring panel 121 at the second target position of the host 200 and the connection of the second interface 1221 to the first interface 22 can be completed simultaneously or with a certain time difference; this embodiment does not limit this.

[0034] It should also be noted that in this embodiment of the application, the monitoring panel 121 and the power panel 111 can be disassembled and assembled independently of each other. That is to say, the power panel 111 and the monitoring panel 121 are independent panels and can be disassembled and assembled independently of each other.

[0035] It should also be noted that the monitoring component 12 can be installed by manually installing the monitoring panel 121 to the second target position and simultaneously connecting the second interface 1221 to the first interface 22, or it can be installed by manually installing the monitoring panel 121 to the second target position and simultaneously connecting the second interface 1221 to the first interface 22. This application embodiment does not limit this.

[0036] It is also understandable that if the pump pipe section 112 and the monitoring pipe section 122 are both integrated on the same mounting panel, on the one hand, the cumulative form and position tolerances formed by actual manufacturing tolerances and assembly tolerances may cause a portion of the pump pipe section 112 and the monitoring pipe section 122 to be unable to be installed properly. On the other hand, when the pump assembly 21 drives the pump pipe section 112 to work, it will cause the mounting panel to vibrate violently. In turn, the vibration of the mounting panel will be transmitted to the monitoring pipe section 122 (such as the second interface 1221 of the monitoring pipe section 122), ultimately affecting the connection between the second interface 1221 and the first interface 22, resulting in incorrect detection results at the monitoring pipe section 122. Therefore, the embodiments of this application can also make the panel kit 100 easy to install and the monitoring assembly 12 have high accuracy.

[0037] The above is an overall description of the technical solutions of the embodiments of this application.

[0038] In some embodiments, the pump pipe section 112 includes a first flexible conduit. When the pump pipe section 112 is adapted to the pump assembly 21, the first flexible conduit abuts against the pump head of the pump assembly 21, so that the rotation of the pump head can drive the first flexible conduit to be wound around the pump head. Therefore, during the installation of the power assembly 11, only the first flexible conduit needs to contact the pump head of the pump assembly 21, eliminating the need for the user to manually wind the pump pipe section 112 around the pump head of the pump assembly 21, thus making the installation of the pump pipe section 112 simpler and more convenient.

[0039] For example, pump assembly 21 may include a peristaltic pump. When the first flexible tubing comes into contact with the pump head of the peristaltic pump, the peristaltic pump first drives the first flexible tubing to wrap around the pump head, and then the peristaltic pump continues to squeeze the first flexible tubing by rotating the pump head, thereby driving the flow of blood or medical fluid in the pump section 112.

[0040] Optionally, the pump section 112 includes a first flexible conduit. When the pump section 112 is adapted to the pump assembly 21, the first flexible conduit is routed to the pump head of the pump assembly 21, so that the rotation of the pump head directly drives the flow of the corresponding blood or medical fluid in the first flexible conduit.

[0041] Understandably, when the pump pipe section 112 is adapted to the pump assembly 21, whether the first flexible pipe is directly wound around the pump head of the pump assembly 21 or the pump assembly 21 needs to work so that the first flexible pipe is wound around the pump head of the pump assembly 21, it means that after the power panel 111 is installed in the first target position, the user does not need to connect the pump pipe section 112 to the pump assembly 21, thus making the installation of the power panel 111 simpler.

[0042] In the first installation method of the power assembly 11, when the power panel 111 is installed in the first preset position of the host 200, the power panel 111 can be driven by the host 200 to move to the first target position, thereby making the pump pipe section 112 compatible with the pump assembly 21.

[0043] Furthermore, for the installation of the power component 11, the user only needs to install the power panel 111 to the first preset position of the host 200, and then the host 200 will automatically drive the power panel 111 to the first target position to realize the automatic installation of the power panel 111, so as to make the installation of the power component 11 simpler.

[0044] Correspondingly, when the power panel 111 is installed in the first preset position, the pump pipe section 112 and the pump assembly 21 may not be adapted. Furthermore, when the power panel 111 is installed in the first preset position, a certain gap can be reserved between the pump pipe section 112 and the pump head so that when the power panel 111 moves toward the first target position, the pump pipe section 112 can move toward the pump head accordingly.

[0045] Furthermore, when the user needs to replace the panel kit 100 on the main unit 200 (i.e., when the panel kit 100 needs to be removed from the main unit 200), the main unit 200 can drive the power panel 111 to retract from the first target position to the first preset position, thereby separating the pump pipe section 112 and the pump head of the pump assembly 21, so that the user can more easily remove the power assembly 11 from the main unit 200.

[0046] Of course, in some other embodiments, when the power panel 111 is installed in the first preset position, the pump pipe section 112 and the pump head of the pump assembly 21 can also be in contact with each other. For example, when the power panel 111 is installed in the first preset position, the first flexible pipe of the pump pipe section 112 can abut against the pump head, and the first flexible pipe can adapt to the terrain changes when the power panel 111 moves toward the first target position.

[0047] Please combine Figure 1 and Figure 3In some embodiments, the power panel 111 is provided with a first connecting part 1111, which is used to connect to the first drive mechanism 23 of the host 200 so that the first drive mechanism 23 can drive the power panel 111 to move from a first preset position to a first target position.

[0048] The first connecting part 1111 can be connected to the first driving mechanism 23 by means of snap-fit, screw-fit or magnetic fixation, etc., and the embodiments of this application do not limit this.

[0049] Taking the first connecting part 1111 as an example, the first driving mechanism 23 may be provided with a first claw 231, which is engaged and fixed with the first connecting part 1111.

[0050] Correspondingly, the first connecting portion 1111 may include a first locking hole, and the first locking claw 231 may engage with the first locking hole. Of course, the first locking claw 231 may also include at least two first locking arms, and the first connecting portion 1111 may be a protruding structure on the power panel 111, so that the first connecting portion 1111 can be engaged between the two first locking arms. This application embodiment does not limit this.

[0051] In some implementations, whether the power panel 111 is installed at the first preset position and / or the first target position can be determined by the first position detection mechanism 24 on the host 200. Furthermore, the position of the power panel 111 can be accurately detected by the first position detection mechanism 24, thereby determining the overall position of the power assembly 11.

[0052] Therefore, the host 200 can determine whether the power panel 111 is properly installed when installed in the first preset position based on the detection result of the first position detection mechanism 24, thereby determining whether to drive the power panel 111 from the first preset position to the first target position via the first drive mechanism 23. Furthermore, after the host 200 drives the power panel 111 from the first preset position to the first target position via the first drive mechanism 23, the host 200 can also determine whether the power panel 111 is properly installed based on the detection result of the first position detection mechanism 24, thereby preventing abnormal installation of the power panel 111.

[0053] In some embodiments, when the power panel 111 is installed at a first preset position and / or a first target position, the power panel 111 blocks or contacts the first position detection mechanism 24, thereby enabling the first position detection mechanism 24 to detect the position of the power panel 111.

[0054] For example, the first position detection mechanism 24 may include photoelectric sensors such as infrared ranging sensors, laser ranging sensors, and photoelectric gates, so that the first position detection mechanism 24 can detect the position of the power panel 111 by detecting the distance of the power panel 111, whether the power panel 111 blocks the corresponding photoelectric gate, etc.

[0055] Optionally, the first position detection mechanism 24 may also include a pressure sensor to detect the position of the power panel 111 by the pressure applied to the first position detection mechanism 24 when the power panel 111 is installed in the first preset position and / or the first target position.

[0056] Of course, in some other embodiments, the first position detection mechanism 24 may also include limit switches, Hall sensors, proximity switches, etc., and this application embodiment does not limit this.

[0057] It is also understood that when the first position detection mechanism 24 is used to detect whether the power panel 111 is installed in the first preset position and the first target position, the first position detection mechanism 24 may include at least two first sensors, at least one first sensor is used to detect whether the power panel 111 is installed in the first preset position, and at least another first sensor is used to detect whether the power panel 111 is installed in the first target position.

[0058] The above describes the first installation method of the power component 11 in the embodiments of this application. The second installation method of the power component 11 in the embodiments of this application will be described below.

[0059] In the second installation method of the power assembly 11, the power assembly 11 can be manually installed so that the power panel 111 is installed to the first target position and the pump pipe section 112 is simultaneously adapted to the pump assembly 21. Therefore, after the power panel 111 is installed to the first target position, the user does not need to manually install the pump pipe section 112 to the pump head, thereby reducing the difficulty for the user when installing the power assembly 11.

[0060] Correspondingly, whether the power panel 111 is installed at the first target position can be determined by the first position detection mechanism 24 on the host 200. Furthermore, the position of the power panel 111 can be accurately detected by the first position detection mechanism 24, thereby determining the overall position of the power assembly 11.

[0061] The specific structure of the first position detection mechanism 24 will not be described in detail here.

[0062] In some embodiments, the power panel 111 may be provided with a first connecting part 1111, which is used to connect to the host 200 so that the power panel 111 can be detachably installed at a first target position.

[0063] For example, a first claw 231 may be fixedly installed on the host 200. The specific structure of the first claw 231 and the first connecting part 1111 will not be described in detail here.

[0064] The above is a description of the second installation method of the power component 11 in the embodiments of this application. The technical solution of the embodiments of this application will be further described below in conjunction with the monitoring component 12 in the embodiments of this application.

[0065] Please continue to combine Figure 1 and Figure 4 In some embodiments, the monitoring panel 121 is further provided with a second connecting part 1211, which is used to engage with the second claw 251 of the host 200 so that the monitoring panel 121 can be detachably installed on the host 200.

[0066] For example, the second connecting portion 1211 may include a second card hole, and the second card claw 251 may be able to engage with the second card hole. Of course, the second card claw 251 may also include at least two second card arms, and the second connecting portion 1211 may be a protruding structure on the monitoring panel 121, so that the second connecting portion 1211 can be engaged between the two second card arms. This application embodiment does not limit this.

[0067] In some implementations, whether the monitoring panel 121 is installed at the second target position can be determined by the second position detection mechanism 26 on the host 200. Furthermore, the second position detection mechanism 26 can accurately detect the position of the monitoring panel 121, thereby determining the overall position of the monitoring component 12. For example, the host 200 can determine whether the monitoring component 12 is installed correctly, thus avoiding erroneous detection results caused by the monitoring component 12 not being installed correctly.

[0068] In some embodiments, when the monitoring panel 121 is installed at the second target position, the monitoring panel 121 blocks or contacts the second position detection mechanism 26, thereby enabling the second position detection mechanism 26 to detect the position of the monitoring panel 121.

[0069] For example, the second position detection mechanism 26 may include photoelectric sensors such as infrared ranging sensors, laser ranging sensors, photoelectric gates, etc., so that the second position detection mechanism 26 can detect the position of the monitoring panel 121 by detecting the distance of the monitoring panel 121, whether the monitoring panel 121 blocks the corresponding photoelectric gate, etc.

[0070] Optionally, the second position detection mechanism 26 may also include a pressure sensor to detect the position of the monitoring panel 121 by monitoring the pressure applied to the second position detection mechanism 26 when the monitoring panel 121 is installed at the second target position.

[0071] Of course, in some other embodiments, the second position detection mechanism 26 may also include limit switches, Hall sensors, proximity switches, etc., and this application embodiment does not limit this.

[0072] It is also understood that when the second position detection mechanism 26 is used to detect whether the monitoring panel 121 is installed in the second preset position and the second target position, the second position detection mechanism 26 may include at least two second sensors, at least one second sensor for detecting whether the monitoring panel 121 is installed in the second preset position, and at least another second sensor for detecting whether the monitoring panel 121 is installed in the second target position.

[0073] In some embodiments, the panel assembly 100 also includes a second flexible conduit, which connects at least one pump section 112 and at least one monitoring section 122.

[0074] Understandably, when the pump assembly 21 of the host 200 drives the pump tubing 112, the pump assembly 21 will not only cause the power panel 111 to vibrate but also pull on the pump tubing 112. Therefore, by separating the power panel 111 from the monitoring panel 121 to avoid the vibration of the power panel 111 being transmitted to the monitoring panel 121, when the pump tubing 112 is pulled, the second flexible tubing can adaptively deform to prevent the pump tubing 112 from pulling on the connected monitoring tubing 122. This avoids the second interface 1221 from being loosened due to interference from the connected second flexible tubing and / or the monitoring panel 121, ultimately improving the accuracy of the blood purification equipment's test results.

[0075] In some implementations, the flow path connecting the pump section 112 and the monitoring section 122 is a flexible hose.

[0076] In some embodiments, the second interface 1221 is fixedly disposed relative to the monitoring panel 121. Therefore, during the installation of the monitoring panel 121, movement of the second interface 1221 relative to the monitoring panel 121 can be avoided, thus preventing the second interface 1221 from colliding with the first interface 22 and failing to be properly installed. Of course, by preventing movement of the second interface 1221 relative to the monitoring panel 121, it is also possible to prevent the second interface 1221 from shaking during the operation of the blood purification equipment, which could cause the second interface 1221 to become loose relative to the first interface 22, thereby improving the accuracy and reliability of the blood purification equipment's test results.

[0077] In some implementations, the second interface 1221 is activating relative to the monitoring panel 121.

[0078] For example, during the installation of the monitoring panel 121 to the second target location, the second interface 1221 is movable relative to the monitoring panel 121 to compensate for the tolerances of at least one of the second interface 1221, the monitoring panel 121, and the host 200.

[0079] Furthermore, by allowing the second interface 1221 to move relative to the monitoring panel 121, the accumulated dimensional and positional tolerances during the manufacturing and assembly of the second interface 1221, the monitoring panel 121, and the main unit 200 can be prevented from causing the second interface 1221 to fail to connect with the first interface 22. Simultaneously, by controlling the movement of the second interface 1221 to a limited range to compensate for tolerances, excessive movement of the second interface 1221 relative to the monitoring panel 121 can be avoided, thus preventing collisions between the second interface 1221 and the first interface 22 and ensuring proper installation. Of course, by preventing excessive movement of the second interface 1221 relative to the monitoring panel 121, it is also possible to prevent the second interface 1221 from shaking during operation of the blood purification equipment, which could lead to its detachment, thereby improving the accuracy and reliability of the blood purification equipment's test results.

[0080] In some implementations, the second interface 1221 is non-detachably connected to the corresponding monitoring pipe segment 122. For example, the second interface 1221 and the corresponding monitoring pipe segment 122 can be connected by means of bonding, integral molding, fusion welding, welding, etc., so as to avoid the second interface 1221 from becoming loose or even falling off, which would lead to inaccurate detection results of the host 200.

[0081] Optionally, in some other embodiments, the second interface 1221 is detachably connected to the corresponding monitoring pipe segment 122. For example, the second interface 1221 and the corresponding monitoring pipe segment 122 are connected by means of screwing, snap-fitting, magnetic fixation, etc., so as to replace the appropriate second interface 1221 according to the model change of the first interface 22 of the host 200.

[0082] In some embodiments, the second interface 1221 is connected to the corresponding monitoring pipe section 122 via a connector. The connector may be a Luer connector or other types of connectors, and this application embodiment does not limit this.

[0083] In some implementations, the monitoring tube segment 122 is non-detachably connected to the monitoring panel 121. For example, the monitoring tube segment 122 and the monitoring panel 121 can be connected by means of bonding, integral molding, fusion welding, welding, etc., so as to avoid the monitoring tube segment 122 from becoming loose or even falling off, which would lead to inaccurate detection results of the host 200.

[0084] Optionally, the monitoring pipe section 122 and the monitoring panel 121 can also be detachably connected. For example, the monitoring pipe section 122 and the monitoring panel 121 can be connected by screwing, snapping, magnetic fixing, etc., so as to replace the appropriate monitoring pipe section 122 or monitoring panel 121 according to the changes of the host 200.

[0085] Please continue to refer to this. Figure 5 In some embodiments, at least one monitoring section 122 includes a pressure monitoring module 1222, which includes a fluid section 1222a, a gas section 1222b, a diaphragm 1222c, and a second interface 1221. A fluid-side cavity defined at least partially by the fluid section 1222a and a gas-side cavity defined at least partially by the gas section 1222b are separated by the diaphragm 1222c. The fluid-side cavity is used for the flow of blood or medical fluid. The second interface 1221 communicates with the gas-side cavity. When the second interface 1221 is connected to the first interface 22, the monitoring section 122 is used by the host 200 to monitor the pressure parameters of the blood or medical fluid flowing through the fluid-side cavity.

[0086] Furthermore, when blood or medical fluid flows through the fluid side cavity, the blood or medical fluid will squeeze the diaphragm 1222c, causing a change in the gas pressure in the gas side cavity. As a result, the first interface 22 on the host 200 can monitor the pressure parameters of the corresponding blood or medical fluid by interfacing with the second interface 1221 to monitor the gas pressure in the gas side cavity. This way, the first interface 22 does not need to come into contact with the corresponding blood or medical fluid, thereby avoiding contamination of the blood or medical fluid.

[0087] Of course, in some other embodiments, at least one monitoring tube segment 122 may be adapted to a contact pressure sensor on the host 200. Thus, the contact pressure sensor on the host 200 can directly contact the diaphragm 1222c or other flexible areas of the monitoring tube segment 122 to monitor the pressure parameters of the corresponding blood or medical fluid. This application embodiment does not limit this.

[0088] In some embodiments, at least two monitoring tube segments 122 are provided with second interfaces 1221, and the number of first interfaces 22 is at least two. The second interfaces 1221 are used to connect to the corresponding first interfaces 22 on the host 200, so that the host 200 can monitor the pressure parameters of the corresponding blood or medical fluid through the monitoring tube segments 122. Furthermore, at least two second interfaces 1221 for monitoring pressure parameters can be connected through the monitoring panel 121, making the installation of the monitoring component 12 more convenient.

[0089] Please continue to refer to this. Figure 6In some embodiments, the blood purification device further includes a first filtration unit 300. The first filtration unit 300 is used to filter the blood flowing through the pump section 112.

[0090] The first filter unit 300 may be disposed on the host 200. After the panel kit 100 is installed on the host 200, the panel kit 100 is then connected to the first filter unit 300 on the host 200. Alternatively, the first filter unit 300 may be disposed on the panel kit 100. During the process of installing the panel kit 100 on the host 200, the first filter unit 300 is fixed to the host 200. This application embodiment does not limit this.

[0091] In some embodiments, when the second interface 1221 is connected to the first interface 22, the monitoring tube segment 122 is used by the host 200 to monitor the pressure parameters of the corresponding blood or medical fluid. At least two monitoring tube segments 122 also include a blood leakage monitoring tube segment 122d, which is used in conjunction with the blood leakage monitoring module on the host 200 to monitor whether blood has permeated from one side of the filter membrane of the first filtration unit 300 to the other side. Furthermore, the monitoring panel 121 allows for the connection of at least one second interface 1221 for monitoring pressure parameters and the installation of the blood leakage monitoring tube segment 122d, making the installation of the monitoring component 12 more convenient.

[0092] In some embodiments, the monitoring section 122 includes at least one of the following: blood pressure monitoring section 122a, filter pre-pressure monitoring section 122b, waste hydraulic pressure monitoring section 122c, and blood leakage monitoring section 122d.

[0093] The blood pressure monitoring tube 122a is used to monitor the pressure parameters of blood drawn from the patient's blood vessels (hereinafter referred to as blood pressure). Thus, the host 200 can determine whether blood is being drawn normally from the patient's blood vessels by monitoring the blood pressure.

[0094] Please continue to refer to this. Figure 7 For example, pump segment 112 includes blood pump segment 1121, which is used to cooperate with pump assembly 21 to drive blood flow. Panel kit 100 also includes a blood drainage path 1301 for connecting the input end of blood pump segment 1121 to a patient's blood vessel, and blood drainage path 1301 is provided with a blood pressure monitoring segment 122a.

[0095] Therefore, when the pump assembly 21 is working, the blood pump tubing 1121 can drive blood from the patient's blood vessels into the blood drainage path 1301, and then the blood will flow through the blood pressure monitoring tubing 122a along the blood drainage path 1301, so that the blood pressure monitoring tubing 122a can monitor the blood pressure.

[0096] The filter pre-pressure monitoring section 122b is used to monitor the pressure parameters of blood flowing from the pump section 112 into the first filtration unit 300 (hereinafter referred to as filter pre-pressure). Furthermore, by monitoring the filter pre-pressure, it can be determined whether blood can flow normally into the first filtration unit 300. For example, if the filter pre-pressure is too high, it may indicate a blockage or clotting within the first filtration unit 300.

[0097] For example, the pump section 112 includes a blood pump section 1121, which is used to cooperate with the pump assembly 21 to drive blood flow. The panel kit 100 also includes a blood pump flow path 1302, which is connected to the output end of the blood pump section 1121 and the blood input end of the first filter unit 300, respectively. The blood pump flow path 1302 is provided with a filter pre-pressure monitoring section 122b.

[0098] Therefore, when the pump assembly 21 is working, the blood in the patient's blood vessels can flow into the first filter unit 300 in sequence through the blood drainage path 1301, the blood pump tube section 1121 and the pump blood flow path 1302, thereby causing the blood flowing into the first filter unit 300 to flow through the filter pre-pressure monitoring tube section 122b.

[0099] Please continue to refer to this. Figure 8 The waste hydraulic pressure monitoring pipe section 122c is used to monitor the pressure parameters of the medical liquid discharged from the first filtration unit 300 (hereinafter referred to as waste hydraulic pressure). Furthermore, by monitoring the waste hydraulic pressure, it can be determined whether the filter membrane of the first filtration unit 300 is clogged.

[0100] For example, the pump section 112 includes a waste hydraulic pump section 1122, which is used to cooperate with the pump assembly 21 to drive the medical liquid in the first filter unit 300 to be discharged. The panel kit 100 also includes a waste liquid flow path 1303, which is connected to the medical liquid output end of the first filter unit 300 and the input end of the waste hydraulic pump section 1122 respectively. The waste liquid flow path 1303 is provided with a waste hydraulic monitoring section 122c.

[0101] Therefore, when the pump assembly 21 is working, the medical liquid in the first filter unit 300 can flow along the waste liquid flow path 1303 to the waste hydraulic pump section 1122, so as to flow through the waste hydraulic monitoring section 122c.

[0102] It should be noted that, compared to placing the waste hydraulic pressure monitoring pipe section 122c downstream of the waste hydraulic pressure pump pipe section 1122, this embodiment places the waste hydraulic pressure monitoring pipe section 122c between the waste hydraulic pressure pump pipe section 1122 and the first filter unit 300. This can prevent other faults downstream of the waste hydraulic pressure pump pipe section 1122 from interfering with the waste hydraulic pressure monitoring pipe section 122c's monitoring of whether the filter membrane of the first filter unit 300 is clogged.

[0103] The blood leakage monitoring section 122d is used in conjunction with the blood leakage monitoring module of the main unit 200 to monitor whether blood has permeated from one side of the filter membrane of the first filtration unit 300 to the other side. Thus, the blood leakage monitoring module can determine whether the filter membrane is damaged, causing blood to permeate through it.

[0104] For example, pump section 112 includes waste hydraulic pump section 1122, which is used to cooperate with pump assembly 21 to drive the medical fluid in the first filter unit 300 to be discharged. Panel kit 100 also includes waste fluid flow path 1303 and collection flow path 1315. Waste fluid flow path 1303 is connected to the medical fluid output end of the first filter unit 300 and the input end of waste hydraulic pump section 1122, respectively. The input end of collection flow path 1315 is connected to the output end of waste hydraulic pump section 1122. Blood leakage monitoring section 122d is provided in waste fluid flow path 1303 or collection flow path 1315.

[0105] Therefore, when the pump assembly 21 is working, the medical fluid in the first filter unit 300 can flow sequentially through the waste fluid flow path 1303, the waste hydraulic pump pipe section 1122, and the collection flow path 1315 before being collected by the external waste fluid collection container. During this process, the leakage monitoring can be performed through the blood leakage monitoring pipe section 122d on the waste fluid flow path 1303 or the collection flow path 1315.

[0106] In some implementations, the blood leakage monitoring module on the host 200 may include a photoelectric sensor, such as a color sensor, to determine the presence of blood components by monitoring the color of the medical fluid discharged from the first filtration unit 300.

[0107] Accordingly, the blood leakage monitoring tube segment 122d may be made of light-shielding material in at least part of its area, or the blood leakage monitoring tube segment 122d may be equipped with light-shielding components to prevent ambient light from affecting the detection results of the blood leakage monitoring module.

[0108] Of course, the blood leakage monitoring module can also be any other module used to detect blood components, and this application embodiment does not limit this.

[0109] It is also understood that the input end of the blood leakage monitoring tube segment 122d can face downwards, so that the medical fluid flows through the blood leakage monitoring tube segment 122d from bottom to top, thereby avoiding the accumulation of air bubbles when the medical fluid flows from top to bottom through the blood leakage monitoring tube segment 122d, which would affect the detection results of the blood leakage monitoring module. Of course, in some other embodiments, the input end of the blood leakage monitoring tube segment 122d can also face other directions, and this application embodiment does not limit this.

[0110] Similarly, at least one of the inlet ends of the monitoring tube 122 can face downwards so that the corresponding medical liquid or blood flows from bottom to top through the monitoring tube 122, thereby preventing air bubbles from accumulating in the monitoring tube 122 and affecting the test results.

[0111] Optionally, in some other embodiments, the panel assembly 100 includes a waste liquid branch for connection to the medical fluid output terminal of the first filtration unit 300. The waste liquid branch is provided with a blood leakage monitoring section 122d, through which medical fluid flowing from the first filtration unit 300 is allowed to pass. The blood leakage monitoring section works in conjunction with a blood leakage monitoring module on the main unit to monitor whether blood has permeated from one side of the filter membrane of the first filtration unit 300 to the other side.

[0112] For example, the waste liquid branch includes a waste liquid flow path 1303 and a collection flow path 1315. Therefore, the blood leakage monitoring tube segment 122d can be located in either the waste liquid flow path 1303 or the collection flow path 1315; this embodiment does not limit the specific location.

[0113] In some embodiments, the waste liquid branch can allow medical liquid flowing from the first filtration unit 300 to flow from bottom to top through the blood leakage monitoring tube section 122d, thereby preventing air bubbles from accumulating in the blood leakage monitoring tube section 122d and affecting the detection results.

[0114] It is also understood that the blood leakage monitoring tube segment 122d can be set on the monitoring panel 121, thus serving as one of the monitoring tube segments 122; the blood leakage monitoring tube segment 122d may also not be set on the monitoring panel 121. For example, the blood leakage monitoring tube segment 122d can be set between the power panel 111 and the monitoring panel 121. This application embodiment does not limit this.

[0115] For example, the blood leakage monitoring pipe section 122d can be set in the waste liquid flow path 1303 and located between the input end of the waste hydraulic pump pipe section 1122 and the output end of the waste hydraulic monitoring pipe section 122c.

[0116] Furthermore, on the one hand, it avoids the need to reserve a large space on the monitoring panel 121 to install the blood leakage monitoring tube segment 122d, thus facilitating the miniaturization design of the monitoring panel 121; on the other hand, it can also reduce the number of monitoring tube segments 122 on the monitoring panel 121, so that the tubing of the panel kit 100 does not need to be bent multiple times on the monitoring panel 121 to construct a large number of monitoring tube segments 122. This not only reduces the manufacturing difficulty of the panel kit 100, but also makes the corresponding blood or medical fluid flow more smoothly in the panel kit 100.

[0117] In addition, when the input end of the waste hydraulic fluid monitoring pipe section 122c is also facing downwards, the input end of the blood leakage monitoring pipe section 122d can also face downwards to connect to the output end of the waste hydraulic fluid monitoring pipe section 122c which is facing upwards. This avoids the accumulation of air bubbles when the medical fluid flows from top to bottom through the blood leakage monitoring pipe section 122d, which would affect the detection results of the blood leakage monitoring module.

[0118] In some embodiments, the number of monitoring components 12 is at least two, and the monitoring components 12 are arranged separately in pairs so that each monitoring component 12 can be independently assembled and disassembled. Each monitoring component 12 has at least two different types of a blood leakage monitoring tube section 122d, a blood pressure monitoring tube section 122a, a filter pre-pressure monitoring tube section 122b, and a waste hydraulic pressure monitoring tube section 122c. Thus, by using at least two monitoring components 12, the panel kit 100 can be adapted to the installation requirements of more different types of host units 200.

[0119] For example, one monitoring component 12 may be provided with a blood pressure monitoring tube section 122a and a filter pre-pressure monitoring tube section 122b, and another monitoring component 12 may be provided with a blood leakage monitoring tube section 122d and a waste hydraulic pressure monitoring tube section 122c. This application embodiment does not limit this.

[0120] Please continue to refer to this. Figure 9 In some embodiments, the blood purification device further includes a second filtration unit 400, which is used to re-filter the blood flowing through the pump section 112. The blood input end of the second filtration unit 400 is connected to the blood output end of the first filtration unit 300 to re-filter the blood flowing out of the blood output end of the first filtration unit 300. The monitoring section 122 also includes a secondary membrane pressure monitoring section 122e for connecting the first filtration unit 300 and the second filtration unit 400, which is used to monitor blood pressure parameters.

[0121] For example, the panel assembly 100 may also include a connecting flow path 1304, which is connected to the blood output end of the first filter unit 300 and the blood input end of the second filter unit 400, respectively, and the secondary membrane pressure monitoring tube segment 122e is disposed in the connecting flow path 1304.

[0122] Accordingly, when there are at least two monitoring components 12, and each monitoring component 12 is separately arranged in pairs so that each monitoring component 12 can be independently assembled and disassembled, then each monitoring component 12 has at least two different types of the following: blood leakage monitoring tube segment 122d, blood pressure monitoring tube segment 122a, filter pre-pressure monitoring tube segment 122b, waste hydraulic pressure monitoring tube segment 122c, and secondary membrane pressure monitoring tube segment 122e. Thus, by using at least two monitoring components 12, the panel kit 100 can adapt to the installation requirements of more different types of main unit 200s.

[0123] In some embodiments, the input end of the collection flow path 1315 is connected to the output end of the waste hydraulic pump pipeline section 1122, and the output end of the collection flow path 1315 is used to connect to the secondary membrane pressure monitoring pipeline section 122e. Thus, the medical liquid in the first filtration unit 300 can flow sequentially along the waste liquid flow path 1303, the waste hydraulic pump pipeline section 1122, and the collection flow path 1315 before flowing into the secondary membrane pressure monitoring pipeline section 122e.

[0124] Please continue to refer to this. Figure 10 In some embodiments, the panel assembly 100 also includes an electrostatic discharge unit 14, which works in conjunction with the host 200 to release static electricity from the panel assembly 100. It is understood that static electricity may also be generated when the pump assembly 21 drives the pump tubing 112; therefore, releasing the static electricity through the electrostatic discharge unit 14 can prevent interference with other simultaneously used devices, such as electrocardiogram monitors.

[0125] In some embodiments, at least one of the power panel 111 and the monitoring panel 121 is provided with an electrostatic discharge unit 14. By integrating the electrostatic discharge unit 14 into the corresponding power panel 111 and / or monitoring panel 121, the electrostatic discharge unit 14 can be adapted to the host 200 through the synchronous installation of the corresponding power panel 111 and / or monitoring panel 121, thereby facilitating the installation of the panel kit 100.

[0126] Of course, in some other embodiments, the electrostatic discharge unit 14 may not be disposed on the power panel 111 or the monitoring panel 121, and this application embodiment does not limit this.

[0127] In some embodiments, the host 200 is provided with a conductive element, and the electrostatic discharge unit 14 is used to connect to the conductive element to release static electricity. For example, the electrostatic discharge unit 14 can form an electrical connection by contacting the conductive element, thereby grounding through the conductive element.

[0128] In some embodiments, a portion of the tube segment of the panel assembly 100 is made of a conductive material to form an electrostatic discharge unit 14. Of course, the electrostatic discharge unit 14 can also be a conductive unit connected to the tube segment of the panel assembly 100, and this application embodiment does not limit this.

[0129] In some embodiments, pump section 112 includes blood pump section 1121. Panel assembly 100 also includes a blood drainage path 1301, a blood pumping path 1302, and a blood return path 1305. The input end of blood drainage path 1301 is connected to the blood drainage point of a patient's blood vessel, and the output end of blood drainage path 1301 is connected to the input end of blood pump section 1121. The input end of blood pumping path 1302 is connected to the output end of blood pumping path 1121, and the output end of blood pumping path 1302 is used to connect to the blood input end of the first filtration unit 300. The input end of blood return path 1305 is used to connect to the blood output end of the first filtration unit 300, and the output end of blood return path 1305 is used to connect to the blood return point of a patient's blood vessel.

[0130] Thus, during the operation of the blood purification device, when the pump assembly 21 of the main unit 200 is working, the blood pump tube 1121 drives the blood to flow sequentially from the blood draw point of the patient's blood vessel through the blood draw path 1301, the blood pump tube 1121, the blood pump path 1302, the first filter unit 300, and the blood return path 1305, and then flows back to the patient's blood vessel from the blood return point, thereby realizing extracorporeal blood circulation therapy for the patient.

[0131] In some embodiments, the panel assembly 100 further includes an injection path 1306, the input of which is connected to an anticoagulant infusion pump, and the output of which is connected to either the drainage path 1301 or the pumping path 1302. Thus, the anticoagulant infusion pump on the host 200 can inject anticoagulant into the blood in the drainage path 1301 or the pumping path 1302 via the injection path 1306, thereby preventing blood clotting in either the drainage path 1301 or the pumping path 1302.

[0132] Anticoagulant drugs may include heparin, citrate, etc., and this application does not limit the specific drugs used.

[0133] It is also understandable that when the injection flow path 1306 is connected to the blood flow path 1302, it can, to some extent, prevent the pump assembly 21 from generating a large negative pressure in the blood flow path 1301 and drawing out the anticoagulant from the anticoagulant injection pump.

[0134] In some embodiments, the pump tubing 112 further includes a pre-pump tubing 1123, and the panel assembly 100 includes a first inlet flow path 1307 and a second inlet flow path 1308. The first inlet flow path 1307, the pre-pump tubing 1123, and the second inlet flow path 1308 are connected sequentially. The input end of the first inlet flow path 1307 is at least used to connect to an anticoagulant drug supply container, and the output end of the second inlet flow path 1308 is connected to the blood draw flow path 1301, the blood pump flow path 1302, or the blood return flow path 1305. Thus, the host 200 can drive the pre-pump tubing 1123 of the blood pump via the pump assembly 21, so that the anticoagulant in the anticoagulant supply container flows sequentially through the first inlet flow path 1307, the pre-pump tubing 1123 of the blood pump, and the second inlet flow path 1308 into the blood drainage flow path 1301, the blood pumping flow path 1302, or the blood return flow path 1305, so as to avoid blood clotting in the blood drainage flow path 1301, the blood pumping flow path 1302, or the blood return flow path 1305.

[0135] It is understandable that when the panel assembly 100 is simultaneously equipped with an injection flow path 1306, a first inlet flow path 1307, a pre-pump tubing section 1123, and a second inlet flow path 1308, the anticoagulant injection pump connected to the injection flow path 1306 and the anticoagulant supply container connected to the first inlet flow path 1307 can be used to supply different anticoagulant drugs. For example, the anticoagulant injection pump can be used to supply heparin, and the anticoagulant supply container can be used to supply citrate, to meet the different anticoagulant requirements in the extracorporeal blood purification process.

[0136] Please continue to refer to this. Figure 11 In some embodiments, the pump section 112 includes a dialysate pump section 1124, and the panel kit 100 also includes a third inlet flow path 1309 and a fourth inlet flow path 1310. The third inlet flow path 1309, the dialysate pump section 1124 and the fourth inlet flow path 1310 are connected in sequence. The input end of the third inlet flow path 1309 is used to connect to the dialysate supply container, and the output end of the fourth inlet flow path 1310 is used to connect to the medical liquid input end of the first filter unit 300.

[0137] Therefore, when the pump assembly 21 on the host 200 is working, the pump assembly 21 can drive the dialysate in the dialysate supply container through the dialysate pump tubing 1124 to flow into the first filter unit 300 in sequence through the third inlet flow path 1309, the dialysate pump tubing 1124, the fourth inlet flow path 1310, and the medical liquid input end of the first filter unit 300.

[0138] In some embodiments, the pump tubing 112 further includes a replacement fluid pump tubing 1125, and the panel assembly 100 further includes a fifth inlet flow path 1311 and a sixth inlet flow path 1312. The fifth inlet flow path 1311, the replacement fluid pump tubing 1125, and the sixth inlet flow path 1312 are connected sequentially. The input end of the fifth inlet flow path 1311 is used to connect to the replacement fluid supply container, and the output end of the sixth inlet flow path 1312 is used to connect to the blood drainage flow path 1301, the blood pumping flow path 1302, or the blood return flow path 1305.

[0139] Therefore, when the pump assembly 21 on the host 200 is working, the pump assembly 21 can drive the replacement fluid in the replacement fluid supply container through the replacement fluid pump pipe section 1125 to flow into the blood drainage flow section 1301, the blood pumping flow section 1302, or the blood return flow section 1305 after passing through the fifth inlet flow path 1311, the replacement fluid pump pipe section 1125 and the sixth inlet flow path 1312.

[0140] The replacement fluid may include commercially available replacement fluids, such as online replacement fluids produced online by hemodialysis filtration machines and manually prepared replacement fluids, etc., and this application does not limit this.

[0141] In some embodiments, the panel kit 100 further includes a heating assembly 15, which is installed in the heating area of ​​the main unit 200 to allow the heating device of the main unit 200 to heat the blood and / or medical fluid within the heating assembly 15. This satisfies the heating requirements of the blood and / or medical fluid. For example, the medical fluid can be heated to prevent excessively cold medical fluid from affecting the blood, such as causing discomfort due to excessively low blood temperature flowing back into the body.

[0142] The heating assembly 15 may include a heating panel 151 and a heating container 152. The heating panel 151 is for detachable installation to the heating area of ​​the main unit 200. The heating container 152 is mounted on the heating panel 151 for installation to the heating area via the heating panel 151, thereby allowing the heating container 152 to be conveniently installed to the main unit 200 via the heating panel 151.

[0143] It is understood that the heating container 152 may include coil-type heating containers, bladder-type heating containers, bottle-type heating containers, bag-type heating containers, etc., and the embodiments of this application do not limit this.

[0144] The heating assembly 15 may also include a liquid outlet path 153. The input end of the liquid outlet path 153 is connected to the output end of the heating container 152. The input end of the liquid outlet path 153 can be mounted on the heating panel 151. Thus, the heating container 152 and the input end of the liquid outlet path 153 can be conveniently mounted to the main unit 200 via the heating panel 151.

[0145] In some embodiments, the pump section 112 includes a dialysate pump section 1124, the heating container 152 includes a first heating container 1521, the input end of the first heating container 1521 is connected to the output end of the fourth inlet flow path 1310, the outlet flow path 153 connected to the first heating container 1521 includes a first outlet flow path 1531 and a second outlet flow path 1532, the first outlet flow path 1531 is connected to the blood return flow path 1305, and the second outlet flow path 1532 is used to connect to the medical liquid input end of the first filter unit 300.

[0146] Therefore, in actual use, the input end of the third fluid inlet flow path 1309 can be connected to either a dialysis fluid supply container or a replacement fluid supply container to meet the diverse usage needs of the blood purification equipment.

[0147] For example, when the input end of the third inlet flow path 1309 is connected to the dialysate supply container, the first outlet flow path 1531 can be disconnected and the second outlet flow path 1532 can be connected by the first pipeline switching device 27 on the host 200. This allows the dialysate in the dialysate supply container to flow into the first filter unit 300 after passing through the third inlet flow path 1309, the dialysate pump pipe section 1124, the fourth inlet flow path 1310, the first heating container 1521, the second outlet flow path 1532, and the medical liquid input end of the first filter unit 300.

[0148] Alternatively, when the input end of the third inlet flow path 1309 is connected to the replacement fluid supply container, the first outlet flow path 1531 can be connected and the second outlet flow path 1532 can be disconnected by the first pipeline switching device 27 on the host 200, so that the replacement fluid in the replacement fluid supply container flows into the blood return flow path 1305 after passing through the third inlet flow path 1309, the dialysate pump pipeline section 1124, the fourth inlet flow path 1310, the first heating container 1521 and the first outlet flow path 1531 in sequence.

[0149] In some embodiments, pump section 112 includes displacement fluid pump section 1125, heating container 152 includes second heating container 1522, the input end of the second heating container 1522 is connected to the output end of the sixth inlet flow path 1312, and the outlet flow path 153 connected to the second heating container 1522 includes a first outlet flow path 1531 and a third outlet flow path 1533, the first outlet flow path 1531 is connected to the blood return flow path 1305, and the third outlet flow path 1533 is connected to the blood drainage flow path 1301 or the blood pumping flow path 1302.

[0150] Therefore, in actual use, the replacement fluid in the second heating container 1522 can selectively flow into the blood return path 1305, the blood drainage path 1301, or the blood pumping path 1302.

[0151] For example, the second pipeline switching device 28 on the host 200 can control the first liquid outlet flow path 1531 to be connected and the third liquid outlet flow path 1533 to be disconnected, so that the replacement fluid in the replacement fluid supply container flows to the blood return flow path 1305 after passing through the fifth liquid inlet flow path 1311, the replacement fluid pump pipe section 1125, the sixth liquid inlet flow path 1312, the second heating container 1522 and the first liquid outlet flow path 1531 in sequence, thereby realizing the injection of replacement fluid into the blood filtered by the first filtration unit 300.

[0152] Alternatively, the second pipeline switching device 28 on the main unit 200 can control the first liquid outlet flow path 1531 to be disconnected and the third liquid outlet flow path 1533 to be connected, so that the replacement fluid in the replacement fluid supply container flows to the blood draw flow path 1301 or the blood pump flow path 1302 after passing through the fifth liquid inlet flow path 1311, the replacement fluid pump pipe section 1125, the sixth liquid inlet flow path 1312, the second heating container 1522 and the third liquid outlet flow path 1533 in sequence, thereby realizing the injection of replacement fluid into the blood that has not been filtered by the first filter unit 300.

[0153] In some embodiments, the power panel 111 and the monitoring panel 121 are both separately disposed from the heating panel 151, so that the heating panel 151 can be independently installed and removed from the power panel 111 and from the monitoring panel 121.

[0154] Please continue to refer to this. Figure 12 In some embodiments, the output end of the first liquid outlet path 1531 may be connected to the blood drainage path 1301 or the blood pumping path 1302, the output end of the second liquid outlet path 1532 may be connected to the medical liquid input end of the first filter unit 300, and the output end of the third liquid outlet path 1533 may be connected to the blood return path 1305.

[0155] Therefore, the replacement fluid in the replacement fluid supply container can be selectively injected into the blood flow path 1301 or the blood pumping flow path 1302 through the first outlet flow path 1531, or into the return flow path 1305 through the third outlet flow path 1533. Furthermore, the input end of the third inlet flow path 1309 can be selectively connected to the dialysate supply container and injected into the filter through the second outlet flow path 1532, or the input end of the third inlet flow path 1309 can be selectively connected to the replacement fluid supply container and injected into the blood flow path 1301 or the blood pumping flow path 1302 through the first outlet flow path 1531.

[0156] In some embodiments, the panel assembly 100 may not include a heating panel 151 and a heating container 152. For example, the output end of the fourth liquid inlet flow path 1310 is connected to the input end of the first liquid outlet flow path 1531 and the input end of the second liquid outlet flow path 1532 via a T-connector or the like, and the output end of the sixth liquid inlet flow path 1312 is connected to the input end of the first liquid outlet flow path 1531 and the input end of the third liquid outlet flow path 1533 via a T-connector or the like.

[0157] At this time, the input terminals of the first liquid outlet flow path 1531, the second liquid outlet flow path 1532, and the third liquid outlet flow path 1533 can be installed on the power panel 111.

[0158] In some embodiments, the blood return path 1305 includes a degassing vessel 1313 and a degassing vessel monitoring unit 1314. The degassing vessel monitoring unit 1314 is connected to the degassing vessel 1313. When the degassing vessel monitoring unit 1314 is connected to the degassing vessel monitoring interface on the main unit 200, the degassing vessel monitoring unit 1314 is used for the blood purification equipment to monitor the pressure inside the degassing vessel 1313. For example, the degassing vessel monitoring unit 1314 may include a Luer connector.

[0159] Please continue to refer to this. Figure 13 In some embodiments, the pump pipe section 112 is arc-shaped. Furthermore, the arc-shaped structure makes it easier for the pump pipe section 112 to be routed around the pump head of the pump assembly 21.

[0160] In some embodiments, the openings formed at both ends of the pump tube section 112 face the outer periphery of the power panel 111, thereby facilitating the connection of both ends of the pump tube section 112 to other corresponding flow paths in the panel assembly 100 by having both ends of all the pump tube sections 112 facing outward.

[0161] Optionally, at least the openings formed at both ends of a portion of the pump pipe section 112 face the inner periphery of the power panel 111, but this embodiment of the application does not limit this.

[0162] In some embodiments, the power panel 111 includes adjacent first regions 1112 and second regions 1113, with the first region 1112 located on one side of the second region 1113 in a horizontal direction. The pump section 112 includes a blood pump section 1121 and multiple medical fluid pump sections 1126. When the blood pump section 1121 is adapted to the pump assembly 21, it drives blood flow under the drive of the pump assembly 21. When the medical fluid pump sections 1126 are adapted to the pump assembly 21, they drive medical fluid flow under the drive of the pump assembly 21. One medical fluid pump section 1126 and the blood pump section 1121 are arranged generally vertically in the first region 1112, and all other medical fluid pump sections 1126 are arranged generally vertically in the second region 1113. Therefore, by arranging the pump pipe sections 112 in two columns, the space on the power panel 111 can be fully utilized.

[0163] The first region 1112 is located on one side of the second region 1113 along the horizontal direction. It can be that the upper end of the first region 1112 is flush with the upper end of the second region 1113, and the lower end of the first region 1112 is flush with the lower end of the second region 1113.

[0164] The first region 1112 is located on one side of the second region 1113 along the horizontal direction. Alternatively, the upper end of the first region 1112 may be higher than the upper end of the second region 1113. In this case, the lower end of the first region 1112 may be lower than the lower end of the second region 1113, or the lower end of the first region 1112 may be higher than the lower end of the second region 1113, or the lower end of the first region 1112 may be flush with the lower end of the second region 1113.

[0165] The first region 1112 is located on one side of the second region 1113 along the horizontal direction. Alternatively, the upper end of the first region 1112 may be lower than the upper end of the second region 1113. In this case, the lower end of the first region 1112 may be lower than the lower end of the second region 1113, or the lower end of the first region 1112 may be higher than the lower end of the second region 1113, or the lower end of the first region 1112 may be flush with the lower end of the second region 1113.

[0166] That is to say, in the embodiments of this application, the first region 1112 is located on one side of the second region 1113 along the horizontal direction. It is not necessary for the upper end of the first region 1112 to be flush with the upper end of the second region 1113, and the lower end of the first region 1112 to be flush with the lower end of the second region 1113.

[0167] In some embodiments, the first region 1112 is located on one side of the second region 1113 along the horizontal direction. This can be that at least half of the first region 1112 along the vertical direction is directly opposite the second region 1113 along the horizontal direction, and / or at least half of the second region 1113 along the vertical direction is directly opposite the first region 1112 along the horizontal direction.

[0168] In some embodiments, when the medical liquid pump tubing segment 1126 is adapted to the pump assembly 21, one of the medical liquid pump tubing segment 1126 located in the first region 1112 and the medical liquid pump tubing segment 1126 located at the lowermost side of the second region 1113 is used to drive the flow of anticoagulant drugs driven by the pump assembly 21, and the other is used to drive the flow of medical liquid out of the first filter unit 300 driven by the pump assembly 21. Alternatively, when the medical liquid pump tubing segment 1126 is adapted to the pump assembly 21, one of the medical liquid pump tubing segment 1126 located in the first region 1112 and the medical liquid pump tubing segment 1126 located in the middle of the second region 1113 is used to drive the flow of anticoagulant drugs driven by the pump assembly 21, and the other is used to drive the flow of medical liquid out of the first filter unit 300 driven by the pump assembly 21.

[0169] For example, the medical liquid pump tubing 1126 used to drive the flow of anticoagulant drugs driven by the pump assembly 21 is the pre-pump pump tubing 1123, and the medical liquid pump tubing 1126 used to drive the flow of medical liquid out of the first filter unit 300 driven by the pump assembly 21 is the waste hydraulic pump tubing 1122.

[0170] On the one hand, whether it is the medical liquid pump tubing segment 1126 located in the first region 1112 or the medical liquid pump tubing segment 1126 located at the bottom of the second region 1113, which is the pre-pump tubing segment 1123, since the pre-pump tubing segment 1123 and the blood pump tubing segment 1121 are adjacent, the blood drainage path 1301 or the blood pumping path 1302 connected to the blood pump tubing segment 1121 can be closer to the second inlet flow path 1308 connected to the pre-pump tubing segment 1123, so that the second inlet flow path 1308 can be made shorter.

[0171] On the other hand, whether it is the medical liquid pump pipe section 1126 located in the first region 1112 or the medical liquid pump pipe section 1126 located at the bottom of the second region 1113, which is a waste hydraulic pump pipe section 1122, in the event of damage to the waste hydraulic pump pipe section 1122, the medical liquid waste leaked from the waste hydraulic pump pipe section 1122 is not likely to contaminate other medical pump pipe sections 112 located above the second region 1113.

[0172] In some embodiments, the number of medical fluid pump tubing segments 1126 may be at least four. For example, medical pump tubing segments 112 include blood pump tubing segment 1121, pre-pump blood pump tubing segment 1123, dialysate pump tubing segment 1124, and replacement fluid pump tubing segment 1125.

[0173] Understandably, the pump body in the pump assembly 21 of the main unit 200 used for pumping blood can be larger than the pump body used for pumping medical fluids to ensure that the pump body used for pumping blood can draw blood from the patient's blood vessels. Correspondingly, the radius of the blood pump tubing segment 1121 is also larger than the radius of the medical fluid pump tubing segment 1126. Therefore, by placing the blood pump tubing segment 112 and one medical fluid pump tubing segment 1126 in the first region 1112, and placing at least three other medical fluid pump tubing segments 1126 in the second region 1113, the space next to the first region 1112 can be fully utilized to integrate at least three medical fluid pump tubing segments 1126, making the structure of the power panel 111 more compact, and correspondingly, the structure of the pump assembly 21 on the main unit 200 can also be more compact.

[0174] For example, the pump tubing segments 112 in the first region 1112 are, from top to bottom, the pre-pump tubing segment 1123 and the blood pump tubing segment 1121, and the pump tubing segments 112 in the second region 1113 are, from top to bottom, the dialysate pump tubing segment 1124, the replacement fluid pump tubing segment 1125 and the waste hydraulic fluid pump tubing segment 1122.

[0175] Alternatively, the pump tubing section 112 in the first region 1112 is, from top to bottom, the pre-pump tubing section 1123 and the blood pump tubing section 1121, and the pump tubing section 112 in the second region 1113 is, from top to bottom, the dialysate pump tubing section 1124, the waste hydraulic fluid pump tubing section 1122 and the replacement fluid pump tubing section 1125.

[0176] Alternatively, the pump tubing section 112 in the first region 1112, from top to bottom, consists of the pre-pump tubing section 1123 and the blood pump tubing section 1121, and the pump tubing section 112 in the second region 1113, from top to bottom, consists of the replacement fluid pump tubing section 1125, the dialysate pump tubing section 1124 and the waste hydraulic fluid pump tubing section 1122.

[0177] Alternatively, the pump tubing section 112 in the first region 1112 consists of the pre-pump tubing section 1123 and the blood pump tubing section 1121 from top to bottom, and the pump tubing section 112 in the second region 1113 consists of the replacement fluid pump tubing section 1125, the waste hydraulic fluid pump tubing section 1122 and the dialysate pump tubing section 1124 from top to bottom.

[0178] Alternatively, the pump tubing section 112 in the first region 1112 consists of the waste hydraulic pump tubing section 1122 and the blood pump tubing section 1121 from top to bottom, and the pump tubing section 112 in the second region 1113 consists of the dialysate pump tubing section 1124, the replacement fluid pump tubing section 1125 and the blood pump pre-pump tubing section 1123 from top to bottom.

[0179] Alternatively, the pump tubing section 112 in the first region 1112 consists of the waste hydraulic pump tubing section 1122 and the blood pump tubing section 1121 from top to bottom, and the pump tubing section 112 in the second region 1113 consists of the dialysate pump tubing section 1124, the blood pump pre-pump tubing section 1123 and the replacement fluid pump tubing section 1125 from top to bottom.

[0180] Alternatively, the pump tubing section 112 in the first region 1112 consists of the waste hydraulic pump tubing section 1122 and the blood pump tubing section 1121 from top to bottom, and the pump tubing section 112 in the second region 1113 consists of the replacement fluid pump tubing section 1125, the dialysate pump tubing section 1124 and the blood pump pre-pump tubing section 1123 from top to bottom.

[0181] Alternatively, the pump tubing section 112 in the first region 1112 consists of the waste hydraulic pump tubing section 1122 and the blood pump tubing section 1121 from top to bottom, and the pump tubing section 112 in the second region 1113 consists of the replacement fluid pump tubing section 1125, the blood pump pre-pump tubing section 1123 and the dialysate pump tubing section 1124 from top to bottom.

[0182] In some embodiments, the first connection portion 1111 of the power panel 111 may be located at least in the first region 1112. For example, the medical liquid pump tubing segment 1126 and at least part of the first connection portion 1111 in the first region 1112 are arranged side by side in the horizontal direction and located above the blood pump tubing segment 1121, thereby making full use of the space above the blood pump tubing segment 1121.

[0183] Secondly, this application also provides a panel kit 100 for a blood purification device, which may include a hemodialysis machine and a continuous renal replacement therapy device, etc., and this application embodiment does not limit this. The blood purification device may also include a main unit 200. The main unit 200 is provided with a pump assembly 21 and a retractable first interface 22.

[0184] The panel kit 100 may include a power component 11 and a monitoring component 12.

[0185] The power assembly 11 includes a power panel 111 and at least two pump tubing segments 112. The power panel 111 is detachably mounted to the main unit 200. At least two pump tubing segments 112 are mounted on the power panel 111. At least one pump tubing segment 112 cooperates with the pump assembly 21 to drive blood flow along the pump tubing segment 112, and at least another pump tubing segment 112 cooperates with the pump assembly 21 to drive medical fluid flow along the pump tubing segment 112. When the power panel 111 is mounted to the first target position on the main unit 200, the pump tubing segments 112 are adapted to the pump assembly 21. When the pump tubing segments 112 are adapted to the pump assembly 21, the pump tubing segments 112 can be driven by the pump assembly 21 to drive the corresponding blood or medical fluid flow. Furthermore, after the power panel 111 is mounted to the first target position, the user does not need to manually install and fix the pump tubing segments 112 to the pump assembly 21, making the installation of the power panel 111 simpler and reducing the risk of incorrect installation of the at least two pump tubing segments 112.

[0186] The monitoring component 12 includes a monitoring panel 121 and at least two monitoring tube segments 122. The monitoring panel 121 is detachably mounted to the main unit 200. The monitoring panel 121 is separate from the power panel 111, allowing independent assembly and disassembly of the two panels. At least two monitoring tube segments 122 are mounted on the monitoring panel 121 and are used to monitor parameter information of blood and / or medical fluids, including at least pressure parameters. At least one monitoring tube segment 122 is provided with a second interface 1221. When the monitoring panel 121 is mounted at a second target position on the main unit 200, a first interface 22 can extend to connect to the second interface 1221. When the second interface 1221 is connected to the first interface 22, the monitoring tube segment 122 is used for the main unit 200 to monitor parameter information. Therefore, the user only needs to install the monitoring panel 121 to the second target position of the host 200, and the first interface 22 on the host 200 can extend to connect with the second interface 1221 of the monitoring pipe section 122. The user does not need to manually connect the first interface 22 and the second interface 1221 after installing the monitoring panel 121 to the second target position of the host 200, which makes the installation of the monitoring component 12 simpler.

[0187] In some embodiments, when the monitoring panel 121 is installed in the second preset position of the host 200, the host 200 can drive the monitoring panel 121 to move to the second target position. Therefore, for the installation of the monitoring component 12, the user only needs to install the monitoring panel 121 in the second preset position of the host 200, and then the host 200 automatically drives the monitoring panel 121 to the second target position to achieve automatic installation of the monitoring panel 121, thus simplifying the installation of the power component 11.

[0188] In some embodiments, when the monitoring panel 121 is installed in the second preset position, the second interface 1221 is not connected to the first interface 22 on the host 200. Furthermore, when the monitoring panel 121 is installed in the second preset position, a certain gap can be reserved between the second interface 1221 and the first interface 22 so that when the monitoring panel 121 moves towards the second target position, the second interface 1221 can move accordingly towards the first interface 22.

[0189] Furthermore, when the user needs to replace the panel kit 100 on the host 200 (i.e., when the panel kit 100 needs to be removed from the host 200), the host 200 can drive the monitoring panel 121 to move from the second target position to the second preset position, thereby separating the second interface 1221 from the first interface 22, so that the user can more easily remove the monitoring component 12 from the host 200.

[0190] In some implementations, whether the monitoring panel 121 is installed at the second preset position and / or installed at the second target position can be detected by the second position detection mechanism 26 on the host 200.

[0191] Then, the host 200 can determine whether the monitoring panel 121 is installed in place when it is installed in the second preset position based on the detection result of the second position detection mechanism 26, thereby determining whether to drive the monitoring panel 121 from the second preset position to the second target position; and, after the host 200 drives the monitoring panel 121 from the second preset position to the second target position, the host 200 can also determine whether the monitoring panel 121 is installed in place based on the detection result of the second position detection mechanism 26.

[0192] In some embodiments, the monitoring panel 121 is provided with a second connection portion 1211, which is connected to the second drive mechanism 25 of the host 200 so that the second drive mechanism 25 can drive the monitoring panel 121 to move from a second preset position to a second target position.

[0193] For example, the second drive mechanism 25 is provided with a second claw 251 so that the second drive mechanism 25 can drive the second claw 251 to move. The specific structure of the second claw 251 and the second connecting part 1211 can be referred to the specific structure of the second claw 251 and the second connecting part 1211 in the first aspect, respectively. The embodiments of this application will not be described in detail here.

[0194] Optionally, the second claw 251 can also be fixedly installed on the host 200, and the corresponding blood purification device does not have a second drive mechanism 25, so that the user can directly install the monitoring panel 121 to the second target position. This application embodiment does not limit this.

[0195] It is understandable that the panel kit 100 of the second aspect differs from the panel kit 100 of the first aspect in that: in the first aspect, the panel kit 100 can be manually installed so that the monitoring panel 121 is installed at the second target position of the host 200 and the second interface 1221 is connected to the first interface 22; while in the second aspect, when the monitoring panel 121 is installed at the second target position of the host 200, the first interface 22 on the host 200 can extend to connect to the second interface 1221.

[0196] Therefore, in some embodiments, other specific structures of the panel kit 100 can be referred to the specific structures corresponding to the panel kit 100 in the first aspect, and will not be described in detail here.

[0197] Thirdly, this application also provides a panel kit 100 for a blood purification device, which may include a hemodialysis machine and a continuous renal replacement therapy device, etc., and this application embodiment does not limit this. The blood purification device may also include a main unit 200. The main unit 200 is provided with a pump assembly 21 and a first interface 22.

[0198] The panel kit 100 may include a power component 11 and a monitoring component 12.

[0199] The power assembly 11 includes a power panel 111 and at least two pump tubing segments 112. The power panel 111 is detachably mounted to the main unit 200. At least two pump tubing segments 112 are mounted on the power panel 111. At least one pump tubing segment 112 cooperates with the pump assembly 21 to drive blood flow along the pump tubing segment 112, and at least another pump tubing segment 112 cooperates with the pump assembly 21 to drive medical fluid flow along the pump tubing segment 112. When the power panel 111 is mounted to the first target position on the main unit 200, the pump tubing segments 112 are adapted to the pump assembly 21. When the pump tubing segments 112 are adapted to the pump assembly 21, the pump tubing segments 112 can be driven by the pump assembly 21 to drive the corresponding blood or medical fluid flow. Furthermore, after the power panel 111 is mounted to the first target position, the user does not need to manually install and fix the pump tubing segments 112 to the pump assembly 21, making the installation of the power panel 111 simpler and reducing the risk of incorrect installation of the at least two pump tubing segments 112.

[0200] The monitoring component 12 includes a monitoring panel 121 and at least two monitoring tube segments 122. The monitoring panel 121 is detachably mounted to the host unit 200. The monitoring panel 121 is separate from the power panel 111, allowing independent assembly and disassembly of the two panels. At least two monitoring tube segments 122 are mounted on the monitoring panel 121 and are used to monitor parameters of blood and / or medical fluids, including at least pressure parameters. At least one monitoring tube segment 122 has a second interface 1221. When the monitoring panel 121 is mounted in a second preset position on the host unit 200, the host unit 200 can drive the monitoring panel 121 to a second target position, so that the second interface 1221 is fixedly connected to the first interface 22. When the second interface 1221 is connected to the first interface 22, the monitoring tube segment 122 is used for the host unit 200 to monitor parameter information. Furthermore, for the installation of the monitoring component 12, the user only needs to install the monitoring panel 121 to the second preset position of the host 200, and then the host 200 will automatically drive the monitoring panel 121 to the second target position to realize the automatic installation of the monitoring panel 121, so as to make the installation of the power component 11 simpler.

[0201] In some embodiments, when the monitoring panel 121 is installed in the second preset position, the second interface 1221 is not connected to the first interface 22 on the host 200. Furthermore, when the monitoring panel 121 is installed in the second preset position, a certain gap can be reserved between the second interface 1221 and the first interface 22 so that when the monitoring panel 121 moves towards the second target position, the second interface 1221 can move accordingly towards the first interface 22.

[0202] Furthermore, when the user needs to replace the panel kit 100 on the host 200 (i.e., when the panel kit 100 needs to be removed from the host 200), the host 200 can drive the monitoring panel 121 to move from the second target position to the second preset position, thereby separating the second interface 1221 from the first interface 22, so that the user can more easily remove the monitoring component 12 from the host 200.

[0203] In some implementations, whether the monitoring panel 121 is installed at the second preset position and / or installed at the second target position can be detected by the second position detection mechanism 26 on the host 200.

[0204] Then, the host 200 can determine whether the monitoring panel 121 is installed in place when it is installed in the second preset position based on the detection result of the second position detection mechanism 26, thereby determining whether to drive the monitoring panel 121 from the second preset position to the second target position; and, after the host 200 drives the monitoring panel 121 from the second preset position to the second target position, the host 200 can also determine whether the monitoring panel 121 is installed in place based on the detection result of the second position detection mechanism 26.

[0205] In some embodiments, the monitoring panel 121 is provided with a second connection portion 1211, which is connected to the second drive mechanism 25 of the host 200 so that the second drive mechanism 25 can drive the monitoring panel 121 to move from a second preset position to a second target position.

[0206] For example, the second drive mechanism 25 is provided with a second claw 251 so that the second drive mechanism 25 can drive the second claw 251 to move. The specific structure of the second claw 251 and the second connecting part 1211 can be referred to the specific structure of the second claw 251 and the second connecting part 1211 in the first aspect, respectively. The embodiments of this application will not be described in detail here.

[0207] It is understandable that the panel kit 100 of the third aspect differs from the panel kit 100 of the first aspect in that: in the first aspect, the panel kit 100 can be manually installed so that the monitoring panel 121 is installed at the second target position of the host 200 and the second interface 1221 is connected to the first interface 22; while in the third aspect, when the monitoring panel 121 is installed at the second preset position of the host 200, the host 200 can drive the monitoring panel 121 to move to the second target position so that the second interface 1221 is connected to the first interface 22.

[0208] Therefore, in some embodiments, other specific structures of the panel kit 100 can be referred to the specific structure of the panel kit 100 in the first aspect, and will not be repeated here in the embodiments of this application.

[0209] Fourthly, this application also provides a panel kit 100 for a blood purification device, which may include a hemodialysis machine and a continuous renal replacement therapy device, etc., and this application embodiment does not limit this. The blood purification device may also include a main unit 200. The main unit 200 is provided with a pump assembly 21 and a first interface 22.

[0210] The panel kit 100 may include a power component 11 and a monitoring component 12.

[0211] The power assembly 11 includes a power panel 111 and at least two pump tubing segments 112. The power panel 111 is detachably mounted to the main unit 200. At least two pump tubing segments 112 are mounted on the power panel 111. At least one pump tubing segment 112 cooperates with the pump assembly 21 to drive blood flow along the pump tubing segment 112, and at least another pump tubing segment 112 cooperates with the pump assembly 21 to drive medical fluid flow along the pump tubing segment 112. When the power panel 111 is mounted to the first target position on the main unit 200, the pump tubing segments 112 are adapted to the pump assembly 21. When the pump tubing segments 112 are adapted to the pump assembly 21, the pump tubing segments 112 can be driven by the pump assembly 21 to drive the corresponding blood or medical fluid flow. Furthermore, after the power panel 111 is mounted to the first target position, the user does not need to manually install and fix the pump tubing segments 112 to the pump assembly 21, making the installation of the power panel 111 simpler and reducing the risk of incorrect installation of the at least two pump tubing segments 112.

[0212] The monitoring component 12 includes a monitoring panel 121 and at least two monitoring tube segments 122. The monitoring panel 121 is detachably mounted to the host unit 200. The monitoring panel 121 is separately configured from the power panel 111, making them independent panels that can be independently installed and removed. At least two monitoring tube segments 122 are mounted on the monitoring panel 121 and are used to monitor parameter information of blood and / or medical fluids, including at least pressure parameters. At least one monitoring tube segment 122 has a second interface 1221. The second interface 1221 is movably configured relative to the monitoring panel 121, and when the monitoring panel 121 is mounted at a second target position on the host unit 200, the second interface 1221 can be manually operated to connect the first interface 22 to the second interface 1221. When the second interface 1221 is connected to the first interface 22, the monitoring tube segment 122 is used for the host unit 200 to monitor parameter information.

[0213] After the monitoring panel 121 is installed, the user can easily connect the first interface 22 and the second interface 1221 manually to avoid misalignment and sealing between the first interface 22 and the second interface 1221.

[0214] In one embodiment, during actual manufacturing, form tolerances are inevitable for each part, and positional tolerances are inevitable between parts during assembly. To address this, after the monitoring panel 121 is installed to the second target position, the user manually connects the first interface 22 and the second interface 1221. This eliminates the need for costly and complex manufacturing processes to ensure that the accumulated form and positional tolerances of the first interface 22, monitoring panel 121, and blood purification equipment are within acceptable limits, allowing for a one-time installation of the first interface 22 and monitoring panel 121. Ultimately, this reduces the manufacturing difficulty of the monitoring component 12 and the difficulty of installing the monitoring component 12 into the device housing 201.

[0215] Furthermore, during the actual assembly of the panel kit 100 into the blood purification equipment, when there are too many parts that need to be installed at once, such as the monitoring panel 121 and the first interface 22, it is difficult to ensure that all these parts can be installed synchronously. Therefore, after the monitoring panel 121 is installed, the user can manually connect the first interface 22 to the second interface 1221, which makes the installation of the panel kit 100 simpler and more convenient.

[0216] In one embodiment, the connection between the first interface 22 and the second interface 1221 can be a sealed connection between the first interface 22 and the second interface 1221.

[0217] In some embodiments, the first interface 22 and the second interface 1221 can be connected by screwing, snapping, plugging, or other means. Based on this, when the monitoring panel 121 is installed at the second target position, the first interface 22 can be manually connected to the second interface 1221 by tightening, pressing, or plugging the first interface 22. This application embodiment does not limit this.

[0218] For example, the first interface 22 is equipped with a knob. When the monitoring panel 121 is installed in the second target position, the first interface 22 can be connected to the second interface 1221 by the user turning the knob.

[0219] In some implementations, the monitoring panel 121 can also be directly installed to the second target location by the user. Therefore, the panel kit 100 of the fourth aspect differs from the panel kit 100 of the first aspect in that: In the first aspect, the panel kit 100 can be manually installed so that the monitoring panel 121 is installed at the second target position of the host 200 and the second interface 1221 is connected to the first interface 22 simultaneously; in the fourth aspect, when the monitoring panel 121 is installed at the second preset position of the host 200, the host 200 can drive the monitoring panel 121 to move to the second target position, and then the user can manually operate it to connect the first interface 22 and the second interface 1221.

[0220] Therefore, in some embodiments, other specific structures of the panel kit 100 can be referred to the specific structure of the panel kit 100 in the first aspect, and will not be repeated here in the embodiments of this application.

[0221] Optionally, the user can manually install the monitoring panel 121 to the second preset position, and then the blood purification equipment can automatically drive the monitoring panel 121 to the second target position. Therefore, the difference between the panel kit 100 in the fourth aspect and the panel kit 100 in the third aspect is: In the third aspect, when the monitoring panel 121 is installed in the second preset position of the host 200, the host 200 can drive the monitoring panel 121 to move to the second target position so that the second interface 1221 can be connected to the first interface 22; and in the fourth aspect, when the monitoring panel 121 is installed in the second preset position of the host 200, the host 200 can drive the monitoring panel 121 to move to the second target position, and then the user can manually operate to connect the first interface 22 and the second interface 1221.

[0222] Therefore, in some embodiments, other specific structures of the panel kit 100 can be referred to the specific structure of the panel kit 100 in the third aspect, and will not be repeated here in the embodiments of this application.

[0223] Fifthly, embodiments of this application also provide a panel kit 100 for a blood purification device. The blood purification device may include a hemodialysis machine and a continuous renal replacement therapy device, etc., and embodiments of this application do not limit this to such devices. The blood purification device includes a main unit 200, which is provided with a pump assembly 21, a first interface 22, and conductive components.

[0224] The panel kit 100 includes a power component 11 and a monitoring component 12.

[0225] The power assembly 11 includes a power panel 111 and at least two pump tubing segments 112. The power panel 111 is detachably mounted to the main unit 200. At least two pump tubing segments 112 are mounted on the power panel 111. At least one pump tubing segment 112 cooperates with the pump assembly 21 to drive blood flow along the pump tubing segment 112, and at least another pump tubing segment 112 cooperates with the pump assembly 21 to drive medical fluid flow along the pump tubing segment 112. When the power panel 111 is mounted to the first target position on the main unit 200, the pump tubing segments 112 are adapted to the pump assembly 21. When the pump tubing segments 112 are adapted to the pump assembly 21, the pump tubing segments 112 can be driven by the pump assembly 21 to drive the corresponding blood or medical fluid flow. Furthermore, after the power panel 111 is mounted to the first target position, the user does not need to manually install and fix the pump tubing segments 112 to the pump assembly 21, making the installation of the power panel 111 simpler and reducing the risk of incorrect installation of the at least two pump tubing segments 112.

[0226] The monitoring component 12 includes a monitoring panel 121, a monitoring tube segment 122, and an electrostatic discharge unit 14. The monitoring panel 121 is detachably mounted to the main unit 200, and is separate from the power panel 111, allowing for independent assembly and disassembly. The monitoring tube segment 122 and the electrostatic discharge unit 14 are both mounted on the monitoring panel 121. The monitoring tube segment 122 monitors parameters of blood and / or medical fluids, including at least pressure parameters. At least one monitoring tube segment 122 has a second interface 1221; the second interface 1221 is fixedly mounted on the monitoring panel 121. The monitoring component 12 can be manually installed so that the monitoring panel 121 is mounted to a second target position on the main unit 200, simultaneously connecting the second interface 1221 to the first interface 22 and connecting the electrostatic discharge unit 14 to a conductive element. When the second interface 1221 is connected to the first interface 22, the monitoring tube segment 122 provides the main unit 200 with the monitored parameter information. When connected to a conductive component, the electrostatic discharge unit 14 can release static electricity from the panel assembly 100. This reduces the need for separate installation steps for the second interface 1221 and the electrostatic discharge unit 14, and improves the accuracy of their installation. Therefore, the panel assembly 100 of this embodiment reduces the difficulty of installing the piping within the panel assembly 100 and lowers the probability of incorrect piping installation.

[0227] It should be noted that the monitoring component 12 can be manually installed so that the monitoring panel 121 is installed at the second target position of the host 200, simultaneously connecting the second interface 1221 to the first interface 22 and the electrostatic discharge unit 14 to the conductive component. This can be understood as follows: by installing the monitoring panel 121 at the second target position, the second interface 1221 is connected to the first interface 22, and the electrostatic discharge unit 14 is connected to the conductive component, thus achieving the installation and fixation of the monitoring panel 121, the second interface 1221, and the electrostatic discharge unit 14 in a single action. During this process, the installation of the monitoring panel 121 at the second target position, the connection of the second interface 1221 to the first interface 22, and the connection of the electrostatic discharge unit 14 to the conductive component can be completed simultaneously or with a certain time difference; this embodiment does not limit this.

[0228] It is understood that the panel kit 100 of the fifth aspect differs from the panel kit 100 of the first aspect in that: in the first aspect, the monitoring panel 121 is provided with at least two monitoring tube segments 122; while in the fifth aspect, the monitoring panel 121 may only be provided with an electrostatic discharge unit 14 and a monitoring tube segment 122, or the monitoring panel 121 may only be provided with an electrostatic discharge unit 14 and multiple monitoring tube segments 122, and the embodiments of this application do not limit this.

[0229] Therefore, in some embodiments, other specific structures of the panel kit 100 can be referred to the specific structure of the panel kit 100 in the first aspect, and will not be repeated here in the embodiments of this application.

[0230] Sixthly, embodiments of this application also provide a panel kit 100 for a blood purification device. The blood purification device may include a hemodialysis machine and a continuous renal replacement therapy device, etc., and embodiments of this application do not limit this. The blood purification device includes a main unit 200, which is provided with a pump assembly 21, a first interface 22, and conductive components.

[0231] The panel kit 100 includes a power component 11 and a monitoring component 12.

[0232] The power assembly 11 includes a power panel 111 and at least two pump tubing segments 112. The power panel 111 is detachably mounted to the main unit 200. At least two pump tubing segments 112 are mounted on the power panel 111. At least one pump tubing segment 112 cooperates with the pump assembly 21 to drive blood flow along the pump tubing segment 112, and at least another pump tubing segment 112 cooperates with the pump assembly 21 to drive medical fluid flow along the pump tubing segment 112. When the power panel 111 is mounted to the first target position on the main unit 200, the pump tubing segments 112 are adapted to the pump assembly 21. When the pump tubing segments 112 are adapted to the pump assembly 21, the pump tubing segments 112 can be driven by the pump assembly 21 to drive the corresponding blood or medical fluid flow. Furthermore, after the power panel 111 is mounted to the first target position, the user does not need to manually install and fix the pump tubing segments 112 to the pump assembly 21, making the installation of the power panel 111 simpler and reducing the risk of incorrect installation of the at least two pump tubing segments 112.

[0233] The monitoring component 12 includes a monitoring panel 121, a monitoring tube segment 122, and an electrostatic discharge unit 14. The monitoring panel 121 is detachably mounted to the main unit 200, and is separately configured from the power panel 111 so that the monitoring panel 121 and the power panel 111 can be independently installed and removed. Both the monitoring tube segment 122 and the electrostatic discharge unit 14 are mounted on the monitoring panel 121. The monitoring tube segment 122 is used to monitor parameter information of blood and / or medical fluids, including at least pressure parameters. At least one monitoring tube segment 122 is provided with a second interface 1221. The second interface 1221 is fixedly disposed on the monitoring panel 121. When the monitoring panel 121 is mounted at a second target position on the main unit 200, the first interface 22 can extend and be fixedly connected to the second interface 1221. The electrostatic discharge unit 14 is electrically connected to a conductive element fixedly disposed on the main unit 200, or the electrostatic discharge unit 14 is connected to a conductive element extending outward from the main unit 200. When the second interface 1221 is connected to the first interface 22, the monitoring pipe segment 122 is used to provide the host 200 with monitoring parameter information. The electrostatic discharge unit 14, when connected to a conductive component, can release static electricity from the panel assembly 100. This reduces the steps required to independently install the second interface 1221 and the electrostatic discharge unit 14, and improves the accuracy of their installation. Therefore, the panel assembly 100 of this embodiment can reduce the difficulty of installing the piping in the panel assembly 100 and reduce the probability of incorrect piping installation.

[0234] It is understood that the panel kit 100 of the sixth aspect differs from the panel kit 100 of the second aspect in that: in the second aspect, the monitoring panel 121 is provided with at least two monitoring tube segments 122; while in the sixth aspect, the monitoring panel 121 may only be provided with an electrostatic discharge unit 14 and a monitoring tube segment 122, or the monitoring panel 121 may only be provided with an electrostatic discharge unit 14 and multiple monitoring tube segments 122. This application embodiment does not limit this.

[0235] Therefore, in some embodiments, other specific structures of the panel kit 100 can be referred to the specific structure of the panel kit 100 in the second aspect, and will not be repeated here in the embodiments of this application.

[0236] In a seventh aspect, embodiments of this application also provide a panel kit 100 for a blood purification device. The blood purification device may include a hemodialysis machine and a continuous renal replacement therapy device, etc., and embodiments of this application do not limit this. The blood purification device includes a main unit 200, which is provided with a pump assembly 21, a first interface 22, and conductive components.

[0237] The panel kit 100 includes a power component 11 and a monitoring component 12.

[0238] The power assembly 11 includes a power panel 111 and at least two pump tubing segments 112. The power panel 111 is detachably mounted to the main unit 200. At least two pump tubing segments 112 are mounted on the power panel 111. At least one pump tubing segment 112 cooperates with the pump assembly 21 to drive blood flow along the pump tubing segment 112, and at least another pump tubing segment 112 cooperates with the pump assembly 21 to drive medical fluid flow along the pump tubing segment 112. When the power panel 111 is mounted to the first target position on the main unit 200, the pump tubing segments 112 are adapted to the pump assembly 21. When the pump tubing segments 112 are adapted to the pump assembly 21, the pump tubing segments 112 can be driven by the pump assembly 21 to drive the corresponding blood or medical fluid flow. Furthermore, after the power panel 111 is mounted to the first target position, the user does not need to manually install and fix the pump tubing segments 112 to the pump assembly 21, making the installation of the power panel 111 simpler and reducing the risk of incorrect installation of the at least two pump tubing segments 112.

[0239] The monitoring component 12 includes a monitoring panel 121, a monitoring tube segment 122, and an electrostatic discharge unit 14. The monitoring panel 121 is detachably mounted to the host unit 200, and is separately configured from the power panel 111 so that the monitoring panel 121 and the power panel 111 can be independently installed and removed. Both the monitoring tube segment 122 and the electrostatic discharge unit 14 are mounted on the monitoring panel 121. The monitoring tube segment 122 is used to monitor parameter information of blood and / or medical fluids, including at least pressure parameters. At least one monitoring tube segment 122 is provided with a second interface 1221. The second interface 1221 is fixedly mounted on the monitoring panel 121. When the monitoring panel 121 is mounted in a second preset position on the host unit 200, the host unit 200 can drive the monitoring panel 121 to a second target position, so that the second interface 1221 is fixedly connected to the first interface 22, and the electrostatic discharge unit 14 is connected to a conductive element. When the second interface 1221 is connected to the first interface 22, the monitoring tube segment 122 is used for the host unit 200 to monitor parameter information. When connected to a conductive component, the electrostatic discharge unit 14 can release static electricity from the panel assembly 100. This reduces the need for separate installation steps for the second interface 1221 and the electrostatic discharge unit 14, and improves the accuracy of their installation. Therefore, the panel assembly 100 of this embodiment reduces the difficulty of installing the piping within the panel assembly 100 and lowers the probability of incorrect piping installation.

[0240] It is understood that the panel kit 100 of the seventh aspect differs from the panel kit 100 of the third aspect in that: in the third aspect, the monitoring panel 121 is provided with at least two monitoring tube segments 122; while in the seventh aspect, the monitoring panel 121 may only be provided with an electrostatic discharge unit 14 and a monitoring tube segment 122, or the monitoring panel 121 may only be provided with an electrostatic discharge unit 14 and multiple monitoring tube segments 122. This application embodiment does not limit this.

[0241] Therefore, in some embodiments, other specific structures of the panel kit 100 can be referred to the specific structure of the panel kit 100 in the third aspect, and will not be repeated here in the embodiments of this application.

[0242] Eighthly, embodiments of this application also provide a panel kit 100 for a blood purification device. The blood purification device may include a hemodialysis machine and a continuous renal replacement therapy device, etc., and embodiments of this application do not limit this to such devices. The blood purification device includes a main unit 200, which is provided with a pump assembly 21, a first interface 22, and conductive components.

[0243] The panel kit 100 may include a power component 11 and a monitoring component 12.

[0244] The power assembly 11 includes a power panel 111 and at least two pump tubing segments 112. The power panel 111 is detachably mounted to the main unit 200. At least two pump tubing segments 112 are mounted on the power panel 111. At least one pump tubing segment 112 cooperates with the pump assembly 21 to drive blood flow along the pump tubing segment 112, and at least another pump tubing segment 112 cooperates with the pump assembly 21 to drive medical fluid flow along the pump tubing segment 112. When the power panel 111 is mounted to the first target position on the main unit 200, the pump tubing segments 112 are adapted to the pump assembly 21. When the pump tubing segments 112 are adapted to the pump assembly 21, the pump tubing segments 112 can be driven by the pump assembly 21 to drive the corresponding blood or medical fluid flow. Furthermore, after the power panel 111 is mounted to the first target position, the user does not need to manually install and fix the pump tubing segments 112 to the pump assembly 21, making the installation of the power panel 111 simpler and reducing the risk of incorrect installation of the at least two pump tubing segments 112.

[0245] The monitoring component 12 includes a monitoring panel 121, a monitoring tube segment 122, and an electrostatic discharge unit 14. The monitoring panel 121 is detachably mounted to the main unit 200. The monitoring panel 121 is separately configured from the power panel 111, making them independent panels that can be independently installed and removed. Both the monitoring tube segment 122 and the electrostatic discharge unit 14 are mounted on the monitoring panel 121. The monitoring tube segment 122 is used to monitor parameter information of blood and / or medical fluids, including at least pressure parameters. At least one monitoring tube segment 122 is provided with a second interface 1221. The second interface 1221 is movably configured relative to the monitoring panel 121, and when the monitoring panel 121 is mounted at a second target position on the main unit 200, the second interface 1221 can be manually operated to connect the first interface 22 to the second interface 1221. When the second interface 1221 is connected to the first interface 22, the monitoring tube segment 122 is used for the main unit 200 to monitor parameter information. When connected to a conductive component, the static discharge unit 14 is able to release static electricity from the panel assembly 100.

[0246] Furthermore, after the monitoring panel 121 is installed, the user can easily connect the first interface 22 and the second interface 1221 manually to avoid misalignment and sealing between the first interface 22 and the second interface 1221. In addition, integrating the electrostatic discharge unit 14 into the monitoring panel 121 also facilitates the installation of the electrostatic discharge unit 14.

[0247] It is understood that the panel kit 100 of the eighth aspect differs from the panel kit 100 of the fourth aspect in that: in the fourth aspect, the monitoring panel 121 is provided with at least two monitoring tube segments 122; while in the eighth aspect, the monitoring panel 121 may only be provided with an electrostatic discharge unit 14 and a monitoring tube segment 122, or the monitoring panel 121 may only be provided with an electrostatic discharge unit 14 and multiple monitoring tube segments 122. This application embodiment does not limit this.

[0248] Therefore, in some embodiments, other specific structures of the panel kit 100 can be found in the specific structure of the panel kit 100 in the fourth aspect, and will not be described in detail here.

[0249] In the above embodiments, the descriptions of each embodiment have different focuses. For parts not described in detail in a certain embodiment, please refer to the relevant descriptions in other embodiments.

[0250] The panel kit 100 for a blood purification device provided in the embodiments of this application has been described in detail above. Specific examples have been used to illustrate the principles and implementation methods of this application. The description of the above embodiments is only for the purpose of helping to understand the method and core ideas of this application. At the same time, for those skilled in the art, there will be changes in the specific implementation methods and application scope based on the ideas of this application. Therefore, the content of this specification should not be construed as a limitation of this application.

Claims

1. A panel kit for a blood purification device, characterized in that, The blood purification device includes a main unit, the main unit being provided with a pump assembly and a first interface, and the panel assembly includes: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least another pump tubing segment cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and A monitoring component includes a monitoring panel and at least two monitoring tube segments. The monitoring panel is detachably mounted to the host computer and is separately disposed from the power panel, making them independent panels that can be independently installed and removed. The at least two monitoring tube segments are mounted on the monitoring panel and are used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. The monitoring component can be manually installed so that the monitoring panel is mounted to a second target position on the host computer and the second interface is simultaneously connected to the first interface. When the second interface is connected to the first interface, the monitoring tube segments are used by the host computer to monitor the parameter information.

2. A panel kit for a blood purification device, characterized in that, The blood purification device includes a main unit, the main unit having a pump assembly and a retractable first interface, and the panel kit includes: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least another pump tubing segment cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and A monitoring component includes a monitoring panel and at least two monitoring tube segments. The monitoring panel is detachably mounted to the host unit and is separately disposed from the power panel, making them independent panels that can be independently installed and removed. The at least two monitoring tube segments are mounted on the monitoring panel and are used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. When the monitoring panel is mounted at a second target position on the host unit, the first interface can extend to connect with the second interface. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information.

3. A panel kit for a blood purification device, characterized in that, The blood purification device includes a main unit, the main unit being provided with a pump assembly and a first interface, and the panel assembly includes: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least another pump tubing segment cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and A monitoring component includes a monitoring panel and at least two monitoring tube segments. The monitoring panel is detachably mounted to the host unit and is separately disposed from the power panel, making them independent panels that can be independently installed and removed. The at least two monitoring tube segments are mounted on the monitoring panel and are used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. When the monitoring panel is mounted in a second preset position on the host unit, the host unit can drive the monitoring panel to a second target position, so that the second interface connects to the first interface. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information.

4. A panel kit for a blood purification device, characterized in that, The blood purification device includes a main unit, the main unit being provided with a pump assembly and a first interface, and the panel assembly includes: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least another pump tubing segment cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and A monitoring component includes a monitoring panel and at least two monitoring tube segments. The monitoring panel is detachably mounted to the host unit and is separately disposed from the power panel, making them independent panels that can be independently installed and removed. The at least two monitoring tube segments are mounted on the monitoring panel and are used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. The second interface is movably disposed relative to the monitoring panel. When the monitoring panel is mounted at a second target position on the host unit, the second interface can be manually operated to connect the first interface and the second interface. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information.

5. The panel kit according to any one of claims 1 to 3, characterized in that, The second interface is fixedly positioned relative to the monitoring panel; or, The second interface is set relative to the monitoring panel.

6. The panel kit according to any one of claims 1 to 4, characterized in that, The pump pipe section includes a first flexible pipe section. When the pump pipe section is adapted to the pump assembly, the first flexible pipe section abuts against the pump head of the pump assembly, so that the rotation of the pump head can drive the first flexible pipe section to be wound around the pump head.

7. The panel kit according to any one of claims 1 to 4, characterized in that, When the power panel is installed in the first preset position of the host, the power panel can be driven by the host to move to the first target position, thereby adapting the pump pipe section to the pump assembly.

8. The panel assembly according to claim 7, characterized in that, When the power panel is installed in the first preset position, the pump pipe section is not compatible with the pump assembly; and / or, Whether the power panel is installed at the first preset position and / or the first target position can be determined by the first position detection mechanism on the host; and / or The power panel is provided with a first connecting part, which is used to connect to the first drive mechanism of the host, so that the first drive mechanism can drive the power panel to move from the first preset position to the first target position.

9. The panel kit according to any one of claims 1 to 4, characterized in that, The power assembly can be manually installed so that the power panel is installed at the first target position and the pump pipe section is simultaneously adapted to the pump assembly.

10. The panel kit according to claim 9, characterized in that, Whether the power panel is installed at the first target position can be determined by the first position detection mechanism on the host.

11. The panel kit according to any one of claims 1, 2, and 4, characterized in that, Whether the monitoring panel is installed at the second target location can be determined by the second location detection mechanism on the host.

12. The panel assembly according to claim 3, characterized in that, When the monitoring panel is installed in the second preset position, the second interface is not connected to the first interface; And / or, Whether the monitoring panel is installed at the second preset position and / or the second target position can be determined by the second position detection mechanism on the host; and / or, The monitoring panel is provided with a second connecting part, which is used to connect to the second drive mechanism of the host, so that the second drive mechanism can drive the monitoring panel to move from the second preset position to the second target position.

13. The panel assembly according to any one of claims 1 to 4, characterized in that, The panel assembly also includes a second flexible tube segment, which connects at least one of the pump tube segments and at least one of the monitoring tube segments.

14. The panel assembly according to any one of claims 1 to 4, characterized in that, At least two of the monitoring tube segments are provided with the second interface, and the number of the first interfaces is at least two. The second interface is used to connect to the corresponding first interface on the host, so that the host can monitor the pressure parameters of the corresponding blood or medical fluid through the monitoring tube segment. And / or, The blood purification device further includes a first filtration unit, which is used to filter the blood flowing through the pump tube section; wherein, when the second interface is connected to the first interface, the monitoring tube section is used for the host to monitor the pressure parameters of the corresponding blood or medical liquid; the at least two monitoring tube sections also include a blood leakage monitoring tube section, which is used in conjunction with the blood leakage monitoring module on the host to monitor whether blood on one side of the filter membrane of the first filtration unit has permeated to the other side.

15. The panel assembly according to any one of claims 1 to 4, characterized in that, The blood purification device further includes a first filtration unit, which is used to filter the blood flowing through the pump tube section; The monitoring tubing includes at least one of the following: a blood leakage monitoring tubing, a blood pressure monitoring tubing, a filter pre-pressure monitoring tubing, and a waste hydraulic pressure monitoring tubing. The blood leakage monitoring tube section is used in conjunction with the blood leakage monitoring module on the host to monitor whether blood on one side of the filter membrane of the first filtration unit has passed to the other side. The blood pressure monitoring tubing is used to monitor the pressure parameters of blood drawn from the patient's blood vessels; The filter pre-pressure monitoring tubing is used to monitor the pressure parameters of blood flowing into the first filtration unit from the pump tubing; The waste hydraulic pressure monitoring pipe section is used to monitor the pressure parameters of the medical liquid discharged from the first filtration unit.

16. The panel assembly according to claim 15, characterized in that, The panel kit also includes an electrostatic discharge unit, at least one of the power panel and the monitoring panel is provided with the electrostatic discharge unit, which is used to cooperate with the host to release static electricity in the panel kit.

17. The panel assembly according to claim 15, characterized in that, The blood purification device further includes a second filtration unit, which is used to re-filter the blood flowing through the pump tube section. The blood input end of the second filtration unit is connected to the blood output end of the first filtration unit to re-filter the blood flowing out of the blood output end of the first filtration unit. The monitoring section further includes a secondary membrane pressure monitoring section for connecting the first filtration unit and the second filtration unit, the secondary membrane pressure monitoring section being used to monitor the pressure parameters of the blood.

18. The panel assembly according to claim 17, characterized in that, The number of monitoring components is at least two, and the monitoring components are set separately from each other so that each monitoring component can be independently assembled and disassembled. Each monitoring component is provided with at least two different types of the following: the blood leakage monitoring tube section, the blood pressure monitoring tube section, the filter pre-pressure monitoring tube section, and the waste hydraulic pressure monitoring tube section.

19. The panel assembly according to claim 15, characterized in that, The pump tubing section includes a blood pump tubing section for cooperating with the pump assembly to drive blood flow. The panel assembly also includes a blood drainage path for connecting the input end of the blood pump tubing section to a patient's blood vessel. The blood drainage path is equipped with the blood pressure monitoring tubing section; and / or, The pump tubing section includes a blood pump tubing section for cooperating with the pump assembly to drive blood flow. The panel kit also includes a blood pump flow path, which is connected to the output end of the blood pump tubing section and the blood input end of the first filtration unit. The blood pump flow path is provided with a pre-filter pressure monitoring section; and / or, The pump section includes a waste hydraulic pump section, which cooperates with the pump assembly to drive the medical fluid in the first filter unit to discharge. The panel kit also includes a waste fluid flow path, which is connected to the medical fluid output end of the first filter unit and the input end of the waste hydraulic pump section. The waste fluid flow path is equipped with the waste hydraulic monitoring section; and / or, The pump section includes a waste hydraulic pump section, which is used to cooperate with the pump assembly to drive the medical fluid in the first filter unit to be discharged. The panel kit also includes a waste liquid flow path and a collection flow path. The waste liquid flow path is connected to the medical fluid output end of the first filter unit and the input end of the waste hydraulic pump section, respectively. The input end of the collection flow path is connected to the output end of the waste hydraulic pump section. The blood leakage monitoring section is located in the waste liquid flow path or the collection flow path.

20. The panel assembly according to any one of claims 1 to 4, characterized in that, At least one of the monitoring segments includes a pressure monitoring module, which includes a fluid section, a gas section, a diaphragm, and the second interface; wherein the diaphragm separates a fluid side cavity defined at least partially by the fluid section and a gas side cavity defined at least partially by the gas section, the fluid side cavity being used for the flow of blood or medical fluid, the second interface communicating with the gas side cavity, and when the second interface is connected to the first interface, the monitoring segment is used by the host to monitor the pressure parameters of the blood or medical fluid flowing through the fluid side cavity.

21. The panel assembly according to any one of claims 1 to 4, characterized in that, The panel kit also includes a heating component for mounting to the heating area of ​​the host unit, so that the heating device of the host unit can heat the blood and / or the medical fluid within the heating component.

22. A panel kit for a blood purification device, characterized in that, The blood purification device includes a main unit, which is equipped with a pump assembly, conductive components, and a first interface. The panel assembly includes: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least one of the pump tubing segments cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and... A monitoring component includes a monitoring panel, a monitoring tube segment, and an electrostatic discharge unit. The monitoring panel is detachably mounted to the host unit and is separate from the power panel, making them independent panels that can be independently installed and removed. The monitoring tube segment and the electrostatic discharge unit are both mounted on the monitoring panel. The monitoring tube segment is used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. The monitoring component allows the monitoring panel to be manually installed to a second target position on the host unit, simultaneously connecting the second interface to the first interface and the electrostatic discharge unit to the conductive element. When the second interface is connected to the first interface, the monitoring tube segment allows the host unit to monitor the parameter information. When the electrostatic discharge unit is connected to the conductive element, it can release static electricity from the panel assembly.

23. A panel kit for a blood purification device, characterized in that, The blood purification device includes a main unit, which is equipped with a pump assembly, conductive components, and a retractable first interface. The panel assembly includes: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least one of the pump tubing segments cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and... A monitoring component includes a monitoring panel, a monitoring tube segment, and an electrostatic discharge unit. The monitoring panel is detachably mounted to the host unit and is separately disposed from the power panel, making them independent panels that can be independently installed and removed. The monitoring tube segment and the electrostatic discharge unit are both mounted on the monitoring panel. The monitoring tube segment is used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. When the monitoring panel is mounted at a second target position on the host unit, the first interface can extend to connect with the second interface. The electrostatic discharge unit is electrically connected to a conductive element fixed on the host unit, or the electrostatic discharge unit is connected to a conductive element extending outward from the host unit. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information. When the electrostatic discharge unit is connected to the conductive element, it can release static electricity from the tube segment of the panel assembly.

24. A panel kit for a blood purification device, characterized in that, The blood purification device includes a main unit, which is equipped with a pump assembly, conductive components, and a first interface. The panel assembly includes: A power assembly, comprising a power panel and at least two pump tubing segments, the power panel being detachably mounted to the main unit, the at least two pump tubing segments being mounted on the power panel, at least one of the pump tubing segments cooperating with the pump assembly to drive blood flow along the pump tubing segment, and at least one of the pump tubing segments cooperating with the pump assembly to drive medical fluid flow along the pump tubing segment; when the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly, and when the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow; and... A monitoring component includes a monitoring panel, a monitoring tube segment, and an electrostatic discharge unit. The monitoring panel is detachably mounted to the host unit and is separately configured from the power panel, making them independent panels that can be independently installed and removed. The monitoring tube segment and the electrostatic discharge unit are both mounted on the monitoring panel. The monitoring tube segment is used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one of the monitoring tube segments has a second interface. When the monitoring panel is mounted in a second preset position on the host unit, the host unit can drive the monitoring panel to a second target position, so that the second interface is connected and fixed to the first interface, and the electrostatic discharge unit is connected to the conductive element. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information. When the electrostatic discharge unit is connected to the conductive element, it can release static electricity from the panel assembly.

25. A panel kit for a blood purification device, the blood purification device including a main unit, the main unit having a pump assembly, a conductive element and a first interface, the panel kit comprising: A power assembly includes a power panel and at least two pump tubing segments. The power panel is detachably mounted to the main unit. The at least two pump tubing segments are mounted on the power panel. At least one pump tubing segment is used to cooperate with the pump assembly to drive blood flow along the pump tubing segment, and at least one pump tubing segment is used to cooperate with the pump assembly to drive medical fluid flow along the pump tubing segment. When the power panel is mounted to a first target position on the main unit, the pump tubing segments are adapted to the pump assembly. When the pump tubing segments are adapted to the pump assembly, the pump tubing segments can be driven by the pump assembly to drive the corresponding blood or medical fluid flow. as well as, A monitoring component includes a monitoring panel, a monitoring tube segment, and an electrostatic discharge unit. The monitoring panel is detachably mounted to the host unit and is separately configured from the power panel, making them independent panels that can be independently installed and removed. The monitoring tube segment and the electrostatic discharge unit are both mounted on the monitoring panel. The monitoring tube segment is used to monitor parameter information of the blood and / or the medical fluid, including at least a pressure parameter. At least one monitoring tube segment has a second interface. The second interface is movably configured relative to the monitoring panel. When the monitoring panel is mounted at a second target position on the host unit, the second interface can be manually operated to connect the first interface and the second interface. When the second interface is connected to the first interface, the monitoring tube segment is used by the host unit to monitor the parameter information. The electrostatic discharge unit, when connected to a conductive element, can release static electricity from the panel assembly.

26. The panel assembly according to any one of claims 22 to 25, characterized in that, The pump pipe section includes a first flexible pipe section. When the pump pipe section is adapted to the pump assembly, the first flexible pipe section abuts against the pump head of the pump assembly, so that the rotation of the pump head can drive the first flexible pipe section to be wound around the pump head.

27. The panel assembly according to any one of claims 22 to 25, characterized in that, The panel assembly also includes a second flexible pipe section, and there is at least one monitoring pipe section, with the second flexible pipe section connecting at least one pump pipe section and at least one monitoring pipe section.

28. The panel assembly according to any one of claims 22 to 25, characterized in that, The number of monitoring tube segments is at least one, and at least one of the monitoring tube segments includes a pressure monitoring module, which includes a fluid section, a gas section, a diaphragm, and the second interface; wherein, a fluid side cavity defined by the fluid section and a gas side cavity defined by the gas section are separated by the diaphragm, the fluid side cavity is used for the flow of blood or medical fluid, and the second interface is in communication with the gas side cavity. When the second interface is connected to the first interface, the monitoring tube segment is used for the host to monitor the pressure parameters of the blood or medical fluid flowing through the fluid side cavity.

29. The panel assembly according to any one of claims 22 to 25, characterized in that, The panel kit also includes a heating component for mounting to the heating area of ​​the host unit, so that the heating device of the host unit can heat the blood and / or the medical fluid within the heating component.

Images