Electronic injector control boosting device with reminding function
By designing an electronic syringe control booster device with reminder function, the problem of inaccurate injection speed control is solved, and the drug solution is injected into the patient's body at a predetermined speed and distance to ensure the treatment effect.
Patent Information
- Application Number
- CN202421854193.2
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-08-01
- Publication Date
- 2025-07-18
- Estimated Expiration
- 2034-08-01
AI Technical Summary
The existing electronic syringe control booster device cannot accurately control the injection speed of the drug solution, causing the staff to mistakenly believe that the injection is completed and fail to inject a predetermined dose of the drug solution into the patient's body.
An electronic syringe control booster device with a reminder function is designed, including the device body, an injection booster assembly, a reminder member and a pressing control assembly. The movement speed and distance of the drive member are accurately controlled through the control member, and a vibration reminder is issued when the injection is completed.
Ensure that the medicine liquid is injected into the patient at a predetermined speed and distance, avoid misoperation, and improve the treatment effect.
Smart Images

Figure CN223112101U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the technical field of electronic syringes, in particular to an electronic syringe control boosting device with a reminder function. Background Art
[0002] During the treatment of patients, it is necessary to inject a predetermined amount of liquid medicine in the syringe into the patient's body to achieve the treatment purpose. However, in order to enable the patient to better absorb the liquid medicine and reduce the discomfort of the patient during the injection process, it is necessary to control the injection speed of the liquid medicine. Since manual operation cannot accurately control the injection speed of the liquid medicine, an electronic syringe control boosting device is used to inject the liquid medicine in the syringe, so as to control the injection speed of the liquid medicine injected by the syringe through the electronic syringe control boosting device. Among them, using an electronic syringe control boosting device can also accurately control the dose of the liquid medicine injected into the patient's body by the syringe.
[0003] In the existing electronic syringe control boosting device, the syringe is installed on the boosting component, and the boosting component presses and pushes the pressing end of the syringe to inject a predetermined amount of liquid medicine in the syringe into the patient's body. Among them, in order to enable the staff to exactly feel the movement of the pressing end of the syringe, the staff will place their finger on the pressing end of the syringe and make the finger follow the movement of the pressing end. However, during the process of the boosting component pushing the pressing end of the syringe, there may be a situation where the staff does not notice and perceive it due to the small pushing speed. At this time, the staff will mistakenly think that the injection is completed, and then mistakenly take out the syringe that has not completed the injection from the boosting component, resulting in the treatment effect not meeting the expectation because the patient has not been injected with a predetermined amount of liquid medicine. Summary of the Utility Model
[0004] To solve the above technical problems and achieve at least one advantage of the present utility model, the present utility model provides an electronic syringe control boosting device with a reminder function, which is used to press the pressing part of the injection part at a predetermined speed and push it a predetermined distance, so as to make the liquid medicine with a predetermined dose in the tube part of the injection part flow out through the channel formed by the injection part of the injection part. The electronic syringe control boosting device with a reminder function includes:
[0005] A device main body, the device main body includes a device body and a control member, and the control member is installed on the device body;
[0006] Injection boosting assembly, the injection boosting assembly includes a holding body, a driving member, a pushing member and at least a pair of port blocking blocks. The holding body is located near the device body. A pair of the port blocking blocks are symmetrically installed on the holding body, and a port fixing groove is formed between the pair of port blocking blocks. One end of the tube portion of the injection member abuts against the port blocking block, and the injection portion connected to the tube portion passes through the port fixing groove. The driving member is arranged on the holding body, and the driving member is connected to the control member to control the moving speed and moving distance of the output end of the driving member through the control member. The pushing member is connected to the output end of the driving member, and the extending direction of the output end of the driving member is a direction that can make the pushing member abut against the pressing portion and press the pressing portion towards the tube portion at a predetermined speed;
[0007] Reminder member, the reminder member is arranged on the injection boosting assembly, and the reminder member is controllably connected to the control member to give a vibration reminder when the pushing member stops pushing the pressing portion;
[0008] Pressing control assembly, the pressing control assembly is located near the device body, the pressing control assembly is connected to the control member, and the pressing control assembly is used to send a signal to the control member to start the driving member, so as to control the output end of the driving member to move a predetermined distance at a predetermined speed through the control member, so as to extrude a predetermined dose of liquid medicine in the tube portion of the injection member from the channel formed by the injection portion at a predetermined speed.
[0009] According to an embodiment of the present invention, the reminder member is installed on the pushing member and communicatively connected to the control member to get rid of the length limitation of the wire and the bondage of the entanglement of the wire itself to the placement position of the reminder member.
[0010] According to an embodiment of the present invention, the injection boosting assembly further includes a tube clamping member, the tube clamping member includes a clamping portion, the clamping portion forms a clamping groove, the inner diameter of the clamping groove matches the outer diameter of the tube portion, the clamping portion is arranged on the holding body, and the tube portion passes through the clamping groove in a manner that can move in the clamping groove.
[0011] According to an embodiment of the present invention, the tube clamping member further includes an anti-detachment portion, the anti-detachment portion is connected to the clamping portion, the holding body has an insertion groove matching the anti-detachment portion, and the anti-detachment portion is detachably arranged in the insertion groove, so as to replace the clamping portion with a clamping groove having a corresponding inner diameter when the outer diameter of the tube portion changes due to replacing different injection members.
[0012] According to an embodiment of the present utility model, the injection boosting assembly further includes an indicating member, the indicating member is disposed on the holding body, and the indicating member is communicatively connected to the control member, and the indicating member is used to emit a bright light reminder when the pushing member is being pushed by the output end of the driving member.
[0013] According to an embodiment of the present utility model, the pressing and controlling assembly includes a pressing main body, a pressing rotating member, a connecting rod, a shielding member, a sensing member, and at least one elastic member. The pressing main body is located near the device body. The pressing rotating member is inserted through the connecting rod and fixed to the connecting rod. Both ends of the connecting rod are rotatably inserted into the pressing main body. The shielding member is connected to the connecting rod in a manner that follows the rotation of the connecting rod. The sensing member is disposed on the pressing main body, and the sensing member is connected to the control member. The sensing member is used to detect the angular data of the shielding member following the rotation of the connecting rod and transmit it to the control member. The elastic member is disposed between the pressing rotating member and the pressing main body in a compressible manner, and both ends of the elastic member respectively abut against the end of the pressing rotating member away from the connecting rod and the pressing main body.
[0014] According to an embodiment of the present utility model, the pressing and controlling assembly further includes a limiting member. The limiting member is disposed on the pressing main body and on the movement path of the shielding member. The limiting member is used to block the shielding member during the rotation of the shielding member following the connecting rod to limit the angle of the shielding member following the rotation of the connecting rod.
[0015] According to an embodiment of the present utility model, the device body further includes at least one mounting member. The mounting member is disposed on the device body, and the mounting member forms a mounting space. The holding body is detachably disposed in the mounting space of the mounting member.
[0016] According to an embodiment of the present utility model, the control member is communicatively connected to the driving member, and the sensing member is communicatively connected to the control member through a signal transmitter.
[0017] According to an embodiment of the present utility model, the device body further includes a control and display member. The control and display member is disposed on the device body, and the control and display member is electrically connected to the control member. The control and display member is used to display the moving speed and moving distance of the output end of the driving member in real time, and the control and display member can be used to adjust the moving speed and moving distance of the output end of the driving member. Description of the Drawings
[0018] Figure 1 A perspective view schematic diagram of a preferred embodiment of the present utility model is shown.
[0019] Figure 2 Shows a perspective view schematic diagram of another perspective of a preferred embodiment of the present utility model.
[0020] Figure 3 Shows a cross-sectional view schematic diagram of a preferred embodiment of the present utility model.
[0021] Figure 4 Shows Figure 3 An enlarged view schematic diagram of part A in
[0022] Figure 5 Shows a perspective view schematic diagram of the pressing control assembly.
[0023] Figure 6 Shows a cross-sectional view schematic diagram of the pressing control assembly.
[0024] Figure 7 Shows a perspective view schematic diagram of the pressing and rotating member, the connecting rod, the shielding member and the rebounding member.
[0025] Figure 8 Shows a perspective view schematic diagram of the injection boosting assembly, wherein the anti-detachment portion of the tube holder is not disposed in the insertion slot.
[0026] Figure 9 Shows a perspective view schematic diagram of the tube holder. Detailed implementation manners
[0027] The following description is used to disclose the present utility model so that those skilled in the art can implement the present utility model. The preferred embodiments described below are only examples, and those skilled in the art can think of other obvious variations. The basic principles defined in the following description can be applied to other implementation schemes, variant schemes, improvement schemes, equivalent schemes and other technical schemes without departing from the spirit and scope of the present utility model.
[0028] Those skilled in the art should understand that in the disclosure of the present utility model, the orientation or positional relationships indicated by the terms "longitudinal", "transverse", "upper", "lower", "front", "rear", "left", "right", "vertical", "horizontal", "top", "bottom", "inner", "outer", etc. are based on the orientation or positional relationships shown in the drawings. It is only for the convenience of describing the present utility model and simplifying the description, rather than indicating or implying that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation. Therefore, the above terms should not be construed as limiting the present utility model.
[0029] It will be appreciated that the term "a" should be construed as "at least one" or "one or more". That is, in one embodiment, the number of an element may be one, while in other embodiments, the number of the element may be multiple. The term "a" should not be construed as a limitation on the number.
[0030] Reference Figures 1 to 9 , a control boosting device of an electronic syringe with a reminder function according to a preferred embodiment of the present invention will be described in detail below. The control boosting device of the electronic syringe with a reminder function is used to press a pressing portion 93 of an injection member 90 at a predetermined speed and push it by a predetermined distance, so as to cause a predetermined dose of liquid medicine in a tube portion 92 of the injection member 90 to flow out through a channel formed by an injection portion 91 of the injection member 90.
[0031] Specifically, the control boosting device of the electronic syringe with a reminder function includes a device main body 10, a reminder member 20, an injection boosting assembly 30, and a pressing control assembly 40.
[0032] The device main body 10 includes a device body 11 and a control member 12. The control member 12 is installed on the device body 11. The injection boosting assembly 30 is located near the device body 11, and the injection boosting assembly 30 is connected to the control member 12 in a manner that can be controlled by the control member 12. The injection member 90 is disposed on the injection boosting assembly 30. Through the control of the control member 12, the injection boosting assembly 30 presses and pushes the pressing portion 93 to squeeze the liquid medicine in the tube portion 92 and cause the liquid medicine to flow out through the channel formed by the injection portion 91. The reminder member 20 is disposed on the injection boosting assembly 30 and is connected to the control member 12. The reminder member 20 is used to give a reminder when the injection boosting assembly 30 stops pressing and pushing the pressing portion 93, so as to prevent the injection boosting assembly 30 from not being noticed by the staff due to a small amplitude when pushing the pressing portion 93.
[0033] Specifically, the injection boosting assembly 30 includes a holding body 31, a driving member 32, a pushing member 33, and at least a pair of port blocking blocks 34. The holding body 31 is located near the device body 11. A pair of the port blocking blocks 34 are symmetrically installed on the holding body 31, and a port fixing groove 3101 is formed between the pair of port blocking blocks 34. One end of the tube portion 92 of the injection member 90 abuts against the port blocking block 34, and the injection portion 91 connected to the tube portion 92 passes through the port fixing groove 3101. The driving member 32 is disposed on the holding body 31, and the driving member 32 is connected to the control member 12 to control the moving speed and moving distance of the output end of the driving member 32 through the control member 12. The pushing member 33 is connected to the output end of the driving member 32. The extending direction of the output end of the driving member 32 is a direction that can make the pushing member 33 abut against the pressing portion 93 while pressing the pressing portion 93 toward the tube portion 92. That is to say, the pushing member 33 abuts against the pressing portion 93 in a manner that can press the pressing portion 93 toward the tube portion 92 under the action of the output end of the driving member 32.
[0034] In this embodiment, the reminder 20 is installed on the pushing member 33, and the reminder 20 is controllably connected to the control member 12.
[0035] In another variant embodiment, the reminder 20 is disposed on the holding body 31, and the reminder 20 is controllably connected to the control member 12.
[0036] Preferably, the reminder 20 is implemented to include a vibration motor to emit vibration when the pushing member 33 stops pushing the pressing portion 93, preventing the situation that the amplitude of the pushing member 33 pushing the pressing portion 93 is too small to be noticed by the staff.
[0037] More preferably, the reminder 20 is communicatively connected to the control member 12 to get rid of the length limitation of the wire and the constraint of the wire's own winding on the place where the reminder 20 can be placed.
[0038] It is worth mentioning that since the reminder 20 is installed on the pushing member 33, when the staff holds the holding body 31 and places the finger on the reminder 20 on the pushing member 33, and the pushing member 33 stops pushing the pressing portion 93, the vibration emitted by the reminder 20 will be easily perceived by the staff, so as to facilitate the staff to know that the predetermined dose of the liquid medicine in the tube portion 92 has been injected into the patient's body.
[0039] Further, since the reminder member 20 is provided on the holding body 31, when the staff holds the holding body 31 and the pushing member 33 stops pushing the pressing portion 93, the vibration emitted by the reminder member 20 is easily perceived by the staff holding the holding body 31, so as to facilitate the staff to know that the predetermined dose of liquid medicine in the tube portion 92 has been injected into the patient's body.
[0040] Preferably, the driving member 32 is implemented to include an electric push rod.
[0041] It should be noted that when the tube portion 92 and the pressing portion 93 are disposed between the pushing member 33 and the port blocking block 34 and the injection portion 91 passes through the port fixing groove 3101, the driving member 32 does not receive the command of the control member 12, that is, the pushing member 33 is not controlled by the output end of the driving member 32 to abut against the pressing portion 93. When the holding body 31 is held and moved, the tube portion 92 and the pressing portion 93 may slip off between the pushing member 33 and the port blocking block 34 due to unstable connection, resulting in the injection portion 91, the tube portion 92 and the pressing portion 93 falling.
[0042] Preferably, the injection boosting assembly 30 further includes a tube clamping member 35. The tube clamping member 35 includes a clamping portion 351. The clamping portion 351 forms a clamping groove 35101, and the inner diameter of the clamping groove 35101 matches the outer diameter of the tube portion 92. The clamping portion 351 is provided on the holding body 31. The tube portion 92 passes through the clamping groove 35101 in a manner that can move in the clamping groove 35101. In other words, the tube portion 92 is fixed by being disposed in the clamping groove 35101 to prevent the tube portion 92 from slipping off between the pushing member 33 and the port blocking block 34.
[0043] More preferably, the tube clamping member 35 further includes an anti - detachment portion 352. The anti - detachment portion 352 is connected to the clamping portion 351. The holding body 31 has an insertion groove 3102 that matches the anti - detachment portion 352. The anti - detachment portion 352 is detachably disposed in the insertion groove 3102, so that when the outer diameter of the tube portion 92 changes due to replacing different injection members 90, the purpose of replacing the clamping portion 351 with a corresponding inner - diameter clamping groove 35101 can be achieved by disassembling the anti - detachment portion 352, avoiding the situation that the tube portion 92 cannot be fixed by the clamping portion 351.
[0044] Further, the injection boosting assembly 30 further includes an indicating member 36. The indicating member 36 is disposed on the holding body 31, and the indicating member 36 is connected to the control member 12. The indicating member 36 is configured to emit light when the pushing member 33 is being pushed by the output end of the driving member 32, so as to prevent the movement speed of the output end of the driving member 32 from being too small to be noticed by the staff.
[0045] Preferably, the indicating member 36 is implemented to include but not limited to a light emitting diode.
[0046] Specifically, the pressing control assembly 40 is located near the device body 11. The pressing control assembly 40 is connected to the control member 12 to send a signal to start the driving member 32 to the control member 12 through the pressing control assembly 40, and control the output end of the driving member 32 to move a predetermined distance at a predetermined speed through the control member 12.
[0047] In this embodiment, the pressing control assembly 40 includes a pressing body 41, a pressing rotating member 42, a connecting rod 43, a shielding member 44 and a sensing member 45. The pressing body 41 is located near the device body 11. The pressing rotating member 42 is inserted through the connecting rod 43, and the pressing rotating member 42 is fixed to the connecting rod 43. Both ends of the connecting rod 43 are inserted through the pressing body 41 in a rotatable manner. That is to say, the pressing rotating member 42 rotates relative to the pressing body 41 with the connecting rod 43 as an axis. The shielding member 44 is connected to the connecting rod 43 in a manner of following the rotation of the connecting rod 43. The sensing member 45 is disposed on the pressing body 41, and the sensing member 45 is connected to the control member 12 to transmit the detected angle data of the shielding member 44 following the rotation of the connecting rod 43 to the control member 12.
[0048] In another variant embodiment, the pressing control assembly 40 includes the pressing body 41, the pressing rotating member 42, the connecting rod 43, the shielding member 44 and the sensing member 45. The pressing body 41 is located near the device body 11. The pressing rotating member 42 is inserted through the connecting rod 43 in a rotatable manner. Both ends of the connecting rod 43 are fixed to the pressing body 41. That is to say, the pressing rotating member 42 rotates relative to the pressing body 41 with the connecting rod 43 as an axis. The shielding member 44 is connected to the pressing rotating member 42 in a manner of following the rotation of the pressing rotating member 42. The sensing member 45 is disposed on the pressing body 41, and the sensing member 45 is connected to the control member 12 to transmit the detected angle data of the shielding member 44 following the rotation of the pressing rotating member 42 to the control member 12.
[0049] To enable those skilled in the art to understand the present utility model, in at least one embodiment of the present utility model, only taking the pressing and rotating member 42 being inserted into the connecting rod 43, and the pressing and rotating member 42 being fixed to the connecting rod 43, and the two end portions of the connecting rod 43 being rotatably inserted into the pressing main body 41, and the shielding member 44 being connected to the connecting rod 43 in a manner of following the rotation of the connecting rod 43 as an example for elaboration.
[0050] Specifically, the pressing control assembly 40 further includes at least one elastic member 46. The elastic member 46 is disposed between the pressing and rotating member 42 and the pressing main body 41 in a compressible manner, and the two end portions of the elastic member 46 respectively abut against the end portion of the pressing and rotating member 42 away from the connecting rod 43 and the pressing main body 41. The elastic member 46 is used to support the end portion of the pressing and rotating member 42 away from the connecting rod 43 when the pressing and rotating member 42 is pressed and rotates around the connecting rod 43, and to make it rotate reversely around the connecting rod 43 to return to the initial position when the pressing and rotating member 42 is no longer pressed.
[0051] Preferably, the elastic member 46 is implemented as a spring.
[0052] In this embodiment, the pressing control assembly 40 further includes a limiting member 47. The limiting member 47 is disposed on the pressing main body 41 and located on the movement path of the shielding member 44 to stop the shielding member 44 during the rotation of the shielding member 44 following the connecting rod 43, thereby preventing the pressing and rotating member 42 from driving the connecting rod 43 to continue rotating. That is to say, the limiting member 47 is used to limit the rotation angle of the shielding member 44 following the connecting rod 43.
[0053] It is worth mentioning that since the compressible amount of the elastic member 46 will change after multiple uses, and since the limiting member 47 is located on the movement path of the shielding member 44 to limit the rotation angle of the shielding member 44 following the connecting rod 43 through the limiting member 47, thereby avoiding the change of the rotatable angle of the pressing and rotating member 42 around the connecting rod 43 due to the change of the compressible amount of the elastic member 46, and finally avoiding the change of the maximum value of the angle data of the shielding member 44 following the connecting rod 43 detected by the sensing member 45.
[0054] It should be noted that since the control member 12 is controlled by the program inside it, when the value transmitted from the sensing member 45 to the control member 12 is not within the range of the program values, the control member 12 may report an error, which may lead to the abnormal operation of the control member 12. Therefore, it is necessary to control the value transmitted from the sensing member 45 to the control member 12 within the range of the program values.
[0055] Preferably, the control member 12 is communicatively connected to the driving member 32, and the sensing member 45 is communicatively connected to the control member 12 through a signal transmitter.
[0056] Those skilled in the art can understand that when the pressing and rotating member 42 rotates around the connecting rod 43 and drives the shielding member 44 to rotate, the sensing member 45 will transmit the detected angle data of the shielding member 44 following the rotation of the connecting rod 43 to the control member 12 through the signal transmitter. The control member 12 will control the output end of the driving member 32 to move a predetermined distance at a predetermined speed, and control the pushing member 33 to push the pressing portion 93, so as to extrude the liquid medicine in the tube portion 92 through the channel formed by the injection portion 91.
[0057] Furthermore, in one embodiment, once the control member 12 receives the change in the angle data detected by the sensing member 45 through the signal transmitter, it will control the output end of the driving member 32 to move a predetermined distance at a predetermined speed.
[0058] Even further, in another embodiment, the control member 12 controls the output end of the driving member 32 to move at different speeds according to the different magnitudes of the angle data values detected by the sensing member 45 received through the signal transmitter. When the control member 12 does not receive the change in the magnitude of the angle data value detected by the sensing member 45 through the signal transmitter, it will immediately stop controlling the movement of the output end of the driving member 32, and start the reminder member 20 to vibrate when stopping to remind the staff.
[0059] It is worth mentioning that since the sensing member 45 is communicatively connected to the control member 12 through the signal transmitter, and the control member 12 is communicatively connected to the driving member 32, when the pressing control assembly 40 is placed on the ground, the bacteria on the ground will not be transmitted to the device main body 10 through the pressing control assembly 40, that is, to avoid the bacteria of the pressing control assembly 40 being transmitted to the device main body 10 and then transmitted to the injection boosting assembly 30 to cause pollution to the injection boosting assembly 30, so that the patient will not be infected by bacteria when being injected with the liquid medicine by the injection member 90, providing guarantee for the patient's life safety.
[0060] Those skilled in the art can understand that since the sensing member 45 is communicatively connected to the control member 12 through the signal transmitter, and the control member 12 is communicatively connected to the driving member 32, the pressing control assembly 40 and the device main body 10, as well as the injection boosting assembly 30 and the device main body 10, will not be restricted by wires and unable to be moved to a predetermined position.
[0061] Among them, the pressing control assembly 40 will not be unable to be placed on the ground due to the entanglement of wires between the pressing control assembly 40 and the device main body 10. And the pressing control assembly 40 will not be unable to be placed on the ground due to the length limitation of the wires because there are obstacles between the pressing control assembly 40 and the device main body 10 that require the wires to bypass. The injection boosting assembly 30 will not be unable to fit the injection part 91 of the injection member 90 to the patient's skin surface due to the restriction of wires between the injection boosting assembly 30 and the device main body 10. This provides convenience for the actual use of the device main body 10, the pressing control assembly 40, and the injection boosting assembly 30.
[0062] Specifically, the pressing and rotating member 42 has at least one anti-slip member 421. The anti-slip member 421 is located on the surface of the pressing and rotating member 42. The anti-slip member 421 is used to prevent the foot from slipping off the surface of the pressing and rotating member 42 during the process of stepping on the pressing and rotating member 42.
[0063] Specifically, the device main body 10 further includes at least one mounting member 13. The mounting member 13 is disposed on the device body 11, and the mounting member 13 forms a mounting space. The holding main body 31 is detachably disposed in the mounting space of the mounting member 13. That is to say, the mounting space is used to accommodate the holding main body 31 so that the holding main body 31 is easy to find after being used.
[0064] Preferably, the device main body 10 further includes a control and display member 14. The control and display member 14 is disposed on the device body 11 and is electrically connected to the control member 12 to display the predetermined speed and predetermined moving distance of the output end of the driving member 32 in real time through the control and display member 14.
[0065] Furthermore, the predetermined speed and predetermined distance of the output end of the driving member 32 can be changed through the control and display member 14.
[0066] The device body 10 further includes a power storage component 15. The power storage component 15 is disposed in the device body 10. The power storage component 15 is electrically connected to the control component 12 to supply power to the control component 12 and the operation display component 14 through the power storage component 15, so that the control component 12 and the operation display component 14 are freed from the dependence on a power source, and the device body 10 can be placed at any desired position.
[0067] Those skilled in the art should understand that the embodiments of the present invention described above and shown in the drawings are only examples and do not limit the present invention. The advantages of the present invention have been fully and effectively realized. The functions and structural principles of the present invention have been shown and described in the embodiments. Without departing from the principle, any deformation or modification can be made to the embodiments of the present invention.
Claims
1. An electronic syringe control boosting device with a reminder function, which is used to press the pressing part of the injection part at a predetermined speed and push it for a predetermined distance, so as to make a predetermined dose of liquid medicine in the tube body part of the injection part flow out through the channel formed by the injection part of the injection part, and is characterized in that, The electronic syringe control boosting device with a reminder function includes: A device main body, which includes a device body and a control member. The control member is installed on the device body; An injection boosting assembly, which includes a holding main body, a driving member, a pushing member, and at least a pair of port blocking blocks. The holding main body is located near the device body. A pair of the port blocking blocks are symmetrically installed on the holding main body, and a port fixing groove is formed between the pair of port blocking blocks. One end of the tube part of the injection member abuts against the port blocking block, and the injection part connected to the tube part passes through the port fixing groove. The driving member is arranged on the holding main body, and the driving member is connected to the control member to control the moving speed and moving distance of the output end of the driving member through the control member. The pushing member is connected to the output end of the driving member. The extending direction of the output end of the driving member is a direction that can make the pushing member abut against the pressing part and press the pressing part towards the tube part at a predetermined speed; A reminder member, which is arranged on the injection boosting assembly, and the reminder member is controllably connected to the control member to emit a vibration reminder when the pushing member stops pushing the pressing part; A pressing control assembly, which is located near the device body. The pressing control assembly is connected to the control member. The pressing control assembly is used to send a signal to the control member to start the driving member, so as to control the output end of the driving member to move a predetermined distance at a predetermined speed through the control member, and realize extruding a predetermined dose of liquid medicine in the tube part of the injection member from the channel formed by the injection part at a predetermined speed.
2. The electronic syringe control boosting device with a reminder function according to claim 1, wherein, The reminder member is installed on the pushing member and communicatively connected to the control member to get rid of the length limitation of the wire and the bondage of the wire's own winding on the placement position of the reminder member.
3. The electronic syringe control boosting device with a reminder function according to claim 2, wherein The injection boosting assembly further includes a tube clamping member, which includes a clamping part. The clamping part forms a clamping groove. The inner diameter of the clamping groove matches the outer diameter of the tube part. The clamping part is arranged on the holding main body, and the tube part passes through the clamping groove in a way that it can move in the clamping groove.
4. The electronic syringe control boosting device with a reminder function according to claim 3, characterized in that, The tube clamping member further includes an anti-detachment part, which is connected to the clamping part. The holding main body has an insertion groove matching the anti-detachment part. The anti-detachment part is detachably arranged in the insertion groove, so as to replace the clamping part with a clamping groove of a corresponding inner diameter when the outer diameter of the tube part changes due to replacing different injection members.
5. The electronic syringe control boosting device with a reminder function according to claim 4, characterized in that, The injection boosting assembly further includes an indicating member, which is arranged on the holding main body, and the indicating member is communicatively connected to the control member. The indicating member is used to emit a light reminder when the pushing member is being pushed by the output end of the driving member.
6. The electronic syringe control boosting device with a reminder function according to any one of claims 1 to 5, characterized in that, The pressing control assembly includes a pressing body, a pressing rotating member, a connecting rod, a shielding member, a sensing member, and at least one elastic member. The pressing body is located near the device body. The pressing rotating member is inserted through the connecting rod and fixed to the connecting rod. Both ends of the connecting rod are rotatably inserted into the pressing body. The shielding member is connected to the connecting rod in a manner that follows the rotation of the connecting rod. The sensing member is disposed on the pressing body, and the sensing member is connected to the control member. The sensing member is used to detect the angular data of the shielding member following the rotation of the connecting rod and transmit it to the control member. The elastic member is disposed between the pressing rotating member and the pressing body in a compressible manner, and both ends of the elastic member respectively abut against the end of the pressing rotating member away from the connecting rod and the pressing body.
7. The electronic syringe control boosting device with a reminder function according to claim 6, characterized in that, The pressing control assembly further includes a limiting member. The limiting member is disposed on the pressing body and on the movement path of the shielding member. The limiting member is used to stop the shielding member during the rotation of the shielding member following the connecting rod to limit the angle of the shielding member following the rotation of the connecting rod.
8. The electronic syringe control boosting device with a reminder function according to claim 7, characterized in that, The device body further includes at least one mounting member. The mounting member is disposed on the device body, and the mounting member forms a mounting space. The holding body is detachably disposed in the mounting space of the mounting member.
9. The electronic syringe control boosting device with a reminder function according to claim 8, characterized in that, The control member is communicatively connected to the driving member, and the sensing member is communicatively connected to the control member through a signal transmitter.
10. The electronic syringe control booster device with a reminder function according to claim 9, characterized in that, The device body further includes a control and display member. The control and display member is disposed on the device body, and the control and display member is electrically connected to the control member. The control and display member is used to display the moving speed and moving distance of the output end of the driving member in real time, and the control and display member can be used to adjust the moving speed and moving distance of the output end of the driving member.