Control boosting device of electronic injector

Through the design of wireless induction parts and electric push rods, the wire entanglement and contamination problems of the electronic syringe control booster device are solved, and the precise control of drug liquid injection and patient safety are achieved.

CN223248583UActive Publication Date: 2025-08-22SHANGHAI HEYATANG MEDICAL EQUIP CO LTD
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Patent Information

Application Number
CN202421857843.9
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2024-08-01
Publication Date
2025-08-22
Estimated Expiration
2034-08-01

AI Technical Summary

Technical Problem

The existing electronic syringe control booster device is easily wound and limited by wire length because the pedal control component and injection booster assembly are connected by wires, resulting in unsuccessful use and contamination risks, which affects the accuracy of drug injection and patient safety.

Method used

The wireless induction piece and electric push rod design is adopted. The movement speed and distance of the electric push rod are controlled by detecting the angle data of the shielding piece, so as to achieve accurate injection of the medicine liquid and avoid wire entanglement and contamination.

Benefits of technology

Accurate control of drug liquid injection, avoiding the risks of wire entanglement and contamination, and improving the flexibility and safety of the device.

✦ Generated by Eureka AI based on patent content.

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Abstract

The utility model discloses an electronic injector control boosting device, the electronic injector control boosting device comprises a device main body, a pressing control assembly and an injection boosting assembly, the device main body comprises a device body and a control piece, the control piece is installed on the device body, and the control piece is installed on the device body. The pressing control assembly and the injection boosting assembly are both located near the device body, the pressing control assembly comprises a pressing main body, a pressing rotating piece, a connecting rod, a shielding piece and a sensing piece, the two ends of the connecting rod rotatably penetrate through the pressing main body, the pressing rotating piece and the shielding piece are both fixed to the connecting rod, and the sensing piece is fixed to the pressing main body. The sensing piece is arranged on the pressing main body and is in communication connection with the control piece, and the sensing piece is used for transmitting rotation angle data of the shielding piece to the control piece; and the injection boosting assembly is controlled by the control piece to extrude a preset dose of liquid medicine in the tube body part from the channel of the injection part at a preset speed.
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Description

Technical Field

[0001] The utility model relates to the technical field of electronic syringes, in particular to a control booster device for an electronic syringe. Background Art

[0002] During the treatment process, a predetermined amount of liquid medicine in a syringe must be injected into the patient's body to achieve the therapeutic purpose. However, in order to better enable the patient to absorb the liquid medicine and reduce the patient's discomfort during the injection process, the injection speed of the liquid medicine must be controlled. However, manual control of the injection speed of the liquid medicine cannot be accurately controlled. Therefore, an electronic syringe control booster device is used to inject the liquid medicine in the syringe. The electronic syringe control booster device can also accurately control the dosage of the liquid medicine injected into the patient's body.

[0003] In the existing electronic syringe control booster device, the pedal control component and the injection booster component are respectively connected to the device body by wires, and the pedal control component is placed on the ground and near the doctor's feet. When the doctor steps on the pedal control component, an electrical signal will be transmitted to the device body, and the device body will control the injection booster component to inject a predetermined dose of liquid medicine in the syringe into the patient's body at a predetermined speed to achieve the injection of the liquid medicine.

[0004] However, because both the pedal control assembly and the injection booster assembly are connected to the device body via wires, if the wires become tangled, the pedal control assembly cannot be placed on the ground and cannot be stepped on, rendering the electronic syringe control booster device inoperable. Furthermore, the length of the wires is limited. Consequently, if an obstacle arises between the pedal control assembly and the device body and the wires need to be routed around, the straight-line distance between the pedal control assembly and the device body is shortened. Consequently, the placement of the pedal control assembly is restricted by the length of the wires, preventing the doctor from freely placing the pedal control assembly where needed.

[0005] Furthermore, although the electronic syringe control booster device is cleaned and disinfected before and after use, since the pedal control component is placed on the ground, the bacteria on the ground will still contaminate the device body along the wires connecting the pedal control component to the device body, and contaminate the injection booster component along the wires connecting the device body to the injection booster component, ultimately causing the syringe set in the injection booster component to be contaminated, causing the patient's health to be threatened when the drug is injected. Utility Model Content

[0006] In order to solve the above technical problems and achieve at least one advantage of the present invention, the present invention provides an electronic syringe control booster device, which is used to press and push the pressing portion of the injection piece at a predetermined speed and a predetermined distance to squeeze a predetermined dose of liquid medicine in the tubular portion of the injection piece out of the channel formed by the injection portion of the injection piece, wherein the electronic syringe control booster device includes:

[0007] A device body, the device body comprising a device body and a control member, the control member being mounted on the device body;

[0008] The pressing and operating component comprises a pressing body, a pressing rotating member, a connecting rod, a shielding member, a sensing member and at least one rebound member, the pressing body being located near the device body, the pressing rotating member being inserted into the connecting rod, and the pressing rotating member being fixed to the connecting rod, the two ends of the connecting rod being rotatably inserted into the pressing body, the shielding member being connected to the connecting rod in a manner of following the rotation of the connecting rod, the sensing member being arranged on the pressing body, the sensing member being communicatively connected to the control member via a signal transmitter, the sensing member being used to detect the angle data of the shielding member following the rotation of the connecting rod and transmitting the data to the control member via the signal transmitter, the rebound member being compressibly arranged between the pressing rotating member and the pressing body, and the two ends of the rebound member respectively abutting against the end of the pressing rotating member away from the connecting rod and the pressing body; and

[0009] An injection booster assembly, the injection booster assembly includes a holding body, a driving member, a pushing member and at least a pair of port stop blocks, the holding body is located near the device body, a pair of the port stop blocks are symmetrically installed on the holding body, and a port fixing groove is formed between the pair of the port stop blocks, one end of the tube body of the injection member abuts against the port stop block, the injection part connected to the tube body passes through the port fixing groove, the driving member is arranged on the holding body, the driving member is communicatively 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 extension direction of the output end of the driving member is such that the pushing member abuts against the pressing part and presses the pressing part toward the tube body.

[0010] According to one embodiment of the present invention, the pressing control assembly also includes a limit member, which is arranged on the pressing body and located on the movement path of the shielding member. The limit member is used to stop the shielding member when the shielding member follows the rotation of the connecting rod to limit the angle of rotation of the shielding member following the connecting rod.

[0011] According to one embodiment of the present invention, the injection booster assembly also includes a tube body clamping member, the tube body 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 body portion, the clamping portion is arranged on the holding body, and the tube body portion passes through the clamping groove in a manner that can move in the clamping groove.

[0012] According to one embodiment of the present invention, the tube body clamping piece also includes an anti-slip portion, which is connected to the clamping portion, and the holding body has an insertion groove matching the anti-slip portion. The anti-slip portion is detachably arranged in the insertion groove so that when the outer diameter of the tube body portion changes due to replacement of different injection pieces, the clamping portion having the clamping groove with the corresponding inner diameter can be replaced.

[0013] According to an embodiment of the present invention, the injection-assisting assembly further includes an alarm component, which is disposed on the pushing component and is communicatively connected to the control component, and is configured to sound an alarm when the pushing component stops moving.

[0014] According to one embodiment of the present invention, the injection boosting assembly further includes an indicator, which is disposed on the holding body and is communicatively connected to the control member, and the indicator is used to emit a bright light when the pushing member is being pushed by the output end of the driving member.

[0015] According to an embodiment of the present invention, the pressing and rotating member has at least one anti-slip member, and the anti-slip member is located on the surface of the pressing and rotating member, and the anti-slip member is used to prevent the pressing and rotating member from slipping when stepping on it.

[0016] According to one embodiment of the present invention, the device body further includes at least one mounting member, which is disposed on the device body and forms an installation space, and the grip body is detachably disposed in the installation space of the mounting member.

[0017] According to one embodiment of the present invention, the device body also includes a control display component, which is arranged on the device body and electrically connected to the control component. The control display component is used to display the moving speed and moving distance of the output end of the driving component in real time, and the control display component can be used to adjust the moving speed and moving distance of the output end of the driving component.

[0018] According to one embodiment of the present invention, the device body further includes a power storage component, which is arranged in the device body and electrically connected to the control component, and is used to supply power to the control component and the operation display component. BRIEF DESCRIPTION OF THE DRAWINGS

[0019] Figure 1 A schematic perspective view of a preferred embodiment of the present invention is shown.

[0020] Figure 2 A schematic perspective view of a preferred embodiment of the present invention is shown in another perspective.

[0021] Figure 3 A schematic cross-sectional view of a preferred embodiment of the present invention is shown.

[0022] Figure 4 Shown Figure 3 Schematic diagram of the enlarged view of point A in the middle.

[0023] Figure 5 A schematic perspective view of the push-to-operate assembly is shown.

[0024] Figure 6 A schematic cross-sectional view of the push-to-operate assembly is shown.

[0025] Figure 7 A schematic structural stereogram of the pressing and rotating member, the connecting rod, the shielding member and the resilient member is shown.

[0026] Figure 8 A schematic perspective view of the injection assist assembly is shown, wherein the anti-slip portion of the tube clamp is not disposed in the insertion groove.

[0027] Figure 9 A schematic perspective view of the tube clamp is shown. DETAILED DESCRIPTION

[0028] The following description is intended to disclose the present invention and enable those skilled in the art to implement the present invention. The preferred embodiments described below are provided for illustrative purposes only, and those skilled in the art will readily appreciate other obvious variations. The basic principles of the present invention as defined in the following description may be applied to other embodiments, variations, improvements, equivalents, and other technical solutions that do not depart from the spirit and scope of the present invention.

[0029] Those skilled in the art should understand that, in the disclosure of the present invention, the terms "longitudinal", "transverse", "up", "down", "front", "back", "left", "right", "vertical", "horizontal", "top", "bottom", "inside", "outside" and the like indicating the orientation or position relationship are based on the orientation or position relationship shown in the accompanying drawings, which are only for the convenience of describing the present invention and simplifying the description, and do not indicate or imply that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation. Therefore, the above terms cannot be understood as limiting the present invention.

[0030] It is to be understood that the term "one" should be understood as "at least one" or "one or more", that is, in one embodiment, the number of an element may be one, while in another embodiment, the number of the elements may be multiple, and the term "one" should not be understood as a limitation on the quantity.

[0031] refer to Figures 1 to 9 According to a preferred embodiment of the present invention, an electronic syringe control booster device will be described in detail below. The electronic syringe control booster device is used to press and push a pressing portion 93 of an injection piece 90 a predetermined distance at a predetermined speed to squeeze a predetermined dose of liquid medicine in a tubular portion 92 of the injection piece 90 out of a channel formed by an injection portion 91 of the injection piece 90.

[0032] Specifically, the electronic syringe control booster device includes a device body 10 , a pressing control component 20 and an injection booster component 30 .

[0033] The device body 10 includes a device body 11 and a control member 12. The control member 12 is mounted on the device body 11.

[0034] In this embodiment, the press control assembly 20 includes a press body 21, a press rotating member 22, a connecting rod 23, a shielding member 24 and a sensing member 25. The press body 21 is located near the device body 11. The press rotating member 22 is inserted into the connecting rod 23, and the press rotating member 22 is fixed to the connecting rod 23. The two ends of the connecting rod 23 are rotatably inserted into the press body 21. In other words, the press rotating member 22 rotates relative to the press body 21 with the connecting rod 23 as the axis. The shielding member 24 is connected to the connecting rod 23 in a manner that rotates with the connecting rod 23. The sensing member 25 is provided on the press body 21 and is communicatively connected to the control member 12 via a signal transmitter, so as to transmit the angle data of the shielding member 24 rotating with the connecting rod 23 detected to the control member 12 via the signal transmitter.

[0035] In another variant embodiment, the pressing control assembly 20 includes the pressing body 21, the pressing rotating member 22, the connecting rod 23, the shielding member 24 and the sensing member 25. The pressing body 21 is located near the device body 11. The pressing rotating member 22 is inserted into the connecting rod 23 in a rotatable manner. The two ends of the connecting rod 23 are fixed to the pressing body 21. In other words, the pressing rotating member 22 rotates relative to the pressing body 21 with the connecting rod 23 as the axis. The shielding member 24 is connected to the pressing rotating member 22 in a manner of following the rotation of the pressing rotating member 22. The sensing member 25 is provided on the pressing body 21 and is communicatively connected to the control member 12 through the signal transmitter, so as to transmit the angle data of the detected shielding member 24 rotating following the pressing rotating member 22 to the control member 12 through the signal transmitter.

[0036] In order to enable those skilled in the art to understand the present invention, in at least one embodiment of the present invention, only the pressing rotating member 22 is inserted into the connecting rod 23, and the pressing rotating member 22 is fixed to the connecting rod 23, the two ends of the connecting rod 23 are rotatably inserted into the pressing body 21, and the shielding member 24 is connected to the connecting rod 23 in a manner of following the rotation of the connecting rod 23 is used as an example for explanation.

[0037] Specifically, the pressing control assembly 20 further includes at least one resilient member 26, which is compressibly disposed between the pressing rotating member 22 and the pressing body 21, with both ends of the resilient member 26 respectively abutting against the end of the pressing rotating member 22 away from the connecting rod 23 and the pressing body 21. The resilient member 26 is used to support the end of the pressing rotating member 22 away from the connecting rod 23 when the pressing rotating member 22 is pressed and rotates around the connecting rod 23, and to cause the pressing rotating member 22 to rotate in the opposite direction around the connecting rod 23 to return to its original position when the pressing rotating member 22 is no longer pressed.

[0038] Preferably, the resilient element 26 is implemented as a spring.

[0039] In this embodiment, the pressing and operating assembly 20 further includes a stopper 27, which is disposed on the pressing body 21 and located along the movement path of the shielding member 24. The stopper 27 is used to stop the shielding member 24 as it rotates following the connecting rod 23, thereby preventing the pressing and rotating member 22 from driving the connecting rod 23 to continue rotating. In other words, the stopper 27 is used to limit the angle at which the shielding member 24 rotates following the connecting rod 23.

[0040] It is worth mentioning that, since the compressibility of the rebound member 26 will change after multiple uses, and since the limiting member 27 is located on the movement path of the shielding member 24, the limiting member 27 limits the angle of rotation of the shielding member 24 following the connecting rod 23, thereby avoiding the change in the compressibility of the rebound member 26 causing the rotatable angle of the pressing rotating member 22 around the connecting rod 23 to change, and ultimately avoiding the change in the maximum value of the angle data of the shielding member 24 following the rotation of the connecting rod 23 detected by the sensing member 25.

[0041] It should be noted that, since the control component 12 is controlled by its internal program, when the value transmitted from the sensor 25 to the control component 12 via the signal transmitter is not within the predetermined program value range, the control component 12 may report an error, thereby causing the control component 12 to be unable to operate normally. Therefore, it is necessary to control the value transmitted from the sensor 25 to the control component 12 via the signal transmitter to be within the predetermined program value range.

[0042] 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 stop blocks 34. The holding body 31 is located near the device body 11. A pair of the port stop blocks 34 are symmetrically mounted on the holding body 31, and a port fixing groove 3101 is formed between the pair of the port stop blocks 34. One end of the tube body 92 of the injection member 90 abuts against the port stop block 34, and the injection portion 91 connected to the tube body 92 passes through the port fixing groove 3101. The driving member 32 is arranged on the holding body 31 and is communicatively connected to the control member 12 so as 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 output end of the driving member 32 extends in a direction that allows the pushing member 33 to abut against the pressing portion 93 while pressing the pressing portion 93 toward the tube portion 92. In other words, the pushing member 33 abuts against the pressing portion 93 under the action of the output end of the driving member 32 in a manner that presses the pressing portion 93 toward the tube portion 92.

[0043] Preferably, the driving member 32 is implemented to include an electric push rod.

[0044] Those skilled in the art will appreciate that when the pressing rotating member 22 rotates with the connecting rod 23 as the axis and drives the shielding member 24 to rotate, the sensing member 25 will transmit the angle data of the shielding member 24 detected following the rotation of the connecting rod 23 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 that the liquid medicine in the tube body portion 92 is squeezed out through the channel formed by the injection portion 91.

[0045] Furthermore, in one embodiment, once the control component 12 receives the change in the angle data detected by the sensor 25 through the signal transmitter, it controls the output end of the driving component 32 to move a predetermined distance at a predetermined speed.

[0046] Furthermore, in another embodiment, the control component 12 receives the difference in the size of the angle data value detected by the sensing component 25 through the signal transmitter, and controls the output end of the driving component 32 to move at different speeds. When the control component 12 does not receive the change in the size of the angle data value detected by the sensing component 25 through the signal transmitter, it will immediately stop controlling the movement of the output end of the driving component 32.

[0047] It is worth mentioning that since the sensing member 25 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 component 20 is placed on the ground, the bacteria on the ground will not be transferred to the device body 10 through the pressing control component 20, that is, it is avoided that the bacteria in the pressing control component 20 is transferred to the device body 10 and then to the injection booster component 30 to contaminate the injection booster component 30, so that the patient will not be infected by bacteria when the medicine is injected by the injection component 90, thereby providing protection for the patient's life safety.

[0048] Those skilled in the art will understand that, since the sensing member 25 is communicatively connected to the control member 12 via the signal transmitter, and the control member 12 is communicatively connected to the driving member 32, the pressing control component 20 and the device body 10 and the injection boosting component 30 and the device body 10 are not restricted by the wires and cannot be moved to the predetermined position.

[0049] The push-to-operate assembly 20 will not be unable to be placed on the ground due to the entanglement of the wires between the push-to-operate assembly 20 and the device body 10. Furthermore, the push-to-operate assembly 20 will not be unable to be placed on the ground due to the length limitation of the wires because of the obstacles between the push-to-operate assembly 20 and the device body 10 and the wires need to be routed around. The injection booster assembly 30 will not be unable to attach the injection portion 91 of the injection piece 90 to the patient's skin surface due to the limitation of the wires between the injection booster assembly 30 and the device body 10. This provides convenience for the actual use of the device body 10, the push-to-operate assembly 20, and the injection booster assembly 30.

[0050] It should be noted that, since the tube body 92 and the pressing portion 93 are arranged between the pushing member 33 and the port stop block 34, and when the injection part 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 press against the pressing portion 93. When the holding body 31 is moved by hand, the tube body 92 and the pressing portion 93 will slip from between the pushing member 33 and the port stop block 34 due to unstable connection, causing the injection part 91, the tube body 92 and the pressing portion 93 to fall.

[0051] Preferably, the injection booster assembly 30 further includes a tube body clamp 35. The tube body clamp 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 body 92. The clamping portion 351 is provided on the holding body 31. The tube body 92 passes through the clamping groove 35101 in a manner that is movable in the clamping groove 35101. In other words, the tube body 92 is fixed by being provided in the clamping groove 35101 to prevent the tube body 92 from slipping off between the pusher 33 and the port stop block 34.

[0052] More preferably, the tube body clamping member 35 further includes an anti-slip portion 352. The anti-slip portion 352 is connected to the clamping portion 351. The gripping body 31 has an insertion groove 3102 that matches the anti-slip portion 352. The anti-slip portion 352 is detachably disposed in the insertion groove 3102, so that when the outer diameter of the tube body 92 changes due to replacement of a different injection component 90, the clamping portion 351 having the clamping groove 35101 with the corresponding inner diameter can be replaced by disassembling the anti-slip portion 352, thereby avoiding the situation where the tube body 92 cannot be fixed by the clamping portion 351.

[0053] Specifically, the injection boost assembly 30 further includes an alarm member 36. The alarm member 36 is disposed on the push member 33 and is communicatively connected to the control member 12. The alarm member 36 is configured to sound an alarm when the push member 33 stops moving, thereby alerting the outside world that the injection of the liquid medicine has been completed.

[0054] Furthermore, the injection boost assembly 30 includes an indicator 37. The indicator 37 is disposed on the grip body 31 and is communicatively connected to the control member 12. The indicator 37 is configured to emit a bright light when the pusher 33 is being pushed by the output end of the driving member 32, thereby preventing the output end of the driving member 32 from moving at a slow speed and being unnoticed by the operator.

[0055] Preferably, the alarm member 36 is implemented to include a vibration motor.

[0056] The indicator 37 is implemented as a light emitting diode.

[0057] Specifically, the pressing and rotating member 22 has at least one anti-slip member 221. The anti-slip member 221 is located on the surface of the pressing and rotating member 22. The anti-slip member 221 is used to prevent the foot from slipping off the surface of the pressing and rotating member 22 when stepping on the pressing and rotating member 22.

[0058] Specifically, the device body 10 further includes at least one mounting member 13. The mounting member 13 is mounted on the device body 11 and forms a mounting space. The grip body 31 is detachably mounted in the mounting space of the mounting member 13. In other words, the mounting space is used to accommodate the grip body 31, making it easy to find after use.

[0059] Preferably, the device body 10 further includes a control display 14. The control display 14 is disposed on the device body 11 and is electrically connected to the control member 12, so as to display the predetermined speed and predetermined moving distance of the output end of the driving member 32 in real time through the control display 14.

[0060] Furthermore, the predetermined speed and the predetermined distance at which the output end of the driving member 32 moves can be changed by the manipulation display member 14 .

[0061] The device body 10 also includes a power storage element 15. The power storage element 15 is disposed within the device body 10 and is electrically connected to the control element 12. The power storage element 15 supplies power to the control element 12 and the control and display element 14 via the power storage element 15, thereby freeing the control element 12 and the control and display element 14 from dependence on a power source and enabling the device body 10 to be placed in any desired location.

[0062] Those skilled in the art will appreciate that the embodiments of the present invention described above and shown in the accompanying drawings are provided for illustrative purposes only and do not limit the present invention. The advantages of the present invention have been fully and effectively realized. The functional and structural principles of the present invention have been demonstrated and illustrated in the embodiments. Any variations or modifications may be made to the embodiments of the present invention without departing from the principles described.

Claims

1. An electronic syringe control booster device is used to press and push the pressing portion of the injection piece at a predetermined speed and a predetermined distance to squeeze a predetermined dose of liquid medicine in the tubular portion of the injection piece out of the channel formed by the injection portion of the injection piece, characterized in that: The electronic injector control booster device comprises: A device body, the device body comprising a device body and a control member, the control member being mounted on the device body; The pressing and operating component comprises a pressing body, a pressing rotating member, a connecting rod, a shielding member, a sensing member and at least one rebound member, the pressing body being located near the device body, the pressing rotating member being inserted into the connecting rod, and the pressing rotating member being fixed to the connecting rod, the two ends of the connecting rod being rotatably inserted into the pressing body, the shielding member being connected to the connecting rod in a manner of following the rotation of the connecting rod, the sensing member being arranged on the pressing body, the sensing member being communicatively connected to the control member via a signal transmitter, the sensing member being used to detect the angle data of the shielding member following the rotation of the connecting rod and transmitting the data to the control member via the signal transmitter, the rebound member being compressibly arranged between the pressing rotating member and the pressing body, and the two ends of the rebound member respectively abutting against the end of the pressing rotating member away from the connecting rod and the pressing body; and An injection booster assembly, the injection booster assembly includes a holding body, a driving member, a pushing member and at least a pair of port stop blocks, the holding body is located near the device body, a pair of the port stop blocks are symmetrically installed on the holding body, and a port fixing groove is formed between the pair of the port stop blocks, one end of the tube body of the injection member is against the port stop block, the injection part connected to the tube body passes through the port fixing groove, the driving member is arranged on the holding body, the driving member is communicatively 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 extension direction of the output end of the driving member is such that the pushing member can be against the pressing part and press the pressing part toward the tube body at a predetermined speed, so as to realize the predetermined dose of liquid medicine in the tube body of the injection member being squeezed out from the channel formed by the injection part at a predetermined speed.

2. The electronic syringe control booster device according to claim 1, characterized in that: The pressing control assembly also includes a limiter, which is arranged on the pressing body and located on the movement path of the shielding member. The limiter is used to stop the shielding member when the shielding member rotates following the connecting rod to limit the angle of rotation of the shielding member following the connecting rod.

3. The electronic syringe control booster device according to claim 2, characterized in that: The injection booster assembly also includes a tube body clamping piece, which includes a clamping portion, the clamping portion forming a clamping groove, the inner diameter of the clamping groove matches the outer diameter of the tube body portion, the clamping portion is arranged on the holding body, and the tube body portion passes through the clamping groove in a manner that can move in the clamping groove.

4. The electronic syringe control booster device according to claim 3, characterized in that: The tube body clamp also includes an anti-slip portion, which is connected to the clamping portion. The holding body has an insertion groove that matches the anti-slip portion. The anti-slip portion is detachably arranged in the insertion groove so that when the outer diameter of the tube body portion changes due to replacement of different injection parts, the clamping portion having the clamping groove with the corresponding inner diameter can be replaced.

5. The electronic syringe control booster device according to claim 4, characterized in that: The injection-assisting assembly further includes an alarm component, which is disposed on the pushing member and is communicatively connected to the control member. The alarm component is configured to sound an alarm when the pushing member stops moving.

6. The electronic syringe control booster device according to claim 5, characterized in that: The injection-assisting assembly further includes an indicator, which is disposed on the grip body and is communicatively connected to the control member. The indicator is configured to emit a bright light when the pushing member is being pushed by the output end of the driving member.

7. The electronic syringe control booster device according to claim 6, characterized in that: The pressing and rotating member has at least one anti-slip member, which is located on the surface of the pressing and rotating member and is used to prevent the pressing and rotating member from slipping when being stepped on.

8. The electronic syringe control booster device according to claim 7, characterized in that: The device body further includes at least one mounting member, which is disposed on the device body and forms a mounting space. The grip body is detachably disposed in the mounting space of the mounting member.

9. The electronic syringe control booster device according to any one of claims 2 to 8, characterized in that: The device body also includes a control display component, which is arranged on the device body and electrically connected to the control component. The control display component is used to display the moving speed and moving distance of the output end of the driving component in real time, and the control display component can be used to adjust the moving speed and moving distance of the output end of the driving component.

10. The electronic syringe control booster device according to claim 9, characterized in that: The device body further includes a power storage component, which is disposed on the device body and electrically connected to the control component. The power storage component is used to supply power to the control component and the operation and display component.