Hyaluronic acid injection equipment
By designing a hyaluronic acid injection device including a fixed part, a support part, a needle and a driving part, the problems of high operational difficulty of existing equipment and high requirements for medical staff are solved, and a more stable and easy injection process is achieved.
Patent Information
- Application Number
- CN202421082828.1
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-05-17
- Publication Date
- 2025-03-21
- Estimated Expiration
- 2034-05-17
AI Technical Summary
The existing hyaluronic acid injection equipment is difficult to operate during facial injection, and requires medical staff to have a high level of operation and are prone to accidents caused by hand shaking.
A hyaluronic acid injection device is designed, including a fixing part, a support part, a needle and a driving part. The fixing part is fixedly connected to the skin tissue, the support part is fixedly connected to the fixing part, and the needle is slidably connected to the support part, and the needle is controlled to slide through the drive member to complete the injection.
By cooperating with the fixing part and the support part, the needle can be stably maintained at the part to be injected. Medical staff can complete the injection by controlling the drive part, reducing the chance of direct contact with the needle from the hand, reducing the difficulty of operation and dependence on the operation level of medical staff.
Smart Images

Figure CN222641017U_ABST
Abstract
Description
Technical Field
[0001] The utility model belongs to the technical field of cosmetic medical equipment, in particular to a hyaluronic acid injection device. Background Art
[0002] Hyaluronic acid is a biochemical drug with high clinical value. It can keep the skin moisturized, smooth, delicate, tender and elastic. It also has anti-wrinkle, anti-wrinkle, beauty and health care, and restores the physiological functions of the skin. Therefore, it is widely used in facial plastic surgery. At present, in the process of facial hyaluronic acid injection, it is generally common to use a syringe directly. During the injection, it is necessary to mark the position on the patient's face to determine the specific location of the needle. When injecting, the syringe is held by the medical staff so that the needle is inserted into the skin tissue at the marked position, and the syringe is pushed with the other hand to complete the injection of hyaluronic acid.
[0003] The particularity of this process is that since the injection site is directly located on the face of the patient, no obvious traces can be left after the injection. In the process of injecting hyaluronic acid with a syringe, when holding the syringe in the hand, it is necessary to ensure that the needle tip is aligned with the marked position, and the shaking or trembling of the hand needs to be overcome during the injection process. If the medical staff is not focused, accidents are inevitable. It can be seen that when injecting through the current equipment, certain operating levels of medical staff are required. In view of this, in order to reduce the difficulty of operation, the present application provides a hyaluronic acid injection device. Utility Model Content
[0004] The purpose of this section is to summarize some aspects of the embodiments of the utility model and briefly introduce some preferred embodiments. Some simplifications or omissions may be made in this section and the specification abstract and utility model name of this application to avoid blurring the purpose of this section, specification abstract and utility model name, and such simplifications or omissions cannot be used to limit the scope of the utility model.
[0005] In view of the following technical problems in the prior art: the current injection device is difficult to operate when completing the injection process of hyaluronic acid on the patient's face, which requires a high level of operation of medical staff and is not convenient to use. In order to solve this technical problem, the utility model provides the following technical solutions:
[0006] A hyaluronic acid injection device, comprising:
[0007] A fixed part that maintains a fixed connection with the skin tissue;
[0008] A supporting portion, fixedly connected to the fixing portion;
[0009] A needle, slidably connected to the support portion and connected to an injection source via a catheter;
[0010] The driving member is softly connected to the needle, and the needle slides through the driving member.
[0011] As a preferred technical solution for a hyaluronic acid injection device, the fixing part is in a sheet-like structure and is made of memory metal, and is adhesively connected to the skin tissue.
[0012] As a preferred technical solution for a hyaluronic acid injection device, the fixing part is connected to the skin tissue via an adhesive patch.
[0013] As a preferred technical solution for a hyaluronic acid injection device, a positioning hole is constructed in the middle of the sheet surface of the fixed part, and the needle points to the positioning hole.
[0014] As a preferred technical solution of a hyaluronic acid injection device, a connecting end is constructed on the fixing part, and the supporting part is connected to the connecting end.
[0015] As a preferred technical solution for a hyaluronic acid injection device, the support portion is in a tubular structure, and a slider is fixedly connected to the circumference of the needle, which slides in cooperation with the inner wall of the support portion.
[0016] As a preferred technical solution for a hyaluronic acid injection device, an air storage cavity is formed between one end of the support portion and the slider, and the driving member is used to supply or inhale air to the air storage cavity.
[0017] As a preferred technical solution for a hyaluronic acid injection device, a guiding structure is constructed on the inner wall of the support portion and acts on the slider.
[0018] The hyaluronic acid injection device provided by the utility model has the beneficial effect that the needle can be fully maintained at the site to be injected on the skin through the cooperation between the fixed part and the supporting part, so that the medical staff can control the needle to slide by controlling the driving part during operation, so as to insert the needle into the target position. Compared with the prior art, during the use of the device, the medical staff does not need to directly touch the needle, thereby fully reducing or avoiding the impact of tremors in the hands during operation, thereby reducing the dependence on the medical staff's operating level. BRIEF DESCRIPTION OF THE DRAWINGS
[0019] In order to more clearly illustrate the technical solutions of the embodiments of the present utility model, the following briefly introduces the drawings required for the description of the embodiments. Obviously, the drawings described below are only some embodiments of the present utility model. For ordinary technicians in this field, other drawings can be obtained based on these drawings without creative labor. Among them:
[0020] Figure 1 It is a three-dimensional diagram of the utility model.
[0021] Figure 2 For the utility model Figure 1 Another perspective view of .
[0022] Figure 3 It is a schematic diagram of the cooperation between the needle head and the supporting part in the utility model.
[0023] Figure 4 For the utility model Figure 3 Another perspective view of .
[0024] Figure numerals: 1. trachea; 2. supporting part; 3. needle; 4. fixing part; 5. catheter; 6. positioning hole; 7. connecting end; 8. slider; 9. air storage chamber; 10. guiding structure. DETAILED DESCRIPTION
[0025] In order to make the above-mentioned purposes, features and advantages of the present invention more obvious and easy to understand, the specific implementation methods of the present invention are described in detail below in conjunction with the accompanying drawings.
[0026] In the following description, many specific details are set forth to facilitate a full understanding of the present invention, but the present invention may also be implemented in other ways different from those described herein, and those skilled in the art may make similar generalizations without violating the connotation of the present invention. Therefore, the present invention is not limited to the specific embodiments disclosed below.
[0027] Secondly, the term "one embodiment" or "embodiment" as used herein refers to a specific feature, structure or characteristic that may be included in at least one implementation of the present invention. The term "in one embodiment" that appears in different places in this specification does not necessarily refer to the same embodiment, nor does it refer to a separate or selective embodiment that is mutually exclusive with other embodiments.
[0028] Secondly, the present invention is described in detail with reference to the schematic diagram. When describing the embodiments of the present invention, for the sake of convenience, the cross-sectional diagrams showing the device structure will not be partially enlarged according to the general scale, and the schematic diagrams are only examples, which should not limit the scope of protection of the present invention. In addition, in actual production, the three-dimensional dimensions of length, width and depth should be included.
[0029] Reference Figure 1 and Figure 2 One embodiment of the utility model provides a hyaluronic acid injection device, comprising the following parts:
[0030] The fixing part 4 is used to form a fixed connection with the skin tissue so as to maintain a fixed position on the skin and can be removed from the skin when not in operation;
[0031] A support portion 2, which is fixedly connected to the fixing portion 4;
[0032] The needle 3 is used for injection and is slidably connected to the support part 2. The root of the needle 3 is connected to the injection source through a soft catheter 5;
[0033] The driving member is softly connected to the needle 3, and the needle 3 will not be touched when the driving member is operated. Its function is that the needle 3 can slide on the support part 2 through the driving member;
[0034] When the utility model cooperates with medical staff to perform hyaluronic acid injection, the fixing part 4 is connected to the position to be injected on the skin tissue, and the tip of the needle 3 is directed to the position to be inserted. By operating the driving member, the needle 3 slides on the support part 2, so as to be inserted into the target position on the skin, and then the injection source is operated to make the hyaluronic acid liquid flow into the needle 3 through the catheter 5, so as to enter the inserted position on the skin to complete the entire injection process. For the injection source involved in the utility model, an injection head with the needle tip removed can still be used and connected to the catheter 5, or some micro pump body structures can be used, and can meet the requirements of precise control;
[0035] Compared with the prior art, during the operation, the alignment process of the needle 3 is achieved by the cooperation of the fixing part 4 and the supporting part 2, and direct contact of the medical staff's hands is avoided, so that during the insertion process, the needle 3 is not affected by the shaking of the staff's hands, and through the soft connection properties at multiple locations, the medical staff will not cause hard contact with the needle 3 during the operation of the driving part and the injection source. Therefore, the requirements for the stability of the medical staff's hands are reduced as a whole, that is, the high requirements for the medical staff's operating level are reduced, making the operation easier and reducing the occurrence of accidents.
[0036] For other structures involved in the utility model, for example:
[0037] The fixing part 4 can be designed as a sheet-like structure. Figure 1 and Figure 2 , and the fixing part 4 is made of memory metal, so that it can be ravaged into a desired shape before connecting with the skin tissue, so as to better adapt to the injection site on the skin. At this time, the fixing part 4 and the skin tissue can be connected by pasting. The sheet-like structural design can increase the contact area between the fixing part 4 and the skin, thereby increasing the stability effect when fixed on the skin;
[0038] Furthermore, the fixing part 4 can be connected to the skin tissue by adhesive tape, such as using double-sided adhesive tape, so that the pasting process is simple and easy, and as a disposable product, the manufacturing cost can also be reduced;
[0039] Furthermore, a positioning hole 6 is also constructed in the middle of the sheet surface of the fixing part 4, such as Figure 1 and Figure 2 As shown, the needle 3 is directed toward the positioning hole 6, so when the fixing part 4 is pasted on the skin, the part to be pierced is located at the positioning hole 6, thereby encircling the part to be pierced, so that the needle insertion part can be better determined in advance, and when the needle 3 exerts force on the skin, the reaction force on the needle 3 is located in the middle of the entire fixing part, so that the phenomenon of deviation on the skin caused by the needle 3 exerting force can be reduced, thereby increasing the stability of the piercing process;
[0040] For the connection between the support portion 2 and the fixing portion 4, a connection end 7 may be constructed on the fixing portion 4. Figure 1 and Figure 2 As shown, the support portion 2 and the connection end 7 can be fixedly connected. Due to the characteristics of the material of the fixing portion 4, the connection end 7 can also be kneaded into a desired shape by a person applying force thereto in advance, so that the direction of the needle 3 can be finely adjusted in advance, so as to further improve the practical effect of the utility model;
[0041] The support portion 2 can be designed as a cylindrical structure. Figure 1-4 As shown, a slider 8 is fixedly connected to the periphery of the needle 3, and the slider 8 is slidably matched with the inner wall of the support portion 2, so as to meet the sliding requirement of the needle 3 on the support portion 2. The cylindrical structure can protect the needle 3, and at the same time, the slider 8 can maintain non-direct contact between the needle 3 and the support portion 2, so as to avoid contamination of the needle 3.
[0042] Furthermore, based on the cylindrical structure, Figure 3 and Figure 4 One end of the support portion 2 is a closed structure, so that an air storage cavity 9 can be formed between one end of the support portion 2 and the slider 8. At this time, the driving member is used to deliver or inhale air to the air storage cavity 9. When delivering air, the slider 8 is pushed to move by gas expansion, thereby realizing the sliding drive of the slider 8. When inhaling air, the slider 8 slides back by creating a negative pressure in the air storage cavity 9, thereby completing the removal of the needle 3 in the skin tissue. For the driving member, for example, an injection head or a pump body structure can still be used, and it can be connected to the air storage cavity 9 through the soft air tube 1;
[0043] Further, see Figure 3 and Figure 4A guide structure 10 is also constructed on the inner wall of the support portion 2. The guide structure 10 is used to make the slider 8 move linearly only along the axial length direction of the cylinder when sliding, thereby playing a directional guiding effect, thereby preventing the needle 3 from spinning when moving. The guide structure 10 can adopt convex or concave linear patterns, and the shape of the slider 8 can be adapted thereto.
[0044] It will be appreciated that in the development of any actual implementation, as in any engineering or design project, numerous implementation-specific decisions may be made. Such a development effort may be complex and time-consuming, but will be a routine task of design, fabrication, and production for those of ordinary skill having the benefit of this disclosure without undue experimentation.
[0045] It should be noted that the above embodiments are only used to illustrate the technical solution of the utility model rather than to limit it. Although the utility model has been described in detail with reference to the preferred embodiments, ordinary technicians in the field should understand that the technical solution of the utility model can be modified or replaced by equivalents without departing from the spirit and scope of the technical solution of the utility model, which should be included in the scope of the claims of the utility model.
Claims
1. A hyaluronic acid injection device, characterized in that: include: A fixing portion (4) which is fixedly connected to the skin tissue; A supporting portion (2) fixedly connected to the fixing portion (4); A needle (3) is slidably connected to the support portion (2) and is connected to an injection source via a catheter (5); The driving member is flexibly connected to the needle (3), and the needle (3) slides via the driving member.
2. The hyaluronic acid injection device according to claim 1, characterized in that: The fixing part (4) is in a sheet-like structure and is made of memory metal, and is adhesively connected to the skin tissue.
3. The hyaluronic acid injection device according to claim 2, characterized in that: The fixing part (4) is connected to the skin tissue via an adhesive patch.
4. The hyaluronic acid injection device according to claim 2, characterized in that: A positioning hole (6) is formed in the middle of the sheet surface of the fixing part (4), and the needle head (3) points to the positioning hole (6).
5. The hyaluronic acid injection device according to claim 2, characterized in that: A connecting end (7) is configured on the fixing portion (4), and the supporting portion (2) is connected to the connecting end (7).
6. The hyaluronic acid injection device according to claim 1, characterized in that: The support portion (2) is of a tubular structure, and a sliding block (8) is fixedly connected to the circumference of the needle head (3) and is slidably matched with the inner wall of the support portion (2).
7. The hyaluronic acid injection device according to claim 6, characterized in that: An air storage chamber (9) is formed between one end of the support portion (2) and the slider (8), and the driving member is used to deliver or inhale air to the air storage chamber (9).
8. The hyaluronic acid injection device according to claim 6, characterized in that: A guide structure (10) is constructed on the inner wall of the support portion (2) and acts on the sliding block (8).