A syringe disassembly assembly and a syringe
By designing the syringe assembly and disassembly components, and utilizing the combination of internal and external threaded grooves and a limiting mechanism, the problem of syringes being unable to adapt to different wound sizes is solved, thus achieving flexible application and stable suction of the syringe.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- THE FIRST AFFILIATED HOSPITAL OF GUANGXI UNIV OF TRADITIONAL CHINESE MEDICINE (GUANGXI TRADITIONAL CHINESE MEDICINE HOSPITAL)
- Filing Date
- 2023-09-18
- Publication Date
- 2026-07-07
AI Technical Summary
Existing syringes have small nipple diameters when drawing venom, making them unsuitable for wounds of different sizes and thus less practical.
A syringe assembly was designed, which uses the cooperation of internal and external threaded grooves to fix the syringe body and the suction part. Combined with a rubber layer and a limiting mechanism, it is suitable for wounds of different sizes and improves practicality.
It achieves a flexible combination of the syringe body and the suction section, making it suitable for wounds of different sizes and improving the practicality and stability of the syringe.
Smart Images

Figure CN224462020U_ABST
Abstract
Description
Technical Field
[0001] This utility model relates to the field of syringe technology, and more specifically, to a syringe disassembly and assembly assembly and a syringe. Background Technology
[0002] Currently, existing syringes draw venom by covering the wound with a nipple and pulling the piston rod to draw the venom from the wound into the syringe. However, wounds vary in size, and the nipple diameter is small, making it unsuitable for different wounds and limiting its practicality.
[0003] Therefore, we have made improvements to this by proposing a syringe disassembly and assembly assembly and a syringe. Summary of the Invention
[0004] The purpose of this invention is to address the issue that existing syringes use a nipple to cover the wound when drawing venom, and then pull the piston rod to draw the venom from the wound into the syringe. However, wounds vary in size, and the nipple diameter is small, making it unsuitable for different wounds and thus impractical.
[0005] To achieve the above-mentioned objectives, this invention provides a syringe disassembly and assembly assembly and a syringe to improve the aforementioned problems.
[0006] The application is as follows:
[0007] A syringe assembly includes a syringe body, a suction section at the top of the syringe body, the suction section being composed of a connecting tube and a nipple, and a disassembly section between the connecting tube and the syringe body for fixing the connecting tube and the syringe body.
[0008] As a preferred technical solution of this application, the bottom end of the nipple is fixedly connected to the middle part of the top end of the connecting cylinder, and the inside of the nipple is connected to the inside of the connecting cylinder, and the bottom end of the connecting cylinder is open.
[0009] As a preferred technical solution of this application, the disassembly part is a rubber layer, the bottom end of the connecting cylinder is provided with an internal thread groove, the top end of the outer side of the syringe body is provided with an external thread groove that matches the internal thread groove, the bottom end of the rubber layer is fixedly connected to the top end of the syringe body, and the top end of the rubber layer is in contact with the top end of the internal thread groove.
[0010] A syringe includes a piston disposed within a cavity formed by a syringe body and a connecting tube. A piston rod is fixedly disposed at the bottom end of the piston, and a limiting mechanism is provided between the piston rod and the syringe body.
[0011] As a preferred technical solution of this application, the limiting mechanism is composed of a first limiting part and a second limiting part.
[0012] As a preferred technical solution of this application, the first limiting part is composed of two limiting blocks and two limiting members.
[0013] As a preferred technical solution of this application, one side of each of the two limiting blocks is fixedly connected to the bottom ends of both sides of the syringe body, and an L-shaped groove is opened in the other side of the limiting block. One side of the limiting member is fixedly installed at one end of the L-shaped groove.
[0014] As a preferred technical solution of this application, the second limiting part is composed of two sliding rods. One side of each sliding rod is fixedly connected to both sides of the piston rod. The other end of each sliding rod is inserted into the L-shaped groove. A plurality of limiting grooves matching the limiting member are equidistantly provided on the other side of the sliding rod.
[0015] As a preferred technical solution of this application, the sealing part includes a sealing cap, and the syringe body is provided with a scale.
[0016] Compared with the prior art, the beneficial effects of this utility model are as follows:
[0017] In the scheme of this application:
[0018] 1. To address the problem that existing syringes, when drawing venom, use a nipple to cover the wound and pull the piston rod to draw the venom into the syringe, but wounds vary in size and the nipple diameter is small, making them unsuitable for different wounds and resulting in low practicality, this application proposes a disassembly / removal part. The internal and external threaded grooves of the disassembly / removal part allow the syringe body to be fixed to the suction part. The nipple of the suction part can be used to draw venom from small wounds, and by removing the suction part, the syringe body, in conjunction with the rubber layer of the disassembly / removal part, can draw venom from large wounds. This design makes it suitable for wounds of different sizes, improving practicality.
[0019] 2. With the setting of the limiting mechanism, as the piston rod moves, the limiting mechanism can be driven to operate. Under the action of the limiting mechanism, the piston rod after it has moved can be fixed, which prevents the piston rod from being sucked back and affecting the absorption of venom, thus improving practicality. Attached Figure Description
[0020] Figure 1 A schematic diagram of the syringe assembly and syringe provided in this application;
[0021] Figure 2 A cross-sectional structural diagram of the syringe assembly and syringe provided in this application;
[0022] Figure 3 A partial cross-sectional structural diagram of the syringe assembly and syringe provided in this application;
[0023] Figure 4 A cross-sectional structural diagram of the syringe assembly and syringe limiting mechanism provided in this application.
[0024] The image shows:
[0025] 1. Syringe body;
[0026] 2. Suction section; 201. Connecting cylinder; 202. Nipple;
[0027] 3. Assembly / disassembly section; 301. Rubber layer; 302. Internal thread groove; 303. External thread groove;
[0028] 4. Piston;
[0029] 5. Piston rod;
[0030] 6. Limiting mechanism; 601. Limiting block; 602. Limiting component; 603. Slide rod;
[0031] 7. Scale. Detailed Implementation
[0032] To enable those skilled in the art to better understand the present invention, the technical solutions of the present invention will be clearly and completely described below with reference to the accompanying drawings of the embodiments. Obviously, the described embodiments are only some embodiments of the present invention, and not all embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those skilled in the art without creative effort should fall within the protection scope of the present invention.
[0033] As in the background art, existing syringes use a nipple to cover the wound when drawing venom, and then pull the piston rod to draw the venom from the wound into the syringe. However, wounds vary in size, and the nipple diameter is small, making it unsuitable for different wounds and thus impractical.
[0034] To solve this technical problem, this utility model provides a syringe disassembly and assembly assembly and a syringe, which are applied to syringes.
[0035] For details, please refer to Figures 1-4 The syringe assembly / disassembly components specifically include:
[0036] The syringe body 1 has a suction part 2 at its top. The suction part 2 consists of a connecting tube 201 and a nipple 202. A disassembly part 3 is provided between the connecting tube 201 and the syringe body 1. The disassembly part 3 is used to fix the connecting tube 201 and the syringe body 1. A needle is attached to the nipple 202. The needle can also slightly puncture the wound for better suction.
[0037] The syringe assembly and syringe provided by this utility model, through the set assembly and disassembly part, can fix the syringe body and the suction part under the action of the internal and external thread grooves of the assembly and disassembly part. The nipple of the suction part can be used to aspirate venom from small wounds. The suction part can be removed, and through the syringe body, in conjunction with the rubber layer of the assembly and disassembly part, venom from large wounds can be aspirated. With this setting, it can be applied to wounds of different sizes, thus improving its practicality.
[0038] To enable those skilled in the art to better understand the present invention, the technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the accompanying drawings.
[0039] It should be noted that, unless otherwise specified, the embodiments and features and technical solutions in the present invention can be combined with each other.
[0040] It should be noted that similar labels and letters in the following figures indicate similar items. Therefore, once an item is defined in one figure, it does not need to be further defined and explained in subsequent figures.
[0041] Example 1
[0042] Please refer to Figures 1-3 A syringe assembly is provided, wherein the bottom end of the nipple 202 is fixedly connected to the middle part of the top end of the connecting tube 201, and the interior of the nipple 202 communicates with the interior of the connecting tube 201, and the bottom end of the connecting tube 201 is open, so that venom from small wounds can be drawn through the nipple 202.
[0043] Please refer to Figures 1-3 A syringe disassembly and assembly assembly includes a disassembly and assembly part 3 consisting of a rubber layer 301. The rubber layer 301 allows for a seal between the connecting cylinder 201 and the syringe body 1. The bottom end of the connecting cylinder 201 has an internal threaded groove 302, and the top end of the syringe body 1 has an external threaded groove 303 that matches the internal threaded groove. The bottom end of the rubber layer 301 is fixedly connected to the top end of the syringe body 1, and the top end of the rubber layer 301 is in contact with the top end of the internal threaded groove 302. The internal threaded groove 302 and the external threaded groove 303 allow for a fixed connection between the connecting cylinder 201 and the syringe body 1.
[0044] Example 2
[0045] The syringe assembly / disassembly component provided in Example 1 has been further optimized, specifically, as follows: Figures 1-4 As shown, a syringe includes a piston 4, which is disposed in a cavity formed by a syringe body 1 and a connecting tube 201. A piston rod 5 is fixedly provided at the bottom end of the piston 4, and a limit mechanism 6 is provided between the piston rod 5 and the syringe body 1.
[0046] Furthermore, such asFigure 3 As shown, the limiting mechanism 6 consists of a first limiting part and a second limiting part.
[0047] Example 3
[0048] The syringe provided in Example 1 or 2 is further optimized, specifically, as follows: Figures 3-4 As shown, the first limiting part consists of two limiting blocks 601 and two limiting members 602.
[0049] Furthermore, such as Figures 3-4 As shown, one side of each of the two limiting blocks 601 is fixedly connected to the bottom of the two sides inside the syringe body 1. An L-shaped groove is opened in the other side of the limiting block 601. One side of the limiting member 602 is fixedly installed at one end of the L-shaped groove. The limiting member 602 is made of a material with a certain degree of toughness.
[0050] Furthermore, such as Figures 3-4 As shown, the second limiting part consists of two slide rods 603. One side of each slide rod 603 is fixedly connected to both sides of the piston rod 5. The slide rod 603 is inserted into the other end of the L-shaped groove. Several limiting grooves matching the limiting member 602 are equidistantly opened on the other side of the slide rod 603.
[0051] Example 4
[0052] The syringes provided in the above embodiments are further optimized, such as... Figures 1-3 As shown, the syringe body 1 has a scale 7, which has two sizes: 10 ml and 20 ml, to accommodate different snake bite wounds.
[0053] The following is the usage process of the syringe disassembly and assembly assembly and the syringe provided by this utility model:
[0054] When treating small wounds, the nipple 202 is placed over the wound, and the piston rod 5 is pulled. The piston rod 5 moves the piston 4, which draws in the venom from the wound. At the same time, the piston rod 5 moves the slide rod 603, which lifts the limiting member 602. The slide rod 603 continues to move, and the limiting member 602 springs back into the next limiting groove. Under the action of the limiting groove, the limiting member 602 is held in place, preventing the piston rod 5 from being sucked back. In this way, the piston rod 5 can be fixed after it has moved, preventing it from being sucked back. When treating large wounds, the connecting cylinder 201 can be removed from the syringe body 1 through the internal thread groove 302 and the external thread groove 303. The end of the syringe body 1 with the rubber layer 301 is placed over the large wound, and the piston rod 5 is pulled to draw in the venom.
[0055] In this utility model, unless otherwise explicitly specified and limited, the terms "installation," "connection," "joining," and "fixing," etc., should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral part; they can refer to a mechanical connection, an electrical connection, or a connection that allows communication between them; they can refer to a direct connection or an indirect connection through an intermediate medium; they can refer to the internal communication of two components or the interaction between two components, unless otherwise explicitly limited. Those skilled in the art can understand the specific meaning of the above terms in this utility model according to the specific circumstances.
[0056] Obviously, the embodiments described above are only some embodiments of this utility model, not all embodiments. The accompanying drawings show preferred embodiments of this utility model, but do not limit the patent scope of this utility model. This utility model can be implemented in many different forms; rather, the purpose of providing these embodiments is to provide a more thorough and comprehensive understanding of the disclosure of this utility model. Although this utility model has been described in detail with reference to the foregoing embodiments, those skilled in the art can still modify the technical solutions described in the foregoing specific embodiments, or make equivalent substitutions for some of the technical features. Any equivalent structures made using the content of this utility model specification and drawings, directly or indirectly applied to other related technical fields, are similarly within the patent protection scope of this utility model.
Claims
1. A syringe disassembly and assembly assembly, characterized in that, The syringe body (1) includes a suction part (2) at the top of the syringe body (1). The suction part (2) is composed of a connecting tube (201) and a nipple (202). A disassembly part (3) is provided between the connecting tube (201) and the syringe body (1). The disassembly part (3) is used to fix the connecting tube (201) and the syringe body (1).
2. The syringe assembly / disassembly component according to claim 1, characterized in that, The bottom end of the nipple (202) is fixedly connected to the middle of the top end of the connecting tube (201), and the inside of the nipple (202) is connected to the inside of the connecting tube (201), and the bottom end of the connecting tube (201) is open.
3. A syringe assembly / disassembly component according to claim 2, characterized in that, The disassembly / assembly part (3) is a rubber layer (301). The bottom end of the connecting cylinder (201) is provided with an internal thread groove (302). The top end of the outer side of the syringe body (1) is provided with an external thread groove (303) that matches the internal thread groove. The bottom end of the rubber layer (301) is fixedly connected to the top end of the syringe body (1), and the top end of the rubber layer (301) is in contact with the top end of the internal thread groove (302).
4. A syringe using a syringe barrel assembly as described in claim 3, characterized in that, Includes a piston (4), which is disposed in a cavity formed by the syringe body (1) and the connecting cylinder (201). A piston rod (5) is fixedly provided at the bottom end of the piston (4), and a limit mechanism (6) is provided between the piston rod (5) and the syringe body (1).
5. A syringe according to claim 4, characterized in that, The limiting mechanism (6) consists of a first limiting part and a second limiting part.
6. A syringe according to claim 5, characterized in that, The first limiting part consists of two limiting blocks (601) and two limiting members (602).
7. A syringe according to claim 6, characterized in that, One side of each of the two limiting blocks (601) is fixedly connected to the bottom of the two sides of the syringe body (1), and an L-shaped groove is provided on the other side of the limiting block (601). One side of the limiting member (602) is fixedly installed at one end of the L-shaped groove.
8. A syringe according to claim 7, characterized in that, The second limiting part consists of two slide rods (603). One side of each slide rod (603) is fixedly connected to both sides of the piston rod (5). The slide rod (603) is inserted into the other end of the L-shaped groove. The other side of the slide rod (603) is provided with several limiting grooves that match the limiting member (602) at equal intervals.
9. A syringe according to claim 8, characterized in that, The syringe body (1) is provided with a scale (7).