Early diagnosis kit for cervical cancer
By introducing a positioning hole, a moving block, and a supporting spring structure into the early cervical cancer diagnostic kit, combined with a sterilization component, the problems of test tube shaking and contamination have been solved, achieving stable positioning and sterilization functions, and improving the safety and convenience of use.
Patent Information
- Application Number
- CN202422648209.0
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-10-31
- Publication Date
- 2025-11-11
- Estimated Expiration
- 2034-10-31
AI Technical Summary
In existing early cervical cancer diagnostic kits, the test tubes are prone to shaking and are inconvenient to handle, and are easily contaminated after opening, leading to a high risk of cross-infection.
A reagent kit comprising a box body and a lid has been designed, with a lower filling layer and an upper filling layer inside. The reagent tubes are stably positioned and easily placed and removed through positioning holes, moving blocks and supporting springs. It is also equipped with a sterilization component to sterilize the inside of the box when the lid is closed.
It achieves stable positioning and convenient handling of test reagent tubes, avoiding contamination and cross-infection, and improving safety and convenience of use.
Smart Images
Figure CN223533924U_ABST
Abstract
Description
Technical Field
[0001] This utility model relates to the field of medical device technology, and in particular to a cervical cancer early diagnostic kit. Background Technology
[0002] Cervical cancer is a common gynecological malignancy, ranking second only to breast cancer in incidence among gynecological tumors. In recent years, the clinical incidence of cervical cancer has shown an increasing trend, and the affected population is gradually becoming younger, posing a serious threat to the physical and mental health of women. The occurrence of cervical cancer is closely related to multiple factors, such as early marriage, early childbirth, multiple pregnancies, and promiscuous sexual activity. For the sake of women's physical and mental health, early diagnosis and screening for cervical cancer are necessary to reduce its incidence and mortality.
[0003] In existing technologies, early diagnosis of cervical cancer usually involves regular testing using test kits. The test kit tubes are typically placed inside the test kit. However, to prevent the test kit tubes from moving around, they are usually secured in a protective layer inside the kit. This makes it inconvenient to remove and place the test kit tubes. Furthermore, since multiple test kit tubes are usually placed inside the kit, opening the lid can easily introduce viruses and bacteria, causing other test kit tubes to become contaminated. Therefore, a test kit that solves the above problems is needed. Utility Model Content
[0004] To address the problems in existing technologies where test tubes are typically secured in a protective layer within the kit to prevent them from shifting, making them inconvenient to handle, and the fact that multiple test tubes are usually placed inside the kit, allowing viruses and bacteria to easily enter after opening the lid, causing other test tubes to become contaminated and prone to re-contamination upon reuse, a new cervical cancer early diagnosis kit has been invented.
[0005] The technical solution of this utility model includes a box body and a box lid. The box body and box lid are respectively provided with a lower filling layer and an upper filling layer. The lower filling layer has several positioning holes, and a test reagent tube is inserted into each positioning hole. A movable hole is provided at the bottom of each positioning hole, and a movable block is movably connected within the movable hole. The bottom of the test reagent tube is inserted into the movable block, and a support spring is connected to the bottom of the movable block. Several positioning heads are connected inside the box lid, and a disinfection component is connected to each positioning head. When the box lid is closed, the disinfection component abuts against the test reagent tube, pressing the test reagent tube into the positioning hole. Simultaneously, the disinfection component can disinfect the inside of the box.
[0006] Preferably, the movable block has a lower insertion hole, and the test reagent tube is inserted into the lower insertion hole.
[0007] Preferably, the upper filling layer has a plurality of upper insertion holes, which are located between the positioning heads, so that when the box cover is opened, the test reagent tube can be inserted into the upper insertion hole to achieve temporary positioning of the test reagent tube.
[0008] Preferably, the disinfection assembly includes an airbag, a connector, a sealing cap, an infusion tube, and an atomizing nozzle. The positioning head has a threaded connection hole at one end away from the box cover. The connector is threaded into the threaded connection hole. The airbag is connected to the connector. The sealing cap is snapped onto the connector. One end of the infusion tube extends through the sealing cap into the airbag, and the other end is connected to the atomizing nozzle.
[0009] Preferably, the outlet of the atomizing nozzle extends into the upper insertion hole, so that when the air bag is compressed, the disinfectant inside the air bag is sprayed from the atomizing nozzle into the upper insertion hole through the infusion tube, and diffuses into the box body through the upper insertion hole.
[0010] The following beneficial effects can be achieved by adopting the technical solution of this utility model: (1) Through the lower filling layer, the upper filling layer and the positioning hole, it is convenient to insert the test reagent tube into the positioning hole, and then use the flexible upper filling layer and the lower filling layer to protect the test reagent tube; (2) Through the moving block and the support spring, the test reagent tube can be pressed into the lower filling layer when the box is closed to protect the test reagent tube. After the box is opened, the test reagent tube is pushed out of the lower filling layer under the elastic force of the support spring, which is convenient for taking and putting away the test reagent tube; (3) Through the positioning head and the disinfection component, the disinfection component abuts against the test reagent tube after the box is closed, pressing the test reagent tube into the positioning hole. At the same time, the disinfection component can be used to disinfect the box; (4) Through the upper insertion hole, it is convenient to insert the test reagent tube into the upper insertion hole after the box is opened, and the test reagent tube can be temporarily positioned. This has a wide range of application prospects in the field of medical device technology. Attached Figure Description
[0011] Figure 1 This is a cross-sectional view of the cervical cancer early diagnostic kit of this invention.
[0012] Figure 2 for Figure 1 Enlarged view of a portion of region A in the middle.
[0013] The components are as follows: 1. Box body, 2. Box cover, 3. Lower filling layer, 4. Positioning hole, 5. Test reagent tube, 6. Moving hole, 7. Moving block, 8. Lower insertion hole, 9. Support spring, 10. Upper filling layer, 11. Upper insertion hole, 12. Positioning head, 13. Threaded connection hole, 14. Connector, 15. Airbag, 16. Sealing cap, 17. Infusion tube, 18. Atomizing nozzle. Detailed Implementation
[0014] The technical solutions of various embodiments of this utility model will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only some embodiments of this utility model, and not all embodiments. Based on the embodiments of this utility model, all other embodiments obtained by those skilled in the art without creative effort are within the scope of protection of this utility model. In the description of this utility model, it should be noted that the terms "center", "upper", "lower", "left", "right", "vertical", "horizontal", "inner", "outer", etc., indicate the orientation or positional relationship based on the orientation or positional relationship shown in the accompanying drawings, and are only for the convenience of describing this utility model and simplifying the description, and do not indicate or imply that the device or element referred to must have a specific orientation, or be constructed and operated in a specific orientation, and therefore should not be construed as a limitation of this utility model.
[0015] Furthermore, the terms "first," "second," and "third" are used for descriptive purposes only and should not be construed as indicating or implying relative importance. In the description of this utility model, it should be noted that, unless otherwise explicitly specified and limited, the terms "installation," "connection," and "joining" should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral connection; they can refer to a mechanical connection or an electrical connection; they can refer to a direct connection or an indirect connection through an intermediate medium; and they can refer to the internal connection of two components. Those skilled in the art can understand the specific meaning of the above terms in this utility model based on the specific circumstances.
[0016] This application discloses a reagent kit for early diagnosis of cervical cancer. (Refer to...) Figure 1 The box includes a box body 1 and a lid 2. The lid 2 is hinged to the opening of the box body 1, connecting the box body 1 and the lid 2 together. This allows the box body 1 to be opened and closed by opening and closing the lid 2. A bag lock is detachably fixed to the ends of the box body 1 and the lid 2 away from the hinge by bolts. This lock prevents the lid 2 from opening automatically. The hinge and bag lock are common types of hinges and locks that can only rotate 90°.
[0017] Reference Figure 1 The box body 1 and the box cover 2 are respectively provided with a lower filling layer 3 and an upper filling layer 10. The lower filling layer 3 has several positioning holes 4, and a test reagent tube 5 is inserted into the positioning holes 4. The upper filling layer 10 and the lower filling layer 3 are made of medical rubber, flexible medical polyurethane foam or movable sponge material, which can facilitate the isolation and protection of the test reagent tube 5 through the positioning holes 4 and the lower filling layer 3 and the upper filling layer 10, so as to avoid damage to the test reagent tube 5.
[0018] Reference Figure 1 A movable hole 6 is provided at the bottom of the positioning hole 4, and a movable block 7 is movably connected within the movable hole 6, allowing the movable block 7 to move up and down within it. The bottom of the test reagent tube 5 is inserted into the movable block 7. Specifically, the movable block 7 has a lower insertion hole 8, and the test reagent tube 5 is inserted into the lower insertion hole 8, connecting the test reagent tube 5 and the movable block 7 together, allowing them to move simultaneously within the movable hole 6. A support spring 9 is connected to the bottom of the movable block 7, providing elasticity to the movable block 7. When the lid 2 is opened, the elasticity of the support spring 9 can push the movable block 7 and part of the test reagent tube 5 out of the positioning hole 4, facilitating the removal and placement of the test reagent tube 5 without affecting the protection of the test reagent tube 5 by the lower filling layer 3.
[0019] Reference Figure 1 , Figure 2 The lid 2 is integrally formed or hot-melt welded with several positioning heads 12, which are connected to the inner end face of the lid 2, allowing them to move simultaneously relative to the box body 1. The positioning heads 12 correspond to the positioning holes 4, so that when the lid 2 is closed, the positioning heads 12 can press the test reagent tube 5 inside the positioning hole 4 into the positioning hole 4. A sterilization component is connected to the positioning head 12, so that when the lid 2 is closed, the sterilization component abuts against the test reagent tube 5, pressing the test reagent tube 5 into the positioning hole 4, while simultaneously sterilizing the inside of the box body 1 using the sterilization component.
[0020] Reference Figure 1 , Figure 2The disinfection assembly includes an airbag 15, a connector 14, a sealing cap 16, an infusion tube 17, and an atomizing nozzle 18. A threaded connection hole 13 is provided at the end of the positioning head 12 furthest from the cover 2. The connector 14 is threaded into the threaded connection hole 13. The airbag 15 is heat-sealed and fixedly connected to the connector 14, thus connecting the airbag 15 and the connector 14 together. This allows the airbag 15 to be stored in the positioning head 12, while simultaneously preventing the airbag 15 from contacting the test reagent tube 5 and avoiding damage to the test reagent tube 5 by the positioning head 12. The sealing cap 16 is snapped onto the end of the connector 14 furthest from the airbag 15, sealing the opening of the connector 14 and preventing leakage of disinfectant from the airbag 15. One end of the infusion tube 17 extends through the sealing cap 16 into the air bladder 15, and the other end is connected to the atomizing nozzle 18. When the lid 2 is closed, the air bladder 15 contacts the test reagent tube 5. As the test reagent tube 5 is pressed downwards, the air bladder 15 is also compressed, allowing the disinfectant inside the air bladder 15 to be delivered through the infusion tube 17 to the atomizing nozzle 18, where it is atomized and sprayed out. The outlet of the atomizing nozzle 18 extends into the upper insertion hole 11, so that when the air bladder 15 is compressed, the disinfectant inside the air bladder 15 is sprayed through the infusion tube 17 from the atomizing nozzle 18 into the upper insertion hole 11, and then diffuses into the box body 1.
[0021] Reference Figure 1 , Figure 2 The upper filling layer 10 has several upper insertion holes 11, which are located between the positioning heads 12. This allows the test reagent tube 5 to be inserted into the upper insertion hole 11 after the box cover 2 is opened, so that the test reagent tube 5 can be temporarily positioned and placed. This facilitates the temporary placement of the test reagent tube 5 through the upper insertion hole 11, which is convenient for screening and detecting cervical cancer.
[0022] Unless otherwise specified, the equipment components involved in the above embodiments are all conventional equipment components, and the structural settings, working methods or control methods involved are all conventional settings, working methods or control methods in the art unless otherwise specified.
[0023] The embodiments described above are merely illustrative of several implementations of this utility model, and while the descriptions are relatively specific and detailed, they should not be construed as limiting the scope of the utility model patent. It should be noted that those skilled in the art can make various modifications and improvements without departing from the concept of this utility model, and these all fall within the protection scope of this utility model. Therefore, the protection scope of this utility model patent should be determined by the appended claims.
Claims
1. A cervical cancer early diagnostic kit, comprising a box body (1) and a box cover (2), characterized in that, The box body (1) and the lid (2) are respectively provided with a lower filling layer (3) and an upper filling layer (10). The lower filling layer (3) is provided with a plurality of positioning holes (4). A test reagent tube (5) is inserted into the positioning hole (4). A moving hole (6) is provided at the bottom of the positioning hole (4). A moving block (7) is movably connected in the moving hole (6). The bottom of the test reagent tube (5) is inserted into the moving block (7). A support spring (9) is connected to the bottom of the moving block (7). A plurality of positioning heads (12) are connected in the lid (2). A disinfection component is connected to the positioning head (12). When the lid (2) is closed, the disinfection component abuts against the test reagent tube (5) and presses the test reagent tube (5) into the positioning hole (4). At the same time, the disinfection component can be used to disinfect the inside of the box body (1).
2. The cervical cancer early diagnostic kit according to claim 1, characterized in that, The movable block (7) has a lower insertion hole (8), and the test reagent tube (5) is inserted into the lower insertion hole (8).
3. The cervical cancer early diagnostic kit according to claim 1, characterized in that, The upper filling layer (10) has several upper insertion holes (11) located between the positioning heads (12), so that when the box cover (2) is opened, the test reagent tube (5) can be inserted into the upper insertion hole (11) to achieve temporary positioning of the test reagent tube (5).
4. The cervical cancer early diagnostic kit according to claim 3, characterized in that, The disinfection assembly includes an airbag (15), a connector (14), a sealing cap (16), an infusion tube (17), and an atomizing nozzle (18). The positioning head (12) has a threaded connection hole (13) at one end away from the box cover (2). The connector (14) is threaded into the threaded connection hole (13). The airbag (15) is connected to the connector (14). The sealing cap (16) is snapped onto the connector (14). One end of the infusion tube (17) extends through the sealing cap (16) into the airbag (15), and the other end is connected to the atomizing nozzle (18).
5. The cervical cancer early diagnostic kit according to claim 4, characterized in that, The outlet of the atomizing nozzle (18) extends into the upper insertion hole (11), so that when the air bag (15) is compressed, the disinfectant in the air bag (15) is sprayed from the atomizing nozzle (18) into the upper insertion hole (11) through the infusion tube (17), and diffuses into the box body (1) from the upper insertion hole (11).