Medical instrument box
By designing a detachable protective shell structure and an internal support mesh, combined with disinfectant expansion rinsing, the problem of bacteria being difficult to clean from the gaps in existing medical device boxes has been solved, achieving convenient and efficient cleaning and protection.
Patent Information
- Application Number
- CN202422950193.9
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-12-02
- Publication Date
- 2026-01-23
- Estimated Expiration
- 2034-12-02
Smart Images

Figure CN223817664U_ABST
Abstract
Description
Technical Field
[0001] This utility model belongs to the field of medical device box technology, and specifically relates to a medical device box. Background Technology
[0002] Medical device cases are used to hold and protect medical devices. For sharp medical devices, protective pads are attached to the inner wall to prevent the sharp ends of the medical devices from colliding with and being damaged by the metal body of the medical device case. However, when the inner protective pads come into contact with the sharp ends of the medical devices, they can be punctured or scratched. The scratches left behind can gather together due to the structure or elasticity of the protective pads themselves, forming tiny gaps that are prone to bacterial growth. When using disinfectant to clean and disinfect the medical device case, the disinfectant has difficulty penetrating into the narrow gaps, making it difficult to clean the bacteria inside the gaps and causing contamination of the medical devices. Utility Model Content
[0003] This invention provides a medical device box that enables more convenient and efficient cleaning of the inner walls of scratched crevices.
[0004] This utility model provides the following technical solution: a medical device box, including a medical device box body, a lower thin-walled protective shell detachably connected to the medical device box body, an upper thin-walled protective shell detachably connected to the top of the lower thin-walled protective shell, an instrument placement protrusion fixedly connected to the inner wall of the bottom end of the upper thin-walled protective shell, an inner support mesh fixedly connected to the inner walls of the lower thin-walled protective shell, the upper thin-walled protective shell and the instrument placement protrusion, an input pipe fixedly connected to one side of the upper thin-walled protective shell, and a clearance groove provided at the top of the instrument placement protrusion.
[0005] The medical device box has a connecting groove plate fixedly connected to its inner wall, and a limit strip fixedly connected to the inner wall at the bottom of the medical device box.
[0006] The lower thin-walled protective shell has a locking positioning strip fixedly connected to its side wall, and the locking positioning strip is inserted into the connecting groove plate.
[0007] The upper thin-walled protective shell has a snap-fit connecting strip fixedly connected to its side wall, and the snap-fit connecting strip is detachably connected to the snap-fit positioning strip.
[0008] The locking positioning strip has a sealing locking groove at its top, and the locking connecting strip has a sealing plug ring fixedly connected to its bottom end. The sealing plug ring is inserted into the sealing locking groove.
[0009] The bottom end of the lower thin-walled protective shell is fixedly connected to a positioning locking strip, which is inserted into the limiting strip.
[0010] The medical device box has a detachable sealing cover at the top.
[0011] The beneficial effects of this utility model are as follows: The hollow protective liner inside the medical device housing, formed by the lower thin-walled protective shell, upper thin-walled protective shell, instrument placement protrusion, and inner support mesh, can protect the sharp parts of the medical device. Furthermore, injecting disinfectant into the lower thin-walled protective shell, upper thin-walled protective shell, and instrument placement protrusion through the inlet pipe allows for rapid inspection to check whether these structures have been scratched. The disinfectant can also be used to expand and rinse any scratches, making it more convenient and efficient to clean the inner walls of any scratches. Additionally, the separate design of the lower and upper thin-walled protective shells facilitates wiping and drying of the disinfectant adhering to the inner walls of these structures, including the instrument placement protrusion and inner support mesh.
[0012] The parts of the device not covered herein are the same as or can be implemented using existing technologies. Attached Figure Description
[0013] Figure 1 This is a schematic diagram of the structure of this utility model;
[0014] Figure 2 for Figure 1 Enlarged view of section A;
[0015] Figure 3 This is a top view of the present invention;
[0016] Figure 4 This is a schematic diagram of the connecting groove plate and the positioning locking strip in this utility model.
[0017] In the diagram: 1. Medical device housing; 11. Connecting groove plate; 12. Limiting strip; 2. Lower thin-walled protective shell; 21. Upper thin-walled protective shell; 22. Device placement protrusion; 23. Inner support grid; 24. Input pipe; 25. Leaving groove; 26. Engaging positioning strip; 261. Sealing engagement groove; 27. Engaging connecting strip; 271. Sealing plug ring; 3. Positioning engagement strip; 4. Sealing cover. Detailed Implementation
[0018] Please see Figures 1-4The present invention provides the following technical solution: a medical device box, including a medical device box body 1, a lower thin-walled protective shell 2 detachably connected inside the medical device box body 1, an upper thin-walled protective shell 21 detachably connected to the top of the lower thin-walled protective shell 2, an instrument placement protrusion 22 fixedly connected to the inner wall of the bottom end of the upper thin-walled protective shell 21, an inner support grid 23 fixedly connected to the inner walls of the lower thin-walled protective shell 2, the upper thin-walled protective shell 21 and the instrument placement protrusion 22, an input pipe 24 fixedly connected to one side of the upper thin-walled protective shell 21, and a clearance groove 25 provided at the top of the instrument placement protrusion 22.
[0019] In this implementation plan: the medical device housing 1 serves as an outer support protective shell. The operator inserts the positioning locking strip 3 into the limiting strip 12, and the locking positioning strip 26 into the connecting groove plate 11. The connecting groove plate 11 and the limiting strip 12 position the lower thin-walled protective shell 2. Then, the operator installs the upper thin-walled protective shell 21 on top of the lower thin-walled protective shell 2, aligning the locking connecting strip 27 with the locking positioning strip 26. The sealing plug ring 271 is inserted into the locking positioning strip 26, and the medical device is aligned and locked within the clearance groove 25. This is achieved with the assistance of the lower thin-walled protective shell 2, the upper thin-walled protective shell 21, the device placement protrusion 22, and the inner support mesh. The grating 23, in conjunction with the inner hollow protective liner of the medical device housing 1, protects the sharp parts of the medical device. When inspecting the lower thin-walled protective shell 2, upper thin-walled protective shell 21, and device placement protrusion 22, the operator uses a syringe aligned with the input tube 24. Disinfectant is injected into the internal space of the lower thin-walled protective shell 2, upper thin-walled protective shell 21, and device placement protrusion 22 using the syringe. When these structures are scratched, the disinfectant is slowly squeezed out from the wound under pressure, expanding and rinsing the scratched area during the process, making inspection more convenient. To efficiently clean the inner walls of the scratched crevices, staff can determine whether the lower thin-walled protective shell 2, upper thin-walled protective shell 21, and instrument placement protrusion 22 have been scratched by observing whether disinfectant has overflowed from their surfaces. Since the lower thin-walled protective shell 2, upper thin-walled protective shell 21, and instrument placement protrusion 22 are all thin-walled structures, their sidewalls are more easily scratched when punctured or scratched by sharp objects. The inner support mesh 23 provides support for the lower thin-walled protective shell 2, upper thin-walled protective shell 21, and instrument placement protrusion 22, ensuring the smooth operation of the structure. Even when scratched, the instrument placement protrusion 22 can still maintain its shape to protect the instrument. With the help of a convenient and efficient disinfection method, the lower thin-walled protective shell 2, the upper thin-walled protective shell 21, and the instrument placement protrusion 22 can still be reused when scratched. When the lower thin-walled protective shell 2, the upper thin-walled protective shell 21, and the instrument placement protrusion 22 are scratched in multiple places and cannot be used, new parts can be replaced. After disinfection, the lower thin-walled protective shell 2 and the upper thin-walled protective shell 21 can be disassembled to facilitate wiping and drying of the disinfectant solution adhering to the inner walls of the lower thin-walled protective shell 2, the upper thin-walled protective shell 21, the instrument placement protrusion 22, and the inner support mesh 23.
[0020] A connecting groove plate 11 is fixedly connected to the inner wall of the medical device box 1, and a limiting strip 12 is fixedly connected to the inner wall of the bottom end of the medical device box 1. By setting the connecting groove plate 11 and the limiting strip 12 together, the lower thin-walled protective shell 2 can be positioned so that the lower thin-walled protective shell 2 can be stably installed in the medical device box 1.
[0021] A snap-fit positioning strip 26 is fixedly connected to the side wall of the lower thin-walled protective shell 2. The snap-fit positioning strip 26 is inserted into the connecting groove plate 11. By setting the snap-fit positioning strip 26, it can cooperate with the connecting groove plate 11 to position the edge of the lower thin-walled protective shell 2. During installation, the staff squeezes the snap-fit positioning strip 26 to insert it into the connecting groove plate 11.
[0022] The upper thin-walled protective shell 21 is fixedly connected to a snap-fit connecting strip 27 on its side wall. The snap-fit connecting strip 27 is detachably connected to the snap-fit positioning strip 26. By setting the snap-fit connecting strip 27, the connection between the upper thin-walled protective shell 21 and the lower thin-walled protective shell 2 can be facilitated. The snap-fit connecting strip 27 and the snap-fit positioning strip 26 are in contact.
[0023] The top of the locking positioning strip 26 has a sealing locking groove 261, and the bottom of the locking connecting strip 27 is fixedly connected to a sealing plug ring 271, which is inserted into the sealing locking groove 261. By setting the sealing locking groove 261 and the sealing plug ring 271, the connection between the lower thin-walled protective shell 2 and the upper thin-walled protective shell 21 can be facilitated. The sealing locking groove 261 and the sealing plug ring 271 can play a sealing role, so that when the staff injects disinfectant into the lower thin-walled protective shell 2, the upper thin-walled protective shell 21 and the instrument placement protrusion 22, the disinfectant will not overflow from the gap between the lower thin-walled protective shell 2 and the upper thin-walled protective shell 21.
[0024] A positioning locking strip 3 is fixedly connected to the bottom end of the lower thin-walled protective shell 2. The positioning locking strip 3 is inserted into the limiting strip 12. By setting the positioning locking strip 3, the connection between the lower thin-walled protective shell 2 and the limiting strip 12 can be facilitated. The positions of the positioning locking strip 3 and the limiting strip 12 correspond.
[0025] The top of the medical device box 1 is detachably connected to a sealing cover 4; by setting the sealing cover 4, the opening at the top of the medical device box 1 can be sealed, thus playing a protective role.
[0026] The working principle and usage process of this utility model are as follows: The operator inserts the positioning locking strip 3 into the limiting strip 12, and the locking positioning strip 26 into the connecting groove plate 11. The connecting groove plate 11 and the limiting strip 12 position the lower thin-walled protective shell 2. Then, the operator installs the upper thin-walled protective shell 21 on top of the lower thin-walled protective shell 2. The locking connecting strip 27 aligns with the locking positioning strip 26, and the sealing plug ring 271 is inserted into the locking positioning strip 26. The medical device is then aligned and locked within the clearance groove 25. The medical device housing 1, consisting of a lower thin-walled protective shell 2, an upper thin-walled protective shell 21, an instrument placement protrusion 22, and an inner support mesh 23, forms a hollow protective liner that protects the sharp parts of the medical device. When inspecting the lower thin-walled protective shell 2, upper thin-walled protective shell 21, and instrument placement protrusion 22, the operator uses a syringe aligned with the input tube 24 and injects disinfectant into the internal space of these structures. When these structures are scratched, the disinfectant is slowly squeezed out under pressure, expanding and rinsing the scratched area. This allows for more convenient and efficient cleaning of the inner walls of the scratched areas. The operator can determine the presence of disinfectant overflow by observing whether it has overflowed from the surfaces of the lower thin-walled protective shell 2, upper thin-walled protective shell 21, and instrument placement protrusion 22. Whether or not it is scratched, it can still be used again if the lower thin-walled protective shell 2, the upper thin-walled protective shell 21 and the instrument placement protrusion 22 are scratched. If the lower thin-walled protective shell 2, the upper thin-walled protective shell 21 and the instrument placement protrusion 22 are scratched in multiple places and cannot be used, new parts should be replaced. After disinfection, the lower thin-walled protective shell 2 and the upper thin-walled protective shell 21 are disassembled, and the disinfectant attached to the inner wall of the lower thin-walled protective shell 2, the upper thin-walled protective shell 21, the instrument placement protrusion 22 and the inner support grid 23 is wiped and dried.
Claims
1. A medical device box, comprising a medical device box body (1), characterized in that: The medical device housing (1) is detachably connected to a lower thin-walled protective shell (2). The top of the lower thin-walled protective shell (2) is detachably connected to an upper thin-walled protective shell (21). The inner wall of the bottom end of the upper thin-walled protective shell (21) is fixedly connected to a device placement protrusion (22). The inner walls of the lower thin-walled protective shell (2), the upper thin-walled protective shell (21), and the device placement protrusion (22) are all fixedly connected to an inner support grid (23). An input pipe (24) is fixedly connected to one side of the upper thin-walled protective shell (21). The top of the device placement protrusion (22) is provided with a clearance groove (25).
2. A medical device box according to claim 1, characterized in that: The inner wall of the medical device box (1) is fixedly connected with a connecting groove plate (11), and the bottom inner wall of the medical device box (1) is fixedly connected with a limit strip (12).
3. A medical device box according to claim 2, characterized in that: The lower thin-walled protective shell (2) has a locking positioning strip (26) fixedly connected to its side wall, and the locking positioning strip (26) is inserted into the connecting groove plate (11).
4. A medical device box according to claim 3, characterized in that: The upper thin-walled protective shell (21) has a snap-fit connecting strip (27) fixedly connected to its side wall, and the snap-fit connecting strip (27) is detachably connected to the snap-fit positioning strip (26).
5. A medical device box according to claim 4, characterized in that: The top of the engagement positioning strip (26) is provided with a sealing engagement groove (261), and the bottom of the engagement connecting strip (27) is fixedly connected with a sealing plug ring (271), which is inserted into the sealing engagement groove (261).
6. A medical device box according to claim 5, characterized in that: The bottom end of the lower thin-walled protective shell (2) is fixedly connected to a positioning locking strip (3), which is inserted into the limiting strip (12).
7. A medical device box according to claim 1, characterized in that: The top of the medical device box (1) is detachably connected to a sealing cover (4).