Severe risk prediction sample collection device
By designing and combining components such as the outer shell of the placement box, the placement rack, the positioning ring, the sample tube, and the sealing sleeve, the problems of limiting and preserving the sample collection device were solved, achieving stable preservation and sealing of the sample, and improving the collection effect.
Patent Information
- Application Number
- CN202520249325.7
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2025-02-17
- Publication Date
- 2026-02-10
- Estimated Expiration
- 2035-02-17
AI Technical Summary
Existing critical illness risk prediction sample collection devices are not easy to limit when faced with different types of samples, which can easily lead to collisions and damage between samples.
A critical illness risk prediction sample collection device was designed, comprising a placement box shell, a placement rack, a positioning ring, sample tubes, a sealing sleeve, and a clamping assembly. Through the coordinated use of these components, the sample can be stably preserved and sealed, avoiding sample loss and collision.
It effectively prevents sample loss and collision during transportation, improves the stability and safety of sample collection, and enhances the collection effect.
Smart Images
Figure CN223888052U_ABST
Abstract
Description
Technical Field
[0001] This utility model belongs to the field of critical illness risk sample collection technology, specifically a critical illness risk prediction sample collection device. Background Technology
[0002] Severe illness risk prediction sample collection covers a variety of types, and different samples have different collection methods and precautions. For example, blood samples, respiratory samples, urine samples and other types of samples all require different collection methods.
[0003] Predicting the risk of severe illness requires comprehensive consideration of multiple factors such as the patient's clinical indicators, underlying diseases, age, and gender, and must be combined with technologies such as artificial intelligence and machine learning to achieve more accurate predictions and provide strong support for clinical treatment.
[0004] After prolonged use, it was found that the existing critical illness risk prediction sample collection device has an overly simplistic sample preservation method. It is not easy to limit the movement of different types of samples, which can easily cause collisions between samples, resulting in sample damage and failure.
[0005] Therefore, this utility model provides a sample collection device for predicting the risk of severe illness. Utility Model Content
[0006] In order to overcome the shortcomings of the prior art, at least one technical problem raised in the background art is solved.
[0007] The technical solution adopted by this utility model to solve its technical problem is as follows: A critical illness risk prediction sample collection device of this utility model includes a placement box shell. A placement rack is provided on the inner side wall of the placement box shell, and the placement rack is evenly distributed on the inner side wall of the placement box shell. A partition plate is installed on the inner side wall of the placement box shell. A positioning ring is provided at the bottom of the inner side wall of the placement box shell, and the positioning ring is evenly distributed at the bottom of the bottom of the inner side wall of the placement box shell. Sample tubes are slidably fitted in the middle of the placement rack, and the sample tubes are evenly distributed in the middle of the placement rack. A sealing sleeve is slidably fitted at the top of the sample tube. A clamping assembly is placed at the bottom of the inner side wall of the placement box shell. During operation, the positioning ring adapts to the sample collection device, the sample tubes preserve the collected samples, the sealing sleeve prevents leakage of the sample from inside the sample tubes, and the clamping assembly holds and fixes the bottom of the sample tubes to prevent sample loss during transport. The placement box shell, rack, and sample tubes allow for the placement and preservation of the collected critical illness prediction samples. The positioning ring adapts to different collection scenarios, and the sealing sleeve seals the samples collected in the sample tubes, enhancing the collection effect of the critical illness risk prediction sample collection device.
[0008] Preferably, the clamping assembly includes a placement ring, with a clamping frame fixedly connected to the top of the placement ring. The clamping frames are evenly distributed on the top of the placement ring, and the clamping frames are in sliding fit with the bottom of the sample tube. During operation, the placement ring and clamping frames can restrain the bottom of the sample tube when it is placed, preventing the sample tube from shaking and breaking when the outer shell of the placement box moves. The placement ring and clamping frames can stabilize the bottom of the sample tube when it is placed, preventing the sample tube from shaking, and further enhancing the sample protection and clamping stability effect of the critical illness risk prediction sample collection device.
[0009] Preferably, a limiting plate is fixed to the outer wall of the bottom of the sample tube. The limiting plates are evenly distributed on the outer wall of the bottom of the sample tube. A limiting groove is formed on the inner wall of the placement ring. The limiting groove and the limiting plate are in sliding fit. During operation, the bottom of the sample tube can be limited by the limiting plate and the limiting groove to prevent the bottom of the sample tube from falling off. The limiting plate and the limiting groove can limit the bottom of the sample tube, which further enhances the limiting stability effect of the critical illness risk prediction sample collection device.
[0010] Preferably, a spring is fixedly connected to the bottom of the inner sidewall of the placement ring; an ejector block is fixedly connected to the end of the spring, and the ejector block is in sliding fit with the inner sidewall of the placement ring. During operation, the sample tube can be ejected by the ejector block and the spring when the limiting plate is rotated to release the limiting position, which facilitates the use and removal of the sample tube. The ejector block and the spring can be used to eject the sample tube after the limiting position is released, which further enhances the portability of the critical illness risk prediction sample collection device.
[0011] Preferably, a protective sleeve is installed on the outer wall of the placement box shell. The protective sleeves are evenly distributed on the outer wall of the placement box shell. A rotating adjustment rod is installed in the middle of each protective sleeve. A suction cup is fixed to the bottom end of the rotating adjustment rod. During operation, the protective sleeve can block and protect the outer wall of the placement box shell. The placement height of the device can be adjusted by the rotating adjustment rod and the suction cup. The protective sleeve can block and protect the outer wall of the placement box shell. The placement height of the device can be adjusted by the rotating adjustment rod and the suction cup, which further enhances the protective and adjustment effect of the critical illness risk prediction sample collection device.
[0012] Preferably, the top of the placement box shell is slidably fitted with a top cover, the outer wall of the top cover is rotatably fitted with a grip, and the inner wall of the top cover is fixedly connected with a sealing gasket. The bottom of the sealing gasket has a placement groove, which is evenly distributed at the bottom of the sealing gasket. During operation, the top of the placement box shell can be sealed by the top cover, and the top cover can be easily opened by the grip. The sealing gasket and placement groove can limit and fix the placed sample tubes and sealing sleeves to avoid collisions caused by sliding. The top cover can seal the top of the placement box shell, and the sealing gasket and placement groove can make the seal of the top cover more complete. The grip can lift and open the top cover, further enhancing the sealing effect of the top of the critical illness risk prediction sample collection device.
[0013] Preferably, an observation plate is slidably fitted in the middle of the side wall of the placement box shell, and a control frame is fixedly connected to the side wall of the observation plate. During operation, the sample collection plate placed inside the placement box shell can be observed through the observation plate, and the position of the observation plate can be controlled through the control frame. The setting of the observation plate allows for observation of the sample collection inside the placement box shell, and the setting of the control frame allows for control of the position of the observation plate, further enhancing the sample observation effect of the critical illness risk prediction sample collection device.
[0014] The beneficial effects of this utility model are as follows:
[0015] 1. The critical illness risk prediction sample collection device of this utility model can store the collected critical illness prediction samples by setting up a box shell, a rack and sample tubes. The positioning ring can adapt to different collection scenarios. The sealing sleeve can seal the samples collected in the sample tubes and enhance the collection effect of the critical illness risk prediction sample collection device.
[0016] 2. The critical illness risk prediction sample collection device of this utility model can stabilize the bottom of the sample tube when it is placed by setting up a placement ring and a clamping frame, so as to avoid shaking of the sample tube and further enhance the sample protection and clamping stability effect of the critical illness risk prediction sample collection device. Attached Figure Description
[0017] The present invention will be further described below with reference to the accompanying drawings.
[0018] Figure 1 This is a perspective view of the present invention;
[0019] Figure 2 This is a schematic diagram of the sample tube structure in this utility model;
[0020] Figure 3 This is a schematic diagram of the limiting groove structure in this utility model;
[0021] Figure 4 This is a schematic diagram of the placement groove structure in this utility model.
[0022] In the diagram: 1. Placement box outer shell; 11. Placement rack; 12. Divider plate; 13. Positioning ring; 14. Sample tube; 15. Sealing sleeve; 2. Placement ring; 21. Clamping frame; 3. Limiting plate; 31. Limiting groove; 4. Ejection block; 41. Spring; 5. Protective sleeve; 51. Rotary adjustment rod; 52. Suction cup; 6. Top cover; 61. Holding frame; 62. Sealing gasket; 63. Placement groove; 7. Observation plate; 71. Control frame. Detailed Implementation
[0023] To make the technical means, creative features, objectives and effects of this utility model easier to understand, the present utility model will be further described below in conjunction with specific embodiments.
[0024] like Figures 1 to 4 As shown in the figure, a sample collection device for predicting the risk of severe illness according to an embodiment of the present invention includes a placement box shell 1. Placement racks 11 are provided on the inner sidewall of the placement box shell 1, and are evenly distributed on the inner sidewall. A partition plate 12 is installed on the inner sidewall of the placement box shell 1. Positioning rings 13 are provided at the bottom of the inner sidewall of the placement box shell 1, and are evenly distributed on the bottom of the inner sidewall. Sample tubes 14 are slidably fitted in the middle of the placement racks 11, and are evenly distributed in the middle of the placement racks 11. A sealing sleeve 15 is slidably fitted at the top of each sample tube 14. A clamping assembly is placed at the bottom of the inner sidewall of the placement box shell 1. During operation, the sample is collected by the positioning rings 13. The collection device is adapted to various configurations. The sample tube 14 can be used to preserve the collected samples. The sealing sleeve 15 can prevent the samples inside the sample tube 14 from leaking out. The clamping assembly can clamp and fix the bottom of the sample tube 14 to prevent sample loss during transportation. The placement box shell 1, placement rack 11 and sample tube 14 can be used to place and preserve the collected critical illness prediction samples. The positioning ring 13 can be adapted to different collection scenarios. The sealing sleeve 15 can seal the samples collected by the sample tube 14 to enhance the collection effect of the critical illness risk prediction sample collection device.
[0025] like Figures 2 to 3As shown, the clamping assembly includes a placement ring 2, with a clamping frame 21 fixedly attached to the top of the placement ring 2. The clamping frames 21 are evenly distributed on the top of the placement ring 2, and the clamping frames 21 are in sliding fit with the bottom of the sample tube 14. During operation, the placement ring 2 and the clamping frame 21 can restrain the bottom of the sample tube 14 when it is placed, preventing the sample tube 14 from shaking and breaking when the outer shell 1 of the placement box moves. The placement ring 2 and the clamping frame 21 can clamp and stabilize the bottom of the sample tube 14 when it is placed, preventing the sample tube 14 from shaking, and further enhancing the sample protection clamping and stabilization effect of the critical illness risk prediction sample collection device.
[0026] like Figure 3 As shown, a limiting plate 3 is fixed to the outer wall of the bottom of the sample tube 14. The limiting plates 3 are evenly distributed on the outer wall of the bottom of the sample tube 14. A limiting groove 31 is opened on the inner wall of the placement ring 2. The limiting groove 31 and the limiting plate 3 are in sliding fit. During operation, the bottom of the sample tube 14 can be limited by the limiting plate 3 and the limiting groove 31 to prevent the bottom of the sample tube 14 from falling off. The setting of the limiting plate 3 and the limiting groove 31 can limit the bottom of the sample tube 14, which further enhances the limiting stability effect of the critical illness risk prediction sample collection device.
[0027] like Figure 3 As shown, a spring 41 is fixedly connected to the bottom of the inner wall of the placement ring 2. A push-out block 4 is fixedly connected to the end of the spring 41. The push-out block 4 and the inner wall of the placement ring 2 are in sliding fit. During operation, the sample tube 14 can be pushed out by the push-out block 4 and the spring 41 when the limiting plate 3 is rotated to release the limit, which facilitates the use and removal of the sample tube 14. The setting of the push-out block 4 and the spring 41 can be used to pop out the sample tube 14 after the limit is released, which further enhances the portability of the critical illness risk prediction sample collection device.
[0028] like Figures 1 to 2 As shown, a protective sleeve 5 is installed on the outer wall of the placement box shell 1. The protective sleeves 5 are evenly distributed on the outer wall of the placement box shell 1. A rotating adjustment rod 51 is installed in the middle of each protective sleeve 5. A suction cup 52 is fixed to the bottom end of the rotating adjustment rod 51. During operation, the protective sleeve 5 can block and protect the outer wall of the placement box shell 1. The placement height of the device can be adjusted by the setting of the rotating adjustment rod 51 and the suction cup 52. The protective sleeve 5 can block and protect the outer wall of the placement box shell 1. The placement height of the device can be adjusted by the setting of the rotating adjustment rod 51 and the suction cup 52, which further enhances the protective adjustment effect of the critical illness risk prediction sample collection device.
[0029] like Figures 1 to 4As shown, a top cover 6 is slidably fitted to the top of the placement box shell 1. A gripping frame 61 is rotatably fitted to the outer wall of the top cover 6. A sealing gasket 62 is fixed to the inner wall of the top cover 6. A placement groove 63 is opened at the bottom of the sealing gasket 62. The placement grooves 63 are evenly distributed at the bottom of the sealing gasket 62. During operation, the top cover 6 can be used to seal the top of the placement box shell 1. The gripping frame 61 can be used to easily open the top cover 6. The sealing gasket 62 and the placement groove 63 can limit and fix the placed sample tube 14 and sealing sleeve 15 to avoid collision caused by sliding. The top cover 6 can seal the top of the placement box shell 1. The sealing gasket 62 and the placement groove 63 can make the seal of the top cover 6 more complete. The gripping frame 61 can be used to lift and open the top cover 6, further enhancing the sealing effect of the top of the critical illness risk prediction sample collection device.
[0030] like Figures 1 to 2 As shown, an observation plate 7 is slidably fitted in the middle of the side wall of the placement box shell 1. A control frame 71 is fixedly connected to the side wall of the observation plate 7. During operation, the sample collection plate placed inside the placement box shell 1 can be observed through the observation plate 7, and the position of the observation plate 7 can be controlled through the control frame 71. The setting of the observation plate 7 allows for observation of the sample collection inside the placement box shell 1, and the setting of the control frame 71 allows for control of the position of the observation plate 7, further enhancing the sample observation effect of the critical illness risk prediction sample collection device.
[0031] During operation, the placement ring 2 and clamping frame 21 can restrain the bottom of the sample tube 14 when it is placed, preventing the sample tube 14 from shaking and breaking when the outer shell 1 of the placement box moves. The placement ring 2 and clamping frame 21 stabilize the bottom of the sample tube 14 during placement, preventing it from shaking and further enhancing the sample protection and stability of the critical illness risk prediction sample collection device. The shaking of test tube 14 further enhances the sample protection and clamping stability of the critical illness risk prediction sample collection device. The limiting plate 3 and limiting groove 31 limit the bottom of the sample test tube 14, preventing it from falling off. The limiting plate 3 and limiting groove 31 further enhance the limiting and stabilizing effect of the critical illness risk prediction sample collection device. The ejector block 4 and spring 41 eject the sample test tube 14 when the limiting plate 3 is rotated to release the limiting, facilitating its use and removal. The ejector block 4 and spring 41 also allow for the ejection operation after the limiting of the sample test tube 14 is released, further strengthening the critical illness risk prediction sample collection device. The portable design of the collection device is enhanced by the protective sleeve 5, which blocks and protects the outer wall of the placement box 1. The placement height of the device can be adjusted using the rotating adjustment rod 51 and suction cup 52. This further strengthens the protective and adjustable effect of the critical illness risk prediction sample collection device. The top cover 6 seals the top of the placement box 1, and the grip 61 facilitates opening the top cover 6. The sealing gasket 62 and placement groove 63 limit and fix the placed sample tube 14 and sealing sleeve 15, preventing slippage. The impact generated by the movement can be sealed by the top cover 6, and the sealing gasket 62 and the placement groove 63 can make the seal of the top cover 6 more complete. The top cover 6 can be lifted and opened by the grip frame 61, which further enhances the sealing effect of the top of the critical illness risk prediction sample collection device. The observation plate 7 can be used to observe the collection sample placed inside the placement box shell 1, and the position of the observation plate 7 can be controlled by the control frame 71. The observation plate 7 can be used to observe the sample collection inside the placement box shell 1, and the position of the observation plate 7 can be controlled by the control frame 71, which further enhances the sample observation effect of the critical illness risk prediction sample collection device.
[0032] The foregoing has shown and described the basic principles, main features, and advantages of this utility model. Those skilled in the art should understand that this utility model is not limited to the above embodiments. The embodiments and descriptions in the specification are merely illustrative of the principles of this utility model. Various changes and modifications can be made to this utility model without departing from its spirit and scope, and all such changes and modifications fall within the scope of the claimed utility model. The scope of protection of this utility model is defined by the appended claims and their equivalents.
Claims
1. A sample collection device for predicting the risk of severe illness, comprising a housing shell (1), characterized in that: The inner wall of the placement box shell (1) is provided with a placement rack (11), the placement rack (11) is evenly distributed on the inner wall of the placement box shell (1), a partition plate (12) is installed on the inner wall of the placement box shell (1), a positioning ring (13) is provided at the bottom of the inner wall of the placement box shell (1), the positioning ring (13) is evenly distributed at the bottom of the inner wall of the placement box shell (1), a sample tube (14) is slidably fitted in the middle of the placement rack (11), the sample tube (14) is evenly distributed in the middle of the placement rack (11), a sealing sleeve (15) is slidably fitted at the top of the sample tube (14), and a clamping assembly is placed at the bottom of the inner wall of the placement box shell (1).
2. The critical illness risk prediction sample collection device according to claim 1, characterized in that: The clamping assembly includes a placement ring (2), and a clamping frame (21) is fixedly attached to the top of the placement ring (2). The clamping frames (21) are evenly distributed on the top of the placement ring (2), and the clamping frames (21) are in sliding fit with the bottom of the sample tube (14).
3. The critical illness risk prediction sample collection device according to claim 2, characterized in that: The sample tube (14) is fixed to the outer wall of the bottom with a limiting plate (3). The limiting plate (3) is evenly distributed on the outer wall of the bottom of the sample tube (14). The inner wall of the placement ring (2) has a limiting groove (31). The limiting groove (31) and the limiting plate (3) are in sliding fit.
4. The critical illness risk prediction sample collection device according to claim 3, characterized in that: A spring (41) is fixed to the bottom of the inner wall of the placement ring (2): a push block (4) is fixed to the end of the spring (41), and the push block (4) is in sliding fit with the inner wall of the placement ring (2).
5. The critical illness risk prediction sample collection device according to claim 4, characterized in that: The outer wall of the placement box shell (1) is equipped with a protective sleeve (5). The protective sleeves (5) are evenly distributed on the outer wall of the placement box shell (1). A rotating adjustment rod (51) is installed in the middle of each protective sleeve (5). A suction cup (52) is fixed to the bottom end of the rotating adjustment rod (51).
6. The critical illness risk prediction sample collection device according to claim 5, characterized in that: The top of the outer shell (1) of the placement box is slidably fitted with a top cover (6), and the outer side wall of the top cover (6) is rotatably fitted with a grip (61). The inner side wall of the top cover (6) is fixedly connected with a sealing gasket (62), and a placement groove (63) is opened at the bottom of the sealing gasket (62). The placement groove (63) is evenly distributed at the bottom of the sealing gasket (62).
7. The critical illness risk prediction sample collection device according to claim 6, characterized in that: An observation plate (7) is slidably fitted in the middle of the side wall of the outer shell (1) of the placement box, and a control frame (71) is fixedly connected to the side wall of the observation plate (7).