Full-automatic glucometer monitoring device

Abstract

The utility model relates to the technical field of automatic glucometers, and discloses a full-automatic glucometer monitoring device which comprises a main body mechanism, a blood sampling mechanism and a detection mechanism, a plurality of through holes are formed in a circle of a rotating disc, and each through hole is provided with a spring seat to provide support for positioning and popping of a needle head or test paper. According to the full-automatic glucometer monitoring device, a highly-automatic blood sampling and detection process is adopted, and a mechanism integrating an electric push rod and an automatic needle replacing mechanism is adopted, so that the device can complete blood glucose detection and automatic loading of test paper from blood sampling without manual intervention, the operation steps are greatly simplified, the operation complexity of a user is reduced, and the working efficiency is improved. Meanwhile, the risk of cross infection is avoided through automatic processing, sanitation and safety in the using process are improved, blood glucose monitoring is more convenient and accurate through the design, and the blood glucose monitoring system is suitable for being used by users of all ages and skill levels.

Description

Technical Field

[0001] The utility model relates to the technical field of automatic blood glucose meters, and particularly relates to a full-automatic blood glucose meter monitoring device. Background Technique

[0002] A blood glucose meter is a medical device used to measure the glucose content in blood. For diabetic patients, it is an important tool for daily blood glucose level management. By regularly monitoring blood glucose, patients can effectively manage their conditions and avoid various health risks caused by too high or too low blood glucose levels. For some people, such as diabetic patients, blood glucose monitoring is an indispensable part of their daily lives. They need to use a blood glucose meter to regularly check their blood glucose levels to ensure they are within a safe range.

[0003] Traditional blood glucose meters have some disadvantages, mainly reflected in the inconvenience and pain during use. Traditional devices usually need to prick the fingertip to obtain a blood sample, and this method will cause pain to patients every time, especially for patients who need to frequently monitor blood glucose. In the long run, it may lead to the risk of callus or infection on the fingertip. In addition, the operation process of these devices is complex, requiring manual adjustment of the device, handling of blood samples and recording of data, which is particularly inconvenient for the elderly or patients with limited hand function. Moreover, traditional blood glucose meters usually cannot provide real-time feedback or the function of automatically recording measurement results. Patients must manually record the data, which to some extent affects the accuracy of the data and the continuity of management. Content of the Utility Model

[0004] (1) Technical Problem to be Solved

[0005] The purpose of the utility model is to provide a full-automatic blood glucose meter monitoring device to solve the problem of the cumbersome use of traditional blood glucose meters mentioned in the above background technique.

[0006] (2) Technical Solution

[0007] To achieve the above object, the present utility model provides the following technical solutions: A fully automatic blood glucose meter monitoring device, which includes a main body mechanism, a blood collection mechanism, and a detection mechanism. The blood collection mechanism is arranged inside the main body mechanism, and the detection mechanism is arranged on the left side of the blood collection mechanism. The main body mechanism includes an equipment housing. A protrusion is provided at the front end of the equipment housing. A cover plate is provided at the upper end of the protrusion. An interaction panel is provided at the upper end of the equipment housing. A speaker is provided at the rear side of the interaction panel. A storage battery is provided inside the equipment housing. A data interface is provided at the left end of the equipment housing. A placement groove is provided at the front end of the equipment housing. The blood collection mechanism includes a first motor. The first motor is arranged near the front inside the equipment housing. A rotating disk is provided below the first motor. A coupling is provided between the rotating disk and the first motor. Several through holes are provided in a circle of the rotating disk. A spring seat is provided at the upper end of each through hole. The main body mechanism includes an equipment housing, which provides structural support and protection for the entire monitoring device. A protrusion is provided at the front end of the equipment housing for installing and fixing other mechanism components. A cover plate is installed at the upper end of the protrusion, which is convenient for users to open to replace parts or perform maintenance. An interaction panel is installed at the upper end of the equipment housing, which provides a user operation interface and a display screen, facilitating users to view information and perform operations. A speaker is installed at the rear side of the interaction panel, which is used to emit operation prompt sounds or warning sounds to ensure that users operate the device correctly. A storage battery is installed inside the equipment housing, which provides necessary power support for the equipment to ensure that the device can work normally without an external power supply. A data interface is installed at the left end of the equipment housing for data transmission and device connection. A placement groove is provided at the front end of the equipment housing for placing accessories or tools required for detection or operation. The first motor drives the rotating disk to rotate to select a new needle or test strip. The rotating disk is connected to the first motor through a coupling to ensure the stability of power transmission. Several through holes are provided in a circle of the rotating disk, and each through hole is equipped with a spring seat to provide support for the positioning and ejection of the needle or test strip.

[0008] Preferably, a connecting rod is provided at the upper end of the spring seat. The inside of the connecting rod is hollow. A guide ring is provided at the upper end of the connecting rod. A first spring is provided between the connecting rod and the guide ring. The connecting rod is used for guiding and supporting the needle. A guide ring is installed at the upper end of the connecting rod to ensure the accurate guiding and insertion of the needle. A first spring is installed between the connecting rod and the guide ring to provide necessary elastic force for the needle to support the rebound of the needle.

[0009] Preferably, an electric push rod is provided on the upper side of the guide ring. A push rod is provided at the lower end of the electric push rod. A limiting end is provided at the lower side of the push rod. The push rod is installed at the lower end of the electric push rod to directly drive the needle to pierce and retract. The limiting end is installed at the lower side of the push rod to limit the maximum extension length of the needle to protect users from being overly stabbed.

[0010] Preferably, a needle is provided at the lower end of the limiting end. The diameter of the needle is smaller than that of the guiding ring. A finger pad is provided inside the placement groove. The needle is used to pierce the user's fingertip to collect a blood sample. The placement groove is equipped with a finger pad to provide a position for the user to place the fingertip and reduce the discomfort during blood collection.

[0011] Preferably, the detection mechanism includes a test strip slot. A test strip slot is provided on the left side of the rotating disk. A second spring is provided inside the rotating disk. A push plate is provided at the lower end of the second spring. Several test strips are provided at the lower end of the push plate.

[0012] Preferably, a second motor is provided at the lower end of the placement groove. A first roller is provided at the upper end of the second motor.

[0013] Preferably, a second roller is provided on the front side of the first roller. A detection device is provided on the front side of the second roller. A waste product slot is provided at the lower end of the detection device. The detection device is used to analyze the blood sample and quickly provide a detection result. The waste product slot is installed at the lower end of the detection device to collect the used test strips, ensure the cleanliness of the device and avoid cross-contamination.

[0014] Compared with the prior art, the beneficial effects of the present utility model are as follows:

[0015] 1. For this fully automatic blood glucose meter monitoring device, with a highly automated blood collection and detection process, by integrating an electric push rod and an automatic needle replacement mechanism, the device can complete blood glucose detection without manual intervention. From blood collection to the automatic loading of test strips, it greatly simplifies the operation steps, reduces the operation complexity of users. At the same time, the automated processing also avoids the risk of cross-infection, increases the hygiene and safety during use. This design makes blood glucose monitoring more convenient and accurate, and is suitable for users of all ages and skill levels;

[0016] 2. For this fully automatic blood glucose meter monitoring device, due to the use of a finely controlled electric push rod and a micro needle, the blood collection process is almost painless, which is a great blessing for diabetic patients who need to frequently detect blood glucose. It reduces the psychological and physiological burden of patients, makes daily blood glucose management easier, and is of great significance for improving patients' compliance with medical advice and improving blood glucose control; BRIEF DESCRIPTION OF THE DRAWINGS

[0017] Figure 1 It is a three-dimensional structural schematic diagram of the blood glucose meter monitoring device of the present utility model;

[0018] Figure 2 It is a top view of the blood collection mechanism of the present utility model;

[0019] Figure 3 It is a structural schematic diagram of the blood collection mechanism of the present utility model;

[0020] Figure 4 Schematic diagram of the structure of the blood collection needle module of the present utility model;

[0021] Figure 5 Schematic cross-sectional structure diagram of the blood collection mechanism of the present utility model;

[0022] Figure 6 Side cross-sectional view of the blood glucose meter monitoring device of the present utility model;

[0023] Figure 7 Schematic cross-sectional structure diagram of the detection mechanism of the present utility model.

[0024] In the figure: 1. Main body mechanism; 101. Equipment housing; 102. Protrusion; 103. Cover plate; 104. Interaction panel; 105. Speaker; 106. Battery; 107. Data interface; 108. Placement groove; 2. Blood collection mechanism; 201. First motor; 202. Rotating disk; 203. Coupling; 204. Through hole; 205. Spring seat; 206. Connecting rod; 207. Guide ring; 208. First spring; 209. Electric push rod; 210. Push rod; 211. Limit end; 212. Needle; 213. Finger pad; 3. Detection mechanism; 301. Test strip slot; 302. Second spring; 303. Push plate; 304. Test strip; 305. Second motor; 306. First roller; 307. Second roller; 308. Detection device; 309. Waste slot. Specific embodiments

[0025] Next, the technical solutions in the embodiments of the present utility model will be clearly and completely described in conjunction with the accompanying drawings in the embodiments of the present utility model. Obviously, the described embodiments are only a part of the embodiments of the present utility model, rather than all the embodiments. Based on the embodiments of the present utility model, all other embodiments obtained by those of ordinary skill in the art without creative efforts shall fall within the protection scope of the present utility model.

[0026] Please refer to Figures 1 - 7, the present utility model provides a technical solution: a fully automatic blood glucose meter monitoring device, which includes a main body mechanism 1, a blood collection mechanism 2, and a detection mechanism 3. The blood collection mechanism 2 is arranged inside the main body mechanism 1, and the detection mechanism 3 is arranged on the left side of the blood collection mechanism 2. The main body mechanism 1 includes a device housing 101. A protrusion 102 is provided at the front end of the device housing 101, a cover plate 103 is provided at the upper end of the protrusion 102, an interaction panel 104 is provided at the upper end of the device housing 101, a speaker 105 is provided at the rear side of the interaction panel 104, a storage battery 106 is arranged inside the device housing 101, a data interface 107 is provided at the left end of the device housing 101, and a placement groove 108 is provided at the front end of the device housing 101. The blood collection mechanism 2 includes a first motor 201. The first motor 201 is arranged at the front inside the device housing 101. A rotating disk 202 is arranged below the first motor 201. A coupling 203 is arranged between the rotating disk 202 and the first motor 201. A plurality of through holes 204 are arranged in a circle on the rotating disk 202. A spring seat 205 is arranged at the upper end of each through hole 204. The device housing 101 provides structural protection and support for the entire blood glucose monitoring device. The protrusion 102 is used for assembling and fixing other components. The cover plate 103 facilitates users to access the internal components for replacement or maintenance. The interaction panel 104 provides a user interface, allowing users to operate the device and view information. The speaker 105 emits sounds for guidance or warnings to assist users in operating. The storage battery 106 powers the device to ensure that the device can still operate without an external power source. The data interface 107 is used for transmitting data and connecting external devices. The placement groove 108 is used for placing relevant accessories or tools. The first motor 201 drives the rotating disk 202. The coupling 203 connects the first motor 201 and the rotating disk 202 to transmit rotational power. The rotating disk 202 is equipped with through holes 204, and the spring seats 205 are installed in the through holes 204.

[0027] The upper end of the spring seat 205 is provided with a connecting rod 206. The inside of the connecting rod 206 is hollow. The upper end of the connecting rod 206 is provided with a guide ring 207. A first spring 208 is arranged between the connecting rod 206 and the guide ring 207. The upper side of the guide ring 207 is provided with an electric push rod 209. The lower end of the electric push rod 209 is provided with a push rod 210. The lower side of the push rod 210 is provided with a limiting end 211. The lower end of the limiting end 211 is provided with a needle 212. The diameter of the needle 212 is smaller than that of the guide ring 207. A finger pad 213 is arranged inside the placement groove 108. The spring seat 205 is used to support the connecting rod 206. The connecting rod 206 is designed to be hollow to guide the movement of the needle. The guide ring 207 is fixed to the top of the connecting rod 206 to ensure that the needle accurately aligns with the blood collection point. The first spring 208 is installed between the connecting rod 206 and the guide ring 207 to provide the necessary elasticity for the needle to rebound. The electric push rod 209 drives the push rod 210, and the push rod 210 directly acts on the needle to control its precise insertion and withdrawal. The limiting end 211 prevents the needle 212 from penetrating excessively and protects the user from harm. The needle 212 performs the blood collection task. The finger pad 213 provides a position for the user to place the finger and improves the comfort of blood collection.

[0028] The detection mechanism 3 includes a test strip slot 301. The test strip slot 301 is arranged on the left side of the rotating disk 202. A second spring 302 is arranged inside the rotating disk 202. The lower end of the second spring 302 is provided with a push plate 303. The lower end of the push plate 303 is provided with several test strips 304. The lower end of the placement groove 108 is provided with a second motor 305. The upper end of the second motor 305 is provided with a first roller 306. The front side of the first roller 306 is provided with a second roller 307. The front side of the second roller 307 is provided with a detection device 308. The lower end of the detection device 308 is provided with a waste slot 309. The test strip slot 301 stores the test strips for convenient and quick replacement. The second spring 302 is part of the pushing system to push the test strip forward. The push plate 303 pushes the test strip 304 towards the detection area. The second motor 305 drives the first roller 306 and the second roller 307 to ensure that the test strip 304 is smoothly fed into the detection device 308. The detection device 308 is responsible for analyzing the blood sample and quickly outputting the blood glucose test result. The waste slot 309 collects the used test strips 304 to keep the device clean and tidy.

[0029] Working principle: This fully automatic blood glucose meter monitoring device achieves user-friendly and efficient blood glucose detection through a series of precise mechanical structures. The overall design makes the device easy and efficient to operate. The main body structure includes the device housing 101, which not only protects the internal precision components from external damage but also provides an operation interface interaction panel 104, enabling users to easily set and monitor the device status. A speaker 105 is provided at the rear of the interaction panel 104 for voice prompting the operation process or warning messages. A built-in battery 106 is installed in the device housing 101 to ensure that the device can work properly even without an external power supply. The data interface 107 supports data transmission and software upgrade. The blood collection mechanism includes a first motor 201 responsible for driving the rotating disk 202. The rotating disk 202 is connected to the first motor 201 through a coupling 203 to ensure smooth and precise movement. The through hole 204 on the rotating disk 202 cooperates with the spring seat 205 and the connecting rod 206 to form a mechanism for automatically replacing the needle. The needle 212 is precisely controlled to move through the guide ring 207 and the electric push rod 209 to achieve painless or minimally painful blood collection. The limiting end 211 ensures the accuracy of the movement of the needle 212 and prevents the needle 212 from penetrating excessively. The detection mechanism automatically provides a new test strip through the test strip slot 301, the second motor 305, and the roller system. The test strip 304 is pushed by the second motor 305 through the first roller 306 and the second roller 307 to the detection device 308. The detection device 308 analyzes the blood sample and quickly provides a blood glucose reading. The waste slot 309 collects the used test strips 304 to ensure hygiene and the cleanliness of the device. During the entire operation process, the user starts the device through the interaction panel 104. After the first motor 201 starts, it drives the rotating disk 202 to rotate, and the new needle 212 and the test strip 304 are automatically loaded in place. The user places the finger on the finger pad 213, and the electric push rod 209 pushes the needle 212 to quickly and accurately complete blood collection. The blood is dropped on the new test strip 304, and the test strip 304 is sent to the detection device 308 for analysis. The entire process has a high degree of automation, reducing the complexity of user operation. At the same time, through precise mechanical control, the pain and inconvenience during use are greatly reduced, and finally, a blood glucose test result is quickly and accurately provided, enhancing the user experience and detection efficiency.

[0030] Finally, it should be noted that the above content is only used to illustrate the technical solution of the present invention, rather than limiting the protection scope of the present invention. Any simple modification or equivalent replacement made by those of ordinary skill in the art to the technical solution of the present invention shall not depart from the essence and scope of the technical solution of the present invention.

Claims

1. A fully automatic blood glucose meter monitoring device, comprising a main body mechanism (1), a blood sampling mechanism (2) and a detection mechanism (3), characterized in that: A blood sampling mechanism (2) is arranged inside the main body (1), a detection mechanism (3) is arranged on the left side of the blood sampling mechanism (2), the main body (1) comprises a device housing (101), a protrusion (102) is arranged at the front end of the device housing (101), a cover plate (103) is arranged at the upper end of the protrusion (102), an interactive panel (104) is arranged at the upper end of the device housing (101), a speaker (105) is arranged at the rear side of the interactive panel (104), a storage battery (106) is arranged inside the device housing (101), and the device housing (101 ) is provided with a data interface (107) at the left end, a placement slot (108) is provided at the front end of the device housing (101), the blood sampling mechanism (2) comprises a first motor (201), the first motor (201) is provided at the front inside the device housing (101), a rotating disk (202) is provided at the lower side of the first motor (201), a coupling (203) is provided between the rotating disk (202) and the first motor (201), a circle of the rotating disk (202) is provided with a plurality of through holes (204), and a spring seat (205) is provided at the upper end of each through hole (204).

2. A fully automatic blood glucose meter monitoring device according to claim 1, characterized in that: A connecting rod (206) is arranged at the upper end of the spring seat (205), the interior of the connecting rod (206) is hollow, a guide ring (207) is arranged at the upper end of the connecting rod (206), and a first spring (208) is arranged between the connecting rod (206) and the guide ring (207).

3. A fully automatic blood glucose meter monitoring device according to claim 2, characterized in that: An electric push rod (209) is arranged on the upper side of the guide ring (207), a push rod (210) is arranged on the lower end of the electric push rod (209), and a limited end (211) is arranged on the lower side of the push rod (210).

4. A fully automatic blood glucose meter monitoring device according to claim 3, characterized in that: A needle head (212) is disposed at the lower end of the limiting end (211), the diameter of the needle head (212) is smaller than the diameter of the guide ring (207), and a finger pad (213) is disposed inside the placement groove (108).

5. The fully automatic blood glucose meter monitoring device according to claim 1, characterized in that: The detection mechanism (3) comprises a test paper slot (301), the test paper slot (301) is arranged on the left side of the rotating disk (202), a second spring (302) is arranged inside the rotating disk (202), a push plate (303) is arranged at the lower end of the second spring (302), and a plurality of test papers (304) are arranged at the lower end of the push plate (303).

6. A fully automatic blood glucose meter monitoring device according to claim 1, characterized in that: A second motor (305) is disposed at the lower end of the placement slot (108), and a first roller (306) is disposed at the upper end of the second motor (305).

7. A fully automatic blood glucose meter monitoring device according to claim 6, characterized in that: A second roller (307) is arranged on the front side of the first roller (306), a detection device (308) is arranged on the front side of the second roller (307), and a waste product slot (309) is arranged at the lower end of the detection device (308).

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