Integrated detection device for perfusion device

By designing an integrated perfusion device including water storage, heating, delivery pump, filtration and testing devices, the problems of low efficiency and safety hazards of existing detection processes are solved, and fully automatic detection of the blood perfusion device is realized, improving the detection accuracy and safety.

CN222774217UActive Publication Date: 2025-04-18昌果生物医药科技河北有限公司
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Patent Information

Application Number
CN202421626193.7
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2024-07-10
Publication Date
2025-04-18
Estimated Expiration
2034-07-10

AI Technical Summary

Technical Problem

The existing blood perfusion device has low efficiency, detection errors and safety risks, and the automated detection device is complex, expensive, and inconvenient to operate and maintain.

Method used

An integrated detection device for perfusion device is designed, including a water storage device, a heating device, a conveying pump, a high temperature 0.22 micron filter device and a testing device to realize fully automatic final flushing, water injection and pressure resistance inspection.

Benefits of technology

The perfusion device detection process is automated, the detection efficiency and accuracy are improved, the risk of product defects or safety accidents caused by human errors is reduced, and the safety of medical products is ensured.

✦ Generated by Eureka AI based on patent content.

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Abstract

The utility model discloses an integrated detection device for a perfusion device, which relates to the technical field related to medical equipment testing, has four modes of disinfection circulation, cleaning, water injection and pressure detection, and mainly comprises a water storage device, a heating device, a delivery pump, a filtering device and a testing device, the conveying pump is connected with the heating device through a water injection pipe and conveys water to the filtering device through the water injection pipe, the upstream of the testing device is connected with the filtering device through the water injection pipe, and the downstream of the testing device is connected with the heating device through a circulating water pipe. By implementing the integrated detection device for the perfusion device, the intervention of manual operation is reduced, so that the risk of product defects or safety accidents caused by human errors is reduced; an automatic system can ensure that each perfusion device reaches a consistent high standard; the automatic system can operate in a sterile environment, the risk of microbial contamination is reduced, and the safety of medical products is ensured.
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Description

Technical Field

[0001] The utility model belongs to the technical field related to medical equipment testing, and specifically relates to an integrated detection device for a perfusion device. Background Art

[0002] In the medical field, hemoperfusion devices are an important blood purification device and are widely used in clinical treatment to remove toxins and metabolic wastes from the blood. The traditional hemoperfusion device detection process includes multiple steps such as final flushing, water injection and pressure resistance test. These steps are usually manually operated by medical staff and have high technical intensity. Not only are they inefficient, but there are also detection errors and safety hazards caused by human factors. During the disinfection process, due to the complex structure of the device, there may be uneven disinfection, resulting in the failure to completely kill microorganisms in certain parts. In order to improve the efficiency and accuracy of detection, the industry has begun to explore automated detection devices in recent years. These devices are designed to achieve automatic final flushing, water injection and pressure resistance test of the perfusion device through integrated design, thereby improving the stability and repeatability of the detection process. Despite this, the existing automated detection devices still have certain limitations, such as high equipment complexity, high cost, and inconvenient operation and maintenance. Therefore, it is necessary to develop a safe and efficient technology related to cleaning, disinfection and testing of medical equipment. Utility Model Content

[0003] In order to solve the problems raised in the above background technology, the purpose of the present utility model is to provide an integrated detection device for a perfusion device.

[0004] In order to achieve the above purpose, the technical solution adopted by the utility model is as follows:

[0005] A perfusion device integrated detection device, characterized in that it includes a water storage device, a heating device, a delivery pump, a high temperature resistant 0.22 micron filter device and a testing device. The water storage device is located at the inlet end of the perfusion device integrated detection device, and is used to store water for equipment and balance the water pressure in the pipeline. The device is designed to be directly connected to the water supply system to ensure a continuous and stable water supply. The water source is selected from physiological saline or heparin saline. The heating device is connected to the water storage device. The working temperature of the heating device is 80°C and is used for heating and sterilization. The delivery pump is connected to the heating device through a water injection pipe, and water is delivered to the high temperature resistant 0.22 micron filter device through the water injection pipe. The upstream of the testing device is connected to the high temperature resistant 0.22 micron filter device through the water injection pipe to flush, inject water and pressure test the perfusion device. The downstream is connected to the heating device through a circulating water pipe for water circulation.

[0006] Furthermore, the testing device includes a perfusion device, a flow sensor, an oscillation motor, a pressure sensor and a fourth pneumatic valve. The perfusion device is located at the core position of the testing device. The flow sensor is located on the water injection pipe between the filtering device and the testing device, and is used to accurately control the flow of the liquid and reduce the waste of water resources. The oscillation motor is located below the perfusion device. The vibration generated by the oscillation motor can enhance the flushing effect of the liquid on the inner wall of the perfusion device, which helps to remove impurities and residues on the surface of the adsorbent and ensure that each part can be fully cleaned. The pressure sensor is located on the circulating water pipe above the perfusion device and is used to detect the pressure value of the perfusion device. A fourth pneumatic valve is provided downstream of the pressure sensor.

[0007] Furthermore, the test device has four modes, namely, disinfection cycle mode, flushing mode, water injection mode, and pressure test mode; Disinfection cycle mode: open the first pneumatic valve, the second pneumatic valve, the third pneumatic valve, the fourth pneumatic valve and the fifth pneumatic valve, control the heating device to maintain the temperature at 80°C, and the delivery pump circulates the water in the heating device through the high temperature resistant 0.22 micron filter device, the irrigation device and the circulating water pipe, and finally returns to the heating device, so as to achieve the disinfection effect and reduce the microorganisms loaded on the equipment to reduce the risk of controlling the microorganisms of the product; Flushing mode: open the first pneumatic valve, the second pneumatic valve, the third pneumatic valve, the fourth pneumatic valve and the fifth pneumatic valve, and control the heating device to maintain the temperature at 80°C. The first pneumatic valve, the second pneumatic valve, the third pneumatic valve, the fourth pneumatic valve and the fifth pneumatic valve are used to add water to the heating device through the water storage device, and the water is delivered to the position of the perfusion device by the delivery pump through the high temperature resistant 0.22 micron filter device. During the flushing process, the adsorbent in the perfusion device is shaken by the oscillation motor to achieve a full flushing effect. The flushing adopts a bottom-up method. The flushing mode is divided into circulation flushing and direct flushing, which saves water to a greater extent; water injection mode: open the first pneumatic valve, the second pneumatic valve, the third pneumatic valve, the fourth pneumatic valve and the fifth pneumatic valve, and inject water from the bottom to the top of the perfusion device through the delivery pump, and the water injection amount is accurately controlled by the flow sensor value. Pressure resistance test mode: open the first pneumatic valve, the second pneumatic valve and the third pneumatic valve, close the fourth pneumatic valve, and continuously inject water into the perfusion device through the delivery pump. After reaching a certain pressure, close the third pneumatic valve, let the product stand at a certain pressure, and observe whether the pressure sensor value is within the safety threshold to achieve the purpose of pressure resistance inspection.

[0008] Furthermore, a water circulation pipe is provided between the fourth pneumatic valve and the heating device, and a drainage pipe is provided on the circulating water pipe, and the drainage pipe is connected to the sixth pneumatic valve and leads to the waste pool.

[0009] Furthermore, a temperature sensor is provided at the connection between the heating device and the circulating water pipe, and the temperature sensor is used to detect the temperature of the heating device; a fifth pneumatic valve is provided near the temperature sensor.

[0010] Furthermore, the perfusion device is fixed using a test fixture, and the test fixture is located at the bottom of the perfusion device.

[0011] Furthermore, the upper and lower connecting tubes of the perfusion device are made of medical silicone tubes, which have high transparency and long service life and are suitable for long-term use.

[0012] Furthermore, a glass cover is provided around the perfusion device to isolate the operator from possible harm from high-pressure spray or debris.

[0013] Furthermore, a waste box is provided below the perfusion device to collect waste or leaked liquid generated during the test.

[0014] Furthermore, an alarm is provided around the perfusion device, and the alarm is connected to a pressure sensor. When the pressure sensor reading is not within a preset safety threshold, a signal is sent to the alarm, and the alarm sounds an alarm.

[0015] Compared with the prior art, the technical progress achieved by the utility model is:

[0016] The utility model can execute preset programs without interruption by realizing the integration and automation of the three processes of fully automatic final flushing, water injection and pressure resistance testing in the production process of the perfusion device, thereby greatly reducing the manpower demand and operation time and improving the overall work efficiency; automation reduces the intervention of human operation, thereby reducing the risk of product defects or safety accidents caused by human errors; by accurately controlling the conditions of flushing, water injection and pressure resistance testing, the automation system can ensure that each perfusion device meets consistent high standards; the automation system can operate in a sterile environment, reduce the risk of microbial contamination, and ensure the safety of medical products. BRIEF DESCRIPTION OF THE DRAWINGS

[0017] The accompanying drawings are used to provide a further understanding of the present invention and constitute a part of the specification. They are used together with the embodiments of the present invention to explain the present invention and do not constitute a limitation to the present invention.

[0018] In the attached picture:

[0019] Figure 1 A schematic diagram of the structure of an integrated detection device for a perfusion device provided in an embodiment of the utility model;

[0020] In the figure:

[0021] 10-water storage device, 20-heating device, 30-delivery pump; 40-high temperature resistant 0.22 micron filter device; 50-testing device; 60-liquid flow direction; 1-first pneumatic valve; 2-second pneumatic valve; 3-third pneumatic valve; 4-fourth pneumatic valve; 5-fifth pneumatic valve; 6-sixth pneumatic valve; 7-temperature sensor; 8-waste pool; 51-flow sensor; 52-medical silicone tube; 53-test fixture; 54-perfusion device; 55 pressure sensor; 56-waste box; 57-oscillation motor; 61-water injection pipe; 62-circulating water pipe; 63-drainage pipe. DETAILED DESCRIPTION

[0022] The following specific embodiments may be combined with each other, and the same or similar concepts or processes may not be described in detail in some embodiments. The following will describe the embodiments of the present utility model in conjunction with the accompanying drawings.

[0023] like Figure 1 As shown, an embodiment of the utility model provides an integrated detection device for a perfusion device, comprising a water storage device 10, a heating device 20, a delivery pump 30, a high temperature resistant 0.22 micron filter device 40 and a testing device 50. The water storage device 10 is located at the inlet end of the perfusion device integrated detection device, and is used to store water for the device and balance the water pressure in the pipeline. The device is responsible for providing sterile saline. The device is designed to be directly connected to the water supply system to ensure a continuous and stable supply of saline. The water source is selected from saline or heparin saline; the water storage device 10 0 is connected to the heating device 20 to ensure that the physiological saline is properly heated during the delivery process. The operating temperature of the heating device 20 is 80°C. The delivery pump 30 is connected to the heating device 20 through the water injection pipe 61, and the physiological saline is delivered to the high temperature resistant 0.22 micron filter device 40 through the water injection pipe 61. The upstream of the testing device 50 is connected to the high temperature resistant 0.22 micron filter device 40 through the water injection pipe 61 to flush, inject water and pressure test the perfusion device 54. The downstream is connected to the heating device 20 through the circulating water pipe 62 for water circulation.

[0024] As a preferred structure, Figure 1As shown, the test device 50 includes a perfusate 54, a flow sensor 51, an oscillation motor 57, a pressure sensor 55 and a fourth pneumatic valve 4. The perfusate 54 is located at the core of the test device 50. The flow sensor 51 is located on the water injection pipe 61 between the high temperature resistant 0.22 micron filter device 40 and the test device 50. The flow sensor 51 is used to accurately control the flow of the liquid and reduce the waste of water resources. The oscillation motor 57 is located below the perfusate 54. The vibration generated by the oscillation motor 57 can enhance the flushing effect of the liquid on the inner wall of the perfusate 54, which helps to remove impurities and residues on the surface of the adsorbent and ensure that each part can be fully cleaned. The pressure sensor 55 is located on the circulating water pipe 62 above the perfusate 54. The fourth pneumatic valve 4 is provided downstream of the pressure sensor 55. 20 groups of test stations (2 in each group) are pre-designed to achieve the improvement of production capacity, and a connection device is reserved to facilitate the addition of equipment stations at any time.

[0025] In a specific embodiment of the present invention, Figure 1 As shown, the test device 50 has four modes, namely, a disinfection cycle mode, a flushing mode, a water injection mode, and a pressure test mode; the disinfection cycle mode is: open the first pneumatic valve 1, the second pneumatic valve 2, the third pneumatic valve 3, the fourth pneumatic valve 4 and the fifth pneumatic valve 5, the delivery pump 30 controls the physiological saline in the heating device 20, and circulates through the high temperature resistant 0.22 micron filter device 40 and the test device 50 to return to the heating device 20, so as to achieve a disinfection effect, reduce the microorganisms loaded on the equipment, and reduce the risk of controlling the microorganisms of the product. Flushing mode: open the first pneumatic valve 1, the second pneumatic valve 2, the third pneumatic valve 3, the fourth pneumatic valve 4 and the fifth pneumatic valve 5, add water to the heating device 20 through the water storage device 10, and the delivery pump 30 delivers the water that has passed through the high temperature resistant 0.22 micron filter device to the position of the irrigation device 54. During the flushing process, the adsorbent in the irrigation device 54 is vibrated by the vibration motor 57 to achieve a sufficient flushing effect. The flushing adopts a bottom-up method. The flushing mode is divided into circulating flushing and direct flushing, which saves water to a greater extent; Water injection mode: open the first pneumatic valve 1, the second The pneumatic valve 2, the third pneumatic valve 3, the fourth pneumatic valve 4 and the fifth pneumatic valve 5 are used to inject water into the irrigation device 54 from bottom to top through the delivery pump 30, and the water injection amount is accurately controlled by the value of the flow sensor 51; the pressure resistance test mode: open the first pneumatic valve 1, the second pneumatic valve 2 and the third pneumatic valve 3, close the fourth pneumatic valve 4, and continuously inject water into the irrigation device 54 through the delivery pump 30. After reaching a certain pressure, close the third pneumatic valve 3, let the product stand at a certain pressure, and observe whether the value of the pressure sensor 55 is within the safety threshold to achieve the purpose of pressure resistance inspection.

[0026] In a specific embodiment of the present invention, Figure 1As shown, a drain pipe 63 is provided on the circulating water pipe 62 , and the drain pipe 63 is connected to the sixth pneumatic valve 6 and leads to the waste pool 8 .

[0027] During specific assembly, a temperature sensor 7 is provided at the connection between the heating device 20 and the circulating water pipe 63 , and the temperature sensor 7 is used to detect the temperature of the heating device 20 ; a fifth pneumatic valve 5 is provided near the temperature sensor 7 .

[0028] like Figure 1 As shown, the perfusate 54 is fixed using a test fixture 53, and the test fixture 53 is located at the bottom of the perfusate 54 to prevent displacement during the process.

[0029] In a specific embodiment of the present invention, Figure 1 As shown, the upper and lower connecting tubes of the perfusion device 54 are medical silicone tubes 52, which have high transparency and long service life and are suitable for long-term use.

[0030] Further optimize the above technical solution, such as Figure 1 As shown, the perfusate 54 is surrounded by a glass cover 58 to isolate the operator from possible harm from high-pressure spray or fragments.

[0031] In a specific embodiment of the present invention, Figure 1 As shown, a waste box 56 is provided below the perfusion device to collect waste or leaked liquid generated during the test.

[0032] To further optimize the above solution, an alarm is provided around the perfusion device 54, and the alarm is connected to the pressure sensor 55. When the pressure sensor 55 reading is not within the preset safety threshold, a signal is sent to the alarm, and the alarm sounds an alarm.

[0033] In summary, the utility model can continuously execute preset programs by realizing the integration and automation of the three processes of fully automatic final flushing, water injection and pressure resistance testing in the production process of the perfusion device, thereby greatly reducing the manpower requirements and operation time and improving the overall work efficiency; automation reduces the intervention of human operation, thereby reducing the risk of product defects or safety accidents caused by human errors; by precisely controlling the conditions of flushing, water injection and pressure resistance testing, the automation system can ensure that each perfusion device meets consistent high standards; the automation system can operate in a sterile environment, reduce the risk of microbial contamination, and ensure the safety of medical products.

[0034] In the description of the present invention, it should be understood that the terms "up", "down", "left", "right", etc. indicating directions or positional relationships are based on the directions or positional relationships shown in the accompanying drawings, and are only for the convenience of describing the present invention and simplifying the description, rather than indicating or implying that the device or element referred to must have a specific direction, be constructed or operated in a specific direction, and therefore should not be understood as a limitation on the present invention.

[0035] In addition, the terms "first" and "second" are used for descriptive purposes only and cannot be understood as indicating or implying relative importance or implicitly indicating the quantity of the indicated technical features.

[0036] Finally, it should be noted that the above description is only a preferred embodiment of the utility model and is not intended to limit the utility model. Although the utility model is described in detail with reference to the aforementioned embodiments, those skilled in the art can still modify the technical solutions described in the aforementioned embodiments or replace some of the technical features therein with equivalents. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the utility model shall be included in the scope of protection of the claims of the utility model.

Claims

1. A perfusion device integrated detection device, characterized in that: It includes a water storage device, a heating device, a delivery pump, a high-temperature resistant 0.22-micron filter device and a testing device. The water storage device is located at the inlet end of the integrated detection device of the perfusion device, and is used to store water for the equipment and balance the water pressure in the pipeline. The heating device is connected to the water storage device and is used for heating and sterilization. The delivery pump is connected to the heating device through an injection pipe, and delivers water to the high-temperature resistant 0.22-micron filter device through the injection pipe. The upstream of the testing device is connected to the filter device through the injection pipe to flush, inject water and pressure test the perfusion device. The downstream is connected to the heating device through a circulating water pipe for water circulation.

2. The integrated detection device for a perfusion device according to claim 1, characterized in that: The testing device includes a perfusion device, a flow sensor, an oscillation motor, a pressure sensor and a fourth pneumatic valve. The perfusion device is located at the core position of the testing device, the flow sensor is located on the water injection pipe between the filtering device and the testing device, the oscillation motor is located below the perfusion device, the pressure sensor is located on the circulating water pipe above the perfusion device, and a fourth pneumatic valve is provided downstream of the pressure sensor.

3. The integrated detection device for a perfusion device according to claim 2, characterized in that: A water circulation pipe is provided between the fourth pneumatic valve and the heating device, and a drainage pipe is provided on the circulating water pipe. The drainage pipe is connected to the sixth pneumatic valve and leads to the waste pool.

4. The integrated detection device for a perfusion device according to claim 3, characterized in that: A temperature sensor is provided at the connection between the heating device and the circulating water pipe, and a fifth pneumatic valve is provided near the temperature sensor.

5. The integrated detection device for a perfusion device according to claim 2, characterized in that: The cartridge is fixed using a test fixture, which is located at the bottom of the cartridge.

6. The integrated detection device for a perfusion device according to claim 2, characterized in that: Medical silicone tubes are used as the upper and lower connecting tubes of the perfusion device.

7. The integrated detection device for a perfusion device according to claim 2, characterized in that: A glass cover is provided around the perfusion device to isolate the operator from possible harm from high-pressure spray or fragments.

8. The integrated detection device for a perfusion device according to claim 2, characterized in that: A waste box is provided below the perfusion device to collect waste or leaked liquid generated during the test.

9. The integrated detection device for a perfusion device according to claim 2, characterized in that: An alarm is arranged around the perfusion device, and the alarm is connected to the pressure sensor.