Pumping type blood transfer bag subpackaging device
By designing a pump-in blood bag packaging device, the problem of difficulty in standardizing manual operations and low degree of automation in the prior art is solved, and the automation and standardization of blood packaging is realized, which improves work efficiency and saves blood resources.
Patent Information
- Application Number
- CN202420824265.2
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-04-19
- Publication Date
- 2025-03-04
- Estimated Expiration
- 2034-04-19
AI Technical Summary
The lack of special blood component dispensing equipment in the prior art makes it difficult to standardize manual operations, large errors in packaging, low efficiency, and impossible to realize automated precise dispensing, automatic thermal bonding and disconnection processes.
A pump-in blood bag dispensing device is designed. By shaking the mother bag smoothly and the child bag suspended weighing unit vertically, and combining the peristaltic blood pumping component, an automated blood bag dispensing operation system is built, which realizes the reasonable positioning between the mother bag and the child bag, blood volume control, process status monitoring and blood braid thermal disconnection.
It realizes the automation and standardization of blood packaging, reduces the difference in manual operations, improves work efficiency, saves blood resources, and reduces the blood consumption costs of infants and children and children.
Smart Images

Figure CN222549797U_ABST
Abstract
Description
Technical Field
[0001] The embodiments of the utility model belong to the technical field of blood preparation, and more specifically, relate to a pump-in type blood bag transfer and filling device. Background Art
[0002] Blood has various specifications, and is usually prepared into blood products of the same specifications according to the specifications of the collected blood. However, for patients such as infants and children who have a small amount of single blood transfusion, even if the smallest specification of blood is used, it is still excessive, which can easily cause blood waste and increase the economic burden on patients. Therefore, for this type of patient group, there has always been a demand for the use of small-specification blood. Since whole blood collection does not have small specifications, it is necessary to use conventional specifications of blood products by weight and divide them equally by transferring bags, but there is currently no dedicated blood component packaging equipment. Therefore, a small-specification blood packaging auxiliary equipment is proposed, which is of great significance for improving the workflow and standardizing the preparation of small-specification blood, as well as maximizing the optimization of blood resources.
[0003] In order to solve the above technical problems, the conventional operation method currently relies on manual operation by staff. The specific operation requires manual mixing and squeezing of blood from the mother bag into the connecting bag, repeated weighing to make the weight of each bag of blood equal, and then disconnecting by heat sealing to achieve the requirement of equal division.
[0004] Although the above method realizes the packaging operation, the following technical problems still exist: (1) Manual operation is difficult to standardize, and because the blood bag has a long blood braid, the weighing process is inaccurate, which increases the distribution error and the quality uniformity of the obtained blood product is poor; (2) Automated equipment is not widely used, and manual operation not only increases the workload, but also lacks efficiency; (3) The existing technology fails to realize the automated operation of precise packaging, automatic heat sealing, and disconnection processes in one machine, so it is possible to consider integrating multi-process auxiliary functions to achieve a significant improvement in work efficiency. Utility Model Content
[0005] In view of the above defects or improvement needs of the prior art, the utility model provides a pump-in blood bag filling device, which vertically arranges the mother bag shaking unit and the child bag hanging weighing unit, and combines it with a peristaltic blood pumping component to completely construct an automated blood bag filling operation system with reasonable positioning between the mother bag and the child bag, control of the packed blood volume, process status monitoring and heat-sealing and disconnection of the blood braid. Compared with the traditional manual filling method, the device realizes the automation and standardization of blood filling and reduces the variability of manual operations.
[0006] In order to achieve the above object, a pump-in blood bag transfer and packaging device is provided, comprising:
[0007] A main shell, a mother bag shaking unit arranged on the top of the main shell, a sub-bag hanging weighing unit arranged on the front side of the main shell, and a blood volume pump control driving unit arranged above the sub-bag hanging weighing unit;
[0008] The mother bag shaking unit comprises an intermediate connecting block horizontally fixedly connected to the top of the main shell, a shaking drive assembly arranged above the intermediate connecting block, and a pressure sensor arranged between the intermediate connecting block and the shaking drive assembly for simultaneously measuring the total mass of the mother bag;
[0009] The sub-bag hanging weighing unit comprises a sub-bag hanging rod for hanging the sub-bag and a mass sensor for contact sensing with the end of the sub-bag hanging rod;
[0010] The blood volume pump control drive unit comprises a pump control device housing fixedly connected to the front side of the main housing, a catheter clamping assembly arranged inside the pump control device housing for easy disassembly and assembly of the blood braid catheter, a peristaltic blood pumping assembly and a heat-closed disconnection assembly;
[0011] The pump control device housing also includes a catheter installation groove opened on its front side and a Carmen slide groove arranged on both sides of the catheter installation groove; the engaging shifting component in the catheter engaging assembly maintains a sliding connection with the Carmen slide groove.
[0012] Preferably, the shaking drive assembly comprises:
[0013] A shake component shell fixed above the pressure sensor, an internal chamber opened inside the shake component shell, an upper support block serving as a shaking actuator and rotatably connected to the side wall of the internal chamber, a blood bag drag chamber opened on the top surface of the upper support block, a bottom guide rod fixed below the upper support block, a vertical slide groove vertically penetrating the bottom guide rod, a sliding block slidably connected to the vertical slide groove, a horizontal connecting rod that maintains a horizontal direction and is fixedly connected to the sliding block, a horizontal sliding block fixedly arranged at both ends of the horizontal connecting rod, a horizontal guide groove opened on the side wall of the shake component shell and slidably connected to the horizontal sliding block, and a horizontal driving assembly for driving the horizontal guide groove to slide horizontally.
[0014] Preferably, the horizontal driving assembly comprises:
[0015] A first connecting rod with one end being rotatably hinged to the horizontal sliding block, a second connecting rod being hinged to the other end of the first connecting rod, a connecting rod driving motor driving the second connecting rod to rotate on a fixed axis, an amplitude modulation nut block fixedly connected to the connecting rod driving motor, an amplitude modulation transmission screw rod maintaining a horizontal transmission connection with the amplitude modulation nut block, and an amplitude modulation driving motor driving the amplitude modulation transmission screw rod to rotate.
[0016] Preferably, the heat-close disconnect assembly comprises:
[0017] A pair of pressing linear motors are fixedly arranged on the side wall of the pump control device housing and maintained in relative direction, and a heat-sealing cutting head is arranged on the protruding end of the pressing linear motors.
[0018] Preferably, the heat-sealed cutting head comprises:
[0019] A base part fixedly connected to the extended end of the pressing linear motor, a center-point heat-sealing part arranged at the front end of the base part, and a heating part fixedly connected to the base part.
[0020] Preferably, the peristaltic blood pump assembly comprises:
[0021] A base mounting block, a base horizontal position control assembly disposed on the side wall of the pump control device housing and used to control the base mounting block to maintain horizontal movement, a transmission sprocket and a transmission chain disposed on the side of the base mounting block, an intermediate connecting rod fixedly disposed on the side of the transmission chain, and a rotating wheel disposed at the protruding end of the intermediate connecting rod; the rotating wheel contacts and squeezes the blood braid pipeline;
[0022] The base horizontal position control component includes a position control transmission nut and a guide slider fixedly arranged on the upper and lower sides of the base mounting block, a position control transmission screw that maintains a horizontal direction and linear thread transmission with the position control transmission nut, a position control drive motor that drives the position control transmission screw to rotate, and a guide light rod that maintains a horizontal direction and a sliding connection with the guide slider.
[0023] Preferably, the catheter engaging assembly comprises:
[0024] A Carmen that maintains horizontal sliding connection with the Carmen slideway, and a linear motor that drives the Carmen to maintain horizontal sliding.
[0025] In general, the above technical solutions conceived by the utility model can achieve the following beneficial effects compared with the prior art:
[0026] (1) The utility model is a pump-in blood transfer bag filling device, which vertically arranges the mother bag shaking unit and the child bag hanging weighing unit, and combines the peristaltic blood pumping component to completely construct an automated blood bag filling operation system with reasonable positioning between the mother bag and the child bag, control of the packed blood volume, process status monitoring, and heat-sealing and disconnection of the blood braid. Compared with the traditional manual filling method, the device realizes the automation and standardization of blood filling, and reduces the differences in manual operation;
[0027] (2) The utility model is a pump-type blood transfer bag filling device, which can greatly improve work efficiency and enhance the ability to prepare small-sized blood, thereby saving blood resources and reducing blood costs for infants and children, and has positive social value. BRIEF DESCRIPTION OF THE DRAWINGS
[0028] Figure 1 This is a schematic diagram of the overall structure of a pump-in blood bag transfer and filling device according to an embodiment of the utility model;
[0029] Figure 2 This is an internal structural diagram of a mother bag shaking unit of a pump-in blood transfer bag filling device according to an embodiment of the utility model;
[0030] Figure 3 This is a partial enlarged view of A of a pump-in blood transfer bag filling device according to an embodiment of the utility model;
[0031] Figure 4 This is a schematic diagram of the internal structure of a blood volume pump control drive unit of a pump-in blood bag transfer and filling device according to an embodiment of the utility model;
[0032] Figure 5 This is a schematic diagram of the structure of the middle tip heat sealing part of a pump-in blood transfer bag filling device according to an embodiment of the utility model;
[0033] In all the drawings, the same reference numerals represent the same technical features, specifically: 1-main shell, 2-mother bag shaking unit, 200-middle connecting block, 210-pressure sensor, 220-shaking drive assembly, 221-shaking assembly shell, 222-internal chamber, 223-upper support block, 224-blood bag drag chamber, 225-bottom guide rod, 226-vertical slide groove, 227-sliding block, 228-horizontal connecting rod, 229-horizontal slider, 2210-horizontal guide groove, 2211-horizontal drive assembly, 22111-first connecting rod, 22112-second connecting rod, 22113-connecting rod drive motor, 22114-amplitude modulation nut block, 22115-amplitude modulation transmission screw, 22116-amplitude modulation drive motor, 3-blood volume pump control drive unit, 300-pump control device shell, 301-catheter Installation slot, 302-Carmen slide, 310-heat-close disconnection assembly, 311-pressing linear motor, 312-heat-close cutting head, 3121-base, 3122-middle tip heat-closed part, 3123-heating part, 320-peristaltic blood pump assembly, 321-drive sprocket, 322-drive chain, 323-middle connecting rod, 324-rotating wheel, 325-base mounting block, 326-position control drive motor, 327-position-controlled transmission screw, 328-position-controlled transmission nut, 329-guide light rod, 3210-guide slider, 330-catheter clamping assembly, 331-linear motor, 332-extension rod, 333-Carmen, 4-sub-bag hanging weighing unit, 401-sub-bag hanging rod, 402-mass sensor, 501-mother bag, 502-mother bag main road, 503-sub-bag branch road, 504-packaging sub-bag. DETAILED DESCRIPTION
[0034] In the description of the present application, it should be understood that the terms "center", "longitudinal", "lateral", "length", "width", "thickness", "up", "down", "front", "back", "left", "right", "vertical", "horizontal", "top", "bottom", "inside", "outside", "clockwise", "counterclockwise" and the like indicate orientations or positional relationships based on the orientations or positional relationships shown in the accompanying drawings, and are only for the convenience of describing the present invention and simplifying the description, and do not indicate or imply that the referred device or element must have a specific orientation, be constructed and operated in a specific orientation, 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 should not be understood as indicating or implying relative importance or implicitly indicating the number of the indicated technical features. Therefore, the features defined as "first" and "second" may explicitly or implicitly include one or more of the features. In the description of the present utility model, the meaning of "plurality" is two or more, unless otherwise clearly and specifically defined.
[0036] In this application, unless otherwise clearly specified and limited, the terms "installed", "connected", "connected", "fixed" and the like should be understood in a broad sense, for example, it can be a fixed connection, a detachable connection, or an integral connection; it can be a mechanical connection or an electrical connection; it can be a direct connection, or it can be an indirect connection through an intermediate medium, or it can be the internal communication of two components. For ordinary technicians in this field, the specific meanings of the above terms in this utility model can be understood according to specific circumstances.
[0037] In order to make the purpose, technical solution and advantages of the utility model more clear, the utility model is further described in detail below in conjunction with the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are only used to explain the utility model and are not used to limit the utility model. In addition, the technical features involved in each embodiment of the utility model described below can be combined with each other as long as they do not conflict with each other.
[0038] like Figures 1 to 5 As shown, in an embodiment of the utility model, a pump-in blood bag transfer and filling device comprises:
[0039] A main housing 1, a mother bag shaking unit 2 arranged on the top of the main housing 1, a sub-bag hanging weighing unit 4 arranged on the front side of the main housing 1, and a blood volume pump control driving unit 3 arranged above the sub-bag hanging weighing unit 4;
[0040] The mother bag shaking unit 2 includes an intermediate connecting block 200 horizontally fixedly connected to the top of the main shell 1, a shaking drive assembly 220 arranged above the intermediate connecting block 200, and a pressure sensor 210 arranged between the intermediate connecting block 200 and the shaking drive assembly 220 for simultaneously measuring the total mass of the mother bag;
[0041] The sub-bag hanging weighing unit 4 comprises a sub-bag hanging rod 401 for hanging the sub-bag and a mass sensor 402 which contacts and senses the end of the sub-bag hanging rod 401 .
[0042] The blood volume pump control driving unit 3 includes a pump control device housing 300 fixedly connected to the front side of the main housing 1, a catheter clamping assembly 330 arranged inside the pump control device housing 300 for easy disassembly of the blood braid catheter, a peristaltic blood pumping assembly 320 and a heat-closed disconnection assembly 310;
[0043] The pump control device housing 300 further includes a catheter installation slot 301 provided on the front side thereof and a Carmen slide slot 302 provided on both sides of the catheter installation slot 301; the engaging shifting part in the catheter engaging assembly 330 is kept in sliding connection with the Carmen slide slot 302;
[0044] In the embodiment of the utility model, by vertically arranging the mother bag shaking unit and the child bag hanging weighing unit and combining with the peristaltic blood pumping component, a complete automated blood bag filling operation system is constructed with reasonable positioning between the mother bag and the child bag, control of the packed blood volume, process status monitoring and heat-sealing and disconnection of the blood braid. Compared with the traditional manual filling method, the present device realizes automation and standardization of blood filling and reduces the variability of manual operation.
[0045] At the same time, the utility model is easy to operate, can greatly improve work efficiency, and enhance the ability to prepare small-sized blood, thereby saving blood resources and reducing blood costs for infants and children, and has positive social value.
[0046] like Figures 1 to 3 As shown, in the embodiment of the present utility model, the shaking drive assembly 220 includes:
[0047] A shaking component shell 221 fixed above the pressure sensor 210, an internal chamber 222 opened inside the shaking component shell 221, an upper support block 223 serving as a shaking actuator and rotatably connected to the side wall of the internal chamber 222, a blood bag drag chamber 224 opened on the top surface of the upper support block 223, a bottom guide rod 225 fixed below the upper support block 223, a vertical slide groove 226 vertically penetrating the bottom guide rod 225, a sliding block 227 slidably connected to the vertical slide groove 226, a horizontal connecting rod 228 that maintains a horizontal direction and is fixedly connected to the sliding block 227, horizontal sliding blocks 229 fixedly arranged at both ends of the horizontal connecting rod 228, a horizontal guide groove 2210 opened on the side wall of the shaking component shell 221 and horizontally slidably connected to the horizontal sliding block 229, and a horizontal driving component 2211 for driving the horizontal guide groove 2210 to slide horizontally.
[0048] like Figure 2 and Figure 3 As shown, in the embodiment of the utility model, the horizontal driving assembly 2211 includes:
[0049] A first connecting rod 22111 having one end pivotally connected to the horizontal slider 229, a second connecting rod 22112 pivotally connected to the other end of the first connecting rod 22111, a connecting rod driving motor 22113 for driving the second connecting rod 22112 to rotate on a fixed axis, an amplitude modulation nut block 22114 fixedly connected to the connecting rod driving motor 22113, an amplitude modulation transmission screw rod 22115 horizontally connected to the amplitude modulation nut block 22114, and an amplitude modulation drive motor 22116 for driving the amplitude modulation transmission screw rod 22115 to rotate.
[0050] like Figure 1 , Figure 4 and Figure 5 As shown, in the embodiment of the utility model, the heat-close disconnection assembly 310 includes:
[0051] A pair of pressing linear motors 311 fixedly arranged on the side wall of the pump control device housing 300 and a heat-sealing cutting head 312 arranged at the protruding end of the pressing linear motors 311 are maintained in relative directions.
[0052] like Figure 4 and Figure 5 As shown, in the embodiment of the utility model, the heat sealing cutting head 312 includes:
[0053] A base portion 3121 fixedly connected to the extended end of the pressing linear motor 311 , a central tip heat sealing portion 3122 provided at the front end of the base portion 3121 , and a heating portion 3123 fixedly connected to the base portion 3121 .
[0054] like Figure 4 As shown, in the embodiment of the utility model, the peristaltic blood pump assembly 320 includes:
[0055] A base mounting block 325, a base horizontal position control assembly provided on the side wall of the pump control device housing 300 and used to control the base mounting block 325 to maintain horizontal movement, a transmission sprocket 321 and a transmission chain 322 provided on the side of the base mounting block 325, an intermediate connecting rod 323 fixedly provided on the side of the transmission chain 322, and a rotating wheel 324 provided on the protruding end of the intermediate connecting rod 323; the rotating wheel 324 contacts and squeezes the blood braid pipeline;
[0056] The base horizontal position control component includes a position control transmission nut 328 and a guide slider 3210 fixedly arranged on the upper and lower sides of the base mounting block 325, a position control transmission screw 327 that maintains a horizontal direction and a linear thread transmission with the position control transmission nut 328, a position control drive motor 326 that drives the position control transmission screw 327 to keep rotating, and a guide light rod 329 that maintains a horizontal direction and a sliding connection with the guide slider 3210.
[0057] like Figure 4 As shown, in the embodiment of the present utility model, the catheter clamping assembly 330 includes:
[0058] A Carmen 333 that maintains a horizontal sliding connection with the Carmen slide slot 302, and a linear motor 331 that drives the Carmen 333 to maintain a horizontal sliding connection.
[0059] The method of using the embodiment of the utility model is as follows: first, complete the installation operation of the mother-child multi-link, place the sub-packaging mother bag above the blood bag drag cavity 224, and hang the child bag on the child bag hanging rod 401, and finally press the child bag branch 503 into the catheter installation groove 301, thereby completing the installation operation; then, start the device, control the catheter clamping assembly 330 to move the card door 333, lock the child bag branch 503 into the catheter installation groove 301 to prevent it from escaping, and control the base horizontal position control assembly to move the rotating wheel 324 horizontally to contact and squeeze the child bag branch 503; then, start the mother bag shaking unit 2 to shake the mother bag to ensure that the blood components in the bag are evenly distributed; after sufficient shaking, control the shaking drive The assembly makes the tube mouth of the mother bag face downward to avoid the output of excess gas in the mother bag during the blood bag transfer process; then, the peristaltic blood pump assembly 320 is controlled to start, and the blood volume is controlled by the squeezing and moving effect of the rotor on the sub-bag branch 503, and the blood flows into the sub-bag; then, the accumulated blood in the sub-bag is continuously weighed by the mass sensor 402. When the predetermined value is reached, the peristaltic blood pump assembly 320 is controlled to run in reverse to extract the air in the sub-bag into the mother bag, and then the sub-bag branch 503 is heat-sealed and disconnected by the heat-sealed disconnection assembly 310 to complete the blood packaging; finally, the catheter clamping assembly 330 and the base horizontal position control assembly are reversely controlled to complete the disassembly of the sub-bag branch, the mother bag, and the sub-bag.
[0060] It should be noted that: the embodiment of the present invention can also be provided with a separate bayonet and heat-sealing device to realize the closing and heat-sealing of the mother bag trunk 502. In this way, when the branch line is blocked by gas or blood clots, the mother bag trunk 502 can be closed, and the blood transfer between the sub-bags can be realized through the peristaltic pump; and if the blood in the mother bag is fully divided into several sub-bags, after the division is completed, the mother bag loses its meaning and can be disconnected and discarded by heat sealing.
[0061] At the same time, the device can also integrate computer control system, touch display screen, code reader, printer and other functions to further improve the automation level of the equipment.
[0062] The above are only preferred embodiments of the present application and are not intended to limit the present application. Any modifications, equivalent replacements and improvements made within the spirit and principles of the present application shall be included in the protection scope of the present application. The above are only preferred implementations of the present application. It should be pointed out that for ordinary technicians in this technical field, several improvements and variations can be made without departing from the technical principles of the present application, and these improvements and variations should also be regarded as the protection scope of the present application.
Claims
1. A pump-in blood transfer bag filling device, characterized in that: include: A main housing (1), a mother bag shaking unit (2) arranged on the top of the main housing (1), a sub-bag hanging weighing unit (4) arranged on the front side of the main housing (1), and a blood volume pump control driving unit (3) arranged above the sub-bag hanging weighing unit (4); The mother bag shaking unit (2) comprises an intermediate connecting block (200) horizontally fixedly connected to the top of the main shell (1), a shaking drive assembly (220) arranged above the intermediate connecting block (200), and a pressure sensor (210) arranged between the intermediate connecting block (200) and the shaking drive assembly (220) for simultaneously measuring the total mass of the mother bag; The sub-bag hanging weighing unit (4) comprises a sub-bag hanging rod (401) for hanging the sub-bag, and a mass sensor (402) for contact sensing with the end of the sub-bag hanging rod (401); The blood volume pump control drive unit (3) comprises a pump control device housing (300) fixedly connected to the front side of the main housing (1), a catheter clamping assembly (330) arranged inside the pump control device housing (300) for facilitating the disassembly and assembly of a blood braid catheter, a peristaltic blood pumping assembly (320) and a heat-closed disconnection assembly (310); The pump control device housing (300) further comprises a catheter installation groove (301) provided on the front side thereof, and a Carmen slide groove (302) provided on both sides of the catheter installation groove (301); the engaging shifting component in the catheter engaging assembly (330) maintains a sliding connection with the Carmen slide groove (302).
2. A pump-in blood bag transfer and filling device according to claim 1, characterized in that: The shaking drive assembly (220) comprises: A shaking assembly housing (221) fixed above the pressure sensor (210), an internal chamber (222) opened inside the shaking assembly housing (221), an upper support block (223) serving as a shaking actuator and rotatably connected to the side wall of the internal chamber (222), a blood bag drag chamber (224) opened on the top surface of the upper support block (223), a bottom guide rod (225) fixed below the upper support block (223), and a vertical slide groove vertically penetrating inside the bottom guide rod (225). (226), a sliding block (227) that is slidably connected to the vertical sliding groove (226), a horizontal connecting rod (228) that is horizontally connected to the sliding block (227), a horizontal sliding block (229) that is fixedly arranged at both ends of the horizontal connecting rod (228), a horizontal guide groove (2210) that is opened on the side wall of the shaking component housing (221) and is horizontally slidably connected to the horizontal sliding block (229), and a horizontal driving component (2211) for driving the horizontal guide groove (2210) to slide horizontally.
3. A pump-in blood bag transfer and filling device according to claim 2, characterized in that: The horizontal driving component (2211) comprises: A first connecting rod (22111) having one end rotatably hinged to the horizontal slider (229), a second connecting rod (22112) hinged to the other end of the first connecting rod (22111), a connecting rod driving motor (22113) driving the second connecting rod (22112) to rotate around a fixed axis, an amplitude modulation nut block (22114) fixedly connected to the connecting rod driving motor (22113), an amplitude modulation transmission screw rod (22115) maintaining a horizontal transmission connection with the amplitude modulation nut block (22114), and an amplitude modulation driving motor (22116) driving the amplitude modulation transmission screw rod (22115) to rotate.
4. A pump-in blood bag transfer and filling device according to claim 1, characterized in that: The heat-close disconnection assembly (310) comprises: A pair of pressing linear motors (311) fixedly arranged on the side wall of the pump control device housing (300) and maintaining relative directions, and a heat-sealing cutting head (312) arranged at the protruding end of the pressing linear motors (311).
5. A pump-in blood bag transfer and filling device according to claim 4, characterized in that: The heat-sealing cutting head (312) comprises: A base portion (3121) fixedly connected to the protruding end of the pressing linear motor (311), a central tip heat sealing portion (3122) provided at the front end of the base portion (3121), and a heating portion (3123) fixedly connected to the base portion (3121).
6. A pump-in blood bag transfer and filling device according to claim 1, characterized in that: The peristaltic blood pump assembly (320) comprises: A base mounting block (325), a base horizontal position control component arranged on the side wall of the pump control device housing (300) and used to control the base mounting block (325) to maintain horizontal movement, a transmission sprocket (321) and a transmission chain (322) arranged on the side of the base mounting block (325), an intermediate connecting rod (323) fixedly arranged on the side of the transmission chain (322), and a rotating wheel (324) arranged at the protruding end of the intermediate connecting rod (323); the rotating wheel (324) contacts and squeezes the blood braid pipeline; The base horizontal position control assembly comprises a position control transmission nut (328) and a guide slider (3210) fixedly arranged on the upper and lower sides of the base mounting block (325), a position control transmission screw (327) which maintains a linear thread transmission with the position control transmission nut (328) in a horizontal direction, a position control drive motor (326) which drives the position control transmission screw (327) to rotate, and a guide light rod (329) which maintains a sliding connection with the guide slider (3210) in a horizontal direction.
7. A pump-in blood bag transfer and filling device according to any one of claims 1 or 6, characterized in that: The catheter clamping assembly (330) comprises: A Carmen (333) that maintains a horizontal sliding connection with the Carmen slide groove (302), and a linear motor (331) that drives the Carmen (333) to maintain a horizontal sliding connection.