CN220938553U - Safe transfusion double-chamber bag - Google Patents
Safe transfusion double-chamber bag Download PDFInfo
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- CN220938553U CN220938553U CN202322027475.7U CN202322027475U CN220938553U CN 220938553 U CN220938553 U CN 220938553U CN 202322027475 U CN202322027475 U CN 202322027475U CN 220938553 U CN220938553 U CN 220938553U
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- infusion
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- 239000007788 liquid Substances 0.000 claims abstract description 111
- 239000000843 powder Substances 0.000 claims abstract description 72
- 238000001802 infusion Methods 0.000 claims abstract description 62
- 238000003466 welding Methods 0.000 claims abstract description 35
- 229910052782 aluminium Inorganic materials 0.000 claims description 19
- 238000011049 filling Methods 0.000 claims description 19
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 17
- 238000000926 separation method Methods 0.000 claims description 6
- 230000009977 dual effect Effects 0.000 claims 2
- 239000003814 drug Substances 0.000 description 41
- 229940079593 drug Drugs 0.000 description 12
- 238000000034 method Methods 0.000 description 7
- 230000008901 benefit Effects 0.000 description 5
- 238000002156 mixing Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 3
- 239000004411 aluminium Substances 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 230000010354 integration Effects 0.000 description 2
- 238000011068 loading method Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 229940126589 solid medicine Drugs 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000006067 antibiotic powder Substances 0.000 description 1
- 238000012864 cross contamination Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000005429 filling process Methods 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000008354 sodium chloride injection Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000005491 wire drawing Methods 0.000 description 1
Landscapes
- Medical Preparation Storing Or Oral Administration Devices (AREA)
Abstract
The utility model discloses a safe transfusion double-chamber bag, which relates to the field of medical devices and comprises a transfusion bag body, wherein the transfusion bag body is divided into a liquid chamber, a powder chamber and a safe chamber, the liquid chamber and the powder chamber form a double-chamber cavity, the safe chamber is arranged at the bottom of the double-chamber cavity, the liquid chamber and the powder chamber are separated by a first weak welding rod, the safe chamber and the double-chamber cavity are separated by a second weak welding rod, and a transfusion port component is connected to the safe chamber. According to the utility model, the safety cavity is arranged under the double-chamber cavity, and the double-chamber cavity and the safety cavity are separated by the second weak welding rod, so that the liquid and the powder are ensured to be uniformly mixed and then enter the safety cavity, the infusion set can be inserted for normal use, and the structure achieves the purpose of avoiding the risk that the liquid in the infusion bag enters the infusion port part after being uniformly mixed, and the liquid input into a human body is nonuniform.
Description
Technical Field
The utility model relates to the field of medical devices, in particular to a safe transfusion double-chamber bag.
Background
When the existing flexible package transfusion product is produced, only liquid is filled, and when the product is used as a basic liquid for treating diseases and applied to the body of a patient, antibacterial powder is often required to be added, after the product is mixed, the product is infused into the human body, as shown in figure 1, the transfusion bag is a single body, different liquid medicines (such as sodium chloride injection) are filled in the liquid chamber 1 according to different specifications, and the powder bottle 15 is filled with therapeutic antibiotic powder; when in clinical use, the injector 16 is used for taking out about 5-10 ml of liquid in the infusion bag through the liquid filling port 7, then the liquid is injected into the powder bottle for dissolution, and then the liquid is led into the infusion bag through the injector 16 after dissolution, the operation is repeated for 2-3 times, the liquid medicine can be mixed, and the infusion hanging hole 10 is hung on the infusion support for infusing to a human body after the liquid medicine is mixed. The existing mode is used for preparing the liquid medicine, an independent preparation center is needed for completing the preparation, the syringe 16 is punctured between two different liquid medicines in the preparation process, the problem that the rubber plug at the medicine adding port 17 is desquamated is easily caused, the holding quality of products such as foreign matters or particles can be influenced, and the same syringe 16 is used for operation, so that a certain risk of cross contamination is also caused. There may be operational risks, and sometimes medical staff may configure not only one infusion bag, but also two or more infusion bags at the same time, which may cause a risk of adding wrong liquid medicine.
Aiming at the above existing different risk problems, a second improvement scheme appears in the prior art, specifically as shown in fig. 2, and on the basis of the scheme, the improvement scheme completes the integration of two kinds of liquid medicine in a factory through industrialized integration, and the working principle is as follows: the powder-liquid infusion bag is produced by a bag making machine, the welding of the first weak welding rod 4 is finished, the powder-liquid infusion bag is sent to a filling part to be finished after the welding, liquid is filled into the liquid chamber 1 through an infusion interface, the combined cover 12 is welded after the liquid is filled, the product of the powder-liquid infusion bag is finished and is sent to sterilization, powder with required proportion is filled into the powder chamber 2 according to the technological requirement after the sterilization, and then the powder is welded and sealed.
The improved scheme has the advantages that the product is integrated into a factory to be uniformly produced, each environment is controlled by the factory, and pollution risks generated in the use process of a user can be avoided; the liquid and the powder are reasonably distributed to two areas, are completely separated and distinguished, and can be opened only when being used again; the mode is convenient to use, only the aluminum film 9 is required to be torn at an easy tearing port, whether the powder has quality problems or not is observed, if the powder has the quality problems, the liquid cavity is extruded by hands, the first weak welding rod 4 can be opened after the powder cavity is extruded forcefully, the liquid enters the powder cavity, the liquid can be contacted with the powder, and the powder can be used after the powder is mixed and is shaken back and forth for about seconds. The liquid medicine is mixed and then used through the transfusion mouth part; the bag folding area 14 can enable the manufactured bag to be folded, and further save the packaging space.
However, the powder chamber 2 has the following defects that the space is larger, the saving of packing materials is not facilitated, and the production cost is increased; the tail arc of the powder chamber 2 is filtered more gently, and when powder and liquid are mixed, certain residues exist, so that the mixing uniformity is affected; the two layers outside the infusion bag body are welded with the aluminum film 9, the welding requirement of the aluminum film 9 is high, secondary damage is easily caused to the welded infusion bag, and powder leakage risk can be caused; the use is not quick, the easy-to-tear film is required to be torn off, and the powder can be used after being checked; it also appears that the operator would squeeze out to mix the liquid medicine without tearing the aluminum film 9; the used combined cover is also required to be heated to a proper melting point with the connector after being filled, and then the combined cover is welded, so that the problems of black edges of the cover and wire drawing of plastic in the process can be solved; the combined cover containing the rubber plug is used, and the risk of introducing medicine is also presented; because the surface of the powder cavity is covered with the aluminum film 9, the liquid can be directly used up under the condition that an operator does not open the first weak welding rod 4 to mix the powder, so that the curative effect is greatly reduced, and the like. Among the above drawbacks, particularly with respect to safety performance, is a problem of great concern to the public patients.
In view of this, the present application has been made.
Disclosure of utility model
The utility model aims to provide a safe transfusion double-chamber bag, which is provided with a safety chamber under a double-chamber cavity, and separates the double-chamber cavity from the safety chamber through a second weak welding rod so as to ensure that liquid and powder are uniformly mixed and then enter the safety chamber to be contacted with a transfusion opening part on the safety chamber, and the transfusion bag can be normally used only by inserting a transfusion device at the moment.
The embodiment of the utility model is realized by the following technical scheme: the utility model provides a safe infusion double-chamber bag, includes the infusion bag body, and the infusion bag body divide into liquid chamber, powder cavity and safe cavity, and liquid chamber constitutes two chambeies with the powder cavity, and safe cavity sets up in the bottom in two chambeies, and liquid chamber and powder cavity are separated by first weak welding rod, and safe cavity separates by the weak welding rod of second with two chambeies, is connected with transfusion mouth part on the safe cavity.
Preferably, the infusion port part comprises a connector tube, one end of the connector tube is communicated with the safety cavity, an easy-tearing film is arranged on the port of the other end of the connector tube, and a liquid separation sheet is arranged in the connector tube.
Preferably, the liquid chamber is provided with a liquid filling port, and the powder chamber is provided with a powder filling port.
Preferably, the liquid chamber is disposed above the powder chamber.
Preferably, the outside of the liquid chamber is sleeved with an aluminum film.
Preferably, the outside of the powder chamber is sleeved with an aluminum film.
Preferably, the inner edges of the liquid chamber, the powder chamber and the safety chamber are all arranged in a circular arc shape.
Preferably, the upper part of the infusion bag body is provided with an infusion hanging hole.
Preferably, the second weak electrode has a greater bearing strength than the first weak electrode.
Preferably, the outer surface of the infusion bag body is provided with an indication mark.
Compared with the prior art, the embodiment of the utility model has the following advantages and beneficial effects:
1. According to the safe transfusion dual-chamber bag provided by the embodiment of the utility model, the safe chamber is arranged below the dual-chamber, the dual-chamber and the safe chamber are separated by the second weak welding rod, when the safe transfusion dual-chamber bag is used, the liquid chamber is extruded firstly to separate the first weak welding rod, the liquid in the liquid chamber and the powder in the powder chamber are mixed in the dual-chamber, the mixed liquid in the dual-chamber is extruded again after the liquid and the powder are uniformly mixed, the second weak welding rod is separated, the mixed liquid enters the safe chamber and can only contact with the transfusion opening part on the safe chamber, and the transfusion device can be inserted into the transfusion device for normal use at the moment, so that the aim of avoiding the non-uniform risk of liquid input into a human body caused by the fact that solid-liquid mixing in the transfusion bag is non-uniform is achieved. At infusion interface handing-over department, design a safe cavity, this cavity keeps apart two chambeies completely, if under the circumstances that takes place misoperation, operating personnel can inspect the product again, confirms why can not have liquid to flow, will inspect, makes the security improve.
2. Compared with the prior art that the liquid filling port is shared by the liquid filling port and the transfusion port part, the liquid filling port is designed on the liquid cavity, the sterile transfusion port can be directly used without a rubber plug in the liquid filling process, the liquid can not be filled, after the easy-tearing film is torn, the needle of the transfusion device is used for puncturing the liquid separation sheet in the port, liquid can be input into a human body through the transfusion device, if an operator has misoperation, the port can leak liquid when the medicine is directly added into the bag, the operator can find out in the first time, the transfusion bag product can not be used, and the medicine using risk is further reduced. Meanwhile, the interface is prefabricated, the outer cover can not be welded, and foreign matters in the cover welding process can be effectively avoided.
3. The protection to the product is strengthened with the aluminium membrane on the bag body surface, and only at most protects two cavities, and the safety cavity outside is not provided with the aluminium membrane, does benefit to the operator and observes whether there is liquid through the safety cavity, if there is not liquid then can not infuse, makes patient's safety more can guarantee.
In general, the safe transfusion dual-chamber bag provided by the embodiment of the utility model has the advantages that the safe chamber is arranged below the dual-chamber, and the dual-chamber and the safe chamber are separated by the second weak welding rod, so that the safe chamber is ensured to be accessed after liquid and powder are uniformly mixed, and the safe transfusion dual-chamber bag can be normally used only by being inserted into a transfusion device.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present utility model, the drawings that are needed in the embodiments will be briefly described below, it being understood that the following drawings only illustrate some embodiments of the present utility model and therefore should not be considered as limiting the scope, and other related drawings may be obtained according to these drawings without inventive effort for a person skilled in the art.
FIG. 1 is a schematic view of a prior art infusion bag in a single unit configuration;
FIG. 2 is a schematic view of the structure of a transfusion bag of the prior art with two chambers;
FIG. 3 is a schematic view of a structure of a safe infusion dual-chamber bag according to an embodiment of the present utility model;
FIG. 4 is a schematic view of another structure of a safe infusion dual-chamber bag according to an embodiment of the utility model;
FIG. 5 is a schematic view of an infusion port component according to an embodiment of the disclosure;
FIG. 6 is a schematic diagram of an infusion set according to an embodiment of the present utility model;
Fig. 7 is a schematic diagram of indication identifier setting provided in an embodiment of the present utility model.
In the drawings, the reference numerals and corresponding part names:
1-liquid chamber, 2-powder chamber, 3-safe chamber, 4-first weak welding rod, 5-second weak welding rod, 6-transfusion mouth part, 61-interface tube, 62-easy tearing film, 63-liquid separation sheet, 7-liquid filling mouth, 8-powder filling mouth, 9-aluminum film, 10-transfusion hanging hole, 11-indication mark, 12-welding combined cover, 13-aluminum film easy tearing mouth, 14-folding area, 15-powder bottle, 16-injector, 17-medicine feeding mouth and 18-transfusion system.
Detailed Description
For the purpose of making the objects, technical solutions and advantages of the embodiments of the present utility model more apparent, the technical solutions of the embodiments of the present utility model will be clearly and completely described below with reference to the accompanying drawings in the embodiments of the present utility model, and it is apparent that the described embodiments are some embodiments of the present utility model, but not all embodiments of the present utility model. The components of the embodiments of the present utility model generally described and illustrated in the figures herein may be arranged and designed in a wide variety of different configurations.
Thus, the following detailed description of the embodiments of the utility model, as presented in the figures, is not intended to limit the scope of the utility model, as claimed, but is merely representative of selected embodiments of the utility model. All other embodiments, which can be made by those skilled in the art based on the embodiments of the utility model without making any inventive effort, are intended to be within the scope of the utility model.
It should be noted that: like reference numerals and letters denote like items in the following figures, and thus once an item is defined in one figure, no further definition or explanation thereof is necessary in the following figures.
In the description of the present utility model, it should be noted that the terms "first," "second," "third," and the like are used merely to distinguish between descriptions and are not to be construed as indicating or implying relative importance.
Examples
As shown in fig. 3, a safe infusion dual-chamber bag comprises an infusion bag body, wherein the infusion bag body is divided into a liquid chamber 1, a powder chamber 2 and a safe chamber 3, the infusion bag body is generally made of transparent plastic materials, the liquid chamber 1 and the powder chamber 2 form a dual-chamber cavity, the liquid chamber 1 is used for loading liquid medicines, the powder chamber 2 is used for loading one or more other medicines or additives, and the liquid medicines can be solid medicines or liquid medicines different from the liquid chamber 1 so as to ensure the stability and safety of the medicines. The safety chamber 3 is arranged at the bottom of the double-chamber cavity, the liquid chamber 1 and the powder chamber 2 are separated by the first weak welding rod 4, the safety chamber 3 and the double-chamber cavity are separated by the second weak welding rod 5, the safety chamber 3 is connected with the transfusion port component 6, when in use, the liquid in the liquid chamber 1 is extruded to the powder chamber 2, the first weak welding rod 4 can be opened, after the medicines in the liquid chamber 1 and the powder chamber 2 are completely mixed, the medicines in the double-chamber cavity are extruded to the safety chamber 3, at the moment, the second weak welding rod 5 is opened, the mixed medicines enter the safety chamber 3 and flow into the transfusion port component 6, and the transfusion device 18 can be normally used after being inserted into the transfusion port component 6. It should be noted that, the sizes of the liquid chamber 1, the powder chamber 2 and the safety chamber 3 may be set according to practical situations, and are not limited herein, in order to avoid wasting space, in the embodiment of the present utility model, the space of the liquid chamber 1 is larger than the space of the powder chamber 2, and the space of the safety chamber 3 is the smallest, so long as it is convenient to observe whether there is a medicine in the safety chamber 3.
In the embodiment of the utility model, a safety chamber 3 is designed at the joint of the infusion interface tube 61, the safety chamber 3 completely isolates the powder double-chamber cavity, and if an operation error occurs, an operator can check the product again to confirm why no liquid flows out, and the inspection can be performed, so that the safety is improved.
Further, the infusion port component 6 includes a port tube 61, one end of the port tube 61 is communicated with the safety chamber 3, an easy-tearing film 62 is arranged on a port of the other end of the port tube 61, a liquid separation sheet 63 is arranged in the port tube 61, specifically, as shown in fig. 5 and 6, the infusion port component 6 has no rubber plug design, liquid can not be added, after the easy-tearing film 62 is torn, a needle of the infusion apparatus 18 is used for puncturing the liquid separation sheet 63 in the port tube 61, and liquid can be input into a human body through the infusion apparatus 18; if the operator fails to operate, the medicine is directly added into the bag, the liquid leakage of the interface tube 61 occurs, the operator finds out at time 1, the bag product is not used, and the medicine application risk is further reduced. Preferably, the infusion port component 6 provided by the embodiment of the utility model is prefabricated, the outer cover is not welded any more, and the generation of foreign matters in the cover welding process can be effectively avoided.
At this time, the liquid filling port 7 may be provided on the liquid chamber 1, the powder filling port 8 may be provided on the powder chamber 2, the medicine may be added through the liquid filling port 7 and the powder filling port 8 during operation, the setting positions of the liquid filling port 7 and the powder filling port 8 may not be specifically limited, may be set on the side surface, may also be set on the top surface, and as long as the medicine in the corresponding state can be conveniently added, the liquid filling port 7 and the powder filling port 8 may be simultaneously set, and also the optional finger may be set to one, so that the structure may not pass through the transfusion port member 6 when the medicine is added.
In order to improve the uniformity of medicine mixing in the double-chamber cavity, the liquid chamber 1 is arranged above the powder chamber 2, when the first weak welding rod 4 is opened, medicine in the powder chamber 2 is positioned at the bottom of the liquid medicine, and when the liquid medicine collides with the medicine in the powder chamber 2, the medicine in the double-chamber cavity can be favorably stirred, the stirring uniformity of the medicine in the double-chamber cavity is improved, and of course, in other embodiments, the liquid chamber 1 and the powder chamber 2 can be designed left and right, the powder chamber 2 can be arranged above the liquid chamber 1, so long as the two chambers can form a double-chamber cavity, and the stirring uniformity in the double-chamber cavity can be realized.
Further, as shown in fig. 4, an aluminum film 9 is sleeved outside the liquid chamber 1, an aluminum film 9 is sleeved outside the powder chamber 2, and the aluminum film 9 can strengthen the protection of products. It should be noted that, the aluminum film 9 outside the liquid chamber 1 and the powder chamber 2 can be set or selected at the same time, and in the actual operation process, the control cost and the protection can be coordinated, so that in order to better protect the infusion bag, in the embodiment of the utility model, the aluminum film 9 is set at the outer sides of the two chambers at the same time, and when in use, only the situation of the safety chamber 3 needs to be observed, so that whether the infusion bag can have medicine output can be judged. When the operator observes that no liquid exists in the safety chamber 3, transfusion is not performed, so that the safety of a patient can be ensured.
In order to further improve the uniformity of medicine mixing in the double-chamber cavity, the edges of the liquid chamber 1, the powder chamber 2 and the safety chamber 3 are all arranged in circular arc shapes, so that solid medicines can be prevented from being accumulated at corners.
Further, the upper portion of the infusion bag body is provided with an infusion hanging hole 10 for hanging the infusion bag on an infusion support or a hook so as to convey the medicine to the patient through the infusion pipeline, and the hanging hole is generally a circular or rectangular opening, so that the infusion bag can be easily hung at a proper position, and by arranging the infusion hanging hole 10, medical staff can more conveniently control the speed and flow of infusion, and ensure that the medicine is conveyed to the patient according to the correct dosage and speed. Simultaneously, the device is also beneficial to reducing the pulling and pressure of the infusion pipeline and improving the comfort and safety of infusion.
Further, the withstand strength of the second weak electrode 5 is greater than that of the first weak electrode 4. Specifically, the second weak welding rod 5 bears the load of the medicines in the liquid chamber 1 and the two chambers in the powder chamber 2, the first weak welding rod 4 bears the load of the medicines in the liquid chamber 1, and obviously the second weak welding rod 5 needs to bear a larger load, and the arrangement of the structure can ensure that the first weak welding rod 4 and the second weak welding rod 5 can be kept stable and are not opened under the condition of ensuring no external force extrusion.
Further, as shown in fig. 7, the outer surface of the infusion bag body is provided with an indication mark 11, and it is to be noted that one or more indication marks 11 may be provided, the setting positions are not limited, and the indication marks may be set according to actual requirements, so as to play a role in indicating and further reducing operation risks, and preferably, in the embodiment of the present utility model, the indication mark 11 is provided at the infusion hanging hole 10, and in order not to obstruct observation, the indication mark 11 may be provided on the aluminum film 9.
The above description is only of the preferred embodiments of the present utility model and is not intended to limit the present utility model, but various modifications and variations can be made to the present utility model by those skilled in the art. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present utility model should be included in the protection scope of the present utility model. It should be noted that the structures or components illustrated in the drawings are not necessarily drawn to scale, and that descriptions of well-known components and processing techniques and procedures are omitted so as not to unnecessarily limit the present utility model.
Claims (10)
1. The utility model provides a safe infusion double-chamber bag, includes infusion bag body, its characterized in that, infusion bag body divide into liquid chamber (1), powder chamber (2) and safe cavity (3), liquid chamber (1) with powder chamber (2) constitute the double-chamber, safe cavity (3) set up the bottom in double-chamber, liquid chamber (1) and powder chamber (2) are separated by first weak welding rod (4), safe cavity (3) with double-chamber is separated by second weak welding rod (5), be connected with infusion mouth part (6) on safe cavity (3).
2. The safe transfusion dual-chamber bag as claimed in claim 1, wherein the transfusion port component (6) comprises a port tube (61), one end of the port tube (61) is communicated with the safe chamber (3), an easy-tearing film (62) is arranged on a port at the other end of the port tube (61), and a liquid separation sheet (63) is arranged in the port tube (61).
3. A safety infusion dual-chamber bag according to claim 1 or 2, wherein the liquid chamber (1) is provided with a filling port (7), and the powder chamber (2) is provided with a powder filling port (8).
4. A safety infusion dual chamber bag according to claim 3, wherein the liquid chamber (1) is arranged above the powder chamber (2).
5. The safe transfusion dual-chamber bag as claimed in claim 1, wherein an aluminum film (9) is sleeved outside the liquid chamber (1).
6. The safe transfusion double-chamber bag as claimed in claim 5, wherein the outer side of the powder chamber (2) is sleeved with an aluminum film (9).
7. A safety infusion dual-chamber bag according to claim 1, wherein the inner edges of the liquid chamber (1), the powder chamber (2) and the safety chamber (3) are all arranged in a circular arc shape.
8. The safe transfusion dual-chamber bag as claimed in claim 1, wherein the transfusion bag body is provided with a transfusion hanging hole (10) at the upper part.
9. A safety infusion dual chamber bag according to claim 1, wherein the second weak welding rod (5) has a higher bearing strength than the first weak welding rod (4).
10. A safety infusion dual-chamber bag according to claim 1, wherein the outer surface of the infusion bag body is provided with an indication mark (11).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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CN202322027475.7U CN220938553U (en) | 2023-07-31 | 2023-07-31 | Safe transfusion double-chamber bag |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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CN202322027475.7U CN220938553U (en) | 2023-07-31 | 2023-07-31 | Safe transfusion double-chamber bag |
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Publication Number | Publication Date |
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CN220938553U true CN220938553U (en) | 2024-05-14 |
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Family Applications (1)
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CN202322027475.7U Active CN220938553U (en) | 2023-07-31 | 2023-07-31 | Safe transfusion double-chamber bag |
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CN (1) | CN220938553U (en) |
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2023
- 2023-07-31 CN CN202322027475.7U patent/CN220938553U/en active Active
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