CN220811811U - Anti-theft finished infusion sealer - Google Patents

Abstract

The utility model provides a tamper-proof finished product infusion sealer which comprises a sealing structure, wherein the sealing structure is used for sealing a finished product infusion bag and a finished product infusion bottle, judging whether the finished product infusion bag/bottle is opened after dispensing is finished, and realizing tamper-proof of the finished product infusion bag/bottle. The utility model can effectively seal the finished product transfusion medicine adding port, prevent the finished product transfusion from being started by mistake before use, ensure the package integrity of the finished product transfusion, and simultaneously, the anti-theft finished product transfusion sealing device has the characteristics of easy operation and use and meeting the sanitary requirement, and improves the safety and the convenience of the finished product transfusion package; the utility model can ensure that the finished product transfusion is in a sterile state before the use of a patient, ensure the package integrity, reduce the pollution risk, ensure the anti-theft state and prevent other people from carrying out any operation or modification on the finished product transfusion.

Description

Anti-theft finished infusion sealer

Technical Field

The utility model belongs to the field of medical appliances, and relates to a tamper-evident finished product transfusion sealing device, in particular to a tamper-evident finished product transfusion sealing cap and a tamper-evident finished product transfusion sealing patch.

Background

The finished infusion is required to be packaged in the process of centralized intravenous administration and the puncture operation is carried out in the process of administration, so that the integrity of an administration port is lost, and the infusion port becomes a risk factor for introducing pollutants from the outside. The finished infusion package can ensure the integrity of finished infusion, isolate the quality risk possibly caused by external pollution factors to the finished infusion, and reduce the microbial challenge before administration. In the past, a sealing patch of a plastic small disc is additionally attached to a puncture port to replace a finished infusion package, but the sealing patch cannot be firmly attached and frequently falls off in the use process, so that a medical institution abandons the means. The field of centralized intravenous drug preparation at present mainly adopts a packaging technology that a finished product transfusion is externally sleeved with a flat pocket and is tied by an adhesive tape.

The traditional flat bag adhesive tape tying packaging technology for finished infusion has a plurality of defects. First, it cannot be completely sealed and is vulnerable to the invasion of external contaminants. Secondly, the packaging process needs to be cooperated by multiple persons, so that the labor cost is increased and the working efficiency is reduced. This is also a major reason why medical institutions with limited human resources have abandoned packaging of finished infusions. When finished infusion packed by the flat bags reaches a clinical sickness area, a treatment nurse also needs to dismantle all the packaging bags before taking the medicine, and huge workload is brought. In addition, flat pocket packaging is not compatible with existing medical automation technology. The flat pocket has color and poor transparency, which affects the recognition of the bar code of the finished infusion label. Importantly, once the flat pocket is opened, the packaged materials are convenient to obtain, so that the flat pocket is easy to repack and difficult to distinguish, and cannot meet the requirement of anti-theft.

For example, patent CN215022344U discloses an infusion bottle convenient for dispensing, and its specification describes that when a part of patients are infused in a hospital, physiological saline and antibiotic powder are needed, when the medicine is prepared, a syringe is firstly inserted into the physiological saline bottle to extract the liquid in the saline bottle, then the liquid is extracted, then the syringe is inserted into the antibiotic powder bottle to push the syringe piston back and forth, after the powder in the powder bottle is dissolved, the mixed liquid is extracted back into the syringe, then the syringe is extracted, then the saline is inserted into the saline bottle again, and then the infusion set is connected for infusion. These descriptions reflect the many shortcomings of the prior art.

Disclosure of utility model

Aiming at the defects of the finished infusion bag and the finished infusion bottle in the prior art in terms of sealing and anti-theft, the sterile sealing cap and the sterile sealing patch which have anti-theft function and are suitable for the finished infusion bag and the finished infusion bottle are designed by combining experience feedback of pharmacists and medical staff in consideration of specific feasibility and product economy of production practice. Specifically, the utility model provides the following technical scheme

The utility model provides a tamper-proof finished product infusion seal, its includes seal structure, seal structure is used for realizing the seal of finished product infusion bag or finished product infusion bottle, is used for judging whether finished product infusion bag or finished product infusion bottle is opened after the dispensing is accomplished, realizes tamper-proof of finished product infusion bag or finished product infusion bottle.

For convenience of description, the (tamper-evident) finished infusion bag and/or the (tamper-evident) finished infusion bottle will hereinafter sometimes be referred to simply as "finished infusion bag/bottle" or "finished infusion bag (bottle"), which may be referred to simply as "infusion bag/bottle" or "infusion bag (bottle)".

In one embodiment, the closure structure is a tamper-evident finished infusion closure, referred to herein as closure assembly one, which is a rolled structure, each unit being in the shape of a label.

Preferably, the first closure assembly comprises a backing layer which is provided in a roll.

The backing layer is release paper, and a support piece is arranged at the center of the roll shape of the backing layer.

The back lining layer is provided with a plurality of seal patch assemblies which can be torn off, and when the seal patch assemblies are used, the seal patch assemblies are torn off from the back lining layer and are stuck on the bottle stopper of the infusion bag or the bottle mouth of the infusion bottle, so that the puncture part of the medicine adding port can be completely covered.

The term "several" means two or more, three or more, four or more, and may be set according to actual needs.

Preferably, the sealing patch assembly is used for protecting the finished infusion bag or the finished infusion bottle after the dispensing is completed, and judging whether the finished infusion bag or the finished infusion bottle is opened or not after the dispensing is completed, so that the finished infusion bag or the finished infusion bottle is prevented from being opened in a theft-proof way.

The sealing patch assembly comprises a sealing patch main body attached to the backing layer, and one side of the sealing patch main body is fixedly connected with a tearing handle.

Preferably, the sealing patch main body comprises a film layer attached to the backing layer, one surface of the film layer, which is far away from the backing layer, is fixedly connected with a printing layer, and one surface of the printing layer, which is far away from the film layer, is fixedly connected with an adhesive layer.

The film layer is connected with the tearing handle, and an indication part is further arranged on the film layer.

The membrane layer is preferably a polymer membrane material, and the polymer membrane material has better performance of blocking oxygen and moisture, so that all factors which are possibly influenced by the outside are isolated.

The indication part is an indication ring arranged on the film layer and used for indicating the position of the drug adding port of the finished infusion bag or the finished infusion bottle.

Alternatively, the printed layer may be provided with a specific base color for differentiating the properties of the finished infusion drug product. For example: the common medicines adopt blue, the antibacterial medicines adopt red, the harmful medicines adopt yellow and the like.

In addition, the printing layer can be added with marks such as characters and the like for warning and explanation.

In another embodiment, the closure structure is a tamper-evident finished infusion closure cap, referred to herein as closure assembly two, which is generally in the shape of a tubular structure or bottle cap.

Preferably, the second sealing component is clamped at the bottle stopper of the finished infusion bag or the bottle mouth of the infusion bottle when in use, so that the puncture part of the medicine adding port can be completely covered, and the anti-theft opening of the finished infusion bag or the finished infusion bottle after the medicine is dispensed can be realized.

The second sealing assembly comprises two sealing cap bodies, two sealing cap bodies are hinged between one sides of the two sealing cap bodies, and bayonets are formed in the tops of the two sealing cap bodies.

Preferably, a first partition plate and a second partition plate are fixedly arranged in one sealing cap body, the second partition plate is positioned below the first partition plate, and a gap is reserved between the second partition plate and the first partition plate.

The other sealing cap body is internally and fixedly provided with a third baffle plate, and the position of the third baffle plate corresponds to a gap between the second baffle plate and the first baffle plate.

Preferably, the top surface and the bottom surface of the third partition board are provided with slopes, and one surface, close to the second partition board, of the first partition board is provided with slopes.

The first baffle is provided with a clamping groove, the three tops of the baffle are fixedly provided with clamping blocks, and the clamping blocks and the clamping grooves are matched to be used for locking when the two sealing cap bodies are folded.

Through holes are formed in the first partition plate, the second partition plate and the third partition plate in a penetrating mode, and the positions of the through holes correspond to the positions of the drug adding ports of the finished infusion bags or the finished infusion bottles.

And a sealing layer is fixedly arranged in the third partition plate on the second partition plate and used for protecting the through hole and protecting the finished infusion bag or the finished infusion bottle after the dispensing is finished so as to judge whether the finished infusion bag or the finished infusion bottle is opened after the dispensing is finished, so that the finished infusion bag or the finished infusion bottle is prevented from being opened in a theft-proof way.

Preferably, the sealing layer can be made of a film or medical rubber, so that the disposable infusion set can be conveniently and directly used for puncturing in the using process.

Optionally, the main body of the sealing cap can adopt a specific base color for distinguishing the properties of the finished infusion medicine. For example, common medicines are blue, antibacterial medicines are red, and harmful medicines are yellow, etc.

In addition, the main body of the sealing cap can be printed with characters and other marks for warning and explanation or marking the adapted infusion manufacturer and specification.

The finished product infusion sealing device can effectively seal the medicine adding port of the finished product infusion bag or the finished product infusion bottle, prevent the finished product infusion bag and the finished product infusion bottle from being started by mistake before use, ensure the package integrity of the finished product infusion bag and the finished product infusion bottle, and simultaneously has the characteristics of easy operation and use and meeting the sanitary requirement, and improve the safety and the convenience of the finished product infusion bag or the finished product infusion bottle; the utility model can ensure that the finished infusion bag or the finished infusion bottle is in a sterile state before the use of a patient, ensure the package integrity, reduce the pollution risk, ensure the anti-theft state and prevent other people from performing any operation or modification on the finished infusion bag or the finished infusion bottle.

Drawings

FIG. 1 is a schematic view of an exemplary embodiment of a tamper-evident finished infusion seal of the present utility model;

FIG. 2 is a schematic diagram of an embodiment of a tamper-evident finished infusion seal;

FIG. 3 is a schematic view of the layered structure of the body of an embodiment of a tamper-evident finished infusion seal;

FIG. 4 is a schematic side view of an embodiment of a tamper-evident finished infusion closure cap of the present utility model;

FIG. 5 is a schematic structural view of the sealing layer of an embodiment of a tamper-evident finished infusion closure cap;

Fig. 6 is another schematic structural view of an embodiment of a tamper-evident finished infusion closure cap.

The reference numerals are explained as follows:

1. a backing layer; 2. a seal assembly; 201. a seal patch main body; 2011. a film layer; 2012. printing a layer; 2013. an adhesive layer; 202. an indication ring; 203. tearing off the handle;

3. A closure cap assembly; 301. a sealing cap body; 302. a bayonet; 303. a first partition board; 304. a second partition board; 305. a third partition board; 306. a clamping block; 307. a clamping groove; 308. a through hole; 309. and (3) a sealing layer.

Detailed Description

In order to prevent the false opening of the finished infusion bag (bottle), the utility model provides a novel sealing structure, and two forms can be selected, wherein one is a tamper-proof finished infusion sealing patch with each unit in the shape of a label, and the other is a tamper-proof finished infusion sealing cap which is approximately in the shape of a bottle cap. The functions are the same, but to reflect the differences, the former is referred to herein as closure assembly one and the latter as closure assembly two.

For simplicity of description, the tamper-evident finished infusion seal may be referred to herein simply as a "finished infusion seal" or "seal". Similarly, the tamper-evident finished infusion cap may be referred to simply as a "finished infusion cap" or "cap".

The two sealing structures can effectively seal the medicine feeding port of the infusion bag and the infusion bottle, prevent the finished infusion bag and the finished infusion bottle from being started by mistake before use and ensure the package integrity of the finished infusion bag and the finished infusion bottle. Meanwhile, the finished infusion bag and the finished infusion bottle can be guaranteed to be in a sterile state before being used, pollution risks are reduced, and anti-theft opening is guaranteed.

The technical scheme of the present utility model will be described below with reference to the accompanying drawings. It is apparent that the described examples are only some, but not all, embodiments of the utility model; and the structures shown in the drawings are merely schematic and do not represent a physical object. It is intended that all other embodiments obtained by those skilled in the art based on these embodiments of the present utility model fall within the scope of the present utility model. Moreover, the embodiments of the present utility model and the features and technical solutions of the embodiments may be combined with each other without collision.

It should be understood 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.

Example 1

Referring to fig. 1-3, a tamper-proof finished product infusion sealer includes a sealing structure for sealing a finished product infusion bag or a finished product infusion bottle after dispensing, for judging whether the finished product infusion bag or the finished product infusion bottle is opened after dispensing is completed, and for tamper-proof of the finished product infusion bag or the finished product infusion bottle.

In one embodiment, the seal is a tamper-evident finished infusion seal, referred to herein as seal assembly one, which is a rolled structure of individual units in the shape of a label.

The first sealing assembly comprises a backing layer 1, and the backing layer 1 is arranged in a roll shape.

The backing layer 1 is release paper, and a supporting piece is arranged at the center of the roll shape of the backing layer 1.

It is noted that the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed.

The back lining layer 1 is provided with a plurality of seal plaster components 2 which can be torn off, when the seal plaster components 2 are used, the seal plaster components are torn off from the back lining layer 1 and pasted on the bottle stopper of the finished infusion bag or the bottle mouth of the infusion bottle, so that the puncture part of the medicine adding port can be completely covered.

The term "several" means two or more, three or more, four or more, and may be set according to actual needs.

The sealing label assembly 2 is used for protecting the finished infusion bag or the finished infusion bottle after the dispensing is finished, and judging whether the finished infusion bag or the finished infusion bottle is opened after the dispensing is finished, so that the finished infusion bag or the finished infusion bottle is prevented from being opened in a theft-proof way.

The seal patch assembly 2 comprises a seal patch main body 201 attached to the backing layer 1, wherein one side of the seal patch main body 201 is fixedly connected with a tearing handle 203, and the seal patch main body 201 can be folded in half and firmly adhered to each other during transfusion and can wrap a transfusion pipeline;

The design of the tearing handle 203 facilitates the tearing of the seal main body 201 from the backing layer 1 or the finished infusion bag or the finished infusion bottle, and once the seal main body 201 is stuck on the finished infusion bag or the finished infusion bottle and then torn, the seal main body 201 can be damaged and cannot be recovered, so that the finished infusion bag or the finished infusion bottle can be judged to be unsealed by naked eyes.

The seal main part 201 includes the rete 2011 of attaching on backing layer 1, the one side fixedly connected with print layer 2012 of backing layer 1 is kept away from to the rete 2011, the one side fixedly connected with adhesive layer 2013 of backing layer 2011 is kept away from to the print layer 2012, adhesive layer 2013 is connected with backing layer 1, this seal design product is through applying print layer 2012 and adhesive layer 2013 as the sign usefulness of distinguishing on the rete 2011, whole seal main part 201 is pasted on backing layer 1, the form of being convenient for take is made in the reel, the rete 2011 is polymer membrane material, polymer membrane material has better separation oxygen and moisture's performance, ensure that isolated everything external perhaps influences the factor of finished product infusion quality.

The print layer 2012 may be provided with different base colors as color codes to distinguish the properties of the finished infusion drug, for example: the common medicines adopt blue, the antibacterial medicines adopt red, the harmful medicines adopt yellow and the like, and marks such as characters and the like can be added into the printing layer 2012 to be used as warning and description.

The film 2011 is connected with the tearing handle 203, and an indication part is further arranged on the film 2011.

The indication part is an indication ring 202 arranged on the film 2011, and the indication ring 202 is used for indicating the position of a medicine feeding port of a finished infusion bag or a finished infusion bottle, so that the medical staff can puncture conveniently during use.

The sealing main body 201 is attached to the bottle stopper of the infusion bag or the bottle mouth of the infusion bottle, so that the puncture part of the medicine feeding mouth can be completely covered. The packaging is complete and sterile, the sealing pasting area is increased while the medicine feeding port is protected, the easily-taken sealing paste main body 201 can be conveniently operated by a single hand, whether a finished infusion bag or a finished infusion bottle is opened or not can be judged according to the state of the sealing paste main body 201 in the clinical use process, the administration mode can be selected to directly use the infusion apparatus to puncture for administration or to dismantle the sealing paste main body 201 for administration, the sealing paste main body 201 can maintain the sterile state after sterilization, and sterile materials required by centralized allocation of intravenous administration are provided.

When the infusion bag or bottle is used, sterile dosing and preparation are completed in a clean environment, a pharmacist or medical staff checks the infusion bag or bottle, the dosing port can be immediately sealed and packaged, a sealing patch main body 201 is picked up from a rolled backing layer 1, the sealing is completed by aligning an indicating ring 202 with the dosing port and attaching the sealing patch main body 201 to the dosing port of the infusion bag or bottle, the operation can be completed by a single person, the finished infusion bag or bottle can be conveyed to clinical various areas for later use, and clinical staff can check whether the sealing patch main body 201 is complete or not to judge whether infusion treatment is performed or not, and can be directly used for dosing after the infusion device is used for puncturing or dosing after the sealing patch main body 201 is detached.

Example 2

Referring to fig. 4-6, a tamper-proof finished product infusion sealer comprises a sealing structure, wherein the sealing structure is used for sealing after dispensing of a finished product infusion bag or a finished product infusion bottle, judging whether the finished product infusion bag or the finished product infusion bottle is opened after dispensing is completed, and achieving tamper-proof of the finished product infusion bag or the finished product infusion bottle.

The sealing structure is a tamper-evident finished infusion sealing cap, which is referred to herein as a second sealing assembly, which is a tubular structure that is generally in the shape of a bottle cap.

The second sealing component is clamped at the bottle stopper of the infusion bag or the bottle mouth of the infusion bottle when in use, can completely cover the dosing mouth, and is used for realizing the anti-theft opening of the finished infusion bag or the finished infusion bottle after the dosage.

The second sealing component comprises two sealing cap bodies 301, one sides of the two sealing cap bodies 301 are hinged, bayonets 302 are formed in the tops of the two sealing cap bodies 301, different base colors can be adopted by the sealing cap bodies 301 for distinguishing the properties of finished infusion medicines, such as blue for common medicines, red for antibacterial medicines, yellow for harmful medicines and the like, and in addition, marks such as characters and characters can be printed on the sealing cap bodies 301 to be used as warning and description or to mark the infusion manufacturers and specifications of the adaptation.

One of the sealing cap bodies 301 is fixedly provided with a first partition plate 303 and a second partition plate 304, the second partition plate 304 is positioned below the first partition plate 303, and a gap is reserved between the second partition plate 304 and the first partition plate 303.

The third partition plate 305 is fixedly installed in the other sealing cap main body 301, and the position of the third partition plate 305 corresponds to the gap between the second partition plate 304 and the first partition plate 303, i.e. when the two sealing cap main bodies 301 are combined together, the third partition plate 305 can be inserted into the gap between the second partition plate 304 and the first partition plate 303.

The top surface and the bottom surface of the third partition plate 305 are respectively provided with a slope, and the surfaces of the first partition plate 303 and the second partition plate 304, which are close to each other, are also provided with slopes, so that the third partition plate 305 can be conveniently inserted into a gap between the second partition plate 304 and the first partition plate 303.

The clamping groove 307 is formed in the first partition plate 303, the clamping block 306 is fixedly arranged at the top of the third partition plate 305, the clamping block 306 and the clamping groove 307 are matched to be used for locking when the two sealing cap main bodies 301 are folded, the sealing cap main bodies cannot be opened after being sealed, meanwhile, the appearance of a joint after being sealed is smooth, and no obvious part capable of being directly applied with force to be opened is arranged on the outer side. The design ensures the safety and the integrity of the seal, has the anti-theft function, and the seal cap assembly 3 has good sealing performance, can effectively block external pollution and ensures the quality of finished transfusion.

Through holes 308 are formed in the first partition plate 303, the second partition plate 304 and the third partition plate 305 in a penetrating mode, and the positions of the through holes 308 correspond to the positions of the medicine feeding ports of the infusion bottles.

The sealing layer 309 is fixedly arranged in the third partition plate 305 on the second partition plate 304, the sealing layer 309 is used for protecting the through hole 308 and protecting the finished infusion bag or the finished infusion bottle after the dispensing is finished so as to judge whether the finished infusion bag or the finished infusion bottle is opened after the dispensing is finished, so that the finished infusion bag or the finished infusion bottle is prevented from being opened in a theft-proof way, the sealing layer 309 can be made of a film or hospital rubber, and the disposable infusion set can be conveniently used for puncturing in the using process.

The finished infusion is finished in a clean environment, sterile dosing and blending are finished, a dosing port can be immediately sealed after checking by a pharmacist or medical staff, a sealing cap assembly 3 is taken, two sealing cap main bodies 301 are folded in half, a bayonet 302 is buckled on the neck of an infusion bottle, a third partition 305 is inserted between a first partition 303 and a second partition 304, a clamping block 306 is clamped into a clamping groove 307 to finish sealing, the operation can be finished by a single person and a single hand, the finished infusion bag or the finished infusion bottle after sealing can be sent to clinical various disease areas for later use, clinical staff can check whether a sealing layer 309 is complete or not, whether secondary puncture exists or not to judge whether infusion treatment is performed, and the infusion bottle can be pierced for drug administration after the sealing layer 309 is pierced by directly using an infusion apparatus.

In the description herein, the terms "front (section)", "lower (side)" refer to a positional relationship with reference to the normal sitting posture of the user, but do not mean that it is necessary to face a certain fixed direction in actual use operation, only for the purpose of showing the positional relationship or connection relationship between the respective components. Similarly, the terms "rear (end)", "upper (portion)", etc. do not constitute absolute spatial relationship limitations, but merely a concept of relative position, as will be readily appreciated by those skilled in the art.

The above description is only of the preferred embodiments of the present utility model; the scope of the utility model is not limited in this respect. Any person skilled in the art, within the technical scope of the present disclosure, may apply to the present utility model, and the technical solution and the improvement thereof are all covered by the protection scope of the present utility model.

Claims (9)

1. The anti-theft finished product transfusion sealer is characterized by comprising a sealing structure, wherein the sealing structure is a first sealing component which is a sealing patch for anti-theft finished product transfusion, and the first sealing component is a coiled structure;

the first sealing assembly comprises a backing layer (1), wherein the backing layer (1) is arranged in a roll shape;

The backing layer (1) is release paper, and a supporting piece is arranged at the center of the roll shape of the backing layer (1), or

The sealing structure is a second sealing component, which is a finished infusion sealing cap capable of preventing illegal opening, and is clamped on the infusion bag bottle stopper or the infusion bottle opening when in use,

The second sealing assembly comprises two sealing cap main bodies (301), one sides of the two sealing cap main bodies (301) are hinged, and the tops of the two sealing cap main bodies (301) are provided with bayonets (302);

A first partition plate (303) and a second partition plate (304) are fixedly arranged in one sealing cap main body (301), the second partition plate (304) is positioned below the first partition plate (303), and a gap is reserved between the second partition plate (304) and the first partition plate (303);

and a third partition plate (305) is fixedly arranged in the other sealing cap main body (301), and the position of the third partition plate (305) corresponds to the gap between the second partition plate (304) and the first partition plate (303).

2. The anti-theft finished product transfusion sealer as claimed in claim 1, wherein a plurality of seal components (2) which can be torn off are arranged on the back lining layer (1) in the seal component I, and the seal components (2) are torn off from the back lining layer (1) and stuck on the transfusion bag bottle stopper or the transfusion bottle opening when in use;

The sealing patch assembly (2) is used for protecting the finished infusion bag or the finished infusion bottle after the dispensing is finished, and judging whether the finished infusion bag or the finished infusion bottle is opened after the dispensing is finished.

3. The tamper-evident finished product infusion sealer according to claim 2, wherein the seal assembly (2) comprises a seal body (201) attached to a backing layer (1), and wherein a tearing handle (203) is fixedly connected to one side of the seal body (201).

4. A tamper-evident finished product infusion sealer according to claim 3, wherein the sealing patch body (201) comprises a film layer (2011) attached to the backing layer (1), one side of the film layer (2011) away from the backing layer (1) is fixedly connected with a printing layer (2012), and one side of the printing layer (2012) away from the film layer (2011) is fixedly connected with an adhesive layer (2013).

5. The tamper-evident finished product infusion sealer according to claim 4, wherein the film (2011) is connected to a tearing handle (203), and an indicator is further provided on the film (2011);

The indication part is an indication ring (202) arranged on the film layer (2011), and the indication ring (202) is used for indicating the position of the medicine feeding port of the infusion bag or the infusion bottle.

6. The anti-theft finished product transfusion sealer as claimed in claim 1, wherein the first partition board (303) is provided with a clamping groove (307), a clamping block (306) is fixedly arranged at the top of the third partition board (305), and the clamping block (306) and the clamping groove (307) are matched for locking when the two sealing cap main bodies (301) are folded.

7. The anti-theft finished product infusion sealer according to claim 6, wherein through holes (308) are formed in the first baffle plate (303), the second baffle plate (304) and the third baffle plate (305) in a penetrating manner, and the positions of the through holes (308) correspond to the positions of the infusion bags or the infusion bottle drug adding ports.

8. The tamper-evident finished infusion sealer as claimed in claim 7, wherein a sealing layer (309) is fixedly installed in a third partition (305) on the second partition (304), the sealing layer (309) is used for protecting the through hole (308) and protecting the finished infusion bag or the finished infusion bottle after the dispensing is completed, so as to determine whether the finished infusion bag or the finished infusion bottle is opened after the dispensing is completed.

9. The tamper-evident finished product fluid transfer closure of claim 4, wherein,

The printing layer (2012) is set to a specific ground color for distinguishing the properties of the finished infusion medicine;

the sealing cap main body (301) adopts specific ground color for distinguishing the properties of finished infusion medicines.