CN220125151U - Sterilizing assembly - Google Patents

Abstract

Embodiments of the present utility model provide a sterilization assembly. The sterilization assembly includes a sterilization wrap. The sterile wrapping cloth in the sterile bag comprises a first folding part, a second folding part, a third folding part, a fourth folding part and a bottom; in the folded state, the first folded part and the bottom part form a first isolation space; the second folding part and the third folding part are overlapped and arranged on one side of the first folding part far away from the bottom, and the second separation space is formed by the second folding part and the third folding part and the first folding part; the fourth folding portion is arranged on one side, far away from the first folding portion, of each of the second folding portion and the third folding portion, and the third isolation space is formed by the fourth folding portion, the second folding portion and the third folding portion. The operation disinfection subassembly sets up in first isolation space, and the disinfection dish subassembly sets up in the second isolation space, and first cover sets up in the third isolation space. According to the utility model, the articles required by central vein catheterization are packaged into a whole, so that the articles can be quickly, conveniently and completely prepared, and the time for preparing the articles can be reduced.

Description

Sterilizing assembly

Technical Field

The utility model relates to the technical field of medical instruments, in particular to a disinfection assembly.

Background

Central venous catheterization is a first-aid technique commonly used clinically. Central venous catheterization is often required for patients with acute and critical diseases such as surgical operation patients, wounds and the like, tumor chemotherapy patients, parenteral nutrition patients and the like, and venous administration routes for rescuing and treating patients are provided. This procedure requires rapid establishment of the central venous access and, in addition, the sterile operating principle to be followed in the catheterization.

However, in the current central venous catheterization process, there is a problem that the time is long or the sterile operation requirement cannot be met.

Disclosure of Invention

Aiming at the defects of the prior art, the utility model provides a disinfection component which is used for solving the technical problems that the prior central vein catheterization process takes longer time or cannot meet the requirement of aseptic operation.

In a first aspect, embodiments of the present utility model provide a sterilization assembly comprising a sterilization wrap; the sterilization bag comprises a sterile wrapping cloth, a first glove, a sterilization tray assembly and an operation sterilization assembly;

the sterile wrapping cloth comprises a first folding part, a second folding part, a third folding part, a fourth folding part and a bottom; in a folded state, the first folded part and the bottom part form a first isolation space; the second folding part and the third folding part are overlapped and arranged on one side, far away from the bottom, of the first folding part, and the second folding part, the third folding part and the first folding part form a second isolation space; the fourth folding part is arranged on one side, far away from the first folding part, of the second folding part and the third folding part, and a third isolation space is formed by the fourth folding part, the second folding part and the third folding part;

the operation disinfection subassembly set up in first isolation space, the disinfection dish subassembly set up in the second isolation space, first cover set up in the third isolation space.

Optionally, the sterile drape is in an unfolded state, the first fold being opposite the fourth fold; the second fold is opposite the third fold.

Optionally, the sanitizing tray assembly comprises a sanitizing treatment tray, a sanitizing solution piece, and at least one sanitizing brush; the disinfection treatment disc comprises a first accommodating space and a second accommodating space, the disinfection solution piece is arranged in the first accommodating space, and the disinfection brush is arranged in the second accommodating space.

Optionally, the sanitizing solution piece comprises chlorhexidine sanitizing solution.

Optionally, the operational sterilization assembly includes a therapeutic towel, a hole towel, a barrier gown, and a second glove.

Optionally, the first glove and the second glove are sterile surgical gloves.

Optionally, the model of the first glove and the model of the second glove are not less than half 6 and not more than 8.

Optionally, the width of the therapeutic towel is not less than 1.2 meters and not more than 1.5 meters, and the length of the therapeutic towel is not less than 1.5 meters and not more than 1.8 meters.

Optionally, the width and length of the hole towel are not less than 1.2 meters and not more than 1.5 meters.

Optionally, the sterilizing bag further comprises a liquid absorbing pad and a sealing bag, wherein the liquid absorbing pad and the sterilizing bag are placed in the sealing bag; the liquid absorbing pad is closer to the opening of the sealing bag than the sterilizing bag.

The technical scheme provided by the embodiment of the utility model has the beneficial technical effects that:

the sterilization bag 1 is formed by arranging more required articles for central vein catheterization, namely the sterilization wrap 11, the first glove 12, the sterilization tray assembly and the operation sterilization assembly, and can be directly taken out in any condition, so that the articles can be quickly, conveniently and completely prepared, and the preparation time of the articles can be reduced.

Further, the sterile wrap 11 in the sterilization wrap 1 is folded to form three isolated spaces, the operation sterilization assembly is disposed in the first isolated space a, the sterilization tray assembly is disposed in the second isolated space B, and the first glove 12 is disposed in the third isolated space C. When the central venous catheterization is performed, the first sleeve 12 is taken in the third isolated space C, the sterilization tray assembly is taken in the second isolated space B for sterilization, and finally the operation sterilization assembly is taken in the first isolated space A. That is, the present utility model can separate the required articles (e.g., the first sleeve 12, the sterilization tray assembly, and the operation sterilization assembly) at different stages according to the central venous catheterization procedure, which can facilitate the operation of the operator, avoid the damage to the sterile principle due to unfamiliar operation procedure, and facilitate the reduction of the risk of infection.

From the above, the required articles for central vein catheterization are placed in the isolation space formed by folding the sterile wrapping cloth, so that the safety and the sanitation can be guaranteed.

Additional aspects and advantages of the utility model will be set forth in part in the description which follows, and in part will be obvious from the description, or may be learned by practice of the utility model.

Drawings

The foregoing and/or additional aspects and advantages of the utility model will become apparent and readily appreciated from the following description of the embodiments, taken in conjunction with the accompanying drawings, in which:

fig. 1 is a schematic view of a sterilization assembly according to an embodiment of the present disclosure;

FIG. 2 is a schematic view of a sterile drape in an unfolded state according to an embodiment of the present utility model;

fig. 3 is a schematic diagram of a folded first folding portion of a sterile drape according to an embodiment of the present utility model;

FIG. 4 is a schematic view of a sterile drape with a first fold folded and a sterile treatment tray placed thereon according to an embodiment of the present utility model;

fig. 5 is a schematic view of a first glove placed after a second folding portion and a third folding portion of a sterile drape according to an embodiment of the present utility model are folded;

fig. 6 is a schematic view of a sterile drape in a folded state according to an embodiment of the present utility model.

Reference numerals illustrate:

1-sterilizing bags;

11-sterile wrapping; 111-a first fold; 112-a second fold; 113-a third fold; 114-fourth fold; 115-bottom; a-a first isolation space; b-a second isolation space; c-a third isolation space;

12-a first glove;

131-sterilizing the treatment tray; 132-sterilizing solution pieces; 133-a disinfection brush; d-a first accommodation space; e-a second accommodation space;

141-a therapeutic towel; 142-hole towel; 143-a barrier coat; 144-second glove;

2-a liquid absorbing pad;

3-sealing the bag; 31-opening.

Detailed Description

Embodiments of the present utility model are described below with reference to the drawings in the present utility model. It should be understood that the embodiments described below with reference to the drawings are exemplary descriptions for explaining the technical solutions of the embodiments of the present utility model, and the technical solutions of the embodiments of the present utility model are not limited.

As used herein, the singular forms "a", "an", "the" and "the" are intended to include the plural forms as well, unless expressly stated otherwise, as understood by those skilled in the art. It should be further understood that the terms "comprises" and/or "comprising," when used in this specification, specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of other features, information, data, steps, operations, elements, components, and/or groups thereof, all of which may be included in the present utility model. The term "and/or" as used herein refers to at least one of the items defined by the term, e.g., "a and/or B" may be implemented as "a", or as "B", or as "a and B".

For the purpose of making the objects, technical solutions and advantages of the present utility model more apparent, the embodiments of the present utility model will be described in further detail with reference to the accompanying drawings.

The development idea of the utility model comprises the following steps: at present, in the actual clinical operation process, the central venous catheterization needs more objects to be prepared, and the time for carrying out the object preparation process is longer. In emergency situations, operators may violate sterility guidelines because some utilities are not fully prepared; moreover, the specifications of the treatment towels and the hole towels prepared by the departments are different, so that the maximization of the sterile barrier recommended by guidelines is difficult to achieve; in addition, the types of the sterilizing liquid used clinically are complicated, and the requirement of sterility cannot be met.

The following describes the technical scheme of the present utility model and how the technical scheme of the present utility model solves the above technical problems in detail with specific embodiments. It should be noted that the following embodiments may be referred to, or combined with each other, and the description will not be repeated for the same terms, similar features, similar implementation steps, and the like in different embodiments.

An embodiment of the present utility model provides a sterilization assembly, which is schematically shown in fig. 1 to 6, and includes a sterilization wrap 1. The sterilization wrap 1 comprises a sterile wrap 11, a first sleeve 12, a sterilization tray assembly and an operation sterilization assembly.

The sterile drape 11 comprises a first fold 111, a second fold 112, a third fold 113, a fourth fold 114, and a bottom 115; in the folded state, the first folded portion 111 and the bottom portion 115 form a first isolated space a; the second folded portion 112 and the third folded portion 113 are overlapped and arranged on one side of the first folded portion 111 away from the bottom 115, and the second folded portion 112 and the third folded portion 113 form a second isolation space B with the first folded portion 111; the fourth folded portion 114 is disposed at a side of both the second folded portion 112 and the third folded portion 113 away from the first folded portion 111, and the fourth folded portion 114 forms a third separation space C with the second folded portion 112 and the third folded portion 113.

The operating sterilization assembly is disposed in the first isolated space a, the sterilization tray assembly is disposed in the second isolated space B, and the first glove 12 is disposed in the third isolated space C.

In this embodiment, many required articles for central venous catheterization, namely, the sterile wrapping 11, the first glove 12, the sterilization tray assembly and the operation sterilization assembly are arranged to form the sterilization bag 1, and in any case, the sterilization bag 1 can be directly taken out, so that the articles can be quickly, conveniently and completely prepared, and the time for preparing the articles can be reduced.

Further, the sterile wrap 11 in the sterilization wrap 1 is folded to form three isolated spaces, the operation sterilization assembly is disposed in the first isolated space a, the sterilization tray assembly is disposed in the second isolated space B, and the first glove 12 is disposed in the third isolated space C. When the central venous catheterization is performed, the first sleeve 12 is taken in the third isolated space C, the sterilization tray assembly is taken in the second isolated space B for sterilization, and finally the operation sterilization assembly is taken in the first isolated space A. That is, the present utility model can separate the required articles (e.g., the first sleeve 12, the sterilization tray assembly, and the operation sterilization assembly) at different stages according to the central venous catheterization procedure, which can facilitate the operation of the operator, avoid the damage to the sterile principle due to unfamiliar operation procedure, and facilitate the reduction of the risk of infection.

From the above, the required articles for central vein catheterization are placed in the isolation space formed by folding the sterile wrapping cloth 11, which is beneficial to ensuring safety and sanitation.

Alternatively, the sterile drape 11 is in an unfolded state, with the first fold 111 opposite the fourth fold 114; the second folded portion 112 is opposite to the third folded portion 113.

In this embodiment, the sterile drape 11 is of a sheet type in the unfolded state. The first folded portion 111 is opposite to the fourth folded portion 114, and the second folded portion 112 is opposite to the third folded portion 113, so that it is beneficial for the first folded portion 111 to form a first isolation space a with the bottom 115 after the first folded portion 111 is folded; next, the second folded portion 112 and the third folded portion 113 are folded, and the second folded portion 112 forms a second separation space B with the third folded portion 113 and the first folded portion 111; finally, the fourth folded portion 114 is folded, and the fourth folded portion 114 forms a third separation space C with the second folded portion 112 and the third folded portion 113.

Illustratively, as shown in fig. 2, the sterile drape 11 is quadrilateral, and the first fold 111, the second fold 112, the third fold 113, and the fourth fold 114 are all four corners of the quadrilateral. The first, second, third and fourth folded portions 111, 112, 113 and 114 are sequentially folded, and the first, second and third isolated spaces a, B and C can be sequentially formed from the inside to the outside.

Optionally, the sanitizing disc assembly includes a sanitizing treatment disc 131, a sanitizing solution piece 132, and at least one sanitizing brush 133; the sterilizing treatment tray 131 includes a first accommodation space D in which the sterilizing solution member 132 is disposed and a second accommodation space E in which the sterilizing brush 133 is disposed.

In this embodiment, the disinfection dish subassembly is placed in the second isolation space B, and disinfection solution piece 132 and disinfection brush 133 are placed in two independent accommodation spaces respectively moreover, can conveniently take, avoid cross infection.

Illustratively, as shown in fig. 4, the sterilization treatment tray 131 has a U-shape, the sterilization treatment tray 131 includes a first receiving space D and a second receiving space E, and the first receiving space D and the second receiving space E are two independent receiving spaces. The sterilizing solution member 132 and the sterilizing brush 133 are respectively provided in different accommodating spaces, so that cross contamination of the sterilizing solution member 132 and the sterilizing brush 133 can be avoided, and the sterilizing solution member 132 and the sterilizing brush 133 can be respectively taken. During the use of the sterilizing solution unit 132, the sterilizing solution in the sterilizing solution unit 132 may be poured into the first receiving space D, and the sterilizing brush 133 is dipped in the sterilizing solution to perform the sterilization.

As shown in fig. 5, the second folded portion 112 and the third folded portion 113 are folded to form a second isolated space B, and the sterilization tray assembly is placed in the second isolated space B.

Illustratively, as shown in fig. 5 and 6, the fourth folded portion 114 is folded to form a third isolated space C in which the first sleeve 12 is placed. It should be noted that L on the schematic diagram of the first glove 12 in fig. 5 represents a left-hand glove, and R represents a right-hand glove. The first glove 12 can be folded and placed in the third isolated space C, and the folded size of the first glove 12 is suitable for the size of the third isolated space C.

Specifically, the number of the sterilizing brushes 133 may be plural, and may be specifically selected according to the actual situation. In fig. 4, 2 disinfection brushes 133 are provided.

Alternatively, the disinfecting brush 133 may be a surgical brush.

In this embodiment, the surgical brush has a large disinfecting contact surface, and the handle of the surgical brush may be configured as a plastic hand for easy grasping by an operator.

Optionally, the sanitizing solution member 132 comprises chlorhexidine sanitizing solution.

In this embodiment, the disinfecting solution member 132 of the disinfecting assembly is uniformly configured as a chlorhexidine disinfecting solution which can reduce contamination and advantageously reduce the risk of infection of the central venous catheter.

Optionally, the operational sterilization assembly includes a treatment towel 141, a hole towel 142, a barrier gown 143, and a second sleeve 144.

In this embodiment, the operation sterilization assembly may include a treatment towel 141, a hole towel 142, a barrier suit 143, and a second sleeve 144, and may further include other articles, which may be omitted according to the actual situation. The treating towel 141, the hole towel 142, the isolation cloth 143 and the second glove 144 of the operation sterilization module can be folded in the first isolated space a, and the folded sizes of the treating towel 141, the hole towel 142, the isolation cloth 143 and the second glove 144 are adapted to the size of the first isolated space a.

Alternatively, the treatment towel 141, the hole towel 142, the barrier gown 143, and the second sleeve 144 may be placed in the first barrier space a in the order of the treatment towel 141, the hole towel 142, the second sleeve 144, and the barrier gown 143 from the outside to the inside.

In this embodiment, the operator places the treatment towel 141 on the operating bed and the hole towel 142 on the affected part of the patient while wearing the first glove 12. The second glove 144 is then taken and the first glove 12 is replaced to ensure sterility of the procedure, and the isolation garment 143 is then donned in preparation for central venous catheterization. This procedure is more advantageous to ensure aseptic operation.

Illustratively, as shown in fig. 3, the first folded portion 111 is folded, and the first folded portion 111 forms a first isolated space a with the bottom 115. The treating towel 141, the hole towel 142, the barrier gown 143 and the second sleeve 144 are folded up to be placed in the first barrier space a. The treating towel 141, the hole towel 142, the barrier gown 143 and the second sleeve 144 in fig. 3 are placed in the same layer in the first barrier space a, whereby the treating towel 141, the hole towel 142, the barrier gown 143 and the second sleeve 144 can be taken according to the habit of the operator. It will be appreciated that the placement positions of the treatment towel 141, the hole towel 142, the isolation suit 143 and the second glove 144 may be set according to actual needs, and the specific placement positions are not limited herein.

Specifically, the isolation garment 143 is made of disposable non-woven fabrics, the front ends of the sleeves are made of narrow sleeves, and the sleeves are made of elastic materials, so that an operator can wear the second sleeves 144 conveniently.

Optionally, first glove 12 and second glove 144 are sterile surgical gloves.

In this embodiment, first glove 12 and second glove 144 are sterile surgical gloves. Sterilization with first glove 12 followed by central venous catheterization with second glove 144 can reduce the risk of infection.

Optionally, in the unfolded state, the first glove 12 and the second glove 144 are no less than half 6 and no greater than 8.

In this embodiment, the first glove 12 and the second glove 144 are both in the above range, and can be adapted to the hand sizes of different operators.

Alternatively, in the unfolded state, the width of the treatment towel 141 is not less than 1.2 meters and not more than 1.5 meters, and the length of the treatment towel 141 is not less than 1.5 meters and not more than 1.8 meters.

In this embodiment, the towel 141 needs to be packed over the entire operating bed to meet the requirements of deep vein catheterization to maximize the sterility barrier. If the width and length of the treatment towel 141 are smaller than the above ranges, the whole operation bed cannot be paved, and the requirement of maximizing the sterile barrier of deep vein catheterization cannot be met; the width and length of the treating towel 141 are outside the above ranges, resulting in increased costs. The width and length of the treating towel 141 are within the above ranges, and can be advantageous in terms of cost saving on the basis of the full operation bed.

Alternatively, in the unfolded state, the hole towel 142 has a width and a length of not less than 1.2 meters and not more than 1.5 meters.

In this embodiment, the hole towel 142 is capable of covering the affected area of the patient. The hole towel 142 can meet the requirement that the hole towel 142 is paved on the affected part of the patient, and the cost can be saved.

Optionally, the disinfection assembly further comprises a liquid suction pad 2 and a sealing bag 3, wherein the liquid suction pad 2 and the disinfection bag 1 are placed in the sealing bag 3; the absorbent pad 2 is closer to the opening 31 of the sealed bag 3 than the sterilization wrap 1.

In this embodiment, as shown in fig. 1, when the central venous catheterization is performed, the absorbent pad 2 is placed under the catheterization, and then the sterilization wrap 1 is taken. Placing the absorbent pad 2 closer to the opening 31 of the sealed bag 3 than the sterilization wrap 1 facilitates access to the absorbent pad 2 prior to access to the sterilization wrap 1.

The liquid absorbing pad 2 and the disinfection bag 1 are placed in the sealing bag 3, so that the regularity of articles can be further ensured, the loss is avoided, and the contact with the external environment is further reduced to reduce pollution.

Optionally, the surfaces of the treatment towel 141, the hole towel 142 and the liquid absorbing pad 2 close to the patient are all water absorbing surfaces, and the surfaces far away from the patient are all waterproof surfaces.

In this embodiment, the surface of the treatment towel 141, the hole towel 142 and the liquid absorbing pad 2, which is close to the patient, is the water absorbing surface, so that the patient can keep dry and comfortable, and the comfort of the patient is improved; the surface of the treatment towel 141, the hole towel 142 and the liquid absorbing pad 2 far away from the patient is waterproof, so that disinfectant and the like can not permeate into the patient.

The preparation process of the sterilization wrap 1 of the present utility model is as follows:

as shown in fig. 2, in the unfolded state of the aseptic package 11, the aseptic package 11 includes a first folded portion 111, a second folded portion 112, a third folded portion 113, a fourth folded portion 114, and a bottom portion 115, the first folded portion 111 being opposite to the fourth folded portion 114; the second folded portion 112 is opposite to the third folded portion 113.

As shown in fig. 3, the first folded portion 111 is folded in the direction of the fourth folded portion 114, and the first folded portion 111 and the bottom portion 115 form a first separation space a. The treatment towel 141, the hole towel 142, the isolation suit 143, the second sleeve 144, and the like are disposed in the first isolated space a.

As shown in fig. 4 and 5, the sterilization tray assembly is placed over the first folded portion 111, the second folded portion 112 is folded in the direction of the third folded portion 113, and the third folded portion 113 is folded in the direction of the second folded portion 112, thereby forming the second insulation space B. The sterilizing tray assembly is now disposed in the second compartment B.

As shown in fig. 5 and 6, the second sleeve 144 is placed over the second folded portion 112, the third folded portion 113, and the bottom portion 115, and the fourth folded portion 114 is folded in the direction of the first folded portion 111, thereby forming the third separation space C. The second sleeve 144 is disposed in the third isolated space C.

The central vein catheterization is carried out, and the use process of the disinfection assembly is as follows:

the sealing bag 3 is opened, the liquid absorbing pad 2 is taken out first and placed under the tube placing part.

The sterilization wrap 1 is taken out, the fourth folded portion 114 is unfolded in a direction away from the first folded portion 111, and the first glove 12 is taken out and worn.

The third folded portion 113 is unfolded in a direction away from the second folded portion 112, the second folded portion 112 is unfolded in a direction away from the third folded portion 113, the sterilizing tray assembly is taken out, the sterilizing solution in the sterilizing solution member 132 is poured into the first accommodating space D, and the sterilizing brush 133 is used for dipping the sterilizing solution to sterilize the skin twice.

The first folding part 111 is unfolded in a direction far away from the fourth folding part 114, the treatment towel 141 is taken out and placed on the operation bed, and the hole towel 142 is placed on the affected part of the patient; the second sleeve 144 is then removed and the first sleeve 12 is replaced, the isolation garment 143 is removed and put on, and the central venous catheter is prepared.

By applying the embodiment of the utility model, at least the following beneficial effects can be realized:

1. according to the embodiment of the utility model, the required articles for central vein catheterization are arranged into the disinfection assembly, and the disinfection assembly can be directly taken out in any condition, so that the articles can be quickly, conveniently and completely prepared, and the time for preparing the articles is reduced.

2. In the embodiment of the utility model, the sterile wrapping cloth in the sterilization bag is folded to form three isolation spaces, the operation sterilization assembly is arranged in the first isolation space, the sterilization tray assembly is arranged in the second isolation space, and the first glove is arranged in the third isolation space. When the central vein catheterization is performed, the first glove is needed to be taken in the third isolation space, the sterilization tray assembly is taken in the second isolation space for sterilization, and finally the operation sterilization assembly is taken in the first isolation space. That is, the utility model can separate the articles at different stages according to the process of central vein catheterization, is beneficial to the operation of operators, can avoid the damage of aseptic principle caused by unfamiliar operation process, and is beneficial to the reduction of infection risk.

3. In the embodiment of the utility model, the disinfection solution piece and the disinfection brush are respectively arranged in the two independent accommodating spaces, so that the disinfection solution piece and the disinfection brush can be conveniently taken out and cross infection is avoided.

4. The disinfecting solution parts of the disinfecting assembly are uniformly configured into the chlorhexidine disinfecting solution, and the chlorhexidine disinfecting solution can reduce pollution and is beneficial to reducing the risk of infection of the central venous catheter.

Those of skill in the art will appreciate that the various operations, methods, steps in the flow, acts, schemes, and alternatives discussed in the present utility model may be alternated, altered, combined, or eliminated. Further, other steps, means, or steps in a process having various operations, methods, or procedures discussed herein may be alternated, altered, rearranged, disassembled, combined, or eliminated. Further, steps, measures, schemes in the prior art with various operations, methods, flows disclosed in the present utility model may also be alternated, altered, rearranged, decomposed, combined, or deleted.

In the description of the present utility model, directions or positional relationships indicated by words such as "center", "upper", "lower", "front", "rear", "left", "right", "vertical", "horizontal", "top", "bottom", "inner", "outer", etc., are based on exemplary directions or positional relationships shown in the drawings, are for convenience of description or simplification of describing embodiments of the present utility model, and do not indicate or imply that the devices or components referred to must have a specific orientation, be configured and operated in a specific orientation, and thus should not be construed as limiting the present utility model.

The terms "first," "second," and the like, are used for descriptive purposes only and are not to be construed as indicating or implying relative importance or implicitly indicating the number of technical features indicated. Thus, a feature defining "a first" or "a second" may explicitly or implicitly include one or more such feature. In the description of the present utility model, unless otherwise indicated, the meaning of "a plurality" is two or more.

In the description of the present utility model, it should be noted that, unless explicitly specified and limited otherwise, the terms "mounted," "connected," and "connected" are to be construed broadly, and may be either fixedly connected, detachably connected, or integrally connected, for example; can be directly connected or indirectly connected through an intermediate medium, and can be communication between two elements. The specific meaning of the above terms in the present utility model will be understood in specific cases by those of ordinary skill in the art.

In the description of the present specification, a particular feature, structure, material, or characteristic may be combined in any suitable manner in one or more embodiments or examples.

It should be understood that, although the steps in the flowcharts of the figures are shown in order as indicated by the arrows, the order in which the steps are performed is not limited to the order indicated by the arrows. In some implementations of embodiments of the utility model, the steps in each flow may be performed in other orders as desired, unless explicitly stated herein. Moreover, some or all of the steps in the flowcharts may include multiple sub-steps or multiple stages based on the actual implementation scenario. Some or all of the sub-steps or stages may be performed at the same time, or may be performed at different times, where the execution sequence of the sub-steps or stages may be flexibly configured according to the requirements, which is not limited by the embodiment of the present utility model.

The foregoing is only a part of the embodiments of the present utility model, and it should be noted that, for those skilled in the art, other similar implementation means based on the technical idea of the present utility model may be adopted without departing from the technical idea of the solution of the present utility model, which is also within the protection scope of the embodiments of the present utility model.

Claims (10)

1. A sterilization assembly comprising a sterilization bag; the sterilization bag comprises a sterile wrapping cloth, a first glove, a sterilization tray assembly and an operation sterilization assembly;

the sterile wrapping cloth comprises a first folding part, a second folding part, a third folding part, a fourth folding part and a bottom; in a folded state, the first folded part and the bottom part form a first isolation space; the second folding part and the third folding part are overlapped and arranged on one side, far away from the bottom, of the first folding part, and the second folding part, the third folding part and the first folding part form a second isolation space; the fourth folding part is arranged on one side, far away from the first folding part, of the second folding part and the third folding part, and a third isolation space is formed by the fourth folding part, the second folding part and the third folding part;

the operation disinfection subassembly set up in first isolation space, the disinfection dish subassembly set up in the second isolation space, first cover set up in the third isolation space.

2. The sterilization assembly of claim 1, wherein the first fold is opposite the fourth fold in the unfolded state of the sterile drape; the second fold is opposite the third fold.

3. The sterilization assembly of claim 1, wherein the sterilization tray assembly includes a sterilization treatment tray, a sterilization solution member, and at least one sterilization brush; the disinfection treatment disc comprises a first accommodating space and a second accommodating space, the disinfection solution piece is arranged in the first accommodating space, and the disinfection brush is arranged in the second accommodating space.

4. A disinfecting assembly as recited in claim 3, characterized in that the disinfecting solution element comprises a chlorhexidine disinfecting solution.

5. The sterilization assembly of claim 1, wherein the operational sterilization assembly comprises a therapeutic towel, a hole towel, a barrier gown, and a second glove.

6. The sterilization assembly of claim 5, wherein the first glove and the second glove are each sterile surgical gloves.

7. The sterilization assembly of claim 6, wherein the first glove and the second glove are of a type no less than half 6 and no greater than 8 in the unfolded state.

8. The sterilization assembly of claim 5, wherein the width of the therapeutic towel in the unfolded state is not less than 1.2 meters and not more than 1.5 meters, and the length of the therapeutic towel is not less than 1.5 meters and not more than 1.8 meters.

9. A disinfecting assembly as recited in claim 5, characterized in that the hole-towel, in the unfolded state, has a width and a length of not less than 1.2 meters and not more than 1.5 meters.

10. The sterilization assembly of claim 1, further comprising a wicking pad and a sealing bag, the wicking pad and the sterilization bag being disposed within the sealing bag; the liquid absorbing pad is closer to the opening of the sealing bag than the sterilizing bag.