Disposable sterile trachea cannula bag sealing device

Through the coordinated operation of the fixing component, limiting component, and driving component, the endotracheal intubation kit achieves precise positioning, adaptive compression, and precise temperature-controlled sealing, improving the efficiency and safety of the sealing device and solving the problems of incomplete sealing and high energy consumption in existing technologies.

CN224045635UActive Publication Date: 2026-03-27SUZHOU AOJIAN SURGICAL&HYGEIAN DISPOSABLES CO LTD
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Patent Information

Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2025-05-12
Publication Date
2026-03-27

AI Technical Summary

Technical Problem

Existing sealing devices suffer from problems such as inaccurate temperature and pressure control, simple fixing components that cannot stably fix endotracheal tube kits of different sizes, poor coordination of drive components, and limited functionality and high energy consumption in the sealing process of endotracheal tube kits.

Method used

The baffle and clamp of the fixed component are used to achieve precise positioning of the endotracheal intubation kit. The telescopic rod and compression spring of the limiting component provide adaptive pressing force. The drive component pushes the heating plate through the cylinder for precise temperature control and sealing. The adjustment panel and display panel of the operation component enable visual adjustment of parameters.

Benefits of technology

Ensure the sealing integrity and sterility of the endotracheal intubation kit, improve sealing efficiency, reduce energy consumption, enhance operational convenience, and improve the sealing quality and safety of medical supply packaging.

✦ Generated by Eureka AI based on patent content.

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Abstract

The utility model provides a disposable sterile trachea cannula bag sealing device, which belongs to the technical field of sealing devices, and comprises an operation component, a placing plate fixedly arranged on the surface of the operation component, a fixing component fixedly connected to the side surface of the operation component, a limiting component matched with the placing plate for use, and a driving component adaptively arranged on the surface of the limiting component, and the limiting rod is inserted into the side surface of the limiting assembly. The trachea cannula bag is ensured to be stably positioned through the matching of the baffle and the clamping plate of the fixing assembly; a telescopic rod of the limiting assembly is in linkage with an extrusion spring to provide self-adaptive pressing force, and uneven sealing pressure is avoided; the driving assembly adopts an air cylinder to push a heating plate, precise temperature control sealing is achieved in cooperation with a hot-pressing rod, and it is ensured that a seal is sterile and good in integrity; an adjusting panel and a display panel of the operation assembly realize visual parameter adjustment, so that the operation convenience is improved; the whole structure works cooperatively, the sealing efficiency is guaranteed, and energy consumption is reduced.
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Description

TECHNICAL FIELD

[0001] The utility model belongs to sealing device technical field, specifically relates to a disposable sterile tracheal cannula package sealing device. BACKGROUND

[0002] Disposable sterile tracheal cannula package sealing device is a kind of intelligent packaging sealing equipment specially designed for medical field, mainly used to ensure the sterility and sealing integrity of tracheal cannula package, its core function is to provide packaging protection meeting sterilization standard for medical consumables by accurate hot-press sealing technology, the device is widely used in emergency department, ICU and operating room, and its sealed finished product can be sterilized by EO (Ethylene Oxide) or radiation, meet YY / T 0698 medical packaging standard, effectively reduce the risk of clinical infection.

[0003] The existing sealing process lacks precise temperature and pressure control, which can easily lead to incomplete sealing or material thermal damage;The fixed assembly has a simple structure, and cannot stably fix tracheal cannula packages of different specifications, affecting the sealing consistency;The heating and pressing mechanism of the driving assembly has poor coordination, low sealing efficiency and high energy consumption;The operation interface has single function, and it is difficult to monitor and adjust sealing parameters in real time;Therefore, a disposable sterile tracheal cannula package sealing device is proposed. UTILITY MODEL CONTENTS

[0004] The utility model aims at providing a disposable sterile tracheal cannula package sealing device, to solve the problems proposed in the above background.

[0005] To achieve the above object, the utility model provides the following technical scheme:

[0006] A disposable sterile tracheal cannula package sealing device, comprising an operating assembly, a placing plate fixedly installed on the surface of the operating assembly, a fixing assembly fixedly connected to the side surface of the operating assembly, a limiting assembly used in cooperation with the placing plate, a driving assembly adaptively installed on the surface of the limiting assembly, and a limiting rod inserted into the side surface of the limiting assembly.

[0007] As a preferred scheme of the utility model, the operating assembly comprises an operating box, a switch fixedly installed on the side wall of the operating box, an adjusting panel fixedly connected to the side surface of the operating box, and a display panel adaptively installed on the side wall of the operating box.

[0008] As a preferred scheme of the utility model, the fixing assembly comprises a baffle fixedly connected to the surface of the operating box, a fixed plate fixedly installed on the side wall of the baffle, and a clamping plate fixedly connected to the side surface of the fixed plate.

[0009] As a preferred scheme of the utility model, the limiting assembly includes an outer shell, a top plate fixedly installed at the bottom of the outer shell, an extrusion spring sleeved on the outer surface of the limiting rod, and a bottom plate fixedly connected at the bottom of the limiting rod.

[0010] As a preferred scheme of the utility model, two telescopic rods are connected at the bottom of the limiting rod and fixedly connected with the limiting rod, extrusion springs are sleeved on the outer walls of the two telescopic rods, and the bottoms of the two telescopic rods are fixedly connected with the bottom plate.

[0011] As a preferred scheme of the utility model, the driving assembly includes a cylinder adaptively installed on the surface of the outer shell, a telescopic cylinder fixedly installed at the output end of the cylinder, a heating plate fixedly connected with the side wall of the telescopic cylinder, and a fixed frame fixedly installed at the bottom of the heating plate.

[0012] As a preferred scheme of the utility model, the driving assembly further includes a rotor rotatably installed on the inner wall of the fixed frame, a conducting rod clamped on the inner surface of the fixed frame, and a hot-pressing rod clamped at the bottom of the conducting rod.

[0013] Compared with the prior art, the utility model has the beneficial effects that: the cooperation of the baffle and the clamping plate of the fixing assembly ensures that the tracheal cannula bag is positioned stably; the telescopic rod and the extrusion spring of the limiting assembly are linked to provide self-adaptive compression force, avoiding uneven sealing pressure; the driving assembly adopts the cylinder to push the heating plate, and cooperates with the hot-pressing rod to realize precise temperature control sealing, ensuring that the sealing is sterile and has good integrity; the adjustment panel and the display panel of the operation assembly realize visual adjustment of parameters, improving operation convenience; the overall structure works cooperatively, ensuring sealing efficiency and reducing energy consumption, improving the sealing quality and safety of medical product packaging. BRIEF DESCRIPTION OF DRAWINGS

[0014] In order to more clearly illustrate the technical scheme of the embodiments of the utility model, the following will briefly introduce the drawings needed to be used in the embodiment description, and obviously, the drawings in the following description are only some embodiments of the utility model, and those skilled in the art can obtain other drawings according to these drawings without paying creative labor. Among them:

[0015] Figure 1 It is the overall structure schematic view of the utility model;

[0016] Figure 2 It is the operation assembly and limiting assembly structure schematic view of the utility model;

[0017] Figure 3 It is the fixing assembly structure schematic view of the utility model;

[0018] Figure 4The utility model discloses a drive assembly structure schematic view.

[0019] In the drawing: 101, operating assembly;102, placing plate;103, fixed component;104, limiting component;105, drive assembly;106, limiting rod;101a, operating box;101b, switch;101c, adjusting panel;101d, display panel;103a, baffle;103b, fixed plate;103c, clamping plate;104a, shell;104b, top plate;104c, extrusion spring;104d, bottom plate;105a, air cylinder;105b, telescopic cylinder;105c, heating plate;105d, fixed frame;105e, rotor;105f, conduction rod;105g, hot-pressing rod. DETAILED DESCRIPTION

[0020] In order to make the above-mentioned purpose, features and advantages of the utility model more apparent, easy to understand, the specific implementation of the utility model is explained in detail below with the attached drawings of the specification.

[0021] In the following description, a lot of specific details are set forth in order to fully understand the utility model, but the utility model can also be implemented in other ways different from the description, and those skilled in the art can make similar generalization without departing from the connotation of the utility model, therefore the utility model is not limited by the specific embodiments disclosed below.

[0022] Secondly, the "one embodiment" or "embodiment" referred to here can include specific features, structures or characteristics in at least one implementation of the utility model. In this specification, "in one embodiment" does not mean the same embodiment, nor is it an independent or alternative embodiment that excludes other embodiments.

[0023] EMBODIMENT

[0024] REFERENCE Figures 1-4 For the embodiment of the utility model, the embodiment provides a disposable sterile tracheal cannula bag sealing device, comprising,

[0025] Operating assembly 101, placing plate 102 fixedly installed on the surface of operating assembly 101, fixed component 103 fixedly connected on the side surface of operating assembly 101, limiting component 104 used in cooperation with placing plate 102, drive assembly 105 adaptedly installed on the surface of limiting component 104 and limiting rod 106 inserted on the side surface of limiting component 104.

[0026] The operation assembly 101 comprises an operation box 101a, a switch 101b fixedly installed on the side wall of the operation box 101a, an adjusting panel 101c fixedly connected to the side surface of the operation box 101a, and a display panel 101d adaptively installed on the side wall of the operation box 101a.

[0027] The fixing assembly 103 comprises a baffle 103a fixedly connected to the surface of the operation box 101a, a fixing plate 103b fixedly installed on the side wall of the baffle 103a, and a clamping plate 103c fixedly connected to the side surface of the fixing plate 103b.

[0028] Specifically, the operator places the tracheal cannula to be sealed on the placement plate 102, and realizes rapid positioning and fixing through the cooperation of the baffle 103a and the clamping plate 103c of the fixing assembly 103; the limiting rod 106 of the limiting assembly 104 is automatically adjusted under the action of the extrusion spring 104c to ensure uniform sealing pressure; after the operator sets the sealing parameters through the adjusting panel 101c, the cylinder 105a of the driving assembly 105 pushes the telescopic cylinder 105b to press down, and the heating plate 105c transmits heat to the hot pressing rod 105g through the transmission rod 105f to complete precise hot pressing sealing under the preset temperature and time; the display panel 101d displays the working state and parameters in real time during the whole process, and the operation box 101a controls the cooperative operation of each component to realize efficient and stable sterile sealing process.

[0029] The limiting assembly 104 comprises a housing 104a, a top plate 104b fixedly installed on the bottom of the housing 104a, an extrusion spring 104c sleeved on the outer surface of the limiting rod 106, and a bottom plate 104d fixedly connected to the bottom of the limiting rod 106.

[0030] The bottom of the limiting rod 106 is connected with two telescopic rods which are fixedly connected with the limiting rod 106, the outer walls of the two telescopic rods are each sleeved with an extrusion spring 104c, and the bottoms of the two telescopic rods are each fixedly connected with the bottom plate 104d.

[0031] The driving assembly 105 comprises a cylinder 105a adaptively installed on the surface of the housing 104a, a telescopic cylinder 105b fixedly installed on the output end of the cylinder 105a, a heating plate 105c fixedly connected to the side wall of the telescopic cylinder 105b, and a fixing frame 105d fixedly installed on the bottom of the heating plate 105c.

[0032] The driving assembly 105 further comprises a rotor 105e rotatably installed on the inner wall of the fixing frame 105d, a transmission rod 105f clamped on the inner surface of the fixing frame 105d, and a hot pressing rod 105g clamped on the bottom of the transmission rod 105f.

[0033] It should be noted that when the tracheal cannula bag is fixed in place, the two telescopic rods of the limiting assembly 104 are driven by the compression spring 104c to stably press down the bottom plate 104d, ensuring that the packaging bag is uniformly stressed; the cylinder 105a of the driving assembly 105 pushes the telescopic cylinder 105b to move vertically, the heating plate 105c adjusts the angle of the transmission rod 105f through the rotor 105e, and the hot pressing rod 105g accurately docks the sealing position; the transmission rod 105f efficiently transfers the heat of the heating plate 105c to the hot pressing rod 105g, and completes the heat sealing under the preset temperature and time parameters; throughout the process, the compression spring 104c provides buffer protection to avoid excessive compression, and the adjustable design of the rotor 105e adapts to different packaging specifications, realizing intelligent and high-precision sterile sealing operation, ensuring the sealing integrity and sterilization reliability of each tracheal cannula bag.

[0034] In use, the tracheal cannula bag is quickly and accurately positioned by the baffle 103a-card plate 103c mechanism of the fixing assembly 103; the double telescopic rod structure of the limiting assembly 104 provides self-adaptive pressure under the action of the compression spring 104c, ensuring that the sealing surface is uniformly stressed; the driving assembly 105 adopts a pneumatic and hot-pressing composite system, the cylinder 105a drives the telescopic cylinder 105b to accurately control the downstroke, and the heating plate 105c accurately transmits heat energy to the hot pressing rod 105g through the adjustable angle transmission rod 105f, realizing the coordinated control of temperature and pressure; the operation assembly 101 integrates parameter setting, process monitoring and data display functions through an electronic control system.

[0035] In summary, the baffle 103a and the card plate 103c of the fixing assembly 103 cooperate to ensure accurate and stable positioning of the tracheal cannula bag; the double telescopic rod and the compression spring 104c of the limiting assembly 104 provide self-adaptive compression force, avoiding sealing defects caused by uneven sealing pressure; the driving assembly 105 combines pneumatic drive and heat conduction technology, and realizes accurate temperature control sealing of the hot pressing rod 105g through the adjustable angle transmission rod 105f, ensuring that the seal is sterile and has good integrity; the intelligent adjustment panel 101c and the display panel 101d of the operation assembly 101 realize visual parameter adjustment and real-time monitoring, greatly improving the operation convenience; the overall structure works cooperatively, ensuring sealing efficiency and reducing energy consumption, significantly improving the sealing quality and sterilization reliability of medical product packaging.

[0036] It is important to note that the construction and arrangements of the application shown in the various exemplary embodiments are illustrative only. Although only a few embodiments have been described in detail in this disclosure, those skilled in the art who review this disclosure will readily appreciate that many modifications can be made to the embodiments without departing from the novel teachings and advantages of the subject matter described herein. For example, elements described as integrated in a single unit can be separated, elements described as separate can be integrated, and the position, number, shape, and arrangements of elements can be varied. Accordingly, all such modifications are intended to be included within the scope of the present inventive subject matter. The order or sequence of any process or method steps can be varied or re-sequenced without departing from the general nature of the claims. Any "means plus function" clauses are intended to cover the structures described herein as performing the recited functionality and not only structural equivalents but also equivalent structures. Other substitutions, modifications, changes, and omissions can be made in the design, operating conditions, and arrangement of the exemplary embodiments without departing from the scope of the present inventive subject matter. Accordingly, the present inventive subject matter is not limited to the particular embodiments described and illustrated herein, but extends to equivalents of which the foregoing describes are intended to cover.

[0037] Furthermore, in order to provide a concise description of the exemplary embodiments, not all features of an actual implementation can be described (i.e., those related to the

[0038] It is understood that in the development of any actual implementation, as in any engineering or design project, numerous implementation-specific decisions can be made. Such development efforts can inevitably lead to modifications, which can be different from those suggested herein, and still fall within the scope of the present inventive subject matter. Those skilled in the art will appreciate the

[0039] It should be noted that the above examples are intended to illustrate the technical solutions of the present application but not limit the present application, and although the present application has been described in detail with reference to the preferred embodiments, those skilled in the art should understand that the technical solutions of the present application can be modified or replaced equivalently without departing from the spirit and scope of the present application, and all should be included in the scope of the claims of the present application.

Claims

1. A disposable sterile tracheal tube pack sealing device, characterized by: The utility model relates to a kind of automatic feeding device for electronic component, including, The operation component (101) includes operation box (101a), fixedly installed in the side wall of the operation box (101a) switch (101b), fixedly connected in the side surface of the operation box (101a) adjusting panel (101c), and display panel (101d) is adaptly installed in the side wall of the operation box (101a).

2. A disposable sterile tracheal tube pack sealing device according to claim 1, wherein: The fixed component (103) includes fixedly connected in the surface of the operation box (101a) baffle (103a), fixedly installed in the side wall of the baffle (103a) fixed plate (103b), and fixedly connected in the side surface of the fixed plate (103b) clamping plate (103c).

3. A disposable sterile tracheal tube pack sealing device according to claim 2, wherein: The limiting component (104) includes shell (104a), top plate (104b) fixedly installed in the bottom of the shell (104a), extrusion spring (104c) is sleeved in the outer surface of the limiting rod (106), and bottom plate (104d) is fixedly connected in the bottom of the limiting rod (106).

4. A sealing device for a single-use sterile tracheal tube pack according to claim 3, characterized in that: The limiting rod (106) bottom is connected with two telescopic rods, and is fixedly connected with the limiting rod (106), the outer wall of two telescopic rods is sleeved with extrusion spring (104c), and the bottom of two telescopic rods is fixedly connected with the bottom plate (104d).

5. A disposable aseptic tracheal cannula package sealing device according to claim 4, characterized in that: The drive component (105) includes that the surface of the shell (104a) is adaptly installed in the cylinder (105a), fixedly installed in the output of the cylinder (105a) telescopic cylinder (105b), fixedly connected in the side wall of the telescopic cylinder (105b) heating plate (105c), and fixed frame (105d) is fixedly installed in the bottom of the heating plate (105c).

6. A one-piece, disposable, sterile, tracheal tube packaging seal according to claim 5, wherein: The drive component (105) further includes rotor (105e) rotationally installed in the inner wall of the fixed frame (105d), is clamped in the inner surface of the fixed frame (105d) conducting rod (105f), and hot-pressing rod (105g) is clamped in the bottom of the conducting rod (105f).

7. A one-piece, disposable, sterile, tracheal tube packaging seal according to claim 6, wherein: ​