Replaceable dressing pasting film and processing technology thereof

By designing and processing a three-layer dressing film, the problems of allergies and pressure caused by dressing film contamination are solved, and the breathability and sterility are improved, ensuring the comfort and safety of using the breast augmentation and correction device.

CN121196900APending Publication Date: 2025-12-26PROMETHEUS MIRACLE (SHENZHEN) MEDICAL TECH CO LTD
View PDF 0 Cites 0 Cited by

Patent Information

Application Number
CN202511263201.5
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2025-09-05
Publication Date
2025-12-26

AI Technical Summary

Technical Problem

The dressings and films used in existing breast augmentation and correction devices are easily contaminated, leading to allergies, itching, and significant local pressure, which affects user comfort.

Method used

The dressing film adopts a three-layer structure: the skin contact layer is medical silicone gel, the protective layer is release paper, and through a precise microporous array design, woven or mesh structure material composite, combined with sterilization treatment and aseptic packaging, the product's breathability and sterility are ensured.

Benefits of technology

It significantly reduces the risk of allergies and itching, alleviates local pressure, improves wearing comfort, prevents microbial invasion, ensures product sterility, and enhances safety and comfort during use.

✦ Generated by Eureka AI based on patent content.

Smart Images

  • Figure CN121196900A_ABST
    Figure CN121196900A_ABST
Patent Text Reader

Abstract

The invention relates to the technical field of dressing films, and discloses a replaceable dressing film and a processing technology thereof.The processing technology comprises the steps that material preparation and quality inspection are conducted, the output of material preparation and quality inspection serves as the input of base film treatment and biological glue coating, and the output of base film treatment and biological glue coating serves as the input of compounding and forming; the output of compounding and forming is used as the input of sterilization and detection, and the output of sterilization and detection is used as the input of film covering and packaging. According to the replaceable dressing pasting film and the processing technology thereof, a precise micropore array is formed on the three layers of elastic base films, excellent air circulation is achieved, allergy, itching and eczema caused by skin closure are reduced, local oppression is relieved due to the low irritation and the softness of medical silicone gel, and the replaceable dressing pasting film has the advantages of being good in breathability and good in breathability. The die cutting and edge cutting process ensures that the edge of the dressing pasting film is neat, the wearing comfort is enhanced, sterilization treatment and sterile packaging effectively prevent microorganism invasion and cross infection, it is ensured that the product is sterile, and the infection risk is prevented.
Need to check novelty before this filing date? Find Prior Art

Description

Technical Field

[0001] This invention relates to the field of dressing and film technology, specifically to a replaceable dressing and film and its processing technology. Background Technology

[0002] As a medical or cosmetic device, the core function of a breast enhancement and correction device involves improving the shape and appearance of the breasts through negative pressure suction or vibration massage, and may promote the growth of breast tissue to some extent.

[0003] Currently, most breast enhancement and correction devices use replaceable dressings, but some unused dressings are easily contaminated and may cause allergies and itching after prolonged use. Some dressings also cause significant local pressure, affecting the user's comfort. Summary of the Invention

[0004] (a) Technical problems to be solved

[0005] To address the shortcomings of existing technologies, this invention provides a replaceable dressing film and its processing technology to solve the problems mentioned in the background section.

[0006] (II) Technical Solution

[0007] To achieve the above objectives, the present invention provides the following technical solution: a replaceable dressing film, comprising a dressing film, wherein the skin contact layer of the dressing film is medical silicone gel, and the protective layer is release paper.

[0008] The present invention also provides a process for processing replaceable dressing films, the process comprising the following steps:

[0009] S1: The output of material preparation and quality inspection serves as the input for base film treatment and bio-adhesive coating;

[0010] S2: The output of the base film treatment and bio-adhesive coating serves as the input for composite and molding;

[0011] S3: The output of the composite and molding process serves as the input for sterilization and detection;

[0012] S4: The output of sterilization and testing serves as the input for coating and packaging.

[0013] Preferably, the material preparation and quality inspection includes raw material preparation, and the material preparation and quality inspection further includes quality inspection. The material is a three-layer structure elastic dressing film, which includes a skin contact layer and a protective layer and is malleable within a temperature range of 80-100 degrees Celsius.

[0014] Preferably, the base film treatment and bio-adhesive coating includes base mold punching, and the base film treatment and bio-adhesive coating is provided with gel coating.

[0015] Preferably, the composite and molding includes a functional layer composite, wherein the functional layer composite is covered with a woven or mesh structure material.

[0016] Preferably, the lamination and molding includes die-cutting and trimming. The lamination and molding further includes release film lamination and roller-assisted molding. The fixture and rubber ring match the arc shape of the dressing film. An irregularly shaped dressing film is provided between the fixture and the rubber ring for auxiliary molding. A heating mold that matches the inner arc shape of the dressing film is selected. The dressing film is placed on the heating mold and pressure is applied to the dressing film in a temperature range of 80-100 degrees Celsius to perform thermoforming, so that it matches the arc surface of the fixture.

[0017] Preferably, the sterilization and testing includes sterilization treatment and sterilization testing, and the sterilization and testing further includes appearance testing and performance testing.

[0018] Preferably, the film and packaging include a surface film, and the film and packaging further encompass aseptic packaging.

[0019] Preferably, the film coating and packaging include packaging integrity testing and packaging sealing testing, wherein the packaging integrity testing and packaging sealing testing adopt a vacuum decay test.

[0020] Preferably, the film and packaging include auxiliary markings, which are printed directly on the outside of the film using a printer.

[0021] Preferably, the film coating and packaging includes finished product warehousing, and the finished product warehousing is internally integrated with temperature and humidity sensors.

[0022] Compared with existing technologies, this invention provides a replaceable dressing film and its processing technology, which has the following beneficial effects: The replaceable dressing film and its processing technology achieve excellent air circulation by forming a precision microporous array on an elastic three-layer base film. Combined with woven or mesh structure materials, this facilitates breathability, significantly reducing allergies, itching, and eczema caused by skin closure. The woven or mesh structure materials also protect and fix the gel. The low irritation and softness of the medical silicone gel further enhance wearing comfort and reduce local pressure. Die-cutting and edge trimming processes ensure neat edges of the dressing film, improving fit and enhancing wearing comfort. Sterilization and aseptic packaging effectively prevent microbial invasion and cross-infection, ensuring product sterility and preventing infection risks. Clear auxiliary markings facilitate user identification and use. The integrated temperature and humidity sensor inside the finished product warehouse further ensures product quality during storage. Attached Figure Description

[0023] Figure 1 This is a flowchart of the manufacturing process for the replaceable dressing film of the present invention;

[0024] Figure 2 This is a schematic diagram illustrating the material preparation and quality inspection process of the present invention.

[0025] Figure 3 This is a schematic diagram of the base film treatment and bio-adhesive coating of the present invention;

[0026] Figure 4 This is a schematic diagram of the composite and molding process of the present invention;

[0027] Figure 5 This is a schematic diagram illustrating the sterilization and detection process of the present invention;

[0028] Figure 6 This is a schematic diagram of the coating and packaging of the present invention;

[0029] Figure 7 This is a schematic diagram of the product structure of the present invention.

[0030] Explanation of reference numerals in the attached diagram: 1. Adhesive ring; 2. Shaped dressing film; 3. Fixture table Detailed Implementation

[0031] The technical solutions of the embodiments of the present invention will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only some embodiments of the present invention, and not all embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those skilled in the art without creative effort are within the scope of protection of the present invention.

[0032] like Figure 1-7 As shown, the present invention provides a technical solution: a replaceable dressing film, comprising a dressing film, wherein the skin contact layer of the dressing film is medical silicone gel, and the protective layer is release paper.

[0033] A process for manufacturing replaceable dressing films includes the following steps:

[0034] S1: The output of material preparation and quality inspection serves as the input for base film treatment and bio-adhesive coating;

[0035] S2: The output of the base film treatment and bio-adhesive coating serves as the input for composite and molding;

[0036] S3: The output of the composite and molding process serves as the input for sterilization and detection;

[0037] S4: The output of sterilization and testing serves as the input for coating and packaging.

[0038] Preferably, the material preparation and quality inspection includes raw material preparation, and the material preparation and quality inspection further includes quality inspection. The material is a three-layer structure elastic dressing film, which includes a skin contact layer and a protective layer and is malleable within a temperature range of 80-100 degrees Celsius.

[0039] Specifically, material preparation and quality inspection serve as the starting point of the entire processing technology. Ensuring that all raw materials used meet medical-grade standards and product usage requirements guarantees the safety, effectiveness, and comfort of the final product. At the same time, accurate raw material specifications are a prerequisite for the smooth progress of subsequent processing steps and can reduce the defect rate.

[0040] Furthermore, the base film treatment and bio-adhesive coating includes base mold punching, and the base film treatment and bio-adhesive coating is provided with gel coating.

[0041] Specifically, the base film is a three-layer elastic dressing film. Using precision laser drilling or mechanical die punching equipment, a uniformly distributed array of micropores is punched into the base film. The numerous micropores allow air to circulate freely, preventing the skin from being in a humid and stuffy environment due to prolonged closure, greatly reducing the risk of allergies, itching, and eczema. The porous structure also makes the film more elastic, reduces the rigidity of the material, makes it softer, and better conforms to shape, making it almost imperceptible when worn, thus improving comfort. The gel uses medical-grade silicone gel, which has the characteristics of low irritation, low risk of allergies, good breathability, and high softness, and can significantly reduce local pressure and frictional heat.

[0042] Furthermore, the composite and molding process includes functional layer composites, which are covered with woven or mesh structure materials.

[0043] Specifically, the use of woven or mesh-like materials in the functional layer composite can improve breathability, enhance the stability of medical silicone gel on the base film while ensuring comfort and softness, improve support capacity, prevent gel deformation, help protect and fix the silicone gel so that it is not easy to fall off, and keep the area in contact with the skin dry. This can prolong the effective adhesion time of the film and prevent the decrease in adhesion or skin problems caused by moisture.

[0044] Furthermore, the lamination and molding process includes die-cutting and trimming, and further encompasses release film lamination and roller-assisted molding. The fixture table 3 and the rubber ring 1 are matched with the arc shape of the dressing film. A special-shaped dressing film 2 is provided between the fixture table 3 and the rubber ring 1 for auxiliary molding. A heating mold that matches the inner arc shape of the dressing film is selected, and the dressing film is placed on the heating mold. Pressure is applied to the dressing film within a temperature range of 80-100 degrees Celsius to perform thermoforming, so that it is highly consistent with the arc surface of the fixture table 3.

[0045] Specifically, die-cutting and trimming remove excess material around the edges. Trimming ensures that the edges of the base film are neat and burr-free, reducing discomfort or scratches to the skin during use or wear. This creates the final appearance and size of the dressing film, perfectly matching the contact surface or breast curve of the breast enhancement device, thus improving the wearer's comfort.

[0046] Furthermore, sterilization and testing include sterilization treatment and sterilization testing, which in turn include appearance testing and performance testing.

[0047] Specifically, sterilization ensures the sterility of the dressing / film product, preventing the introduction of pathogens during use and thus avoiding infection. Sterilization testing detects any residues, ensuring they remain within safe limits. Appearance and performance testing eliminate cosmetic defects and verify core functions. Visual inspection and imaging technology identify and remove products with cosmetic defects such as impurities, bubbles, adhesive residue, dimensional deviations, and scratches, ensuring product cleanliness and aesthetics. Sampling tests are conducted on key performance aspects such as breathability and comfort to ensure the product meets design standards and effectively and safely fulfills its intended physiological or corrective functions.

[0048] Furthermore, the film and packaging include surface film, and the film and packaging further encompass aseptic packaging.

[0049] Specifically, surface coating provides a smooth, flat surface that is easy to print on. Aseptic packaging, by packaging in a sterile environment and using coating materials that provide an effective barrier, can effectively prevent the invasion of microorganisms, reduce the risk of contamination during operation, and ensure the safety and effectiveness of dressings.

[0050] Furthermore, the lamination and packaging process includes packaging integrity testing and packaging seal testing, which employs a vacuum decay test.

[0051] Specifically, packaging integrity testing and packaging seal testing ensure the physical integrity of the product and prevent gas, liquid, or microorganisms from entering the interior through the edges of the packaging. Vacuum decay testing assesses the sealing performance of the packaging by measuring the rate at which the vacuum level inside the packaging decreases, preventing microbial intrusion and maintaining sterility.

[0052] Furthermore, the lamination and packaging include auxiliary markings, which are printed directly on the outside of the lamination using a printer.

[0053] Specifically, auxiliary labels can clearly indicate the product name, model, specifications, production date, expiration date, batch number, instructions for use, precautions, and manufacturer information, providing users with necessary product identification and traceability information.

[0054] Furthermore, the film coating and packaging process includes finished product warehousing, and the finished product warehousing is equipped with integrated temperature and humidity sensors.

[0055] Specifically, temperature and humidity sensors can continuously record temperature and humidity data in the warehouse, ensuring that environmental conditions meet product storage requirements, ensuring that products maintain their original quality during storage, extending shelf life, and ensuring that products meet usage requirements.

[0056] Working Principle: First, material preparation and quality inspection ensure the biocompatibility, safety, and dimensional accuracy of all raw materials from the source. Second, the base film treatment and bio-adhesive coating involve precision microporous array processing of the base film. These micropores allow free air circulation, effectively preventing the skin from being in a closed, humid environment, thus significantly reducing the risk of skin allergies, itching, or eczema. In the lamination and molding process, a layer of woven or mesh functional layer is laminated with the adhesive-coated base film to enhance stability and support. Die-cutting and edge trimming processes ensure smooth and neat product edges. Sterilization and testing ensure that all microorganisms are completely eliminated through reliable sterilization treatment, ensuring the product's sterile state and eliminating the risk of infection due to the introduction of pathogens during use. Finally, surface coating and sterile barrier packaging in a sterile environment create a sealed microenvironment, blocking the intrusion of external microorganisms and contaminants. Auxiliary labeling provides clear product information and usage instructions, while temperature and humidity sensors can monitor environmental data in real time, ensuring the product is stored under suitable conditions.

[0057] Although embodiments of the invention have been shown and described, it will be understood by those skilled in the art that various changes, modifications, substitutions and alterations can be made to these embodiments without departing from the principles and spirit of the invention, the scope of which is defined by the appended claims and their equivalents.

Claims

1. A replaceable dressing film, comprising a dressing film, characterized in that: The skin contact layer of the dressing film is a medical silicone gel, and the protective layer is isolation paper.

2. The replaceable dressing patch of claim 1, wherein: The processing technology comprises the following steps: S1: material preparation and quality inspection output as the input of base film processing and biological glue coating; S2: the output of the base film processing and biological glue coating as the input of compounding and molding; S3: the output of the compounding and molding as the input of sterilization and detection; S4: the output of the sterilization and detection as the input of film coating and packaging.

3. The process of claim 1, wherein: The material preparation and quality inspection include raw material preparation, and further cover quality inspection, and the material selected is an elastic dressing film with a three-layer structure, which contains a skin contact layer and a protective layer and has plasticity at a temperature of 80-100 degrees.

4. The process of claim 1, wherein: The base film processing and biological glue coating include base film punching, and are provided with gel coating.

5. The process of claim 1, wherein: The compounding and molding include functional layer compounding, which adopts woven or mesh structure material covering.

6. The process of claim 1, wherein: The compounding and molding include die cutting and edge cutting, and further cover release film fitting and roller assisted molding, the jig table (3) and the rubber ring (1) match the arc surface shape of the dressing film, and the jig table (3) and the rubber ring (1) are provided with a special-shaped dressing film piece (2) for auxiliary molding, and a heating mold matched with the inner arc surface shape of the dressing film is selected, the dressing film is placed on the heating mold, and pressure is applied to the dressing film in a temperature range of 80-100 degrees for hot forming, so that the dressing film is matched with the arc surface height of the jig table (3).

7. The process of claim 1, wherein: The sterilization and detection include sterilization treatment and sterilization detection, and further include appearance detection and performance detection.

8. The process of claim 1, wherein: The film coating and packaging include surface film coating, and further cover sterile packaging.

9. The process of claim 1, wherein: The film coating and packaging include packaging integrity detection and packaging sealing detection, which adopts vacuum decay test.

10. The process of claim 1, wherein: The film coating and packaging include auxiliary identification, which is directly printed on the outside of the film coating by a printer.