KR20110110531A - Hydrogen peroxide plasma sterilization indicator label and manufacturing method thereof - Google Patents

Abstract

The present invention relates to a hydrogen peroxide plasma sterilization identification label having various sterilization information such as sterilization date, expiration date, as well as identification of sterilization, and a method of manufacturing the same. Hydrogen peroxide plasma sterilization identification label of the present invention is a sheet of paper made of a material capable of printing in the form of a roll, moisture permeability that can pass through the water vapor due to hydrogen peroxide in the plasma sterilization process without absorbing moisture And a sterilization identification mark formed by printing on one side of the sheet surface, and printed by a sterile identification ink which is discolored by radicals generated in the hydrogen peroxide plasma sterilization process, and printed on the surface of the sheet other than the sterilization identification mark to sterilize information. In addition, it is composed of a sterilization information display unit that provides a space for typing the sterilization information through the label. The invention facilitates the classification of articles according to sterilization information, enables sterilization information tracking, and enables objective and efficient documentation.

Description

Hydrogen peroxide plasma sterilization identification label and manufacturing method {Hydrogen peroxide plasma sterilization indicator label and manufacturing method

The present invention relates to a hydrogen peroxide plasma sterilization identification label, and more particularly, to a hydrogen peroxide plasma sterilization identification label having various sterilization information such as sterilization date, expiration date, as well as identification of sterilization, and a method of manufacturing the same.

Currently used sterilization methods include steam sterilization, EO sterilization, formalin sterilization and plasma sterilization.

Steam sterilization (steam sterilization) is the most commonly used method of sterilizing articles by killing bacteria using high temperature and high pressure thermal energy. Steam sterilization puts saturated steam into the pressure vessel containing the article to be sterilized, so that the steam contacting the article condenses into water and a large amount of thermal energy is transferred to the bacteria present on the surface of the article as the state of the substance changes. To kill. Such steam sterilization is standardized by exposure at 134 ° C. for 3 minutes and exposure at 121 ° C. for 15 minutes. On the other hand, in order to obtain a high temperature of more than 100 ℃ to increase the pressure of the steam above the atmospheric pressure, in the case of 134 ℃ 3 bar, 121 ℃ 2 bar is required. Steam sterilization is also used to sterilize instruments, fabrics, and other materials that are not subject to thermal deformation.

Such steam sterilization is very fast and low cost of sterilization and can sterilize various articles. In addition, a variety of processes have been developed for a long time and recently has the most widely available advantages of all sterilization systems, such as increasing the permeability of steam and shorten the time. However, steam sterilization is a high-temperature, high-pressure sterilization system that can not sterilize instruments and articles that are susceptible to heat and is sensitive to changes in pressure.

EO sterilization (Ethylene Oxide gas sterilization) is a method using a relatively low temperature ethylene oxide (C ₂ H ₄ O) chemical reaction (Scheme 1) of 38 ~ 54 ℃.

Scheme 1

Ethylene oxide acts to destroy bacteria by reducing hydrogen in the same structure as in Scheme 1 present in various cells of bacteria. Ethylene oxide gas has high reactivity and relatively low molecular weight, so it is easy to penetrate and has excellent sterilization ability.

EO sterilization is a method using 100% EO gas and a method using a certain ratio of mixed gas. Since EO gas is highly reactive and explosive, 100% EO gas cannot be used when the volume of the sterilizer is larger than 225L. Therefore, in the case of a large-capacity sterilizer of 225 L or more, a stabilizing gas is mixed and used at a constant rate. Mixed gases include EO / CO ₂ (20: 80%) and EO / HCFC (10: 90%). Here, in the case of CO ₂ gas is inexpensive, special equipment is required for pressure control and attention to gas use is necessary. EO / HCFC is an Oxyfume product from Honeywell, which is easy to use and has a constant gas quality, but at a very high price.

In EO sterilization, put the goods inside the pressure vessel, increase the humidity to 30% or more and inject gas, and expose it for a certain time according to the temperature (38 ℃: 6 hours, 55 ℃: 2 hours) and exhaust process (38 ℃: 36 hours or more, 55 ° C .: 10 hours or more).

EO sterilization as described above has the advantage of good gas penetration and excellent sterilization ability. However, sterilization process time is longer than at least 12 hours, and the risk of leakage of toxic substances is high and is currently disappearing in the US and Europe. In addition, there is a disadvantage that a safety facility for toxic gas exhaust is required.

Formalin sterilization is the official name is LTSF (Low Temperature Steam Formaldehyde) sterilization, using a formaldehyde chemical reaction in the LTSF sterilizer is carried out at 65 ℃ ~ 80 ℃ sterilization. Here, the material used for sterilization is an aqueous solution containing 35 to 38% of Formaldehyde (CH ₂ O: 30.03).

Formalin sterilization is performed by vacuuming a pressure vessel containing sterilized articles, generating formalin gas at a temperature of 65 to 80 ° C, mixing it with steam, and injecting it into a vacuum pressure vessel, exposing it for about 30 minutes after gas injection. Carry out 4 to 5 hours of exhaust. Formalin sterilization takes about 8-9 hours.

Formalin sterilization as described above has the advantage of low cost of sterilization. However, there is a risk in use because it uses toxic substances and a long exhaust time for detoxification is required. In addition, there is a limit of sterilization capacity and is not only widely used internationally, such as used in some European countries, but also used in some large hospitals in Korea.

Plasma refers to a state of matter other than a solid-liquid-gas and is generally called a fourth state as a state of a material in which ions are separated. Plasma is a high temperature plasma which separates ions by applying enormous heat to a gas and a low temperature plasma which forms a strong magnetic field at a relatively low temperature to separate ions. Plasma sterilization utilizes low temperature plasma. Plasma destroys microorganisms and bacteria in a highly energetic state with very strong reactivity, and has a sterilizing effect through active interaction.

Currently widely used plasma sterilization systems use hydrogen peroxide as a sterilization medium. The chemical reaction of hydrogen peroxide used for sterilization is represented by the following chemical formula. In general, hydrogen peroxide used for plasma sterilization is a strong oxidant, separated into water and oxygen, using a mixture of water (58% hydrogen peroxide).

The gaseous hydrogen peroxide is separated into two hydroxyl groups with very strong reactivity through the plasma process, and the hydroxyl groups kill bacteria very quickly.

Hydroxyl groups are highly reactive and bind to water to stabilize into a hydrogen peroxide / water mixture. Therefore, water must be removed to increase sterilization effect. For effective sterilization, it is desirable to increase the concentration of hydrogen peroxide to 90% or more when injecting sterilizing agents.

Plasma sterilization is performed using 58% hydrogen peroxide as a sterilant, and sterilization at 42-48 ° C., but once per 55-72 minutes according to the program. The process of plasma sterilization is as follows. First, the inside of the pressure vessel is made in a high vacuum state to increase the penetration of the sterilant to the article and to increase the concentration of plasma. Then, hydrogen peroxide is injected into the vaporization chamber to vaporize. At this time, the concentration of hydrogen peroxide is increased by using the difference between the boiling point of water and hydrogen peroxide. Then, the vaporized hydrogen peroxide is introduced into the vacuum vessel containing the article, and then a high frequency of 13.5 MHz is applied between the electrodes in the pressure vessel to activate the hydrogen peroxide so that sterilization is actively performed. The sterilization is then completed by injecting air through the filter into the pressure vessel and returning to atmospheric pressure.

Plasma sterilization as described above can reduce the sterilization time by at least 30 minutes depending on the program and sterilization situation, the sterilization time is shorter than other low temperature sterilization system, the installation conditions are simple, and no harmful substances are discharged. There is this. By the way, the material that absorbs water, such as paper, cloth is not sterilized there is a limitation of the sterilized article, there is a disadvantage that the capacity is limited as the sterilizer is released to the current 200L class.

Hereinafter, a general process of sterilization in a hospital will be described with reference to FIG. 1.

Goods used in the operating room and other patients are classified as contaminated and washed first and then sent to a central supply room for sterilization or to a sterile part of the operating room. Items sent to a central supply room for sterilization are subjected to a second wash. After second cleaning, completely dried items are packaged prior to sterilization. Here, the role of packaging prevents the sterilized article from being exposed to the air and re-infecting the germ and keeping the article for a certain period of time. Sterile identification strips are inserted inside to check whether the items are sterilized during packaging, and sterile tape or sterile identification labels are placed on the outside.

On the other hand, materials frequently used or urgently used in surgery, instruments and systems that require attention in handling are directly sterilized by packaging in the sterilization part of the operating room. Packaged items are sterilized by a sterilizer and the sterilized items are stored in a fixed place. Sterile articles are distinguished from non-sterile articles by color changes, such as identification tapes or identification labels attached to the outside of the package.

In general, steam sterilization uses a reusable fabric package as a packaging material. By the way, all the packaging has some degree of breathability and storage capacity is poor when used a lot or over time. Accordingly, sterile packages have a limit of storage and have a shelf life.

Recently, the use of disposable pouches is increasing due to the deterioration of packaging using fabric. In general, the front side of the pouch is made of visible vinyl and the back side is made of paper so that steam, EO, formalin and hydrogen peroxide can penetrate. Pouches can be stored for a longer period of time compared to fabric packages for one-time use and have the advantage of checking the contents, and are widely used for low temperature sterilization such as EO, formalin, and plasma.

As the days of storage of articles increase, the contact of contaminants increases and the probability of bacterial growth increases. Therefore, the expiration date must be set in detail according to the type of packaging and storage place, and the set expiration date must be strictly observed. All sterilization information is recorded in the sterilization log. The sterilization log records all sterilization information, including sterilizer number, number and times of sterilization, test of sterilization performance, sterilization identification information (tape, label, etc.), sterilization numerical records, print records, personnel, etc. for each sterilization. It is kept as a reference. This data is also used as evidence for the sterilization process in the event of an infection. Sterile identification labels play an important role in the classification and documentation of articles in this sterilization process and contain a great deal of information about sterilization.

Products currently used to identify plasma sterilization (indicators) include indicator tapes and indicator strips.

Indicator tape is a product that is attached to the surface of a sterile package or article to identify sterilization by changing the color of the printed part on the surface of the tape. In addition, the indicator strip is a product that can be checked with the sterilized product is packaged with the sterile inside the package.

The above products can be identified whether or not sterilization, but since the sterilization date, expiration date, personnel, etc. can not be identified, it is difficult to classify the goods and can not classify the products beyond the expiration date due to long-term storage. In addition, reuse of wrapping paper can lead to confusion about identification and accidents that often result in the use of unsterilized items.

On the other hand, in the case of plasma indicators, since most product materials are plastic, it is difficult to record sterilization information by hand. In addition, handwritten records are difficult to secure objectivity for information, and false recording and manipulation of information can be easily made later.

As described above, the plasma sterilization identification system is merely a classification of sterilization until now, and there is no system capable of specifically identifying sterilization information. In addition, the sterile identification system is not properly established in the operating room that uses a large number of plasma systems, and infections are frequently generated accordingly.

In order to establish a sterilization identification system and establish an infection prevention system, various information on sterilization should be recorded and maintained, and a documentation system that can trace the sterilization route in detail in case of an infection accident is required. In other words, not only the identification of sterilization, but also the items stored for a certain period of time through the sterilization date and the expiration date should be sterilized again.The sterilizer number confirms which sterilizer has been sterilized and how many times of the day It should be possible to identify who has been sterilized and who is responsible for sterilization. Furthermore, in case of an infection, it should be able to be used as a backtracking system that enables the traceback of sterilization to identify the exact cause.

Accordingly, an object of the present invention is to provide a hydrogen peroxide plasma sterilization identification label having various sterilization information such as sterilization date, expiration date as well as identification of sterilization and a method of manufacturing the same.

Hydrogen peroxide plasma sterilization identification label of the present invention is a sheet of paper made of a material capable of printing in the form of a roll, moisture permeability that can pass through the water vapor due to hydrogen peroxide in the plasma sterilization process without absorbing moisture And a sterilization identification mark formed by printing on one side of the sheet surface, and printed by a sterile identification ink which is discolored by radicals generated in the hydrogen peroxide plasma sterilization process, and printed on the surface of the sheet other than the sterilization identification mark to sterilize information. In addition, it characterized in that it comprises a sterilization information display unit that provides a space for typing the sterilization information through the label.

The sheet of the invention may be Tyvek ^® (Tyvek) fabric supplied by DuPont ^™ .

The sterile identification ink of the present invention may be formed by mixing an organometallic compound, an adsorption indicator, a metal indicator, a fixative, and a discoloration aid.

The sterilization information display unit of the present invention may be described sterilization type, sterilization identification display color change information, sterilization date and expiration date.

The sterilization information display unit of the present invention may further describe the device number, sterilization sequence number, person in charge or article code.

The method of manufacturing the hydrogen peroxide plasma sterilization identification label of the present invention comprises the steps of performing a double-sided adhesive tape and a sticker fuji operation on the back of the sheet-shaped sheet fabric, and a step of cutting the fabric to the label printing machine standard after the sticker fuji operation; Printing a sterile identification ink on a portion of the cut fabric and forming a sterile identification mark and drying the ink; printing a sterile identification ink on the printed fabric to form a sterile information display; and a sterile identification display and sterilization information. It may include the step of producing a label by cutting the cutting part to have a display unit.

This invention facilitates the classification of articles according to sterilization information. That is, it is possible to classify sterile articles and non-sterile articles according to the color change of the sterile identification ink, and it is possible to classify items that have passed the storage period by checking the expiration date.

In addition, the invention can be sterilized information tracking. In other words, the date, device number, and sterilization number on the label can be used to determine when and from which sterilization process the sterilization process can be performed.

In addition, the present invention enables objective and efficient documentation. Not only can you record the date and sterilization information by hand, but also you can record more information than handwriting. Can be.

1 is a sterilization process in a general hospital,
2 is a conceptual diagram of a hydrogen peroxide plasma sterilization identification label according to an embodiment of the present invention,
3 is a photograph of a label roll on which the contents of the label shown in FIG. 2 are printed;
4 is a photograph of the labeling machine fitted with the label roll shown in FIG.
FIG. 5 is a detailed view of a label in which various sterilization degrees are recorded on the label shown in FIG. 2 by the labeler shown in FIG. 4;
FIG. 6 is a process chart photographing the manufacturing process of the label shown in FIG.
Figure 7 is a photograph of a series of processes experimented in a hydrogen peroxide plasma sterilizer after producing the label of this embodiment.

In the following, with reference to the accompanying drawings, preferred embodiments of the hydrogen peroxide plasma sterilization identification label and a method of manufacturing the same according to the present invention will be described in detail.

2 is a conceptual diagram of a hydrogen peroxide plasma sterile identification label according to an embodiment of the present invention, FIG. 3 is a photograph of a label roll on which the contents of the label shown in FIG. 2 are printed, and FIG. 4 is a label roll shown in FIG. This is a photograph of the fitted labeling machine, and FIG. 5 is a detail view of a label in which various degrees of sterilization are recorded on the label shown in FIG. 2 by the labeling machine shown in FIG. 4.

Hydrogen peroxide plasma sterilization to which this embodiment is applied not only sterilizes water-absorbing materials such as paper and cloth, but also prevents sterilization when using water-absorbing materials. In addition, when the label of this embodiment is made of a material that absorbs moisture, when the ink printed on the label changes color by reacting with hydrogen peroxide, the color of the label does not occur smoothly due to chemical reactions caused by moisture contained in the label. Change is impossible.

Therefore, the label of this embodiment has the flexibility to be wound in the form of a label roll as shown in FIG. 3, and the moisture permeability through which hydrogen peroxide can pass through without absorbing moisture. do. For example, the sheet of the label of this example may use Tyvek ^® (Tyvek) fabric supplied by DuPont ^™ . Currently, Tyvek is being used to make packaging pouches for use in plasma sterilizers. That is, Tyvek is a material of the packaging sterilizer packaging pouch, it can be seen that the material does not absorb moisture. On the other hand, Tyvek is a polyethylene material that does not absorb water, and because of its strong chemical resistance, it is possible to print without affecting plasma sterilization. Thus, Tyvek is suitable as a fabric for producing the label of this embodiment.

Tyvek is generally a very tough and soft sheet of multi-layered polyethylene made of high density polyethylene. In addition, due to a number of excellent properties such as waterproof, moisture permeability, radiant heat shielding is installed in the construction field with the insulation between the wall and the roofing material is used to significantly reduce the energy cost by minimizing heat loss.

In addition, Tyvek has a unique fibrous structure of porous sheet paper made of ultrafine fibers (0.5 ~ 1.0㎛), which increases the thermal insulation effect when used with thermal insulation materials. There is a characteristic.

In addition, this embodiment requires a sterile identification ink that can be printed on a label and that changes color to vivid when reacted with hydrogen peroxide. In other words, the sterile identification ink of this embodiment is a color changing ink in response to hydrogen peroxide used as a sterilizing agent for plasma sterilization, which can be printed on Tyvek fabric for making a label and must be naturally free from color change in other chemicals and the atmosphere. . In addition, the sterile identification ink must be visually vivid in response to vaporized hydrogen peroxide, so that anyone can distinguish whether it is before or after sterilization. That is, the sterile identification ink of this embodiment may use an ink discolored by radicals generated in the hydrogen peroxide plasma sterilization.

The sterile identification ink according to this embodiment uses a mixture of organometallic compounds, adsorption indicators, chelate titration metal indicators, fixatives and discoloration aids. Here, the organometallic compound reacts with an acid to form metal ions, and the adsorption indicator reacts with the metal ions to discolor to show color sterilization results. The chelate titration metal indicator reacts with metal ions to form irreversible compounds, determines the color before discoloration, including organic dyes, and discolors by displacing it with metal ions. In addition, the fixing agent is generally added to the synthetic resin used in ink manufacturing to enable printing.

Looking at the process of discoloring the sterile identification ink of this embodiment configured as described above in the hydrogen peroxide plasma sterilization process as follows.

First, when the plasma sterilization process is started, hydrogen peroxide is vaporized to produce a high concentration of hydrogen peroxide gas. High concentrations of gaseous hydrogen peroxide are separated (2OH ⁻ ) into two hydroxyl groups via a plasma step for strong oxidation. That is, the hydroxyl group, which is a strong oxidant, oxidizes the organometallic compound of the sterile identification ink to form metal ions. The metal ions thus formed are stabilized by reacting with the chelate titration metal indicator and discoloring from the existing color to other colors and forming a chelating compound. That is, discoloration occurs irreversibly. On the other hand, the adsorption indicator also reacts with the metal ions to discolor to show the sterilization results in color change.

As shown in Figure 2, the hydrogen peroxide plasma sterile identification label 100 of this embodiment is a sheet paper 110 formed by cutting a Tyvek fabric to a certain size, and the sterilization printed with a sterile identification ink on one side of the sheet paper 110 The identification display unit 120 and the sterilization information display unit 130, which is printed on a predetermined position of the sheet 110 other than the sterilization identification display unit 120, respectively, so that the sterilization information can be typed through the labeling device. Here, the sterilization information display unit 130, "Plasma" indicating the type of sterilization, "Pink-> Yellow" indicating the color change of the sterilization identification display unit 120, "LOT ▲" indicating the sterilization date, distribution as shown in FIG. "EXP ▼" indicating the deadline, "Chamber" indicating the manufacturer of the label is printed by the general ink, and the sterilization date and the expiration date and equipment number, sterilization order, person in charge or item code through the labeling machine as shown in FIG. Spaces can be formed respectively.

The following describes the process of producing a label according to this embodiment using the Tyvek fabric and sterile identification ink adopted as described above.

FIG. 6 is a process chart photographing the manufacturing process of the label shown in FIG. 2. As shown in FIG. 6, the double-sided adhesive tape work and the sticker fuji (back paper attachment) work are performed on the back of the roll-type Tyvek fabric. At this time, the Tyvek fabric is supplied in the form of a roll of 1020mmX5000m size. After printing the sticker, the Tyvek fabric is cut to meet the label printing machine's specifications by 130mmX500m for label printing. Then, a sterile identification ink is printed on a section of a Tyvek fabric cut in units of 130 mm × 500 m through a rotary rotary copper plate printing method (gravure printing) to form a sterile identification display unit 120 of FIG. 2 and then naturally dried. In other words, the sterile identification ink is printed by drying the Tyvek fabric printed at 70m or more transfer distance, and the natural dried Tyvek fabric is wound again in the form of a roll. Here, the gravure printing is printing with a concave plate made by applying a photographic technique during the concave plate printing, and fills the liquid ink in the concave portion of the wire and removes the ink in the other portions to print. Sterilization identification display unit 120 of this embodiment is also possible through other methods than the gravure printing method.

The background of the label corresponding to the sterilization information display unit 130 of FIG. 2 is printed on the tyvek fabric on which the sterile identification ink is printed by a general flexographic printing method. Here, the background of the label means a character or a term indicating the type of sterilization, the date of sterilization, the expiration date, the company name, etc., and the label 100 includes "Plasma, (Pink-> Yellow), LOT ▲, EXP ▼, Chamber "and the like can be described.

After the background printing as described above, put a cut operation to put in the labeling machine. At this time, the cutting work is to make a label with a width of 26mmX length of 28mm, but the tyvek fabric that has been printed and cut is cut to 26mmX16.8m so that the label is 500 ~ 800EA, and the diameter 30mmX width 22mm paper pipe (label roll) Wind on By doing so, the production of the label according to this embodiment is completed.

In the use of the label, the label roll is inserted into the label, and the sterilization information such as device number, sterilization number, person or item code, sterilization date, and expiration date is printed on the label to be attached to the sterilized product. Can be used.

Hereinafter, an example of actually producing a hydrogen peroxide plasma sterilization identification label according to this embodiment and experimenting with a hydrogen peroxide plasma sterilizer will be described.

Figure 7 is a photograph of a series of processes experimented in a hydrogen peroxide plasma sterilizer after producing the label of this embodiment.

Sheet paper was produced in the same manner as described above to have a basis weight of 42.5g / m ² , a Tyvek fabric of 130㎛ thickness, but having a size of 26mm x 28mm in height, and then type the sterilization information on the label through a labeling machine. The label with the sterilization information typed was then attached to the plasma sterilization pouch (75 mm x 90 mm). At this time, the plasma sterilization indicator tape "ASP" of the company was attached to the side for reference. On the other hand, using the basis weight of 70g / m ^2, 100㎛ the mojoji thickness, basis weight 90g / m ^2, thickness 110㎛ poly coated paper was tested by making the same label as the embodiment.

At this time, the test was performed on the Sterrad 200 model of "ASP" and PS100 model of "SHINVA". As a result of the experiment, the general label using paper (imitation paper) showed the color change vaguely, and the result was slightly different according to the difference between the sterilizer and the parameter. For reference, the paper may affect the sterilization itself and thus may not be manufactured as an indicator for identifying the hydrogen peroxide plasma sterilization. Polyart paper and Tyvek are synthetic papers, and it can be seen that the color change of sterile identification ink is relatively clear. However, in the case of polyart paper, it is difficult to use the ink due to the ink spreading phenomenon occurs. By the way, in the case of the label made of Tyvek of this embodiment, there was no bleeding phenomenon, so printing was easy and color change of ink was clear.

The above description of the hydrogen peroxide plasma sterilization identification label of the present invention and the technical details of the manufacturing method thereof have been described with the accompanying drawings, but the exemplary embodiments of the present invention have been described by way of example and are not intended to limit the present invention.

In addition, it is obvious that any person skilled in the art can make various modifications and imitations within the scope of the appended claims without departing from the scope of the technical idea of the present invention.

100: label 110: sheet paper
120: sterilization identification display unit 130: sterilization information display unit

Claims (6)

Sheet paper made of a material that can be rolled and has a flexibility to be wound, the moisture permeable moisture through the hydrogen peroxide in the plasma sterilization process without absorbing moisture, can pass through,
Sterile identification display unit is formed by printing on one side of the surface of the sheet, but printed by printing with a sterile identification ink discolored by radicals generated in the hydrogen peroxide plasma sterilization process, and
Hydrogen peroxide plasma sterilization identification label comprising a sterilization information display unit for printing the surface of the sheet other than the sterilization identification display unit to display sterilization information and to provide a space for typing sterilization information through a label. The method according to claim 1,
The sheet is hydrogen peroxide plasma sterile identification label, characterized in that the Tyvek ^® (Tyvek) fabric supplied by DuPont ^TM . The method according to claim 2,
The sterile identification ink is a hydrogen peroxide plasma sterile identification label, characterized in that consisting of a mixture of organometallic compound, adsorption indicator, metal indicator, fixative and discoloration aid. The method according to claim 3,
The sterilization information display unit is a hydrogen peroxide plasma sterilization identification label, characterized in that the type of sterilization, color change information, sterilization date and the expiration date of the sterilization identification display. The method of claim 4,
The sterilization information display unit is a hydrogen peroxide plasma sterilization identification label, characterized in that the device number, sterilization order, personnel or article code is further described. As a manufacturing method of the hydrogen peroxide plasma sterilization identification label of any one of Claims 1-5,
Performing a double-sided adhesive tape operation and a sticker fuji operation on the back of the roll-shaped sheet fabric;
Cutting the fabric to a label printing machine standard after the sticker fuji work;
Printing the sterile identification ink on some sections of the cut fabric to form and dry the sterile identification display unit;
Printing the sterilized identification ink on the printed fabric to form the sterilized information display unit, and
Method of producing a hydrogen peroxide plasma sterile identification label comprising the step of producing a label by cutting the sterilization identification display unit and the sterilization information display unit together.

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