Otorhinolaryngological disease treatment device using infrared rays

Abstract

The present disclosure relates to a physical disease treatment device using infrared rays and, more specifically, to a treatment device for caring for otorhinolaryngological diseases including diseases of the nose and ears of a user by utilizing infrared rays. The otorhinolaryngological disease treatment device according to various embodiments of the present disclosure comprises: an infrared device that emits infrared rays onto a part of the body including the nose of a user; a controller that supplies power to the infrared device and controls the operation of the infrared device; and a line cable that has one end connected to the controller and the other end connected to the infrared device, and transmits the power and control signals generated by the controller to the infrared device, wherein the line cable includes therein a contact section provided with a flexible wire that can be freely deformed to conform to the facial curvature of the user.

Description

Infrared treatment device for ENT diseases

[0001] The present disclosure relates to a device for treating physical ailments using infrared rays, and more specifically, to a treatment device for caring for otolaryngological diseases, including the user's nose and ears, using infrared rays.

[0002] The technology of treating various diseases by irradiating the body with infrared rays is already being utilized in a wide range of medical devices and treatment equipment. Infrared rays are known to penetrate deep into body tissues, improving blood circulation, promoting cell regeneration, and reducing inflammation; based on these characteristics, they are used as an adjunctive treatment for various conditions, including muscle pain, arthritis, and inflammatory diseases. Infrared therapy plays an important role in medical and home treatment devices due to the advantage of being a non-invasive and relatively safe method.

[0003] Recently, there has been increasing interest in treating various nose-related diseases such as rhinitis, sinusitis, and respiratory diseases. When infrared rays are applied to the nose and absorbed into the body through the mucous membranes inside the nostrils, they have effects such as improving blood flow, reducing inflammation, and promoting cell regeneration. Consequently, there is a growing trend of using infrared rays to treat ENT diseases.

[0004] Conventional infrared ENT treatment devices generally have large and complex shapes, making it uncomfortable for users to insert or wear them in their nostrils for extended periods. Furthermore, conventional ENT treatment devices have limited control over the intensity and angle of the irradiated infrared rays and are not tailored to the individual user's nostril shape and size, making personalized treatment difficult and resulting in inconsistent treatment effects. Additionally, there is a problem where the treatment device easily falls out due to fluid inside the nostrils.

[0005] Therefore, to solve these problems, there is a need for an infrared therapy device that causes minimal discomfort when inserted into the user's nostrils, allows for customized treatment, and does not easily fall off when worn.

[0006] [Prior Art Literature]

[0007] [Patent Document] Republic of Korea Patent Publication No. 10-2021-0114739

[0008] The purpose of the present disclosure is to provide an ENT disease treatment device that improves wearing comfort and prevents the infrared device from falling off by using a flexible wire inside the line cable to allow the user to operate and maintain the line cable according to the shape of the user's face.

[0009] In addition, the objective of the present disclosure is to provide an otolaryngological disease treatment device that includes a silicone cap to prevent the infrared device from falling off due to secretions inside the user's nose.

[0010] In addition, the objective of the present disclosure is to provide an ENT disease treatment device that can be easily worn by anyone regardless of the user's nose width by adjusting the spacing of the first module of the infrared device in correspondence with the distance between the user's nostrils.

[0011] In addition, the objective of the present disclosure is to provide an otolaryngology disease treatment device capable of treating both nose and ear-related diseases of a user with a single device by selectively combining a first module with a second module or a third module.

[0012] The purposes of this specification are not limited to those mentioned above, and other purposes and advantages of this specification not mentioned may be understood from the following description and will be more clearly understood by the embodiments of this specification. Furthermore, it will be readily apparent that the purposes and advantages of this specification can be realized by the means and combinations thereof set forth in the claims.

[0013] An otolaryngological disease treatment device according to various embodiments of the present disclosure comprises an infrared device that irradiates infrared rays onto a part of a user's body including the nose, a controller that supplies power to the infrared device and controls the operation of the infrared device, and a line cable having one end connected to the controller and the other end connected to the infrared device to transmit power and control signals generated by the controller to the infrared device, wherein the line cable includes a contact section having a flexible wire that is freely deformable to correspond to the curvature of the user's face.

[0014] In addition, in various embodiments of the present disclosure, the contact section includes a first section mounted on one side of the user's ear and supported by a section behind the earlobe, and a second section extending from the first section and mounted in contact with the user's face.

[0015] In addition, in various embodiments of the present disclosure, the first section further includes a silicone pad formed at a position corresponding to the outer ear to disperse and relieve pressure applied to the user's ear.

[0016] In addition, in various embodiments of the present disclosure, the infrared device includes a first module that is inserted into a plurality of the user's nose and fixedly supported through lateral pressure or tensile force, and a second module that extends from a line cable and is positioned below the user's nose so that the plurality of first modules can be detachably attached.

[0017] Additionally, in various embodiments of the present disclosure, the first module comprises an infrared lamp that emits infrared rays, an electronic circuit that controls at least one of the wavelength of the infrared rays, the intensity of the infrared rays, and the on / off of the infrared lamp according to a control signal of a controller, a cover member that covers the infrared lamp and the electronic circuit to protect the infrared lamp and the electronic circuit, an insertion tube coupled to the top of the cover member and having a hollow formed in the center so that the emitted infrared rays are irradiated into the nose of the user, and a base module that is received inside the second module and is coupled to and fixedly supported by the infrared lamp, the electronic circuit, the cover member, and the insertion tube.

[0018] Additionally, in various embodiments of the present disclosure, the insertion tube further includes a silicone cover surrounding the outer surface that contacts the user's nose.

[0019] Additionally, in various embodiments of the present disclosure, the insertion tube is formed of a transparent glass material, and the infrared rays pass through or are reflected from the insertion tube and scattered in at least one direction of the nose.

[0020] Additionally, in various embodiments of the present disclosure, the base module is formed to enable left and right rotational movement of the insertion tube, and the insertion tube rotates left and right at predetermined intervals corresponding to the width of the user's nose.

[0021] Additionally, in various embodiments of the present disclosure, the first module includes a silicone cap that is detachably fitted to the end of the insertion tube, and the silicone cap is fixedly supported inside the nose by filling the spaced-apart space between the inner surface of the user's nose and the insertion tube.

[0022] In addition, in various embodiments of the present disclosure, the silicone cap is formed of a mesh material so as not to obstruct the user's breathing.

[0023] Additionally, in various embodiments of the present disclosure, the silicone cap is formed in a multi-layer shape so that the first module is transported by the user's internal nasal secretions and does not fall out of the user's nose.

[0024] Additionally, in various embodiments of the present disclosure, the contact section includes a third module having a groove formed to a predetermined depth so that the first module can be coupled thereto, and when the first module is coupled to the third module, the insertion tube is inserted into the user's ear to treat a disease related to the user's ear.

[0025] An otolaryngological disease treatment device according to various embodiments of the present disclosure can improve wearing comfort and prevent the infrared device from falling off by using a flexible wire inside the line cable to allow the user to operate and maintain the line cable according to the shape of the user's face.

[0026] In addition, an otolaryngology treatment device according to various embodiments of the present disclosure may include a silicone cap to prevent the infrared device from falling off due to secretions inside the user's nose.

[0027] In addition, the otolaryngology treatment device according to various embodiments of the present disclosure can be easily worn by anyone regardless of the user's nose width by adjusting the spacing of the first module of the infrared device in correspondence with the distance between the user's nostrils.

[0028] In addition, an otolaryngology disease treatment device according to various embodiments of the present disclosure can treat both nose and ear-related diseases of a user with a single device by selectively combining a first module with a second module or a third module.

[0029] FIG. 1 is a block diagram of an otolaryngological disease treatment device according to various embodiments of the present disclosure.

[0030] FIG. 2 is a drawing showing the wearing state of an otolaryngological disease treatment device according to various embodiments of the present disclosure.

[0031] FIG. 3 is a block diagram of an infrared device in various embodiments of the present disclosure.

[0032] FIGS. 4 to 11 are drawings showing the configuration of an infrared device in various embodiments of the present disclosure.

[0033] FIG. 12 is a drawing showing a line cable in various embodiments of the present disclosure.

[0034] FIG. 13 is a drawing showing a silicone pad included in a line cable in various embodiments of the present disclosure.

[0035] FIGS. 14 and 15 are drawings showing the state in which a first module is combined with a third section of a line cable in various embodiments of the present disclosure.

[0036] The present invention is susceptible to various modifications and may have various embodiments; specific embodiments are illustrated in the drawings and described in detail in the detailed description. However, this is not intended to limit the invention to specific embodiments, and it should be understood that the invention includes all modifications, equivalents, and substitutions that fall within the spirit and scope of the invention. Similar reference numerals have been used for similar components in the description of each drawing.

[0037] Terms such as first, second, A, B, etc., may be used to describe various components, but said components should not be limited by said terms. These terms are used solely for the purpose of distinguishing one component from another. For example, without departing from the scope of the present invention, the first component may be named the second component, and similarly, the second component may be named the first component. The term "and / or" includes a combination of a plurality of related described items or any of a plurality of related described items.

[0038] When it is stated that one component is "connected" or "connected" to another component, it should be understood that while it may be directly connected or connected to that other component, there may also be other components in between. On the other hand, when it is stated that one component is "directly connected" or "directly connected" to another component, it should be understood that there are no other components in between.

[0039] The terms used in this application are used merely to describe specific embodiments and are not intended to limit the invention. The singular expression includes the plural expression unless the context clearly indicates otherwise. In this application, terms such as "comprising" or "having" are intended to specify the presence of the features, numbers, steps, actions, components, parts, or combinations thereof described in the specification, and should be understood as not precluding the existence or addition of one or more other features, numbers, steps, actions, components, parts, or combinations thereof.

[0040] Unless otherwise defined, all terms used herein, including technical or scientific terms, have the same meaning as generally understood by those skilled in the art to which the present invention pertains. Terms such as those defined in commonly used dictionaries should be interpreted as having a meaning consistent with their meaning in the context of the relevant technology, and should not be interpreted in an ideal or overly formal sense unless explicitly defined in this application.

[0041] Here, the user may refer to a person who uses an ENT disease treatment device and has an ENT-related disease, such as a nasal disease or an ear disease, or a person who wishes to prevent the disease.

[0042] Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the attached drawings.

[0043] FIG. 1 is a block diagram of an otolaryngological disease treatment device according to various embodiments of the present disclosure, and FIG. 2 is a drawing showing the wearing state of an otolaryngological disease treatment device according to various embodiments of the present disclosure.

[0044] Referring to the drawing, the ENT disease treatment device (10) includes an infrared device (100), a line cable (200), and a controller (300).

[0045] The infrared device (100) irradiates infrared rays onto a part of the user's body. The user's body refers to a body part related to the otolaryngology, but is not necessarily limited thereto and may include any body part capable of treating diseases through infrared rays. However, for convenience of explanation, the user's body part irradiated with infrared rays is defined as the nose and ears below.

[0046] One end of the line cable (200) is connected to the controller (300), and the other end is connected to the infrared device (100) to transmit power and control signals generated by the controller (300) to the infrared device (100). As the line cable (200) is used with a portion of the infrared device (100) and the controller (300) spanning the user's ear area, the section from the ear to the infrared device (100) may be maintained in contact with the user's face, and a flexible wire may be provided inside the contact section, and the length of the flexible wire may be formed to correspond to the length of the contact section (210).

[0047] Here, the flexible wire refers to a wire made of a material that possesses the flexibility to curve and can be deformed into various shapes, including curved shapes. That is, when an external force is applied to a straight wire, it can be deformed into a curved shape, and then restored to a straight shape through an external force in the opposite direction. Through this, by using the flexible wire, the shape of the line cable (200) can be deformed to correspond to the curvature of the user's face.

[0048] The controller (300) supplies power to the infrared device (100) and controls the operation of the infrared device (100), and to this end, may include a power supply module (310), a signal generation module (320), an operation module (330), and a display (340).

[0049] The power supply module (310) can generate power to supply to the infrared device (100) and controller (300) through a general battery such as a manganese battery or an alkaline battery, or a rechargeable secondary battery such as a lead-acid battery, nickel-cadmium, nickel-manganese, or lithium-ion battery.

[0050] The signal generation module (320) generates a control signal that controls the operation of the infrared device (100) according to user input or information (temperature, humidity, etc.) sensed from the sensor module (116). The generated power and control signals are transmitted to the infrared device (100) through the line cable (200).

[0051] The operation module (330) receives various inputs according to the user's operation. The inputs may be, for example, the wavelength of the infrared light, the intensity of the infrared light, the on / off operation of the infrared lamp, and the current time, and the input information and current status information may be displayed through a display (340) provided on one side of the controller (300) so that the user can recognize them.

[0052] Specific details regarding the infrared device (100), line cable (200), and controller (300) will be explained in detail below with reference to the drawings.

[0053] FIG. 3 is a block diagram of an infrared device in various embodiments of the present disclosure, and FIGS. 4 to 11 are drawings showing the configuration of an infrared device in various embodiments of the present disclosure.

[0054] Referring to FIGS. 3 to 5, the infrared device (100) may include a first module (110) that is inserted into the user's nose and fixedly supported by lateral pressure or tensile force, and a second module (120) that extends from a line cable (200) and is positioned at the lower part of the user's nose and has a receiving structure formed inside so that a plurality of first modules (110) can be attached and detached.

[0055] Specifically, the first module (110) may be two in number corresponding to the number of nostrils, and each of the first modules (110) includes an infrared lamp (111), an electronic circuit (112), a cover member (113), an insertion tube (114), a base module (115), and a sensor module (116).

[0056] The infrared lamp (111) generates infrared rays and emits them outside the first module (110), and the electronic circuit (112) controls at least one of the wavelength of the infrared rays, the intensity of the infrared rays, and the on / off of the infrared lamp according to a control signal from the controller (300). In various embodiments, the infrared lamp (111) may emit infrared rays with a wavelength of 660 nm.

[0057] The cover member (113) covers the infrared lamp (111) and the electronic circuit (112) to protect the infrared lamp (111) and the electronic circuit (112) from being damaged by physical pressure. The cover member (113) may be formed of a transparent or opaque material, and since the infrared lamp (111) and the electronic circuit (112) are components with a high risk of damage, the durability of the first module (110) can be improved through the cover member (113).

[0058] The insertion tube (114) is a member formed with a predetermined length in one direction and inserted directly into the user's nose, and is coupled to the top of the cover member (113). The insertion tube (114) has a hollow formed longitudinally in the center so that emitted infrared rays can be guided along the hollow and irradiated into the user's nose.

[0059] In various embodiments, the insertion tube (114) may be formed of a transparent glass material. As the insertion tube (114) is formed of a glass material, infrared rays pass through or are reflected from the insertion tube (114) and scattered in at least one direction of the nose, and the infrared rays are irradiated onto a wide area inside the nostril, thereby improving the performance of rhinitis treatment, such as improving blood flow. Meanwhile, if formed of a transparent glass material, infrared rays can be transmitted to the outside even without a hollow, so the end of the insertion tube (114) may be formed in a shielded form without a hollow.

[0060] Additionally, in various embodiments, the insertion tube (114) may further include a silicone cover surrounding the outer surface that contacts the user's nose. The silicone cover may be made of a transparent or opaque material, and since the insertion tube (114) is the part that is directly inserted into and contacts the user's nose, it can be used hygienically through the silicone cover. In various embodiments, the silicone cover may not be fixed integrally with the insertion tube (114) but may be formed separately to facilitate cleaning and replacement.

[0061] Additionally, as illustrated in FIG. 6, the insertion tube (114) may include a silicone cap that is detachably fitted to the end. The width of the nostrils and the size of the nose may vary from user to user, and if the insertion tube (114) is significantly smaller than the width of the nostrils, it may easily fall out of the nose. The silicone cap can be fixedly supported inside the nose by filling the spaced-apart space between the inner side of the user's nose and the insertion tube (114), and can be customized and used regardless of the size of the user's nose by being composed of various sizes.

[0062] In addition, in various embodiments, the silicone cap may be formed in a multi-layer shape so that the first module (110) is transported by the user's nasal secretions and does not fall out of the user's nose. Referring to FIG. 7, the silicone cap may be formed in a circular three-layer structure, with the diameter of the first layer being the smallest and the diameter gradually increasing as it goes to the third layer. In addition, in this embodiment, the silicone cap may have a shape in which each individual layer has a narrow upper surface area and a wide lower surface area.

[0063] Typically, a person's nose has the widest area at the entrance of the nostril and has a structure that narrows as it goes deeper. By using the structure of such a silicone cap, it can be matched to the structure of the nose to minimize the feeling of unfamiliarity when inserted, and even after wearing the insertion tube (114), it can be prevented from easily falling out of the nose due to the shape of the individual layers, which have a narrow upper area and a wide lower area.

[0064] Additionally, as shown in FIG. 8, the silicone cap can be formed from a mesh material. Since the mesh has pores that allow air to flow through them, using a silicone cap made of mesh material has the advantage of allowing the ENT disease treatment device (10) to be used without obstructing the user's breathing.

[0065] The base module (115) is housed in a receiving structure (121) inside the second module (120) and is fixedly supported by being combined with an infrared lamp (111), an electronic circuit (11), a cover member (113), and an insertion tube (114).

[0066] In various embodiments, the base module (115) has a structure that is detachable from the receiving structure (121) of the second module (120), as shown in FIG. 9, and with reference to FIG. 10, the base module (115) combined with the second module (120) is formed to be rotatable left and right so that the insertion tube (114) can be rotated left and right at a predetermined interval corresponding to the user's nose width through a groove formed on the upper surface of the second module (120).

[0067] Specifically, as shown in FIG. 11 (a), for a user with a wide nose, each of the first modules (110) can be rotated in a spreading direction, and as shown in FIG. 11 (b), for a user with a narrow nose, each of the first modules (110) can be rotated in a closing direction. That is, when each of the first modules (110) is rotated in a spreading direction, a tensile load is generated so that the infrared device (100) is supported by the outer wall of the nostrils so that it does not fall off, and conversely, when each of the first modules (110) is rotated in a closing direction, a compressive load is generated so that the infrared device (100) is supported by the inner wall of the nostrils so that it does not fall off. In other words, since the spacing of the first modules of the infrared device can be adjusted in correspondence with the distance between the user's nostrils through the rotation of the base module (115), the infrared device (100) can be prevented from falling off regardless of the user's nose width.

[0068] The sensor module (116) is provided at one end of the first module (110) to sense the temperature inside the nose or to sense humidity. The sensor module (116) may be, for example, a humidity sensor and a temperature sensor. The signal generation module (320) can generate a control signal that, if the temperature inside the nose exceeds a preset temperature as a result of sensing, turns off the power of the infrared lamp, or, if the humidity inside the nose exceeds a preset humidity, instructs the fan (122) to dry the nose first. In this way, the otolaryngology disease treatment device (10) can not only prevent nose burns and improve safety through the sensor module (116), but also provide optimal conditions for using the device.

[0069] Meanwhile, in various embodiments, the second module (120) may include a fan (122) with an open exterior. When the first module (110) is removed from the second module (120), operating the fan (122) dries the user's nose with air, thereby preventing the first module (110) from slipping off due to secretions inside the nose.

[0070] FIG. 12 is a drawing showing a line cable in various embodiments of the present disclosure, FIG. 13 is a drawing showing a silicone pad included in a line cable in various embodiments of the present disclosure, and FIG. 14 and FIG. 15 are drawings showing a state in which a first module is coupled with a third section of a line cable in various embodiments of the present disclosure. Hereinafter, the line cable will be described in detail with reference to FIG. 12 to FIG. 15.

[0071] As described above, the line cable (200) includes a contact section (210), and the contact section (210) is provided with a flexible wire that is freely deformable to correspond to the curvature of the user's face, with a length corresponding to the contact section.

[0072] Specifically, the contact section (210) may include a first section (211) mounted on one side of the user's ear and supported by the back of the earlobe, and a second section (212) extending from the first section (211) and mounted in contact with the user's face. The line cable (200) of the present disclosure allows for stable wearing because the first section (211) is supported by the user's ear, the infrared device (100) is supported by the user's nose, and the second section (212) is supported by the frictional force of contact with the user's face.

[0073] In addition, in various embodiments, as shown in FIG. 13, the first section (211) may further include a silicone pad (S) formed at a position corresponding to the outer ear to disperse and relieve pressure applied to the user's ear. The silicone pad (S) may include a light and soft material inside to improve comfort, and may be, for example, memory foam or latex.

[0074] In various embodiments, the contact section (210) may include a third module (213) having a groove formed to a predetermined depth so that the first module (110) can be coupled. Specifically, the third module (213) may be located at the back of the user's ear as shown in FIG. 14, or at a portion of the section (upper ear) corresponding to the second section (212) as shown in FIG. 15. Alternatively, the third module (213) may be formed on one side of the silicone pad (S), and the location of the third module (213) is not limited and may be formed in various positions and shapes.

[0075] When the first module (110) is combined with the third module (213), the insertion tube (114) connected to the first module (110) is inserted into the user's ear and irradiates infrared rays to treat a disease related to the user's ear (e.g., otitis media).

[0076] That is, since the first module (110) is separately combined with the second module (120) and the third module (213), the user can selectively combine and use the first module (110) according to the desired disease area (ear or nose), thereby maximizing the usability of the device.

[0077] As described above, the otolaryngology treatment device according to various embodiments of the present disclosure can improve wearing comfort and prevent the infrared device from falling off by using a flexible wire inside the line cable to allow the user to operate and maintain the line cable according to the shape of the user's face.

[0078] In addition, an otolaryngology treatment device according to various embodiments of the present disclosure may include a silicone cap to prevent the infrared device from falling off due to secretions inside the user's nose.

[0079] In addition, the otolaryngology treatment device according to various embodiments of the present disclosure can be easily worn by anyone regardless of the size of the user's nostrils by adjusting the spacing of the first module of the infrared device in correspondence with the size of the user's nostrils.

[0080] Although the present invention has been described above with reference to the illustrated drawings, the present invention is not limited by the embodiments and drawings disclosed in this specification, and it is obvious that various modifications can be made by a person skilled in the art within the scope of the technical concept of the present invention. Furthermore, even if the effects of the configuration of the present invention were not explicitly described while explaining the embodiments of the present invention above, it is natural to acknowledge that the effects predictable by said configuration should also be recognized.

Claims

1. An infrared device that irradiates infrared rays onto a part of the user's body, including the nose; A controller that supplies power to the infrared device and controls the operation of the infrared device; and It includes a line cable in which one end is connected to the controller and the other end is connected to the infrared device to transmit power and control signals generated by the controller to the infrared device. The above-described line cable includes a contact section having a flexible wire provided therein that is freely deformable to correspond to the contours of the user's face. Treatment device for otolaryngological diseases.

2. In Paragraph 1, The above contact section is A first section mounted on one side of the user's ear and supported by the rear section of the earlobe, and a second section extending from the first section and mounted in contact with the user's face. Treatment device for otolaryngological diseases.

3. In Paragraph 2, The above first section is Further comprising a silicone pad formed at a position corresponding to the auricle to disperse and relieve pressure applied to the user's ear Treatment device for otolaryngological diseases.

4. In Paragraph 1, The above infrared device is A first module inserted in multiple places inside the nose of the user and fixedly supported through lateral pressure or tensile force, and A second module extending from the above-mentioned line cable and positioned below the user's nose, formed to allow the plurality of first modules to be detachably attached. Treatment device for otolaryngological diseases.

5. In Paragraph 4, The above first module is Infrared lamp that emits infrared rays; An electronic circuit that controls at least one of the wavelength of the infrared light, the intensity of the infrared light, and the on / off of the infrared lamp according to a control signal of the above controller; A cover member that covers the infrared lamp and the electronic circuit to protect the infrared lamp and the electronic circuit; An insertion tube coupled to the top of the above-mentioned cover member and having a hollow formed in the center so that the emitted infrared rays are irradiated into the user's nose; and A base module that is housed inside the second module and is coupled to and fixedly supported by the infrared lamp, the electronic circuit, the cover member, and the insertion tube. Treatment device for otolaryngological diseases.

6. In Paragraph 5, The above insertion tube A silicone cover further comprising surrounding the outer surface that contacts the user's nose. Treatment device for otolaryngological diseases.

7. In Paragraph 5, The above insertion tube It is formed of a transparent glass material, and the infrared rays pass through or are reflected from the insertion tube and scattered in at least one direction of the nose. Treatment device for otolaryngological diseases.

8. In Paragraph 5, The above base module is The insertion tube is formed to be capable of left and right rotational movement, and the insertion tube rotates left and right at predetermined intervals corresponding to the user's nose width. Treatment device for otolaryngological diseases.

9. In Paragraph 5, The above first module is It includes a silicone cap that is detachably fitted to the end of the insertion tube, and The above silicone cap fills the spaced-apart space between the inner side of the user's nose and the insertion tube, and is fixedly supported inside the nose. Treatment device for otolaryngological diseases.

10. In Paragraph 9, The above silicone cap is Formed of mesh material so as not to obstruct the breathing of the aforementioned user Treatment device for otolaryngological diseases.

11. In Paragraph 9, The above silicone cap is The first module is formed in a multi-layer form so that it is transported by the user's internal nasal secretions and does not fall out of the user's nose. Treatment device for otolaryngological diseases.

12. In Paragraph 5, The above contact section is It includes a third module having a groove formed to a predetermined depth so that the first module can be coupled thereto, and When the first module is coupled to the third module, the insertion tube is inserted into the user's ear to treat a disease related to the user's ear. Treatment device for otolaryngological diseases.

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