A breast infrared therapy device, a therapy bra and a therapy bandage

Abstract

The application relates to the technical field of medical devices, and particularly provides a breast infrared treatment device, a treatment chest garment and a treatment bandage, which comprise a controller and a plurality of infrared treatment pieces, a plurality of electric control ports are arranged on the controller, the plurality of infrared treatment pieces are plug-in connected to the electric control ports of the controller through cables, the plurality of infrared treatment pieces are controlled by the controller and used for emitting infrared rays to the breast, and the infrared treatment piece is a near-infrared treatment device or a far-infrared medicine bag treatment device. The breast near / far-infrared treatment device in the application is used for treatment in an office or at home, so that the patient can continuously perform the breast infrared treatment according to the doctor's advice.

Description

Technical Field

[0001] This utility model relates to the field of medical device technology, and in particular to a breast infrared treatment device, a treatment bra, and a treatment bandage. Background Technology

[0002] Most women have a history of breast pain (such as cyclical pain due to breast hyperplasia, mastitis pain, breast pain caused by psychological factors, and postoperative breast pain and scar hyperplasia). Some women experience severe and prolonged breast pain, which can affect their work, studies, and daily life.

[0003] In existing technologies, breast treatment involves irradiating the breast with near / far-infrared rays. Infrared rays can penetrate the skin surface (to a depth of approximately 1-5 mm), reaching a depth of 2-5 cm. Infrared rays are absorbed by mitochondria in cells, promoting ATP production, enhancing cell metabolism, aiding tissue repair, and reducing inflammation. After being absorbed by breast tissue, infrared rays are converted into heat energy, relieving muscle spasms and reducing pain; they may also act by regulating cell function (such as reducing inflammatory factors); and they can promote local recovery after breast surgery, reducing scar hyperplasia. When patients require breast infrared therapy, the equipment used is relatively complex and inconvenient to move, requiring patients to visit a hospital outpatient clinic. Each treatment session lasts 10-20 minutes, once daily, for 10-15 days as one course of treatment. Because the treatment cycle is relatively long, typically ranging from two weeks to several months, the fast pace of modern life makes it difficult for patients to take time off work to visit the clinic every day, leading to inconsistent treatment and affecting the treatment's effectiveness.

[0004] Therefore, existing technologies still need to be improved and developed. Utility Model Content

[0005] In view of the shortcomings of the prior art, the purpose of this application is to provide a breast infrared therapy device, a treatment bra and a treatment bandage to solve the problem that patients need to repeatedly go to medical clinics for treatment in the existing solutions. With the breast infrared therapy device, treatment bra and treatment bandage of this application, treatment can be performed in the office or at home, thereby ensuring that patients can continue to receive breast infrared therapy for the full course of treatment as prescribed by the doctor.

[0006] The technical solution adopted by this application to solve the technical problem is as follows: A breast infrared treatment device, comprising:

[0007] A controller, wherein the controller is provided with multiple electrical control ports;

[0008] Multiple infrared therapy devices are provided, and the multiple infrared therapy devices are detachably connected to the electrical control port of the controller via cables.

[0009] Multiple infrared therapeutic devices are controlled by the controller to emit infrared rays toward the breast, and the infrared therapeutic devices are near-infrared therapeutic devices or far-infrared medicated pack therapeutic devices.

[0010] Furthermore, when the far-infrared medicine pack therapy device is electrically connected to the controller, the far-infrared medicine pack therapy device includes:

[0011] An infrared emitter, wherein the heated side of the infrared emitter is used to emit infrared rays toward the mammary gland;

[0012] A medicine pack holder is detachably mounted on the heating side of the infrared emitter to heat the medicine pack holder when the infrared emitter emits infrared rays.

[0013] Furthermore, the medicine package holder includes:

[0014] A drug pack, wherein the drug pack is detachably mounted on the heating side of the infrared emitter;

[0015] A first connector is mounted on the drug package and is detachably connected to the infrared emitter.

[0016] Furthermore, the first connector includes a restraint strap, which is connected to the medicine pack;

[0017] The drug package is attached to the infrared emitter via the restraint strap;

[0018] The restraint strap is a binding strap or an elastic band.

[0019] Furthermore, the infrared emitter has side slots on both sides for the restraint strap to be inserted;

[0020] The infrared emitter has an insertion direction, and the restraint strap is fitted into the side slot along the insertion direction;

[0021] The side slot has a first inner side and a second inner side along the insertion direction, and the height of the first inner side is less than the height of the second inner side.

[0022] Furthermore, the infrared emitter has a rear slot on the side opposite to the heating side for the restraint strap to be inserted;

[0023] The rear slot is provided with limiting teeth to prevent the first connector from disengaging from the rear slot when the first connector is engaged in the rear slot.

[0024] Furthermore, the infrared emitter is fan-shaped.

[0025] Furthermore, the drug package includes:

[0026] A support layer is provided on the heating side of the infrared emitter;

[0027] A placement slot is provided on the support layer for placing drugs;

[0028] A shielding layer is attached to the support layer and is used to open or close the placement slot.

[0029] A therapeutic bra includes a bra body and a breast infrared treatment device. When the infrared treatment component is a far-infrared medicine pack therapy device, the infrared emitter of the far-infrared medicine pack therapy device is further provided with a second connector so as to install the breast infrared treatment device on the bra body through the second connector.

[0030] A therapeutic bandage includes a bandage body and a breast infrared treatment device. When the infrared treatment component is a far-infrared medicated pack therapy device, a third connector is further provided on the infrared emitter of the far-infrared medicated pack therapy device to install the breast infrared treatment device on the bandage body via the third connector.

[0031] Beneficial Effects: This application provides a breast infrared therapy device, a treatment bra, and a treatment bandage. The infrared therapy components are controlled by a controller to treat the breast. Multiple infrared therapy components are used simultaneously during treatment to enhance the therapeutic effect. The infrared therapy components are connected to an external controller via cables, allowing the user to hold the controller and directly control multiple infrared therapy components, improving portability. This eliminates the need for repeated visits to medical clinics; patients can perform treatment at home or in the office under a doctor's guidance, ensuring continuous treatment and maintaining effectiveness. Furthermore, the infrared therapy components are divided into near-infrared therapy devices and far-infrared medicated pack therapy devices, making breast treatment more targeted and further improving its effectiveness. Attached Figure Description

[0032] Figure 1 This is a schematic diagram of a breast infrared therapy device according to an embodiment of this application;

[0033] Figure 2 This is a schematic diagram of the infrared emitter in an embodiment of this application;

[0034] Figure 3 This is a schematic diagram of the infrared emitter from another angle in an embodiment of this application;

[0035] Figure 4 This is a schematic diagram of the medicine package placement component in an embodiment of this application;

[0036] Figure 5 This is a schematic diagram showing the inner shielding layer of the medicine pack placement component being torn from the support layer in an embodiment of this application;

[0037] Figure 6 This is a schematic diagram of a therapeutic bra as described in an embodiment of this application;

[0038] Figure 7 This is a schematic diagram of the treatment bandage in an embodiment of this application.

[0039] Explanation of reference numerals in the attached figures:

[0040] 10. Infrared therapy component; 100. Infrared emitter; 110. Side slot; 120. Rear slot; 121. Limiting tooth; 130. Placement slot; 140. Second connector; 200. Medicine pack placement component; 210. Medicine pack; 211. Support layer; 212. Placement slot; 213. Shielding layer; 220. First connector; 20. Controller; 21. Electrical control port; 22. Cable; 23. Temperature sensor; 30. Bra body; 40. Bandage body. Detailed Implementation

[0041] To make the objectives, technical solutions, and advantages of this application clearer and more explicit, the following detailed description of this application is provided with reference to the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are merely illustrative of this application and are not intended to limit this application.

[0042] In the description of this application, it should be understood that the terms "center," "longitudinal," "lateral," "upper," "lower," "front," "rear," "left," "right," "vertical," "horizontal," "top," "bottom," "inner," and "outer," etc., indicating orientation or positional relationships based on the orientation or positional relationships shown in the accompanying drawings, are used only for the convenience of describing this application and simplifying the description, and do not indicate or imply that the device or element referred to must have a specific orientation, or be constructed and operated in a specific orientation, and therefore should not be construed as a limitation on this application. Furthermore, the terms "first" and "second" are used for descriptive purposes only and should not be construed as indicating or implying relative importance or implicitly specifying the number of indicated technical features. Thus, a feature defined as "first" or "second" may explicitly or implicitly include one or more of that feature. In the description of this application, unless otherwise stated, "a plurality of" means two or more.

[0043] In the description of this application, it should be noted that, unless otherwise expressly specified and limited, the terms "installation," "connection," and "linking" should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral connection; they can refer to a mechanical connection or an electrical connection; they can refer to a direct connection or an indirect connection through an intermediate medium; and they can refer to the internal connection between two components. Those skilled in the art can understand the specific meaning of the above terms in this application based on the specific circumstances.

[0044] Example 1

[0045] This embodiment provides a breast infrared therapy device, such as Figures 1 to 7 As shown, this invention addresses the problem of patients needing to visit medical clinics for treatment in existing solutions. By using a breast infrared therapy device, treatment bra, and treatment bandage as described in this application, treatment can be performed in the office or at home, ensuring continuous breast infrared therapy for patients. Specifically, the breast infrared therapy device includes multiple infrared therapy elements 10 and a controller 20. The infrared therapy elements 10 emit infrared rays to the breast, and the multiple infrared therapy elements 10 are pluggable and detachable onto the electrical control port 21 of the controller 20 via cables 22. The controller 20 controls the operation of the infrared therapy elements 10. To make the treatment more targeted, the infrared therapy elements 10 can be near-infrared therapy devices or far-infrared medicated pack therapy devices.

[0046] Near-infrared therapy devices use wavelengths of 600-850nm and power densities of 50-200mW / cm². 2 The near-infrared light or near-infrared composite light can directly irradiate the breast lesions of the patient. The infrared light source generated by the near-infrared therapy device directly acts on the lesions. Alternatively, the near-infrared therapy device can be connected to a patch; the patch does not block the near-infrared light but only provides an attachment function, and is applied to the lesion area of ​​the breast. In this embodiment, the near-infrared therapy device consists of multiple 10-20 infrared LEDs (Light Emitting Diodes), 5-10mm in size or SMD (Surface Mount Device), arranged in a circular or rectangular array. The total power is 1-5W, the forward voltage is 1.2V-1.8V, and the radiation intensity is 10-500mW / sr. The near-infrared therapy device can be directly fixed to the skin with medical adhesive, or first fixed to the bra body 30 or bandage body 40 with Velcro, and then the treatment bra or bandage is worn by the patient. The near-infrared therapy device is connected to a connector via cable 22, which is connected to the electrical control port 21 of the controller 20, enabling the controller 20 to control the operation of the near-infrared therapy device.

[0047] The far-infrared herbal pack therapy device includes an infrared emitter 100 and a herbal pack holder 200. The heating side of the infrared emitter 100 emits infrared rays towards the mammary gland. The herbal pack holder 200 is detachably installed on the heating side of the infrared emitter 100, so that the herbal pack holder 200 also faces the mammary gland and is in contact with it. When the infrared emitter 100 emits infrared rays, it heats the herbal pack holder 200, allowing the traditional Chinese medicine to enter the patient's body. Heating makes it easier for the medicine to penetrate into the patient's acupoints, relieving pain and inflammation, thus achieving traditional Chinese medicine treatment. The infrared emitter 100 emits far-infrared light with a wavelength of 10μm±0.5μm and a fixed power of 1.5W / cm². 2 The red light emitted has a shallow penetration of less than 1 cm, so it is mainly used to heat the medicine inside the medicine pack 200, allowing the medicine to enter the patient's body for treatment. Specifically, the medicine is directed to the area of ​​the breast lesion, or to acupoints such as Tanzhong, Rugen, Qimen, Yunmen, Dabao, Ganshu, Geshu, Shenshu, and Weishu, which are effective in treating breast diseases, thereby treating the breast through the medicine. The infrared emitter 100 is made of alumina ceramic heating element coated with a silicon carbide radiation layer; all far-infrared emission units use a constant current drive circuit with a fixed output current of 0.6A, a voltage of 5V, and a power density of 1.5W / cm². 2 Meanwhile, the infrared emitter 100 is connected to a connector via cable 22, which connects to the electrical control port 21 of the controller 20, enabling the controller 20 to control the operation of the infrared emitter 100. Since multiple infrared treatment devices 10 need to be applied to the patient simultaneously during breast infrared therapy to improve treatment effectiveness, the controller 20 is equipped with multiple electrical control ports 21. These multiple infrared treatment devices 10 are connected to connectors via cables 22, and these connectors connect to the electrical control ports 21 of the controller 20, allowing the controller 20 to control the operation of the multiple infrared treatment devices 10 applied to the patient, further improving the therapeutic effect of breast infrared therapy. Furthermore, temperature control is necessary during treatment to avoid weakening the treatment effect due to excessively low temperature and causing burns to the patient due to excessively high temperature. Therefore, in this application, the treatment temperature needs to be controlled between 45-55℃. To achieve temperature control, the controller 20 also includes a temperature sensor 23, which is installed on the infrared treatment device 10. The temperature sensor 23 detects the temperature in real time, enabling the controller 20 to control the operation of the infrared treatment device 10 based on the monitoring data of the temperature sensor 23.

[0048] To achieve portability of the breast infrared therapy device, the controller 20 is battery-powered, eliminating the need for a power cord and thus freeing it from placement restrictions. Furthermore, the cable 32 is long enough that the controller 20 does not need to be in close proximity to the infrared therapy unit 10, allowing it to be placed in the patient's pocket or other location, or held in the hand. The user can directly control multiple infrared therapy units with the handheld controller. To accommodate pocket placement or handheld use, the controller 20's size is significantly reduced compared to existing infrared therapy devices. In this application, its length, width, and height are 17cm, 8cm, and 3cm respectively, enhancing portability. In other embodiments, it is similar in size to a mobile phone. Additionally, the controller 20 is equipped with a display screen that shows current temperature information and treatment time, and allows for timely adjustments to the operation of the infrared therapy unit 10 based on the displayed information.

[0049] When the far-infrared medicated pack therapy device is applied to the breast to treat the breast, it is necessary to keep the medicated pack placement component 200 fixed to the infrared emitter 100 to prevent the medicated pack placement component 200 from falling off the infrared emitter 100 and thus preventing the infrared emitter 100 from heating the medicated pack placement component 200, which would affect the therapeutic effect on the breast. Therefore, the medicated pack placement component includes a medicated pack 210 and a first connecting component 220. The medicated pack 210 is detachably installed on the heating side of the infrared emitter and contains medication for treating the breast. The first connecting component 220 is installed on the medicated pack 210 and is detachably connected to the infrared emitter 100. Therefore, when installing the medicine pack holder 200 on the heating side of the infrared emitter 100, first align the medicine pack 210 with the heating side of the infrared emitter 100, and then install the first connector 220 on the infrared emitter 100 to keep the positions of the medicine pack 210 and the infrared emitter 100 relatively fixed; when it is necessary to replace the medicine pack holder 200, first remove the first connector 220 from the infrared emitter 100, and then remove the medicine pack 210 from the heating side of the infrared emitter 100. Specifically, in this application, the first connecting member 220 is a restraint strap, with both ends of the restraint strap fixedly installed on both sides of the medicine pack 210. Therefore, when the medicine pack placement piece 200 is installed on the infrared emitter 100, after aligning the medicine pack 210 with the heating side of the infrared emitter 100, the restraint strap is used to secure the medicine pack 210. When it is necessary to remove the medicine pack placement piece 200, the restraint strap is readjusted and removed from the infrared emitter 100, thereby finally removing the medicine pack 210 and completing the removal of the medicine pack placement piece 200. Specifically, the restraint strap is a binding strap or an elastic band. When the restraint strap is a binding strap, after it is placed on the infrared emitter 100, the two ends of the binding strap are tied to secure it to the infrared emitter 100. When the restraint strap is an elastic band, the elasticity of the elastic band secures the restraint strap placed on the infrared emitter 100 to the infrared emitter.

[0050] In addition, in other embodiments, the first connector 220 may also be a Velcro fastener, which is installed on the side of the medicine pack 210 near the heating side, and the medicine pack 210 is attached to the infrared emitter 100 by the Velcro fastener to keep the medicine pack 210 fixed.

[0051] To prevent the first connector 220 from sliding along the outer wall of the infrared emitter 100 and detaching from the infrared emitter 100 during patient movement, which could lead to the detachment of the medicine pack holder 200 and affect the treatment effect, side slots 110 are provided on both sides of the infrared emitter 100 for the first connector 220 to be inserted. Specifically, the infrared emitter 100 has an insertion direction, and the restraint strap is inserted from the outside of the infrared emitter 100 along the insertion direction, so that it can be tightened and embedded in the side slots 110. For example, the insertion direction can be from top to bottom, with the heating side facing forward, and the side slots 110 are provided on the left and right sides of the infrared emitter 100.

[0052] When the restraint strap is fitted onto the infrared emitter 100, the first connectors 220 located on both sides of the infrared emitter 100 are fitted into the side slots 110 along the fitting direction, thereby preventing the restraint strap from falling off the infrared emitter 100 when the breast infrared treatment device moves.

[0053] The side slot 110 has a first inner side 111 and a second inner side 112 along the insertion direction. For example, the first inner side 111 is located on the upper side and the second inner side 112 is located on the lower side. The height of the first inner side 111 (the distance between the top edge and the bottom surface of the side slot 110) is less than the height of the second inner side 112. In this way, when the first connector 220 is fitted onto the side slot 110, the first connector 220 can be further prevented from detaching from the infrared emitter 100, and the relative fixation between the medicine pack holder 200 and the infrared emitter 100 can be maintained.

[0054] Furthermore, the infrared emitter 100 has a rear slot 120 on the side facing away from the heating side for the first connector 220 to be inserted. Therefore, when the first connector 220 is fitted onto the infrared emitter 100, the first connectors 220 on both sides of the infrared emitter 100 are inserted into the side slots 110, while the first connector 220 on the side of the infrared emitter 100 facing away from the heating side is inserted into the rear slot 120. The first connector 220 is kept fitted onto the infrared emitter 100 by the action of the side slots 110 and the rear slot 120. Only when it is necessary to remove the medicine pack holder 200 can the first connector 220 be pulled out from the side slots 110 and the rear slot 120 to facilitate the removal of the medicine pack holder 200.

[0055] Since the area of ​​the side of the infrared emitter 100 facing away from the heating side is larger than the area of ​​its side surface, even if the position of the first connector 220 is fixed by embedding it into the rear slot 120, the first connector 220 may still slip out of the rear slot 120. Therefore, in order to further fix the first connector 220 embedded in the rear slot 120, a limiting tooth 121 is provided in the rear slot 120 so that when the first connector 220 is embedded in the rear slot 120, the first connector 220 is further embedded in the fixing groove formed by the limiting tooth 121, thus preventing the first connector 220 from detaching from the rear slot 120. When removing the medicine pack holder 200 by removing the first connector 220 from the infrared emitter 100, the first connector 220 needs to be removed from the fixing groove formed by the limiting tooth 121 while moving the first connector 220 out of the side slot 110, and then the first connector 220 needs to be moved out of the rear slot 120. Finally, the first connector 220 is completely removed from the infrared emitter 100, so that the medicine pack 210 can be removed and the medicine pack holder 200 can be removed.

[0056] To better match the breast infrared therapy device to the breast, the infrared emitter 100 is fan-shaped, thus avoiding contact with the nipple when applied to the breast. Alternatively, the infrared emitter 100 can also be square, disc-shaped, etc.

[0057] In addition, since the medicine pack placement component 200 has a certain thickness after being filled with medicine, it can cause discomfort to the patient when it is applied to the breast. Therefore, in order to reduce the patient's discomfort, a placement groove 130 is provided on the heating side of the infrared emitter 100 for the placement component 200 to be placed. When the medicine pack placement component 200 is placed in the placement groove 130, the protrusion height of the medicine pack placement component 200 relative to the infrared emitter 100 can be reduced, thereby reducing the patient's discomfort. The placement groove 130 can also better align the medicine pack placement component 200 with the infrared emitter 100, so that the medicine pack placement component 200 can be installed in the designated position on the infrared emitter 100, thereby further improving the therapeutic effect of the breast infrared therapy device.

[0058] The drug package 210 includes a support layer 211, a placement slot 212, and a shielding layer 213, such as Figure 4 and Figure 5As shown, the support layer 211 is square and made of a mesh knitted fabric. The first connector 220 is installed on both sides of the support layer 211. A placement groove 212 is provided on the support layer 211 for placing medication. The medication can be in various states such as powder or solid block. In this application, the placement groove 212 is circular; in other embodiments, it may have a different shape. One side of the shielding layer 213 is fixed to the support layer 211, and the other side of the shielding layer 213 is attached to the other side of the shielding layer 212. When medication needs to be placed into the placement groove 212, the shielding layer 213 attached to the support layer 211 is first peeled off to expose the placement groove 212. After the medication is placed, the shielding layer 213 is reattached to the support layer 211. Finally, the medication package 210 is placed into the placement sink 130 for the subsequent step of installing the medication package placement component 200 on the infrared emitter 100. In addition, the shielding layer 213 is also made of mesh knitted material. When the infrared emitter 100 heats the drug pack 210 by emitting infrared rays, the drug in the placement slot 212 is gradually heated and then passes through the shielding layer 213 made of mesh knitted material to enter the patient's body to treat the breast.

[0059] A therapeutic bra includes a bra body 30 and a breast infrared treatment device. When the infrared treatment component 10 is a far-infrared medicine pack therapy device, the infrared emitter 100 of the far-infrared medicine pack therapy device is further provided with a second connector 140. The breast infrared treatment device is mounted on the bra body 30 via the second connector 140. Therefore, after the medicine pack placement component 200 is mounted on the infrared emitter 100, the infrared emitter 100 is then mounted on the bra body 30 via the second connector 140, specifically on the side of the bra body 30 facing the breast. Finally, the bra body 30 is worn by the patient, so that the breast infrared treatment device is aligned with the breast, thereby treating the breast. In this application, the second connector 140 is a Velcro fastener, which is used to attach the breast infrared treatment device to the bra body 30. Other structures may be used in other embodiments.

[0060] In addition, a therapeutic bandage includes a bandage body 40 and a breast infrared treatment device. When the infrared treatment component 10 is a far-infrared medicated pack therapeutic device, the infrared emitter 100 of the far-infrared medicated pack therapeutic device is further provided with a second connector 140. The breast infrared treatment device is mounted on the bandage body 40 via the second connector 140. Therefore, after the medicated pack placement component 200 is mounted on the infrared emitter 100, the infrared emitter 100 is then mounted on the bandage body 40 via the second connector 140, specifically on the side of the bandage body 40 facing the breast. Finally, the bandage body 40 is bound to the patient, so that the breast infrared treatment device is aligned with the breast, thereby treating the breast. In this application, the second connector 140 is a Velcro strap; in other embodiments, it can be of other structures.

[0061] Therefore, when using the breast infrared treatment device of this application for breast treatment, when the infrared treatment component 10 is a far-infrared medicine pack treatment device, first tear the shielding layer 213 off the support layer 211 so that medicine can be placed into the placement slot 212 inside the medicine pack 210. After the medicine is placed, reattach the shielding layer 213 to the support layer 211, then place the medicine pack placement component 200 into the placement sink 130, and pull the first connecting component 220 so that the first connecting component 220 is engaged in the side slot 110 and the rear slot 12. Within the limiting tooth 121 of 0, the medicine pack placement component 200 is installed on the infrared emitter 100. After installation, the infrared emitter 100 is connected to the controller 20. Then, the breast infrared treatment device is installed on the bra body 30 or the bandage body 40 through the second connector 140. The bra body 30 is either worn on the patient or the bandage body 40 is tied to the patient, so that the breast infrared treatment device is aligned with the breast. Finally, the operation of the infrared emitter 100 is started through the controller 20, so as to start the treatment of the breast.

[0062] When the infrared treatment device 10 is a near-infrared treatment device, the near-infrared treatment device is connected to the controller 20, and then the breast infrared treatment device is installed on the bra body 30 or the bandage body 40 through Velcro. The bra body 30 is either worn on the patient or the bandage body 40 is tied to the patient, so that the breast infrared treatment device is aligned with the breast. Finally, the operation of the infrared emitter 100 is started through the controller 20 to begin treating the breast.

[0063] For example, patients with lower back pain can use the aforementioned infrared therapy device to install on an elastic waistband and fix it to the patient's lower back. The infrared rays and the Chinese medicine pack will act on acupoints such as Shenshu, Mingmen, Yaoyangguan, Weizhong, Dachangshu, Huantiao, and Ashi points.

[0064] For patients with dysmenorrhea, the aforementioned infrared therapy device can be installed on an elastic waistband and fixed to the patient's waist and abdomen. The infrared rays and Chinese medicine packs act on acupoints such as Qihai, Sanyinjiao, Taichong, Guanyuan, Baliao, Xuehai, Wushu, and Qugu.

[0065] It should be understood that the application of this utility model is not limited to the examples above. Those skilled in the art can make improvements or modifications based on the above description, and all such improvements and modifications should fall within the protection scope of the appended claims.

Claims

1. A breast infrared therapy device, characterized in that, include: A controller, wherein the controller is provided with multiple electrical control ports; Multiple infrared therapy devices are provided, and the multiple infrared therapy devices are detachably connected to the electrical control port of the controller via cables. Multiple infrared therapeutic devices are controlled by the controller to emit infrared rays toward the breast, and the infrared therapeutic devices are near-infrared therapeutic devices or far-infrared medicated pack therapeutic devices.

2. The breast infrared therapy device according to claim 1, characterized in that, When the far-infrared medicine pack therapy device is electrically connected to the controller, the far-infrared medicine pack therapy device includes: An infrared emitter, wherein the heated side of the infrared emitter is used to emit infrared rays toward the mammary gland; A medicine pack holder is detachably mounted on the heating side of the infrared emitter to heat the medicine pack holder when the infrared emitter emits infrared rays.

3. The breast infrared therapy device according to claim 2, characterized in that, The medicine package holder includes: A drug pack, wherein the drug pack is detachably mounted on the heating side of the infrared emitter; A first connector is mounted on the drug package and is detachably connected to the infrared emitter.

4. The breast infrared therapy device according to claim 3, characterized in that, The first connector includes a restraint strap, which is attached to the medicine pack; The drug package is attached to the infrared emitter via the restraint strap; The restraint strap is a binding strap or an elastic band.

5. The breast infrared therapy device according to claim 4, characterized in that, The infrared emitter has side slots on both sides for the restraint strap to be inserted. The infrared emitter has an insertion direction, and the restraint strap is fitted into the side slot along the insertion direction; The side slot has a first inner side and a second inner side along the insertion direction, and the height of the first inner side is less than the height of the second inner side.

6. The breast infrared therapy device according to claim 4, characterized in that, The infrared emitter has a rear slot on the side opposite to the heating side for the restraint strap to be inserted. The rear slot is provided with limiting teeth to prevent the first connector from disengaging from the rear slot when the first connector is engaged in the rear slot.

7. The breast infrared therapy device according to any one of claims 2 to 5, characterized in that, The infrared emitter is fan-shaped.

8. The breast infrared therapy device according to claim 3, characterized in that, The drug package includes: A support layer is provided on the heating side of the infrared emitter; A placement slot is provided on the support layer for placing drugs; A shielding layer is attached to the support layer and is used to open or close the placement slot.

9. A therapeutic bra, characterized in that, The device includes a bra body and a breast infrared treatment device as described in any one of claims 1 to 8. When the infrared treatment component is the far-infrared medicine pack therapy device, the infrared emitter of the far-infrared medicine pack therapy device is further provided with a second connector so as to install the breast infrared treatment device on the bra body through the second connector.

10. A therapeutic bandage, characterized in that, The device includes a bandage body and a breast infrared treatment device as described in any one of claims 1 to 8. When the infrared treatment component is the far-infrared medicated pack therapy device, the infrared emitter of the far-infrared medicated pack therapy device is further provided with a third connector so as to install the breast infrared treatment device on the bandage body through the third connector.

Images