Hemostatic ice compress device for face

Abstract

The utility model provides a hemostasis ice compress device for the face, and belongs to the technical field of medical supplies. Comprising a first bandage body and a second bandage body, one end of the first bandage body is forked to obtain a first fork opening and a second fork opening, the length of the first fork opening is smaller than that of the second fork opening, one end of the second bandage body is forked to obtain a third fork opening and a fourth fork opening, and the length of the third fork opening is smaller than that of the fourth fork opening; the first fork opening and the third fork opening are rotationally connected with first binding buckles correspondingly, and the second fork opening and the fourth fork opening are rotationally connected with the same second binding buckle correspondingly. The shaping assembly is used for shaping the ice bag to adapt to the skeleton contour of the wound position of a patient, the shaping assembly is connected with the first binding buckle and the second binding buckle, and the shaping assembly can be adjusted to adapt to the distance between the eyebrow arch and the nasal bone of different patients. Meanwhile, the use comfort of the patient can be improved under the cooperation of all parts in the shaping assembly.

Description

Technical Field

[0001] This utility model relates to the field of medical supplies technology, and in particular to a hemostatic ice pack device for the face. Background Technology

[0002] Nasal cyst anastomosis, also known as dacryocystorhinostomy, is an ophthalmic surgery primarily used to treat chronic dacryocystitis and nasolacrimal duct obstruction. The goal of the surgery is to create a new tear drainage pathway by directly anastomosing the lacrimal sac to the nasal cavity, allowing tears and secretions to flow smoothly into the nasal cavity. This eliminates purulent lesions in the lacrimal sac and resolves epiphora (excessive tearing).

[0003] After intranasal capsular anastomosis surgery, patients typically receive ice pack therapy to relieve postoperative pain and quickly stop bleeding. In clinical practice, ophthalmologists usually fill rubber medical gloves with water and freeze them to make ice packs. Since the incision for intranasal capsular anastomosis surgery is located on the bridge of the nose, and the frozen rubber medical gloves are palm-shaped, they are not easily fixed to the bridge of the nose. Therefore, patients need to hold the ice pack and apply it to the incision for extended periods, which can cause hand soreness and discomfort. Therefore, this invention provides a hemostatic ice pack device for the face to meet this need. Utility Model Content

[0004] This utility model provides a hemostatic ice pack device for the face. By setting a shaping component, the two ends of the first buckle and the second buckle are respectively fixedly connected to the shaping component. The shaping component can shape the ice pack and can also be adjusted to adapt to the distance from the brow bone to the nasal bone of different patients. At the same time, the cooperation of various components in the shaping component can also improve the patient's comfort. The structure of the shaping component is closely connected and complementary in function. The overall structure of the plate is made of ABS plastic material, which is not only inexpensive but also simple to process and easy to manufacture.

[0005] To solve the above-mentioned technical problems, this utility model provides the following technical solution:

[0006] A hemostatic ice pack device for the face includes a first strap and a second strap. A front Velcro is fixedly connected to the bottom outer wall of the first strap, and a back Velcro is fixedly connected to the top outer wall of the second strap. One end of the first strap is forked to form a first fork and a second fork, the length of the first fork being shorter than the length of the second fork. One end of the second strap is forked to form a third fork and a fourth fork, the length of the third fork being shorter than the length of the fourth fork.

[0007] The first fork and the third fork are respectively rotatably connected to a first buckle, and the second fork and the fourth fork are both rotatably connected to the same second buckle;

[0008] A shaping component for shaping an ice pack to fit the bone contour of the patient's wound location, the shaping component being connected to the first buckle and the second buckle respectively.

[0009] Optionally, the shaping component includes a first skeleton fixedly connected to both ends of the first buckle, and a second skeleton fixedly connected to one end of the first skeleton.

[0010] Optionally, a first support plate and a second support plate are fixedly connected to the inner walls of the middle part of the first frame near the top and near the bottom, respectively.

[0011] Optionally, a first arc-shaped plate is fixedly connected to the top outer wall on both sides of the first frame, and a second arc-shaped plate is fixedly connected to the bottom outer wall on both sides of the first frame.

[0012] Optionally, a rubber sleeve is fitted on the inner wall of the first skeleton and the second skeleton, and the rubber sleeve is filled with purified water containing alcohol, wherein the alcohol and purified water are mixed in a ratio of 1:3.

[0013] Optionally, a sliding plate is slidably connected to the outer wall of the first frame, and elastic clips are symmetrically fixedly connected to the outer walls on both sides of the sliding plate.

[0014] Optionally, a third support plate is fixedly connected to one end of the sliding plate, and four limiting plates are fixedly connected to the other end of the sliding plate.

[0015] Optionally, two first elastic plates are fixedly connected to the top outer wall of the other end of the third support plate, and a plurality of first limiting teeth are fixedly connected to one side outer wall of the first elastic plates.

[0016] Optionally, a second elastic plate is fixedly connected to the outer wall of the other side of the first elastic plate.

[0017] Optionally, a limiting hole is provided on the outer wall of the middle top of the second skeleton, and second limiting teeth are symmetrically fixedly connected on the inner walls on both sides of the limiting hole.

[0018] Compared with the prior art, this utility model has at least the following beneficial effects:

[0019] In the above solution, a shaping component is set up. The two ends of the first and second buckles are respectively fixedly connected to the shaping component. The shaping component can shape the ice pack and can also be adjusted to fit the distance from the brow bone to the nasal bone of different patients. At the same time, the cooperation of various components in the shaping component can also improve the patient's comfort. The structure of the shaping component is closely connected and complementary in function. The overall structure of the board is made of ABS plastic material, which is not only inexpensive but also has a simple processing technology and is easy to manufacture.

[0020] By setting up a first skeleton, a sliding plate, and a second skeleton, the overall outline of the first skeleton can be adjusted using the sliding plate to fit the distance from the patient's brow bone to the nasal bone. This setup allows for easy adaptation to different patients after a simple operation, improving the work efficiency of medical staff.

[0021] By setting up elastic clips, medical gauze can be held in place, preventing it from accidentally falling off while the patient is moving around, thus avoiding direct contact between the rubber sheath and the patient's skin, which could cause frostbite. In addition, the elastic clips can also prevent condensation droplets on the rubber sheath from falling onto the patient's skin and causing wound infection.

[0022] By setting limit plates, the bottom outer walls of the two limit plates near the top of the sliding plate can slide along the top outer wall of the first support plate, while the top outer walls of the two limit plates near the bottom of the sliding plate can slide along the bottom outer wall of the second support plate. This can prevent the sliding plate from deviating from the preset sliding track during the sliding process. Attached Figure Description

[0023] The accompanying drawings, which are incorporated herein and form part of the specification, illustrate embodiments of the present invention and, together with the specification, further serve to explain the principles of the present invention and enable those skilled in the art to implement and use the present invention.

[0024] Figure 1 A first-person perspective three-dimensional structural diagram of a hemostatic ice pack device for use on the face;

[0025] Figure 2 A second-view three-dimensional structural diagram of a hemostatic ice pack device for use on the face;

[0026] Figure 3 A magnified three-dimensional structural diagram showing the combination of the first frame, the second frame, and the sliding plate;

[0027] Figure 4 for Figure 3 Enlarged 3D structural diagram at point A;

[0028] Figure 5A magnified first-view three-dimensional structural diagram showing the combination of the first and second skeletons;

[0029] Figure 6 for Figure 5 Enlarged 3D structural diagram at point B;

[0030] Figure 7 A magnified schematic diagram of the second-view stereoscopic structure for the cooperation of the first and second skeletons;

[0031] Figure 8 An enlarged three-dimensional structural diagram of the sliding plate and the third support plate in combination;

[0032] Figure 9 for Figure 8 Enlarged 3D structural diagram at point C.

[0033] Figure label:

[0034] 1. First strap; 101. Second strap; 102. Front Velcro; 103. Back Velcro; 2. First buckle; 201. Second buckle; 3. First frame; 301. First curved plate; 302. Second curved plate; 303. First support plate; 304. Second support plate; 4. Second frame; 401. Limiting hole; 402. Second limiting tooth; 5. Sliding plate; 501. Elastic clip; 502. Third support plate; 503. First elastic plate; 504. First limiting tooth; 505. Limiting plate; 6. Second elastic plate.

[0035] As shown in the figure, specific structures and devices are marked in the figure to clearly illustrate the structure of the embodiment of this utility model. However, this is only for illustrative purposes and is not intended to limit this utility model to this specific structure, device and environment. Those skilled in the art can adjust or modify these devices and environments according to specific needs. Detailed Implementation

[0036] The following is a detailed description of a hemostatic ice pack device for the face provided by this utility model, with reference to the accompanying drawings and specific embodiments. It should be noted that, to make the embodiments more detailed, the following embodiments are the best and preferred embodiments; those skilled in the art can also use other alternative methods to implement some known technologies; and the accompanying drawings are only for more specific description of the embodiments and are not intended to specifically limit this utility model.

[0037] It should be noted that the use of terms such as "an embodiment," "an embodiment," "an exemplary embodiment," and "some embodiments" in the specification indicates that the described embodiment may include a specific feature, structure, or characteristic, but not every embodiment necessarily includes that specific feature, structure, or characteristic. Furthermore, when a specific feature, structure, or characteristic is described in connection with an embodiment, implementing such a feature, structure, or characteristic in conjunction with other embodiments (whether explicitly described or not) should be within the knowledge of those skilled in the art.

[0038] Generally, terms can be understood at least partly from their use in context. For example, depending at least partly on the context, the term "one or more" as used herein can be used to describe any feature, structure, or characteristic in a singular sense, or a combination of features, structures, or characteristics in a plural sense. Additionally, the term "based on" can be understood not necessarily to convey an exclusive set of factors, but rather, alternatively, depending at least partly on the context, to allow for the presence of other factors that are not necessarily explicitly described.

[0039] It is understood that the meanings of “on”, “above”, and “above” in this utility model should be interpreted in the broadest manner, such that “on” not only means “directly on” something, but also includes the meaning of being “on” something with an intervening feature or layer, and that “above” or “above” not only means “on” something, but also includes the meaning of being “on” something without an intervening feature or layer.

[0040] Furthermore, spatially related terms such as “below,” “under,” “lower,” “above,” and “upper” are used herein for convenience to describe the relationship of one element or feature to one or more other elements or features, as illustrated in the accompanying drawings. Spatially related terms are intended to cover different orientations in the use or operation of the device other than those depicted in the accompanying drawings. The device may be oriented in other ways, and the spatially related descriptive terms used herein can be interpreted similarly.

[0041] like Figures 1 to 9 As shown, an embodiment of the present invention provides a hemostatic ice pack device for the face, including a first strap 1 and a second strap 101. A front Velcro 102 is fixedly connected to the bottom outer wall of the first strap 1, and a reverse Velcro 103 is fixedly connected to the top outer wall of the second strap 101. One end of the first strap 1 is forked to form a first fork and a second fork, the length of the first fork being shorter than the length of the second fork. One end of the second strap 101 is forked to form a third fork and a fourth fork, the length of the third fork being shorter than the length of the fourth fork.

[0042] The first and third forks are rotatably connected to the first buckle 2, and the second and fourth forks are rotatably connected to the same second buckle 201. Specifically, the overall outline of the first strap 1 and the second strap 101 is "Y" shaped and made of nylon. The front hook and loop fastener 102 and the back hook and loop fastener 103 are respectively fixedly connected to the bottom outer wall of the first strap 1 away from the fork and the top outer wall of the second strap 101 away from the fork. The front hook and loop fastener 102 and the back hook and loop fastener 103 are both existing technologies and will not be described in detail.

[0043] The outer walls of the two first buckles 2 are rotatably connected to the ends of the first strap 1 away from the front Velcro 102. This setting allows the Velcro to be adjusted according to the size of the patient's head. The outer walls of the two first buckles 2 are rotatably connected to the first and third forks. The outer walls of the two ends of the second buckle 201 are rotatably connected to the second and fourth forks, respectively. The first buckle 2 is a "U"-shaped plastic cylinder. The second buckle 201 consists of three parts: two plastic cylinders and a plastic semi-circular ring.

[0044] The hemostatic ice pack device also includes a shaping component, which is used to shape the ice pack to fit the patient's wound location. The shaping component is connected to the first buckle 2 and the second buckle 201 respectively. By setting the shaping component, the two ends of the first buckle 2 and the second buckle 201 are fixedly connected to the shaping component. The shaping component can shape the ice pack and can also be adjusted to fit the distance from the brow bone to the nasal bone of different patients. At the same time, the cooperation of various components in the shaping component can also improve the patient's comfort.

[0045] like Figures 1 to 9As shown, the shaping component includes a first skeleton 3 fixedly connected to both ends of the first buckle 2. A second skeleton 4 is fixedly connected to one end of the first skeleton 3. A limiting hole 401 is provided on the outer wall of the top middle part of the second skeleton 4. Second limiting teeth 402 are symmetrically fixedly connected to the inner walls on both sides of the limiting hole 401. Specifically, the two ends of the two first buckles 2 are respectively fixedly connected to the outer walls of the two ends of the first skeleton 3. The first skeleton 3 is composed of two "ε"-shaped plastic plates and is made of plastic. The top and bottom outer walls of the middle part of the first skeleton 3 are respectively provided with semi-circular weakening grooves. The weakening grooves facilitate the shaping process. When the first frame 3 is bent, it will deform along its bending direction when subjected to force. The two ends of the second frame 4 are fixedly connected to the two ends of the first frame 3. The second frame 4 is a plastic straight plate. When the first frame 3 and the second frame 4 are put together, the outline is "T" shaped. The limiting hole 401 is set on the outer wall near the top of the middle of the second frame 4. The overall outline of the limiting hole 401 is square. The second limiting teeth 402 are symmetrically fixedly connected to the inner walls on both sides of the limiting hole 401. The overall outline of the limiting teeth is a quarter-cylinder shape and is made of plastic. This setting can adapt to the contour of the patient's brow bone and nasal bone.

[0046] A first support plate 303 and a second support plate 304 are fixedly connected to the inner walls of the middle part of the first frame 3 near the top and bottom, respectively. A first arc-shaped plate 301 is fixedly connected to the top outer walls of both sides of the first frame 3, and a second arc-shaped plate 302 is fixedly connected to the bottom outer walls of both sides of the first frame 3. Rubber sleeves are fitted on the inner walls of the first frame 3 and the second frame 4. The rubber sleeves are filled with purified water containing alcohol, wherein the alcohol and purified water are mixed in a ratio of 1:3. Specifically, the first support plate 303 and the second support plate 304 are fixedly connected to the inner walls of the middle part of the first frame 3 near the top and bottom, respectively. The first support plate 303 and the second support plate 304 are both made of plastic and are the same size and shape, consisting of two parts: a "V" shaped plastic straight plate and a "C" shaped plastic plate. When the first frame 3 is bent, the first support plate 303 and the second support plate 304 will deform in the direction of bending.

[0047] Two first arc-shaped plates 301 are fixedly connected to the top outer wall of the middle part of the first frame 3 on one side, and are distributed in a mirror image. The first arc-shaped plate 301 is a plastic plate with an arc and a segmented groove on the other side. Two second arc-shaped plates 302 are fixedly connected to the bottom outer wall of the middle part of the first frame 3 on one side, and are distributed in a mirror image. The second arc-shaped plate 302 is a plastic plate with an arc and a segmented groove on the other side. When the second arc-shaped plate 302 is attached to the patient's nasal bone, the side with the segmented groove is open. During the process of attaching to the patient's nasal bone, it will be deformed in the direction of the nasal bone bulge under force. With the setting of the segmented groove, it can adapt to the contour of the patient's nasal bone.

[0048] A rubber sleeve is fitted onto the inner wall of the first frame 3 and the second frame 4. Purified water mixed with alcohol is filled into the rubber sleeve. Since the alcohol and purified water are mixed in a 1:3 ratio, the ice pack made in this way can maintain a certain degree of softness after freezing, making it easy to use later. The rubber sleeve is a prior art and will not be described in detail. After the device is placed in the freezer, the purified water mixed with alcohol in the rubber sleeve will freeze into ice. By bending the first frame 3 and the second frame 4, the ice block near the first support plate 303 and the second support plate 304 is relatively thin due to the restriction of the first support plate 303 and the second support plate 304. With the help of the weakening grooves set on the first frame 3 and the second frame 4, the ice block can be broken. This structural design makes it easy to adapt to the patient's nasal bone contour and improve the patient's wearing comfort.

[0049] like Figures 1 to 9As shown, a sliding plate 5 is slidably connected to the outer wall of the first frame 3. Elastic clips 501 are symmetrically fixedly connected to the outer walls of both sides of the sliding plate 5. A third support plate 502 is fixedly connected to one end of the sliding plate 5, and four limiting plates 505 are fixedly connected to the other end of the sliding plate 5. Specifically, the sliding plate 5 is slidably connected to the outer wall of the first frame 3. The overall outline of the sliding plate 5 is a flat "8" shape, made of plastic. This shape allows the sliding plate 5 to deform along its bending direction as the first frame 3 is bent. Two elastic clips 501 are symmetrically fixedly connected to the outer walls of both sides of the sliding plate 5. The elastic clips 501 are "S"-shaped plastic plates, with one end of each clip fixed... The sliding plate 5 is connected to the outer wall of the sliding plate 5, and its other end is open, so that sterile gauze can be clamped when applying ice to the patient. One end of the four limiting plates 505 is fixedly connected to the outer wall of the sliding plate 5 away from the second skeleton 4, and they are symmetrical in pairs. The limiting plates 505 are plastic plates in the shape of "7". The bottom outer walls of the two limiting plates 505 near the top of the sliding plate 5 can slide with the sliding plate 5 on the top outer wall of the first support plate 303, while the top outer walls of the two limiting plates 505 near the bottom of the sliding plate 5 can slide with the sliding plate 5 on the bottom outer wall of the second support plate 304. This can prevent the sliding plate 5 from deviating from the preset sliding track during the sliding process.

[0050] Two first elastic plates 503 are fixedly connected to the top outer wall of the other end of the third support plate 502. Several first limiting teeth 504 are fixedly connected to one side outer wall of the first elastic plate 503. A second elastic plate 6 is fixedly connected to the other side outer wall of the first elastic plate 503. Specifically, one end of the third support plate 502 is fixedly connected to the outer wall of the sliding plate 5 near the second frame 4. The third support plate 502 is a "V"-shaped plastic straight plate. Two first elastic plates 504 are fixedly connected to the top outer wall of the other end of the third support plate 502. The first elastic plate 503 consists of two mirror-image distributed first elastic plates 503, which are composed of three parts: an arc-shaped plastic plate, a straight plastic plate, and an S-shaped plastic plate. The part of the first elastic plate 503 with the S-shaped plastic plate is fixedly connected to the top outer wall of the third support plate 502, while the other end with the arc-shaped plastic plate is open. When the end of the first elastic plate 503 with the arc-shaped plastic plate is pinched, the part of the first elastic plate 503 with the S-shaped plastic plate will be deformed along its bending direction under force.

[0051] On the side opposite to the straight portion of the first elastic plate 503, several linearly distributed first limiting teeth 504 are provided. The overall outline of the first limiting teeth 504 is a quarter-cylinder shape, made of plastic, with its curved outer wall facing the side of the first elastic plate 503 with the curved plastic plate. A second elastic plate 6 is fixedly connected between the outer walls of the opposite sides of the straight portion of the first elastic plate 503. The second elastic plate 6 is a plastic plate with an overall "C" shape. When the end of the first elastic plate 503 with the curved plastic plate is pinched, the second elastic plate 6 will be subjected to force and deform along its bending direction. The first limiting teeth 504 will move in accordance with the deformation of the first elastic plate 503. Displacement occurs when the sliding plate 5 is pushed away from the second skeleton 4, without being restricted by the second limiting tooth 402. When the first elastic plate 503 is released, the second elastic plate 6, no longer under force, will recover its deformation under its own elasticity and push the first elastic plate 503 back to its original position. The first limiting tooth 504 will then move along with the reset of the first elastic plate 503. The outer wall of the first limiting tooth 504 without curvature will abut against the outer wall of the second limiting tooth 402 without curvature, thus limiting the sliding plate 5. The above structure can be used to adjust the contour of the first skeleton 3 through the sliding plate 5 to adapt to the distance from the patient's brow bone to the nasal bone.

[0052] The working principle of the technical solution provided by this utility model is as follows:

[0053] In use, first slide the sliding plate 5 according to the distance from the patient's brow bone to the nasal bone to adjust the contour of the first skeleton 3. When the distance from the patient's brow bone to the nasal bone is long, push the sliding plate 5 towards the direction of the second skeleton 4. At this time, the curved outer wall of the first limiting tooth 504 will slide on the curved outer wall of the second limiting tooth 402, which will give the first elastic plate 503 a compressive force, causing the first elastic plate 503 to be stressed. The part with the S-shaped plastic plate will be stressed and deform along its bending direction. At the same time, the first elastic plate 503... 3. During the deformation process, the second elastic plate 6 will be subjected to force and deform along its bending direction until the sliding plate 5 slides to the appropriate position. Then, the curved outer wall of the first limiting tooth 504 will no longer abut against the curved outer wall of the second limiting tooth 402. The second elastic plate 6, no longer subjected to force, will recover its deformation under its own elasticity and push the first elastic plate 503 back to its original position. The first limiting tooth 504 will then follow the reset of the first elastic plate 503 and undergo displacement. The first frame 3 will then move along the direction of the sliding plate 5 during its sliding process. The first skeleton 3 deforms in the direction of its curvature, elongating its overall outline. Since the outer wall of the first limiting tooth 504 (without curvature) abuts against the outer wall of the second limiting tooth 402 (without curvature), it limits the sliding plate 5, preventing the first skeleton 3 from recovering its deformation under its own elasticity. This forces the sliding plate 5 to shift away from the second skeleton 4. When the distance from the patient's brow bone to the nasal bone is small, the sliding plate 5 is pushed away from the second skeleton 4. Because the first limiting tooth 504 (without curvature)... The curved outer wall will abut against the non-curved outer wall of the second limiting tooth 402, forming a limit on the sliding plate 5. When the end of the first elastic plate 503 with the curved plastic plate is pinched, the second elastic plate 6 will be subjected to force and deformed along its curvature direction. The first limiting tooth 504 will move with the deformation of the first elastic plate 503. At this time, the sliding plate 5 can be easily pushed away from the second skeleton 4 to adjust the overall contour of the first skeleton 3 to match the distance from the brow bone to the nasal bone of the patient.

[0054] The adjusted device is then placed in a medical freezer for freezing. After the patient's surgery, the purified water containing alcohol inside the rubber sleeve of the device also freezes. The first frame 3 and the second frame 4 are then bent. Due to the limitations of the first support plate 303 and the second support plate 304, the ice block near the first support plate 303 and the second support plate 304 inside the rubber sleeve is relatively thin. Using the weakening grooves on the first frame 3 and the second frame 4, the ice block can be broken off, ready for subsequent ice application to the wound. At this time, the two sides of medical gauze can be clamped in the elastic clips 501 on both sides of the sliding plate 5. First, the elastic clips 501 are bent away from the sliding plate 5, causing the elastic clips 501 to deform along their bending direction under force. Then, one side of the medical gauze is placed on the inner wall of the elastic clip 501. Under the elasticity of the clip 501 itself, it recovers its shape and clamps the medical gauze. This prevents the medical gauze from accidentally falling off during the patient's movement, thus preventing the rubber sleeve from directly contacting the patient's skin and causing frostbite. In addition, the medical gauze can also prevent condensation droplets on the rubber sleeve from falling onto the patient's skin and causing wound infection. After clamping the medical gauze on the elastic clip 501, the device can be placed on the patient's wound. As the strap is tied, the second arc-shaped plate 302 with segmented grooves will conform to the patient's nasal bone and adapt to the patient's nasal bone contour, thereby improving the patient's wearing comfort.

[0055] This utility model encompasses any substitutions, modifications, equivalent methods, and solutions made within the spirit and scope of this utility model. To provide the public with a thorough understanding of this utility model, specific details are described in detail in the preferred embodiments; however, those skilled in the art can fully understand this utility model without these details. Furthermore, to avoid unnecessary confusion regarding the essence of this utility model, well-known methods, processes, procedures, components, and circuits are not described in detail.

[0056] The above description is only a preferred embodiment of the present utility model. It should be noted that for those skilled in the art, several improvements and modifications can be made without departing from the principle of the present utility model, and these improvements and modifications should also be considered within the protection scope of the present utility model.

Claims

1. A hemostatic ice pack device for a face, characterized by, The utility model provides a binding belt, including first binding band and second binding band, the bottom outer wall of first binding band is fixedly connected with positive magic tape, the top outer wall of second binding band is fixedly connected with negative magic tape, first binding band one end sets bifurcation to get first prong and second prong, and the length of first prong is shorter than the length of second prong, and second binding band one end sets bifurcation to get third prong and fourth prong, and the length of third prong is shorter than the length of fourth prong, The first prong and the third prong are rotatably connected with a first buckle respectively, and the second prong and the fourth prong are rotatably connected with a second buckle. A shaping assembly is used for shaping the ice bag to fit the bone contour of the patient's wound position, and the shaping assembly is connected with the first buckle and the second buckle respectively.

2. The hemostatic ice pack device for face according to claim 1, characterized in that, The first skeleton of the shaping assembly is fixedly connected at both ends of the first buckle, and one end of the first skeleton is fixedly connected with a second skeleton.

3. The hemostatic ice pack device for face according to claim 2, characterized in that, The inner wall of the middle part of the first skeleton close to the top and close to the bottom is fixedly connected with a first support plate and a second support plate respectively.

4. The hemostatic ice pack device for face according to claim 2, characterized in that, The outer wall of the top of both sides of the first skeleton is fixedly connected with a first arc-shaped plate respectively, and the outer wall of the bottom of both sides of the first skeleton is fixedly connected with a second arc-shaped plate respectively.

5. The hemostatic ice pack device for face according to claim 2, wherein A rubber sheath is sleeved on the inner wall of the first skeleton and the second skeleton, purified water with alcohol added is filled in the rubber sheath, and the alcohol and the purified water are mixed in a ratio of 1:

3.

6. The hemostatic ice pack device for face according to claim 2, wherein A sliding plate is slidably connected to the outer wall of the first skeleton, and elastic clamps are fixedly connected to the outer wall of both sides of the sliding plate symmetrically.

7. The hemostatic ice pack device for face according to claim 6, characterized in that, One end of the sliding plate is fixedly connected with a third support plate, and the other end of the sliding plate is fixedly connected with four limiting plates.

8. The hemostatic ice pack device for face according to claim 7, characterized in that, The other end of the third support plate is fixedly connected with two first elastic plates on the outer wall of the top, and a plurality of first limiting teeth are fixedly connected to the outer wall of one side of the first elastic plate.

9. The hemostatic ice pack device for face according to claim 8, characterized in that, A second elastic plate is fixedly connected to the outer wall of the other side of the first elastic plate.

10. The hemostatic ice pack device for face according to claim 2, characterized in that, A limiting hole is arranged on the outer wall of the top of the middle part of the second skeleton, and second limiting teeth are fixedly connected to the inner wall of both sides of the limiting hole symmetrically.

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