Medical protective restraint glove
By installing a grip ball and a limiting component on a medical protective restraint glove to fix the pulse oximeter lead wire, the problem of cumbersome operation in the existing technology is solved, achieving the effect of simplifying operation and improving the convenience of monitoring.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- CHENGDE CENT HOSPITAL
- Filing Date
- 2025-01-14
- Publication Date
- 2026-06-09
AI Technical Summary
Existing medical restraint gloves are cumbersome to use when monitoring patients' blood oxygen saturation, increasing the workload of nursing staff.
A medical protective restraint glove was designed. The glove body has perforations for fingers to pass through and grip balls. An installation part is fixed on the back of the hand. The installation part has an installation groove and a limiting member for fixing the pulse oximeter's wires. The limiting member clamps the wires through an elastic element, simplifying the operation process.
It simplifies the operating procedures for nursing staff, improves the convenience of blood oxygen monitoring and the stability of gloves, and reduces the workload of nursing staff.
Smart Images
Figure CN224331104U_ABST
Abstract
Description
Technical Field
[0001] This application relates to the field of medical device technology, and more specifically, to a medical protective restraint glove. Background Technology
[0002] The content in this section provides only background information related to this application and may not constitute prior art.
[0003] Medical protective restraint gloves are safety devices used in medical environments to help manage agitated patient behavior. Neurological patients often experience uncontrolled hand movements due to abnormal electrical activity in their brains, clinically manifesting as involuntary movements such as tremors, convulsions, or other abnormal actions. In such cases, restraint gloves are needed to restrain the patient's hands to prevent them from harming themselves or others, or to prevent them from removing medical devices (such as catheters, IV lines, etc.).
[0004] Existing restraint gloves typically consist of a glove body with a rigid plate in the palm area. In practice, the patient's hand is inserted into the glove, with the rigid plate against the palm. The glove is then secured at the wrist opening using a strap or zip ties. This prevents hand movement as the patient's palm remains in contact with the rigid plate. However, this existing technology has several drawbacks. In practice, the patient's entire hand is inside the glove. For patients requiring long-term monitoring, real-time blood oxygen saturation monitoring is necessary. In such cases, the only option is to unzip the glove's back side and attach the oxygen clip to the patient's fingertips, a cumbersome procedure that increases the workload of caregivers. Utility Model Content
[0005] In order to solve the above-mentioned technical problems, the purpose of this application is to provide a medical protective restraint glove that can simplify the operation process of nursing staff and reduce their workload.
[0006] The objective of this application is achieved through the following technical solution:
[0007] A medical protective restraint glove includes a glove body with perforations at the fingertips for fingers to pass through. A grip ball is provided in the palm of the glove body and is detachably connected to the glove body. A fixing part is fixedly provided on the back of the glove body, and an installation part is rotatably provided on the side of the fixing part near the fingertips. An installation block is provided on the installation part, and an installation groove is provided on the top of the installation block. The installation groove extends through both sides and is used for the passage of a pulse oximeter's lead wire. A limiting member is provided on the installation block to limit the position of the lead wire within the installation groove.
[0008] In some possible embodiments, the limiting member is configured as a limiting block, and a groove is formed on the inner wall of the mounting groove near the fingertip. There are two grooves, which are symmetrically distributed on the inner walls of both sides of the mounting groove. A limiting member is provided in each groove. One end of the limiting member is rotatably disposed in the groove. The side of the limiting member away from the groove is used to abut against the wire. An elastic member is provided in the groove, which is used to drive the limiting member to deflect in a direction that brings them closer together.
[0009] In some possible embodiments, a receiving groove is provided at the end of the limiting member away from the groove, and a roller is rotatably disposed in the receiving groove, the roller being used for the rolling contact of the wire.
[0010] In some possible embodiments, the limiting block includes a connecting part and a limiting part, and an installation shaft is rotatably disposed in the groove. One end of the connecting part is fixedly connected to the installation shaft, and the limiting part is fixedly disposed at the end of the connecting part away from the installation shaft. The connecting part and the limiting part are arranged at an inclined and staggered manner.
[0011] In some possible embodiments, a mounting hole is provided on the connecting part, the mounting shaft passes through the mounting hole and is fixedly connected to the connecting part, a notch is provided on the connecting part, the elastic element is set as a torsion spring, the elastic element is sleeved on the end of the mounting shaft, one end of the elastic element is fixedly connected to the inner wall of the notch, and the other end is fixedly connected to the inner wall of the groove.
[0012] In some possible embodiments, an abutment block is slidably disposed in the groove in a horizontal direction, the abutment block being used to abut against the side wall of the connecting part, and a driving member is disposed on the mounting block, the driving member being used to drive the abutment block to move in the groove.
[0013] In some possible embodiments, the driving component is configured as a driving block, with a connecting hole inside the mounting block, a connecting rod slidably disposed within the connecting hole, a strip-shaped hole on the bottom wall of the groove communicating with the connecting hole, a strip-shaped block slidably disposed within the strip-shaped hole, the top of the strip-shaped block being fixedly connected to the bottom of the abutment block, the bottom of the strip-shaped block being fixedly connected to the connecting rod, the end of the connecting rod away from the abutment block extending out of the connecting hole, and the driving block being fixedly disposed at the end of the connecting rod away from the abutment block.
[0014] In some possible embodiments, a connecting plate is fixedly provided on the side wall of the drive block, the connecting plate fixing the two drive blocks together, and an anti-slip pad is provided on the side wall of the connecting plate away from the connecting rod, and the anti-slip pad is provided with anti-slip texture.
[0015] In some possible embodiments, a groove is provided horizontally at the top of the mounting part, and a slider is slidably disposed in the groove. The top of the slider is fixedly connected to the bottom of the mounting block. The groove is a T-shaped groove, and the slider is a T-shaped block adapted to the groove. A sliding layer is provided on the side wall of the slider, and the sliding layer is used to slide and connect with the inner wall of the groove.
[0016] In some possible embodiments, a guide block is fixedly provided on the top of the fixing part, and a guide groove is provided on the guide block. The two ends of the guide groove are provided through the guide groove, and the guide groove is used for the wire to pass through. The guide groove is T-shaped.
[0017] In summary, the technical solutions of this application have at least the following advantages and beneficial effects:
[0018] 1. In actual use, the glove body is put on the patient's hand, with the patient's fingertips protruding through the perforations. The pulse oximeter body can then be clamped onto the patient's fingertips. The pulse oximeter's lead wire passes through the mounting slot on the mounting block, and then the position of the lead wire within the mounting slot is limited by the limiting component. After completing the above operations, the grip ball is installed in the palm of the glove body to facilitate the patient's grip. In subsequent patient use, on the one hand, the grip ball allows the patient to hold the glove, and on the other hand, it makes it easier to monitor the patient's blood oxygen in real time. This effectively simplifies the operation process for nursing staff and reduces their workload.
[0019] 2. When the wire is inserted into the mounting groove, the limiting component tends to deflect towards each other under the action of the elastic component. This clamps and positions the wire in the mounting groove, preventing it from falling out and improving the overall stability and reliability of the device during actual use. Furthermore, during use, the wire slides along the length of the mounting groove as the patient's fingers move, ensuring that the wire moves accordingly when the patient grips the grip ball, thus preventing the pulse oximeter from falling out.
[0020] 3. The position of the wire in the mounting groove is limited by the limiting component. Under the action of the elastic component, the limiting component deflects towards the wire, thereby causing the roller to roll into contact with the wire. This transforms the sliding friction between the wire and the limiting component into rolling friction, effectively reducing the friction between the wire and the limiting component and facilitating the displacement of the wire in the mounting groove. At the same time, since the limiting component is designed with mutually inclined and staggered connecting and limiting parts, it can further improve the limiting effect on the position of the wire in the mounting groove, preventing the wire from leaving the mounting groove from the top opening of the mounting groove, and further improving the practicality and reliability of the device in actual use.
[0021] 4. When installing the wire into the mounting slot, the driving component moves the connecting rod within the connecting hole. The connecting rod then moves the abutment block within the groove. The abutment block moves the connecting part, which in turn moves the entire limiting component away from each other, thus increasing the distance between the ends of the two limiting components. This makes it easier for the operator to place the wire into the mounting slot. After the wire installation is complete, the driving component is released. The limiting component then deflects towards the wire under the action of the elastic component, causing the end of the limiting component to abut against the limiting component to define the wire's position. By moving the connecting plate, both driving components can be moved simultaneously, causing the abutment blocks in the two grooves to move synchronously. This allows for synchronous deflection of the two limiting components, simplifying the operator's steps and making operation more convenient. When pressing the connecting plate, the anti-slip pad effectively increases the friction between the operator's hand and the connecting part, making it easier for the operator to move the connecting plate. Attached Figure Description
[0022] Figure 1 This is a schematic diagram of the overall structure of an embodiment of this application;
[0023] Figure 2 This is a schematic diagram of the grip ball according to an embodiment of this application;
[0024] Figure 3 This is a schematic diagram of the fixing part and the mounting part according to an embodiment of this application;
[0025] Figure 4 This is a cross-sectional view of the mounting section according to an embodiment of this application;
[0026] Figure 5 for Figure 4 Enlarged view of part A in the image;
[0027] Figure 6 This is a schematic diagram of the structure of the driver component according to an embodiment of this application;
[0028] Figure 7This is a schematic diagram of the slide groove structure according to an embodiment of this application. Icons: 1. Glove body; 11. Perforation; 12. Grip ball; 2. Fixing part; 21. Mounting part; 22. Mounting block; 23. Mounting groove; 24. Groove; 25. Elastic element; 3. Limiting element; 31. Connecting part; 32. Limiting part; 33. Mounting shaft; 34. Mounting hole; 35. Notch; 4. Receiving groove; 41. Roller; 5. Abutment block; 6. Driving element; 61. Connecting hole; 62. Connecting rod; 63. Strip hole; 64. Strip block; 65. Connecting plate; 66. Anti-slip pad; 67. Anti-slip texture; 7. Slide groove; 71. Slider; 8. Guide block; 81. Guide groove; 9. Pulse oximeter; 91. Wire. Detailed Implementation
[0029] To make the objectives, technical solutions, and advantages of the embodiments of this application clearer, the technical solutions of the embodiments of this application will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only some embodiments of this application, and not all embodiments. The components of the embodiments of this application described and shown in the accompanying drawings can generally be arranged and designed in various different configurations.
[0030] The following is for reference Figures 1 to 7 This application will be described in further detail.
[0031] Reference Figure 1 A medical protective restraint glove includes a glove body 1, with perforations 11 at the fingertips for fingers to pass through, and a grip ball 12 in the palm of the glove body 1, which is detachably connected to the glove body 1.
[0032] Reference Figure 3 A fixing part 2 is fixedly provided on the back of the glove body 1. A mounting part 21 is rotatably provided on the side of the fixing part 2 near the fingertips. A mounting block 22 is provided on the mounting part 21. A mounting groove 23 is provided on the top of the mounting block 22. The mounting groove 23 is provided through on both sides and is used for the wire 91 of the pulse oximeter 9 to pass through. A limiting member 3 (such as...) is provided on the mounting block 22. Figure 5 As shown), the limiting member 3 is used to limit the position of the wire 91 in the mounting groove 23.
[0033] In one possible implementation of this application, the grip ball 12 and the glove body 1 are detachably connected by a hook-and-loop fastener. In other possible implementations, the grip ball 12 and the glove body 1 can also be connected by buttons, connecting straps, or other easily detachable methods, such as... Figure 2The size and specific installation position of the grip ball 12 shown are for illustrative purposes only. In actual use, the size, material (which affects its force recovery), and installation position in the palm of the hand of the grip ball 12 can be adjusted according to actual needs, making it suitable for patients with different conditions.
[0034] Reference Figure 4 and Figure 5 As one embodiment of this application, the limiting member 3 is configured as a limiting block. A groove 24 is provided on the inner wall of the mounting groove 23 near the fingertip. There are two grooves 24, which are symmetrically distributed on the inner walls of both sides of the mounting groove 23. A limiting member 3 is provided in each groove 24. One end of the limiting member 3 is rotatably disposed in the groove 24. The side of the limiting member 3 away from the groove 24 is used to abut against the wire 91. An elastic member 25 is provided in the groove 24. The elastic member 25 is used to drive the limiting member 3 to deflect in a direction that brings them closer to each other.
[0035] When the wire 91 is inserted into the mounting groove 23, the limiting member 3, under the action of the elastic member 25, tends to deflect towards each other, thereby clamping and positioning the wire 91 in the mounting groove 23 to a certain extent, preventing the wire 91 from falling out of the mounting groove 23, and improving the overall stability and reliability of the device in actual use. At the same time, during use, as the patient's fingers move, the wire 91 can slide along the length of the mounting groove 23, ensuring that when the patient holds the grip ball 12, the wire 91 can move accordingly with the movement of the patient's fingers, which also helps to avoid the risk of the pulse oximeter 9 falling out.
[0036] Reference Figure 5 A receiving groove 4 is provided at the end of the limiting member 3 away from the groove 24. A roller 41 is rotatably arranged in the receiving groove 4. The roller 41 is used for the rolling contact of the wire 91.
[0037] Reference Figure 5 The limiting block includes a connecting part 31 and a limiting part 32. An installation shaft 33 is rotatably arranged in the groove 24. One end of the connecting part 31 is fixedly connected to the installation shaft 33. The limiting part 32 is fixedly arranged at the end of the connecting part 31 away from the installation shaft 33. The connecting part 31 and the limiting part 32 are arranged at an angle and alternately.
[0038] The position of the wire 91 in the mounting groove 23 is limited by the limiting member 3. Under the action of the elastic member 25, the limiting member 3 deflects towards the direction closer to the wire 91, thereby causing the roller 41 to roll into contact with the wire 91. This transforms the sliding friction between the wire 91 and the limiting member 3 into rolling friction, effectively reducing the friction between the wire 91 and the limiting member 3. This facilitates the displacement of the wire 91 in the mounting groove 23. At the same time, since the limiting member 3 is set as a connecting part 31 and a limiting part 32 that are inclined and staggered to each other, the limiting effect on the position of the wire 91 in the mounting groove 23 can be further improved, preventing the wire 91 from leaving the mounting groove 23 through the top opening of the mounting groove 23. This further improves the practicality and reliability of the device in actual use.
[0039] Reference Figure 5 A mounting hole 34 is provided on the connecting part 31, and the mounting shaft 33 passes through the mounting hole 34 and is fixedly connected to the connecting part 31. A notch 35 is provided on the connecting part 31. As one embodiment of this application, the elastic member 25 is set as a torsion spring. The elastic member 25 is sleeved on the end of the mounting shaft 33. One end of the elastic member 25 is fixedly connected to the inner wall of the notch 35, and the other end is fixedly connected to the inner wall of the groove 24.
[0040] Reference Figure 6 An abutment block 5 is slidably disposed in the groove 24 along the horizontal direction. The abutment block 5 is used to abut against the side wall of the connecting part 31. A driving member 6 is disposed on the mounting block 22. The driving member 6 is used to drive the abutment block 5 to move in the groove 24.
[0041] As one embodiment of this application, refer to Figure 6 The driving component 6 is configured as a driving block. A connecting hole 61 is provided inside the mounting block 22. A connecting rod 62 is slidably disposed in the connecting hole 61. A strip hole 63 is provided on the bottom wall of the groove 24. The strip hole 63 is connected to the connecting hole 61. A strip block 64 is slidably disposed in the strip hole 63. The top of the strip block 64 is fixedly connected to the bottom of the abutment block 5. The bottom of the strip block 64 is fixedly connected to the connecting rod 62. The end of the connecting rod 62 away from the abutment block 5 extends out of the connecting hole 61. The driving block is fixedly disposed at the end of the connecting rod 62 away from the abutment block 5.
[0042] When the wire 91 is installed into the mounting slot 23, the driving member 6 drives the connecting rod 62 to move in the connecting hole 61. The connecting rod 62 drives the abutment block 5 to move in the groove 24. The abutment block 5 drives the connecting part 31 and then drives the entire limiting member 3 to move in a direction away from each other, thereby increasing the distance between the ends of the two limiting members 3. This makes it easier for the staff to put the wire 91 into the mounting slot 23. After the installation of the wire 91 is completed, the driving member 6 is released. At this time, the limiting member 3 deflects towards the direction of the wire 91 under the action of the elastic member 25, thereby causing the end of the limiting member 3 to abut against the limiting member 3 to limit the position of the wire 91.
[0043] Reference Figure 6 A connecting plate 65 is fixedly installed on the side wall of the drive block, and the connecting plate 65 fixes the two drive blocks together. An anti-slip pad 66 is provided on the side wall of the connecting plate 65 away from the connecting rod 62, and anti-slip texture 67 is provided on the anti-slip pad 66.
[0044] By moving the connecting plate 65, two driving components 6 can be moved simultaneously, thereby driving the abutment blocks 5 in the two grooves 24 to move synchronously, and thus enabling the synchronous deflection of the two limiting components 3. This simplifies the operation steps for the operator to a certain extent and makes the operation more convenient. When pressing the connecting plate 65, the anti-slip pad 66 can effectively increase the friction between the operator's hand and the connecting part 31, making it easier for the operator to move the connecting plate 65.
[0045] Reference Figure 7 A groove 7 is provided horizontally at the top of the mounting part 21. A slider 71 is slidably disposed in the groove 7. The top of the slider 71 is fixedly connected to the bottom of the mounting block 22. The groove 7 is a T-shaped groove. The slider 71 is a T-shaped block adapted to the groove 7. A sliding layer is provided on the side wall of the slider 71. The sliding layer is used to slide and connect with the inner wall of the groove 7.
[0046] Reference Figure 4 A guide block 8 is fixedly installed on the top of the fixing part 2. A guide groove 81 is provided on the guide block 8. Both ends of the guide groove 81 are provided through. The guide groove 81 is used for the wire 91 to pass through. The guide groove 81 is T-shaped.
[0047] As one embodiment of this application, the fixing part 2 and the mounting part 21 are detachably connected to the glove body 1 by a snap fastener. In actual use, the fixing part 2 and the mounting part 21 can be removed from the glove body 1. At the same time, the back of the hand part of the glove body 1 is set to be transparent or open, so that the blood vessels and skin condition of the patient's back of the hand can be easily observed in time, thereby improving the protection effect on the patient.
[0048] As one possible implementation of this application, a strap can be provided on the wrist of the glove body 1. In actual use, the glove body is put on the patient's hand, and then the patient's hand can be bound to the hospital bed by the strap, which can play a certain binding and fixing effect on the patient's hand.
[0049] In addition, as another possible implementation of this application, a cover is provided on the back of the fingers of the glove body 1. The cover is connected to the glove body by a snap fastener. One end of the cover is fixedly connected to the glove body. In actual use, the pulse oximeter's wire is placed between the cover and the glove body, and then the cover is connected to the glove body by a snap fastener, thereby fixing the pulse oximeter's wire. At the same time, in actual use, considering various situations, the pulse oximeter needs to be worn on different fingertips of the patient to avoid pressure sores caused by wearing it on the same fingertips for a long time. Therefore, the cover is provided on all five fingers of the glove body 1.
[0050] As one possible implementation of this application, the material of the glove body 1 can be cotton, which is relatively thick; as another possible implementation of this application, the material of the glove body 1 can be leather, which is relatively thin.
[0051] In actual use, when the patient is agitated, a thicker cotton glove (body 1) is placed on the patient's hands. At this time, because the glove body 1 is thicker, the patient's hand movements are restricted, which can further reduce the range of motion of the patient's hand movements and improve the protection of the patient's hand. When the patient is calmer, a thinner leather glove (body 1) is placed on the patient's hands. At this time, because the glove body 1 is thinner, the patient's hand can have more complex and greater range of motion, which can facilitate the patient's hand movements and promote further recovery.
[0052] The implementation principle of the medical protective restraint glove proposed in this application embodiment is as follows:
[0053] In actual use, the glove body 1 is put on the patient's hand, and the patient's fingertips are passed through the perforations 11. The pulse oximeter 9 body can then be clamped on the patient's fingertips. The pulse oximeter 9's lead wire 91 passes through the mounting groove 23 on the mounting block 22. Then, the position of the lead wire 91 in the mounting groove 23 is limited by the limiting member 3. After completing the above operations, the grip ball 12 is installed in the palm of the glove body 1 to facilitate the patient's grip. In subsequent patient use, the grip ball 12 allows the patient to hold the glove and makes it easier to monitor the patient's blood oxygen in real time. This effectively simplifies the operation process for nursing staff and reduces their workload.
[0054] The above are merely preferred embodiments of this application and are not intended to limit this application. Various modifications and variations can be made to this application by those skilled in the art. Any modifications, equivalent substitutions, improvements, etc., made within the spirit and principles of this application should be included within the protection scope of this application.
Claims
1. A medical protective restraint glove, characterized in that: The glove body (1) includes a glove body (1) with a finger hole (11) for the finger to pass through. A grip ball (12) is provided in the palm of the glove body (1). The grip ball (12) is detachably connected to the glove body (1). A fixing part (2) is fixedly provided on the back of the glove body (1). An installation part (21) is rotatably provided on the side of the fixing part (2) near the finger. An installation block (22) is provided on the installation part (21). An installation groove (23) is provided on the top of the installation block (22). The installation groove (23) is provided through both sides. The installation groove (23) is used for the wire (91) of the pulse oximeter (9) to pass through. A limiting member (3) is provided on the installation block (22). The limiting member (3) is used to limit the position of the wire (91) in the installation groove (23).
2. The medical protective restraint glove according to claim 1, characterized in that: The limiting member (3) is set as a limiting block. A groove (24) is provided on the inner wall of the mounting groove (23) near the fingertip. There are two grooves (24), which are symmetrically distributed on the inner walls of both sides of the mounting groove (23). A limiting member (3) is provided in each groove (24). One end of the limiting member (3) is rotatably set in the groove (24). The side of the limiting member (3) away from the groove (24) is used to abut against the wire (91). An elastic member (25) is provided in the groove (24). The elastic member (25) is used to drive the limiting member (3) to deflect towards each other.
3. The medical protective restraint glove according to claim 2, characterized in that: A receiving groove (4) is provided at one end of the limiting member (3) away from the groove (24), and a roller (41) is rotatably provided in the receiving groove (4). The roller (41) is used for the rolling contact of the wire (91).
4. A medical protective restraint glove according to claim 3, characterized in that: The limiting block includes a connecting part (31) and a limiting part (32). An installation shaft (33) is rotatably arranged in the groove (24). One end of the connecting part (31) is fixedly connected to the installation shaft (33). The limiting part (32) is fixedly arranged at the end of the connecting part (31) away from the installation shaft (33). The connecting part (31) and the limiting part (32) are arranged in an inclined and staggered manner.
5. A medical protective restraint glove according to claim 4, characterized in that: A mounting hole (34) is provided on the connecting part (31). The mounting shaft (33) passes through the mounting hole (34) and is fixedly connected to the connecting part (31). A notch (35) is provided on the connecting part (31). The elastic element (25) is set as a torsion spring. The elastic element (25) is sleeved on the end of the mounting shaft (33). One end of the elastic element (25) is fixedly connected to the inner wall of the notch (35), and the other end is fixedly connected to the inner wall of the groove (24).
6. A medical protective restraint glove according to claim 4, characterized in that: An abutment block (5) is slidably disposed in the groove (24) along the horizontal direction. The abutment block (5) is used to abut against the side wall of the connecting part (31). A driving member (6) is disposed on the mounting block (22). The driving member (6) is used to drive the abutment block (5) to move in the groove (24).
7. A medical protective restraint glove according to claim 6, characterized in that: The driving component (6) is configured as a driving block. A connecting hole (61) is provided inside the mounting block (22). A connecting rod (62) is slidably disposed in the connecting hole (61). A strip hole (63) is provided on the bottom wall of the groove (24). The strip hole (63) is connected to the connecting hole (61). A strip block (64) is slidably disposed in the strip hole (63). The top of the strip block (64) is fixedly connected to the bottom of the abutment block (5). The bottom of the strip block (64) is fixedly connected to the connecting rod (62). The end of the connecting rod (62) away from the abutment block (5) extends out of the connecting hole (61). The driving block is fixedly disposed at the end of the connecting rod (62) away from the abutment block (5).
8. A medical protective restraint glove according to claim 7, characterized in that: A connecting plate (65) is fixedly installed on the side wall of the drive block. The connecting plate (65) connects the two drive blocks. An anti-slip pad (66) is provided on the side wall of the connecting plate (65) away from the connecting rod (62). Anti-slip texture (67) is provided on the anti-slip pad (66).
9. A medical protective restraint glove according to claim 1, characterized in that: A groove (7) is provided horizontally at the top of the mounting part (21). A slider (71) is slidably disposed in the groove (7). The top of the slider (71) is fixedly connected to the bottom of the mounting block (22). The groove (7) is a T-shaped groove. The slider (71) is a T-shaped block adapted to the groove (7). A sliding layer is provided on the side wall of the slider (71). The sliding layer is used to slide and connect with the inner wall of the groove (7).
10. A medical protective restraint glove according to any one of claims 1-9, characterized in that: A guide block (8) is fixedly installed on the top of the fixing part (2). A guide groove (81) is provided on the guide block (8). Both ends of the guide groove (81) are provided through. The guide groove (81) is used for the wire (91) to pass through. The guide groove (81) is a T-shaped groove.