This application claims priority to Taiwanese Invention patent application Ser. No. 11/212,4348, filed on Jun. 29, 2023.
The disclosure relates to an actuator, and more particularly to a magnetic actuator and a rehabilitation device having the magnetic actuator.
Nowadays, a conventional rehabilitation machine for wrist rehabilitation generally includes a driving system and an actuator that have high stiffness. Therefore, it may be difficult for a physical therapist to fit a patient's injured arm into the conventional rehabilitation machine because degrees of joint stiffness and position of wrist vary from patients to patients. In addition, during rehabilitation, if the patient suddenly feels pain and then resists movements of the conventional rehabilitation machine, the conventional rehabilitation machine may not be able to stop generating torque exerted on the patient because the actuator is not elastic/soft enough.
Furthermore, the movements of the conventional rehabilitation machine include continuous passive motion (CPM) and active-resisted movement (ARM). The continuous passive motion is a therapy in which the patient is urged by the conventional rehabilitation machine to move repetitively so as to relieve joint stiffness and to regain muscle tension, and is a therapy that is commonly used in an early stage of the rehabilitation (i.e., a therapy for patients with a high degree of joint stiffness). The active-resisted movement is a therapy that helps the patients whose joint mobility has started to recover by providing the patients with weight training exercises so that the patients' muscles may grow, their activities of daily living (ADL) may restart, and the same injury may be prevented. All in all, these therapies require the conventional rehabilitation machine to generate and exert forces on the patients. However, size of the conventional rehabilitation machine may be too large when it includes an apparatus used for adjusting the exerted forces during the active-resisted movement.
Therefore, an object of the disclosure is to provide a magnetic actuator that can alleviate at least one of the drawbacks of the prior art.
According to the disclosure, the magnetic actuator includes a base seat, a motor, a rotating unit, and a magnetic coupling unit. The motor is disposed on the base seat. The rotating unit includes a rotating shaft that is rotatably disposed on the base seat, a rotating member that is sleeved on the rotating shaft, and an angle position sensor that is sleeved on the rotating shaft. The magnetic coupling unit is connected to the motor and is drivable by the motor to rotate. The magnetic coupling unit includes two magnetic coupling subunits that are respectively connected to the motor and the rotating shaft. Each of the magnetic coupling subunits includes a magnetic ring that has a plurality of N pole portions and a plurality of S pole portions which are alternately arranged about a center of the magnetic ring. The N pole portions of the magnetic ring of one of the magnetic coupling subunits respectively correspond in position to the S pole portions of the magnetic ring of the other one of the magnetic coupling subunits. When one of the magnetic coupling subunits that is connected to the motor is driven by the motor to rotate, the other one of the magnetic coupling subunits that is connected to the rotating shaft is urged to rotate by attraction between the magnetic rings of the magnetic coupling subunits such that the rotating shaft and the rotating member rotate.
Another object of the disclosure is to provide a rehabilitation device that can alleviate at least one of the drawbacks of the prior art.
According to an aspect of the disclosure, the rehabilitation device is adapted for wrist rehabilitation, and includes two of the magnetic actuators as mentioned above, a movable frame unit, and two pairs of cables. The movable frame unit includes two standing plates, a first movable frame, and a second movable frame. The standing plates are spaced apart from each other in a first direction. The first movable frame is rotatably mounted to the standing plates, and is rotatable relative to the standing plates about a first axis extending in the first direction. The second movable frame is rotatably mounted to the first movable frame, and is rotatable relative to the first movable frame about a second axis of the first movable frame orthogonal to the first axis. The first movable frame includes a first frame body, and a first rotation member that is fixedly mounted to the first frame body and that is rotatably mounted to one of the standing plates. The second movable frame includes a second frame body, and a second rotation member that is fixedly mounted to the second frame body, that is rotatably mounted to the first frame body, and that is located below the first frame body. One of the pairs of the cables interconnects the first rotation member and one of the magnetic actuators so that the first movable frame is drivable by the one of the magnetic actuators to rotate. The other one of the pairs of the cables interconnects the second rotation member and the other one of the magnetic actuators so that the second movable frame is drivable by the other one of the magnetic actuators to rotate.
According to another aspect of the disclosure, the rehabilitation device is adapted for finger rehabilitation, and includes the magnetic actuator as mentioned above, a base frame unit, a linkage unit, a joint actuation unit, and two cables. The base frame unit includes a lower abutting plate, two side standing plates that are disposed on the lower abutting plate and that are spaced apart from each other, a sliding block that is movably disposed between the side standing plates and that has two opposite ends, and a first pushing member that is movably disposed on the lower abutting plate. The linkage unit interconnects the sliding block and the first pushing member, and is movable relative to the base frame unit. The joint actuation unit is adapted for a finger of a patient to abut against. The joint actuation unit interconnects the first pushing member and the linkage unit. The joint actuation unit is adapted to urge the finger of the patient to bend when being pushed by the first pushing member and the linkage unit. One of the cables interconnects the magnetic actuator and one of the ends of the sliding block. The other one of the cables interconnects the magnetic actuator and the other one of the ends of the sliding block. The magnetic actuator is operable to urge the sliding block to move so that the sliding block urges the linkage unit and the first pushing member to move. The joint actuation unit is adapted to urge the finger of the patient to bend when the linkage unit and the first pushing member are urged by the sliding block to move, to push the joint actuation unit, and to urge the joint actuation unit to bend.
Other features and advantages of the disclosure will become apparent in the following detailed description of the embodiment(s) with reference to the accompanying drawings. It is noted that various features may not be drawn to scale.
Before the disclosure is described in greater detail, it should be noted that where considered appropriate, reference numerals or terminal portions of reference numerals have been repeated among the figures to indicate corresponding or analogous elements, which may optionally have similar characteristics.
It should be noted herein that for clarity of description, spatially relative terms such as “top,” “bottom,” “upper,” “lower,” “on,” “above,” “over,” “downwardly,” “upwardly” and the like may be used throughout the disclosure while making reference to the features as illustrated in the drawings. The features may be oriented differently (e.g., rotated 90 degrees or at other orientations) and the spatially relative terms used herein may be interpreted accordingly.
Referring to
Each of the magnetic actuator 10 includes a base seat 1, a motor 2, a rotating unit 3, and a magnetic coupling unit 4. The base seat 1 includes a main plate 11, a first bearing plate 12, a second bearing plate 13, a third bearing plate 14, and a mounting plate 15. The first bearing plate 12 is disposed on the main plate 11. The second bearing plate 13 is disposed on the main plate 11 and is spaced apart from the first bearing plate 12. The third bearing plate 14 is disposed on the main plate 11 and is spaced apart from the second bearing plate 13. The mounting plate 15 is disposed on the main plate 11, and is located between the second bearing plate 13 and the third bearing plate 14. The motor 2 includes a motor main body 21 that is disposed on the first bearing plate 12 of the base seat 1, and a motor output shaft 22 that is connected to the motor main body 21, that extends through the first bearing plate 12, and that is connected to the magnetic coupling unit 4.
For each of the magnetic actuators 10, the rotating unit 3 includes a rotating shaft 31 that is rotatably disposed on the base seat 1, a rotating member 32 that is sleeved on the rotating shaft 31, and an angle position sensor 33 that is sleeved on the rotating shaft 31. The rotating shaft 31 is elongated in a longitudinal direction (D1), extends through the second bearing plate 13 and the mounting plate 15, and is inserted into the third bearing plate 14. It is noted that, in one embodiment, the rotating shaft 31 may extend through the third bearing plate 14. The angle position sensor 33 is disposed on the mounting plate 15. The rotating member 32 has two grooves 321 that are formed in an outer circumferential surface thereof. The cables (W) in each pair wind around the grooves 321 of the rotating member 32 of a respective one of the magnetic actuators 10.
For each of the magnetic actuators 10, the magnetic coupling unit 4 is connected to the motor 2 and is drivable by the motor 2 to rotate. The magnetic coupling unit 4 includes two magnetic coupling subunits 41 that are respectively connected to the motor 2 and the rotating shaft 31. The magnetic coupling subunits 41 are located between the first bearing plate 12 and the second bearing plate 13. Each of the magnetic coupling subunits 41 includes a magnetic ring 411, an outer housing 412 that covers the magnetic ring 411, and an interconnecting member 413 that is connected to the outer housing 412. For each of the magnetic actuators 10, the interconnecting member 413 of the one of the magnetic coupling subunits 41 that is connected to the motor 2 interconnects the outer housing 412 of the one of the magnetic coupling subunits 41 and the motor 2, and the interconnecting member 413 of the other one of the magnetic coupling subunits 41 that is connected to the rotating shaft 31 interconnects the outer housing 412 of the other one of the magnetic coupling subunits 41 and the rotating shaft 31. For each of the magnetic actuators 10, the magnetic rings 411 are spaced apart from each other in the longitudinal direction (D1), and each of the magnetic ring 411 has a plurality of N pole portions 411a and a plurality of S pole portions 411b that are alternately arranged about a center of the magnetic ring 411. For each of the magnetic actuators 10, the N pole portions 411a of the magnetic ring 411 of one of the magnetic coupling subunits 41 respectively correspond in position to the S pole portions 411b of the magnetic ring 411 of the other one of the magnetic coupling subunits 41 (not shown). For each of the magnetic actuators 10, when the one of the magnetic coupling subunits 41 that is connected to the motor 2 is driven by the motor 2 to rotate, the other one of the magnetic coupling subunits 41 that is connected to the rotating shaft 31 is urged to rotate by magnetic attraction between the magnetic rings 411 of the magnetic coupling subunits 41 such that the rotating shaft 31 and the rotating member 32 rotate.
Referring further to
Referring to
The second movable frame 54 includes a second frame body 541, and a second rotation member 542 that is fixedly mounted to the second frame body 541, that is rotatably mounted to the first frame body 531, and that is located below the lower plate 531a of the first frame body 531. The second frame body 541 includes two movable plates 541a, two wing plates 541b, two pivot shafts 541c, two slide rails 541d, two slide blocks 541e, and a handle 541f. The movable plates 541a are respectively connected to the lower plate 531a and the upper plate 531c of the first frame body 531. The wing plates 541b are respectively connected to the movable plates 541a. The slide rails 541d are respectively disposed on the movable plates 541a. The slide blocks 541e are respectively and movably disposed on the slide rails 541d. The handle 541f is fixedly mounted to the slide blocks 541e. One of the pivot shafts 541c extends through the second rotation member 542, the lower plate 531a, the respective one of the movable plates 541a that is connected to the lower plate 531a, and the respective one of the wing plates 541b that is connected to the respective one of the movable plates 541a which is connected to the lower plate 531a, and is connected to the second rotation member 542. The other one of the pivot shafts 541c extends through the upper plate 531c, the respective one of the movable plates 541a that is connected to the upper plate 531c, and the respective one of the wing plates 541b that is connected to the respective one of the movable plates 541a which is connected to the upper plate 531c. The pivot shafts 541c cooperatively define the second axis (Y1). The handle 541f is adapted to be gripped by the patient. By virtue of the slide blocks 541e being respectively and movably disposed on the slide rails 541d, and by virtue of the handle 541f being fixedly mounted to the slide blocks 541e, the patient may adjust a distance between the handle 541f and the supporting frame 55, according to a length of the patient's arm, via movements of the slide blocks 541e relative to the slide rails 541d. The second rotation member 542 has two grooves 542a that are formed in an outer circumferential surface thereof. The cables (W) in the other one of the pairs wind around the grooves 542a of the second rotation member 542.
The tension regulator 6 is disposed on the base plate 51.
The one of the pairs of the cables (W) interconnects the first rotation member 532 and one of the magnetic actuators 10 so that the first movable frame 53 is drivable by the one of the magnetic actuators 10 to rotate. The other one of the pair of the cables (W) interconnects the second rotation member 542 and the other one of the magnetic actuators 10 so that the second movable frame 54 is drivable by the other one of the magnetic actuators 10 to rotate. Each of the cables (W) in each of the pairs extends through the tension regulator 6 so that the tension regulator 6 is operable to adjust tension of each of the cables (W). When the patient grips the handle 541f and when the first movable frame 53 rotates relative to the standing plates 52, the wrist of the patient is urged to move toward an ulnar side of the wrist (i.e., ulnar deviation) or a radial side of the wrist (i.e., radial deviation) for wrist rehabilitation. In this embodiment, when the patient grips the handle 541f in a common manner, the wrist of the patient is urged to move upwardly when being urged to move toward the radial side, and is urged to move downwardly when being urged to move toward the ulnar side. When the patient grips the handle 541f with his/her left hand and when the second movable frame 54 rotates relative to the first movable frame 53, the wrist of the patient is urged to move toward a right side of the patient (i.e., extension of the wrist) or a left side of the patient (i.e., flexion of the wrist) for wrist rehabilitation.
By virtue of the rehabilitation device 100 transmitting torque from the motor 2 to the rotating shaft 31 via the magnetic coupling unit 4 of each of the magnetic actuators 10, and by virtue of the magnetic rings 411 of each of the magnetic coupling subunits 41 being spaced apart from each other, the magnetic actuators 10 may serve as elastic/soft actuators for the rehabilitation device 100, and elasticity of each of the magnetic actuators 10 may be easily adjusted by adjusting a distance between the magnetic rings 411 of the magnetic actuator 10. In addition, each of the magnetic actuators 10 may have a particular limit for its output no matter how great an input from the motor 2 thereof is. Therefore, a force that is generated by the rehabilitation device 100 and that is exerted on the patient may be limited without using an electric control device or a torque limiter so the patient is protected. Even when the magnetic rings 411 of each of the magnetic actuators 10 are misaligned, the angle position sensor 33 of the magnetic actuator 10 may detect misalignment between the magnetic rings 411 and compensate the misalignment. Thus, the rehabilitation device 100 may not stop operating because of overload protection when the magnetic rings 411 of any one of the magnetic actuators 10 are repeatedly misaligned so that there may be no need to reset the rehabilitation device 100, thereby preventing malfunction of the rehabilitation device 100 and preventing the patient from injuries. Moreover, a torque for the misalignment between the magnetic rings 411 of each of the magnetic actuators 10 may be easily adjusted by adjusting the distance between the magnetic rings 411 of the magnetic actuator 10 as well.
Generally, a conventional rehabilitation device that is common on the market is either for a therapy that involves continuous passive motion (CPM) in which the patient is urged by the conventional rehabilitation machine to move repetitively, or a therapy that involves active-resisted movement (ARM) and that helps the patient by providing weight training exercises. However, by virtue of each of the magnetic actuators 10 having adjustable elasticity, the rehabilitation device 100 may be operable to provide both of the therapies, which makes the rehabilitation device 100 multifunctional.
With predetermined magnetic parameters of each of the magnetic rings 411, the angle position sensor 33 of each of the magnetic actuators 10 may detect a load on each of the magnetic rings 411 of the magnetic actuator 10 according to the misalignment between the magnetic rings 411 of the magnetic actuator 10. Therefore, the angle position sensor 33 of each of the magnetic actuators 10 may serve as a force detector. Muscle tone of the patient may thus be detected and quantified so that the muscle tone may be evaluated when values thereof is analyzed.
Moreover, for each of the magnetic actuators 10, because the torque is transmitted from the motor 2 to the rotating shaft 31 by the attraction between the magnetic rings 411 that are spaced apart from each other, and because the magnetic parameters of each of the magnetic rings 411 may be predetermined, the magnetic rings 411 of the magnetic coupling subunits 41 may be adjusted to be misaligned when the torque that is transmitted from the motor 2 to the magnetic coupling subunit 41 connected to the motor 2 is greater than a predetermined limit torque that the magnetic coupling subunit 41 connected to the rotating shaft 31 may transmit. That is to say, each of the magnetic actuators 10 may have the particular limit for its output. Therefore, even when someone operates the rehabilitation device 100 in a wrong way, or when the rehabilitation device 100 accidentally malfunctions, the patient may still be protected from injuries. Such protection mechanism involving magnetic attraction may react faster and may be more trustworthy than a protection mechanism involving a system control software, an electric control device, or a force detector.
Referring to
The base frame unit 7 includes a lower abutting plate 71, two side standing plates 72, a sliding block 73, a first pushing member 74, a front roller 75, and two rear rollers 76. The side standing plates 72 are disposed on the lower abutting plate 71 and are spaced apart from each other. The sliding block 73 is movably disposed between the side standing plates 72, and has two opposite ends. The first pushing member 74 is movably disposed on the lower abutting plate 71, and is connected to the joint actuation unit 9. The front roller 75 is disposed between the side standing plates 72. The rear rollers 76 are disposed between the side standing plates 72, and are opposite to the front roller 75. The lower abutting plate 71 has a curved protrusion 711 that is formed on an upper surface thereof. Each of the side standing plates 72 has a first slide slot 722 that is curved, a second slide slot 723 that is curved and that is located above the first slide slot 722, and a third slide slot 721 that is elongated in a plate direction (P1). The second slide slot 723 of each of the side standing plates 72 is located between the first slide slot 722 and the third slide slot 721 of the side standing plate 72. The third slide slot 721 of each of the side standing plates 72 has a first end 721a that is adjacent to the rear rollers 76, and a second end 721b that is opposite to the first end 721a in the plate direction (P1). A length of the second slide slot 723 of each of the side standing plates 72 is greater than a length of the first slide slot 722 of the side standing plate 72. The first slide slot 722 of each of the side standing plates 72 has a first end 722a that is adjacent to the rear rollers 76, and a second end 722b that is opposite to the first end 722a in the plate direction (P1). The second slide slot 723 of each of the side standing plates 72 has a first end 723a that is adjacent to the rear rollers 76, and a second end 723b that is opposite to the first end 723a in the plate direction (P1).
The sliding block 73 includes a block body portion 731 that is substantially cuboid and that has the ends of the sliding block 73, an insertion portion 732 that extends downwardly from the body portion 731, and four protrusions 733 (only two of the protrusions 733 are visible due to the viewing angle) that are formed at two opposite sides of the block body portion 731 and that extend into the slide slots 721 of the side standing plates 72. Specifically, two of the protrusions 733 extend into one of the slide slots 721, and the remaining two of the protrusions 733 extend into the other one of the slide slots 721. The insertion portion 732 has a through hole 732a. The first pushing member 74 has a curved segment 741 that is coupled to the protrusion 711 of the lower abutting plate 71, a connecting segment 742 that extends from the curved segment 741 and that is connected to the joint actuation unit 9, and a through hole 743 that extends through one end of the curved segment 741 opposite to the connecting segment 742. Each of the side standing plates 72 has two opposite ends that are respectively proximate to and distal from the joint actuation unit 9. The front roller 75 is located between the ends of the side standing plates 72 proximate to the joint actuation unit 9. The rear rollers 76 are located between the ends of the side standing plates 72 distal from the joint actuation unit 9, and are spaced apart from each other in an up-down direction (U1) orthogonal to the plate direction (P1). One of the cables (W) is fixedly mounted to one of the ends of the block body portion 731 of the sliding block 73, abuts against the upper one of the rear rollers 76, and interconnects the magnetic actuator 10 and the one of the ends of the block body portion 731. The other one of the cables (W) is fixedly mounted to the other one of the ends of the block body portion 731, extends around the front roller 75, abuts against the lower one of the rear rollers 76, and interconnects the magnetic actuator 10 and the other one of the ends of the sliding block 73. The cables (W) are operable to pull the sliding block 73 in opposite directions so that the sliding block 73 is movable along the third slide slot 721 in the plate direction (P1).
The linkage unit 8 interconnects the sliding block 73 and the first pushing member 74, and is movable relative to the base frame unit 7. The linkage unit 8 includes two slot-interconnecting links 81, two first links 82, a first slide rod 83, a second slide rod 84, two second links 85, two third links 86, two fourth links 87, and a second pushing member 88. Each of the first links 82 is rotatably connected to an end of a respective one of the slot-interconnecting links 81. The first slide rod 83 extends through the first slide slots 722 of the side standing plates 72 and the through hole 743 of the first pushing member 74, interconnects the slot-interconnecting rods 81, and is movable along the first slide slots 722. The second slide rod 84 extends through the second slide slots 723 of the side standing plates 72 and the through hole 732a of the sliding block 73, interconnects the slot-interconnecting links 81, and is movable along the second slide slots 723. Each of the second links 85 is rotatably connected to an end of a respective one of the first links 82. Each of the third links 86 is rotatably connected to an end of a respective one of the second links 85. Each of the fourth links 87 is rotatably connected to an end of a respective one of the third links 86. The second pushing member 88 is rotatably connected to an end of each of the fourth links 87. Each of the slot-interconnecting links 81 has a first pivot portion 811 that is rotatably connected to the first slide rod 83, a second pivot portion 812 that is rotatably connected to the second slide rod 84, and a third pivot portion 813 that is rotatably connected to the respective one of the first links 82. Each of the second links 85 has an upper connecting portion 851 that is rotatably connected to the respective one of the third links 86, a middle connecting portion 852 that is rotatably connected to the respective one of the first links 82, and a lower connecting portion 853. Each of the fourth links 87 is bent, and has a first linkage portion 871, a vertex portion 872 that is rotatably connected to the respective one of the third linkage rods 86, and a second linkage portion 873 that is rotatably connected to the second pushing member 88. Each of the fourth links 87 is bent at the vertex portion 872 thereof.
The joint actuation unit 9 is adapted for the finger of the patient to abut against. The joint actuation unit 9 interconnects the first pushing member 74 and the linkage unit 8. The joint actuation unit 9 is adapted to urge the finger of the patient to bend when being pushed by the pushing member 74 and the linkage unit 8. The joint actuation unit 9 includes a first actuation member 91, a second actuation member 92, a third actuation member 93, and a rotation seat 94. The first actuation member 91 is fixedly mounted to the first pushing member 74, and is rotatably connected to the first linkage portion 871 of each of the fourth links 87. The second actuation member 92 is rotatably mounted to the first actuation member 91. The third actuation member 93 is rotatably mounted to the second actuation member 92, and is fixedly mounted to the second pushing member 88. The rotation seat 94 is disposed on the first actuation member 91, is adjacent to the first pushing member 74, and has two opposite sides. The lower connecting portions 853 of the second links 85 are respectively and rotatably connected to the opposite sides of the rotation seat 94. For each of the second links 85, the upper connecting portion 851 is located at the end thereof opposite to the rotation seat 94 (i.e., each of the third links 86 is rotatably connected to the end of the respective one of the second links 85 opposite to the rotation seat 94). When the finger of the patient abuts against the joint actuation unit 9, the first, second, and third actuation members 91, 92, 93 respectively correspond in position to a proximal phalanx, a middle phalanx, and a distal phalanx of the finger. In addition, a junction between the first actuation member 91 and the first pushing member 74 substantially corresponds in position to a metacarpophalangeal joint of the finger, a junction between the second actuation member 92 and the first actuation member 91 substantially corresponds in position to a proximal interphalangeal joint of the finger, and a junction between the third actuation member 93 and the second actuation member 92 substantially corresponds in position to a distal interphalangeal joint of the finger.
Referring to
In summary, by virtue of the magnetic actuator 10 transmitting the torque by the attraction between the magnetic rings 411 of the magnetic coupling subunits 41, and by virtue of the angle position sensor 33 detecting the load on each of the magnetic rings 411 according to the misalignment between the magnetic rings 411, the output of the magnetic actuator 10 may be adjusted when a rotational speed of the motor 2 is adjusted, and may be set to a predetermined value when the motor 2 is kept rotating at a specific speed. In addition, by adjusting the distance between the magnetic rings 411 of the magnetic actuator 10, by adjusting a distance among the magnetic pole portions in each of the magnetic rings 411, or by adjusting effective magnetic field between the magnetic rings 411, the attraction between the magnetic rings 411 may be adjusted so that the elasticity of the magnetic actuator 10 is adjusted, and that the output limit of the magnetic actuator 10 for the protection mechanism is also adjusted. That is to say, the force generated by the magnetic actuator 10 and exerted on the patient may be adjusted easily and swiftly, and therefore the purpose of the disclosure is achieved.
In the description above, for the purposes of explanation, numerous specific details have been set forth in order to provide a thorough understanding of the embodiment(s). It will be apparent, however, to one skilled in the art, that one or more other embodiments may be practiced without some of these specific details. It should also be appreciated that reference throughout this specification to “one embodiment,” “an embodiment,” an embodiment with an indication of an ordinal number and so forth means that a particular feature, structure, or characteristic may be included in the practice of the disclosure. It should be further appreciated that in the description, various features are sometimes grouped together in a single embodiment, figure, or description thereof for the purpose of streamlining the disclosure and aiding in the understanding of various inventive aspects; such does not mean that every one of these features needs to be practiced with the presence of all the other features. In other words, in any described embodiment, when implementation of one or more features or specific details does not affect implementation of another one or more features or specific details, said one or more features may be singled out and practiced alone without said another one or more features or specific details. It should be further noted that one or more features or specific details from one embodiment may be practiced together with one or more features or specific details from another embodiment, where appropriate, in the practice of the disclosure.
While the disclosure has been described in connection with what is (are) considered the exemplary embodiment(s), it is understood that this disclosure is not limited to the disclosed embodiment(s) but is intended to cover various arrangements included within the spirit and scope of the broadest interpretation so as to encompass all such modifications and equivalent arrangements.
Number | Date | Country | Kind |
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112124348 | Jun 2023 | TW | national |