Genital examination sampler

By designing the forceps, auxiliary components and self-locking components of the genital examination sampler, the problem of tissue adhesion damage caused by insufficient angle or force in the cervical biopsy is solved, and safe and efficient cutting of living tissue is achieved.

CN120345932APending Publication Date: 2025-07-22贵州航天医院
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Patent Information

Application Number
CN202510468177.2
Authority / Receiving Office
CN · China
Patent Type
Applications(China)
Current Assignee / Owner
Filing Date
2025-04-15
Publication Date
2025-07-22

AI Technical Summary

Technical Problem

During the cervical biopsy, the sampling forceps fail to cut and separate after picking up the tissue due to improper operating angle or insufficient closing force, which may cause tissue adhesion, traction damage, local bleeding and mucosal tear.

Method used

A genital examination sampler is designed, including a clamping component, an auxiliary component, a self-locking component and a support component. The clamping component increases the closing force, assists the cutting, and the self-locking component records and locks the operation, and the support component provides support and guidance to prevent tissue adhesion damage.

Benefits of technology

It effectively prevents pulling damage caused by tissue adhesion, ensures safe cutting of living tissue, timely identifying the problem of sampling clamp instruments, and improves the safety and accuracy of operation.

✦ Generated by Eureka AI based on patent content.

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Abstract

The invention relates to the technical field of medical instruments, and particularly discloses a genital examination sampler which comprises a fixed handle and further comprises a clamping assembly arranged on the inner side of the fixed handle and used for clamping living tissue; the auxiliary assembly is arranged on one side of the clamping assembly, and when the clamping assembly fails to cut the living tissue, the auxiliary assembly assists the clamping assembly in cutting the living tissue. According to the cervical biopsy forceps, the movable handle is held to rotate close to the fixed handle, the upper forceps head is driven to rotate close to the lower forceps head through the clamping assembly, cervical biopsy is cut through the upper forceps head and the lower forceps head, and when the biopsy is not cut and separated by the upper forceps head and the lower forceps head through the clamping assembly, the cervical biopsy is cut and separated through the auxiliary assembly. By means of the auxiliary device, the clamping assembly can be assisted to cut the living tissue, the closing force between the upper clamp head and the lower clamp head is automatically increased, the living tissue is cut and separated, and traction damage caused by tissue adhesion is prevented.
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Description

Technical Field

[0001] The present invention relates to the technical field of medical devices, and specifically relates to a genital examination sampler. Background Technique

[0002] Gynecology is a diagnostic and treatment subject in medical institutions, which is a professional department for diagnosing and treating female gynecological diseases. It is divided into Western medicine gynecology and traditional Chinese medicine gynecology. Gynecological diseases include diseases of the female reproductive system, including vulvar diseases, genital diseases, uterine diseases, fallopian tube diseases, ovarian diseases, etc. The female reproductive system mainly includes the genital organs, the uterus, and the ovaries. Among them, the genital organs and the uterus are very susceptible to diseases. For example, in the examination and treatment of the cervix, the sampling and examination of cervical biopsy specimens play an important role. Therefore, in cervical biopsy, sampling forceps are usually used to take biopsy specimens.

[0003] In cervical biopsy, usually the vagina is first dilated with a speculum to facilitate the doctor to observe the vaginal wall and the cervical morphology. Then the doctor holds the sampling forceps and inserts them into the vagina. The sampling forceps are used to cut and take the biopsy specimen, and then the sampling forceps are taken outwards to complete the sampling of the cervical biopsy specimen. However, during this process, due to improper operation angle or insufficient closing force of the sampling forceps, the sampling forceps may not be able to cut and separate the tissue after clamping the tissue. When taking out the sampling forceps outwards, it may cause traction injury due to tissue adhesion, resulting in local bleeding, mucosal tearing or increased pain of the patient, and may aggravate cervical injury. For this reason, we propose a genital examination sampler. Summary of the Invention

[0004] The purpose of the present invention is to provide a genital examination sampler to solve the problem that during cervical biopsy, due to improper operation angle or insufficient closing force of the sampling forceps, the sampling forceps may not be able to cut and separate the tissue after clamping the tissue, and when taking out the sampling forceps outwards, it may cause traction injury due to tissue adhesion as mentioned in the above background technique.

[0005] To achieve the above purpose, the present invention provides the following technical solution: A genital examination sampler, comprising: a fixed handle, an activity handle is hinged to the fixed handle, an outer tube is fixedly arranged on one side of the fixed handle, a lower clamp head is fixedly arranged on one side of the outer tube, and an upper clamp head is hinged to one side of the lower clamp head.

[0006] Further comprising: a clamping component, the clamping component is arranged inside the fixed handle, and the clamping component is used for clamping biopsy specimens.

[0007] An auxiliary component, the auxiliary component is arranged on one side of the clamping component, and when the clamping component fails to cut the biopsy specimen, the auxiliary component assists the clamping component to cut the biopsy specimen.

[0008] The self-locking component is arranged on one side of the fixed handle. When the clamping component fails to cut the living tissue multiple times, the fixed handle and the movable handle are automatically locked by the self-locking component.

[0009] The support component is arranged on the outer side of the outer tube. The support component is used for supporting and guiding the sampling forceps during use.

[0010] Among them, the clamping component includes a sleeve rod hinged to the movable handle. A push rod member is slidably arranged in the sleeve rod. Activity grooves adapted to the push rod member are symmetrically arranged on the inner side of the upper clamping head. One end of the push rod member close to the upper clamping head is movably arranged along the activity groove. A first spring fixedly arranged on the inner side of the sleeve rod is fixedly arranged on one side of the push rod member. An installation shell is fixedly arranged on the lower side of the sleeve rod. A first electromagnetic block is fixedly arranged in the installation shell. An insertion rod member adsorbed by the first electromagnetic block is slidably arranged in the installation shell. The insertion rod member movably penetrates through the lower side of the sleeve rod. A second spring fixedly arranged with the insertion rod member is fixedly arranged on the lower side of the sleeve rod. A camera module is installed on the outer tube.

[0011] Among them, the auxiliary component includes a first connecting piece fixedly arranged with the push rod member. A rotating piece is movably arranged on the lower side of the first connecting piece. A second connecting piece is movably arranged on the lower side of the rotating piece. A support column fixedly arranged with the fixed handle is rotatably arranged on the rotating piece. An adsorption block slidably arranged with the fixed handle is fixedly arranged on the lower side of the second connecting piece. A limiting groove adapted to the adsorption block is arranged on the inner side of the fixed handle. The adsorption block is slidably arranged along the limiting groove.

[0012] Among them, a second electromagnetic block is fixedly arranged on one side of the fixed handle where the adsorption block is located. After being energized, the second electromagnetic block adsorbs with the adsorption block. A pressure sensor is installed on the upper clamping head. A control board is arranged on one side of the fixed handle. A first switch is installed on one side of the control board.

[0013] Among them, the self-locking component includes a connection shell fixedly arranged with the fixed handle. A third electromagnetic block is fixedly arranged in the connection shell. A first shell adsorbed by the third electromagnetic block is slidably arranged in the connection shell. A first guide groove adapted to the first shell is arranged in the connection shell. The first shell is slidably arranged along the first guide groove. A sixth spring fixedly arranged on the inner side of the connection shell is fixedly arranged on one side of the first shell. A second shell is fixedly arranged in the connection shell. Limiting tooth blocks are slidably arranged in both the first shell and the second shell. Pull rods are fixedly arranged on the sides of the two limiting tooth blocks away from each other. Fifth springs sleeved on the pull rods are fixedly arranged on one side of the two limiting tooth blocks.

[0014] Among them, a helical tooth block slidably arranged with the connection shell is arranged between the two limiting tooth blocks. A second guide groove adapted to the helical tooth block is arranged in the connection shell. The helical tooth block is slidably arranged along the second guide groove. A fourth spring fixedly arranged on the inner side of the connection shell is fixedly arranged on one side of the helical tooth block.

[0015] Wherein, a limiting post is slidably arranged on the other side of the helical gear block, a third spring fixedly arranged with the helical gear block is fixedly arranged inside the limiting post, a through hole adapted to the limiting post is arranged through one side of the fixed handle, and a limiting hole adapted to the limiting post is arranged on one side of the movable handle.

[0016] Wherein, the support assembly includes a support block arranged on the lower side of the outer tube, a support member is movably arranged on the lower side of the support block, an installation member is fixedly arranged at the lower end of the support member, rack bars are rotatably arranged on both sides of the installation member, sliding sleeves are sleeved on the outer sides of the two rack bars, support rods are rotatably arranged on one side of the two sliding sleeves, and fixing members are fixedly arranged on one side of the two support rods away from the sliding sleeves.

[0017] Wherein, a speculum is arranged between the two fixing members, the speculum includes an upper forceps arm and a lower forceps arm, the upper forceps arm and the lower forceps arm are hinged, and the two fixing members are respectively fixedly arranged on the two outer sides of the lower forceps arm.

[0018] Wherein, a screw rod is rotatably arranged on one side of the support block, a clamping member is arranged on the upper side of the screw rod in a threaded manner, a limiting rod fixedly arranged with the support block is arranged through and slidably on one side of the clamping member, a plurality of balls are movably arranged at equal intervals between the clamping member and the inner side of the support block, fixing shells are fixedly arranged on one side of the two sliding sleeves, a fourth electromagnetic block is fixedly arranged inside the fixing shells, a second switch is arranged on one side of the installation member, a toothed block adsorbed by the fourth electromagnetic block is slidably arranged inside the fixing shells, the toothed block is matched with the rack bar, and seventh springs fixedly arranged with the fixing shells are symmetrically fixedly arranged on one side of the toothed block.

[0019] The present invention at least has the following beneficial effects:

[0020] In the present invention, by holding the movable handle and rotating it close to the fixed handle, and through the clamping component, the upper clamping head is driven to rotate close to the lower clamping head, and the cervical living tissue is cut by the upper clamping head and the lower clamping head. When the upper clamping head and the lower clamping head fail to cut and separate the living tissue through the clamping component, through the auxiliary component, the auxiliary clamping component can cut the living tissue, automatically increasing the closing force between the upper clamping head and the lower clamping head to cut and separate the living tissue, preventing traction damage caused by tissue adhesion. When the clamping component fails to cut and separate the living tissue, the self-locking component will record. When the number of times recorded by the self-locking component reaches the set number of times, the fixed handle and the movable handle will be automatically locked and fixed, so that the doctor can no longer hold the movable handle and rotate it close to the fixed handle. At this time, the doctor needs to check the sampling forceps and check whether the cutting edges of the upper clamping head and the lower clamping head are dull, and whether it is due to the improper closing of the sampling forceps itself that the living tissue cannot be cut and separated. That is, when the clamping component fails to cut the living tissue multiple times, it may not be an operation problem of the doctor using the sampling forceps due to insufficient closing force, but may be a problem of the sampling forceps itself; through the support component, it can be used in cooperation with the speculum, support and guide the sampling forceps during use, facilitate the doctor to adjust to a suitable operation angle and cutting angle when cutting the living tissue, and can maintain a suitable support position to further ensure the cutting of the living tissue. Description of the Drawings

[0021] Figure 1 is a three-dimensional structural schematic diagram of the present invention;

[0022] Figure 2 is a structural schematic diagram of a partial cross-section of the fixed handle of the present invention;

[0023] Figure 3 is a structural schematic diagram of a partial cross-section of the outer tube on the side close to the upper clamping head of the present invention;

[0024] Figure 4 is an exploded structural schematic diagram of the upper clamping head and the push rod member of the present invention;

[0025] Figure 5 is a cross-sectional structural schematic diagram of the sleeve rod and the mounting shell of the present invention;

[0026] Figure 6 is a partial structural schematic diagram of the auxiliary component of the present invention;

[0027] Figure 7 is a structural schematic diagram of another view of the connection of the fixed handle of the present invention;

[0028] Figure 8 is a cross-sectional structural schematic diagram of the fixed handle, the movable handle and the connection shell of the present invention;

[0029] Figure 9 In the present inventionFigure 8 Schematic diagram of the enlarged structure at A in the middle;

[0030] Figure 10 Schematic diagram of another perspective of the cross-section of the connection shell of the present invention;

[0031] Figure 11 Schematic diagram of the support assembly of the present invention;

[0032] Figure 12 Schematic diagram of the connection between the support assembly and the speculum of the present invention;

[0033] Figure 13 Schematic diagram of the explosion of the support block and the support member of the present invention;

[0034] Figure 14 Schematic diagram of the cross-section of the sliding sleeve and the fixed shell of the present invention.

[0035] In the figure: 11, fixed handle; 12, movable handle; 13, outer tube; 14, lower jaw head; 15, upper jaw head; 2, clamping component; 21, sleeve rod; 22, push rod member; 23, first spring; 24, camera module; 25, mounting shell; 26, first electromagnetic block; 27, inserting rod member; 28, second spring; 29, movable groove; 3, auxiliary component; 31, first connecting member; 32, rotating member; 33, support column; 34, second connecting member; 35, adsorption block; 36, second electromagnetic block; 37, limiting groove; 38, pressure sensor; 39, control board; 310, first switch; 4, self-locking component; 41, connection shell; 42, first housing; 43, helical tooth block; 44, second housing; 45, first guide groove; 46, second guide groove; 47, limiting post; 48, third spring; 49, fourth spring; 410, limiting tooth block; 411, pull rod; 412, fifth spring; 413, sixth spring; 414, third electromagnetic block; 415, through hole; 416, limiting hole; 5, support assembly; 51, support block; 52, support member; 53, mounting member; 54, toothed rod; 55, sliding sleeve; 56, support rod member; 57, fixing member; 58, seventh spring; 59, screw; 510, limiting rod; 511, clamping member; 512, ball; 513, fixed shell; 514, fourth electromagnetic block; 515, toothed block; 516, second switch; 6, speculum; 61, lower clamp arm; 62, upper clamp arm. Detailed implementation manners

[0036] Next, the technical solutions in the embodiments of the present invention will be clearly and completely described in conjunction with the accompanying drawings in the embodiments of the present invention. Obviously, the described embodiments are only a part of the embodiments of the present invention, rather than all the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those of ordinary skill in the art without creative efforts shall fall within the protection scope of the present invention.

[0037] Example 1

[0038] Please refer to Figures 1 to 14 , the present invention provides a technical solution: a genital examination sampler, comprising: a fixed handle 11, a movable handle 12 is hingedly arranged on the fixed handle 11, an outer tube 13 is fixedly arranged on one side of the fixed handle 11, a lower clamp head 14 is fixedly arranged on one side of the outer tube 13, and an upper clamp head 15 is hingedly arranged on one side of the lower clamp head 14 through a hinge shaft.

[0039] It further comprises: a clamping component 2, the clamping component 2 is arranged inside the fixed handle 11, and the clamping component 2 is used for clamping living tissue;

[0040] An auxiliary component 3, the auxiliary component 3 is arranged on one side of the clamping component 2, and when the clamping component 2 fails to cut living tissue, the auxiliary component 3 assists the clamping component 2 to cut living tissue;

[0041] A self-locking component 4, the self-locking component 4 is arranged on one side of the fixed handle 11, and when the clamping component 2 fails to cut living tissue for multiple times, the self-locking component 4 automatically locks the fixed handle 11 and the movable handle 12;

[0042] A support component 5, the support component 5 is arranged outside the outer tube 13, and the support component 5 is used for supporting and guiding the sampling forceps during use.

[0043] A reed is arranged between the fixed handle 11 and the movable handle 12. By holding the movable handle 12 and rotating it close to the fixed handle 11, and through the clamping component 2, the upper clamping head 15 is driven to rotate close to the lower clamping head 14. The upper clamping head 15 and the lower clamping head 14 are used to cut the cervical living tissue. When the upper clamping head 15 and the lower clamping head 14 fail to cut and separate the living tissue through the clamping component 2, through the auxiliary component 3, it can assist the clamping component 2 to cut the living tissue, automatically increase the closing force between the upper clamping head 15 and the lower clamping head 14, so as to cut and separate the living tissue, and prevent traction damage caused by tissue adhesion. When the clamping component 2 fails to cut and separate the living tissue, the self-locking component 4 will record. When the number of times recorded by the self-locking component 4 reaches the set number of times, it will automatically lock and fix the fixed handle 11 and the movable handle 12, so that the doctor can no longer hold the movable handle 12 and rotate it close to the fixed handle 11. At this time, the doctor needs to check the sampling forceps and check whether the cutting edges of the upper clamping head 15 and the lower clamping head 14 are blunt, and whether it is due to the improper closing of the sampling forceps itself that the living tissue cannot be cut and separated. That is, when the clamping component 2 fails to cut the living tissue multiple times, it may not be an operation problem of the doctor using the sampling forceps due to insufficient closing force, but a problem of the sampling forceps itself; through the support component 5, it can be used in cooperation with the speculum 6 to support and guide the sampling forceps during use, so that it is convenient for the doctor to adjust to the appropriate operation angle and cutting angle when cutting the living tissue, and can maintain the appropriate support position to further ensure the cutting of the living tissue.

[0044] The clamping component 2 includes a sleeve rod 21 hinged to the movable handle 12 through a hinge shaft. A push rod member 22 is slidably arranged in the sleeve rod 21. The push rod member 22 passes through the inside of the outer tube 13. Activity grooves 29 are symmetrically arranged inside the upper clamping head 15. The activity grooves 29 are adapted to one end of the push rod member 22 close to the upper clamping head 15. One end of the push rod member 22 close to the upper clamping head 15 is movably arranged along the activity grooves 29, so that when the push rod member 22 pushes the upper clamping head 15 to move, the upper clamping head 15 can be rotated downward close to or upward away from the lower clamping head 14; A first spring 23 fixedly arranged on the inner side of the sleeve rod 21 is fixedly arranged on one side of the push rod member 22. An installation shell 25 is fixedly arranged on the lower side of the sleeve rod 21. A first electromagnetic block 26 is fixedly arranged inside the installation shell 25. A plug rod member 27 adsorbed to the first electromagnetic block 26 is slidably arranged inside the installation shell 25. The plug rod member 27 movably penetrates through the lower side of the sleeve rod 21. A second spring 28 fixedly arranged with the plug rod member 27 is fixedly arranged on the lower side of the sleeve rod 21. A jack adapted to the upper side of the plug rod member 27 is arranged on the lower side of the push rod member 22. Initially, the upper end of the plug rod member 27 is inserted into the jack to limit and fix the push rod member 22 and the sleeve rod 21; A camera module 24 is installed on the outer tube 13. The camera module 24 is located on one side close to the upper clamping head 15. Through the camera module 24, the doctor can easily observe the position of the living tissue during clamping, which is convenient for cutting the living tissue.

[0045] By holding the movable handle 12 and rotating it close to the fixed handle 11, the sleeve rod 21 can be pushed to move close to the outer tube 13, and the push rod member 22 is driven to move synchronously, so as to drive the upper clamp head 15 to rotate downward close to the lower clamp head 14, and the living tissue is cut by the upper clamp head 15 and the lower clamp head 14.

[0046] The auxiliary component 3 includes a first connecting member 31 fixedly arranged with the push rod member 22. A rotating member 32 is movably arranged on the lower side of the first connecting member 31. A second connecting member 34 is movably arranged on the lower side of the rotating member 32. The rotating member 32 is provided with movable through grooves at the positions of the first connecting member 31 and the second connecting member 34. The first connecting member 31 and the second connecting member 34 are respectively movably arranged with the rotating member 32 through the movable through grooves on both sides of the rotating member 32. A support column 33 fixedly arranged with the fixed handle 11 is rotatably arranged on the rotating member 32. The support column 33 is located on the side close to the first connecting member 31. When the adsorption block 35 is adsorbed by the second electromagnetic block 36, the push rod member 22 and the upper clamp head 15 are driven, so that when cutting, the upper clamp head 15 and the lower clamp head 14 are closed more tightly, or when increasing the closing force between the upper clamp head 15 and the lower clamp head 14, through the lever principle of the rotating member 32, it is more convenient to drive the push rod member 22 and the upper clamp head 15; A second connecting member 34 is fixedly arranged with an adsorption block 35 slidably arranged with the fixed handle 11 on the lower side. A limiting groove 37 adapted to the adsorption block 35 is arranged inside the fixed handle 11. The adsorption block 35 is slidably arranged along the limiting groove 37;

[0047] A second electromagnetic block 36 is fixedly arranged on one side of the fixed handle 11 where the adsorption block 35 is located. After being energized, the second electromagnetic block 36 adsorbs the adsorption block 35. A pressure sensor 38 is installed on the upper clamp head 15. A control board 39 is arranged on one side of the fixed handle 11. Control elements are installed inside the control board 39. A first switch 310 is installed on one side of the control board 39;

[0048] When the living tissue is clamped by holding the movable handle 12 and rotating it close to the fixed handle 11, the movement of the push rod 22 will drive the movement of the first connecting member 31, first rotating the upper side of the rotating member 32 toward the outer tube 13 by a certain amplitude, so that the lower side of the rotating member 32 drives the second connecting member 34 and the adsorption block 35 to move a certain distance close to the second electromagnetic block 36. When the upper clamp head 15 and the lower clamp head 14 fail to cut and separate the living tissue through the clamping assembly 2, the living tissue will be pulled due to tissue adhesion, which will conflict with the pressure sensor 38. That is, when the pressure sensor 38 detects pressure, indicating that the living tissue cannot be cut and separated, the first electromagnetic block 26 will be controlled to be energized to produce an adsorption effect on the plug rod 27, so that the plug rod 27 moves downward out of the insertion hole on the lower side of the push rod 22, the second spring 28 stretches, and controls the second electromagnetic block 36 to be energized to produce an adsorption effect on the plug rod 27. The adsorption effect of the attachment block 35 causes the adsorption block 35 and the second connecting member 34 to move close to the second electromagnetic block 36, and through the rotating member 32, the first connecting member 31 and the push rod member 22 are pushed close to the upper clamp head 15, and the first spring 23 is extended, thereby continuing to drive the upper clamp head 15 to rotate downward to cut the living tissue, so that the upper clamp head 15 and the lower clamp head 14 are closed more tightly during cutting, or the adsorption effect of the second electromagnetic block 36 on the adsorption block 35 can increase the closing force between the upper clamp head 15 and the lower clamp head 14, thereby assisting in cutting and separating the living tissue and preventing traction damage caused by tissue adhesion. After the living tissue is taken out, the first switch 310 can be pressed to de-energize the first electromagnetic block 26 and the second electromagnetic block 36, and under the elastic force of the second spring 28 and the first spring 23, the insertion rod member 27 is reinserted into the jack on the lower side of the push rod member 22.

[0049] The self-locking assembly 4 includes a connection shell 41 fixedly arranged with the fixed handle 11. A third electromagnetic block 414 is fixedly arranged inside the connection shell 41. A first shell 42 adsorbed to the third electromagnetic block 414 is slidably arranged inside the connection shell 41. A first guide groove 45 adapted to the first shell 42 is arranged inside the connection shell 41. The first shell 42 is slidably arranged along the first guide groove 45. A sixth spring 413 fixedly arranged with the inner side of the connection shell 41 is fixedly arranged on one side of the first shell 42. A second shell 44 is fixedly arranged inside the connection shell 41. Limiting tooth blocks 410 are slidably arranged inside both the first shell 42 and the second shell 44. Pulling rods 411 are fixedly arranged on one side of the two limiting tooth blocks 410 away from each other. The pulling rod 411 inside the first shell 42 movably penetrates the first shell 42 and one side of the connection shell 41 and can be slidably arranged along the movable penetration part of the connection shell 41. The pulling rod 411 inside the second shell 44 movably penetrates the second shell 44 and one side of the connection shell 41. Fifth springs 412 sleeved on the outer sides of the pulling rods 411 are fixedly arranged on one side of the two limiting tooth blocks 410. One end of the fifth spring 412 inside the first shell 42 away from the limiting tooth block 410 is fixed to the inner side of the first shell 42. One end of the fifth spring 412 inside the second shell 44 away from the limiting tooth block 410 is fixed to the inner side of the second shell 44;

[0050] A helical tooth block 43 slidably arranged with the connection shell 41 is arranged between the two limiting tooth blocks 410. The helical tooth block 43 cooperates with the limiting tooth blocks 410 on both sides. A second guide groove 46 adapted to the helical tooth block 43 is arranged inside the connection shell 41. The helical tooth block 43 is slidably arranged along the second guide groove 46. A fourth spring 49 fixedly arranged with the inner side of the connection shell 41 is fixedly arranged on one side of the helical tooth block 43. A limiting column 47 is slidably arranged on the other side of the helical tooth block 43. A limiting protrusion is arranged inside the limiting column 47, which can play a role in limiting and guiding the limiting column 47. A third spring 48 fixedly arranged with the helical tooth block 43 is fixedly arranged inside the limiting column 47. A through hole 415 adapted to the limiting column 47 is arranged through one side of the fixed handle 11. A limiting hole 416 adapted to the limiting column 47 is arranged on one side of the movable handle 12;

[0051] When it is impossible to cut and separate the living tissue, when the second electromagnet 36 is controlled to be energized by the pressure sensor 38, the third electromagnet 414 can be controlled to be energized simultaneously to generate an adsorption effect on the first housing 42, so that the first housing 42 moves close to the third electromagnet 414 along the first guide groove 45, and the sixth spring 413 elongates. When the first housing 42 moves to the other end of the first guide groove 45, the first housing 42 stops moving. The movement of the first housing 42 can drive the limit tooth block 410 inside it to move synchronously. Through the engagement of the first housing 42 and the helical tooth block 43, the helical tooth block 43 can be driven to move the same distance close to the fixed handle 11, and the fourth spring 49 elongates. At the end of this cutting, when the first switch 310 is pressed, the third electromagnet 414 can be controlled to be powered off simultaneously. Under the elastic force of the sixth spring 413, the first housing 42 is driven to move reversely and reset. And through the limiting effect of the limit tooth block 410 in the second housing 44 on the helical tooth block 43, the reverse movement of the helical tooth block 43 can be blocked. In this way, every time the living tissue fails to be cut and separated, the helical tooth block 43 can be made to move a certain distance close to the fixed handle 11, so that the number of times the living tissue fails to be cut and separated can be converted into the distance that the helical tooth block 43 moves close to the fixed handle 11 for recording. When the living tissue fails to be cut and separated many times, the movement of the helical tooth block 43 will drive the limit post 47 through the through hole 415, and under the action of the third spring 48, the limit post 47 abuts against one side of the movable handle 12. After the movable handle 12 is reset, under the elastic force of the third spring 48, the limit post 47 is inserted into the limit hole 416, so as to limit the movable handle 12 from rotating again, lock and fix the fixed handle 11 and the movable handle 12, so that the doctor cannot hold the movable handle 12 and rotate it close to the fixed handle 11. At this time, the doctor needs to check the sampling forceps and check whether the cutting edges of the upper jaw 15 and the lower jaw 14 are blunt, and whether it is due to the improper closing of the sampling forceps itself that the living tissue cannot be cut and separated, that is, when the clamping component 2 fails to cut the living tissue many times, it may not be an operation problem of the doctor using the sampling forceps due to insufficient closing force, but may be a problem of the sampling forceps itself. When the self-locking component 4 locks the movable handle 12, the number of times the sampling forceps fails to cut the living tissue is preferably three times;

[0052] After checking the relevant situation, by simultaneously pushing the two pull rods 411 outward, the two limit tooth blocks 410 can be disengaged from the helical tooth block 43. Under the elastic force of the fourth spring 49, the helical tooth block 43 moves reversely and resets, and the limit post 47 resets, releasing the lock on the movable handle 12.

[0053] Embodiment 2

[0054] The support assembly 5 includes a support block 51 disposed on the lower side of the outer tube 13. A support member 52 is movably disposed under the support block 51. A spherical groove adapted to the support member 52 is provided on the lower side of the support block 51. The upper end of the support member 52 is movably disposed in the spherical groove, so that the support block 51 can be adjusted in multiple directions and angles through the support member 52, thereby improving the flexibility of the operation angle adjustment when the biopsy forceps cut the living tissue. An installation member 53 is fixedly provided at the lower end of the support member 52. Rack bars 54 are rotatably provided on both sides of the installation member 53. Slide sleeves 55 are slidably sleeved on the outer sides of the two rack bars 54. One side of each of the two slide sleeves 55 is rotatably provided with a support rod member 56 through a hinge shaft. Fixing members 57 are fixedly provided on the sides of the two support rod members 56 away from the slide sleeves 55. The support rod member 56 and the fixing member 57 are fixed by screws, which facilitates the installation and disassembly between the support rod member 56 and the fixing member 57.

[0055] A speculum 6 is provided between the two fixing members 57. The speculum 6 includes an upper forceps arm 62 and a lower forceps arm 61. The upper forceps arm 62 and the lower forceps arm 61 are hinged. The two fixing members 57 are respectively fixedly provided on the two outer sides of the lower forceps arm 61. During cervical biopsy, the vagina can be dilated through the speculum 6, so that the doctor can cut the living tissue through the biopsy forceps. The support rod member 56 can be fastened to the fixing member 57 by screws, and the speculum 6 and the support assembly 5 are used to assist in supporting and guiding the biopsy forceps.

[0056] A screw rod 59 is rotatably provided on one side of the support block 51. A clamping member 511 is threadedly provided on the upper side of the screw rod 59. A limiting rod 510 fixedly provided with the support block 51 penetrates and slides through one side of the clamping member 511. The inner sides of the clamping member 511 and the support block 51 are set to be arc-shaped adapted to the outer tube 13. Ball beads 512 are evenly and movably provided on the inner sides of the arc-shaped clamping member 511 and the support block 51. After the outer tube 13 is clamped by the clamping member 511 and the support block 51, the ball beads 512 abut against the outer side of the outer tube 13. Fixed shells 513 are fixedly provided on one side of each of the two slide sleeves 55. A fourth electromagnetic block 514 is fixedly provided in the fixed shell 513. A second switch 516 is installed on one side of the installation member 53. The control element can be arranged in the installation member 53. A toothed block 515 adsorbed to the fourth electromagnetic block 514 is slidably provided in the fixed shell 513. The toothed block 515 movably penetrates through the fixed shell 513 and one side of the slide sleeve 55. The toothed block 515 cooperates with the rack bar 54. Seventh springs 58 fixedly provided with the fixed shell 513 are symmetrically fixedly provided on one side of the toothed block 515.

[0057] In use, the outer tube 13 can be inserted into the clamping member 511 and the support block 51 from the side end. By rotating the screw 59, the clamping member 511 moves downward along the limiting rod 510 to clamp the outer tube 13 between the support block 51 and the clamping member 511. When inserting or removing the sampling forceps, the outer tube 13 moves along the ball 512 on the inner arc of the clamping member 511 and the support block 51, and the ball 512 rolls. Thus, through the arrangement of the ball 512, the flexibility of the sampling forceps when moving inward or outward can be ensured. The support block 51 can be adjusted in multiple directions and angles through the support member 52, enabling the sampling forceps to be flexibly adjusted at multiple angles. When the sampling forceps move in the up-down or left-right directions, the second switch 516 can be pressed to control the fourth electromagnet 514 to be energized to generate an adsorption effect on the toothed block 515, causing the toothed block 515 to disengage from the toothed rod 54 and releasing the limiting effect on the toothed rod 54. The seventh spring 58 is compressed. Thus, when the sampling forceps are adjusted in the up-down or left-right directions, the sliding sleeve 55 and the support rod member 56 can rotate, and the toothed rod 54 slides along the sliding sleeve 55. Thereby, the flexibility of the operation angle adjustment when the sampling forceps cut the living tissue can be ensured, facilitating the doctor to adjust the sampling forceps to the appropriate operation angle and cutting angle when cutting the living tissue. Then, the second switch 516 can be pressed again to cut off the power supply of the fourth electromagnet 514. Under the elastic force of the seventh spring 58, the toothed block 515 is engaged with the toothed rod 54. Thus, through the limiting effect of the two toothed blocks 515 on the toothed rod 54, that is, restricting the sliding of the toothed rod 54 along the sliding sleeve 55, the support position where the sampling forceps are located at this time can be maintained, improving the stability when the doctor cuts the living tissue and facilitating the adjustment to the appropriate operation angle and cutting angle. Thereby, the cutting of the living tissue can be further ensured.

[0058] It should be noted that in this text, relational terms such as first and second are only used to distinguish one entity or operation from another entity or operation, and do not necessarily require or imply any actual relationship or order between these entities or operations. Moreover, the terms "include", "comprise" or any other variant thereof are intended to cover non-exclusive inclusion, so that a process, method, article or device including a series of elements not only includes those elements but also includes other elements not expressly listed, or further includes elements inherent to such process, method, article or device.

[0059] Although the embodiments of the present invention have been shown and described, for those of ordinary skill in the art, it can be understood that various changes, modifications, substitutions and variations can be made to these embodiments without departing from the principles and spirit of the present invention. The scope of the present invention is defined by the appended claims and their equivalents.

Claims

1. A genital examination sampler, comprising: A fixed handle (11), the fixed handle (11) is hinged with a movable handle (12), one side of the fixed handle (11) is fixedly provided with an outer tube (13), one side of the outer tube (13) is fixedly provided with a lower jaw (14), and one side of the lower jaw (14) is hinged with an upper jaw (15). It is characterized in that: it further includes: a clamping component (2), the clamping component (2) is arranged inside the fixed handle (11), and the clamping component (2) is used for clamping living tissues; An auxiliary component (3), the auxiliary component (3) is arranged on one side of the clamping component (2), and when the clamping component (2) fails to cut living tissues, the auxiliary component (3) assists the clamping component (2) to cut living tissues; A self-locking component (4), the self-locking component (4) is arranged on one side of the fixed handle (11), when the clamping component (2) fails to cut living tissues for multiple times, the fixed handle (11) and the movable handle (12) are automatically locked through the self-locking component (4); A support component (5), the support component (5) is arranged outside the outer tube (13), and the support component (5) is used for supporting and guiding the sampling forceps during use.

2. The genital examination sampler according to claim 1, wherein: The clamping component (2) includes a sleeve rod (21) hinged with the movable handle (12), a push rod member (22) is slidably arranged inside the sleeve rod (21), movable grooves (29) adapted to the push rod member (22) are symmetrically arranged inside the upper jaw (15), one end of the push rod member (22) close to the upper jaw (15) is movably arranged along the movable groove (29), a first spring (23) fixedly arranged with the inner side of the sleeve rod (21) is fixedly arranged on one side of the push rod member (22), an installation shell (25) is fixedly arranged on the lower side of the sleeve rod (21), a first electromagnetic block (26) is fixedly arranged inside the installation shell (25), a plug rod member (27) adsorbed with the first electromagnetic block (26) is slidably arranged inside the installation shell (25), the plug rod member (27) movably penetrates through the lower side of the sleeve rod (21), a second spring (28) fixedly arranged with the plug rod member (27) is fixedly arranged on the lower side of the sleeve rod (21), and a camera module (24) is installed on the outer tube (13).

3. The genital examination sampler according to claim 2, characterized in that: The auxiliary component (3) includes a first connecting member (31) fixedly arranged with the push rod member (22), a rotating member (32) is movably arranged on the lower side of the first connecting member (31), a second connecting member (34) is movably arranged on the lower side of the rotating member (32), a support column (33) fixedly arranged with the fixed handle (11) is rotatably arranged on the rotating member (32), an adsorption block (35) slidably arranged with the fixed handle (11) is fixedly arranged on the lower side of the second connecting member (34), a limiting groove (37) adapted to the adsorption block (35) is arranged inside the fixed handle (11), and the adsorption block (35) is slidably arranged along the limiting groove (37).

4. The genital examination sampler according to claim 3, characterized in that: The fixed handle (11) is fixedly provided with a second electromagnetic block (36) on one side of the adsorption block (35). After being energized, the second electromagnetic block (36) adsorbs to the adsorption block (35). A pressure sensor (38) is installed on the upper jaw (15), and a control board (39) is arranged on one side of the fixed handle (11). A first switch (310) is installed on one side of the control board (39).

5. The genital examination sampler according to claim 1, characterized in that: The self-locking assembly (4) includes a connection shell (41) fixedly provided with the fixed handle (11). A third electromagnetic block (414) is fixedly provided inside the connection shell (41). A first shell (42) that adsorbs to the third electromagnetic block (414) is slidably arranged inside the connection shell (41). A first guide groove (45) adapted to the first shell (42) is arranged inside the connection shell (41). The first shell (42) is slidably arranged along the first guide groove (45). A sixth spring (413) fixedly provided on the inner side of the connection shell (41) is fixedly provided on one side of the first shell (42). A second shell (44) is fixedly provided inside the connection shell (41). Limit tooth blocks (410) are slidably arranged inside both the first shell (42) and the second shell (44). Pull rods (411) are fixedly provided on one side of the two limit tooth blocks (410) facing away from each other. Fifth springs (412) sleeved outside the pull rods (411) are fixedly provided on one side of the two limit tooth blocks (410).

6. The genital examination sampler according to claim 5, characterized in that: An inclined tooth block (43) slidably arranged with the connection shell (41) is arranged between the two limit tooth blocks (410). A second guide groove (46) adapted to the inclined tooth block (43) is arranged inside the connection shell (41). The inclined tooth block (43) is slidably arranged along the second guide groove (46). A fourth spring (49) fixedly provided on the inner side of the connection shell (41) is fixedly provided on one side of the inclined tooth block (43).

7. The genital examination sampler according to claim 6, wherein: A limit post (47) is slidably arranged on the other side of the inclined tooth block (43). A third spring (48) fixedly provided with the inclined tooth block (43) is fixedly provided inside the limit post (47). A through hole (415) adapted to the limit post (47) is arranged through one side of the fixed handle (11). A limit hole (416) adapted to the limit post (47) is arranged on one side of the movable handle (12).

8. The genital examination sampler according to claim 1, wherein: The support assembly (5) includes a support block (51) arranged on the lower side of the outer tube (13). A support member (52) is movably arranged on the lower side of the support block (51). A mounting member (53) is fixedly provided at the lower end of the support member (52). Rack bars (54) are rotatably arranged on both sides of the mounting member (53). Slide sleeves (55) are slidably sleeved outside the two rack bars (54). Support rods (56) are rotatably arranged on one side of the two slide sleeves (55). Fixing members (57) are fixedly provided on one side of the two support rods (56) away from the slide sleeves (55).

9. The genital examination sampler according to claim 8, characterized in that: A speculum (6) is arranged between the two fixing members (57). The speculum (6) includes an upper clamping arm (62) and a lower clamping arm (61). The upper clamping arm (62) and the lower clamping arm (61) are hinged. The two fixing members (57) are respectively fixed on the two outer sides of the lower clamping arm (61).

10. The genital examination sampler according to claim 9, characterized in that: A screw rod (59) is rotatably arranged on one side of the support block (51). A clamping member (511) is threadedly arranged on the upper side of the screw rod (59). A limiting rod (510) fixedly arranged with the support block (51) is slidably arranged through one side of the clamping member (511). A plurality of balls (512) are evenly arranged in the inner sides of the clamping member (511) and the support block (51) in a movable manner. Fixing shells (513) are fixedly arranged on one side of the two sliding sleeves (55). A fourth electromagnetic block (514) is fixedly arranged in the fixing shell (513). A second switch (516) is installed on one side of the mounting member (53). A toothed block (515) adsorbed by the fourth electromagnetic block (514) is slidably arranged in the fixing shell (513). The toothed block (515) is matched with a toothed rod (54). Seventh springs (58) fixedly arranged with the fixing shell (513) are symmetrically fixedly arranged on one side of the toothed block (515).