CN113576552B - Early integrated painless section sampler of female reproductive organ pathological change - Google Patents

Abstract

The present application relates to the field of medical equipment, in particular to an integrated painless slice sampler for early stage lesions of female reproductive organs, which includes: two sets of first sampling assemblies, wherein the two sets of first sampling assemblies are arranged close to or away from each other; a second A sampling assembly, which is located between the two sets of the first sampling assemblies; a connecting assembly, where the second sampling assembly and the two sets of the second sampling assemblies are connected through the connecting assembly, along with the two sets of the first sampling assemblies move away from each other, the connecting assembly drives the second sampling assembly to protrude from one end of the first sampling assembly. The present application has the advantages of simultaneously sampling the inner wall of the genitalia and the uterine cavity, improving sampling efficiency, reducing sampling times, and optimizing patient experience.

Description

An integrated painless slice sampler for early stage of female reproductive organ lesions

technical field

The present application relates to the field of medical equipment, in particular to an integrated painless slice sampler for the early stage of female reproductive organ lesions.

Background technique

Diseases of female reproductive organs include ovarian tumors, fallopian tube tumors, uterine tumors and other tumors, cervical cancer and other cancerous diseases, as well as various infectious diseases. For reproductive diseases of female reproductive organs, regular routine screening, early diagnosis, Early surgical treatment enables the tube to reduce the morbidity and mortality of female reproductive organs, and its screening method is through brushing technology, toilet technology and extraction technology, so the sampler has become one of the indispensable tools in the process of screening and treatment.

In the related art, cotton swabs or sponges are usually used to wipe the genitals, and the samples of the inner wall of the genitals are adhered, so as to take out the cell samples in the genitals, which is convenient for subsequent detection and diagnosis.

However, when sampling the genitals of patients with genital lesions, if the method of swabbing is used, the sample capacity of each sampling is limited, and only a certain depth can be sampled. In this case, multiple samplings are required, the efficiency of multiple samplings is slow, and the patient needs to endure the pain during sampling multiple times, so the patient's experience is poor.

SUMMARY OF THE INVENTION

The embodiments of the present application provide an integrated painless slice sampler for the early stage of female reproductive organ lesions, so as to solve the technical problems of wiping sampling in the related art, which require more sampling times, lower efficiency, and affect the experience of patients.

An integrated painless slice sampler for the early stage of female reproductive organ lesions, comprising:

Two sets of first sampling assemblies, the two sets of first sampling assemblies are arranged close to or away from each other;

a second sampling component located between the two sets of the first sampling components;

A connecting assembly, the second sampling assembly and the two sets of the second sampling assemblies are connected through the connecting assembly, and the connecting assembly drives the second sampling assembly as the two sets of the first sampling assemblies move away from each other Extends from one end of the first sampling assembly.

In some embodiments, the first sampling component includes a first sampling piece, the interior of which is hollow, and a surface of the first sampling piece is provided with a first sampling hole that communicates with the inside thereof.

In some embodiments, the first sampling assembly further includes a connecting rod, and the first sampling piece is connected to an end surface of the connecting rod.

In some embodiments, the integrated painless slice sampler for the early stage of female reproductive organ lesions further includes a collection tube, the first sampling assembly further includes a collection tube, and the two ends of the collection tube are respectively connected with the collection tube and the collection tube. The first coupon is connected.

In some embodiments, the integrated painless slice sampler for the early stage of female genital lesions further includes two guide rods, both of which are connected with the peripheral outer side of the collection tube, and the two guide rods are The rods are respectively penetrated through the two connecting rods, so that the two groups of the first sampling components are arranged close to or away from each other.

In some embodiments, the integrated painless slice sampler for the early stage of female genital lesions further includes an air suction part, which is communicated with the collection tube, so as to reduce the air pressure in the collection tube.

In some embodiments, the second sampling assembly includes a second sampling piece, the interior of which is hollow, and the second sampling hole is opened on the surface of the second sampling piece and communicated with the inside thereof.

In some embodiments, the second sampling assembly further includes an anesthesia bulb, and the anesthesia bulb is arranged in communication with the second sampling piece.

In some embodiments, the second sampling assembly further includes a liquid storage tube, and the liquid storage tube is arranged in communication with the anesthesia bulb.

In some embodiments, the connecting assembly includes two connecting rods, and two ends of the connecting rods are hinged with the collecting pipe and the liquid storage pipe respectively. As the two collecting pipes move away from each other, the connecting rods become The second sampling assembly is driven to move, so that the second sampling piece protrudes from the end of the first sampling piece.

The beneficial effects brought by the technical solution provided by this application include:

The embodiment of the present application provides an integrated painless slice sampler for early stage lesions of female genital organs. When sampling, the sampler extends into the genitalia, and the first sampling component performs sampling operation on the inner wall of the genitalia. Go deep into the genitals, by keeping the two groups of first sampling assemblies away from each other, under the action of the connecting assembly, the second sampling assembly is driven to protrude from one end of the first sampling assembly, so that the second sampling assembly can be extended into the uterine cavity. Sampling can simultaneously sample the inner wall of the genitalia and the uterine cavity in one sampling process, which improves the sampling efficiency, reduces the number of sampling times, and optimizes the patient's experience.

Description of drawings

In order to illustrate the technical solutions in the embodiments of the present application more clearly, the following briefly introduces the drawings that are used in the description of the embodiments. Obviously, the drawings in the following description are only some embodiments of the present application. For those of ordinary skill in the art, other drawings can also be obtained from these drawings without creative effort.

1 is a schematic diagram of the overall structure of an integrated painless slice sampler in the early stage of female reproductive organ lesions provided by the embodiment of the present application;

Fig. 2 is the enlarged view of A place in Fig. 1;

Fig. 3 is the enlarged view at B in Fig. 1;

FIG. 4 is a longitudinal sectional view of the integrated painless slice sampler in the early stage of female reproductive organ lesions provided by the embodiment of the present application;

FIG. 5 is a schematic diagram of a getter provided by an embodiment of the present application.

In the figure: 1, the first sampling assembly; 101, the first sampling piece; 1011, the first sampling hole; 102, the connecting rod; 103, the handle; 104, the collection tube; 2, the second sampling assembly; 201, the second sampling sheet; 2011, the second sampling hole; 202, anesthesia bulb; 2021, micro anesthesia gasket; 203, the liquid storage tube; 3, the connecting assembly; 4, the collection tube; 5, the guide rod; 6, the suction part; 7, Pressure relief pipe; 701, pressure relief hole; 8, cover.

Detailed ways

In order to make the purposes, technical solutions and advantages of the embodiments of the present application clearer, the technical solutions in the embodiments of the present application will be described clearly and completely below with reference to the drawings in the embodiments of the present application. Obviously, the described embodiments It is a part of the embodiments of this application, but not all of the embodiments. Based on the embodiments in the present application, all other embodiments obtained by those of ordinary skill in the art without creative work shall fall within the protection scope of the present application.

The embodiment of the present application provides an integrated painless slice sampler for the early stage of female genital organ lesions, which can solve the problem of wiping sampling in the related art, which requires more sampling times, has low efficiency, and affects the experience of patients. question.

An integrated painless slice sampler for the early stage of female reproductive organ lesions, comprising:

Two groups of first sampling assemblies 1, and the two groups of first sampling assemblies 1 are arranged close to or away from each other;

a second sampling assembly 2, which is located between the two sets of the first sampling assemblies 1;

The connecting assembly 3, the second sampling assembly 2 and the two groups of the second sampling assemblies 2 are connected through the connecting assembly 3, and the connecting assembly 3 drives the movement of the two groups of the first sampling assemblies 1 away from each other. The second sampling assembly 2 protrudes from one end of the first sampling assembly 1 .

Referring to FIG. 1 , the integrated painless slice sampler for the early stage of female reproductive organ lesions includes: a second sampling assembly 2 , a connecting assembly 3 and two sets of first sampling assemblies 1 .

Referring to FIG. 1 , two groups of first sampling assemblies 1 are disposed close to or away from each other. After the first sampling assemblies 1 extend into the genitals, the first sampling assemblies 1 sample the inner wall of the genitals.

Referring to FIG. 1 , the second sampling assembly 2 is located between the two first sampling assemblies 1 , and is connected with the two sets of first sampling assemblies 1 through the connecting assembly 3 . Since the second sampling assembly 2 is located between the two first sampling assemblies 1, when the first sampling assembly 1 samples the inner wall of the genitalia, the second sampling assembly 2 is shielded by the first sampling assembly 1, and the second sampling assembly 2 The inner wall of the genitals is not sampled.

1 and 2, the connecting assembly 3 connects the second sampling assembly 2 with the two groups of first sampling assemblies 1, and as the two first sampling assemblies 1 move away from each other, the connecting assembly 3 drives the second sampling assembly 2 from the first sampling assembly 2. The end of a sampling assembly 1 protrudes, so that the second sampling assembly 2 can be extended into the uterine cavity and sample the uterine cavity. After the sampling of the second sampling assembly 2 is completed, the two groups of first sampling assemblies 1 move close to each other, and the connecting assembly 3 drives the second sampling assembly 2 to retract, so that the first sampling assembly 1 shields the second sampling assembly 2. During the sampling process, the second sampling component 2 is not easy to sample the inner wall of the genitalia. Therefore, the samples of the inner wall of the genitalia and the uterine cavity are stored in the first sampling assembly 1 and the second sampling assembly 2 respectively, which are not easily mixed, and are convenient for subsequent inspection and diagnosis.

In this way, when sampling, the sampler extends into the genitalia, and the first sampling assembly 1 performs sampling operation on the inner wall of the genitalia. Under the action of the connecting assembly 3, the second sampling assembly 2 is driven to protrude from one end of the first sampling assembly 1, so that the second sampling assembly 2 can be extended into the uterine cavity for sampling. Sampling the inner wall of the genitals and the uterine cavity improves sampling efficiency, reduces the number of samplings, and optimizes the patient experience.

Optionally, the first sampling assembly 1 includes a first sampling piece 101 , the interior of which is hollow, and a surface of the first sampling piece 101 is provided with a first sampling hole 1011 that communicates with the inside thereof.

1 and FIG. 4 , the first sampling assembly 1 includes a first sampling piece 101 , the first sampling piece 101 is arranged in the shape of a circular arc, and the edges and corners of the first sampling piece 101 are all arranged in a transitional arc. The interior of the first sample piece 101 is hollow, and the outer surface of the first sample piece 101 is provided with a plurality of first sampling holes 1011 , and the first sampling holes 1011 communicate the inside and outside of the first sample piece 101 . As the first sampling piece 101 is in contact with the inner wall of the genitalia, the sample enters the first sampling piece 101 through the first sampling hole 1011 to complete the sampling operation of the inner wall of the genitalia.

1 and 4 , when sampling the inner wall of the genitalia, one end of the two first sampling pieces 101 abuts against each other, so as to limit the contact of the second sampling assembly 2 with the inner wall of the genitalia. When it is necessary to sample the uterine cavity, the two first sampling pieces 101 are separated, so that the second sampling assembly 2 can be extended from the end of the first sampling piece 101, so that the second sampling assembly 2 can be extended into the uterine cavity for performing sampling.

Optionally, the first sampling assembly 1 further includes a connecting rod 102 , and the first sampling piece 101 is connected with the end surface of the connecting rod 102 .

1 and 4 , the first sampling assembly 1 further includes a connecting rod 102 and a handle 103 , and the two end surfaces of the connecting rod 102 are respectively fixed to the first sampling piece 101 and the handle 103 . The connecting rod 102 and the handle 103 are both formed by bending medical 316 stainless steel, and the edges and corners are all processed with arc transitions. By holding the handle 103, it is convenient to extend the first sample piece 101 into the genitalia, and the connecting rod 102 increases the extending length of the first sample piece 101, which facilitates sampling at different depths. At the same time, it is convenient to extend the second sampling assembly 2 to the position of the uterine cavity, so as to facilitate the extension of the second sampling assembly 2 into the uterine cavity.

The sampler needs to be sterilized before use. The traditional 430 stainless steel is made of iron + 18% chromium without nickel, which can prevent oxidation caused by natural factors, but cannot resist oxidation caused by chemical substances in the air. 430 stainless steel After infrequent use for a period of time, there will still be oxidation and rust due to unnatural factors. Due to the safety requirements of medical equipment to ensure the highest performance safety, 430 stainless steel and 430 stainless steel are not suitable for use as sampler connecting rods 102 and 100. Handle 103 is made, 304 stainless steel is made of iron + 18% chromium + 8% nickel, which can resist chemical oxidation, but there are more and more chemical components in the air, and even 304 will rust in some places with serious pollution , so the connecting rod 102 and handle 103 of the sampler are made of medical 316 stainless steel + 18% chromium + 10% nickel to make it more durable and corrosion-resistant, and there is no metal ion precipitation at all, which improves the safety of the sampler.

Optionally, the integrated painless slice sampler for the early stage of female reproductive organ lesions further includes a collection tube 4, and the first sampling assembly 1 further includes a collection tube 104, two ends of the collection tube 104 are respectively connected to the collection tube. 4 is in communication with the first sample piece 101 .

Referring to FIGS. 1 and 4 , the collection cylinder 4 is located between the two connecting rods 102 , and the two groups of second sampling assemblies 2 are evenly distributed around the axis of the collection cylinder 4 . The first sampling assembly 1 further includes a collection tube 104, the two ends of the collection tube 104 are communicated with the collection cylinder 4 and the first sample piece 101 respectively, and the communication between the collection tube 104 and the collection tube 4 and the first sample piece 101 is sealed. . The two collection tubes 104 in the first sampling assembly 1 of the two groups are evenly distributed around the axis of the collection cylinder 4 .

In this way, when the first sampling piece 101 is sampling, the sample on the inner wall of the genitalia enters the first sampling piece 101 through the first sampling hole 1011 , and then flows into the collecting tube 4 through the collecting tube 104 for storage. Meanwhile, the collection cylinder 4 includes a cylinder body and a cover body threadedly connected to the cylinder body, and the sample stored in the collection cylinder 4 can be taken out by removing the cover body.

Optionally, the integrated painless slice sampler for the early stage of female genital lesions also includes two guide rods 5, both of which are connected to the peripheral outer side of the collection tube 4, and the two guide rods 5 are The guide rods 5 are respectively penetrated through the two connecting rods 102 , so that the two groups of the first sampling assemblies 1 are arranged close to or away from each other.

Referring to FIGS. 1 and 4 , one end surface of the guide rod 5 is fixed to the outer side wall of the collection cylinder 4 , and the length direction of the guide rod 5 is consistent with the radial direction of the collection cylinder 4 . The two guide rods 5 are evenly distributed on the circumference of the axis of the collecting cylinder 4, and the two guide rods 5 are respectively penetrated through the two connecting rods 102, wherein the connecting position of the connecting rod 102 and the guide rod 5 is located at the connecting rod 102 close to the handle 103. one end. Therefore, the connecting rod 102 slides on the guide rod 5 so as to be close to or away from the collecting cylinder 4, and the two connecting rods 102 can slide close to or away from each other, so that the two sets of first sampling assemblies 1 are set close to or away from the sliding. One end of the guide rod 5 facing away from the collecting cylinder 4 is integrally formed with a limit head, and the cross-sectional area of the limit head is larger than that of the guide rod 5 to restrict the connecting rod 102 from being separated from the guide rod 5 .

When the two connecting rods 102 are disposed closest to the collecting cylinder 4 , the two first sampling pieces 101 are abutted and disposed, so as to shield the second sampling assembly 2 . When the two connecting rods 102 are farthest away from the collection tube 4, the two first sampling pieces 101 are separated, and the second sampling assembly 2 protrudes from between the two first sampling pieces 101, so as to measure the uterine cavity. sampling.

Optionally, the integrated painless slice sampler for the early stage of female genital lesions further includes an air suction member 6 which is communicated with the collection cylinder 4 to reduce the air pressure in the collection cylinder 4 .

Referring to FIGS. 1 and 4 , the suction member 6 is located between the two first sampling assemblies 1 and communicated with the collection cylinder 4 . In this embodiment, the axis of the collection cylinder 4 is consistent with the axis of the suction member 6 . The suction part 6 includes a balloon or an aspirator. In this embodiment, the suction part 6 includes a balloon, and the balloon is arranged in communication with the collecting cylinder 4 . Before the first sampling piece 101 is extended into the genitals, the balloon is in a pre-compressed state. When sampling is required, the balloon is expanded to inhale, so that the air pressure in the collecting cylinder 4 is reduced, which is convenient for the sample in the first sampling piece 101. Suction into the collection tube 4 to complete the sampling process of the inner wall of the genitalia.

Referring to FIG. 5 , a pressure relief tube 7 is communicated with the suction member 6 , and the pressure relief tube 7 is integrally formed with the balloon, so that the inside and outside of the balloon are communicated through the pressure relief tube 7 . The upper cover of the pressure relief pipe 7 is provided with a shielding cover 8 , the peripheral outer wall of the pressure relief pipe 7 is provided with threads, and the shielding cover 8 is connected with the pressure relief pipe 7 through the threads. The circumferential side wall of the pressure relief pipe 7 is also provided with a plurality of pressure relief holes 701 . When the shielding cover 8 cooperates with the pressure relief pipe 7 , the pressure relief holes 701 are also blocked by the shielding cover 8 . When the balloon is in the collapsed state, the pressure relief hole 701 is blocked by the cover 8, the air pressure in the collection cylinder 4 can be reduced by restoring the balloon, and the sample flows into the collection cylinder 4 from the first sample piece 101. . If the amount of sample entering the collection cylinder 4 is small during the recovery process of the balloon, the shielding cover 8 can be opened, the balloon can be re-compressed, and the gas in the balloon will flow from the pressure relief hole 701 to the atmosphere, and then By restoring the balloon again, the sample in the first coupon 101 is sucked into the collection tube 4 again.

Optionally, the second sampling assembly 2 includes a second sampling piece 201 , the interior of which is hollow, and a second sampling hole 2011 is opened on the surface of the second sampling piece 201 , which communicates with the inside thereof.

1 and FIG. 3 , wherein, the second sampling assembly 2 includes a second sampling piece 201 , and the second sampling piece 201 is arranged in an arc-shaped sheet, and its interior is hollow. The outer surface of the second sample piece 201 is provided with a plurality of second sampling holes 2011 which communicate the inside and outside of the second sample piece 201 . When the second sampling piece 201 is sampling, the sample enters the second sampling piece 201 through the second sampling hole 2011 . The second coupon 201 is located between the two first coupons 101 . As the first coupons 101 move away from each other, the connecting assembly 3 drives the second coupon 201 to protrude from between the two first coupons 101 , and The second sampling piece 201 is extended into the uterine cavity to complete sampling.

Optionally, the second sampling assembly 2 further includes an anesthesia bulb 202 , and the anesthesia bulb 202 is arranged in communication with the second sampling piece 201 .

Referring to FIG. 1 , FIG. 3 and FIG. 4 , the second sampling assembly 2 further includes an anesthesia ball 202 , and the anesthesia ball 202 is made of rubber material. The second sampling piece 201 is communicated with the anesthesia bulb 202 , and the sample in the second sampling piece 201 flows into the anesthesia bulb 202 . The anesthesia bulb 202 is in the shape of a fusiform cone, and a plurality of micro anesthesia spacers 2021 are fixed on its outer surface. Before sampling, the anesthesia ball 202 is soaked in a 0.5% lidocaine solution, so that the micro-hemp pad 2021 is coated with the lidocaine solution. As the second sampling piece 201 extends into the uterine cavity, the anesthesia ball 202 also extends into the uterine cavity to perform anesthesia treatment on the sampling position, thereby reducing the pain during sampling.

Optionally, the second sampling assembly 2 further includes a liquid storage tube 203 , and the liquid storage tube 203 is arranged in communication with the anesthesia bulb 202 .

Referring to FIGS. 1 and 3 , the liquid storage tube 203 is arranged in communication with the anesthesia bulb 202 , and the liquid storage tube 203 is threadedly connected to the anesthesia bulb 202 . The sample in the anesthesia bulb 202 flows into the liquid storage tube 203 for storage, and by disassembling the liquid storage tube 203 and the anesthesia bulb 202 , it is convenient to take out the sample in the liquid storage tube 203 .

Optionally, the connecting assembly 3 includes two connecting rods, two ends of the connecting rods are hinged with the collecting pipe 104 and the liquid storage pipe 203 respectively. The connecting rod drives the second sampling assembly 2 to move, so that the second sampling piece 201 protrudes from the end of the first sampling piece 101 .

1 and 2, the connecting assembly 3 includes two connecting rods, two ends of the connecting rods are hinged with the liquid storage pipe 203 and the collecting pipe 104 respectively. In this embodiment, the connecting rod and the liquid storage pipe 203 are away from the second connecting rod. One end of the coupon 201 is hinged, and the acute-angle opening formed by the two connecting rods is disposed toward the second coupon 201 . As the two first collecting tubes 104 move away, the angle between the two connecting rods gradually increases, which drives the liquid storage tube 203 to move. 101, so that the second sampling piece 201 can be extended into the uterine cavity for sampling.

In the description of this application, it should be noted that the orientation or positional relationship indicated by the terms "upper", "lower", etc. is based on the orientation or positional relationship shown in the accompanying drawings, and is only for the convenience of describing the application and simplifying the description, Rather than indicating or implying that the referred device or element must have a particular orientation, be constructed and operate in a particular orientation, it should not be construed as a limitation on the application. Unless otherwise expressly specified and limited, the terms "installed", "connected" and "connected" should be understood in a broad sense, for example, it may be a fixed connection, a detachable connection, or an integral connection; it may be a mechanical connection, It can also be an electrical connection; it can be a direct connection, an indirect connection through an intermediate medium, or an internal connection between two components. For those of ordinary skill in the art, the specific meanings of the above terms in this application can be understood according to specific situations.

It should be noted that, in this application, 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 such actual relationship or sequence exists between these entities or operations. Moreover, the terms "comprising", "comprising" or any other variation thereof are intended to encompass a non-exclusive inclusion such that a process, method, article or device that includes a list of elements includes not only those elements, but also includes not explicitly listed or other elements inherent to such a process, method, article or apparatus. Without further limitation, an element qualified by the phrase "comprising a..." does not preclude the presence of additional identical elements in a process, method, article or apparatus that includes the element.

The above descriptions are only specific embodiments of the present application, so that those skilled in the art can understand or implement the present application. Various modifications to these embodiments will be readily apparent to those skilled in the art, and the generic principles defined herein may be implemented in other embodiments without departing from the spirit or scope of the present application. Therefore, this application is not intended to be limited to the embodiments shown herein, but is to be accorded the widest scope consistent with the principles and novel features claimed herein.

Claims (6)

1. an early integration painless slice sampler for female reproductive organ lesions, is characterized in that, it comprises: Two sets of first sampling assemblies (1), the two sets of first sampling assemblies (1) are arranged close to or away from each other; A second sampling assembly (2), which is located between the two sets of the first sampling assemblies (1), when the first sampling assembly (1) performs sampling, the second sampling assembly (2) is located between the two sets of the first sampling assembly (1). Under the shielding of the first sampling assembly (1), the second sampling assembly (2) does not perform sampling; The connecting assembly (3), the second sampling assembly (2) and the two sets of the first sampling assemblies (1) are connected through the connecting assembly (3), along with the two sets of the first sampling assemblies (1). moving away from each other, the connecting assembly (3) drives the second sampling assembly (2) to protrude from one end of the first sampling assembly (1), so as to facilitate the sampling of the second sampling assembly (2); After the sampling of the second sampling assembly (2) is completed, as the two groups of the first sampling assemblies (1) move closer to each other, the connecting assembly (3) drives the second sampling assembly (2) to retract, so that the second sampling assembly (2) is retracted. The first sampling assembly (1) shields the second sampling assembly (2); The first sampling assembly (1) comprises a first sampling piece (101), the interior of which is hollow, and the surface of the first sampling piece (101) is provided with a first sampling hole (1011) communicating with the interior thereof; The first sampling assembly (1) further comprises a connecting rod (102), and the first sampling piece (101) is connected with the end face of the connecting rod (102); It also includes a collection cylinder (4), the first sampling assembly (1) further includes a collection tube (104), and the two ends of the collection tube (104) are respectively connected with the collection cylinder (4) and the first sampling The sheet (101) is connected; It also includes a suction member (6), which is communicated with the collecting cylinder (4) to reduce the air pressure in the collecting cylinder (4), and the suction member (6) is communicated with a pressure relief pipe (7), The upper cover of the pressure relief pipe (7) is provided with a shielding cover (8), the peripheral outer side wall of the pressure relief pipe (7) is provided with threads, and the shielding cover (8) is connected to the The pressure relief pipe (7) is connected, the circumferential side wall of the pressure relief pipe (7) is further provided with a plurality of pressure relief holes (701), and the shielding cover (8) is matched with the pressure relief holes (701). When the blocking cover (8) blocks the pressure relief hole (701), when the blocking cover (8) is opened, the blocking cover (8) does not block the pressure relief hole (701). 2. The integrated painless slice sampler for early stage of female reproductive organ lesions according to claim 1, characterized in that it further comprises two guide rods (5), both of which are connected with the collection The peripheral outer sides of the cylinder (4) are connected, and the two guide rods (5) are respectively penetrated through the two connecting rods (102), so that the two groups of the first sampling components (1) are close to or away from settings. 3. The integrated painless slice sampler in the early stage of female genital lesions according to claim 1, wherein the second sampling assembly (2) comprises a second sampling plate (201), the interior of which is hollow and provided, and A second sampling hole (2011) communicated with the inside of the second sampling piece (201) is formed on the surface of the second sampling piece (201). 4. The integrated painless slice sampler for early stage of female genital lesions according to claim 3, wherein the second sampling assembly (2) further comprises an anesthesia ball (202), and the anesthesia ball (202) It is arranged in communication with the second sample piece (201). 5. The integrated painless slice sampler for the early stage of female genital lesions according to claim 4, wherein the second sampling assembly (2) further comprises a liquid storage tube (203), and the liquid storage tube ( 203) is communicated with the anesthesia ball (202). 6. The integrated painless slice sampler for early stage of female genital lesions according to claim 5, wherein the connecting assembly (3) comprises two connecting rods, and two ends of the connecting rods are respectively connected to the The collection tube (104) and the liquid storage tube (203) are hinged, and as the two collection tubes (104) gradually move away from each other, the connecting rod drives the second sampling assembly (2) to move, so that the first Two coupons (201) protrude from the end of the first coupon (101).

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