A detection device

Abstract

The utility model provides a kind of detection device, it is related to measurement detection equipment technical field, the detection device includes carrier, resist pressure subassembly and clamping component. Carrier is provided with storage groove, and storage groove is used to place the medical accessory to be detected, resist pressure subassembly is provided with resist pressure piece, and resist pressure piece is set above storage groove, and resist pressure piece moves to the direction close to storage groove to make resist pressure piece abut the medical accessory to be detected, clamping component is provided with clamping piece and detection piece, clamping piece is set above carrier and with resist pressure piece can mutually close or mutually far away, and the end of clamping piece away from carrier is provided with detection piece. The utility model can detect the tension and pressure of the medical accessory to be detected respectively, realize the purpose of tension detection and pressure detection to the medical accessory to be detected in turn, with higher degree of automation, and then improve detection efficiency.

Description

Technical Field

[0001] This utility model relates to the field of measurement and testing equipment technology, and more specifically, to a testing device. Background Technology

[0002] When performing performance testing on the connection structure of valve bodies and connectors for materials, axial tensile or compressive forces are applied between the valve body and connector to simulate the tensile load on the valve body and connector under actual working conditions. Tensile strength, compressive strength, and other properties are measured to verify whether the material meets safety and durability requirements. A common testing method involves personnel using clamps to fix the material, allowing only individual pressure or tensile tests. This method has a low degree of automation, results in a limited range of testing types, and low testing efficiency. Utility Model Content

[0003] The purpose of this invention is to provide a testing device that, with the cooperation of a clamping component and a testing component, can separately test the tensile and compressive forces of the medical accessory to be tested, eliminating the need for manual handling of the accessory. This achieves the goal of sequentially testing the tensile and compressive forces of the medical accessory, resulting in a high degree of automation and improved testing efficiency.

[0004] A first aspect of this utility model provides a detection device, the detection device comprising: The carrier is equipped with a storage compartment for placing medical accessories to be tested; A pressing assembly, wherein the pressing assembly is provided with a pressing member, the pressing member is disposed above the storage slot, and the pressing member moves toward the storage slot to press against the medical accessory to be tested; A clamping assembly is provided with a clamping element and a detection element. The clamping element is positioned above the carrier and can move close to or away from the pressing element. The detection element is provided at the end of the clamping element away from the carrier.

[0005] In one possible embodiment of the present invention, the clamping member is provided with a first clamping member and a second clamping member, and the pressing member is located between the first clamping member and the second clamping member, and the first clamping member and the second clamping member can move closer to each other or further away from each other.

[0006] In one possible embodiment of the present invention, there is a gap between the first clamping member and the second clamping member, and the pressing member is disposed in the gap.

[0007] In one possible embodiment of this utility model, the first clamping member is provided with a first slot, and the second clamping member is provided with a second slot. When the first clamping member and the second clamping member abut against each other, the first slot is provided corresponding to the second slot and surrounds and defines a receiving hole, and the valve body of the medical accessory to be tested passes through the receiving hole.

[0008] In one possible embodiment of the present invention, the carrier includes a carrier platform, and a positioning member is provided on the side of the carrier platform near the clamping assembly. The positioning member is provided with a third slot, the opening of the third slot is oriented toward the clamping member, and the third slot is configured to correspond to the receiving hole.

[0009] In one possible embodiment of the present invention, the detection device is further provided with a support component, which is located at the end of the carrier away from the clamping component, and the support component can be close to or away from the storage slot.

[0010] In one possible embodiment of the present invention, the detection device further includes a frame and a moving component, the clamping component further includes a mounting plate, the moving component is fixedly disposed on the frame, the clamping member is mounted on the side of the mounting plate near the carrier, and the side of the mounting plate opposite to the clamping member is fixedly connected to the driving end of the moving component.

[0011] In one possible embodiment of the present invention, the moving component includes a fixed plate and a first driving member. The fixed plate is fixed to the frame and arranged side by side with the first driving member. The fixed plate is slidably connected to the mounting plate.

[0012] In one possible embodiment of this utility model, the pressing component has multiple pressing members arranged side by side, the number of storage slots is multiple, the number of clamping members is multiple, the multiple clamping members are arranged side by side, each pressing member is arranged above a storage slot, and each pressing member is arranged with a clamping member.

[0013] Compared with the prior art, the beneficial effects of this utility model are as follows: The detection device provided by this utility model has a placement slot of a carrier for placing and supporting medical accessories to be tested. The connector in the medical accessory to be tested passes through the valve body. The pressing members can be moved to the position of the placement slot to abut and limit the corresponding connector of the medical accessory to be tested. The moving component drives the clamping member of the clamping component to move. The clamping member is used to clamp the valve body of the medical accessory to be tested, so that the clamping member clamps the valve body of the corresponding medical accessory to be tested to facilitate the detection of the connection tension or pressure between the valve body and the connector. With the cooperation of the clamping member and the detection member, the tension and pressure of the medical accessory to be tested can be detected separately without the need for manual handling of the medical accessory to be tested again. This achieves the purpose of sequentially testing the tension and pressure of the medical accessory to be tested, with a high degree of automation, thereby improving the detection efficiency. Attached Figure Description

[0014] To more clearly illustrate the technical solutions of the embodiments of this utility model, the drawings used in the embodiments will be briefly introduced below. It should be understood that the following drawings only show some embodiments of this utility model and should not be regarded as a limitation on the scope. For those skilled in the art, other related drawings can be obtained based on these drawings without creative effort.

[0015] Figure 1 This is a three-dimensional structural diagram of the detection device provided in some embodiments of the present invention. Figure 1 ; Figure 2 This is a three-dimensional structural diagram of the detection device provided in some embodiments of the present invention. Figure 2 ; Figure 3 It shows Figure 2 Schematic diagram of the structure of section A; Figure 4 This is a side view of the detection device provided in some embodiments of the present invention; Figure 5 This is a schematic diagram of the structure of the medical accessory to be tested provided in some embodiments of this utility model.

[0016] Explanation of key component symbols; 100 - Detection device; 110 - Carrier; 111 - Carrier platform; 112 - Storage slot; 113 - Positioning component; 1131 - Third slot; 114 - Support assembly; 1141 - Support component; 1142 - Third driving component; 120 - Pressing assembly; 121 - Pressing component; 122 - Second driving component; 130 - Moving assembly; 131 - Fixing plate; 132 - First driving component; 140 - Clamping assembly; 141 - Clamping component; 1411- First clamping component; 1411a- First slot; 1412- Second clamping component; 1412a- Second slot; 1413- Receiving hole; 1414- Gap; 142- Fourth driving component; 143- Mounting plate; 144- Detection component; 150- Frame; 200- Medical accessory to be tested; 210- Valve body; 220- Connector; X- Width direction; Y- Vertical direction; Z- Thickness direction. Detailed Implementation

[0017] To make the objectives, technical solutions, and advantages of the embodiments of this utility model clearer, the technical solutions of the embodiments of this utility model will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only some embodiments of this utility model, and not all embodiments. The components of the embodiments of this utility model described and shown in the accompanying drawings can generally be arranged and designed in various different configurations.

[0018] Therefore, the following detailed description of the embodiments of the present invention provided in the accompanying drawings is not intended to limit the scope of the claimed invention, but merely to illustrate selected embodiments of the invention. All other embodiments obtained by those skilled in the art based on the embodiments of the present invention without inventive effort are within the scope of protection of the present invention.

[0019] It should be noted that similar labels and letters in the following figures indicate similar items. Therefore, once an item is defined in one figure, it does not need to be further defined and explained in subsequent figures.

[0020] In the description of this utility model, it should be noted that the terms "center," "upper," "lower," "left," "right," "vertical," "horizontal," "inner," and "outer," etc., indicate the orientation or positional relationship based on the orientation or positional relationship shown in the accompanying drawings, or the orientation or positional relationship commonly used when the product of this utility model is in use. They are only for the convenience of describing this utility model and simplifying the description, and do not indicate or imply that the device or element referred to must have a specific orientation, or be constructed and operated in a specific orientation. Therefore, they should not be construed as limitations on this utility model. In addition, the terms "first," "second," and "third," etc., are only used to distinguish descriptions and should not be construed as indicating or implying relative importance.

[0021] Furthermore, terms such as "horizontal," "vertical," and "sag" do not imply that components must be absolutely horizontal or suspended, but rather that they can be slightly tilted. For example, "horizontal" simply means that its direction is more horizontal relative to "vertical," and does not mean that the structure must be completely horizontal, but can be slightly tilted.

[0022] In the description of this utility model, it should also be noted that, unless otherwise explicitly specified and limited, the terms "set," "install," "connect," and "link" should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral connection; they can refer to a mechanical connection or an electrical connection; they can refer to a direct connection or an indirect connection through an intermediate medium; and they can refer to the internal connection of two components. Those skilled in the art can understand the specific meaning of the above terms in this utility model based on the specific circumstances.

[0023] The following detailed description, in conjunction with the accompanying drawings, outlines some embodiments of the present invention. Unless otherwise specified, the following embodiments and features can be combined with each other.

[0024] In related technologies, when performing performance testing on the connection structure of valve bodies and connectors of materials, axial tensile or compressive forces are applied between the valve body and connector to simulate the tensile load of the valve body and connector under actual working conditions. Tensile strength, compressive strength, and other properties are measured to verify whether the material meets safety and durability requirements. Some testing requirements necessitate high-frequency testing. Common testing methods involve personnel using clamps to fix the material, allowing only individual pressure or tensile tests. This method has low automation, results in limited testing types, and low testing efficiency.

[0025] To solve the above problems, please refer to... Figure 1 As shown, an embodiment of this application provides a detection device 100, which includes a carrier 110, a pressing component 120, and a clamping component 140.

[0026] refer to Figure 1 and Figure 2 As shown, the detection device 100 has a width direction X, a vertical direction Y, and a thickness direction Z, wherein the width direction X, vertical direction Y, and thickness direction Z are arranged perpendicularly to each other. For example, the width direction X refers to the width of the detection device 100, the vertical direction Y refers to the height of the detection device 100, and the thickness direction Z refers to the thickness of the detection device 100. It is understood that the above definitions are only for ease of understanding the relative positional relationships of the various parts in the detection device 100 and should not be construed as limitations on this application.

[0027] Specifically, in combination Figure 1 and Figure 2As shown, the carrier 110 is provided with a storage slot 112 for placing the medical accessory 200 to be tested. The pressing assembly 120 is provided with a pressing member 121, which is positioned above the storage slot 112. The pressing member 121 moves towards the storage slot 112 to abut against the medical accessory 200 to be tested. The clamping assembly 140 is provided with a clamping member 141 and a detection member 144. The clamping member 141 is positioned above the carrier 110 and can move closer to or further away from the pressing member 121. The detection member 144 is provided at the end of the clamping member 141 away from the carrier 110. Correspondingly, the storage slot 112 of the carrier 110 is used for... The medical accessory 200 to be tested is placed and supported. The connector 220 of the medical accessory 200 to be tested passes through the valve body 210. The pressing member 121 can be moved to the position of the storage slot 112 to abut and limit the corresponding connector 220 of the medical accessory 200 to be tested. The moving component 130 drives the clamping member 141 of the clamping component 140 to move. The clamping member 141 clamps the valve body 210 of the medical accessory 200 to be tested, so as to perform tensile or compressive testing at the connection between the valve body 210 and the connector 220. With the cooperation of the clamping member 141 and the testing member 144, tensile and compressive tests are performed on the medical accessory 200 to be tested, so as to realize the detection of the amount of silicone oil applied at the connection between the connector 220 and the valve body 210.

[0028] Among them, such as Figure 5 As shown, the medical accessory 200 to be tested includes a valve body 210 and a connector 220. The connector 220 passes through the valve body 210, and the connector 220 and the valve body 210 have a first assembly position and a second assembly position with relative positioning. When in the first assembly position, the two ends of the connector 220 are exposed outside the valve body 210; when in the second assembly position, at least one end of the connector 220 can be received inside the valve body 210.

[0029] As is easily understood, the pressing member 121 is used to abut and press against the connector 220, and the clamping member 141 is used to clamp the valve body 210. When the clamping member 141 moves closer to the pressing member 121 in the vertical direction Y, the connector 220 and the valve body 210 change from the second assembly position to the first assembly position. During this process, the clamping force of the clamping member 141 is detected by the detection member 144. The clamping force of the clamping member 141 is the tension between the connector 220 and the valve body 210. The detection member 144 can be a force sensor, and the detected data is transmitted to the controller to ensure the clamping force. Within a preset reasonable range, when the clamping member 141 moves away from the pressing member 121 in the vertical direction Y, causing the connector 220 and valve body 210 to change from the first assembly position to the second assembly position, the clamping force of the clamping member 141 is the pressure between the connector 220 and the valve body 210. Since lubricating silicone oil is provided between the connector 220 and the valve body 210 to reduce the tension or pressure between the connector 220 and the valve body 210, when the tension or pressure is detected to exceed the set threshold, the detection device 100 issues an alarm indicating that the content of lubricating silicone oil does not meet the standard.

[0030] In addition, the pressing assembly 120 also includes a second driving member 122, which may be a miniature cylinder. The second driving member 122 is connected to the pressing member 121 in a transmission manner. The second driving member 122 is used to drive the pressing member 121 to descend or rise in the vertical direction Y, so that the pressing member 121 abuts against or moves away from the joint 220. For example, when the medical accessory 200 to be tested is placed in the storage slot 112, the second driving member 122 drives the pressing member 121 to move in the vertical direction Y toward the storage slot 112 until it abuts against the end face of the joint 220 of the medical accessory 200 to be tested, thereby limiting and fixing the joint 220.

[0031] Optionally, such as Figure 3 As shown, the clamping member 141 is provided with a first clamping member 1411 and a second clamping member 1412. The first clamping member 1411 and the second clamping member 1412 are arranged opposite to each other. The pressing member 121 is located between the first clamping member 1411 and the second clamping member 1412. The first clamping member 1411 and the second clamping member 1412 can move closer to each other or further away from each other to realize the clamping or releasing action of the clamping member 141. The assembly is relatively compact and the space utilization rate is high.

[0032] Further, refer to Figure 3 and Figure 4 As shown, there is a gap 1414 between the first clamping member 1411 and the second clamping member 1412. The pressing member 121 is disposed in the gap 1414. The pressing member 121 can press the connector 220 toward the storage groove 112 through the gap 1414.

[0033] Optionally, such as Figure 3 As shown, the first clamping member 1411 is provided with a first slot 1411a, and the second clamping member 1412 is provided with a second slot 1412a. When the first clamping member 1411 and the second clamping member 1412 abut against each other, the first slot 1411a corresponds to the second slot 1412a and surrounds and defines a receiving hole 1413. The valve body 210 of the medical accessory 200 to be tested passes through the receiving hole 1413, thereby achieving clamping and fixing of the valve body 210. For example, the first slot 1411a is a semi-circular groove structure, and the second slot 1412a is a semi-circular groove structure. The depth and width of the slots match the diameter of the valve body 210. After combination, a circular receiving hole 1413 is formed, ensuring a tight fit during clamping and preventing damage to the surface of the valve body 210.

[0034] For example, there are two first slots 1411a and two second slots 1412a. Each first slot 1411a corresponds to one second slot 1412a, defining one receiving hole 1413. That is, the two receiving holes 1413 respectively limit the valve body 210 of the medical accessory 200 to be tested at opposite ends, ensuring the balance of the valve body 210 during the tensile test or pressure test, and preventing the valve body 210 from tilting or shifting to one side.

[0035] In addition, the clamping assembly 140 also includes a fourth drive member 142, which is used to drive the first clamping member 1411 and the second clamping member 1412 to move closer to each other or further away from each other, so that the clamping member 141 clamps or releases the valve body 210.

[0036] In one embodiment, optionally, combining Figure 2 and Figure 3 As shown, the carrier 110 includes a carrier platform 111. The carrier 110 includes a carrier platform 111. A positioning member 113 is provided on the side of the carrier platform 111 near the clamping assembly 140. The positioning member 113 is provided with a third slot 1131. The opening of the third slot 1131 is set towards the clamping member 141. The third slot 1131 can be set to correspond to the receiving hole 1413 and is used to carry the medical accessory 200 to be tested. The positioning member 113 is used to assist in positioning the valve body 210 of the medical accessory 200 to be tested, and to ensure the clamping accuracy of the clamping member 141 on the valve body 210.

[0037] Furthermore, the carrier platform 111 is provided with a plurality of storage slots 112 spaced apart along its width x its length. Each storage slot 112 corresponds to a placement position of a medical accessory 200 to be tested. On the side of the carrier platform 111 near the clamping assembly 140, a plurality of positioning members 113 are provided. Each positioning member 113 is provided with a third slot 1131. The opening of the third slot 1131 faces the clamping member 141. Each positioning member 113 corresponds to one clamping member 141. The number of positioning members 113 is the same as the number of storage slots 112, and each positioning member 113 corresponds to one storage slot 112. One third slot 1131 can correspond to one receiving hole 1413.

[0038] Optionally, refer to Figure 2 As shown, the detection device 100 is also provided with a support component 114. The support component 114 is located at the end of the carrier 110 away from the clamping component 140. The support component 114 can move closer to or further away from the storage slot 112. The support component 114 is used to support the carrier platform 111, reduce the shaking of the carrier platform 111 when external force is applied to the medical accessory 200 to be tested on the storage slot 112, prevent the carrier platform 111 from being suspended, and ensure the accuracy of the detection. The support component 114 can reciprocate along the vertical direction Y to support the carrier platform 111 or move away from the carrier platform 111, so that the carrier platform 111 can be rotated or flipped after the detection is completed. For example, the support component 114 is driven by a cylinder or a linear module.

[0039] Furthermore, multiple support components 114 are spaced apart along the width direction X. The support components 114 are located at the end of the carrier platform 111 away from the clamping component 140. Each support component 114 can be close to or away from one of the storage slots 112 along the vertical direction Y.

[0040] For example, the support component 114 includes a support member 1141 and a third drive member 1142. The third drive member 1142 is used to drive the support member 1141 to move relative to each other in the vertical direction Y, so that the support member 1141 moves closer to or further away from the storage slot 112, so that the support member 1141 provides support for the storage slot 112.

[0041] In one embodiment, alternatively, referencing Figure 2 and Figure 3As shown, the detection device 100 further includes a frame 150 and a moving component 130. The clamping component 140 further includes a mounting plate 143. The moving component 130 is fixedly mounted on the frame 150. The clamping member 141 is mounted on the side of the mounting plate 143 near the carrier 110. The side of the mounting plate 143 away from the clamping member 141 is fixedly connected to the driving end of the moving component 130. The mounting plate 143 serves as an intermediate carrier for power transmission. The output end of the moving component 130 is used to drive the mounting plate 143 to move relative to the vertical direction Y, causing the clamping member 141 on the mounting plate 143 to rise or fall, so that the clamping member 141 can move closer to or away from the medical accessory 200 to be tested. For example, the fourth driving component 142 serves as a power source and can drive the clamping member 141 to complete the clamping action by means of machinery, hydraulics, or motor.

[0042] Optionally, refer to Figure 2 and Figure 4 As shown, the moving component 130 includes a fixed plate 131 and a first driving member 132. The fixed plate 131 is fixed to the frame 150 and arranged side by side with the first driving member 132. The fixed plate 131 is slidably connected to the mounting plate 143. The mounting plate 143 can move relative to the fixed plate 131 along the vertical direction Y. The fixed plate 131 provides support and guidance, allowing the mounting plate 143 to rise or fall along the vertical direction Y, thereby adjusting the height of the clamping member 141 and moving it to the corresponding clamping position of the medical accessory 200 to be tested. For example, the sliding connection between the fixed plate 131 and the mounting plate 143 can be a slide rail structure, a slide groove structure, etc., and no specific limitation is made here.

[0043] Optionally, the pressing assembly 120 has multiple pressing members 121 arranged side-by-side along the width direction X; the number of storage slots 112 is multiple, arranged along the width direction X; the number of clamping members 141 is multiple, arranged side-by-side along the width direction X; each pressing member 121 is positioned above a storage slot 112, and each pressing member 121 is positioned corresponding to a clamping member 141; the multiple pressing members 121 can be moved to the positions of the storage slots 112 to press against the corresponding medical accessories 200 to be tested. The connector 220 engages and limits contact, and the multiple clamping members 141 of the clamping assembly 140 move to clamp the valve body 210 of the medical accessory 200 to be tested, so that any clamping member 141 clamps the corresponding valve body 210 of the medical accessory 200 to be tested, so as to perform tensile or compressive testing on the connection between the valve body 210 and the connector 220. With the cooperation of the clamping member 141 and the testing member 144, the tensile and compressive forces of the medical accessory 200 to be tested are tested separately, so as to achieve the purpose of simultaneously testing the medical accessories 200 to be tested on multiple storage slots 112, thereby improving the testing efficiency.

[0044] During the operation of the testing device 100, the medical accessories 200 to be tested (the assembly structure of valve body 210 and connector 220) are placed one by one on the storage slot 112 of the carrier 110, so that the valve body 210 is positioned on the storage slot 112 and the connector 220 extends towards the side of the pressing component 120; at the same time, the drive support component 114 moves towards the storage slot 112 in the vertical direction Y to support the carrier platform 111, and drives the pressing component 121 to move towards the storage slot 112 in the vertical direction Y until each pressing component 121 abuts against the end face of the connector 220 of the medical accessory 200 to be tested on the corresponding storage slot 112, thus completing the limiting and fixing of the connector 220. The first driving member 132 drives the mounting plate 143 to move vertically Y toward the carrier 110, and drives the clamping member 141 to move closer to the storage slot 112. When the first clamping member 1411 and the second clamping member 1412 of the clamping member 141 move to the outside of the valve body 210, the first clamping member 1411 and the second clamping member 1412 approach each other, so that the valve body 210 passes into the receiving hole 1413 formed by the first slot 1411a and the second slot 1412a, until the first clamping member 1411 and the second clamping member 1412 abut against each other, and the clamping and fixing of the valve body 210 is completed. At this time, the third slot 1131 of the positioning member 113 corresponds to the receiving hole 1413, further assisting in positioning the valve body 210. After the clamping member 141 clamps the valve body 210, the first driving member 132 drives the clamping assembly 140 to move away from the carrier 110 in the vertical direction Y, so that a relative tension is generated between the valve body 210 and the connector 220; or the first driving member 132 drives the clamping assembly 140 to move closer to the carrier 110 in the vertical direction Y, so that a relative pressure is generated between the valve body 210 and the connector 220. During this process, the detection member 144 detects the clamping force of the clamping member 141 on the valve body 210 in real time and synchronously feeds back the tension / pressure data between the valve body 210 and the connector 220.

[0045] As an example, the detection device 100 also includes a controller, which is electrically connected to the carrier 110, the pressing component 120, the moving component 130 and the clamping component 140 respectively. The controller can control the opening and movement of each component. The controller can also have functions such as timing control of multiple components, force value processing, threshold judgment and status feedback. The controller can be a PLC (programmable logic controller) or an industrial-grade microcontroller, which is installed in the electrical control box of the detection device 100.

[0046] In summary, the carrier 110 of the testing device 100 has multiple placement slots 112 for placing and supporting the medical accessory 200 to be tested. The valve body 210 of the medical accessory 200 is inserted into the valve body. Multiple abutment members 121 can be moved to the positions of the placement slots 112 to abut and limit the corresponding connector 220 of the medical accessory 200 to be tested. The first driving member 132 drives multiple clamping members 141 of the clamping assembly 140 to move. The clamping members 141 are used to clamp the valve body 210 of the medical accessory 200 to be tested, so as to detect the connection tension or pressure between the valve body 210 and the connector 220. The medical accessory 200 is tested under the cooperation of the clamping members 141 and the testing members 144. The tensile and compressive forces of the medical accessory 200 are tested separately, and the amount of silicone oil applied at the connection between the connector 220 and the valve body 210 is detected. With the cooperation of the clamping part 141 and the testing part 144, the tensile and compressive forces of the medical accessory 200 to be tested can be tested separately without the need for manual handling of the medical accessory 200 to be tested. It has a high degree of automation, thereby improving the testing efficiency. Furthermore, the limiting of the pressing part 121, the auxiliary positioning of the positioning part 113, and the real-time monitoring of the testing part 144 ensure the testing accuracy and material safety. It is suitable for tensile / compression testing scenarios of batch medical accessories 200 (the assembly structure of valve body 210 and connector 220) to be tested.

[0047] In all examples shown and described herein, any specific values ​​should be interpreted as merely exemplary and not as limitations; therefore, other examples of exemplary embodiments may have different values.

[0048] The embodiments described above are merely examples of several implementations of this utility model, and while the descriptions are relatively specific and detailed, they should not be construed as limiting the scope of this utility model. It should be noted that those skilled in the art can make various modifications and improvements without departing from the concept of this utility model, and these modifications and improvements all fall within the protection scope of this utility model.

Claims

1. A detection device, characterized in that, include: The carrier (110) is provided with a storage slot (112) for placing the medical accessories (200) to be tested. A pressure assembly (120) is provided with a pressure member (121), which is disposed above the storage slot (112). The pressure member (121) moves toward the storage slot (112) so that the pressure member (121) abuts against the medical accessory (200) to be tested. The clamping assembly (140) is provided with a clamping member (141) and a detection member (144). The clamping member (141) is disposed above the carrier (110) and can be close to or far away from the pressing member (121). The detection member (144) is provided at the end of the clamping member (141) away from the carrier (110).

2. The detection device according to claim 1, characterized in that, The clamping member (141) is provided with a first clamping member (1411) and a second clamping member (1412), and the pressing member (121) is located between the first clamping member (1411) and the second clamping member (1412). The first clamping member (1411) and the second clamping member (1412) can move closer to each other or further away from each other.

3. The detection device according to claim 2, characterized in that, There is a gap (1414) between the first clamping member (1411) and the second clamping member (1412), and the pressing member (121) is disposed in the gap (1414).

4. The detection device according to claim 2, characterized in that, The first clamping member (1411) is provided with a first slot (1411a), and the second clamping member (1412) is provided with a second slot (1412a). When the first clamping member (1411) and the second clamping member (1412) abut against each other, the first slot (1411a) is provided with corresponding second slot (1412a) and surrounds and defines a receiving hole (1413). The valve body (210) of the medical accessory (200) to be tested passes through the receiving hole (1413).

5. The detection device according to claim 4, characterized in that, The carrier (110) includes a carrier platform (111), and a positioning member (113) is provided on the side of the carrier platform (111) near the clamping assembly (140). The positioning member (113) is provided with a third slot (1131), the opening of the third slot (1131) is provided facing the clamping assembly (141), and the third slot (1131) is provided corresponding to the receiving hole (1413).

6. The detection device according to claim 1, characterized in that, The detection device is also provided with a support component (114), which is located at the end of the carrier (110) away from the clamping component (140) and can be close to or away from the storage slot (112).

7. The detection device according to claim 1, characterized in that, The detection device (100) further includes a frame (150) and a moving component (130). The clamping component (140) further includes a mounting plate (143). The moving component (130) is fixedly mounted on the frame (150). The clamping member (141) is mounted on the side of the mounting plate (143) near the carrier (110). The side of the mounting plate (143) away from the clamping member (141) is fixedly connected to the driving end of the moving component (130).

8. The detection device according to claim 7, characterized in that, The moving component (130) includes a fixed plate (131) and a first driving member (132). The fixed plate (131) is fixed to the frame (150) and arranged side by side with the first driving member (132). The fixed plate (131) is slidably connected to the mounting plate (143).

9. The detection device according to any one of claims 1 to 8, characterized in that, The pressing component (120) has multiple pressing members (121) arranged side by side. There are multiple storage slots (112) and multiple clamping members (141). The multiple clamping members (141) are arranged side by side. Each pressing member (121) is positioned above a storage slot (112), and each pressing member (121) is positioned corresponding to a clamping member (141).

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