Safe blood sample classification device

Abstract

The utility model relates to the technical field of storage devices, and discloses a safe blood specimen classification device which comprises a storage container, a storage end cover is installed at the top end of the storage container in a sealed mode, and a plurality of sets of separation assemblies are arranged in the storage container. According to the safe classification device for the blood samples, through the buffer limiting seat and the distance adjusting supporting element, the buffer limiting seat elastically deforms in the placing process of the blood sampling test tubes so that the outer diameters of the top ends and the bottom ends of the blood sampling test tubes can be matched; meanwhile, the blood sampling test tube drives two groups of buffer limiting seats to move along the inner walls of the separation container and the separation end cover through a longitudinal structure of the blood sampling test tube, the buffer limiting seats drive the distance adjusting supporting elements to elastically deform, and the deformed distance adjusting supporting elements clamp and fix the blood sampling test tube through the buffer limiting seats; the convenience of the device for storing the blood sampling test tubes with different sizes is greatly enhanced, the adaptability of the device to the blood sampling test tubes with different purposes is effectively improved, and thus the practicability of the device is enhanced.

Description

Technical Field

[0001] The utility model relates to the technical field of storage devices, in particular to a blood specimen safety classification device. Background Art

[0002] After searching, Chinese patent number CN219135005U discloses a specimen and blood specimen classification storage device, which relates to the technical field of storage devices, specifically a specimen and blood specimen classification storage device, including an insulated box, an inner wall of the insulated box is fixedly connected to a partition, a storage tray is arranged inside the insulated box, the upper surface of the storage tray is provided with a groove and a first through hole, a positioning box is arranged inside the groove, a second through hole is provided on the top of the positioning box, a first vertical plate is fixedly connected to the top and on both sides of the second through hole, a telescopic rod is fixedly connected to the side wall of one side of the first vertical plate, a movable end of the telescopic rod is fixedly connected to the second vertical plate, a spring is fixedly connected between the first and second vertical plates, and a semi-cylinder is fixedly connected to the bottom end of the second vertical plate. In the utility model, pulling the two second vertical plates causes the springs and the telescopic rod on both sides to retract, so that the two semi-cylinders are moved away, and each test tube is taken out separately. The removal of each test tube will not affect other test tubes and will not cause contamination to other test tubes.

[0003] When the specimen and blood specimen classification storage device in the prior art is in use, the two second vertical plates are pulled to contract the springs and telescopic rods on both sides, so that the two semi-cylinders are moved away, and each test tube is taken out individually. The removal of each test tube will not affect other test tubes and will not cause contamination to other test tubes. However, due to the different sizes of blood collection tubes for different purposes, such as culture tubes, blood glucose test tubes, ordinary blood collection tubes, routine blood collection tubes, coagulation blood collection tubes, anticoagulant blood collection tubes and blood culture tubes, it is difficult for the device to conveniently accommodate multiple groups of blood collection tubes of different sizes at the same time, which reduces the adaptability of the device to blood collection tubes for different purposes, thereby affecting the practicality of the device.

[0004] Based on this, the utility model designs a blood specimen safety classification device to solve the above problems. Utility Model Content

[0005] (1) Technical problems solved

[0006] In view of the deficiencies of the prior art, the present invention provides a blood specimen safety classification device, which solves the problems raised in the above-mentioned background technology.

[0007] (2) Technical solution

[0008] To achieve the above-mentioned purpose, the present invention provides the following technical solutions: a blood specimen safety classification device, comprising a storage container, a storage end cover is sealedly installed on the top of the storage container, a plurality of groups of partition components are arranged inside the storage container, each group of the partition components includes a partition container, a partition end cover is sealedly installed on the top of each group of the partition containers, a buffer limit seat is slidably inserted into the inner wall of each group of the partition containers and the partition end cover, a distance-adjusting support element is provided at the outer end of each group of the buffer limit seat, the inner wall of each group of the partition containers and the partition end cover is fixedly connected to the outer end of the corresponding distance-adjusting support element, a temperature control component is provided inside the storage container, a temperature storage medium is provided inside the temperature control component, and an insulation sleeve is provided on the outer surface of the storage container and the storage end cover.

[0009] Preferably, the outer surface of each group of the thermal insulation sleeves is provided with a disassembly and assembly grip ring, and the outer surface of each group of the disassembly and assembly grip rings is provided with multiple groups of anti-slip grooves.

[0010] Preferably, the bottom end of the storage container is provided with multiple groups of embedded positioning seats, and the top end of the storage end cover is provided with multiple groups of positioning bosses that can be plugged into the embedded positioning seats.

[0011] Preferably, two groups of reinforcing rings are inserted into the interior of the storage container, and multiple groups of limiting holes are opened on the top of each group of reinforcing rings. The outer surface of each group of partition components and temperature adjustment components is inserted into the inner wall of the corresponding limiting hole.

[0012] Preferably, two groups of deflection seats are provided on the top of the storage end cover, and a folding handle is rotatably inserted between the inner walls of the two groups of deflection seats.

[0013] Preferably, an information sign is provided on the top of the upper insulation sleeve, and an indication mark is provided on the top of the information sign.

[0014] (3) Beneficial effects

[0015] Compared with the existing technology, the present invention provides a blood specimen safety classification device with the following beneficial effects:

[0016] 1. The blood specimen safety classification device uses a buffer limit seat and a distance-adjusting support element to enable the buffer limit seat to elastically deform during the placement of the blood collection test tube to adapt to the outer diameters of the top and bottom ends of the blood collection test tube. At the same time, the blood collection test tube drives the two groups of buffer limit seats to move along the inner walls of the separation container and the separation end cover respectively through its own longitudinal structure. The buffer limit seat drives the distance-adjusting support element to elastically deform. The deformed distance-adjusting support element clamps the blood collection test tube through the buffer limit seat, which greatly enhances the convenience of the device for storing blood collection test tubes of different sizes, effectively improves the adaptability of the device to blood collection test tubes for different purposes, and thus enhances the practicality of the device.

[0017] 2. The blood specimen safety classification device uses a buffer limit seat and a distance-adjustable support element. When the device is subjected to external impact, the blood collection tube is displaced under the impact. During the displacement process, the blood collection tube drives the distance-adjustable support element to elastically deform through the buffer limit seat. During the deformation process, the distance-adjustable support element drives the blood collection tube to move back and forth. At the same time, the buffer limit seat buffers and reduces the impact force through deformation, effectively improving the device's protection capability for the blood collection tube, greatly enhancing the safety of the device during operation, and thus enhancing the applicability of the device.

[0018] 3. The blood specimen safety classification device forms a separation space through a sealed separation container and a separation end cover, making it difficult for external pollutants to contaminate the blood collection tubes in the separation space. At the same time, when an abnormality occurs in the blood collection tube, the blood in the blood collection tube is confined inside the separation space. When it is necessary to take out the corresponding blood collection tube, the personnel separates the separation end cover from the separation container, and then takes out the blood collection tube in the separation space. At this time, the remaining blood collection tubes are sealed inside the remaining separation components, thereby effectively reducing the chance of the blood collection tubes being contaminated or contaminated by each other, thereby enhancing the practicality of the device. BRIEF DESCRIPTION OF THE DRAWINGS

[0019] Figure 1 This is a schematic diagram of the structure of the utility model;

[0020] Figure 2 It is a front view of the structure of the utility model;

[0021] Figure 3 It is a cross-sectional view of the structure of the present utility model.

[0022] In the figure: 1. Storage container; 2. Storage end cover; 3. Partition assembly; 4. Partition container; 5. Partition end cover; 6. Buffer limit seat; 7. Distance adjustment support element; 8. Temperature control component; 9. Temperature storage medium; 10. Temperature insulation sleeve; 11. Disassembly and assembly grip ring; 12. Anti-slip groove; 13. Embedded positioning seat; 14. Positioning boss; 15. Reinforcement ring; 16. Deflection seat; 17. Folding handle; 18. Information sign. DETAILED DESCRIPTION

[0023] The following will be combined with the drawings in the embodiments of the present invention to clearly and completely describe the technical solutions in the embodiments of the present invention. Obviously, the embodiments described are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without making creative efforts are within the scope of protection of the present invention.

[0024] See also Figure 1-3The utility model provides a technical solution: a blood specimen safety classification device, comprising a storage container 1, a storage end cap 2 is sealedly installed on the top of the storage container 1, and the installation methods between the storage container 1 and the storage end cap 2 include but are not limited to screw installation, interference fit installation and card installation. A plurality of groups of partition components 3 are arranged inside the storage container 1, each group of partition components 3 includes a partition container 4, and a partition end cap 5 is sealed on the top of each group of partition containers 4. The installation methods between the partition container 4 and the partition end cap 5 include but are not limited to screw installation, interference fit installation and card installation. The partition container 4 and the partition end cap 5 after sealed installation constitute a partition space, and the blood collection test tube is located inside the partition space. When it is necessary to take out the corresponding blood collection tube, the personnel separates the separation end cover 5 from the separation container 4, and then takes out the blood collection tube relative to the separation space. At this time, the remaining blood collection tubes are sealed inside the remaining separation components 3, thereby effectively reducing the chance of the blood collection tubes being contaminated or contaminated with each other. The inner walls of each group of separation containers 4 and separation end covers 5 can be slidably plugged with a buffer limit seat 6 that adapts to the outer diameters of the top and bottom ends of the blood collection tube through its own elastic deformation. The outer ends of each group of buffer limit seats 6 are provided with a distance-adjusting support element 7 that adjusts its own length through elastic deformation. The distance-adjusting support element 7 with changed length drives the buffer limit seat 6 to move along the inner wall of the separation container 4 or the separation end cover 5. After the two groups of relative buffer limit seats 6 move to a relative distance, they adapt the blood collection tubes. At the same time, the deformed distance-adjusting support element 7 clamps the blood collection tubes through the buffer limit seat 6. When the device is subjected to external impact, the blood collection tubes are displaced under the impact. During the displacement process, the blood collection tubes drive the distance-adjusting support element 7 to elastically deform through the buffer limit seat 6. During the deformation process, the distance-adjusting support element 7 drives the blood collection tubes to move back and forth. At the same time, the buffer limit seat 6 buffers and reduces the impact force through deformation. The inner walls of each group of separation containers 4 and separation end covers 5 are fixedly connected to the outer ends of the corresponding distance-adjusting support elements 7. The interior of the storage container 1 is provided with a space for exchanging with the air in the storage container 1. A temperature regulating component 8 for heat exchange is provided. During a set period of time, the temperature regulating component 8 keeps the temperature in the space formed by the storage container 1 and the storage end cover 2 within a set range. A temperature storage medium 9 is provided inside the temperature regulating component 8 for increasing the stored energy value. The temperature storage medium 9 includes but is not limited to salt water with a concentration of 23.1%. The outer surfaces of the storage container 1 and the storage end cover 2 are both provided with an insulating sleeve 10 for reducing their heat conduction efficiency, thereby making it difficult for the air in the space between the storage container 1 and the storage end cover 2 to exchange heat with the outside. In conjunction with the temperature regulating component 8, the temperature in the device is kept within the set range for as long as possible, effectively increasing the storage time of blood in the blood collection tube in the device.

[0025] In the present invention, in order to improve the convenience during the disassembly and assembly process of the storage container 1 and the storage end cover 2, a disassembly and assembly grip ring 11 is provided on the outer surface of each set of thermal insulation sleeves 10 for enhancing the friction between it and the hands of the person, and the outer surface of each set of disassembly and assembly grip rings 11 is provided with multiple sets of anti-slip grooves 12 for increasing its friction coefficient, thereby improving the convenience during the disassembly and assembly process of the storage container 1 and the storage end cover 2.

[0026] In the present invention, in order to improve the stability of multiple groups of devices during stacking, multiple groups of embedded positioning seats 13 are provided at the bottom end of the storage container 1, and multiple groups of positioning bosses 14 that can be inserted into the embedded positioning seats 13 are provided at the top end of the storage end cover 2. During the stacking of multiple groups of devices, the embedded positioning seats 13 are inserted into the relative positioning bosses 14. After the inserted and installed embedded positioning seats 13 and positioning bosses 14 limit the lateral movement pairs between adjacent devices, thereby improving the stability of multiple groups of devices during stacking.

[0027] In the present utility model, in order to reduce the probability of displacement of the partition component 3 and the temperature regulating component 8 in the storage container 1, two groups of reinforcing rings 15 for providing limiting stress in the middle of the partition component 3 and the temperature regulating component 8 are inserted into the interior of the storage container 1, and each group of reinforcing rings 15 is provided with multiple groups of limiting holes on the top, and the outer surface of each group of partition components 3 and temperature regulating components 8 is inserted into the inner wall of the corresponding limiting hole, thereby reducing the probability of displacement of the partition component 3 and the temperature regulating component 8 in the storage container 1.

[0028] In the present invention, in order to improve the convenience during the transportation and transfer of the device, two groups of deflection seats 16 for limiting the movement of the folding handle 17 are provided on the top of the storage end cover 2, so that the folding handle 17 can change its position during use or standby. The folding handle 17 for providing a gripping position during the transportation and transfer of the device is rotatably inserted between the inner walls of the two groups of deflection seats 16, thereby improving the convenience during the transportation and transfer of the device.

[0029] In the present invention, in order to improve the convenience of distinguishing the differences between devices, an information sign 18 is provided on the top of the upper insulation sleeve 10, and an indicator mark is provided on the top of the information sign 18. By storing the indicator mark for distinguishing new types on the top of the information sign 18, personnel can quickly determine the differences between multiple groups of devices, thereby improving the convenience of distinguishing the differences between devices.

[0030] When in use, first insert the blood collection tube into the separation container 4. At this time, the bottom end of the blood collection tube fits with the engaging end of the buffer limit seat 6 in the separation container 4. Then the separation end cover 5 is fixedly installed to the top of the separation container 4. During this process, the engaging end of the buffer limit seat 6 in the separation end cover 5 fits with the top of the blood collection tube. At the same time, the blood collection tube drives the two groups of buffer limit seats 6 to move along the inner walls of the separation container 4 and the separation end cover 5 respectively through its own longitudinal structure. The buffer limit seat 6 drives the distance adjustment support element 7 to elastically deform. The deformed distance adjustment support element 7 clamps the blood collection tube through the buffer limit seat 6. When the device is subjected to external impact, the blood collection tube is displaced under the impact. During the displacement process, the blood collection tube is driven by the buffer limit seat 6 The distance-adjusting support element 7 deforms elastically, and the distance-adjusting support element 7 during the deformation process drives the blood collection tube to move back and forth. At the same time, the buffer limit seat 6 buffers and reduces the impact force through deformation. At the same time, the sealed and installed separation container 4 and the separation end cover 5 form a separation space. The blood collection tube is located inside the separation space, and external pollutants are difficult to contaminate the blood collection tube in the separation space. At the same time, after the blood collection tube has an abnormality, the blood in the blood collection tube is constrained inside the separation space. When the corresponding blood collection tube needs to be taken out, the personnel separates the separation end cover 5 from the separation container 4, and then takes out the blood collection tube relative to the separation space. At this time, the remaining blood collection tubes are all sealed inside the remaining separation components 3, thereby effectively reducing the chance of the blood collection tubes being contaminated or contaminated by each other.

[0031] Although the embodiments of the present invention have been shown and described, it will be understood by those skilled in the art that various changes, modifications, substitutions and variations may be made to these embodiments without departing from the principles and spirit of the present invention, and the scope of the present invention is defined by the appended claims and their equivalents.

Claims

1. A blood specimen safety classification device, comprising a storage container (1), wherein a storage end cap (2) is sealedly mounted on the top end of the storage container (1), and characterized in that: The storage container (1) is provided with a plurality of groups of partition components (3), each group of the partition components (3) includes a partition container (4), the top of each group of the partition containers (4) is sealed with a partition end cover (5), the inner wall of each group of the partition containers (4) and the partition end cover (5) can be slidably plugged with a buffer limit seat (6), the outer end of each group of the buffer limit seat (6) is provided with a distance adjustment support element (7), the inner wall of each group of the partition containers (4) and the partition end cover (5) is fixedly connected to the outer end of the corresponding distance adjustment support element (7), the storage container (1) is provided with a temperature adjustment component (8), the interior of the temperature adjustment component (8) is provided with a heat storage medium (9), and the outer surfaces of the storage container (1) and the storage end cover (2) are provided with a temperature insulation sleeve (10).

2. A blood specimen safety classification device according to claim 1, characterized in that: The outer surface of each group of the thermal insulation sleeves (10) is provided with a disassembly grip ring (11), and the outer surface of each group of the disassembly grip rings (11) is provided with multiple groups of anti-slip grooves (12).

3. The blood specimen safety classification device according to claim 1, characterized in that: The bottom end of the storage container (1) is provided with multiple groups of embedded positioning seats (13), and the top end of the storage end cover (2) is provided with multiple groups of positioning bosses (14) that can be inserted into the embedded positioning seats (13).

4. The blood specimen safety classification device according to claim 1, characterized in that: Two groups of reinforcing collars (15) are inserted into the interior of the storage container (1), and a plurality of limiting holes are provided on the top of each group of reinforcing collars (15). The outer surfaces of each group of the partitioning components (3) and the temperature regulating components (8) are inserted into the inner walls of the corresponding limiting holes.

5. The blood specimen safety classification device according to claim 1, characterized in that: Two groups of deflection seats (16) are provided on the top of the storage end cover (2), and a folding handle (17) is rotatably inserted between the inner walls of the two groups of deflection seats (16).

6. The blood specimen safety classification device according to claim 1, characterized in that: An information sign (18) is provided on the top of the upper insulation sleeve (10), and an indication mark is provided on the top of the information sign (18).

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