A umbilical cord blood plasma bag flared drainage device
By designing an umbilical cord blood plasma bag expansion drainage device, and using components such as cylindrical drainage tubes and blunt insertion tubes, the problems of cross-infection and low operation efficiency were solved, and a low-cost and efficient sampling process was achieved.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- GUANGZHOU MUNICIPALITY TIANHE NUOYA BIO-ENG CO LTD
- Filing Date
- 2025-08-06
- Publication Date
- 2026-07-21
AI Technical Summary
Existing technologies for umbilical cord blood sampling pose risks of cross-infection, high costs of consumables, low operational efficiency, and significant occupational exposure risks, and the sampling process is prone to spillage.
A device for expanding and draining umbilical cord blood plasma bags was designed, including an expanding component and a drainage component. It adopts a cylindrical hollow drainage tube, a blunt insertion tube, a limiting ring, a flow control valve, etc., to realize an independent drainage channel without contacting the culture bottle, reducing the risk of cross-infection. The device also improves the operation efficiency by expanding the orifice diameter with a conical blunt tip and adjusting the flow rate with a press-type clamping structure.
This approach avoids cross-infection, reduces costs and risks, improves ease of operation and efficiency, and reduces the number of punctures and the risk of leakage.
Smart Images

Figure CN224535490U_ABST
Abstract
Description
Technical Field
[0001] This utility model relates to the field of medical device technology, specifically to a device for expanding and draining umbilical cord blood plasma bags. Background Technology
[0002] Umbilical cord blood or plasma bags need to be sampled by puncture with a syringe for inoculation into bacterial culture bottles to detect microorganisms. After sampling, if necessary, the remaining blood or plasma should be transferred to containers such as cryovials.
[0003] Currently, there is a risk of cross-infection when collecting umbilical cord blood. If the original syringe is used again for sampling, the culture medium in the culture bottle may remain in the syringe, causing sample contamination. Frequent replacement of new syringes will increase the cost of consumables, and frequent puncture operations are prone to occupational exposure (such as needlestick injuries). In addition, the original puncture site is small, and the liquid flow rate is slow and easy to spill when poured directly, requiring repeated adjustment of the angle, resulting in low operation efficiency.
[0004] There is an urgent need for a device to expand and drain umbilical cord blood plasma bags to address the technical deficiencies mentioned above. Utility Model Content
[0005] The purpose of this invention is to provide a device for expanding and draining umbilical cord blood plasma bags to solve the problem of cross-infection risk mentioned in the background art.
[0006] To achieve the above objectives, this utility model provides the following technical solution: an umbilical cord blood plasma bag dilation and drainage device, comprising a dilation assembly and a drainage assembly. The dilation assembly consists of a drainage tube, a limiting ring, and a blunt insertion tube. The limiting ring is fixedly connected to the top end of the drainage tube. The drainage assembly includes an extension catheter and an optional flexible tube. A flow control valve is fixedly installed on the optional flexible tube. A connection opening is fixedly connected to the end of the optional flexible tube. A sealing ring is fixedly connected to the inner side of the connection opening. A cryotube is provided below the connection opening. The outside of the drainage tube is provided with anti-slip texture.
[0007] As a further technical solution of this utility model, the main body of the drainage tube is a cylindrical hollow structure, and the blunt insertion tube is connected to the drainage tube in a through manner.
[0008] As a further technical solution of this utility model, the blunt insertion tube adopts a tapered blunt head, and the limiting ring is disposed below the blunt insertion tube.
[0009] As a further technical solution of this utility model, the drainage tube and the extension catheter are connected in a through connection.
[0010] As a further technical solution of this utility model, the extension conduit and the optional hose are connected in a through connection.
[0011] As a further technical solution of this utility model, the flow control valve adopts a press-type clamping structure control valve.
[0012] As a further technical solution of this utility model, both the flaring component and the drainage component are made of medical-grade polypropylene.
[0013] As a further technical solution of this utility model, the connecting opening is threadedly connected to the top end of the freezing tube.
[0014] Compared with the prior art, the beneficial effects of this utility model are: the umbilical cord blood plasma bag dilation and drainage device not only achieves the function of avoiding cross-infection and reducing costs and risks, but also achieves the function of simple and efficient operation.
[0015] (1) The device is equipped with a flaring assembly, a drainage assembly, an extension catheter, an optional hose, anti-slip texture, a drainage tube, a limiting ring, and a blunt insertion tube. The main body of the drainage tube of the flaring assembly is a cylindrical hollow structure. The anti-slip texture on the surface of the drainage tube can improve the friction of holding the hand during insertion and enhance the stability of insertion. The blunt insertion tube at the top of the drainage tube adopts a conical blunt tip, which is used to insert into the original puncture site of the blood plasma bag and enlarge the aperture to avoid secondary damage or leakage caused by sharp structures. The limiting ring at the bottom of the blunt insertion tube prevents the plasma bag from being damaged due to excessive insertion. The device consists of a flaring assembly, a drainage assembly, and an extension catheter. The dedicated drainage channel is independent of the sampling syringe and does not need to contact the culture bottle, thus eliminating cross-contamination between the sample and the culture medium.
[0016] (2) By setting up a flaring component, a drainage component, an extension catheter and a cryotube, the flaring component and the drainage component are both made of medical-grade polypropylene. The overall consumable volume of the drainage device is only one-fifth of that of a traditional syringe, and the cost is reduced by more than 60%. The blunt insertion tube adopts a conical round head structure design and integrated operation to reduce the number of punctures and reduce the risk of occupational exposure. This structure achieves the function of reducing costs and risks.
[0017] (3) By setting up optional hoses, flow control valves, connecting openings and cryotubes, the flaring assembly can quickly enlarge the original puncture site and extend the catheter directly to the target container. The flow control valve on the optional hose adopts a press-type clamping structure, which can be used to adjust the liquid flow rate. The liquid flow rate is increased by 3 to 5 times. During sampling, umbilical cord blood flows directly into the interior of the cryotube along the optional hose. The connecting opening is closed and connected to the opening of the cryotube, which is not easy to spill during transportation. The operation can be completed by a single person. This structure realizes the functions of convenient and efficient operation. Attached Figure Description
[0018] Figure 1 This is a frontal cross-sectional view of the present invention.
[0019] Figure 2This is a front view structural diagram of the flared assembly of this utility model;
[0020] Figure 3 This is a front view schematic diagram of the connection opening structure of this utility model;
[0021] Figure 4 This is a schematic diagram of the flow control valve structure of this utility model.
[0022] In the diagram: 1. Flaring assembly; 2. Drainage assembly; 3. Extension tube; 4. Optional hose; 5. Flow control valve; 6. Connection opening; 7. Cryotube; 8. Sealing ring; 9. Anti-slip texture; 10. Drainage tube; 11. Limiting ring; 12. Blunt insertion tube. Detailed Implementation
[0023] The technical solutions of the present utility model will be clearly and completely described below with reference to the accompanying drawings of the embodiments. Obviously, the described embodiments are only some embodiments of the present utility model, and not all embodiments. Based on the embodiments of the present utility model, all other embodiments obtained by those of ordinary skill in the art without creative effort are within the protection scope of the present utility model.
[0024] Please see Figure 1-4 An embodiment of this utility model provides: a umbilical cord blood plasma bag expansion and drainage device, including an expansion assembly 1 and a drainage assembly 2. The expansion assembly 1 consists of a drainage tube 10, a limiting ring 11 and a blunt insertion tube 12. The limiting ring 11 is fixedly connected to the top end of the drainage tube 10. The drainage assembly 2 includes an extension conduit 3 and an optional hose 4. A flow control valve 5 is fixedly installed on the optional hose 4. A connection opening 6 is fixedly connected to the end of the optional hose 4. A sealing ring 8 is fixedly connected to the inner side of the connection opening 6. A cryotube 7 is provided below the connection opening 6. Anti-slip texture 9 is provided on the outside of the drainage tube 10.
[0025] The main body of the drainage tube 10 is a cylindrical hollow structure. The blunt insertion tube 12 is connected to the drainage tube 10 in a through manner. The blunt insertion tube 12 adopts a conical blunt head, and the limiting ring 11 is set below the blunt insertion tube 12.
[0026] Specifically, such as Figure 1 and Figure 2As shown, the main body of the drainage tube 10 of the flaring assembly 1 is a cylindrical hollow structure. The anti-slip texture 9 on the surface of the drainage tube 10 can improve the friction of holding the hand during insertion and enhance the stability of insertion. The blunt insertion tube 12 at the top of the drainage tube 10 adopts a conical blunt tip, which is used to insert into the original puncture site of the blood plasma bag and enlarge the aperture to avoid secondary damage or leakage caused by sharp structures. The limiting ring 11 at the bottom of the blunt insertion tube 12 prevents the plasma bag from being damaged due to excessive insertion. The flaring assembly 1, the drainage assembly 2 and the extension catheter 3 are composed of a dedicated drainage channel that is independent of the sampling syringe and does not need to contact the culture bottle, thus eliminating cross-contamination between the sample and the culture medium.
[0027] The drainage tube 10 is connected to the extension tube 3 in a through connection, the extension tube 3 is connected to the optional hose 4 in a through connection, and the flow control valve 5 adopts a press-type clamping structure control valve.
[0028] Specifically, such as Figure 1 and Figure 4 As shown, the flaring assembly 1 can quickly enlarge the original puncture site, and the extension catheter 3 can be directly connected to the target container. The flow control valve 5 on the optional tubing 4 adopts a press-type clamping structure, which can be used to adjust the liquid flow rate, increasing the liquid flow rate by 3 to 5 times. During sampling, the umbilical cord blood flows directly into the interior of the cryotube 7 along the optional tubing 4. The connecting opening 6 is closed and connected to the opening of the cryotube 7, making it less prone to leakage during transportation. The operation can be completed by a single person.
[0029] Both the flaring assembly 1 and the drainage assembly 2 are made of medical-grade polypropylene, and the connecting opening 6 is threadedly connected to the top of the cryotube 7.
[0030] Specifically, such as Figure 1 and Figure 3 As shown, both the flaring assembly 1 and the drainage assembly 2 are made of medical-grade polypropylene. The overall consumable volume of the drainage device is only one-fifth that of a traditional syringe, reducing the cost by more than 60%. The blunt insertion tube 12 adopts a conical round head structure design and integrated operation to reduce the number of punctures and reduce the risk of occupational exposure.
[0031] Working principle: First, connect the 1.8ml cryotube 7 to the connection opening 6 at the bottom of the optional tubing 4. Then, use the flaring assembly 1 to insert it into the umbilical cord blood plasma bag. The main body of the drainage tube 10 of the flaring assembly 1 is a cylindrical hollow structure. The anti-slip texture 9 on the surface of the drainage tube 10 can improve the friction of holding the hand during insertion and enhance the stability of insertion. The blunt insertion tube 12 at the top of the drainage tube 10 adopts a conical blunt tip, which is used to insert into the original puncture site of the blood plasma bag and enlarge the diameter, avoiding secondary damage or leakage caused by sharp structures. The limiting ring 11 at the bottom of the blunt insertion tube 12 prevents the plasma bag from being damaged due to excessive insertion. The flaring assembly 1, drainage assembly 2 and extension catheter 3 are composed of a dedicated drainage channel that is independent of the sampling syringe, does not need to contact the culture bottle, and eliminates cross-contamination between the sample and the culture medium. The plasma inside the plasma bag flows through the dedicated drainage channel. The flow channel enters the cryotube 7 for sampling. Both the flaring assembly 1 and the drainage assembly 2 are made of medical-grade polypropylene. The overall consumable volume of the drainage device is only one-fifth that of a traditional syringe, reducing costs by more than 60%. The blunt insertion tube 12 adopts a conical round head structure design and integrated operation to reduce the number of punctures and reduce occupational exposure risks. The flaring assembly 1 can quickly enlarge the original puncture site, and the extension catheter 3 can be directly connected to the target container. The flow control valve 5 on the optional tubing 4 adopts a press-type clamping structure, which can be used to adjust the liquid flow rate, increasing the liquid flow rate by 3 to 5 times. During sampling, umbilical cord blood flows directly into the cryotube 7 through the optional tubing 4. The connecting opening 6 is closed to the opening of the cryotube 7, making it less prone to leakage during delivery. The operation can be completed by a single person. This structure achieves convenient and efficient operation.
[0032] It will be apparent to those skilled in the art that this invention is not limited to the details of the exemplary embodiments described above, and that it can be implemented in other specific forms without departing from the spirit or essential characteristics of this invention. Therefore, the embodiments should be considered illustrative and non-limiting in all respects, and the scope of this invention is defined by the appended claims rather than the foregoing description. Thus, it is intended that all variations falling within the meaning and scope of equivalents of the claims be included within this invention. No reference numerals in the claims should be construed as limiting the scope of the claims.
Claims
1. Umbilical cord blood plasma bag flare drainage device comprising a flare assembly (1) and a drainage assembly (2), characterized in that: The flaring assembly (1) consists of a drainage tube (10), a limiting ring (11) and a blunt insertion tube (12). The limiting ring (11) is fixedly connected to the top end of the drainage tube (10). The drainage assembly (2) includes an extension conduit (3) and an optional hose (4). A flow control valve (5) is fixedly installed on the optional hose (4). A connection opening (6) is fixedly connected to the end of the optional hose (4). A sealing ring (8) is fixedly connected to the inside of the connection opening (6). A cryotube (7) is provided below the connection opening (6). Anti-slip texture (9) is provided on the outside of the drainage tube (10).
2. The umbilical cord blood plasma bag flare drainage device according to claim 1, characterized in that: The main body of the drainage tube (10) is a cylindrical hollow structure, and the blunt insertion tube (12) is connected to the drainage tube (10) in a through connection.
3. The umbilical cord blood plasma bag flare drainage device according to claim 1, characterized in that: The blunt insertion tube (12) has a tapered blunt tip, and the limiting ring (11) is located below the blunt insertion tube (12).
4. The umbilical cord blood plasma bag flare drainage device according to claim 1, wherein: The drainage tube (10) and the extension catheter (3) are connected in a continuous manner.
5. The umbilical cord blood plasma bag flare drainage device of claim 1, wherein: The extension conduit (3) is connected in a through manner to the optional hose (4).
6. The umbilical cord blood plasma bag flare drainage device of claim 1, wherein: The flow control valve (5) adopts a press-type clamping structure control valve.
7. The umbilical cord blood plasma bag flare drainage device of claim 1, wherein: Both the flaring component (1) and the drainage component (2) are made of medical-grade polypropylene.
8. The umbilical cord blood plasma bag flare drainage device of claim 1, wherein: The connection opening (6) is threadedly connected to the top end of the freezing tube (7).