Multifunctional needle assembly for skin operation
By designing a multifunctional needle assembly including a suction adapter, injection joint and adjustment part, the problems of drug leakage and over-applied in the prior art are solved, and efficient injection of drugs and skin cleaning are achieved.
Patent Information
- Application Number
- CN202421816582.6
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-07-30
- Publication Date
- 2025-06-27
- Estimated Expiration
- 2034-07-30
AI Technical Summary
In existing skin surgery, the multi-needle assembly will leak medication before the needle protrudes to the skin, causing the medication to be over-applied onto the skin, and the medication will leak to the outside before the needle is inserted into the skin, causing waste of medication.
A multifunctional needle assembly is designed, including a suction adapter, injection joint and adjustment section. The suction adapter prevents the drug from leaking before the needle is inserted into the skin through the partition wall and needle holder structure; the injection joint is connected through close contact and threaded connection to ensure that the drug is only injected when the needle is inserted into the skin; the adjustment part is connected through threaded connection to adjust the protruding length of the needle to control the depth of the drug injection.
It effectively prevents the drug from leaking through the syringe before the operation, avoids excessive application of the drug on the skin, realizes a comfortable surgical process, and reduces waste of drugs. At the same time, it inhales and discharges blood and other liquids from the skin through the inhalation port, keeping the skin clean.
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Figure CN223026530U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the technical field of medical devices, in particular to a multifunctional needle assembly for skin surgery. Background Art
[0002] Generally, a surgical method of perforating a plurality of fine holes in the skin to allow drugs, etc. to enter the body (hereinafter referred to as "porous surgical method") can eliminate various skin problems such as wrinkles, moles, scars, striae distensae, acne, freckles, pigmentation, etc., maintain hair health, improve hair loss, and is applicable to obesity treatment, etc.
[0003] This porous surgical method utilizes the self-generating force of damaged skin tissue to cause the skin to grow new flesh or allow drugs, etc. to penetrate into the body through fine holes, thereby achieving a rapid surgical effect.
[0004] The inventor of the present application has applied for a Korean patent for an injection device for skin surgery, with the application number 10-2019-0003802. In this patent, a cylinder combined with a needle is moved by being threadedly connected to a suction adapter, and the exposed length of the needle is adjusted by rotation, so that the depth of the needle on the skin can be accurately adjusted.
[0005] However, in the conventional multi-needle assembly for skin surgery, drugs flow out before the needles protrude into the skin, so that they are overly smeared on the skin, causing inconvenience to patients. Also, before the needles protrude or before the needles are inserted into the skin, in a state where the drugs are not injected into the skin, the drugs supplied from the needles flow into the inside of the suction adapter and leak to the outside through the gaps at the combined part of the main body threadedly combined with the suction adapter, resulting in waste of drugs. Summary of the Utility Model
[0006] The purpose of the utility model is to provide a multifunctional needle assembly for skin surgery to solve the problems in the above-mentioned background art.
[0007] To solve the above technical problems, the technical solution adopted by the utility model is as follows:
[0008] A multifunctional needle assembly for skin surgery includes a suction adapter, an injection joint part, and an adjustment part.
[0009] The suction adapter includes a main body with openings at both ends and a partition wall. The main body includes a needle insertion section and a fastening pipe section. The partition wall is arranged inside the needle insertion section. A needle holder and a suction hole are arranged on the partition wall. A needle hole is arranged on the needle holder. An air suction port is arranged on the side wall of the needle insertion section.
[0010] The injection joint portion includes an introduction tube body, a support plate, and a side plate. A needle member is provided on one side of the support plate, and the side plate is provided on the other side of the support plate. The side plate is in close contact with the inner peripheral surface of the fastening tube body section, and the side of the side plate away from the support plate is connected to the introduction tube body;
[0011] The injection joint portion is inserted into one end of the aspiration adapter, and the needle member is inserted into the needle holder, and the support plate is adapted to the needle holder;
[0012] The adjustment portion is provided on the outer peripheral surface of the fastening tube body section, and the adjustment portion can adjust the length of the needle member protruding in the needle holder.
[0013] Further, the adjustment portion is annular and is connected to the fastening tube body section by a thread.
[0014] Further, a blocking wall is provided between the through hole of the suction port and the needle holder.
[0015] Further, a positioning protrusion is provided at one end of the adjustment portion away from the needle insertion section, and a positioning groove adapted to the positioning protrusion is provided on the side plate.
[0016] Further, the adjustment portion is annular with a blocking plate, and the injection joint portion is inserted into the aspiration adapter through the blocking plate.
[0017] Further, the injection joint portion is threadedly connected to the blocking plate.
[0018] Further, an inlet is provided on the side of the introduction tube body away from the side plate, and the inlet is connected to the discharge port of the syringe.
[0019] Further, an airtight device is provided at a position on the side plate close to the needle holder.
[0020] Further, the airtight device is a sealing ring, and the sealing ring is connected to the outer surface of the side plate and also to the inner surface of the fastening tube body section.
[0021] Further, the suction port is connected to a suction device through a suction hose, the end of the suction hose is connected to a suction motor, and a filter is installed on the suction hose.
[0022] Beneficial effects:
[0023] The utility model can improve the sealing structure of the needle assembly, prevent the leakage of liquid medicine through the needle tube before the operation, prevent the excessive application of the medicine on the skin, thereby realizing a comfortable operation, prevent the waste of the medicine, and provide that during the operation of injecting the medicine into the subcutaneous tissue through the needle tube, the liquid such as blood flowing out of the skin is inhaled and discharged through the suction port, and it can be satisfactory by preventing skin residues. Description of the Drawings
[0024] Figure 1 is a perspective view of a multi-needle assembly for skin surgery according to the first embodiment of the utility model.
[0025] Figure 2 is an exploded perspective view of a multi-needle assembly for skin surgery according to the first embodiment of the utility model.
[0026] Figure 3 is a perspective view of a multi-needle assembly for skin surgery according to the first embodiment of the utility model observed from the front.
[0027] Figure 4 is a cross-sectional view of a multi-needle assembly for skin surgery according to the first embodiment of the utility model.
[0028] Figure 5 is an exploded perspective view of a multi-needle assembly for skin surgery according to the second embodiment of the utility model.
[0029] Figure 6 is a cross-sectional view of a multi-needle assembly for skin surgery according to the second embodiment of the utility model.
[0030] Figure 7 is a suction device connected to the multi-needle assembly for skin surgery of the utility model.
[0031] Wherein: A, multi-needle assembly; W, internal accommodation space; T, suction device;
[0032] 100, syringe; 110, discharge port;
[0033] 2, suction adapter; 20, multiple needles; 200, main body; 202, front end opening; 210, side wall; 22, needle holder; 220, needle hole; 24, suction port; 240, through hole; 25, blocking wall; 26, partition wall; 260, suction hole; 27, suction hose; 270, fastening tube section; 272, second thread; 28, suction motor; 29, filter; 30, drain pipe;
[0034] 4, injection joint; 40, introduction tube body; 42, support plate; 44, side plate; 402, introduction port; 403, third thread;
[0035] 5, airtight device;
[0036] 6. Adjusting part; 603. First thread; 62. Insertion port; 64. Baffle plate; 640. Connection hole. Detailed implementation mode
[0037] In the description of the present utility model, it should be noted that the orientation or positional relationship indicated by terms such as "front", "rear", "inner", etc. is based on the orientation or positional relationship shown in the drawings. It is only for the convenience of describing the present utility model and simplifying the description, rather than indicating or implying that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation. Therefore, it should not be construed as a limitation to the present utility model. In addition, unless otherwise clearly specified and defined, terms such as "installation" and "connection" should be understood in a broad sense. For example, it can be a fixed connection, a detachable connection, or an integral connection; it can be directly connected, indirectly connected through an intermediate medium, or the communication inside two elements. For those of ordinary skill in the art, the specific meanings of the above terms in the present utility model can be understood according to specific situations.
[0038] In addition, unless otherwise specified, the components used in the following embodiments are all existing components, and their corresponding connection methods can also be realized by conventional technical means, which will not be elaborated one by one in this application.
[0039] The present utility model will be further described in detail below in conjunction with the drawings and specific implementation modes.
[0040] Embodiment
[0041] Embodiment 1
[0042] A multifunctional needle assembly for skin surgery, as Figures 1 to 4 shown, the multi-needle assembly A includes a suction adapter 2, an injection joint part 4, and an adjusting part 6.
[0043] The suction adapter 2 includes a main body 200 with openings at both ends and a partition wall 26. The main body 200 includes a needle insertion section and a fastening tube section 270. A partition wall 26 is arranged inside the needle insertion section. A needle holder 22 and a suction hole 260 are arranged on the partition wall 26. A needle hole 220 is arranged on the needle holder 22. An air suction port 24 is arranged on the side wall 210 of the needle insertion section.
[0044] Specifically, the suction adapter 2 forms an internal accommodation space W through the side wall 210. A partition wall 26 is arranged inside the internal accommodation space W. A plurality of conical needle holders 22 are arranged on the partition wall 26, and the needle holders 22 are also accommodated inside the internal accommodation space W. Needle holes 220 are arranged inside the needle holders 22 for inserting a plurality of needle members 20 respectively. A plurality of suction holes 260 are also arranged on the partition wall 26. The needle holders 22 and the suction holes 260 are arranged at intervals. Residual drugs or blood (hereinafter referred to as "liquid") on the skin can be sucked through the needle holes 220 and the suction holes 260. During use, the front end opening 202 of the main body 200 is in close contact with the skin, so that a space capable of sucking pressure is formed between the front end opening 202 and the internal partition wall 26 of the main body 200. Therefore, when a suction pressure is formed between the front end opening 202 and the skin, during the surgical process of inserting the needle member 20 into the skin and injecting drugs, the liquid flowing out will remain inside the front end opening 202 or in the internal space behind the partition wall 26, that is, on the side far from the front end opening 202, and then is sucked out through the suction port 24. Among them, the suction adapter 2 can be cylindrical tubular or rectangular tubular.
[0045] The injection joint part 4 includes an introduction tube body 40, a support plate 42 and a side plate 44. A needle member is arranged on one side of the support plate 42, and a side plate 44 is arranged on the other side of the support plate 42. The side plate 44 is in close contact with the inner peripheral surface of the fastening tube body section 270, and the side of the side plate 44 away from the support plate 42 is connected to the introduction tube body 40. The injection joint part 4 is inserted at one end of the suction adapter 2, and the needle member is inserted into the needle holder 22, and the support plate 42 is adapted to the needle holder 22.
[0046] Specifically, the injection joint part 4 is inserted into the internal accommodation space W from the end of the suction adapter 2 away from the front end opening 202, and can be adapted to the needle holder 22 through the support plate 42, wherein the needle member 20 on the support plate 42 is inserted into the needle holder 22 to complete the injection.
[0047] An adjustment part 6 is arranged on the outer peripheral surface of the fastening tube body section 270. The adjustment part 6 can adjust the length of the needle member 20 protruding in the needle holder 22 to adjust the injection depth of the needle member 20.
[0048] Preferably, in this embodiment, the adjustment part 6 is annular, is connected to the fastening tube body section 270 by thread, and a positioning protrusion is arranged at the end of the adjustment part 6 away from the needle member insertion section, and a positioning groove adapted to the positioning protrusion is arranged on the side plate 44.
[0049] Specifically, a first thread 603 is provided on the inner surface of the adjusting portion 6, and a second thread 272 adapted to the first thread 603 is provided on the outer surface of the fastening pipe body section 270. Moreover, the side plate 44 of the adjusting portion 6 and the injection joint portion 4 are fixedly connected through positioning protrusions and positioning grooves. Therefore, by rotating the adjusting portion 6, the suction adapter 2 can be moved away from or closer to the injection joint portion 4 to achieve the protruding length of the needle member 20 at the front end outlet 202.
[0050] Preferably, a blocking wall 25 is provided between the through hole 240 of the air inlet port 24 and the needle holder 22. Specifically, one end of the blocking wall 25 is connected to the outer surface of the needle holder 22, and the other end is connected to the inner surface of the main body 200, which can block the through hole 24 of the air inlet port 24 from communicating with the internal accommodation space W, thus serving as a pipeline for moving the drug. During operation, the drug is inhaled through the inhalation hole 260, moves along the internal flow path, and is inhaled and discharged through the upper air inlet port 24. Due to the obstruction of the blocking wall 25, direct inhalation around the through hole 240 of the air inlet port 24 is avoided, thereby preventing the liquid from concentrating around the through hole 240.
[0051] Preferably, an inlet 402 is provided on the side of the introducing pipe body 40 away from the side plate 44, and the inlet 402 is connected to the discharge port 110 of the syringe 100. Specifically, the introducing pipe body 40 is connected to the syringe 100 to complete the injection work.
[0052] Preferably, an airtight device 5 is provided at the position of the side plate 44 close to the needle holder 22. The airtight device 5 can be a sealing ring, which is connected to the outer surface of the side plate 44 and also to the inner surface of the fastening pipe body section 270.
[0053] Preferably, as Figure 7 shown, the air inlet port 24 is connected to the suction device T through a suction hose 27. The end of the suction hose 27 is connected to a suction motor 28, and a filter 29 is installed on the suction hose 27. Specifically, the air inlet port 24 protrudes from the outer surface of the suction adapter 2 and communicates with the internal accommodation space W through the through hole 240. The suction device T is connected to the air inlet port 24 of the suction adapter 2 through the suction hose 27. The suction motor 28 can generate negative pressure to complete the suction work, and the filter 29 can filter foreign substances such as drugs. The filtered air is discharged through the drain pipe 30, and finally, the leaked drug during the operation is recovered through the filter 29. When the unfiltered foreign substances in the filter 29 accumulate on one side of the suction motor 28, causing the negative pressure to weaken, at this time, clean water can be sucked into the suction hose 27, and the clean water flows out through the drain pipe 30 to complete the cleaning and restore the normal negative pressure.
[0054] Usage process: First, insert the injection joint part 4 into and connect it to the inside of the aspiration adapter 2. Then, insert the adjustment part 6 through the fastening tube body section 270 of the aspiration adapter 2. The introduction tube body 40 of the injection joint part 4 is connected to the discharge port 110 of the syringe 100 to complete the preparation work. During injection, by rotating the adjustment part 6, the aspiration adapter 2 moves back and forth, so as to finely adjust the protruding length of the needle part 20 relative to the front end opening 202. Inject the drug through the syringe 100. With the aspiration adapter 2 closely attached to the skin, the needle part 20 will protrude and penetrate the skin, so that the drug is injected into the skin from the port of the needle part 20. During the operation, the drug will flow out of the skin again, and at the same time, the drug will remain on the skin in a state of being mixed with blood. In order to remove these liquids, start the aspiration motor 28, so that the aspiration hose 27 connected to the aspiration port 24 generates negative pressure to suck out the excess drug remaining on the skin.
[0055] Embodiment 2
[0056] As Figure 5 And Figure 6 shown, the difference from Embodiment 1 is that the method of adjusting the protruding length of the adjustment needle part 20 relative to the front end outlet 202 in this embodiment is different.
[0057] In this embodiment, the adjustment part 6 is a ring with a baffle plate 64. The injection joint part 4 passes through the baffle plate 64 and is inserted into the aspiration adapter 2, and the injection joint part 4 is threadedly connected to the baffle plate 64.
[0058] Specifically, the adjustment part 6 is inserted through the insertion port 602 on the outer periphery of the fastening tube body section 207 of the aspiration adapter 2. A connection hole 640 is provided on the baffle plate 64. The injection joint part 4 passes through the connection hole 640 and is inserted into the inside of the aspiration adapter 2 to be adapted to the needle holder 22. A third thread 403 is provided on a section of the injection joint part 4 in contact with the connection hole 640, and a fourth thread adapted to the third thread is provided on the surface of the connection hole 640 in contact with the injection joint part 4. Therefore, the injection joint part 4 can be moved back and forth by rotation to realize the protruding length of the needle part 20 relative to the front end outlet 202.
[0059] Although the embodiments of the present invention are described in the specification, these embodiments are only for reference and should not limit the protection scope of the present invention. All kinds of omissions, substitutions and changes within the scope not departing from the gist of the present invention should be included in the protection scope of the present invention.
Claims
1. A multifunctional needle assembly for skin surgery, characterized in that: It includes a suction adapter, an injection joint and an adjustment part. The suction adapter comprises a main body with openings at both ends and a partition wall, the main body comprises a needle insertion section and a fastening tube section, the partition wall is arranged inside the needle insertion section, a needle holder and a suction hole are arranged on the partition wall, a needle holder is arranged with a needle hole, and a suction port is arranged on the side wall of the needle insertion section; The injection joint comprises an introduction tube body, a support plate and a side plate, a needle is arranged on one side of the support plate, the side plate is arranged on the other side of the support plate, the side plate is in close contact with the inner circumference of the fastening tube body section, and the side of the side plate away from the support plate is connected to the introduction tube body; The injection joint is inserted into one end of the suction adapter, and the needle is inserted into the needle holder, and the support plate is adapted to the needle holder; The outer circumferential surface of the fastening tube section is provided with the adjusting portion, and the adjusting portion can adjust the protruding length of the needle in the needle holder.
2. The multifunctional needle assembly for skin surgery according to claim 1, characterized in that: The adjusting portion is annular and is connected to the fastening pipe body section via threads.
3. The multifunctional needle assembly for skin surgery according to claim 2, characterized in that: A blocking wall is arranged between the through hole of the suction port and the needle holder.
4. The multifunctional needle assembly for skin surgery according to claim 2, characterized in that: A positioning protrusion is arranged at one end of the adjusting portion away from the needle insertion section, and a positioning groove matched with the positioning protrusion is arranged on the side plate.
5. The multifunctional needle assembly for skin surgery according to claim 1, characterized in that: The adjusting portion is in a ring shape with a blocking plate, and the injection coupling portion passes through the blocking plate and is inserted into the suction adapter.
6. The multifunctional needle assembly for skin surgery according to claim 5, characterized in that: The injection joint is connected to the blocking plate via threads.
7. The multifunctional needle assembly for skin surgery according to claim 1, characterized in that: An introduction port is arranged on a side of the introduction tube body away from the side plate, and the introduction port is connected to the discharge port of the syringe.
8. The multifunctional needle assembly for skin surgery according to claim 1, characterized in that: An airtight device is arranged at a position of the side plate close to the needle holder.
9. The multifunctional needle assembly for skin surgery according to claim 8, characterized in that: The airtight device is a sealing ring, which is connected to the outer surface of the side plate and also connected to the inner surface of the fastening pipe body section.
10. The multifunctional needle assembly for skin surgery according to claim 1, characterized in that: The suction port is connected to the suction device through a suction hose, the end of the suction hose is connected to a suction motor, and a filter is installed on the suction hose.