CN211270927U - Biological glue suture line for medical cosmetology - Google Patents
Biological glue suture line for medical cosmetology Download PDFInfo
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- CN211270927U CN211270927U CN201921648435.1U CN201921648435U CN211270927U CN 211270927 U CN211270927 U CN 211270927U CN 201921648435 U CN201921648435 U CN 201921648435U CN 211270927 U CN211270927 U CN 211270927U
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- clamping groove
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Abstract
The utility model discloses a biological glue suture line for medical treatment is cosmetic, including the suture group, the one end of suture group is connected with the sewing needle, suture group and sewing needle formula structure as an organic whole, the suture group includes a plurality of intertwine's suture single line, the sewing needle is the crotch form, and the sewing needle is equipped with a plurality of centre gripping banks that are used for the centre gripping. The utility model discloses a plurality of single lines of sewing up twine and constitute the group of sewing up, guarantee the toughness of group of sewing up, prevent to sew up in the fracture, secondly, set up the centre gripping bank of cells at the sewing needle, the convenience is to the centre gripping of sewing up the needle when sewing up, avoids skidding.
Description
Technical Field
The utility model belongs to the field of medical supplies, concretely relates to a biological glue suture line for medical cosmetology.
Background
The medical suture experiences the following history from the development of materials: silk thread, catgut thread, chemical synthetic thread, pure natural collagen suture thread; from the physical form, the fiber can be divided into single fiber and multi-fiber; the suture is divided into two types, namely natural suture (animal tendon suture, catgut suture, silk and cotton silk) and artificial suture (nylon, polyethylene, polypropylene, PGA, stainless steel wire and metal tantalum wire) according to the source of raw materials; from an absorbent perspective, non-absorbent sutures and absorbable sutures were experienced.
Suturing the epidermis, especially the facial skin, with non-absorbent sutures leaves scars. The absorbable suture is particularly important for suturing medical cosmetic eyelid-doubling operations, eyebrow lifting operations, external pouch surgery and the like, the pain of a patient caused by secondary operation is avoided, the infection chance of wounds is reduced, and meanwhile the working efficiency of medical staff is accelerated, so that the absorbable suture is pursued to be used in various plastic surgery operations.
SUMMERY OF THE UTILITY MODEL
An object of the utility model is to provide a biological glue suture line for medical treatment is cosmetic, through the improvement to its structure for biological glue suture line not only can be absorbed by the human body, and secondly, can also play the operation of being convenient for, resumes advantage such as effectual.
In order to solve the above problems existing in the prior art, the utility model discloses the technical scheme who adopts is:
a biological glue suture line for medical cosmetology comprises a suture line group, wherein one end of the suture line group is connected with a suture needle, and the suture line group and the suture needle are of an integrated structure.
The suture group includes a plurality of suture strands entangled with each other.
The suture needle is in a hook shape and is provided with a plurality of clamping groove groups for clamping.
The suture group is formed by winding a plurality of suture single lines, the toughness of the suture group is guaranteed, the suture group is prevented from being broken in sewing, secondly, the suture needle is provided with the clamping groove group, the clamping of the suture needle is convenient when the suture is performed, and the slippage is avoided.
The existing antiskid suture needle carries out antiskid treatment on the surface of the suture needle to roughen the surface of the suture needle, and when the suture needle is used, the surface is not smooth enough, so that tissues are dragged when the suture needle is sutured, and the pain of a patient is increased.
The suture line group and the suture needle are designed into an integrated structure, so that burrs of the suture line group are prevented from being formed during needle threading, and meanwhile, the operation time is effectively saved.
The unitary construction of the suture sets and needles is prior art and is referred to herein directly.
Furthermore, the single suture line is made of the polylactic acid, the single suture line is made of collagen, the polylactic acid is adopted as the single suture line, after suture, the single suture line can be absorbed by a human body, the suture does not need to be removed, and secondary damage is avoided.
Furthermore, the outer side of the single suture line is provided with an antibacterial coating which is a nano-silver antibacterial coating, and the nano-silver antibacterial coating is adopted to release nano-silver particles, so that germs contacting with the nano-silver particles are inhibited and killed, and the effect of promoting skin healing is achieved.
Furthermore, the suture group is connected with a plurality of annular lubricating layers, each lubricating layer comprises a variable-diameter section and an equal-diameter section, the variable-diameter section is arranged on one side, close to the suture needle, of the equal-diameter section, the larger end of the variable-diameter section is connected to the equal-diameter section, the diameter of the smaller end of the variable-diameter section is equal to that of the suture group, the diameter of the larger end of the variable-diameter section is equal to that of the equal-diameter section, through the lubricating layer, the suture group is smooth and easy to penetrate through tissues, the suture time can be shortened, pain of a patient is relieved, the lubricating layers are designed into the variable-diameter section and the equal-diameter section, after the lubricating layer contacts the wound, the thread rope penetrates through the wound, the lubricating layers are blocked by tissues around the wound at the moment and cannot penetrate through the tissue around the wound, and when subsequent suture groups pass through.
Furthermore, the lubricating layer is made of polylactam-calcium stearate.
Further, the suture needle comprises a connecting end connected to the suture group and a puncturing end far away from the suture group, and the diameter of the connecting end is equal to that of the suture group.
Furthermore, the suture needle is an arc-shaped needle, the cross section of the suture needle is circular, the side wall of the suture needle is a smooth curved surface, the clamping groove group is arranged on the side wall of the arc-shaped needle and comprises a first clamping groove group, a second clamping groove group and a third clamping groove group, the third clamping groove group is arranged between the first clamping groove group and the second clamping groove group, the suture needle is conveniently clamped by arranging a plurality of clamping groove groups, and no matter the head part or the tail part of the suture needle is in the tissue, at least one clamping groove group can clamp the suture needle, so that the suture needle is prevented from slipping.
Furthermore, the first clamping groove group comprises two first clamping grooves, the two first clamping grooves are respectively arranged on two opposite sides of the suture needle, the second clamping groove group comprises two second clamping grooves, the two second clamping grooves are respectively arranged on two opposite sides of the suture needle, the third clamping groove group comprises two third clamping grooves, the two third clamping grooves are respectively arranged on two opposite sides of the suture needle, and the clamping grooves are arranged on two opposite sides of the axis of the suture needle, so that the clamping is convenient to carry out during operation.
Furthermore, the first clamping groove and the second clamping groove are arranged on the same side of the axis of the suture needle, the third clamping groove is arranged on a surface different from the first clamping groove and the second clamping groove, multi-angle clamping can be facilitated, the first clamping groove group is rotated by 90 degrees along the axis of the suture needle, and the first clamping groove group and the third clamping groove group are located on the same side of the axis of the suture needle.
The utility model has the advantages that:
(1) the utility model discloses a plurality of single lines of sewing up twine and constitute the group of sewing up, guarantee the toughness of group of sewing up, prevent to sew up in the fracture, secondly, set up the centre gripping bank of cells at the sewing needle, the convenience is to the centre gripping of sewing up the needle when sewing up, avoids skidding.
(2) Sew up the single line and adopt poly levorotatory lactic acid to sew up the single line, sewing up the back, the single line can be absorbed by the human body, need not the stitches that take out, avoids causing the secondary damage.
(3) The utility model discloses a set up the lubricant film, make the suture group more level and smooth, very easily pierce through the tissue, but the time of reducible sewing, alleviate patient's misery, will the lubricant film design is for becoming diameter section and equal diameter section, and after the wound is contacted to the lubricant film, the cotton rope passes the wound, and the lubricant film is blockked by the wound tissue on every side and can't pass this moment, and follow-up suture group is through, is lubricated by the lubricant film for the suture group is more level and smooth.
(4) The utility model discloses a set up a plurality of centre gripping banks at the sewing needle, conveniently carry out the centre gripping to the sewing needle, no matter sewing needle head portion still sews up the needle afterbody in organizing, always have at least one centre gripping bank of cells can the centre gripping, avoid sewing the needle and skid.
Drawings
Fig. 1 is a schematic structural view of the present invention;
FIG. 2 is an enlarged view of a portion of the present invention;
FIG. 3 is an enlarged view of a portion A of FIG. 2;
FIG. 4 is a left side view of FIG. 2;
FIG. 5 is a partial enlarged view of portion B of FIG. 4;
fig. 6 is a schematic structural diagram of a single line in the present invention.
In the figure: 11-group of suture; 111-sewing a single thread; 112-an antimicrobial coating; 12-a variable diameter section; 13-equal diameter section; 2-suture needle; 21-a first clamping groove; 22-a second clamping groove; 23-third clamping groove.
Detailed Description
The present invention will be further explained with reference to the accompanying drawings and reference numerals.
In the present invention, unless otherwise expressly specified or limited, the terms "mounted," "connected," and "fixed" are to be construed broadly and may, for example, be fixedly connected, detachably connected, or integrally connected; can be mechanically or electrically connected; they may be connected directly or indirectly through intervening media, or they may be interconnected between two elements. The specific meaning of the above terms in the present invention can be understood according to specific situations by those skilled in the art.
In the description of the present invention, it should be noted that the terms "center", "upper", "lower", "left", "right", "vertical", "horizontal", "inner", "outer", and the like indicate orientations or positional relationships based on the orientations or positional relationships shown in the drawings, and are only for convenience of description and simplification of description, but do not indicate or imply that the device or element referred to must have a specific orientation, be constructed and operated in a specific orientation, and thus, should not be construed as limiting the present invention. Furthermore, the terms "first," "second," and "third" are used for descriptive purposes only and are not to be construed as indicating or implying relative importance.
The following detailed description of the embodiments of the present invention will be made with reference to the accompanying drawings. It is to be understood that the description of the embodiments herein is for purposes of illustration and explanation only and is not intended to limit the invention.
Example 1:
as shown in fig. 1 and 2, a biological glue suture for medical beauty comprises a suture group 11, a suture needle 2 is connected to one end of the suture group 11, and the suture group 11 and the suture needle 2 are of an integrated structure.
The suture group 11 includes a plurality of suture strands 111 wound around each other.
The sewing needle 2 is in a hook shape, and the sewing needle 2 is provided with a plurality of clamping groove groups for clamping.
The suture group 11 is formed by winding a plurality of suture single lines 111, the toughness of the suture group 11 is guaranteed, the suture is prevented from being broken, secondly, the suture needle 2 is provided with a clamping groove group, the suture needle 2 is conveniently clamped when in suture, and the slippage is avoided.
The existing antiskid suture needle 2 carries out antiskid treatment on the surface of the suture needle 2, so that the surface of the suture needle 2 is roughened, and when the suture needle 2 is used, the surface is not smooth enough, so that tissues are dragged when the suture needle 2 is sutured, and the pain of a patient is increased.
The suture line group 11 and the suture needle 2 are designed into an integral structure, so that burrs of the suture line group 11 are prevented from being formed during needle threading, and meanwhile, the operation time is effectively saved.
Example 2:
as shown in fig. 1 to 3, a biological glue suture for medical beauty comprises a suture group 11, a suture needle 2 is connected to one end of the suture group 11, and the suture group 11 and the suture needle 2 are of an integrated structure.
The suture group 11 includes a plurality of suture strands 111 wound around each other.
The sewing needle 2 is in a hook shape, and the sewing needle 2 is provided with a plurality of clamping groove groups for clamping.
The suture group 11 is formed by winding a plurality of suture single lines 111, the toughness of the suture group 11 is guaranteed, the suture is prevented from being broken, secondly, the suture needle 2 is provided with a clamping groove group, the suture needle 2 is conveniently clamped when in suture, and the slippage is avoided.
The existing antiskid suture needle 2 carries out antiskid treatment on the surface of the suture needle 2, so that the surface of the suture needle 2 is roughened, and when the suture needle 2 is used, the surface is not smooth enough, so that tissues are dragged when the suture needle 2 is sutured, and the pain of a patient is increased.
The suture line group 11 and the suture needle 2 are designed into an integral structure, so that burrs of the suture line group 11 are prevented from being formed during needle threading, and meanwhile, the operation time is effectively saved.
The unitary construction of the suture package 11 and the needle 2 is prior art and is referred to herein directly.
The suture thread 111 is made of collagen.
The outer side of the suture thread 111 is provided with an antibacterial coating 112.
The antibacterial coating 112 is a nano silver antibacterial coating.
The nano silver antibacterial coating is adopted, and nano silver particles are released by utilizing the nano silver antibacterial coating, so that germs contacting with the nano silver particles are inhibited and killed, and the effect of promoting skin healing is achieved.
The suture group 11 is connected with a plurality of annular lubricating layers, each lubricating layer comprises a variable diameter section 12 and an equal diameter section 13, and the variable diameter section 12 is arranged on one side of the equal diameter section 13 close to the suture needle 2.
The larger end of the variable diameter section 12 is connected to the equal diameter section 13, the smaller end of the variable diameter section 12 has a diameter equal to the diameter of the suture set 11, and the larger end of the variable diameter section 12 has a diameter equal to the diameter of the equal diameter section 13.
By providing a lubricating layer, the suture set 11 is smoother and easily penetrates the tissue, thereby shortening the suture time and alleviating the pain of the patient.
The lubricating layer is designed into a variable diameter section 12 and an equal diameter section 13, after the lubricating layer contacts the wound, the thread rope passes through the wound, the lubricating layer is blocked by tissues around the wound and cannot pass through the wound, and when the subsequent suture group 11 passes through the lubricating layer, the thread rope is lubricated by the lubricating layer, so that the suture group 11 is smoother.
The lubricating layer is made of polylactam-calcium stearate.
The suture needle 2 includes a connection end connected to the suture group 11 and a piercing end distant from the suture group 11, and the connection end has a diameter equal to that of the suture group 11.
The sewing needle 2 is an arc-shaped needle, the section of the sewing needle 2 is circular, and the side wall of the sewing needle 2 is a smooth curved surface.
Example 3:
as shown in fig. 1 to 6, a biological glue suture for medical beauty comprises a suture group 11, a suture needle 2 is connected to one end of the suture group 11, and the suture group 11 and the suture needle 2 are of an integrated structure.
The suture group 11 includes a plurality of suture thread lines 111 wound around each other, and the plurality of suture thread lines 111 are wound in a spatial spiral shape.
The sewing needle 2 is in a hook shape, and the sewing needle 2 is provided with a plurality of clamping groove groups for clamping.
The suture group 11 is formed by winding a plurality of suture single lines 111, the toughness of the suture group 11 is guaranteed, the suture is prevented from being broken, secondly, the suture needle 2 is provided with a clamping groove group, the suture needle 2 is conveniently clamped when in suture, and the slippage is avoided.
The existing antiskid suture needle carries out antiskid treatment on the surface of the suture needle 2, so that the surface of the suture needle 2 is roughened, and the surface is not smooth enough, so that tissues are dragged when the suture needle 2 is sutured, and the pain of a patient is increased.
The suture thread group 11 and the suture needle 2 are designed into an integral structure, so that burrs of the suture thread group 11 during threading are avoided, and meanwhile, the operation time is effectively saved.
The unitary construction of the suture package 11 and the needle 2 is prior art and is referred to herein directly.
The suture thread 111 is a poly-L-lactic acid thread.
The single suture line 111 is made of poly-L-lactic acid, after suture, the poly-L-lactic acid single line can be absorbed by a human body, and the suture does not need to be removed, so that secondary damage is avoided.
The outer side of the suture thread 111 is provided with an antibacterial coating 112.
The antibacterial coating 112 is a nano silver antibacterial coating.
The nano silver antibacterial coating is adopted, and nano silver particles are released by utilizing the nano silver antibacterial coating, so that germs contacting with the nano silver particles are inhibited and killed, and the effect of promoting skin healing is achieved.
The suture group 11 is connected with a plurality of annular lubricating layers, each lubricating layer comprises a variable diameter section 12 and an equal diameter section 13, and the variable diameter section 12 is arranged on one side of the equal diameter section 13 close to the suture needle 2.
The larger end of the variable diameter section 12 is connected to the equal diameter section 13, the smaller end of the variable diameter section 12 has a diameter equal to the diameter of the suture set 11, and the larger end of the variable diameter section 12 has a diameter equal to the diameter of the equal diameter section 13.
By providing a lubricating layer, the suture set 11 is smoother and easily penetrates the tissue, thereby shortening the suture time and alleviating the pain of the patient.
The lubricating layer is designed into a variable diameter section 12 and an equal diameter section 13, after the lubricating layer contacts the wound, the thread rope passes through the wound, the lubricating layer is blocked by tissues around the wound and cannot pass through the wound, and when the subsequent suture group 11 passes through the lubricating layer, the thread rope is lubricated by the lubricating layer, so that the suture group 11 is smoother.
The lubricating layer is made of polylactam-calcium stearate.
The suture needle 2 includes a connection end connected to the suture group 11 and a piercing end distant from the suture group 11, and the connection end has a diameter equal to that of the suture group 11.
The sewing needle 2 is an arc-shaped needle, the section of the sewing needle 2 is circular, and the side wall of the sewing needle 2 is a smooth curved surface.
The clamping groove group is arranged on the side wall of the arc-shaped needle and comprises a first clamping groove group, a second clamping groove group and a third clamping groove group, and the third clamping groove group is arranged between the first clamping groove group and the second clamping groove group.
Through set up a plurality of centre gripping groove groups at sewing needle 2, conveniently carry out the centre gripping to sewing needle 2, no matter 2 heads of sewing needle or 2 afterbody of sewing needle organize, always have at least one centre gripping groove group can the centre gripping, avoid sewing needle 2 to skid.
The first clamping groove group comprises two first clamping grooves 21, and the two first clamping grooves 21 are respectively arranged on two opposite sides of the suture needle 2.
The second clamping groove group comprises two second clamping grooves 22, and the two second clamping grooves 22 are respectively arranged on two opposite sides of the suture needle 2.
The third clamping groove group comprises two third clamping grooves 23, and the two third clamping grooves 23 are respectively arranged on two opposite sides of the suture needle 2.
The clamping grooves are arranged on two opposite sides of the axis of the suture needle 2, so that the suture needle is convenient to clamp during operation.
The first holding groove 21 and the second holding groove 22 are provided on the same side of the axis of the suture needle 2.
The third clamping groove 23 is provided on a different surface from the first clamping groove 21 and the second clamping groove 22, which facilitates multi-angle clamping.
The first holding groove 21 group is rotated 90 degrees along the axis of the sewing needle 2, that is, the third holding groove 23 group is positioned on the same side of the axis of the sewing needle 2.
The specific working principle is as follows:
when the device is used, the clamping groove is clamped through an instrument, the stability of the suture needle 2 is guaranteed, the suture needle 2 penetrates through tissues to be sutured, the suture line group 11 penetrates through the tissues, the lubricating layer is blocked and cannot penetrate through the tissues along with the suture line group 11, the subsequent suture line group 11 is lubricated by the lubricating layer when passing through, the smoothness of the suture line group 11 is guaranteed, and the suture line group can smoothly penetrate through the tissues. After the suture is finished, the antibacterial coating 112 releases the nano silver particles for sterilization, which is beneficial to wound recovery, and finally the suture group 11 is absorbed by the human body without removing the suture.
The present invention is not limited to the above-mentioned optional embodiments, and any other products in various forms can be obtained by anyone under the teaching of the present invention, and any changes in the shape or structure thereof, all the technical solutions falling within the scope of the present invention, are within the protection scope of the present invention.
Claims (8)
1. A biogel suture for medical cosmetology, characterized in that: the novel sewing machine comprises a sewing thread group (11), wherein one end of the sewing thread group (11) is connected with a sewing needle (2), and the sewing thread group (11) and the sewing needle (2) are of an integrated structure;
the suture group (11) includes a plurality of intertwined suture strands (111);
the suture needle (2) is in a hook shape, and the suture needle (2) is provided with a plurality of clamping groove groups for clamping.
2. A biogel suture for medical cosmetology according to claim 1, characterized in that: the suture single thread (111) is a poly-L-lactic acid single thread.
3. A biogel suture for medical cosmetology according to claim 2, characterized in that: the outer side of the suture single line (111) is provided with an antibacterial coating (112).
4. A biogel suture for medical cosmetology according to claim 1, characterized in that: the suture needle (2) comprises a connecting end connected to the suture group (11) and a puncturing end far away from the suture group (11), and the diameter of the connecting end is equal to that of the suture group (11).
5. A biogel suture for medical cosmetology according to claim 4, characterized in that: the sewing needle (2) is an arc-shaped needle, the section of the sewing needle (2) is circular, and the side wall of the sewing needle (2) is a smooth curved surface.
6. A biogel suture for medical cosmetology according to claim 5, characterized in that: the clamping groove group is arranged on the side wall of the arc-shaped needle and comprises a first clamping groove group, a second clamping groove group and a third clamping groove group, and the third clamping groove group is arranged between the first clamping groove group and the second clamping groove group.
7. A biogel suture for medical cosmetology according to claim 6, characterized in that: the first clamping groove group comprises two first clamping grooves (21), and the two first clamping grooves (21) are respectively arranged at two opposite sides of the suture needle (2);
the second clamping groove group comprises two second clamping grooves (22), and the two second clamping grooves (22) are respectively arranged at two opposite sides of the suture needle (2);
the third clamping groove group comprises two third clamping grooves (23), and the two third clamping grooves (23) are respectively arranged on two opposite sides of the suture needle (2).
8. A biogel suture for medical cosmetology according to claim 7, characterized in that: the first clamping groove (21) and the second clamping groove (22) are arranged on the same side of the axis of the suture needle (2).
Priority Applications (1)
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CN201921648435.1U CN211270927U (en) | 2019-09-29 | 2019-09-29 | Biological glue suture line for medical cosmetology |
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CN201921648435.1U CN211270927U (en) | 2019-09-29 | 2019-09-29 | Biological glue suture line for medical cosmetology |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115844477A (en) * | 2022-11-22 | 2023-03-28 | 中国人民解放军总医院第六医学中心 | Achilles tendon sewing tool |
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2019
- 2019-09-29 CN CN201921648435.1U patent/CN211270927U/en active Active
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115844477A (en) * | 2022-11-22 | 2023-03-28 | 中国人民解放军总医院第六医学中心 | Achilles tendon sewing tool |
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