CN211534616U - Plugging device and system - Google Patents

Abstract

The utility model relates to a plugging device and system, the plugging device includes the body, the body is including design silk and spring coil, the metal wire of design silk for having the resilience to be configured to have predetermined shape, the spring coil cover is established on the design silk, so that the body forms predetermined shape. The shaping wire is used for restraining the shape of the body, so that the body can effectively block a laceration in the treatment of the aortic dissection.

Description

Plugging device and system

Technical Field

The utility model relates to the technical field of medical equipment, concretely relates to plugging device and system.

Background

Aortic Dissection (AD) refers to a state in which blood in the aortic lumen enters the aortic media from the aortic intimal tear to separate the media, and expands along the major axis of the aorta to separate the two true and false lumens of the aortic wall. AD is a cardiovascular acute disease, has the advantages of acute onset, rapid progress and extremely high mortality rate. Currently, endovascular aortic angioplasty (EVAR) is the most widely used treatment for AD in the clinic. The EVAR adopts the principle that an implant is sent into an aorta, the primary laceration is blocked in the aorta cavity by utilizing the implant, so that the blood flow in a false cavity is slowed down or even disappears to form thrombosis, and the thrombosis is gradually organized and absorbed so as to recover the true cavity form, namely the blood supply of visceral arteries, and finally the aim of aortic remodeling is achieved. Compared with other treatment means (such as open surgery), the EVAR has the advantages of small trauma, low perioperative mortality, quick recovery and the like.

Theoretically, after the primary laceration is blocked in the aorta main lumen, the blood flow entering the false lumen from the primary laceration disappears, the pressure in the false lumen is suddenly reduced, the compression on the main lumen is also reduced, the false lumen is gradually thrombosed and organized to be absorbed along with the time, and the shape of the main lumen can be recovered. However, in actual treatment, the aorta of some AD patients cannot be ideally reshaped after the EVAR is performed, the main reason is that the EVAR only blocks the primary laceration near the heart end, and most AD patients often have multiple concurrent lacerations, and most of the lacerations are located around the visceral artery (i.e. the lacerations are most of the distal lacerations). At present, the treatment methods for the far-end crevasses mainly include: (1) adding an implant to close the distal laceration; (2) aortic replacement; (3) conservative treatment, close observation. The treatment (1) may cause insufficient blood supply in visceral areas and endanger the life of patients, the treatment (2) has high risks of postoperative mortality and paraplegia, and the treatment (3) causes poor postoperative dilatation of the true lumen of the distal aorta, continuous perfusion of the false lumen, and serious influence on benign remodeling of the distal aorta and late prognosis of patients.

For AD, the ideal operation mode is to repair the whole-course laceration of the aorta and promote the thrombopoiesis of the false cavity, and the plugging device is widely used for plugging the distal laceration in the prior art. The occluder treatment belongs to the targeted treatment in the intracavity treatment field, aims to isolate the breach without influencing the blood supply of the adjacent important branch artery, and has lower probability of the ischemia and organ infarction of the important branch artery after operation, so the occluder has a plurality of advantages in the AD treatment aspect, and has wide clinical application value. However, the occluder for occluding lacerations in the prior art has many problems, for example, the occluder has loose form after being released, the occlusion effect is not good, and the occluder is not fixed by a fixing device in the blood vessel, so that the occluder is displaced under the impact of blood flow, and the occlusion purpose cannot be realized.

SUMMERY OF THE UTILITY MODEL

An object of the utility model is to provide a plugging device and system, this plugging device can keep predetermined form after the release to ensure the shutoff effect, promote false chamber and tie, realize remodeling in real chamber.

In order to achieve the above object, the utility model provides a pair of occluder, which comprises a body, the body includes stock wire and spring coil, the metal wire of stock wire for having the resilience to be configured to have predetermined shape, the spring coil cover is established on the stock wire, so that the body forms predetermined shape.

Optionally, the occluder further comprises an anchoring mechanism, the anchoring mechanism is connected with one end of the sizing wire, the anchoring mechanism can wind the axis of the sizing wire to rotate, and the anchoring mechanism is used for fixing the body on a target object.

Optionally, the sizing wire is coiled into a continuous curvilinear structure to form the predetermined shape.

Optionally, the predetermined shape is a spiral, the sizing wire being helically wound along an axis to form the spiral.

Optionally, the predetermined shape is a conical shape, the sizing wire is wound into a plurality of arc-shaped sections which are connected in sequence, in the axial direction of the conical shape, the plurality of arc-shaped sections are arranged in sequence, and two adjacent arc-shaped sections are eccentrically arranged.

Optionally, the body has a first end and a second end opposite to each other in the axial direction of the cone, the radial cross section of the cone gradually increases along the direction from the first end to the second end, the radial dimension of each arc segment gradually increases, and the anchoring mechanism is arranged on the second end.

Optionally, the predetermined shape is spherical or hexahedral.

Optionally, the anchoring mechanism includes a positioning portion, the positioning portion is a barb or a fixed disk, and the positioning portion is used for being connected with the target object.

Optionally, the positioning part is provided with a tip structure, and the tip structure is used for penetrating into the inner wall of the blood vessel to fix the body.

Optionally, the occluding device further comprises thrombogenic hairs attached to the body.

Optionally, the embolism promotion fluff is wound on the sizing wire and is clamped and fixed by the spring ring.

Optionally, at least two of the embolism promotion villi are arranged on the sizing silk at intervals, and the distance between two adjacent embolism promotion villi in the axis direction of the sizing silk is 5mm-10 mm.

Optionally, the length of the thrombogenic hairs is 15mm-25 mm.

Optionally, the spring ring has an inner diameter of 0.5mm to 1.0 mm.

In order to achieve the above object, the present invention further provides a plugging system, comprising a support and at least one plugging device as described in any one of the preceding claims, said plugging device being connected to said support.

Compared with the prior art, the utility model discloses a plugging device and system have following advantage:

first, aforementioned occluder includes the body, wherein the body is including sizing silk and spring coil, sizing silk is the wire that has the resilience to be configured to have predetermined shape, the spring coil cover is established sizing silk is last, so that the body forms predetermined shape. The shape of the body is kept through the shaping wire, so that the plugging device can effectively plug the crevasses.

Secondly, the occluder further comprises an anchoring mechanism, wherein the anchoring mechanism is made of metal with resilience, and the anchoring mechanism is arranged on the body and used for fixing the body on a target object. The position of the body is fixed by an anchoring mechanism so as to achieve the aim of avoiding the displacement of the body.

Thirdly, the anchoring mechanism is connected with one end of the sizing wire, and the anchoring mechanism can rotate around the axis of the sizing wire so as to counteract the torsion effect generated by the spring ring when the occluder is delivered into the aorta and released.

Drawings

FIG. 1 is a cross-sectional view of a blood vessel in a patient in the region of aortic dissection;

fig. 2 is a schematic structural diagram of the occluder according to the first embodiment of the present invention, in which a ball head is not shown;

FIG. 3 is a schematic view of the occlusion system implanted in the aorta and occluding a laceration according to the first embodiment of the present invention, showing only one occluding device;

fig. 4 is a schematic structural diagram of a shaping wire of the occluder according to the first embodiment of the present invention;

fig. 5 is a schematic structural view of a spring coil of the occluder according to the first embodiment of the present invention, wherein the spring coil is not disposed on the shaping wire;

fig. 6 is a schematic structural diagram of a body of an occluder according to a first embodiment of the present invention;

figure 7 is a schematic view of the occluding device according to the first embodiment of the present invention, wherein the occluding device is shown stretched to a linear configuration and wherein the anchoring mechanism is not shown;

figure 8a is a schematic view of the anchoring mechanism of the occluding device according to the first embodiment of the present invention;

figure 8b is a schematic view of a variant of the anchoring mechanism of the occluding device shown in figure 8 a;

figure 8c is a schematic view of another alternative configuration of the anchoring mechanism of the occluding device shown in figure 8 a;

figure 8d is a schematic view of yet another alternative configuration of the anchoring mechanism of the occluding device shown in figure 8 a;

fig. 9 is a schematic view showing the connection relationship between the anchoring mechanism and the shaping wire of the occluder according to the first embodiment of the present invention;

figure 10 is a schematic view of the anchoring mechanism of the occluding device according to the first embodiment of the present invention connected to the stent;

fig. 11a is a schematic view of the connection between the occluder and the lead-in system according to the first embodiment of the present invention;

fig. 11b is a schematic view of another connection between the occluder and the lead-in system according to the first embodiment of the present invention;

fig. 12 is a schematic structural view of an occluder according to a second embodiment of the present invention;

FIG. 13 is a schematic view of the occlusion system implanted in the aorta and occluding the laceration according to the second embodiment of the present invention, showing only one occluding device;

fig. 14 is a schematic structural view of an occluder according to a third embodiment of the present invention;

FIG. 15 is a schematic view of the occlusion system implanted in the aorta and occluding the laceration according to the third embodiment of the present invention, showing only one occluding device;

fig. 16a is a schematic structural view of an occluder according to a fourth embodiment of the present invention in one direction;

figure 16b is a schematic view of the occluding device shown in figure 16a in another orientation;

figure 16c is a schematic view of the occluding device shown in figure 16a in a further orientation;

FIG. 17 is a schematic view of the occlusion system implanted in the aorta and occluding a laceration according to the fourth embodiment of the present invention, showing only one occluding device;

fig. 18 is a schematic structural view of an occluder according to a fifth embodiment of the present invention;

fig. 19 is a schematic view of the occlusion system implanted in the aorta and occluding the laceration according to the fifth embodiment of the present invention, showing only one occluding device.

[ reference numerals are described below ]:

100-an occluder;

110-a body;

111-shaping wire, 112-spring ring, 113-ball head;

120-an anchoring mechanism;

121-positioning part, 122-tip structure, 123-sleeve pipe, 124-first limiting part;

130-thrombogenic villi;

200-a scaffold;

210-hollow structure;

300-a lead-in device;

310-a disengagement mechanism;

10-true lumen, 20-false lumen, 30-laceration.

Detailed Description

To make the objects, advantages and features of the present invention clearer, the present invention will be described in further detail with reference to the accompanying drawings. It should be noted that the drawings are in simplified form and are not to precise scale, and are provided for convenience and clarity in order to facilitate the description of the embodiments of the present invention.

As used in this specification, the singular forms "a", "an" and "the" include plural referents, and the plural forms "a plurality" includes more than two referents unless the content clearly dictates otherwise. As used in this specification, the term "or" is generally employed in its sense including "and/or" unless the content clearly dictates otherwise, and the terms "mounted," "connected," and "connected" are to be construed broadly, e.g., as meaning either fixedly connected, detachably connected, or integrally connected. Either mechanically or electrically. Either directly or indirectly through intervening media, either internally or in any other relationship. The specific meaning of the above terms in the present invention can be understood according to specific situations by those skilled in the art. The same or similar reference numbers in the drawings identify the same or similar elements.

Herein, the terms "proximal" and "distal" are relative orientations, relative positions, and directions of elements or actions with respect to each other from the perspective of a clinician using the medical device, and although "proximal" and "distal" are not intended to be limiting, the term "proximal" generally refers to the end that is closer to the clinician during normal operation, and the term "distal" generally refers to the end that is first introduced into a patient.

Fig. 1 shows a cross-sectional view of a blood vessel in a patient in the region of aortic dissection. As shown in fig. 1, when aortic dissection occurs in a patient, an aortic intima tears, so that media separates to form a true lumen 10 and a false lumen 20 in a blood vessel, and the true lumen 10 and the false lumen 20 communicate through a laceration 30. An object of the embodiment of the utility model is to provide an occluder, occluder can be used for packing in the treatment of aortic dissection the false chamber 20 and shutoff breach 30 to the separation blood flow gets into the false chamber 20 promotes false chamber 20 thrombopoiesis.

Fig. 2 is a schematic structural diagram of an occluder 100 according to a first embodiment of the present invention. As shown in fig. 2, the occluding device 100 comprises a body 110, wherein the body 110 comprises a sizing wire 111 and a spring coil 112, the sizing wire 111 is a metal wire with resilience and is configured to have a predetermined shape; the spring ring 112 is sleeved on the shaping wire 111.

When the aortic dissection is treated, the body 110 is filled in the prosthetic cavity 20 and blocks the laceration 30. Regard as through the adoption wire that has the resilience the sizing wire 111, and sizing wire 111 is configured into predetermined shape, works as the cover of spring coil 112 is established in order to form on sizing wire 111 when body 110, body 110 also appears to be predetermined shape. During the delivery of the occluding device 100 to the blood vessel, the shape of the body 110 is changed, and after the occluding device 100 is released in the blood vessel, the body 110 is restored to the predetermined shape by the resilient force of the shaping wire 111. That is, the embodiment of the present invention maintains the shape of the body 110 by the shaping wire 111, so that it effectively blocks the laceration 30.

Further, the occluder 100 further comprises an anchoring mechanism 120, the anchoring mechanism 120 is made of metal with resilience, just the anchoring mechanism 120 set up in on the body 110, with the one end of sizing wire is connected, just the anchoring mechanism can wind the axis of sizing wire is rotatory, the anchoring mechanism be used for with the body 110 is fixed in on the target.

Referring with emphasis to fig. 3, the occluding device 100 can be used with a stent 200 for treatment of aortic dissection. When the occluding device 100 and the stent 200 are used together to treat an aortic dissection as shown in figure 3, the stent 200 is used to be positioned in the true lumen 10 and support the true lumen 10 to reduce the compression of the false lumen 20 on the true lumen 10. The occluding device 100 is implanted within the prosthetic cavity 20 and positioned at the breach 30 to reduce or even block blood flow into the prosthetic cavity 20, promoting thrombolysis of the prosthetic cavity 20. The occluding device 100 comprises an anchoring mechanism 120, and the occluding device 100 is connected with the stent 200 through the anchoring mechanism 120. Specifically, the stent 200 has a hollow structure 210, and the anchoring mechanism 120 can be inserted into the hollow structure 210 and connected to the stent 200 (the stent 200 is the target object), so that the occluder 100 is kept at the laceration 30 to position the body 110, and the body 110 is prevented from deviating from the laceration 30 due to blood flow impact, thereby affecting the treatment effect.

The following describes the specific structure and fabrication of the occluding device 100 of the present embodiment.

The shaping wire 111 may be made of shape memory alloy (such as nickel-titanium alloy, copper-nickel alloy, copper-zinc alloy, etc.), cobalt-chromium alloy, or stainless steel. The shaping wire 111 is coiled to have the predetermined shape, and the shaping wire 111 is heat-treated to have the predetermined shape in a natural state. When the sizing wire 111 receives external force, the shape of the sizing wire 111 can be changed, but when the external force is cancelled, the sizing wire 111 can be restored to the predetermined shape.

Preferably, the shaping wire 111 is coiled into a continuous and smooth curve structure, so that when the body 110 is finally formed, the body 110 has no sharp break angle, so as to avoid scratching blood vessels when the blood vessels are implanted and causing secondary damage.

As shown in fig. 5, the spring coil 112 is formed by winding a metal wire into a spring structure along a mandrel and then heat setting both ends of the metal wire. The spring ring 112 can be made of nickel-titanium wire, platinum-tungsten wire, stainless steel wire, etc. According to actual requirements, the outer diameter of the mandrel is 0.5mm-1.0mm, so that the inner diameter of the spring ring 112 is 0.5-1.0 mm.

Then, an acting force is applied to the shaping wire 111 to stretch the shaping wire 111 in a predetermined shape, and then the spring ring 112 is sleeved on the shaping wire 111. After the force is removed, the shaping wire 111 returns to the predetermined shape by its own resilience, thereby obtaining the body 110 with the predetermined shape (i.e., as shown in fig. 6). Preferably, two ends of the spring coil 112 are respectively connected with two ends of the sizing wire 111, so as to prevent the spring coil 112 from unwinding during the release of the occluding device 100.

Further, in the present embodiment, the predetermined shape is a spiral shape. For example, referring to fig. 2 in conjunction with fig. 4, the shaping wire 111 is helically wound around an axis to form a conical helical structure. As such, the body 110 has a first end and a second end opposite to each other along the extension direction of the axis, and the radial cross section of the body 110 gradually increases from the first end to the second end. The anchoring mechanism 120 is disposed on the second end of the body 110, and a ball (not shown in fig. 2 and 4) is disposed on the first end of the body 110. In another implementation, the sizing wire may also be helically wound about an axis to form a cylindrical helical structure (not shown).

The anchoring mechanism 120 may be made of shape memory alloys (e.g., nitinol, copper-nickel alloy, copper-zinc alloy, etc.), cobalt-chromium alloy, or stainless steel, etc. As shown in fig. 8a to 8d, the anchoring mechanism 120 has a positioning portion 121, in some embodiments, as shown in fig. 8a, 8b and 8c, the positioning portion 121 is a barb, and in other embodiments, the positioning portion 121 may be a fixed disk, and the fixed disk may be formed by a plurality of rods bent into a V shape and arranged in sequence around an axis (as shown in fig. 8 d). Of course, the anchoring mechanism 120 may be other structures as long as it can be connected to the bracket 200, and this embodiment is not limited thereto.

Further, as shown in fig. 8c, the positioning portion 121 is further provided with a tip structure 122, and when the positioning portion 121 is connected to the stent 200 and the occluder 100 cannot be positioned at the laceration 30, the tip structure 122 is used for piercing the inner wall of the blood vessel to keep the occluder 100 at the laceration 30.

Will when the vascular is implanted to occluder 100, anchoring mechanism 120 has born great effort, for avoiding anchoring mechanism 120 transmits the effort to spring coil 112 and leads to spring coil 112 is followed break away from on the sizing wire 111, anchoring mechanism 120 preferably with sizing wire 111 connects, and anchoring mechanism 120 can wind the axis of sizing wire 111 is rotatory.

Referring to fig. 9, the anchoring mechanism 120 further includes a sleeve 123, the positioning portion 121 is fixedly disposed on the sleeve 123, and the sleeve 123 has a first inner cavity. The one end of sizing silk 111 is inserted in the first inner chamber of sleeve pipe 123, just be equipped with first spacing portion 124 in the first inner chamber, the tip of sizing silk 111 is equipped with the spacing portion of second (not mark in the picture), the spacing portion of second with first spacing portion 124 cooperatees, so that sizing silk 111 with sleeve pipe 123 keeps relative standstill in the axial, but in circumference, sizing silk 111 with but relative rotation between the sleeve pipe 123. The advantage of this arrangement is that, referring to fig. 3 and 10, after the occluding device 100 is delivered into a blood vessel, the anchoring mechanism 120 needs to be inserted into the hollow structure 210 to connect the anchoring mechanism 120 with the stent 200. And the occluder 100 is when carrying the design silk 111 is stretched straight, releases in the blood vessel behind the occluder 100, the design silk 111 recovers under the effect of its self resilience power to the in-process of predetermined shape, the design silk 111 appears twisting, the sleeve pipe 123 can with it offsets the design silk 111 through relative rotation between the design silk 111 and twists the adverse effect that brings to anchoring mechanism 120's posture adjustment to make anchoring mechanism 120 get into smoothly in the hollow out structure 210 of support 200.

Further, as shown in fig. 2 and 7, the occluding device 100 further comprises thrombogenic hairs 130, and the thrombogenic hairs 130 are attached to the body 110 to increase the filling area of the occluding device 100 and promote thrombopoiesis of the prosthetic cavity 20. The material of the thrombus-promoting floss 130 can be at least one of polyethylene terephthalate (PET), Polyamide (PA), Polyethylene (PE), polypropylene (PP), Polyurethane (PU), polylactic acid (PLA), or other high polymer materials. The polymer material is made into 300-700D fully-drawn or stretch-deformed filament, and then the shaping filament 111 is wound two to three turns and clamped and positioned by two adjacent turns of the spring coil 112, so as to form the thrombogenic hairs 130 (as shown in fig. 7). Further, on the body 110, the thrombogenic piles 130 are arranged at intervals along the axial direction of the sizing filament 111, and the axial distance between two adjacent thrombogenic piles 130 is 5mm-10 mm. In addition, the length of each of the thrombogenic piles 130 (the length of the thrombogenic piles 130 from the connecting point on the shaping wire 111 to the free end of the thrombogenic piles 130) is 15mm to 25 mm.

Referring to fig. 11a, the occluding device 100 is implanted into a blood vessel through an introduction device 300 when performing aortic dissection treatment. The introducer 300 has a second lumen for receiving the occluding device 100, the second lumen extending in the axial direction of the introducer 300 and having opposite proximal and distal ends, wherein the distal end is provided with a release mechanism 310. Upon implantation of the occluding device 100 in a blood vessel, the occluding device 100 is stretched and disposed in the second lumen, and in some embodiments, the ball 113 on the first end of the occluding device 100 is connected to the release mechanism 310 as the occluding device 100 is delivered from the true lumen 10 into the false lumen 20. After the occluder 100 is delivered to the site, the introduction system 300 releases the occluder 100 and releases the connection between the release mechanism 310 and the ball 113. Alternatively, as shown in fig. 11b, in other embodiments, the anchoring mechanism 120 of the occluder 100 is connected to the release mechanism 310 in such a way that the occluder 100 is transported from the prosthetic cavity 20 to the breach 30.

Fig. 12 shows a schematic structural diagram of an occluder 100 according to a second embodiment of the present invention, and only the differences between this embodiment and the first embodiment will be described in the following description, and other structures may have the same configuration as the first embodiment, and thus will not be described herein again.

As shown in fig. 12, in the present embodiment, the shaping wire 111 is wound around the outer contour of a spherical structure (the spherical structure herein includes a spherical structure in a geometric sense and also includes a substantially spherical structure), so that the body 110 has a spherical structure. One end of the sizing wire 111 extends outside the spherical structure to facilitate connection of the anchoring mechanism 120.

As shown in fig. 13, the occluding device 100 provided by the present embodiment can also be used with a stent 200 to treat aortic dissection.

Fig. 14 shows a schematic structural diagram of an occluder 100 according to a third embodiment of the present invention. As shown in fig. 14, the shaping wire 111 is wound to the outer contour of the regular hexahedron structure in this embodiment. As shown in fig. 15, the occluder 100 provided in this embodiment can be used with a stent 200 for treating aortic dissection.

Fig. 16a to 16c show a schematic structural diagram of an occluder 100 according to a fourth embodiment of the present invention. As shown in fig. 16a to 16c, the body 110 of the occluder 100 in this embodiment is generally conical, which is different from the first embodiment in that the shaping wire is bent to form a plurality of sequentially connected arc segments, and the plurality of arc segments are sequentially arranged in the axial direction, and two adjacent arc segments are eccentrically disposed. This has the advantage that there is no large void in the body 110, so that the occluder 100 can better occlude the laceration 30. And, from the first end to the second end, each of the arcuate segments progressively increases in radial dimension such that the arcuate segments of lesser radial dimension are closer to the vessel wall. Further, each of the curved sections is approximately circular, and the smaller the radial dimension of the curved section is, the more difficult the spring coil 112 of the section is to kink when the occluding device 100 is released, which is beneficial to improving the usability of the occluding device 100.

As shown in fig. 17, the occluder 100 provided in the present embodiment can be used together with a stent 200 for aortic dissection treatment.

Fig. 18 shows a schematic structural diagram of an occluder 100 according to a fifth embodiment of the present invention. As shown in fig. 18, the occluding device 100 is a spherical structure which differs from the second embodiment in that a portion of the sizing wire 111 is coiled around the outer contour of the spherical structure and another portion of the sizing wire 111 is coiled in the inner cavity of the spherical structure. One end of the sizing wire 111 extends outside the spherical structure to facilitate connection with the anchoring mechanism 120.

The shaping wire 111 is coiled into a plurality of arc sections, and is a plurality of the arc sections constitute spherical structure. Further, it is preferable that each of the arc-shaped sections is approximately circular. In this embodiment, design silk 111 coils and is spherical structure, and spherical structure's inside also coils design silk 111, works as spring coil 112 cover is established design silk 111 is last in order to constitute during body 110, body 110 does not have great space to be favorable to the separation blood flow. Meanwhile, when the shaping wire 111 with the spherical structure is released, even if the arc-shaped section is twisted, enough space is provided for the twisted arc-shaped section to reverse, and the twisted arc-shaped section is restored to a preset position under the action of the resilience force of the shaping wire 111, so that the whole structure of the body 110 is not influenced, and the plugging effect of the plugging device 100 is ensured.

As shown in fig. 19, the occluder 100 provided in this embodiment can be used together with a stent 200 for aortic dissection treatment.

Based on the aforementioned occluder 100, it is another object of the present invention to provide an occlusion system for aortic dissection treatment. Referring to fig. 3, fig. 13, fig. 15, fig. 17 and fig. 19, the occlusion system includes an occluding device 100 and a stent 200, the stent 200 is positioned in a true lumen 10 and has a hollow structure 210, the occluding device 100 is implanted in a false lumen 20 and positioned at a laceration 30, and an anchoring mechanism 120 on the occluding device 100 is inserted into the hollow structure 210 and connected with the stent 200.

Further, the occlusion system comprises at least one of the occluders 100, and in fact the stent 200 preferably has a length that covers all of the crevasses 30, and the number of the occluders 100 may be equal to the number of the crevasses 30, so that one occluder 100 is provided at each of the crevasses 30 to obstruct blood flow into the prosthetic cavity 20 and promote thrombolysis of the prosthetic cavity 20.

The embodiment of the utility model provides an occluder 100 and system, wherein occluder 100 includes body 110 and anchoring mechanism 120, body 110 includes sizing wire 111 and spring coil 112, sizing wire 111 is the wire that has the resilience to be configured into and have predetermined shape, spring coil 112 cover is established sizing wire 111 is last so that body 110 forms into predetermined shape, anchoring mechanism 120 sets up on body 110 for be connected with target (support 200). Through the resilience of the sizing wire 111, the body 110 can keep a preset shape after being released, so as to ensure the sealing of the lacerated opening 30, and meanwhile, the anchoring mechanism 120 is used for positioning the sealing device 100 at the lacerated opening 30, so that the sealing effect is prevented from being influenced by the displacement of the sealing device 100 caused by the blood flow impact.

Although the present invention is disclosed above, it is not limited thereto. Various modifications and alterations of this invention may be made by those skilled in the art without departing from the spirit and scope of this invention. Thus, if such modifications and variations of the present invention fall within the scope of the claims and their equivalents, the present invention is also intended to include such modifications and variations.

Claims (15)

1. The utility model provides a plugging device, its characterized in that, includes the body, the body is including sizing silk and spring coil, sizing silk is the wire that has the resilience to be configured to have predetermined shape, the spring coil cover is established sizing silk is last, so that the body forms predetermined shape.

2. The occlusion device of claim 1, further comprising an anchoring mechanism connected to one end of the sizing wire, and rotatable about an axis of the sizing wire, the anchoring mechanism configured to secure the body to a target.

3. The occlusion device of claim 2, wherein the sizing wire is coiled into a continuous curvilinear configuration to form the predetermined shape.

4. The occlusion device of claim 3, wherein the predetermined shape is a spiral, the sizing wire being helically wound along an axis to form the spiral.

5. The occlusion device of claim 3, wherein the predetermined shape is a conical shape, the sizing wire is wound into a plurality of sequentially connected arc-shaped segments, the plurality of arc-shaped segments are sequentially arranged in the axial direction of the conical shape, and two adjacent arc-shaped segments are eccentrically arranged.

6. The occluder of claim 5, wherein said body has opposite first and second ends in the direction of said conical axis, said conical radial cross-section increasing in the direction from said first end to said second end, each of said arcuate segments increasing in radial dimension, said anchoring mechanism being disposed at said second end.

7. The occlusion device of claim 3, wherein the predetermined shape is spherical or hexahedral.

8. The occlusion device of claim 2, wherein the anchoring mechanism includes a positioning portion that is a barb or a fixation disk, the positioning portion configured to connect with the target.

9. The occlusion device of claim 8, wherein the positioning portion is provided with a pointed structure for penetrating an inner wall of a blood vessel to secure the body.

10. The occluder of any one of claims 1-9, further comprising thrombogenic hairs attached to said body.

11. The occlusion device of claim 10, wherein the thrombogenic hairs are wrapped around the sizing wire and held in place by the spring coil.

12. The occlusion device of claim 11, wherein at least two of said thrombogenic hairs are disposed on said sizing wire at intervals, and a distance between two adjacent thrombogenic hairs in an axial direction of said sizing wire is 5mm to 10 mm.

13. The occlusion device of claim 12, wherein the thrombogenic hairs are 15mm-25mm in length.

14. The occluder of any of claims 1-9, wherein the inner diameter of said coil is between 0.5mm and 1.0 mm.

15. An occlusion system comprising a stent and at least one occluding device of any of claims 1 to 14 attached to the stent.

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