CN211325298U

CN211325298U - Plugging device

Info

Publication number: CN211325298U
Application number: CN201921006169.2U
Authority: CN
Inventors: 李安宁; 刘建勇
Original assignee: Lifetech Scientific Shenzhen Co Ltd
Current assignee: Lifetech Scientific Shenzhen Co Ltd
Priority date: 2019-06-28
Filing date: 2019-06-28
Publication date: 2020-08-25
Anticipated expiration: 2029-06-28

Abstract

The utility model relates to a plugging device, including the sealed dish, and be connected with the sealed dish and be located the mount of sealed dish one side, the mount includes the connecting portion of being connected with the sealed dish, and at least one supporter, at least one supporter radiates out and extends towards the near-end from connecting portion, thereby form a plurality of supporting sections, be equipped with the at least first about portion of at least one and the at least about portion of at least one second on the mount, the at least first about portion of at least one links to each other through at least one about part with the at least about portion of at least one second, move towards the direction of keeping away from the mount to at least one supporting section and retrain. The utility model discloses a plugging device can give the certain radial restraint of a plurality of supporting sections of umbelliform mount to avoid the supporting section excessively outwards to open the risk of bringing.

Description

Plugging device

Technical Field

The utility model relates to an intervene medical instrument technical field, especially relate to an internal open-ended plugging device for shutoff human or animal body.

Background

Plugging devices such as left atrial appendage occluders, atrial septal defect occluders, aneurysm occluders and the like are increasingly trusted by doctors and patients due to the characteristics that the plugging device has excellent plugging realization structure and almost no complications which can endanger life exist after being implanted into the bodies of the patients. Particularly, the occluder with the umbrella-shaped structure fixing frame, such as a cantilever occluder, the suspended parts of the supporting rods of the fixing frame, such as the supporting section parts, have no constraint with each other, so that the occluder can be better adapted to parts to be occluded with different structures in the body.

However, just because the unsettled part of each bracing piece does not have the restraint each other, use the shutoff of left auricle as an example, after implanting internal, probably because the influence of the structure of the inside cavity of left auricle and pectinate muscle, and cause the outside open angle of partial supporting section too big, not only can not make the inner wall of bracing piece effective laminating left auricle, and the end of supporting section probably contacts with the inner wall of left auricle, thereby at the in-process that the heart beats, because there is the looks mutual friction, can make the inner wall of left auricle damaged, and then lead to appearing the pericardial effusion and even grind the operation risk of wearing through the inner wall of left auricle.

In addition, the fixing frame is formed by weaving and heat setting the weaving silk into an umbrella-shaped weaving net, the near end of the fixing frame is in an opening shape after the heat setting, and a support body part (namely, a support section) positioned near the opening of the near end provides support for the fixing. In the releasing process of the blocking device, a part of the supporting section of the fixing frame is excessively expanded outwards to influence the fixation of the fixing frame in the body, and a certain operation risk is also brought.

SUMMERY OF THE UTILITY MODEL

In view of the above, it is necessary to provide a new occlusion device to solve the technical problem that when the existing umbrella-shaped occlusion device is implanted into the body, a part of the support section is excessively expanded outwards.

An embodiment of the utility model provides a plugging device, including the sealed dish, and with the sealed dish is connected and is located the mount of sealed dish one side, the mount include with connecting portion and at least one supporter that the sealed dish is connected, at least one supporter follows connecting portion radiation-out and extend towards the near-end to form a plurality of supporting sections, be equipped with at least one first about the portion and at least one second about the portion, at least one on the mount first about the portion with at least one about the portion of second links to each other through at least one about the piece, with to at least one the supporting section is towards keeping away from the direction of mount removes retrains.

In one embodiment, the support body provided with the first constraining portion is the same as or different from the support body provided with the second constraining portion.

In one embodiment, at least one of the first and second constraining portions is provided on different ones of the supporting sections.

In one embodiment, at least one anchor is provided on at least one of the support sections, the anchor facing the seal disk, and the root of the anchor is fixedly connected to the support section, and at least one of the first restraint portion and/or the second restraint portion is provided on the support section within a range of 0.1 mm to 2 mm from the root of the anchor.

In one embodiment, at least one of the first restraints is disposed on the support section; at least one second restraint part is arranged at one of the following positions of the fixing frame: the supporting section, the part of the supporting body except the supporting section and the connecting part.

In one embodiment, at least one of the support sections further comprises a curved section, the first constraint being disposed on the curved section.

In one embodiment, at least two adjacent support sections are connected in series by at least one restraint along the circumferential direction of the fixing frame.

In one embodiment, at least one flow-blocking film or woven mesh is arranged on the fixing frame, and at least one part of the edge of the at least one flow-blocking film or woven mesh wraps the tail end of the supporting section.

In one embodiment, the restraint member is provided with at least one buffer part, and the buffer part has elasticity and variable length.

In one embodiment, the first constraint part is a first through hole and/or the second constraint part is a second through hole, one end of the constraint piece passes through the first through hole and/or the second through hole, and at least one part of the constraint piece can slide in the first through hole and/or the second through hole.

According to the plugging device, the fixing frame is provided with at least one first constraint part and at least one second constraint part, and the at least one first constraint part and the at least one second constraint part are connected through the at least one constraint part, so that the plurality of supporting sections on the fixing frame can be constrained to move towards the direction far away from the fixing frame, and the supporting sections are prevented from being excessively opened outwards.

Drawings

FIG. 1 is a schematic view of the external structure of the occluding device of example 1;

FIG. 2 is a schematic view of the mounting bracket of the occluding device of FIG. 1 as viewed from the proximal end to the distal end thereof;

FIG. 3 is a schematic view of a portion of the fastening frame of the plugging device of FIG. 1;

FIG. 4 is a partial structural view of another fixing frame of the occluding device of the embodiment 1;

fig. 5 is another schematic structural view of the first constraining section or the second constraining section provided on the support body in the occluding device of example 1;

fig. 6 is another schematic structural view of the first constraining section or the second constraining section provided on the support body in the occluding device of example 1;

fig. 7 is another schematic structural view of the first constraining section or the second constraining section provided in the support body in the occluding device of example 1;

fig. 8 is another schematic structural view of the first constraining section or the second constraining section provided on the support body in the occluding device of example 1;

FIG. 9 is another schematic structural view of the occluding device of embodiment 1;

FIG. 10 is another schematic structural view of the occluding device of example 1;

FIG. 11 is another schematic structural view of the occluding device of example 1;

FIG. 12 is a schematic structural view of the occluding device of example 2;

FIG. 13 is a schematic structural view of the occluding device of example 3;

fig. 14 is a schematic structural view of a holder of the occluding device of embodiment 4;

FIG. 15 is a schematic structural view of the occluding device of example 5; wherein, for the convenience of observation, the fixing frame is bent towards one side;

fig. 16 is a schematic structural view of a holder of the occluding device of embodiment 6;

fig. 17 is another structural schematic view of the holder of the occluding device of embodiment 6.

Detailed Description

In order to make the objects, technical solutions and advantages of the present invention more clearly understood, the present invention is further described in detail below with reference to the accompanying drawings and embodiments. It should be understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention.

In the field of interventional medical devices, the end of a medical device implanted in a human or animal body closer to an operator is generally referred to as the "proximal end", the end farther from the operator is referred to as the "distal end", and the "proximal end" and the "distal end" of any component of the medical device are defined according to this principle. "axial" generally refers to the length of the medical device as it is being delivered, and "radial" generally refers to the direction of the medical device perpendicular to its "axial" direction, and defines both "axial" and "radial" directions for any component of the medical device in accordance with this principle.

The technical solution of the present invention will be further described in detail with reference to the following specific examples. The occlusion device of the present invention can be implanted in the body tissue of a human or animal body having an opening for occluding the opening, preferably, but not limited to, left atrial appendage occlusion and aneurysm occlusion.

Example 1

Embodiment 1 provides a plugging device 100, referring to fig. 1 and 2 together, comprising a flexible sealing disc 110 and a flexible holder 120 connected to the sealing disc 110 and located on one side of the sealing disc 110, wherein the sealing disc 110 and the holder 120 can be connected directly or via at least one connector. The connecting member may be a flexible or rigid connecting member, which may be connected to one end of each of the sealing plate 110 and the fixing frame 120 by a sleeving connection or a welding connection. In this embodiment, the sealing plate 110 is directly connected to the fixing frame 120, and specifically, the distal end of the sealing plate 110 extends into the connecting portion 121 at the proximal end of the fixing frame 120 and is fixed.

The sealing disc 110 may be made of at least one metal wire (e.g. nitinol wire) with superelasticity and shape memory or biocompatible polymer wire, and after being woven into a mesh tube, the two ends of the mesh tube are respectively closed and fixed by a sleeve 111, and then heat-shaped into a flat shape or a disc shape, etc., which is not limited as long as the shape can seal the tissue opening after being implanted in vivo. The sleeve 111 at the proximal end of the sealing disk 110 may not only capture the proximal end of the wire, but may also be removably attached, such as by threading, to the distal end of a delivery device that delivers the occluding device 100. A sleeve (not shown) at the distal end of the sealing disc 110 is used not only to constrict the distal end of the wire but also to connect with the proximal end of the fixation frame 120. The inside of the sealing disk 110 is provided with at least one thin film body (not shown) to enhance the sealing performance of the sealing disk 110. Wherein, the thin film body can be a PET film or other polymer film, and the sealing disc 110 provided with the thin film body can prevent blood flowing from one side of the sealing disc 110 to the other side through the sealing disc 110.

In another embodiment, the sealing disc 110 may be made of at least one metal tube with super-elasticity and shape memory properties, such as a nitinol tube, which is laser cut and then heat set into a flat or disc shape, etc., without limitation, so long as it is capable of sealing a tissue opening after being implanted in a body. In another embodiment, the sealing disk 110 may be formed of at least one metal rod having superelastic and shape memory properties, such as a disk shape, but is not limited to a shape that will occlude a tissue opening after implantation in a body.

The fixing frame 120 includes a connecting portion 121 connected to the sealing disk 110, and a plurality of supports 122. The connecting portion 121 may be a hollow nitinol tube, or a hollow tubular member woven from at least one nitinol wire. The supporting bodies 122 radiate from the distal end of the connecting portion 121 to the distal end and cooperate to form a recessed area, and then extend to the proximal end by bending to form a plurality of spaced suspended supporting sections 123, and the ends of the supporting sections 123 enclose to form a proximal opening. The suspended support section 123 may be formed of a suspended portion of one end of a single support body 122, which is not connected to the connection portion 121, or may be formed of suspended portions of two or more support bodies 122 that are gathered together, and may also be formed of suspended portions of two or more support bodies 122 that are crossed together.

In this embodiment, the supporting section 123 is formed by the suspended portions of the two supporting bodies 122 gathered together in fig. 1. Specifically, referring to fig. 2, the portion of each supporting body 122 except its supporting section 123 includes an outgoing section 124 connected to the connecting portion 121, and two branch sections 125 located between the outgoing section 124 and the supporting section 123, and one branch section 125 of one supporting body 122 and the branch section 125 of another supporting body 122 adjacent to the supporting body 122, which is closest to the branch section 125, converge at the proximal end, thereby forming one supporting section 123. The suspended support sections 123 are arranged at intervals along the circumferential direction C of the fixing frame 120. In practical production, a plurality of struts 122 may be cut from one end of a nitinol tube in a direction toward the other end, and then the struts 122 are expanded by a mold and then heat-treated to be shaped, wherein the uncut portion of the nitinol tube is the connecting portion 121.

In other embodiments, the supporting body 122 may also be made of at least one metal wire (e.g., a nickel-titanium wire) having superelasticity and shape memory property, specifically, the supporting body 122 may be a single nickel-titanium wire, or may be formed by winding or weaving two or more metal wires; one end of the plurality of supporting bodies 122 is connected to the connecting portion 121, and the rest is in an umbrella shape by heat setting, thereby obtaining the fixing frame 120 having a distal recessed area and a proximal opening.

In other embodiments, the fixing frame 120 may include a connection portion 121 and a supporting body 122 connected to the connection portion 121. The fixing frame 120 with a recessed distal end region and an open proximal end region can be obtained by cutting a flared or tubular elastic material and then heat-setting the material into an umbrella shape, wherein the connecting portion 121 is located at the end of the elastic material with the smaller outer diameter, the portion of the elastic material except the connecting portion 121 is a supporting body 122, the supporting body 122 occupies most of the elastic material, and the suspended portion obtained by cutting is the supporting section 123. The wall of the support 122 may or may not have a plurality of openings evenly distributed.

In other embodiments, at least one support 122 radiates from the connecting portion 121 and extends towards the proximal end, and may not form a recessed area on the fixing frame 120 as in the present embodiment, for example, may radiate from the distal end of the connecting portion 121 in parallel and then bend outward and extend towards the proximal end, and a plurality of spaced apart hanging support sections 123 can also be formed. Here, the specific situation that at least one supporting body 122 radiates from the connecting portion 121 is not listed, as long as a plurality of spaced apart suspended supporting sections 123 can be formed after extending towards the proximal end.

In this embodiment, please refer to fig. 1 and fig. 3 together, the fixing frame 120 is provided with a plurality of first constraining portions 131 and a plurality of second constraining portions 132, the first constraining portions 131 and the second constraining portions 132 are respectively disposed on different supporting sections 123, and only one first constraining portion 131 or one second constraining portion 132 is disposed on one supporting section 123, that is, the supporting body 122 provided with the first constraining portion 131 and the supporting body 122 provided with the second constraining portion 132 are not the same supporting body 122. The first constraining portions 131 and the second constraining portions 132 are sequentially distributed at intervals along the circumferential direction C of the fixing frame 120, all the first constraining portions 131 and all the second constraining portions 132 are connected by one constraining member 140, and all the supporting sections 123 are connected in series by the constraining member 140 along the circumferential direction C of the fixing frame 120. So as to restrain all the supporting sections 123 on the fixing frame 120 from moving away from the fixing frame 120. It is understood that all the first constraining portions 131 and all the second constraining portions 132 may also be connected by two or more constraining members 140, and all the supporting sections 123 are connected in series by two or more constraining members 140 along the circumferential direction C of the fixing frame 120, so that the constraining members 140 are connected with the first constraining portions 131 and the second constraining portions 132 by this series connection.

It should be noted that the first constraining portion 131 and the second constraining portion 132 may be constrained positions defined on the fixing frame 120 and acted on by the constraining member 140, for example, the constraining member 140 may be connected to at least the two constraining positions of the first constraining portion 131 and the second constraining portion 132 by binding, welding, adhering, etc. The first constraining portion 131 and the second constraining portion 132 may also be a solid structure defined on the fixing frame 120, for example, the first constraining portion 131 may be a through hole, a protruding structure, a groove structure, etc., and the manner of connecting with the corresponding solid structure may be through connection with the through hole, may be binding with the protruding structure, may be binding with the groove structure, etc., which is not described herein again.

In other embodiments, two or more first constraining portions 131 or second constraining portions 132 may be disposed on each supporting section 123, and two or more constraining members 140 may also be disposed, so as to increase the connection strength between the supporting body 122 and the constraining members 140. Taking the example of providing two constraining members 140 and two first constraining portions 131 or second constraining portions 132 on each supporting section 123 at intervals along the axial direction of the supporting section 123, one of the constraining members 140 may be used to sequentially connect the plurality of first constraining portions 131 and the plurality of second constraining portions 132 of the supporting section 123 near the end thereof along the circumferential direction C of the fixing frame 120, and the other constraining member 140 may be used to sequentially connect the plurality of first constraining portions 131 and the plurality of second constraining portions 132 of the supporting section 123 near the distal end thereof along the circumferential direction C of the fixing frame 120, and the two constraining members 140 may not cross each other along the axial direction of the supporting section 123, and in some cases may be approximately parallel.

Further, in another embodiment, referring to fig. 4, the two constraining members 140 may connect the first constraining portion 131 and the second constraining portion 132 in a crossed manner along the circumferential direction C of the fixing frame 120. Further, in other embodiments, a plurality of constraining members 140 may be provided, and at least one first constraining portion 131 and at least one second constraining portion 132 on two or more supporting sections 123 adjacent in the circumferential direction C of the fixing frame 120 are connected by at least one constraining member 140. Other arrangements are similar to those of the above embodiments, and all the supporting sections 123 on the fixing frame 120 can be restricted from moving away from the fixing frame 120, which is not illustrated here.

In this embodiment, each supporting segment 123 is provided with an anchor 150 facing the sealing disk 110, the root of the anchor 150 is fixedly connected to the supporting segment 123, and each of the first and second constraining

portions

131 and 132 is disposed near a corresponding one of the anchors 150, for example, at a position of the supporting segment 123 more distal than the root of the anchor 150 as shown in fig. 1. Preferably, the distance between the supporting section 123 and the root of the anchor is in the range of 0.1 mm to 2 mm, so that the radial movement of the supporting section 123 is restrained more effectively, and the radial restraint of all the supporting sections 123 on the fixing frame 120 on the whole is more stable. Further, in other embodiments, the first constraining portion 131 and/or the second constraining portion 132 may be openings left after the anchor 150 is cut out of the supporting body 122, respectively, to avoid reducing the supporting strength of the bearing section 123. In other embodiments, at least one anchor 150 facing the sealing plate 110 may be disposed on each of the partial supporting sections 123 of the fixing frame 120, and at least one first constraint portion 131 and/or at least one second constraint portion 132 may be disposed adjacent to each of the at least one anchor 150 corresponding thereto, so as to provide better radial constraint for the partial supporting sections 123. In other embodiments, the anchor 150 may not be disposed on the fixation frame 120, and the fixation frame 120 itself may provide support for the occluding device 100 after release within the cavity, thereby securing at least a portion of the occluding device 100 within the cavity of the left atrial appendage.

The first constraining portion 131 and the second constraining portion 132 are both a through hole formed in the fixing frame 120, and can be formed by punching the fixing frame 120. Further, the through hole disposed on the supporting body 122 is preferably located on the central axis of the supporting body 122, and since the through hole is located relatively centrally, the metal rod at the location of the through hole is relatively weak and is not easily broken. In other embodiments, referring to fig. 5, the through holes (i.e. the first constraining portion 131 or the second constraining portion 132) disposed on the supporting body 122 are located at the side edge of the supporting body 122, and the outer diameter of the portion of the supporting body 122 where the through holes are disposed is larger than the outer diameter of the portion where the through holes are not disposed, so that the portion where the through holes are disposed still has sufficient supporting strength and is not easy to break. The specific form of the through hole is not limited, and may be a circular hole or an elliptical hole, or may be a long strip disposed along the axial direction of the support body 122. The specific manner of connecting one end or a part of the constraining member 140 to the first constraining part 131 or the second constraining part 132 of the supporting body 122 may be to tie or wind after passing through the through hole, or to fuse one end of the constraining member 140 into a ball shape after passing through the through hole, and at least a part of the constraining member 140 having a tip configured into a ball shape may slide in the through hole.

The elongated through hole has a long length along the axial direction of the supporting body 122 and a small width, so that the supporting strength of the portion of the supporting body 122 where the through hole is provided is not excessively affected, and the constraining member 140 engaged with the through hole can have a certain degree of freedom along the axial direction of the supporting body 122, so that when the fixing frame 120 enters and exits the sheath, the length of the constraining member 140 between the first constraining portion 131 and the second constraining portion 132 can change in compliance with the deformation of the supporting body 122, and at the same time, the radial movement of the supporting section 123 can be properly constrained.

In other embodiments, referring to fig. 6 to 8, the first constraining portion 131 may also be at least one protrusion disposed on the fixing frame 120, and the second constraining portion 132 may also be at least one protrusion disposed on the fixing frame 120. The shape of the projection is not limited and may be a circle or other irregular shape, preferably a shape having no sharp point. The projections may be imperforate or may be annular and have a perforated configuration (similar to that shown in figure 5). Various combinations of the specific forms of the first constraining part 131 and the second constraining part 132 are not described herein.

The constraining member 140 in this embodiment is made of at least a linear member, which can be made of a polymer material, such as PET polyester thread, PP suture, PA suture, etc., or a metal material, such as nickel titanium, stainless steel, etc. In other embodiments, the restriction member 140 can be a mesh member made of a wire having superelasticity and shape memory, such as the annular mesh 140 shown in fig. 9, and the annular mesh 140 can be a separate mesh or can be a unitary structure with the mesh 141 coated on the outer surface of the fixing frame 120, as shown in fig. 10. The annular mesh grid 141 may be provided as desired along the axial length of the occluding device 100, preferably along the axial length of the occluding device 100 from the root of the anchor 150 to the tip of the bearing segment 123. Further, in other embodiments, at least one woven mesh (i.e., the constraining member 140) is disposed on the fixing frame 120, and at least a portion of an edge of the at least one woven mesh wraps the end of the supporting section 123, that is, the woven mesh wraps the entire fixing frame 120 and the edge of the end of the woven mesh wraps the end of the supporting section 122, so that a certain radial constraint can be better given to the supporting section 123 of the fixing frame 120 to prevent the supporting section 123 from being excessively opened outward.

In other embodiments, the constraining member 140 can also be a polymer film made of polymer material, such as the ring-shaped film 140 shown in fig. 11, and the ring-shaped film 140 can be a separate film provided on the supporting section 123, or can be an integral structure with the film body 142 covering the outer surface of the fixing frame 120. The annular membrane 140 can be disposed along the axial length of the occluding device 100 as desired, preferably along the axial length of the occluding device 100 from the root of the anchor 150 to the end of the bearing section 123. The annular membrane 140 not only radially restrains the outward expansion of each support segment 123, but also prevents the portion of each support 122 covered by the annular membrane 140 from being scratched due to direct contact with the tissue inside the body. Further, in other embodiments, at least one film body (i.e., the constraining member 140) is disposed on the fixing frame 120, and at least a portion of an edge of the at least one film body wraps the end of the supporting section 123, that is, the film body wraps the entire fixing frame 120 and an end edge of the obstructing film wraps the end of the supporting body 122. The thin film body not only can enable the fixing frame 120 to have a good sealing effect, but also can provide certain radial constraint for each supporting section 123, so that the situation that one or more supporting sections 123 are too outwards opened compared with other supporting sections 123 after the plugging device 100 is released is avoided, and due to the soft characteristic of the thin film body, the supporting body 122 can be prevented from directly contacting the tissues in the body to scratch the tissues in the body. Specifically, the thin film body has the characteristics of softness, thinness, compressibility and elasticity, so that in the process that the fixing frame 120 is pushed out after being put into a conveying device such as a sheath tube, the thin film body is always attached to the supporting body 122 of the fixing frame 120 and folded and unfolded along with the supporting body 122, thereby reducing or even avoiding the risk of kinking between the supporting bodies 122 and ensuring smooth operation.

In other embodiments, the constraining member 140 may also be any combination of a wire member, a net member, a polymer film, etc., for example, at least one wire member is further disposed on the fixing frame 120 at a suitable position on the net member or the polymer film, or at least one polymer film is further disposed on the fixing frame 120 at a suitable position on the net member, etc., which are not listed here. The length of the constraining members 140 may be set as desired, so long as all of the constraining members 140 can cooperate with each other without affecting the transition of the fixing frame 120 between the compressed state and the expanded state.

In other embodiments, the first constraining unit 131 may be disposed on a portion of one supporting body 122 close to the supporting section 123 except the supporting section 123, for example, on the branch section 125, and the closer to the distal end of the supporting section 123, the better the constraining effect. In other embodiments, the second constraining section 132 may be disposed at a position of a portion of one supporting body 122 other than the supporting section 123 thereof (e.g., the leading-out section 124 or the branch section 125), or the connecting section 121 of the fixing frame 120, or the like. The specific combination of the positions of the first constraining portions 131 and the positions of the second constraining portions 132 engaged therewith is not illustrated, as long as at least one first constraining portion 131 and at least one second constraining portion 132 engaged therewith can be connected by at least one constraining member 140 to constrain the movement of at least one supporting segment 123 corresponding to the first constraining portion 131 and the second constraining portion 132 in a direction away from the fixed frame 120.

In this embodiment, each support segment 123 further comprises a curved segment 126, the curved segment 126 being formed by bending the tip of the support segment 123 towards the interior of the occlusion device 100 to reduce friction or damage to the in vivo tissue caused by the tip of the support segment 123. In other embodiments, the support section 123 of the fixing frame 120 is not provided with the bending section 126, or only a part of the support section 123 of the fixing frame 120 includes the bending section 126.

Further, in other embodiments, at least one of the constraining members 140 may be provided with at least one buffer portion having elasticity and a variable length. The buffer portion may be in a spiral line shape or a wavy line shape, and the specific shape is not limited. The buffer portion can ensure that the arranged constraining member 140 does not affect the transformation of the fixing frame 120 between the compressed state and the expanded state, thereby ensuring the transportation and normal use of the occlusion device.

The occluding device 100 of any of the above embodiments is constrained to be approximately linear by the lumen of a delivery device such as a sheath when delivered from the outside of the body to the inside of the body, and is thus compressed. Taking the sheath as an example, when releasing in vivo, the sheath is withdrawn towards the proximal end, the fixing frame 120 located at the distal end firstly extends out from the cavity of the sheath, and the distal end of each supporting body 122 on the fixing frame 120 is firstly expanded radially outwards, then is bent towards the proximal end, and continues to extend towards the proximal end along with the release of the proximal end part of the fixing frame 120 from the sheath until the fixing frame returns to the heat-set shape, thereby being in the unfolding state. The released anchor 120 may be fixed to the inner wall of the body tissue having the cavity, such as the left atrial appendage, to fix the occluding device 100 to the body tissue. Thereafter, the sheath is further withdrawn toward the proximal end, and the sealing disk 110 protruding from the cavity of the sheath is expanded to a flat or disk shape after heat setting, thereby covering the opening of the site to be plugged and smoothly achieving plugging.

Example 2

The same parts of the occluding device 200 of the embodiment 2 and the occluding device 100 of the embodiment 1 are not repeated here, and the main difference is that in the embodiment 2, at least two adjacent supporting segments are connected in series by at least one constraining member along the circumferential direction C of the fixing frame. Specifically, referring to fig. 12, only some of the support sections 223 of the fixing frame 220 are respectively provided with a first constraining portion 231 or a second constraining portion 232, and the first constraining portion 231 and the second constraining portion 232 cooperating therewith are respectively provided on two adjacent support sections 223 along the circumferential direction C of the fixing frame 220, and the plurality of constraining members 240 are dispersedly and alternately provided along the circumferential direction C of the fixing frame 220, instead of being continuously provided in embodiment 1. Such an occlusion device 200 achieves a radial movement restriction of some of the support segments 223 of the holder 220, and prevents the support segments 223 from being excessively expanded outward.

In other embodiments, at least one first constraining unit 231 or at least one second constraining unit 232 may be disposed along the circumferential direction C of the fixing frame 220 at three or more adjacent supporting sections 223 or other portions of the supporting body near the distal end thereof, respectively, and the plurality of constraining units 240 may be disposed at intervals along the circumferential direction C of the fixing frame 220 after being fixed to the fixing frame 220. This arrangement also enables the radial movement of some of the bearing segments 223 of the holder 220 to be restricted to avoid excessive outward splaying of these bearing segments 223.

Example 3

The same portions of the occluding device 300 of example 3 as those of the occluding device 100 of example 1 are not described again, and the main difference is that in example 3, the first constraining portions and the second constraining portions are respectively provided at arbitrary positions of the curved sections. Further, the first constraining portion and the second constraining portion are respectively disposed at the ends of the bending section, and may be implemented by punching holes at the ends of the bending section or by providing at least one protrusion at the ends of the bending section, as long as one end or a part of the constraining member can be fixed at the ends of the supporting section.

Specifically, referring to fig. 13, the end of the bending section 326 is provided with a ball (not shown), which may be achieved by thermally fusing the end of the bending section 326 or fixedly connecting a ball to the end of the bending section 326. A through hole is formed in the ball head, and one end or a part of at least one restraint piece 340 passes through the through hole, so that the restraint piece 340 is fixed on the tail end of the supporting section in a knotting or hot melting mode, or a winding mode and the like. Such an arrangement uses less material for the restraints 340 and greater radial restraint between the various support sections.

It can be appreciated that the first and second constraining portions and the at least one constraining member 340 provided at the end of the curved section 326 in example 2 can be added to the occluding device 100 of example 1 to further enhance the effect of constraining the supporting sections of the stent from moving away from the stent.

Example 4

The same portions of the occluding device of example 4 as those of the occluding device 100 of example 1 are not described again, but the difference is mainly that in example 4, the support body provided with the first restraining portion is the same as the support body provided with the second restraining portion. For example, referring to fig. 14, the fixing frame 420 is provided with a first constraining portion 431 on each supporting section 423 of the supporting body 422, and for each first constraining portion 431, a second constraining portion 432 is provided at a position of the supporting body 422 where the first constraining portion 431 is located, the position being close to the connecting portion 421, so that all the supporting sections 423 of the fixing frame 420 are constrained to move in a direction away from the fixing frame 420.

At least one buffer part 441 is arranged on the at least one restraint member 440, and the buffer part 441 has elasticity and is variable in length. The buffer portion 441 may have a spiral shape or a wavy shape, and the specific shape is not limited. The buffer 441 can ensure that the arranged constraining member 440 does not affect the transformation of the fixing frame 420 between the compressed state and the expanded state, thereby ensuring the transportation and normal use of the occluding device. In other embodiments, the buffer 441 may not be provided, and the length of the constraining member 440 may be adjusted without affecting the conversion of the fixing frame 420 between the compressed state and the expanded state.

In other embodiments, the fixing frame 420 may be provided with at least one first constraining portion 431 on only one or a part of the supporting bodies 422, and at least one second constraining portion 432 on the corresponding supporting body 422 or connecting portion 421. For example, at least one first constraint part 431 is provided on the supporting section 423 of the same supporting body 422, and at least one second constraint part 432 is provided at a position of the supporting body 422 close to the connecting part 421, so as to realize the constraint of radial movement of the single supporting section 423 and avoid the supporting section 423 from being excessively expanded outwards. The arrangement of two or more supports 422 is similar and is not further described herein.

Example 5

The same parts of the occluding device 500 of example 5 as those of the occluding device 100 of example 1 are not described again, but the main difference is that in example 5, at least two supporting sections adjacent to each other in the circumferential direction C of the fixation frame are connected to the same support body except for the supporting sections thereof by at least one restraining member.

Specifically, referring to fig. 15, for each group of two supporting segments 523 adjacent to each other in the circumferential direction C of the fixing frame 520, a first constraining portion 531 is respectively disposed, a second constraining portion 532 is disposed on the leading-out segment 524 between the two supporting segments 523, the constraining member 540 is radial and has three ends, and each end of the constraining member 540 is respectively connected to the two first constraining portions 531 and the second constraining portion 532, so as to constrain the movement of all the supporting segments 523 of the fixing frame 520 in the direction away from the fixing frame 520.

In other embodiments, the first constraining portions 531 may be respectively disposed on a plurality of groups of the support sections 523 adjacent to each other in the circumferential direction C of the fixed frame 520, each group of the support sections 523 includes two or more support sections 523, and the support sections 523 of the same group are connected to the same extraction section 524, or connected to at least two extraction sections 524, or connected to the connection portion.

Example 6

The same parts of the occluding device of embodiment 6 as those of any one of the above-described embodiments are not described again, but the embodiment 6 mainly differs therefrom in that the fixing frame 600 comprises a structure in which at least one support body 622 is woven and then heat-set into an umbrella shape, and a connecting part 621 which is located at one end of the umbrella shape and is connected with the sealing disk. In this embodiment, as shown in fig. 16 and 17, the supporting body 622 may be a nitinol wire having superelasticity and shape memory, and the connecting portion 621 may be a metal sleeve capable of restraining the wire. The supporting bodies 622 between the distal end and the proximal end of the fixing frame 600 are supporting sections 623, and one supporting body 622 comprises at least one supporting section 623. The ends of the support sections 623 are bent toward the interior of the mount 600 to form bent sections 626. There are several support sections 623 with such curved sections, and a curved section 626 may also be provided on each support section 623. In the circumferential direction of the fixing frame 600, the ends of two or more adjacent curved sections 626 can be fixedly connected, for example, in fig. 16, the ends of two adjacent curved sections 626 are fixedly connected to form a V-shaped curve. The function of the V-shaped bend is the same as that of the bend section in any of the embodiments described above. The V-shaped bent portion in fig. 16 can be actually formed by knitting the same support 622.

The first restraint portion 631 and the second restraint portion 632, which are similar to those of any of the above embodiments, are provided on the plurality of supporting bodies 622, respectively, to fix the restraint 640 to the fixing frame 600. For example, in fig. 16, at least one binding element 640 is fixed to each support section 623 after being wound or bound several times in the circumferential direction of the fastening frame. In other embodiments, the specific structure, the arrangement position and the connection manner of the first constraining portion 631 and the second constraining portion 632 are the same as or similar to those of any of the above embodiments, and are not repeated herein. The constraining member 640 is also the same as the constraining member in any of the above embodiments, for example, the constraining member 640 is a thread or a polymer film. The constraining member 640 may further include a buffering portion 641 similar to any of the above embodiments.

The technical features of the embodiments described above may be arbitrarily combined, and for the sake of brevity, all possible combinations of the technical features in the embodiments described above are not described, but should be considered as being within the scope of the present specification as long as there is no contradiction between the combinations of the technical features.

The above-mentioned embodiments only represent some embodiments of the present invention, and the description thereof is specific and detailed, but not to be construed as limiting the scope of the present invention. It should be noted that, for those skilled in the art, without departing from the spirit of the present invention, several variations and modifications can be made, which are within the scope of the present invention. Therefore, the protection scope of the present invention should be subject to the appended claims.

Claims

1. The utility model provides a plugging device, including the sealed dish, and with the sealed dish is connected and is located the mount of sealed dish one side, the mount include with connecting portion and at least one supporter that the sealed dish is connected, at least one supporter is followed connecting portion radiate out and extend towards the near-end to form a plurality of supporting segments, its characterized in that, be equipped with at least one first restraint portion and at least one second restraint portion on the mount, at least one first restraint portion and at least one the restraint portion of second links to each other through at least one restraint piece, with to at least one the supporting segment is towards keeping away from the direction of mount removes and retrains.

2. The occlusion device of claim 1, wherein the support body provided with the first constraint is the same or different from the support body provided with the second constraint.

3. The occlusion device of claim 2, wherein at least one of the first and second constraints is disposed on different ones of the support sections.

4. The occlusion device of claim 3, wherein at least one of the support sections is provided with at least one anchor spike facing the sealing disc, the root of the anchor spike being fixedly attached to the support section, and wherein at least one of the first restraint portion and/or the at least one of the second restraint portion is provided on the support section within a range of 0.1 mm to 2 mm from the root of the anchor spike.

5. The occlusion device of claim 1 or 2, wherein at least one of the first restrictions is disposed on the support section; at least one second restraint part is arranged at one of the following positions of the fixing frame: the supporting section, the part of the supporting body except the supporting section and the connecting part.

6. The occlusion device of claim 1, wherein at least one of the support sections further comprises a curved section, the first constraint being disposed on the curved section.

7. The occlusion device of claim 1, wherein at least two of the support sections that are adjacent are connected in series by at least one of the restraints in a circumferential direction of the fixation frame.

8. The occlusion device of claim 1, wherein the fixation frame is provided with at least one flow-blocking membrane or mesh, and wherein at least a portion of an edge of the at least one flow-blocking membrane or mesh wraps around the distal end of the support section.

9. The occlusion device of claim 1, wherein the constraint is provided with at least one bumper portion that is resilient and variable in length.

10. The occlusion device of claim 1, wherein the first restraint portion is a first through-hole and/or the second restraint portion is a second through-hole, wherein an end of the restraint passes through the first through-hole and/or the second through-hole, and wherein at least a portion of the restraint is slidable within the first through-hole and/or the second through-hole.