CN219921286U - Stent assembly structure, catheter assembly and delivery system - Google Patents

Abstract

The utility model relates to a support assembly structure, wherein a fixing part is provided with an axially-through fixing inner cavity, the fixing inner cavity is used for penetrating an inner core tube, the fixing part is provided with a distal fixing part, the distal fixing part is used for fixing a valve support, a guiding part is provided with an axially-through guiding inner cavity, the guiding inner cavity is used for penetrating the inner core tube, the proximal end of the guiding part is connected with the distal end of the fixing part, so that the guiding inner cavity is communicated with the fixing inner cavity, and the guiding part is used for supporting the valve support outside the inner core tube. The guide part is utilized to provide a guide effect, so that the valve stent is convenient to load, and moreover, as the valve stent is directly supported with the guide part and is not directly supported by the inner core tube with smaller diameter, the guide part can fill a gap between the valve stent and the inner core tube, the inner core tube with smaller diameter plays a role in supporting and protecting, the inner core tube is prevented from being folded in the process of transporting or loading the valve stent, and the passing of a guide wire and the stability of the release of the valve stent are ensured.

Description

Stent assembly structure, catheter assembly and delivery system

Technical Field

The utility model relates to the technical field of medical instruments, in particular to a bracket assembly structure, a catheter assembly and a conveying system.

Background

The heart valve replacement surgery is characterized in that valves such as mitral valve, tricuspid valve and pulmonary valve are delivered to target positions such as aortic root through a delivery system to perform valve positioning release, so that the heart valve replacement surgery replaces the original valves, is a hot-hand leading edge technology in the field of valve heart disease treatment, and creates a milestone of aortic valve disease minimally invasive interventional therapy. The heart valve replacement can treat the aortic valve disease without opening chest and stopping heart, and avoids the huge trauma to patients caused by traditional surgical chest opening operation, heart stopping and the like.

At present, a self-expanding valve stent is commonly used in heart valve replacement, most of conveying systems for conveying the self-expanding valve stent are composed of multilayer tubes, such as an inner core tube of an inner layer, an inner catheter of a middle layer and an outer sheath tube of an outer layer, the inner core tube of the conveying system is provided with a guide wire inner cavity, the pre-operation self-expanding valve stent is stored in a space between the outer sheath tube and the inner core tube in a compressed state, and as the structure of the self-expanding valve stent is petal-shaped, namely, the head end of the self-expanding valve stent is provided with each claw which is in petal shape and is opened, wherein except for two symmetrical hangers which are used for hooking the self-expanding valve stent in cooperation with the inner core tube of the conveying system, other claws mainly play a supporting role after expansion.

However, since the outer diameter of the tube section on the inner core tube for assembling the self-expanding valve stent is generally very thin, when the self-expanding valve stent is loaded or recovered during operation, the tube section with the relatively thin outer diameter is easily folded before operation, which affects the passing of the guide wire and the stability of releasing the self-expanding valve stent, and the jaws of the self-expanding valve stent are easily overlapped and twisted, thereby easily damaging and scratching the outer sheath tube of the delivery system, which affects the success of operation.

Disclosure of Invention

In view of the above, it is desirable to provide a stent assembly structure, a catheter assembly, and a delivery system that address at least one of the technical problems mentioned above.

The present utility model provides a bracket assembly structure, comprising:

the fixing component is provided with an axially-through fixing inner cavity, the fixing inner cavity is used for penetrating the inner core tube, the fixing component is provided with a distal fixing part, and the distal fixing part is used for fixing the valve bracket;

the guide component is provided with a guide inner cavity which is penetrated axially and used for penetrating an inner core tube, the proximal end of the guide component is connected with the distal end of the fixing component, so that the guide inner cavity is communicated with the fixing inner cavity, and the guide component is used for supporting a valve bracket outside the inner core tube;

and a partition member provided on the guide member for separating and supporting the plurality of branch sections of the valve holder.

In one embodiment, the bracket assembly structure includes:

a sealing member provided to the guide member, the sealing member being for sealing a gap between a guide lumen of the guide member and an outer wall of the inner core tube; or alternatively, the process may be performed,

the inner cavity bulge is positioned on the inner wall of the guide inner cavity and is used for being in sealing contact with the outer wall of the inner core tube.

In one embodiment, the guide member comprises a distal guide section and a proximal guide section, each of the distal and proximal guide sections being a cylindrical tube, the maximum outer diameter of the distal guide section being smaller than the minimum outer diameter of the proximal section; and/or the number of the groups of groups,

the fixation component includes a distal fixation section and a proximal fixation section, both of which are cylindrical tubes, the maximum outer diameter of the distal fixation section being smaller than the minimum outer diameter of the proximal section.

In one embodiment, the separation member is located at the proximal guide section;

and/or the number of the groups of groups,

a transition guide section is connected between the distal guide section and the proximal guide section, the transition guide section is a cylindrical tube, wherein the outer diameter of the transition guide section gradually increases from the distal end to the proximal end.

In one embodiment, the separation member comprises a plurality of unit spacers, the unit spacers are arranged on the outer wall of the proximal guide section along the circumference of the proximal guide section in a surrounding manner, and unit separation spaces are formed between adjacent unit spacers and are used for accommodating the branch sections of the valve stent.

In one embodiment, the cell separator is employed as a separator plate, wherein the separator plate increases in height relative to the outer wall of the proximal guide section in the distal to proximal direction.

In one embodiment, the proximal end of the guide member and the distal end of the fixing member are provided with a first connection portion and a second connection portion, respectively, through which the proximal end of the guide member and the distal end of the fixing member are connected;

alternatively, the proximal end of the guide member and the distal end of the fixation member are adhesively secured.

In one embodiment, the first connection part is a plug hole formed at the proximal end of the guiding component, the second connection part is a plug connector arranged at the distal end of the fixing component, and the plug connector is assembled with the plug hole in a plug manner; or alternatively, the process may be performed,

the first connecting part is a threaded hole formed in the proximal end of the guide part, the second connecting part is a threaded head arranged at the distal end of the fixing part, and the threaded head is in threaded connection with the threaded hole.

The present utility model also provides a catheter assembly comprising:

the inner core tube is provided with an axially-through guide wire inner cavity, and the guide wire inner cavity is used for penetrating a guide wire;

an inner catheter having an axially-through catheter lumen, the inner core tube fitting within the catheter lumen with a distal end of the inner core tube beyond a distal end of the inner catheter;

the inner core pipe exceeds the pipe section of the inner guide pipe and is sleeved in the fixing inner cavity of the fixing part and the guiding inner cavity of the guiding part;

the outer sheath tube is provided with a sheath tube inner cavity which is axially penetrated, and the inner core tube, the inner catheter and the bracket assembly structure are assembled in the sheath tube inner cavity.

The present utility model also provides a conveying system comprising:

the bracket assembly structure; alternatively, the catheter assembly.

In the support assembly structure, the catheter assembly and the conveying system, the guide part can be sleeved on the inner core pipe, when the valve support is loaded by the inner core pipe with a smaller diameter, the guide part can be used for providing a guide effect in the loading process of the valve support, so that the valve support is convenient to load, and moreover, as the valve support is directly supported by the guide part and is not directly supported by the inner core pipe with a smaller diameter, the guide part can fill a gap between the valve support and the inner core pipe, the inner core pipe with a smaller diameter plays a role in supporting and protecting the inner core pipe, the inner core pipe is prevented from being folded in the process of transporting or loading the valve support, and the passing of a guide wire and the stability of the release of the valve support are ensured.

Drawings

Fig. 1 is a schematic diagram of an assembly structure of a bracket according to an embodiment of the present utility model.

Fig. 2 is a schematic diagram of an assembly structure of a bracket according to another embodiment of the present utility model.

Fig. 3 is a schematic view of an assembly structure of a bracket assembly structure according to another embodiment of the present utility model.

Fig. 4 is a schematic structural view of a guide member according to an embodiment of the present utility model.

Fig. 5 is a schematic structural view of a guide member according to another embodiment of the present utility model.

Fig. 6 is a schematic diagram of an assembly structure of a valve stent according to an embodiment of the present utility model.

Reference numerals:

1000. a fixing member; 2000. a guide member; 3000. an inner core tube; 4000. a distal introducer; 5000. a valve stent; 6000. an inner catheter;

1000a, distal fixation section; 1000b, proximal fixation section; 1100. a distal end fixing portion; 1200. a first connection portion; 1300. a second connecting portion;

2000a, distal guide section; 2000b, proximal guide section; 2000c, a transition boot section; 2100. a sealing member; 2200. an inner cavity bulge; 2300. a unit spacer; 2300a, unit isolation space;

5100. and (5) branching the segments.

Detailed Description

In order that the above objects, features and advantages of the utility model will be readily understood, a more particular description of the utility model will be rendered by reference to the appended drawings. In the following description, numerous specific details are set forth in order to provide a thorough understanding of the present utility model. The present utility model may be embodied in many other forms than described herein and similarly modified by those skilled in the art without departing from the spirit of the utility model, whereby the utility model is not limited to the specific embodiments disclosed below.

In the description of the present utility model, it should be understood that, if any, these terms "center", "longitudinal", "transverse", "length", "width", "thickness", "upper", "lower", "front", "rear", "left", "right", "vertical", "horizontal", "top", "bottom", "inner", "outer", "clockwise", "counterclockwise", "axial", "radial", "circumferential", etc., are used herein with respect to the orientation or positional relationship shown in the drawings, these terms refer to the orientation or positional relationship for convenience of description and simplicity of description only, and do not indicate or imply that the apparatus or element referred to must have a particular orientation, be constructed and operated in a particular orientation, and therefore should not be construed as limiting the utility model.

Furthermore, the terms "first," "second," and the like, if any, are used for descriptive purposes only and are not to be construed as indicating or implying a relative importance or implicitly indicating the number of technical features indicated. Thus, a feature defining "a first" or "a second" may explicitly or implicitly include at least one such feature. In the description of the present utility model, the terms "plurality" and "a plurality" if any, mean at least two, such as two, three, etc., unless specifically defined otherwise.

In the present utility model, unless explicitly stated and limited otherwise, the terms "mounted," "connected," "secured," and the like are to be construed broadly. For example, the two parts can be fixedly connected, detachably connected or integrated; can be mechanically or electrically connected; either directly or indirectly, through intermediaries, or both, may be in communication with each other or in interaction with each other, unless expressly defined otherwise. The specific meaning of the above terms in the present utility model can be understood by those of ordinary skill in the art according to the specific circumstances.

In the present utility model, unless expressly stated or limited otherwise, the meaning of a first feature being "on" or "off" a second feature, and the like, is that the first and second features are either in direct contact or in indirect contact through an intervening medium. Moreover, a first feature being "above," "over" and "on" a second feature may be a first feature being directly above or obliquely above the second feature, or simply indicating that the first feature is level higher than the second feature. The first feature being "under", "below" and "beneath" the second feature may be the first feature being directly under or obliquely below the second feature, or simply indicating that the first feature is less level than the second feature.

It will be understood that if an element is referred to as being "fixed" or "disposed" on another element, it can be directly on the other element or intervening elements may also be present. If an element is referred to as being "connected" to another element, it can be directly connected to the other element or intervening elements may also be present. The terms "vertical," "horizontal," "upper," "lower," "left," "right," and the like as used herein, if any, are for descriptive purposes only and do not represent a unique embodiment.

Referring to fig. 1, an embodiment of the present utility model provides a stent assembly structure, which includes a fixing member 1000 and a guiding member 2000, wherein the fixing member 1000 has a fixing lumen passing through axially, the fixing lumen is used for passing through an inner core tube 3000, the fixing member 1000 has a distal fixing portion 1100, the distal fixing portion 1100 is used for fixing a valve stent 5000, the guiding member 2000 has a guiding lumen passing through axially, the guiding lumen is used for passing through the inner core tube 3000, a proximal end of the guiding member 2000 is connected with a distal end of the fixing member 1000, such that the guiding lumen is communicated with the fixing lumen, and the guiding member 2000 is used for supporting the valve stent 5000 outside the inner core tube 3000.

The fixing member 1000 may have various structures, for example, the fixing member 1000 may have a stepped structure as shown in fig. 1, for example, the fixing member 1000 includes a distal fixing section 1000a and a proximal fixing section 1000b, the distal fixing section 1000a and the proximal fixing section 1000b are both cylindrical tubes, the maximum outer diameter of the distal fixing section 1000a is smaller than the minimum outer diameter of the proximal section, besides, the distal fixing section 1000a and the proximal fixing section 1000b may be configured as other structures according to the requirement of the fixing valve support 5000, such as regular or irregular shapes such as prism, hemisphere, etc., so long as the stepped structure can be configured by the two sections of the distal fixing section 1000a and the proximal fixing section 1000b included in the fixing member 1000, which can be set arbitrarily by a person skilled in the art.

The distal fixing portion 1100 of the fixing member 1000 may be in various structural forms such as a groove structure and a through hole structure, so long as the distal fixing portion 1100 can fix the valve support 5000, and the shapes of the groove structure and the through hole structure can be matched according to connection structures such as lugs on the valve support 5000, so that the fixing member is suitable for stable assembly of the valve support 5000, and when the valve support 5000 with a valve is fixed, the distal fixing portion 1100 can limit movement of the valve support 5000, for example, limit movement of the valve support 5000 in circumferential, axial and other directions. In addition, those skilled in the art may choose to assemble the valve holder 5000 in other similar or existing manners as desired, without limitation.

With continued reference to fig. 1, the guide member 2000 may be sleeved on the inner core tube 3000, when the valve stent 5000 is loaded by using the inner core tube 3000 with a smaller diameter, the guide member 2000 may be used to provide a guiding function during the loading process of the valve stent 5000, so that the loading of the valve stent 5000 is facilitated, and since the valve stent 5000 is directly supported by the guide member 2000, and is not directly supported by the inner core tube 3000 with a smaller diameter, the guide member 2000 may fill the gap between the valve stent 5000 and the inner core tube 3000, and support and protect the inner core tube 3000 with a smaller diameter, so as to avoid the inner core tube 3000 from being folded during the transportation or loading of the valve stent 5000.

Because the guide wire needs to be threaded in the guide wire inner cavity of the inner core tube 3000, the guide wire is used to guide the advancing direction in the conveying process of the conveying system, wherein the guide wire can be abutted against the vessel wall, the conveying system is arranged along the guiding track and direction of the guide wire, and the guide wire can be passively bent along with the bending of the inner core tube 3000 in the bending control process of the catheter. Therefore, the bending failure of the inner core tube 3000 is avoided, and the guide wire inner cavity of the inner core tube 3000 is ensured to be always in a through state, which is favorable for ensuring the smooth passing of the guide wire in the guide wire inner cavity, and the channel of the guide wire inner cavity is not broken due to the bending of the inner core tube 3000, so that the guide wire cannot pass through smoothly. Moreover, avoiding the failure of the inner core tube 3000 to bend will also ensure the stability of the release of the valve stent.

Referring to fig. 1 to 3, in one embodiment, the bracket assembly structure includes a sealing member 2100, a cavity boss 2200, and the like. As shown in fig. 1, the sealing member 2100 is disposed on the guiding member 2000, for example, the sealing member 2100 may be disposed at a distal end of the guiding member 2000, and the sealing member 2100 may be made of any material capable of achieving a sealing effect, so that the sealing member 2100 may be used to seal a gap between a distal end position of the guiding lumen of the guiding member 2000 and an outer wall of the inner core tube 3000, as shown in fig. 1, by sealing a gap between a distal end position of the guiding lumen of the guiding member 2000 and the outer wall of the inner core tube 3000 by using the sealing member 2100. For example, in this case, the sealing member 2100 may be made of an adhesive material such as glue, and the adhesive material may seal the gap between the distal end position of the guide lumen and the outer wall of the inner core tube 3000 and fix the guide member 2000 and the inner core tube 3000 to each other so that the guide member 2000 and the inner core tube 3000 cannot be rotated at will.

With continued reference to fig. 2, the stent-mounting structure may further include a lumen projection 2200, the lumen projection 2200 being located on an inner wall of the guide lumen, the lumen projection 2200 being adapted to be in sealing contact with an outer wall of the inner core tube 3000, whereby the lumen projection 2200 is in fact a circumferentially surrounding annular projection, the annular lumen projection 2200 being capable of sealing a gap between the inner wall of the guide lumen and the outer wall of the inner core tube 3000 without dead angles in the circumferential direction, and whereby the lumen projection 2200 is in sealing contact with only the outer wall of the inner core tube 3000, but does not completely restrict the relative movement between the guide member 2000 and the inner core tube 3000, such as primarily not restricting the relative axial movement therebetween.

With continued reference to fig. 3, the sealing member 2100 may be located at a proximal end of the guide member 2000, for example, the sealing member 2100 may be located between the fixing member 1000 and the guide member 2000, and in this case, the sealing member 2100 may be made of a sealing ring or the like, and a material capable of having a sealing effect, such as rubber, may be used for sealing a gap between a guide lumen of the guide member 2000 and an outer wall of the inner core tube 3000. In addition, those skilled in the art may seal the gap between the guide lumen of the guide member 2000 and the outer wall of the inner core tube 3000 in other sealing manners, and select whether to restrict the mutual rotation between the guide member 2000 and the inner core tube 3000, which is not limited herein.

The proximal end of the guide member 2000 and the distal end of the fixation member 1000 may be attached in a variety of ways, such as by adhesively securing the proximal end of the guide member 2000 and the distal end of the fixation member 1000 as shown with reference to fig. 1 and 2. Still alternatively, referring to fig. 3, in one embodiment, the proximal end of the guide member 2000 and the distal end of the fixing member 1000 are provided with a first connection portion 1200 and a second connection portion 1300, respectively, and the proximal end of the guide member 2000 and the distal end of the fixing member 1000 are connected by the first connection portion 1200 and the second connection portion 1300. The first connection portion 1200 may be a socket formed at a proximal end of the guide member 2000, and the second connection portion 1300 may be a socket disposed at a distal end of the fixing member 1000, where the socket is assembled with the socket. Alternatively, the first connection part 1200 may be a threaded hole formed at the proximal end of the guide member 2000, and the second connection part 1300 may be a screw head provided at the distal end of the fixing member 1000, the screw head being screw-coupled with the threaded hole.

The guide member 2000 may be made of a polymer material by injection molding, such as pebax, silica gel, etc., and the guide member 2000 may be made of various structures, for example, the guide member 2000 may be made of a stepped structure, as shown in fig. 4, for example, the guide member 2000 includes a distal guide section 2000a and a proximal guide section 2000b, both the distal guide section 2000a and the proximal guide section 2000b are cylindrical tubes, the maximum outer diameter of the distal guide section 2000a is smaller than the minimum outer diameter of the proximal section, besides, the distal guide section 2000a and the proximal guide section 2000b may be made of other structures according to the requirement of the support valve support 5000, such as a prism, a hemisphere, etc. in regular or irregular shape, as long as the stepped structure can be made by the two sections, i.e. the distal guide section 2000a and the proximal guide section 2000b, which are included in the guide member 2000, can be set arbitrarily by a person skilled in the art, and the present utility model is not limited thereto. Further, as shown in fig. 4, a transition guide section 2000c may be connected between the distal guide section 2000a and the proximal guide section 2000b, and the transition guide section 2000c is a cylindrical tube, wherein the outer diameter of the transition guide section 2000c gradually increases from the distal to the proximal direction.

With continued reference to fig. 5 and 6, in one embodiment, to better support the valve stent 5000, a partition member may be further disposed on the proximal guide section 2000b to prevent the branch sections 5100 of the valve stent 5000 from overlapping and twisting, the valve stent 5000 has an expanded state and a contracted state, as shown in fig. 6, the valve stent 5000 has the branch sections 5100, that is, a plurality of claws at the ends of the valve stent 5000, and when the valve stent 5000 is assembled in the contracted state between the fixing member 1000 and the guide member 2000 of the stent assembly structure, the fixing member 1000 is used to fix a part of the branch sections 5100, and the remaining branch sections 5100 can be separated by the partition member, so that the plurality of branch sections 5100 of the valve stent 5000 can be separated and supported by the partition member, and overlapping and twisting between the plurality of branch sections 5100 can be prevented after each of the branch sections 5100 are separated.

The partition member may have various structures, for example, the partition member may be a complete structure disposed on the proximal guide section 2000b, or the partition member may include a plurality of unit structures disposed on the proximal guide section 2000b, as shown in fig. 5, in one embodiment, the partition member may include a plurality of unit spacers 2300 disposed around an outer wall of the proximal guide section 2000b along a circumferential direction of the proximal guide section 2000b, a unit isolation space 2300a is formed between adjacent unit spacers 2300, the unit isolation space 2300a is used for accommodating a branch segment 5100 of the valve stent 5000, and after the branch segment 5100 is accommodated in the unit isolation space 2300a, the current unit isolation space 2300a is used for guiding the valve stent 5000, so as to prevent twisting, dislocation and overlapping between the plurality of branch segments 5100, and improve stability of releasing and recovering the valve stent 5000.

The unit spacer 2300 may be of any structure, and the unit spacer space 2300a may be configured in any space shape as long as it can stably accommodate the branch segment 5100, as shown in fig. 5, in one embodiment, the unit spacer 2300 is configured as a spacer plate, wherein the height of the spacer plate with respect to the outer wall of the proximal guide section 2000b increases from the distal end to the proximal end. In addition, the unit spacer 2300 may have other reasonable structures such as a barrier net structure and a protrusion structure, and may be selected by those skilled in the art according to the needs without limitation.

The utility model also provides a catheter assembly, which comprises an inner core tube 3000, an inner catheter 6000, a stent assembly structure and an outer sheath tube, wherein the inner core tube 3000 is provided with an axially-through guide wire inner cavity, the guide wire inner cavity is used for penetrating a guide wire, the inner catheter 6000 is provided with an axially-through catheter inner cavity, the inner core tube 3000 is assembled in the catheter inner cavity, the outer sheath tube is provided with an axially-through sheath tube inner cavity, and the inner core tube 3000, the inner catheter 6000 and the stent assembly structure are assembled in the sheath tube inner cavity. Wherein the distal end of the inner core tube 3000 exceeds the distal end of the inner catheter 6000, the section of the tube section of the distal end of the inner core tube 3000 exceeding the distal end of the inner catheter 6000 may be referred to as an assembly tube section, which may be used to assemble the valve stent 5000, i.e. indirectly load the valve stent 5000 with the guide member 2000, with the valve stent 5000 being located between the inner core tube 3000 and the outer sheath. With continued reference to fig. 1, the inner core tube 3000 may be simultaneously sleeved in the guide lumen of the guide member 2000 and the fixation lumen of the fixation member 1000. The distal end of the inner core tube 3000 is provided with a distal introducer 4000, and the distal introducer 4000 may have a tapered head or the like to facilitate guiding the advancement of the entire catheter assembly.

The utility model also provides a conveying system, which comprises a bracket assembly structure; or the delivery system includes a catheter assembly. Since the specific structure, functional principle and technical effect of the stent assembly structure and the catheter assembly are described in detail above, the description is omitted herein, and any technical content related to the stent assembly structure and the catheter assembly can be referred to in the description above.

The technical features of the above embodiments may be arbitrarily combined, and all possible combinations of the technical features in the above embodiments are not described for brevity of description, however, as long as there is no contradiction between the combinations of the technical features, they should be considered as the scope of the description.

The foregoing examples illustrate only a few embodiments of the utility model, which are described in detail and are not to be construed as limiting the scope of the claims. It should be noted that it will be apparent to those skilled in the art that several variations and modifications can be made without departing from the spirit of the utility model, which are all within the scope of the utility model. Accordingly, the scope of protection of the present utility model is to be determined by the appended claims.

Claims (10)

1. A bracket assembly structure, characterized in that the bracket assembly structure comprises:

the fixing component is provided with an axially-through fixing inner cavity, the fixing inner cavity is used for penetrating the inner core tube, the fixing component is provided with a distal fixing part, and the distal fixing part is used for fixing the valve bracket;

the guide component is provided with a guide inner cavity which is penetrated axially and used for penetrating an inner core tube, the proximal end of the guide component is connected with the distal end of the fixing component, so that the guide inner cavity is communicated with the fixing inner cavity, and the guide component is used for supporting a valve bracket outside the inner core tube;

and a partition member provided on the guide member for separating and supporting the plurality of branch sections of the valve holder.

2. The bracket assembly structure of claim 1, wherein the bracket assembly structure comprises:

a sealing member provided to the guide member, the sealing member being for sealing a gap between a guide lumen of the guide member and an outer wall of the inner core tube; or alternatively, the process may be performed,

the inner cavity bulge is positioned on the inner wall of the guide inner cavity and is used for being in sealing contact with the outer wall of the inner core tube.

3. The stent assembly structure of claim 1, wherein the guide member comprises a distal guide section and a proximal guide section, the distal guide section and the proximal guide section each being a cylindrical tube, a maximum outer diameter of the distal guide section being less than a minimum outer diameter of the proximal section; and/or the number of the groups of groups,

the fixation component includes a distal fixation section and a proximal fixation section, both of which are cylindrical tubes, the maximum outer diameter of the distal fixation section being smaller than the minimum outer diameter of the proximal section.

4. The stent assembly structure of claim 3, wherein the spacer member is located at the proximal guide section;

and/or the number of the groups of groups,

a transition guide section is connected between the distal guide section and the proximal guide section, the transition guide section is a cylindrical tube, wherein the outer diameter of the transition guide section gradually increases from the distal end to the proximal end.

5. The stent assembly structure of claim 4, wherein the partition member comprises a plurality of cell spacers disposed around an outer wall of the proximal guide section along a circumference of the proximal guide section, cell isolation spaces being constructed between adjacent cell spacers, the cell isolation spaces being for accommodating the branch sections of the valve stent.

6. The stent assembly structure of claim 5, wherein the cell separator is a separator plate, wherein the separator plate increases in height relative to the outer wall of the proximal guide section in a distal-to-proximal direction.

7. The stent assembly structure of claim 1, wherein the proximal end of the guide member and the distal end of the fixing member are provided with a first connection portion and a second connection portion, respectively, through which the proximal end of the guide member and the distal end of the fixing member are connected;

alternatively, the proximal end of the guide member and the distal end of the fixation member are adhesively secured.

8. The bracket assembly structure according to claim 7, wherein the first connection portion is a plug hole formed at a proximal end of the guide member, the second connection portion is a plug head formed at a distal end of the fixing member, and the plug head is plug-fitted with the plug hole; or alternatively, the process may be performed,

the first connecting part is a threaded hole formed in the proximal end of the guide part, the second connecting part is a threaded head arranged at the distal end of the fixing part, and the threaded head is in threaded connection with the threaded hole.

9. A catheter assembly, the catheter assembly comprising:

the inner core tube is provided with an axially-through guide wire inner cavity, and the guide wire inner cavity is used for penetrating a guide wire;

an inner catheter having an axially-through catheter lumen, the inner core tube fitting within the catheter lumen with a distal end of the inner core tube beyond a distal end of the inner catheter;

the stent assembly structure of any one of claims 1-8, wherein a tube section of the inner core tube beyond the inner catheter fits within the fixation lumen of the fixation member and the guide lumen of the guide member;

the outer sheath tube is provided with a sheath tube inner cavity which is axially penetrated, and the inner core tube, the inner catheter and the bracket assembly structure are assembled in the sheath tube inner cavity.

10. A conveyor system, the conveyor system comprising:

the stent mounting structure of any one of claims 1-8; or alternatively, the process may be performed,

the catheter assembly of claim 9.