Abstract: An ablation device is provided, including a main body structure (110), electrodes (130), and a plurality of supporting arms (120), where the supporting arm (120) is inclined outward relative to the main body structure (110) and includes a contact portion (121); the contact portion (121) has an arcuate structure, and a convex surface of the arcuate structure faces a side of the supporting arm (120) away from a center of the main body structure (110); the electrode (130) is mounted on the contact portion (121) and covers at least a part of an outer side wall of the contact portion (121). Thus, when the supporting arm (120) is squeezed by an air tube (300), the contact portion (121) forms an arcuate structure, and the convex surface of the arcuate structure faces the side of the supporting arm (120) away from the main body structure (110), causing the contact portions (121) on different supporting arms (120) to at least partially attach to a gap (340) between cartilages (330) of the air tube (300).

Abstract: An ablation apparatus (20) is provided, including: a catheter (21) and an ablation portion (22) connected to a distal end of the catheter (21), where the ablation portion (22) has an expansible property and includes a plurality of ablation members (22a); each ablation member (22a) includes a supporting unit (24), a wall attachment unit (23), and an energy release unit provided on the wall attachment unit (23); a plurality of supporting units (24) are deployed radially outwardly and extend toward the distal end of the ablation portion (22) to be connected to a plurality of wall attachment units (23); when the ablation portion (22) is in a naturally expanded state, at least one wall attachment unit (23) in the ablation portion (22) is independently deformed relative to the adjacent wall attachment units (23). The ablation apparatus (20) can adapt to the morphology of a target tissue and attach well to the target tissue.

Abstract: A puncture device, including a handle assembly and a puncture assembly that is received in the handle assembly and fixedly connected to the handle assembly, where the puncture assembly includes a puncture member; the handle assembly further includes a first control element for controlling the puncture member; and when the first control element rotates, the first control element controls the puncture member to move close to or away from the handle assembly. The first control element controls the puncture member to move close to or away from the handle assembly to facilitate the first control element to control the puncture member to pass out of the handle assembly, which is easy to operate, and it is convenient for controlling the puncture member to carry out puncture surgery. The puncture member can be prevented from continuously moving and harming the body due to inertia after a successful puncture during puncture surgery.

Abstract: A nerve ablation apparatus is provided, including supporting bodies (110, 210, 310, 410) and mounting members (120, 220, 420); the mounting members (120, 220, 420) are provided along the circumferences of the supporting bodies (110, 210, 310, 410) and of mesh structures; the mounting members (120, 220, 420) include first regions (121, 222) and second regions (122, 223) provided along the circumferences of the supporting bodies (110, 210, 310, 410) and include the mesh structures formed by a plurality of mesh wires; in the first regions (121, 222), the plurality of mesh wires intersect and at least a portion of the mesh wires are fixedly connected at intersections.

Abstract: A filter, including a main body part. The main body part includes a heart-proximal end, a plurality of connecting segments, and a first filter mesh connecting between the heart-proximal end and the plurality of connecting segments. An end of the connecting segments that is connected to the first filter mesh is bent towards a central longitudinal axis of the filter to form a bending part. A vertical distance between a proximal end of the bending part and the central longitudinal axis of the filter is less than a vertical distance between a distal end of the bending part and the central longitudinal axis of the filter.

Abstract: An embolic protection device includes a frame, an edge filter screen, and a plurality of supporting rods that are arranged at intervals. Each supporting rod includes a first tail end, a second tail end, and at least one head end that faces a distal end. The first tail end and the second tail end are separately connected to two opposite sides of the frame. The first tail end and the second tail end separately form a first line segment and a second line segment with the head end. The first line segment extends in a direction from the first tail end to the head end and gradually moves away from the frame, and the second line segment extends in a direction from the second tail end to the head end and gradually moves away from the frame, such that the plurality of supporting rods support the edge filter screen, which covers the plurality of supporting rods, in a direction facing away from the frame.

Abstract: A medical device, including a fixing part, and having a compressed state and a deployed state after self-expansion, where the fixing part is provided with at least one anchoring member configured to be clamped in a gap on body tissue after the medical device is implanted into the body tissue, so as to anchor the medical device in the body. The medical device prevents damage to human tissue by providing anchoring members that are clamped in the gap in the human tissue rather than piercing through the human tissue after the medical device is implanted into the human body, thereby further preventing wound damage from enlarging due to movement of the human tissue. Normal operation of the medical device is achieved while ensuring good anchoring ability.

Abstract: A left atrial appendage (LAA) occluder and an occluding system are provided. The LAA occluder includes a sealing portion and an ablation portion arranged in the sealing portion, as well as a hollow proximal connector at a proximal end of the sealing portion. The ablation portion is connected to the proximal connector. The ablation portion is used to freeze an LAA after being injected with cryogen so as to form an annular isolation band on an inner wall of the LAA for blocking the conduction of electrical signals between the LAA and a left atrium.

Abstract: A left atrial appendage occluder (200) comprises a sealing part (220), a fixing part (210) disposed at one side of the sealing part (220), and a connection part (230) for connecting the sealing part (220) and the fixing part (210). The radial deformation capacity of the sealing part (220) is greater than the radial deformation capacity of the fixing part (210), and/or, the axial deformation capacity of the sealing part (220) is greater than the axial deformation capacity of the fixing part (210). In the left atrial appendage occluder (200), the radial or axial deformation capacity of the sealing part (220) is configured to be greater than the radial or axial deformation capacity of the fixing part (210), thereby avoiding the situation in which the sealing part (220) is not optimally fitted with the opening of the left atrial appendage (10) when the fixing part (210) is placed inside of the left atrial appendage (10), which in turn enhances the occlusion effect.

Abstract: A left atrial appendage (LAA) occluder includes a sealing portion and a fixing portion connected to the sealing portion, and one or more sealed seed sources encapsulated with radioactive particles. The sealed seed sources are arranged on the sealing portion and/or the fixing portion (20) and configured for forming an annular isolation band on an inner wall of an LAA after the radioactive particles are released. The annular isolation band is configured for blocking the electrical signal conduction between the LAA and a left atrium. In the LAA occluder, the annular isolation band is formed on the inner wall of the LAA by the release of the radioactive particles in the sealed seed sources arranged on the sealing portion and/or the fixing portion.

Abstract: An occlusion device includes a fixing portion with a plurality of supporting bodies; the plurality of supporting bodies include a plurality of supporting sections spaced apart along a circumferential direction of the fixing portion, where tail ends of at least two adjacent supporting sections bend and extend towards the interior of the fixing portion to form a convergence section, by which the tail ends of the at least two adjacent supporting sections are connected; the at least two adjacent supporting sections and the corresponding convergence section form a set of suspended sections, which are spaced and suspended along the circumferential direction of the fixing portion. The suspended sections can adaptively deform according to different internal tissue structures, and prevent a single supporting section from being locally deformed to a large extent, and buffer the supporting section.

Abstract: A measuring device includes a hollow catheter and a guide wire which is insertable into the hollow catheter, where a catheter developing structure is arranged on the catheter, a distance of the catheter developing structure from a distal end of the catheter being less than a length of diseased tissue; a guide wire developing structure is arranged on a distal end of the guide wire, and a scale mark zone is arranged on the guide wire, a proximal end of the catheter can enter into the scale mark zone; the scale mark zone is configured to directly or indirectly measure a distance between the proximal end of the catheter and the end portion of the guide wire, and further measure the length of the diseased tissue.

Abstract: An occlusion device includes a sealing disc, and a fixing frame connected to the sealing disc and located on one side of the sealing disc. The fixing frame includes a connecting portion connected to the sealing disc and at least one supporting body. The at least one supporting body radiates from the connecting portion and extends towards a proximal end to form a plurality of supporting sections. The supporting section is provided with at least one first restraint portion. The fixing frame is provided with at least one second restraint portion. The occlusion device further includes at least one restraint member. The restraint member is connected to the first and second restraint portion so a portion of the restraint member between the first and second restraint portion generates a restraint force that restrains movement of at least the supporting section.

Abstract: A left atrial appendage occluder (200) comprises a sealing part (220), a fixing part (210) disposed at one side of the sealing part (220), and a connection part (230) for connecting the sealing part (220) and the fixing part (210). The radial deformation capacity of the sealing part (220) is greater than the radial deformation capacity of the fixing part (210), and/or, the axial deformation capacity of the sealing part (220) is greater than the axial deformation capacity of the fixing part (210). In the left atrial appendage occluder (200), the radial or axial deformation capacity of the sealing part (220) is configured to be greater than the radial or axial deformation capacity of the fixing part (210), thereby avoiding the situation in which the sealing part (220) is not optimally fitted with the opening of the left atrial appendage (10) when the fixing part (210) is placed inside of the left atrial appendage (10), which in turn enhances the occlusion effect.

Abstract: The present invention relates to a left atrial appendage occluder having a sealing disc and a fixing bracket which is connected to the sealing disc and located at one side of the sealing disc; the fixing bracket comprising a connecting portion connected to the sealing disc, and a plurality of supports. After radiating out distally from the connecting portion, the plurality of supports are bent to extend proximally to form a plurality of spaced suspended supporting segments. The left atrial appendage occluder further includes a thin film, with all the supports being connected through the thin film.

Abstract: A plugging device, including a first part, and a second part connected to the first part. The first part or the second part includes a plurality of braiding filaments and a gathering member; portions of the braiding filaments that are close to one ends of the braiding filaments cooperate to form a disc face. The plugging device further includes a film member. The film member at least covers part of an outer surface of the disc face; the gathering member includes an inner sleeve and an outer sleeve, both of which are hollow and sleeved; and one end of each braiding filament and at least part of a gathering region of the film member are all fixed to the gathering member.

Abstract: A left atrial appendage (LAA) occluder includes a sealing portion and a fixing portion connected to the sealing portion, and one or more sealed seed sources encapsulated with radioactive particles. The sealed seed sources are arranged on the sealing portion and/or the fixing portion (20) and configured for forming an annular isolation band on an inner wall of an LAA after the radioactive particles are released. The annular isolation band is configured for blocking the electrical signal conduction between the LAA and a left atrium. In the LAA occluder, the annular isolation band is formed on the inner wall of the LAA by the release of the radioactive particles in the sealed seed sources arranged on the sealing portion and/or the fixing portion.

Abstract: A conveyor for an implant having at least one cavity, including a conveying handle, a conveying cable, and a core wire. The conveying cable is a tubular body, a proximal end of the core wire is connected to the conveying handle, and a distal end of the core wire penetrates a distal end of the conveying cable from a proximal end of the conveying cable; a first control is provided on the conveying handle, and when the implant is connected to the distal end of the conveying cable, the first control controls the distal end of the core wire to extend into the implant to straighten the curved implant, or the first control controls the core wire to withdraw from the implant to restore the implant to a preset shape. The conveyor can load and release the implant on the conveyor, and be used in the entire implanting process.

Abstract: An occluding device includes a sealing disc. The sealing disc includes a proximal disc surface and a distal disc surface, as well as an edge connecting the proximal disc surface and the distal disc surface. The sealing disc is provided with at least one buffer member. The at least one buffer member is distributed along the edge. The occluding device can reduce the damage inflicted on internal tissues caused by the edge of the sealing disc, better protect the internal tissues and reduce the risk of surgery.

Abstract: A delivery sheath and a medical device. The delivery sheath includes an outer canal and a traction structure. The outer canal includes a connecting canal, a canal body, and a distal canal. The canal body is located between the connecting canal and the distal canal. The canal body includes a first flexible canal, a spacer canal, and a second flexible canal. The spacer canal is provided between a distal end of the first flexible canal and a proximal end of the second flexible canal. The hardness of the connecting canal is greater than that of the first and second flexible canals, and the hardness of the spacer canal is greater than that of the first and second flexible canals. The traction structure includes a first traction fiber and a second traction fiber.