Abstract: An occluder and an occlusion device, including: a mesh occlusion body, which defines a cavity, and a proximal end bolt head; the proximal end bolt head configured with a locking hole which penetrates the cavity; the occluder further having a locking member, a distal end of the locking member being connected to a distal end of the occlusion body; the locking member having a connecting portion which is connected to the occlusion body; the diameter of a circumscribed circle of a projection of the first bending portion on a cross section perpendicular to a length direction thereof being smaller than the diameter of the smallest inscribed circle of a locking hole, and the width of a projection of the first bending portion on a plane perpendicular to longitudinal central axis direction of the locking hole being larger than the diameter of the largest inscribed circle of the locking hole.

Abstract: A lung volume-reducing elastic implant (2) and a lung volume-reducing instrument; the lung volume-reducing elastic implant (2) is tubular and comprises a proximal implant end (201), an elastic deformation part (205) and a distal implant end (202); the elastic deformation part (205) is located between the proximal implant end (201) and the distal implant end (202), and the elastic deformation part (205) has a shape memory characteristic; the lung volume-reducing elastic implant (2) is opened at the proximal implant end (201); the elastic deformation part (205) is provided with a plurality of grooves (204) at intervals along the longitudinal direction thereof; each groove (204) communicates with the tube cavity of the elastic deformation part (205); the lung volume-reducing instrument comprises the lung volume-reducing elastic implant (2) and a delivery device (1) matching same; the delivery device (1) comprises a guidewire (101) and a hollow push piece (110); the lung volume-reducing elastic implant (2) is det

Abstract: A heart valve prosthesis device includes a tubular stent body having an inflow end and an outflow end; a leaflet disposed in the lumen of the stent body; and fixing structures connected with the stent body and configured to fix the leaflet on the stent body. The leaflet includes at least two halves, and a connecting portion(s) connecting two adjacent halves. The fixing structure includes a closed hollow portion located on the stent body, and a fixing rod disposed in the hollow portion; one end of the fixing rod is connected to the hollow portion, and the other end is a free end; the connecting portion is hung on the fixing rod from the free end so as to fix the leaflet on the stent body.

Abstract: An intervention guidance device (10) includes a main body portion (100) and a guidance portion (200). The guidance portion (200) has a contracted configuration and an expanded configuration. In the expanded configuration, the guidance portion (200) has a central area (201) and a closed outer edge (202). In the contracted configuration, the outer edge (202) is farther away from the main body portion (100) than the central area (201), and the guidance portion (200) is restorable from the contracted configuration to the expanded configuration. In the intervention guidance device (10), the radial dimension of the guidance portion (200) is larger than the distance between the chordae tendineae, so that an effective access path that does not cross the chordae tendineae can be established, the subsequent implantation of a heart valve prosthesis does not pass through the chordae tendineae, and the success rate of a heart valve prosthesis implantation surgery can be improved.

Abstract: A covered stent, including a proximal end end surface, a distal end end surface and a peripheral surface located between the proximal end end surface and the distal end end surface, the peripheral surface including an inner surface and an outer surface. The outer surface is covered with a first coating membrane, and the inner surface is covered with a second coating membrane. The covered stent further includes a stent main body, which is between the first coating membrane and the second coating membrane. At least one of two ends of the first coating membrane and the second coating membrane fold inward or outward so as to wrap at least one from among the proximal end end surface and the distal end end surface.

Abstract: A conveyor and a conveyor system are provided. The conveyor comprises a lumen assembly and a self-locking mechanism connected to the lumen assembly, wherein the lumen assembly comprises an inner core tube, a recovery sheath movably surrounding the inner core tube, and an outer sheath movably surrounding the recovery sheath; the self-locking mechanism is connected to the recovery sheath; and the outer sheath can move relative to the inner core tube in an axial direction of the conveyor. The self-locking mechanism has a self-locked state and an unlocked state, wherein when the self-locking mechanism is in the unlocked state, the recovery sheath can move relative to the inner core tube in the axial direction of the conveyor; and when the self-locking mechanism is in the self-locked state, the recovery sheath maintains stationary relative to the inner core tube.

Abstract: An anti-shrinkage device for a conveyor and a conveyor thereof, wherein the anti-shrinkage device is sleeved on a sheath core tube of a conveyor and is located between an end head of the conveyor and a push rod. The anti-shrinkage device includes at least two hollow anti-retraction members, and the at least two anti-retraction members are arranged at an interval along the length direction of the sheath core tube. The anti-shrinkage device further includes a connection member that connects any two adjacent anti-retraction members among the at least two anti-retraction members.

Abstract: A left atrial appendage occluder, including a closure disc, a bracket located on one side of the closure disc, and a connecting member connecting the closure disc and the bracket; the bracket includes a first fixing connection member, a second fixing connection member, and a number of support rods; the first ends of the plurality of support rods are collapsed and secured by the first fixing connection member; the second ends of the plurality of support rods are collapsed and secured by the second fixing connection member; a connecting member is connected to the first fixing connection member. The bracket is arranged such that the two ends constituted by at least two support rods have a closed structure, thus increasing the area of contact between the outer surface of the bracket and the left atrial appendage.

Abstract: An implant (500) comprises an elastic deformation portion (51) and a connection portion (52) connected with the proximal end (511) of the elastic deformation portion (51), wherein the elastic deformation portion (51) is covered by an elastic outer layer (55); the proximal end of the connection portion (52) is surrounded by a tightening ring (58); and the proximal end of the elastic outer layer (55) is covered by the tightening ring (58). Since the proximal end of the elastic outer layer (55) of the implant (500) is surrounded by a tightening ring (58), the elastic outer layer (55) is closely attached on the connecting portion (52) of the implant (500), such that the elastic outer layer (55) can be prevented from being rolled over from the surface of the implant (500) when the implant (500) is implanted, thereby improving safety of lung volume reduction surgery.

Abstract: The invention belongs to the field of interventional medical instruments, and relates in particular to a thrombus removal device used for removing a thrombus in a blood vessel. The thrombus removal device includes an elongated delivery member and a plurality of thrombus removal members disposed on the elongated delivery member; the thrombus removal member has a compressed configuration and an expanded configuration formed from the compressed configuration by means of self-expansion; and at least one thrombus removal member among the plurality of thrombus removal members is rotatably connected to the elongated delivery member. By means of causing the thrombus removal member to have rotational degrees of freedom, the thrombus removal device provided by the present invention enables a thrombus to enter the thrombus removal member more easily by means of a thrombus entrance so that the thrombus removal member may fully contact the thrombus, thereby achieving effective capture of the thrombus.

Abstract: An occluder, including an occlusion unit and an occlusion head connected to the occlusion unit. The occlusion unit has a central axis passing through a distal end and a proximal end of the occluder; the occluder further includes a marking structure, the marking structure includes a distal marker and at least two first markers, the distal marker is provided on the occlusion head, all the first markers located in the same placement plan are connected to the occlusion unit, the placement plane is perpendicular to the central axis, the distal marker is located outside the placement plane, projection points of all the first markers in a projection plane perpendicular to the placement plane is located on a straight line segment, and when the occluder is in a natural state, connection lines between the distal marker and two end points of the straight line segment form a triangle.

Abstract: A tube stent includes a first tube body. The first tube body includes a first section, a second section, and a transition section located between the first section and the second section. One end of the transition section is connected to the first section, and the other end is connected to the second section. The shortening rate of the first section and the shortening rate of the second section are smaller than the shortening rate of the transition section. By using the tube stent, the pulsations of aortas are buffered by the transition section, so that vibration deformations of the tube stent are confined to the first section and the transition section, and accordingly the relative stability of the second section and branch blood vessels can be ensured, and the stimulations to walls of the branch blood vessels can be reduced.

Abstract: A filter (10) includes a proximal end (1), a distal end (2) and a main filter body connected between the proximal end (1) and the distal end (2). The main filter body has a first filter unit (3) and a second filter unit (4), both being conical mesh structures, as well as multiple intermediate connection posts (5) connecting the first filter unit and the second filter unit. The intermediate connection posts (5) have provided thereon support posts (6). A support post (6) includes a transition segment (61) extending from an intermediate connection post (5) to a blood vessel wall, and a support segment bent and extending from the transition segment (61), and at least partially abutting the blood vessel wall. The support segment has a main body (62) bent and extending from the end of the transition segment (61) and a flexible segment (63) bent and extending from the main body (62).

Abstract: The present application provides an implantation method of an artificial heart valve. The implantation method can include forming an incision in the left chest to expose the ventricle; advancing a guide wire kept away from chordae tendineaes through the atrium into the ventricle; advancing a guide wire catcher into the ventricle from the incision to pull out the distal end of the guide wire from the ventricle; and advancing the artificial heart valve into the ventricle from the distal end of the guide wire with a valve deliverer, and placing the artificial heart valve at a primary valve between the ventricle and the atrium along the guide wire. The artificial heart valve may avoid the chordae tendineaes in the heart system through the guide wire track during implantation.

Abstract: A method for implanting an interventional medical device, including the following steps: delivering the distal end of the puncture needle into the right atrium via the inferior vena cava; locating the puncture site on atrial septum under X-ray fluoroscopy in a first perspective angle and a second perspective angle, and puncturing the atrial septum by the puncture needle through the puncture site; delivering the medical device to the left atrial appendage or left atrium for release under X-ray fluoroscopy in a first perspective angle. The implanting method of the disclosure does not require the use of a TEE device during implementation and provides benefits of a simple operation, short operation time, and easy implementation conditions, while also be easy to promote and popularize.

Abstract: Disclosed is a catcher (100), comprising an catching ring (11) and at least one connecting rod (15), wherein both ends of the connecting rod (15) are connected to the catching ring (11), and the connecting line between the two ends of the connecting rod (15) is located within the catching ring (11). Compared with catching loops in the prior art, the catching ring (11) of the catcher (100) is a ring structure supported by the connecting rod (15), thereby having a relatively high stability and not easily being deformed under erosion by a blood flow, so as to facilitate accurate positioning by a doctor during clinical operations and improve the success rate of withdrawal.

Abstract: An implantation method of a stent system, and the implantation method including implanting a main stent; introducing a catcher; introducing a long sheath and a guiding catheter along a preset guide wire, so as to make the distal end of the long sheath and the distal end of the guiding catheter extend out from the distal end of the inner branch; the distal end of the long sheath and the distal end of the guiding catheter to respectively enter a target branch blood vessel; withdrawing the guiding catheter, and introducing a branch stent delivery along the long sheath to complete the implantation of the branch stent. The method greatly shortens the implantation time of the stent system by simplifying the path of the preset guide wire in the implantation process and fully utilizing the characteristics of the preset guide wire with double soft heads.

Abstract: An artificial heart valve stent including: a tubular stent body having an inflow side end and an outflow side end, the inflow side end and the outflow side end being opposite to each other; an inflow side skirt surrounding the external wall of the stent body; and an outflow side skirt surrounding the external wall of the stent body. In a spread state, free ends of the inflow side skirt and the outflow side skirt extend toward the inflow side end; and the inflow side skirt cooperates with the outflow side skirt to clamp heart valve tissues. The artificial heart valve stent can be steadily arranged on heart valve tissues, prolong the service life of an artificial heart valve and reduce the risk of another artificial heart valve replacement for the patient.

Abstract: An occluder includes a first occluder disc, a second occluder disc, a waist portion connecting the first occluder disc and the second occluder disc, and at least one soft and fibrous strand bundle structure. The strand bundle structure is disposed on at least one of a disc surface of the first occluder disc and a disc surface of the second occluder disc, the two disc surfaces faces each other, and the strand bundle structure is disposed near the waist portion. By disposing the strand bundle structure to be immediately adjacent to the waist portion, a defect opening can be occluded after implantation, thereby effectively blocking blood from flowing from one side of the defect to the other side thereof, and preventing a shunt from being formed.

Abstract: A double-layer blood vessel stent. A skirt-sided stent is provided on a main body stent. A first developing member and a second developing member are provided on the main body stent. The first developing member includes a first developing portion and a second developing portion, where the first developing portion and the second developing portion are flush with a free end at a position where the distance between the intersections on a plane perpendicular to the direction of an axis of the main body stent is the minimum distance; and an end, away from a first end, of the second developing member is flush with an end away from a tapered section of an extending section. This structure allows for accurate positioning of the double-layer vessel stent.