Abstract: A stent graft, including multiple wavy rings. The stent graft includes, in a circumferential direction, a region A and a region B connected to the region A. Each wavy ring includes a first wavy section located in the region A, and a second wavy section located in the region B. The wave included angle of the first wavy section is about 70°-120°; the ratio of the wave height of the first wavy section to the spacing between adjacent first wavy sections is 1/4-3; the wave included angle of the second wavy section is 30°-60°, the ratio of the wave height of the second wavy section to the spacing between adjacent second wavy sections is 1/4-3/2, and the ratio of the wave height of the first wavy section to the wave height of the second wavy section is greater than or equal to 1/3 and less than 1.

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: 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: A luminal stent, including a tubular body and a skirt sleeved on the tubular body. One end of the skirt is a fixed end, and the fixed end is sealedly connected to the outer surface of the tubular body; the other end of the skirt is a free end; on a section passing through the central axis of the tubular body, the ratio of the distance between the fixed end and the free end located on the same side of the central axis of the tubular body to the vertical distance between two points of the free end on both sides of the central axis of the tubular body along the radial direction of the skirt is less than 1/2.

Abstract: A stent graft. The stent graft is provided in the axial direction thereof with at least one region T, and the region T includes a number of wavy rings; in the circumferential direction, the region T includes a region A and a region B that is connected to the region A, the ratio of the area of the region A to the area of the region T being ¼-?, the ratio of the coverage rate of the wavy rings in the region A to the coverage rate of the wavy rings in the region B being ?- 9/10, and the ratio of the coverage rate of the wavy rings within any circular region having a diameter of 20 mm within the region A to the coverage rate of the wavy rings in the region A being 0.7-1.3.

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: Disclosed are an implantable medical device, a preparation method thereof and an implantable medical device preform for the preparation of the implantable medical device. The implantable medical device comprises a metal basal body (21) and a polymer film layer (22) covering the surface of the metal basal body (21) and preventing endothelium growth and covering, and also comprises a transitional body (23), which is located between the metal basal body (21) and the polymer film layer (22) and covers at least part of the surface of the metal basal body (21), wherein the transitional body (23) is connected to the polymer film layer (22) and the metal basal body (21). By arranging the transitional body (23) to be connected to the polymer film layer (22) and the metal basal body (21), the polymer film layer (22) will not easily fall off when being implanted into a human body.

Abstract: A temporary cardiac pacemaker including an acquisition module for acquiring an intracavity electrocardiography signal; a pre-processing module, connected to the acquisition module, for pre-processing the intracavity electrocardiography signal; a storage module, connected to the pre-processing module, for storing the pre-processed intracavity electrocardiography signal in real time; and a display control module, connected to the storage module, for display control. The display control module includes a display and an instruction determination unit for detecting whether a pacing parameter adjustment instruction is triggered and to call and display the intracavity electrocardiography signal stored in real time on a pacing parameter adjustment interface, which displays the intracavity electrocardiography signal stored in real time and the pacing adjustment parameter on the display; and the displayed information includes intracavity electrocardiography and electrocardiography event markers.

Abstract: A heart valve prosthesis, including a valved stent and valve leaflets, where the valve leaflets are accommodated in the valved stent, at least two valve leaflets are provided and centrosymmetrically distributed along the circumferential direction of an inner surface of the valve leaflet stent, one ends of each of two adjacent valve leaflets are combined together on the valve leaflet stent to form a valve corner, the valved stent is provided with a positioning member, and the projections of a perpendicular line of one of the valve corners to the axis of the valved stent and a perpendicular line of the positioning member to the axis of the valved stent are coincident on a plane perpendicular to the axis of the valved stent. The heart valve prosthesis can considerably reduce regurgitation at the center.

Abstract: A lung-volume-reduction elastic implant (500) is tubular and at least the proximal end of the implant has an opening. The implant (500) comprises an elastic deforming part (51) and a flexible guiding part (53) connected to the distal end of the elastic deforming part (51). The elastic deforming part (51) has a shape memory property. The elastic deforming part (51) is provided in the lengthwise direction thereof with several slots (514) at intervals, wherein each slot (514) communicates with the tubular cavity of the elastic deforming part (51). Under the same externally applied force, the flexible guiding part (53) deforms more easily than the elastic deforming part (51). An implant delivering instrument (600) comprises an implant (500) and a matching delivering means (700). The delivering means (700) comprises a core wire (71) and a hollow pushing member (73). The implant (500) is detachably connected to the distal end of the pushing member (73) by means of the proximal end of the implant.

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: 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: An absorbable iron-based implantable device, including an iron-based substrate and an iron absorption promoter that is attached to the iron-based substrate. The iron absorption promoter is a polymer containing an antioxidant structural unit on the molecular chain thereof. The antioxidant is gradually released as the iron absorption promoter is gradually degraded or broken, and may promote the absorption of iron.

Abstract: A lung volume reduction elastic implant (500) and a lung volume reduction instrument are provided. The lung volume reduction elastic implant (500) has an elastic deformation part (51), and a flexible guide (53, 53a) connected to the distal end of the elastic deformation part (51). The flexible guide (53, 53a) is provided with a first flexible part (531). The first flexible part (531) has an insert part (5312) and a distal part (5311). The insert part (5312) is connected to the distal end of the elastic deformation part (51). The distal end of the distal part (5311) of the first flexible part (531) is the distal end of the lung volume reduction elastic implant (500). The first flexible part (531) is internally provided with a radiograph component (56).

Abstract: An absorbable iron-based instrument is provided having an iron-based substrate, a zinc-containing protector in contact with the iron-based substrate, and a degradable polyester in contact with the iron-based substrate and/or the zinc-containing protector. The range of the ratio of the mass of the zinc-containing protector to the mass of the iron-based substrate is 1:200 to 1:2. In the degradable polyester, the mass fraction of a low-molecular-weight part with a molecular weight of less than 10,000 is less than or equal to 5%; alternatively, in the degradable polyester, the mass fraction of a residual monomer is less than or equal to 2%.

Abstract: A luminal stent includes a tube body (10) that can be compressed and expanded in the radial direction, and an anti-leakage structure (20); the tube body (10) is divided by the anti-leakage structure (20) into a first tube body (11) positioned on one side of the anti-leakage structure (20) and a second tube body (12) positioned on the other side of the anti-leakage structure (20), at least part of the first tube body (11) being encircled by the anti-leakage structure (20).

Abstract: Provided is an occluder, comprising a first disk-shaped structure (10) with a grid, wherein the first disk-shaped structure (10) is woven from at least two groups of braided wires, the two groups of braided wires are crossed to form multiple rings of crossing points, a blocking membrane (20) is also arranged in the disk-shaped structure (10), an edge of the blocking membrane (20) is connected to the outermost ring of crossing points (100) of the multiple rings of crossing points through a sewing wire, and the number of crossing points in the outermost ring of crossing points (100) sewn with the blocking membrane (20) is smaller than the number of all the crossing points in the outermost ring of the crossing points (100), and a position of the blocking membrane (20) near the edge thereof is connected to a ring of crossing points within the outermost ring of crossing points (100) in the multiple rings of crossing points through the sewing wire.

Abstract: An absorbable iron-based alloy implantable medical device includes an iron-based alloy matrix, a degradable polymer coating disposed on the surface of the iron-based alloy matrix, and a corrosion inhibition layer disposed on the surface of the iron-based alloy matrix. The corrosion inhibition layer can delay early-stage corrosion of the iron-based alloy matrix, ensure mechanical performance of a medical device in the early stage of the implantation, prevent degradation of a polymer in the early stage of the implantation of the medical device, and reduce the usage of the degradable polymer, thereby reducing risks of inflammatory reactions.

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: An absorbable metal stent includes an absorbable metal substrate; the absorbable metal substrate includes a plurality of wave-shaped annular structures and a plurality of axial connecting portions, two ends of each axial connecting portion being connected to two adjacent wave-shaped annular structures, respectively, so as to axially connect the plurality of wave-shaped annular structures; a corrosion-promoting coating is formed on each axial connecting portion, the corrosion-promoting coating containing a corrosion-promoting substance, and the corrosion-promoting substance being selected from at least one of a degradable polymer and a degradable polymer antioxidant; the corrosion-promoting coatings cause the corrosion of the axial connecting portions to occur earlier than the corrosion of the plurality of wave-shaped annular structures. The absorbable metal stent has good bending performance and may prevent the problems of secondary hyperplasia after implantation and stenosis caused thereby.