CN109009562B - Improved aortic arch tectorial membrane stent type blood vessel - Google Patents
Improved aortic arch tectorial membrane stent type blood vessel Download PDFInfo
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- CN109009562B CN109009562B CN201810982118.7A CN201810982118A CN109009562B CN 109009562 B CN109009562 B CN 109009562B CN 201810982118 A CN201810982118 A CN 201810982118A CN 109009562 B CN109009562 B CN 109009562B
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- aortic
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- 210000002376 aorta thoracic Anatomy 0.000 title claims abstract description 23
- 210000002489 tectorial membrane Anatomy 0.000 title claims abstract description 11
- 210000004204 blood vessel Anatomy 0.000 title abstract description 28
- 239000012528 membrane Substances 0.000 claims description 21
- 238000005452 bending Methods 0.000 claims description 3
- 230000017531 blood circulation Effects 0.000 description 5
- 210000001168 carotid artery common Anatomy 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 210000002168 brachiocephalic trunk Anatomy 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- -1 polytetrafluoroethylene Polymers 0.000 description 2
- 238000002601 radiography Methods 0.000 description 2
- 210000003270 subclavian artery Anatomy 0.000 description 2
- 229910000531 Co alloy Inorganic materials 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 210000001367 artery Anatomy 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 229910001285 shape-memory alloy Inorganic materials 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001256 stainless steel alloy Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 231100000216 vascular lesion Toxicity 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/04—Hollow or tubular parts of organs, e.g. bladders, tracheae, bronchi or bile ducts
- A61F2/06—Blood vessels
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2250/00—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2250/0058—Additional features; Implant or prostheses properties not otherwise provided for
- A61F2250/0096—Markers and sensors for detecting a position or changes of a position of an implant, e.g. RF sensors, ultrasound markers
- A61F2250/0098—Markers and sensors for detecting a position or changes of a position of an implant, e.g. RF sensors, ultrasound markers radio-opaque, e.g. radio-opaque markers
Landscapes
- Health & Medical Sciences (AREA)
- Gastroenterology & Hepatology (AREA)
- Pulmonology (AREA)
- Cardiology (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Prostheses (AREA)
Abstract
The utility model provides an improved generation aortic arch tectorial membrane support formula blood vessel, including an aortic stent blood vessel and three branch arterial stent blood vessel, aortic stent blood vessel is by near heart end section, sunken section and distal end section splice gradually and is formed a nearly curved multistage line structure, opening one has been seted up to near heart end section, opening two has been seted up to sunken section roof, opening three has been seted up to distal end section, opening one, opening two and opening three respectively correspond to be fixed with respectively and correspond in interior chimney support one, interior chimney support two and interior chimney support three, three interior chimney support staggers in axial distribution, three branch arterial stent blood vessel partial shipment is in three interior chimney supports. The application can prevent the mutual interference when two inner chimney brackets at the near-heart end are compressed, so that the aortic stent vessels are easier to compress and put into a conveying system with smaller diameter, and the guide wires and the guide pipes are easier to respectively select the inner chimney brackets, thereby facilitating the conveying and releasing of the branched arterial stent vessels.
Description
Technical Field
The application relates to the field of implantable blood vessels, in particular to an improved aortic arch covered stent type blood vessel.
Background
The Chinese patent with the publication number of CN 102973303B is an aortic arch tectorial membrane stent type blood vessel invented by the inventor, and comprises an aortic stent type blood vessel and three branch arterial stent type blood vessels, wherein a section of concave part is formed on the aortic stent type blood vessel, the concave part comprises a left side wall close to a proximal end, a right side wall far away from the proximal end and a bottom wall connected with the left side wall and the right side wall, the left side wall of the concave part is provided with two openings, the right side wall is provided with one or two openings, an inner chimney stent with the caliber equivalent to that of the opening is fixed in each opening, the inner chimney stent extends along the side wall of the aortic stent type blood vessel deviating from the direction of the concave part, and the branch arterial stent type blood vessel is subpackaged in the inner chimney stent.
During operation, the aortic stent in a compressed state is delivered to the position of vascular lesions through a delivery system with a smaller tube diameter. However, since two inner chimney stents on the same side wall in the aortic stent extend along the side wall of the vessel of the aortic stent facing away from the recess, the two inner chimney stents interfere with each other in the radial direction when compressed, affecting the compression of the entire vessel of the aortic stent. After the aortic stent is released, the two inner chimney stents are mutually overlapped in the radial direction, which brings difficulty to the delivery and release of the branched arterial stent vessels and possibly causes that the two branched arterial stent vessels are simultaneously delivered and released in the same inner chimney stent. In addition, most of the existing aortic stents have a linear tubular structure, and after the aortic stent is delivered into the aortic arch part for release, the resilience force generated at the two ends of the aortic stent is large, so that the vessels at the corresponding positions of the aortic stent are greatly pressed, and even the vessels are ruptured. To this end, the present inventors have proposed an improved aortic arch stent graft.
Disclosure of Invention
The application provides an improved aortic arch tectorial membrane stent type blood vessel, which aims to solve the defects that the compression of the whole aortic stent blood vessel is affected by the mutual interference of two inner chimney stents which are arranged in parallel in the radial direction when the existing aortic arch tectorial membrane stent type blood vessel is compressed, and the two inner chimney stents are mutually overlapped in the axial direction, so that the difficulty is brought to the transportation and the release of branch arterial stent blood vessels.
The application adopts the following technical scheme:
the improved aortic arch tectorial membrane stent type blood vessel comprises an aortic stent blood vessel and three branch arterial stent blood vessels, wherein the aortic stent blood vessel is formed by sequentially splicing a proximal end section, a sunken section and a distal end section to form an approximately arc-shaped multi-section line structure, the left end part and the right end part of the sunken section are respectively connected with the right side wall of the proximal end section and the left side wall of the distal end section through a tectorial membrane I and a tectorial membrane II, the middle upper part of the right side wall of the proximal end section is provided with a first opening, the top surface of the bottom wall of the sunken section close to the left side wall of the distal end section is vertically upwards provided with a second opening, the middle upper part of the left side wall of the distal end section is provided with a third opening, the first opening, the second opening and the third opening are respectively correspondingly fixed with an inner chimney stent, the second inner chimney stent and the third inner chimney stent, the third inner chimney stent is respectively sewed along the side wall of the aortic stent in the direction deviating from the sunken section, the second chimney stent is fixedly sewed on the lower end surface of the top wall of the sunken section, the second chimney stent is formed by the second opening is vertically upwards provided with a third opening, the left chimney stent extends towards the third chimney stent and the inner chimney stent, and the third chimney stent extends towards the inner chimney stent.
Further, a large bending side is arranged below the connection of the second inner chimney bracket and the second opening.
Further, the left side wall of the distal end section is an inclined surface, the inclined surface and the top wall of the concave section form an obtuse angle structure, and the opening III is an inclined notch formed on the inclined surface.
Further, the longitudinal section of the top wall of the concave section is in an upward convex arc shape, or the longitudinal section of the concave section is in a circular shape.
Further, the first and second films are ring structures with wide upper part and narrow lower part, and the maximum lengths of the upper parts of the first and second films are 3-12 mm.
Further, the right end part of the first inner chimney bracket protrudes out of the first opening, and the protruding length of the first inner chimney bracket is 3-5 mm.
Further, the top end, the bottom end, the front end and the rear end of the outer circumference of the inner chimney support fixed at the opening one are respectively provided with an 8-shaped developing mark, and the top end, the bottom end, the front end and the rear end of the outer circumference of the front end of the inner chimney support protruding out of the opening one are respectively provided with an 8-shaped developing mark.
Further, the left end, the right end, the front end and the rear end of the outer circumference of the inner chimney bracket fixed at the two positions of the opening are respectively provided with an 8-shaped developing mark.
The top end, the bottom end, the front end and the rear end of the outer circumference of the inner chimney bracket fixed at the three openings are respectively provided with an 8-shaped developing mark.
Further, the aortic stent vessel is composed of a tubular membrane I and a plurality of annular waveform stents I which are sewn in the tubular membrane I at intervals, the inner chimney stent I, the inner chimney stent II and the inner chimney stent III all comprise a tubular membrane II and a plurality of annular waveform stents II which are sewn in the tubular membrane II at intervals, wherein the aortic stent vessel part corresponding to the axial projection of the inner chimney stent II is only provided with the tubular membrane I, the outer sides of two adjacent annular waveform stents II in the inner chimney stent I and the inner chimney stent III are correspondingly provided with the annular waveform stent I, and the sum of the widths of the two annular stents II is equal to the width of the corresponding annular waveform stent I.
As can be seen from the above description of the structure of the present application, compared with the prior art, the present application has the following advantages:
1. the aortic stent vessel is formed by splicing the proximal end section, the concave section and the distal end section, each section is provided with an opening, each opening is internally provided with an inner chimney stent correspondingly, and the three inner chimney stents are distributed in an axial staggered manner, so that the two inner chimney stents at the proximal end can be prevented from interfering with each other when being compressed, the aortic stent vessel is easier to compress and put into a conveying system with smaller diameter, and a guide wire and a guide tube are easier to select each inner chimney stent respectively, thereby facilitating the conveying and release of the branched arterial stent vessels and preventing a plurality of branched arterial stent vessels from entering the same inner chimney stent.
2. The aortic stent vessel is spliced by the proximal end section, the concave section and the distal end section to form a multi-section line structure which is approximately arc-shaped in a natural state, so that the resilience force of the two end parts of the aortic stent vessel is smaller after the aortic arch part is released, and the phenomenon of vessel rupture caused by compression of the corresponding vessel is avoided.
3. The aortic stent vessel part corresponding to the axial projection of the inner chimney stent II is only provided with the tubular membrane I and does not contain the annular waveform stent I, so that the inner chimney stent II is ensured not to be blocked by the annular waveform stent I on the aortic stent vessel during radiography, and the guide wire and the guide tube are enabled to rapidly select the inner chimney stent II.
Drawings
Fig. 1 is a front view of an aortic stent vessel in accordance with the present application.
Fig. 2 is a schematic view showing a state in which the aortic stent graft of the present application is stretched into a straight line.
Fig. 3 is a cross-sectional view taken along the direction A-A in fig. 2.
Fig. 4 is a sectional view in the direction B-B of fig. 2.
Fig. 5 is a schematic diagram showing the structure of the stent-type blood vessel of the present application after the stent-type blood vessel is released in the thoracic aorta and three branch blood vessels branch the arterial blood vessel.
Detailed Description
Specific embodiments of the present application will be described below with reference to the accompanying drawings.
The application discloses an improved aortic arch covered stent-graft, which comprises an aortic stent-graft 1 and three branch aortic stent-grafts 2, referring to figures 1 and 5. The aortic stent graft 1 is formed by sequentially splicing a proximal section 10, a concave section 20 and a distal section 30 to form an approximately arc-shaped multi-section line structure, wherein the left end and the right end of the concave section 20 are respectively connected with the right side wall of the proximal section 10 and the left side wall of the distal section 30 through a first coating 201 and a second coating 202.
Referring to fig. 1 to 4, an opening one 100 is formed in the upper middle portion of the right side wall of the proximal section 10, an opening two 200 is vertically formed on the top surface of the bottom wall of the concave section 20 close to the left side wall of the distal section 30, an opening three 300 is formed in the upper middle portion of the left side wall of the distal section 30, an inner chimney support one 31, an inner chimney support two 32 and an inner chimney support three 33 are respectively and correspondingly fixed in the opening one 100, the opening two 200 and the opening three 300, the inner chimney support one 31 and the inner chimney support three 33 are respectively sewn along the side wall of the aortic stent vessel 1 deviating from the direction of the concave section 20, the inner chimney support two 32 is fixedly sewn on the lower end surface of the top wall of the concave section 20, the inner chimney support two 32 extends from the opening two 200 to the direction of the left end of the concave section 20, and the three branch arterial stent vessels 2 are respectively arranged in the inner chimney support one 31, the inner chimney support two 32 and the inner chimney support three 33. The embodiment shows that the blood flow channels of the brachiocephalic trunk, the left common carotid artery and the left subclavian artery are respectively implanted into branch artery stent blood vessels from the inner chimney stent I, the inner chimney stent II and the inner chimney stent III. Of course, for some patients with the brachiocephalic trunk and left common carotid artery blood flow channel at a relatively short distance, in order to prevent the blood flow supply from being affected by the excessive bending angle of the branch arterial stent vessels, the blood flow channels of the left common carotid artery and the left subclavian artery can be implanted into the branch arterial stent vessels from the inner chimney stent III and the inner chimney stent II respectively.
Referring to fig. 1, the lower portion of the second inner chimney stent 32 connected to the second opening 200 has a large curved side, so that the branch arterial stent vessel 2 installed in the second inner chimney stent 31 is correspondingly curved and deformed, and the resistance of the blood flow flowing out of the branch arterial stent vessel can be reduced.
With continued reference to fig. 1, the first and second films 201 and 202 are ring-shaped structures with wide upper portions and narrow lower portions, and the maximum lengths of the upper portions of the first and second films 201 and 202 are 3-12 mm. The right end of the first inner chimney bracket 31 protrudes out of the first opening 100, and the protruding length is 3-5 mm, so that the right end of the first inner chimney bracket 31 can be found quickly during radiography. The longitudinal section of the top wall of the concave section 20 is in an upwardly convex arc shape, or the longitudinal section of the concave section 20 is in a circular shape.
Referring to fig. 2 and 4, the left side wall of distal section 30 is an inclined surface, and opening three 300 is an oblique cut formed on the inclined surface, and the inclined surface forms an obtuse angle structure with the top wall of recessed section 20, so that branch arterial stent vessel 2 can select inner chimney stent three 33.
Referring to fig. 1, the aortic stent vessel 1 is composed of a tubular membrane one 101 and a plurality of annular wave stents one 102 sewn in the tubular membrane one 101 at intervals, the inner chimney stent one 31, the inner chimney stent two 32 and the inner chimney stent three 33 each comprise a tubular membrane two 301 and a plurality of annular wave stents two 302 sewn in the tubular membrane two 301 at intervals, wherein only the tubular membrane one 101 is arranged at the aortic stent vessel 1 position corresponding to the axial projection of the inner chimney stent two 32, one annular wave stent one 102 is correspondingly arranged at the outer sides of two adjacent annular wave stents two 302 in the inner chimney stent one 31 and the inner chimney stent three 33, and the sum of the widths of the two annular wave stents two 302 is equal to the width of the corresponding annular wave stent one 102. The first annular wave bracket 102 and the second annular wave bracket 302 are made of medical stainless steel alloy rings with good biocompatibility, chemical stability, mechanical and physical properties, such as nickel-based alloy, cobalt-based alloy, 316 medical stainless steel, shape memory alloy or degradable high polymer materials; and the tubular membrane is polytetrafluoroethylene membrane, polyester fiber membrane, polyamide membrane or polypropylene membrane.
Referring to fig. 1, the top, bottom, front and rear ends of the outer circumference of the inner chimney support 31 fixed at the opening one 100 are respectively provided with an 8-shaped developing mark 12, and the top, bottom, front and rear ends of the outer circumference of the front end of the inner chimney support 31 protruding from the opening one 100 are respectively provided with a v-shaped developing mark 12. The left end, the right end, the front end and the rear end of the outer circumference of the inner chimney bracket II 32 fixed at the opening II 200 are respectively provided with an 8-shaped developing mark 12. The top end, the bottom end, the front end and the rear end of the outer circumference of the inner chimney bracket three 33 fixed at the opening three 300 are also respectively provided with an 8-shaped developing mark 12. The 8-shaped developing marks 12 are all obliquely arranged along the axial direction of the aortic stent graft 1. The figure 8 shaped imaging marker 12 is an inherent component of the stent itself, or a material with good biocompatibility and X-ray opaque properties.
The foregoing is merely illustrative of specific embodiments of the present application, but the design concept of the present application is not limited thereto, and any insubstantial modification of the present application by using the design concept shall fall within the scope of the present application.
Claims (10)
1. An improved aortic arch covered stent-graft vessel, comprising an aortic stent vessel and three branch aortic stent vessels, and is characterized in that: the aortic stent vessel is formed by splicing a near-heart end section, a concave section and a distal end section in sequence to form an approximate arc-shaped multi-section line structure, the left end part of the concave section is connected with the right side wall of the near-heart end section through a first tectorial membrane, the right end part of the concave section is connected with the left side wall of the distal end section through a second tectorial membrane, an opening I is formed in the middle upper part of the right side wall of the near-heart end section, an opening II is formed in the top surface of the top wall of the concave section, which is close to the left side wall of the distal end section, an opening III is formed in the middle upper part of the left side wall of the distal end section, an inner chimney bracket I, an inner chimney bracket II and an inner chimney bracket III are respectively and correspondingly fixed in the opening I, the inner chimney bracket II and the inner chimney bracket III, the inner chimney bracket III are respectively sewed along the side wall of the aortic stent vessel deviating from the direction of the concave section, the inner chimney bracket II is fixedly sewed on the lower end surface of the top wall of the concave section, the opening II extends towards the left end part of the concave section, and the opening III is divided into the inner chimney bracket I, the inner chimney bracket and the inner chimney bracket III.
2. The improved aortic arch stent graft as set forth in claim 1, wherein: and a large bending side is arranged below the connection of the inner chimney bracket II and the opening II.
3. The improved aortic arch stent graft as set forth in claim 1, wherein: the left side wall of the distal end section is an inclined surface, the inclined surface and the top wall of the concave section form an obtuse angle structure, and the opening III is an inclined notch formed on the inclined surface.
4. The improved aortic arch stent graft as set forth in claim 1, wherein: the longitudinal section of the top wall of the concave section is in an upward convex arc shape, or the longitudinal section of the concave section is in a circular shape.
5. The improved aortic arch stent graft as set forth in claim 1, wherein: the first and second films are ring structures with wide upper part and narrow lower part, and the maximum lengths of the upper parts of the first and second films are 3-12 mm.
6. The improved aortic arch stent graft as set forth in claim 5, wherein: the right end part of the first inner chimney bracket protrudes out of the first opening, and the protruding length of the first inner chimney bracket is 3-5 mm.
7. The improved aortic arch stent graft as set forth in claim 6, wherein: the top end, the bottom end, the front end and the rear end of the outer circumference of the inner chimney support fixed at the opening one are respectively provided with an 8-shaped developing mark, and the top end, the bottom end, the front end and the rear end of the outer circumference of the front end of the inner chimney support protruding out of the opening one are respectively provided with an 8-shaped developing mark.
8. The improved aortic arch stent graft as set forth in claim 1, wherein: the left end, the right end, the front end and the rear end of the outer circumference of the inner chimney bracket fixed at the two openings are respectively provided with an 8-shaped developing mark.
9. The improved aortic arch stent graft as set forth in claim 1, wherein: the top end, the bottom end, the front end and the rear end of the outer circumference of the inner chimney bracket fixed at the three openings are respectively provided with an 8-shaped developing mark.
10. The improved aortic arch stent graft as set forth in claim 1, wherein: the aortic stent vessel consists of a tubular membrane I and a plurality of annular waveform stents I which are sewn in the tubular membrane I at intervals, wherein the inner chimney stent I, the inner chimney stent II and the inner chimney stent III all comprise a tubular membrane II and a plurality of annular waveform stents II which are sewn in the tubular membrane II at intervals, wherein the aortic stent vessel part corresponding to the axial projection of the inner chimney stent II is only provided with the tubular membrane I, the outer sides of two adjacent annular waveform stents II in the inner chimney stent I and the inner chimney stent III are correspondingly provided with the annular waveform stent I, and the sum of the widths of the two annular stents II is equal to the width of the corresponding annular waveform stent I.
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CN201810982118.7A CN109009562B (en) | 2018-08-27 | 2018-08-27 | Improved aortic arch tectorial membrane stent type blood vessel |
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CN201810982118.7A CN109009562B (en) | 2018-08-27 | 2018-08-27 | Improved aortic arch tectorial membrane stent type blood vessel |
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CN109009562B true CN109009562B (en) | 2023-11-21 |
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Families Citing this family (7)
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CN209808643U (en) * | 2019-01-31 | 2019-12-20 | 陈宏伟 | Aorta stent type blood vessel |
CN111407463B (en) * | 2020-03-19 | 2022-08-12 | 湖南埃普特医疗器械有限公司 | Covered stent system |
CN113712702A (en) * | 2020-05-12 | 2021-11-30 | 上海微创心脉医疗科技(集团)股份有限公司 | Covered stent |
EP4205701A1 (en) * | 2020-10-13 | 2023-07-05 | Hangzhou Endonom Medtech Co., Ltd | Covered stent |
CN112402060A (en) * | 2020-11-02 | 2021-02-26 | 金仕生物科技(常熟)有限公司 | Delivery system of intervention valve |
CN115137526A (en) * | 2021-03-31 | 2022-10-04 | 上海微创心脉医疗科技(集团)股份有限公司 | Covered stent and medical device |
CN116492108A (en) * | 2023-03-01 | 2023-07-28 | 中国医学科学院阜外医院 | Branched artery reconstruction auxiliary device and S-C branched priority aortic reconstruction system |
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