Kit Which Is Intended to Be Implanted in a Blood Vessel, and Associated Tubular Endoprosthesis
First Claim
1. Kit which is intended to be implanted in a blood vessel, of the type comprising:
- a tubular endoprosthesis which has an inner surface which delimits a channel having a longitudinal axis; and
a prosthetic valve which is intended to be implanted in the channel, the valve comprising;
a carrier reinforcement which has an outer surface which is intended to be pressed against the inner surface of the endoprosthesis, the reinforcement being able to be deformed radially from a folded position for placement to a deployed position for implantation;
a flexible shutter which is connected to the reinforcement and which can be deformed between a blocking position in which it is extended transversely and a release position in which it is contracted transversely under the action of the flow moving in the channel;
characterised in that at least one of the inner and outer surfaces has at least two portions having a variable cross-section along the longitudinal axis, the portions forming a proximal stop and a distal stop, respectively, to block the axial displacement of the outer surface along the inner surface in two opposing directions.
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Accused Products
Abstract
The invention concerns a kit (11) comprising a tubular endoprosthesis (19) having an inner surface (57) delimiting a channel (58) with longitudinal axis (X-X′). It comprises a prosthetic valve (17) designed to be implanted in the channel (58). The valve (17) comprises a supporting frame (25) having an outer surface (35A, 35B) designed to be pressed against the inner surface (57), and a flexible cover (39) connected to the frame (25). The inner surface (57) has at least two segments (65, 67) with variable cross-section along the longitudinal axis (X-X′). The segments (65, 67) form respectively a proximal stop (71) and a distal stop (73) to lock the axial displacement of the outer surface (35A, 35B) along the inner surface (57) along two opposite directions.
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Citations
20 Claims
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1. Kit which is intended to be implanted in a blood vessel, of the type comprising:
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a tubular endoprosthesis which has an inner surface which delimits a channel having a longitudinal axis; and a prosthetic valve which is intended to be implanted in the channel, the valve comprising; a carrier reinforcement which has an outer surface which is intended to be pressed against the inner surface of the endoprosthesis, the reinforcement being able to be deformed radially from a folded position for placement to a deployed position for implantation; a flexible shutter which is connected to the reinforcement and which can be deformed between a blocking position in which it is extended transversely and a release position in which it is contracted transversely under the action of the flow moving in the channel;
characterised in that at least one of the inner and outer surfaces has at least two portions having a variable cross-section along the longitudinal axis, the portions forming a proximal stop and a distal stop, respectively, to block the axial displacement of the outer surface along the inner surface in two opposing directions. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 12, 13, 14, 15, 16, 17, 18, 19, 20)
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10. Tubular endoprosthesis, of the type having an inner surface which delimits a channel having a longitudinal axis, characterised in that the inner surface has at least two portions which have a variable cross-section along the longitudinal axis, the portions forming a proximal stop and a distal stop, respectively, to block the axial displacement in two opposing directions of an outer surface provided on a prosthetic valve which is intended to be implanted on the inner surface.
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11. Prosthetic valve which is intended to be implanted in a channel of a tubular endoprosthesis, comprising:
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a carrier reinforcement which has an outer surface which is intended to be pressed against the inner surface of the endoprosthesis, the reinforcement being able to be radially deformed from a folded position for placement to a deployed position for implantation; a flexible shutter which is connected to the reinforcement and which can be deformed between a blocking position in which it is extended transversely and a release position in which it is contracted transversely under the action of the flow moving in the channel;
characterised in that the outer surface of the carrier reinforcement has at least two portions having a variable cross-section along the longitudinal axis, the portions forming a proximal stop and a distal stop, respectively, to block the axial displacement of the valve relative to the tubular endoprosthesis.
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Specification