Abstract: The device includes at least a tubular endoprosthesis (6), deployable between a retracted state and a dilated state, and a hollow support (10) which extends longitudinally between a proximal end (18) and a distal end (16). The support (10) is provided, in the vicinity of the distal end (16), with at least a transverse retention opening. The device includes at least a releasable threadlike tie (12, 14) for holding the endoprosthesis (6) on the support (10). The tie is engaged in the retention opening (28) and actuated from the proximal end (18) of the support (10) to release the endoprosthesis (6). The support (10) includes, over at least a portion of its length, a spring (24) forming the support. The spring (24) has contiguous turns over at least a portion of its length.

Abstract: The invention relates to a system for injecting a liquid into a body, comprising an implantable chamber disposed under the skin and an injection device including: a base bearing an injection needle having a free end that is intended to be inserted into the chamber; an injection conduit connected to the needle; means for extracting the needle; means that can be actuated to generate excess pressure in the injection conduit; synchronization means between the extraction means and the generation means for actuating the generation means during a needle extraction phase. The synchronization means can essentially only actuate the generation means when the free end of the needle is located in the chamber during the needle extraction phase.

Abstract: A tubular prosthesis is radially deformable and includes a lattice that is deformable between a retracted state of small diameter and an expanded state of larger diameter. The prosthesis includes at least two outer hooks delimiting between them a clamp for engaging in an outer tissue. The two hooks are carried by the lattice and can be moved between a spaced-apart position in which the clamp is open and a closer-together position in which the clamp is closed. The prosthesis includes a guiding member for moving at least one of the hooks during deformation of the prosthesis. The guiding member delimits a guide passage in which at least one of the hooks is engaged.

Abstract: This device (10) includes an implant (20) which has a tubular endoprosthesis (30) with a radially deployable framework (36). The implant (20) includes a flexible interposition member (24) mounted movably on the endoprosthesis (30) so as to be interposed between the outer surface (40) and a blood circulation conduit (14). The device (10) includes a deployment tool (26) which can adopt a configuration for insertion of the implant (20) and a configuration for release of the implant (20). In the configuration for insertion of the implant (20), the flexible member (24) includes at least one free part (68) held axially away from the outer surface (40) in order to minimize the radial dimension of the implant (20). The free part (68) is at least partly displaceable against the outer surface (40) when the tool (26) moves from its configuration for insertion to its configuration for release.

Abstract: This device comprises a tubular endoprosthesis (11) of axis (X-X?) and a stent (13) of axis (Y-Y?) defining a distal retention opening (23A) and a proximal retention opening (23B). The device comprises a distal wire-like tie (33A) and a proximal wire-like tie (33B). Each tie (33A, 33B) forms a retaining loop (43) running around the endoprosthesis (11). Each retaining loop (43) can stretch between a configuration in which the endoprosthesis (11) is kept in a contracted state against the stent (13) and a configuration in which the endoprosthesis (11) is released. When each retaining loop (43) is in its releasing configuration, the axis (X-X?) of the endoprosthesis (11) is inclined with respect to the axis (Y-Y?) of the stent (13) when no external stresses are applied. The axis (X-X?) of the endoprosthesis (11) intersects the axis (Y-Y?) of the stent in the internal line (18) defined by the endoprosthesis (11).

Abstract: A kit for implanting in a duct, which includes a tubular endoprosthesis and a prosthetic valve is disclosed. The prosthetic valve includes a carrier frame that is radially deformable in elastic manner relative to a central axis of the tubular endoprosthesis between a deployed, implanted position, and a folded, implanting position. The carrier frame is urged elastically towards its deployed position. A flexible shutter is connected to the carrier frame. The shutter is deformable between an obstruction position in which it is extended transversely, and a release position in which it is contracted transversely under to allow a fluid to flow through the carrier frame. The carrier frame also includes an integrated centripetal compressing mechanism for centripetally compressing the carrier frame towards folded position.

Abstract: A kit includes an implantable treatment element (13) which can be radially deformed between a retracted state and a deployed state, and a sheath (15) for maintaining the treatment element (13) in its retracted state. The kit also includes a member (19) for pulling the treatment element (13) into the sheath (15), which includes a sleeve (17) for receiving the treatment element (13) which can slide in relation to the sheath (15) between an expanded position for receiving the treatment element (13) and a compressed interposed position between the treatment element (13) and the sheath (15). The treatment element (13) is substantially axially fixed in relation to the receiving sleeve (17) when the sleeve (17) moves between its receiving and interposed positions. The kit can be used to insert endoprostheses into a blood vessel.

Abstract: This implant comprises an endoprosthesis having an axis which can be spontaneously deployed in a radial manner between a compressed configuration and a dilated configuration. The implant comprises at least one radial runner which comprises a separation surface which extends radially with respect to an outer surface of the endoprosthesis and a member which can be deployed away from the axis. The runner is arranged so as to delimit a confinement housing which extends between the separation surface and the outer surface and a radial spacer which is defined by the separation surface and the deployable member. When the implant is retained in a state of radial compression, the maximum radial width of the housing is less than the maximum radial width of the spacer which is not equal to zero.

Abstract: A device includes a support defining at least one opening for retaining an implant situated in the vicinity of the distal end thereof, and at least one threadlike link for retaining the implant. The link includes a control portion engaged in the support and a tightening loop of the implant which projects outside the support through the retention opening. A component is provided for placing each tightening loop around the implant. The placement component includes a rigid member and at least one flexible cord integral with the member and engaged releasably around the tightening loop.

Abstract: The invention relates to a system for injecting a liquid into a body, comprising an implantable chamber disposed under the skin and an injection device including: a base bearing an injection needle having a free end that is intended to be inserted into the chamber; an injection conduit connected to the needle; means for extracting the needle; means that can be actuated to generate excess pressure in the injection conduit; synchronization means between the extraction means and the generation means for actuating the generation means during a needle extraction phase. The synchronization means can essentially only actuate the generation means when the free end of the needle is located in the chamber during the needle extraction phase.

Abstract: A tubular endoprosthesis can be radially deployed between a retracted state and an expanded state. It includes an axially rigid support which has at least one retention opening. The device further includes at least one filamentary connection which has a region for clamping the endoprosthesis, at least partially surrounding the endoprosthesis, and a control region which is connected to the clamping region via the retention opening. The support is permanently fixed to the endoprosthesis.

Abstract: The device includes at least a tubular endoprosthesis (6), deployable between a retracted state and a dilated state, and a hollow support (10) which extends longitudinally between a proximal end (18) and a distal end (16). The support (10) is provided, in the vicinity of the distal end (16), with at least a transverse retention opening. The device includes at least a releasable threadlike tie (12, 14) for holding the endoprosthesis (6) on the support (10). The tie is engaged in the retention opening (28) and actuated from the proximal end (18) of the support (10) to release the endoprosthesis (6). The support (10) includes, over at least a portion of its length, a spring (24) forming the support. The spring (24) has contiguous turns over at least a portion of its length.

Abstract: This device (10) includes an implant (20) which has a tubular endoprosthesis (30) with a radially deployable framework (36). The implant (20) includes a flexible interposition member (24) mounted movably on the endoprosthesis (30) so as to be interposed between the outer surface (40) and a blood circulation conduit (14). The device (10) includes a deployment tool (26) which can adopt a configuration for insertion of the implant (20) and a configuration for release of the implant (20). In the configuration for insertion of the implant (20), the flexible member (24) includes at least one free part (68) held axially away from the outer surface (40) in order to minimise the radial dimension of the implant (20). The free part (68) is at least partly displaceable against the outer surface (40) when the tool (26) moves from its configuration for insertion to its configuration for release.

Abstract: The invention relates to a prosthetic valve which is endoluminally placeable and comprises a tubular support radially deformable with respect to a main axis (X-X) from an unfolded implanting position to a folded setting position. A flexible plug connected to the tubular support and deformable between a blocking position in which it is transversally stretched and a releasing position in which it is transversally contracted by the action of a flow circulating through said tubular support. The inventive valve also comprises a rigid chord which extends generally along the generatrix of the tubular support and is connected thereto at least at two points which are remote from each other along the axis thereof.

Abstract: A kit includes a tubular endoprosthesis having an inner surface which delimits a channel with a longitudinal axis. The kit includes a prosthetic valve to be implanted in the channel. The valve includes a supporting framework having an outer surface to be applied against the inner surface, and a flexible obturator which is connected to the framework. The endoprosthesis includes a stop for locking the supporting framework in order to block the axial displacement of the outer surface along the inner surface in at least a first direction. The stop includes at least one flexible connection extending transversely in the channel between two connection points, which are located on the inner surface and are angularly spaced about the axis.

Abstract: A valve prosthesis includes a flexible plug and an annular bearing reinforcement which is embodied such that it is radially rigid and surgically implantable in the area of a heart valve. The valve prosthesis is provided with an interchangeable prosthetic valve, is independent of the bearing reinforcement, endoluminally placeable and includes a tubular support which is radially deformable between a folded setting position and an unfolded position for implanting into a bearing structure and the flexible plug connected to a tubular support. The bearing reinforcement forms an annular support devoid of any plug capable of univocally limiting a blood flow circulation.

Abstract: The injection device (10) comprises: a needle support (24); an injection needle (22) which is fixedly joined to the needle support (24) and which has a free end (28) which is arranged with spacing from the needle support (24); and a mechanism (50) for extracting the injection needle (22), comprising a base (52) and a pushing member (54) which can be moved relative to the base (52) between a position in which the needle (22) is used and a position in which the needle (22) is extracted. The base (52) is permanently connected to the needle support (24) and can be moved relative to the needle support (24) between an inactive position of the extraction mechanism (50) and an active position of the extraction mechanism (50). Use for injection of doses of medication.

Abstract: The invention relates to a prosthetic valve (50) which is endoluminally placeable and comprises a tubular support (52) radially deformable with respect to a main axis (X-X) from an unfolded implanting position to a folded setting position a flexible plug (52) connected to the tubular support (52) and deformable between a blocking position in which it is transversally stretched and a releasing position in which it is transversally contracted by the action of a flow circulating, through said tubular support (52). The inventive valve also comprises a rigid chord (90) which extends generally along the generatrix of the tubular support (52) and is connected thereto at least at two points (92A, 92B) which are remote from each other along the axis thereof.

Abstract: The kit comprises a tubular endoprosthesis and a prosthetic valve which comprises a carrier frame that is radially deformable in elastic manner relative to a main axis between a deployed, implanted position and a folded, implanting position. The carrier frame is urged elastically towards its deployed position. A flexible shutter is connected to the carrier frame. It is deformable between an obstruction position in which it is extended transversely, and a release position in which it is contracted transversely under the action of the flow flowing through the carrier frame. The frame includes means integrated therein for centripetally compressing said carrier frame towards its folded position against the elastic action.

Abstract: A flanged prosthesis (10) comprises a tubular body (18) equipped at one end with an external flange (19) designed for the anastomosis of the prosthesis to a tubular duct equipped with an opening. The flange (19) is made of a textile material and comprises at least one seam (324, 360, 362) shaping it at the end of the tubular body (18).