A medical balloon for deployment of stents is disclosed. The medical balloon includes a central section; a proximal and a distal cone section; a proximal and a distal shaft section; a proximal sleeve which is arranged coaxial to and radially inside the proximal shaft section. The proximal end of the proximal shaft section is permanently connected and/or unitarily formed with the proximal end of the proximal sleeve, and distal thereto, at least part of the proximal cone section is connected with the proximal sleeve by an adhesive bond, and a distal sleeve which is arranged coaxial to and radially inside the distal shaft section. Methods of manufacturing a medical balloon are disclosed.
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
2.
ELECTROLYTE COMPOSITION AND METHOD FOR THE ELECTROPOLISHING TREATMENT OF NICKEL-TITANIUM ALLOYS AND/OR OTHER METAL SUBSTRATES INCLUDING TUNGSTEN, NIOB AND TANTAL ALLOYS
The present invention relates to an electrolyte composition and an electropolishing method in the presence of said composition, which is directed towards the surface treatment of medical devices. The electrolyte composition comprises methanesulfonic acid and a surface selective (anode specific) masking agent. The medical devices in question are formed from high-strength medical grade alloys, wherein the metals comprising said alloys are selected from a group of Nickel, Titanium, Cobalt, Chromium, Tantalum, Niobium, Tungsten, and whereas said alloys may contain one or more of said metals.
The invention relates to a catheter (1) for delivery of a self-expanding stent (7) into a body lumen, comprising a shaft (3) having a distal end and a proximal end, the shaft (3) defining a lumen (5) and a stent accommodating portion at its outside for carrying a self-expanding stent (7), a catheter tip (4) arranged at the distal end of the shaft (3), a sheath (6) arranged concentrically to the shaft (3), a pusher coil (8) arranged concentrically in between the shaft (3) and the sheath (6), and proximal to the stent accommodating portion, wherein the sheath (6) comprises an inside layer (22), an outside layer (25), and a wire layer (23) of interwoven wires (26, 27), the wire layer (23) being arranged in between the inside layer (22) and the outside layer (25).
A61F 2/966 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes possédant une gaine extérieure avec un mouvement longitudinal relatif entre la gaine extérieure et la prothèse, p. ex. utilisant une tige poussoir
The application relates to a shaft (10) for medical devices comprising an inner tube (11) and an outer tube (12), wherein the inner tube (11) and the outer tube (12) extend concentrically with a common longitudinal axis from a proximal end (15) to a distal end (16) of the shaft (10), and a spiral wall (13) projecting radially outwards from the inner tube (11). Further, the application relates to a catheter having such a shaft (10).
The invention relates to a stent graft, adapted for being inserted into a blood vessel, and to a method for forming a stent graft. The stent graft (1) comprises a first stent (2) comprising a plurality of first rings (4) being connected by at least one first connector, wherein the first stent (2) is arranged at least partly in an inner part of the stent graft (1), a second stent (3) comprising a plurality of second rings (5) being connected by at least one second connector, wherein the second stent (3) is arranged at least partly in an outer part of the stent graft (1), and a graft layer is arranged at least partly between the first stent (2) and the second stent (3), wherein the first stent (2) and the second stent (3) having each a predetermined length and the plurality of first rings (4) and the plurality of second rings (5) are axially arranged along the length such that the plurality of second rings (5) fit into the plurality of first rings (4). In this way, a possibility is provided to avoid the problem of integrity in connection with having as less as possible interaction between the first stent and the second stent and thus to minimize the risks of shear effects.
A61F 2/90 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles
A61F 2/00 - Filtres implantables dans les vaisseaux sanguinsProthèses, c.-à-d. éléments de substitution ou de remplacement pour des parties du corpsAppareils pour les assujettir au corpsDispositifs maintenant le passage ou évitant l'affaissement de structures corporelles tubulaires, p. ex. stents
A61F 2/852 - Dispositifs maintenant le passage ou évitant l’affaissement de structures tubulaires du corps, p. ex. stents constitués d’au moins deux stents distincts se chevauchant
A61F 2/89 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles les éléments filiformes comprenant au moins deux anneaux adjacents reliés de manière flexible par des éléments séparés
A61F 2/915 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles fabriquée à partir de feuilles perforées ou de tubes perforés, p. ex. perforés par découpe au laser ou gravés avec des bandes présentant une structure en méandre, des bandes adjacentes étant reliées l’une à l’autre
6.
SYSTEM AND METHOD FOR DETECTING STRUCTURAL DEFECTS WITHIN A STENT
The invention relates to a system (1) for detecting defects (12) within a structure of struts (2) forming a stent (3), the system comprising a power supply (8) for applying an electrical potential to a proximal end (9) and to a distal end (10) of said stent (3) in order to establish an electrical current flow between said proximal end (9) and said distal end (10), and a temperature sensor (7) such as a infrared camera, adjacent to said stent (3) for detecting a defect (12) within said structure of struts (2), said temperature sensor (7) being adapted to measure a temperature profile of said stent (3). Further, the invention relates to a respective method for detecting those defects (12).
The present invention refers to medical devices comprising a non-metallic micro tube containing FRP (fiber reinforced polymer), especially to respective tubings, used for constructing catheters like balloon dilation catheters, stent delivery catheters, guiding catheters and diagnostic catheters.
A61L 29/12 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent
A61L 29/18 - Matériaux au moins partiellement opaques aux rayons X ou au laser
A body lumen filter includes a plurality of bistable anchors configured to move between a stable pre-deployed state and a stable deployed state. In the stable deployed state the stable pre-deployed diameter the bistable anchors define a pre- deployed anchor diameter and in the stable deployed diameter the bistable anchors define a deployed anchor diameter, the deployed diameter being larger than the pre-deployed diameter. A filtering structure is operatively associated with the bistable anchors.
The present invention refers to medical devices comprising a modified Co-Polymer or to the modified Co-Polymer itself having high flexibility and high stress resistance, especially tensile strength or tear resistance, in addition to the good physical characteristics of a Block-Co-Polymers of a polyamide and a polycarbonate diamine.
C08L 69/00 - Compositions contenant des polycarbonatesCompositions contenant des dérivés des polycarbonates
C08L 77/00 - Compositions contenant des polyamides obtenus par des réactions créant une liaison amide carboxylique dans la chaîne principaleCompositions contenant des dérivés de tels polymères
A balloon catheter comprising a catheter tube, an inflatable and deflatable balloon fixed to the catheter tube and a refolding device for folding the balloon onto the catheter tube during balloon deflation, wherein the refolding device includes at least one flap arrangement being fixed on the catheter tube and being disposed within the balloon.
An interluminal medical treatment device (100) configured to treat a targeted treatment site within a body lumen. The interluminal medical treatment device can include an elongated generally tubular outer member (110). The outer member can include an expandable distal portion (110b), an expandable proximal portion (110a), and a central portion (110c) of limited expandability. The interluminal medical treatment device can include at least one membrane (120). The outer member and at least one membrane may define a housing area positioned between the proximal portion and distal portion of the outer member. The outer member and at least one membrane can be configured to redirect fluid flow within a body lumen away from the housing area inner member or inner passageway.
Apparatus for enhancing pushability and minimizing kinking of a balloon catheter is provided, wherein a catheter comprises inner (44) and outer tubes (42), and a balloon (55) that is proximally affixed to the outer tube and distally affixed to the inner tube. The catheter of the present invention further comprises a tubular member (100) imposed on the inner tube which is configured to form a reversible mechanical linkage between inner tube and outer tube while an axially compressive load is applied to the catheter tip.
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
The present invention refers to medical devices comprising a non-metallic micro tube containing FRP (fiber reinforced polymer), especially to respective tubings, used for constructing catheters like balloon dilation catheters, stent delivery catheters, guiding catheters and diagnostic catheters.
A61L 29/12 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent
a) a higher adhesion strength than the inner layer (4), and its use in a variety of medical procedures to treat medical conditions in animal and human patients.
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
The present invention refers to medical devices comprising a modified Co-Polymer or to the modified Co-Polymer itself having high flexibility and high stress resistance, especially tensile strength or tear resistance, in addition to the good physical characteristics of a Block-Co-Polymers of a polyamide and a polycarbonate, either polycarbonate diol or polycarbonate diamine.
C08L 69/00 - Compositions contenant des polycarbonatesCompositions contenant des dérivés des polycarbonates
C08L 77/00 - Compositions contenant des polyamides obtenus par des réactions créant une liaison amide carboxylique dans la chaîne principaleCompositions contenant des dérivés de tels polymères
The present disclosure is directed to an apparatus (100) for applying a graft material to a stent. (4) The apparatus may include a hollow mandrel (3) adapted to receive a stent. The mandrel (3) may include apertures adapted to allow a vacuum to be applied in order to temporarily affix the graft material sheath (20) to the stent. A forming roller (8) lying axially parallel to and in contact with the stent (4) may be included. Rotation of the forming roller may rotate the stent about its longitudinal axis. A second roller (9) for applying the sheath (20) of graft material to the stent as the stent (4) is rotated about its axis may be included. Further, the present disclosure is directed to a method of manufacturing stent grafts.
B29C 63/06 - Garnissage ou gainage, c.-à-d. application de couches ou de gainages préformés en matière plastiqueAppareils à cet effet avec des matières sous forme de feuilles ou de nappes par pliage, enroulement, cintrage ou par des opérations similaires autour d'objets tubulaires
An apparatus and method are described for electropolishing metallic stents. The apparatus may include an electropolishing container made from material of low thermal conductivity. The apparatus may include at least one spiral cathode for optimization of solution agitation and/or voltage distribution in the electrolytic solution. Further, an electrolytic solution is described. A method for improved polishing to consistently produce smooth surfaces is described.
An apparatus and method are described for electropolishing metallic stents made of high strength medical alloys. The apparatus may include an electropolishing container made from material of low thermal conductivity. The apparatus may include at least one spiral cathode for optimization of solution agitation and/or voltage distribution in the electrolytic solution. Further, an electrolytic solution is described. A method for improved polishing to consistently produce smooth surfaces is described.
As described herein, a body lumen filter is provided that includes a body configured to move between a pre-deployed state and a deployed state, a filtering structure operatively associated with the body to filter particulates, and a blending structure operatively associated with the body. The blending structure can be configured to break up at least one of the particulates.
A filter retrieval system is described. The filter retrieval system may include a capture structure having an interior space bounded by an at least partially closed distal end and an open proximal end. The filter retrieval system may include an elongate retrieval member slidably disposable within at least a portion of the interior space. The elongate retrieval member may include a retrieval structure adapted to releasably engage at least a portion of a filter. Methods of using the same are disclosed.
An implantable lumen filter (100) is described. The implantable lumen filter includes a proximal portion (103a) having a generally -tapered outer surface defined by a plurality of outer struts (106). The implantable lumen filter may also include a distal portion (103b) having a generally-tapered outer surface defined by a plurality of outer struts (106b) coupled together at the distal end (102b) of the distal portion. The implantable lumen filter may also include an apex (105) comprising the connection between the proximal and distal portions. The apex may define an outer dimension of the implantable lumen filter. The outer surface of the proximal portion is dimensioned to direct particulates towards the outer dimension.
An implantable lumen filter is described. The filter may include a body formed from an elongate member. The body may include loops encircling an axis extending along the length of the body. The body may be sized to be implanted into a body lumen. The body may be capable of transitioning from a collapsed state to a deployed state. The filter may include a first group of a plurality of members positioned around at least one loop of said body. At least a portion of the plurality of members may be oriented towards the axis. The plurality of members may be arranged to capture and/or lyse particulates of a selected size and/or to inhibit the particulates from passing through the body. Methods of making, deploying, and retrieving the same are described.
As described herein, a body lumen filter (100) is provided that includes a body configured to move between a pre-deployed state and a deployed state. In the deployed state, the body has filtering openings (150) defined therein. The body lumen filter also includes at least one anchor (140) coupled to the body, the anchor including a base and a bulbed (170) portion, having a major cross-sectional dimension that is larger than a major cross-sectional dimension of the base.
An expandable stent (1) for implantation in a body lumen, such as coronary- artery, and methods for manufacturing such a stent are provided, whereby the stent comprises at least one radially expandable cylindrical crown (3) covered with a polymeric tube (12). The at least one crown is generally aligned on a longitudinal axis of the stent and connected to at least one further stent segment with highly flexible connectors (4) formed from the same or different polymeric material as the crown covering material. In a preferred embodiment the cylindrical crown is loaded or coated with a therapeutic active agent.
A61F 2/86 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles
A61F 2/89 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles les éléments filiformes comprenant au moins deux anneaux adjacents reliés de manière flexible par des éléments séparés
A61F 2/91 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles fabriquée à partir de feuilles perforées ou de tubes perforés, p. ex. perforés par découpe au laser ou gravés
A61F 2/915 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles fabriquée à partir de feuilles perforées ou de tubes perforés, p. ex. perforés par découpe au laser ou gravés avec des bandes présentant une structure en méandre, des bandes adjacentes étant reliées l’une à l’autre
The present invention relates to a stent delivery system and a process for mounting a stent onto a delivery system. More specifically, the present invention relates to a method of loading a stent onto a balloon and mounting the stent balloon assembly onto a catheter. The premounting of the stent onto the balloon subassembly allows the stent to be crimped in a way that the crimping recoil can be compensated and stent retention is kept at a maximum.
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
A61F 2/95 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes
The present invention provides an apparatus (1) for processing a medical stent, comprising: a holding device (2) for holding a stent (S), and a processing device (3) for processing the stent held by the holding device (2). The holding device (2) comprises a first chamber (5) for a fluid medium adapted to exert pressure around the stent. The first chamber (5) for the fluid medium at least partially, and preferably fully, surrounds or encompasses the stent in the holding device (2). The holding device (2) desirably comprises a housing (4) which substantially encloses the first chamber (5) for the fluid medium, wherein the holding device (2) further includes a second chamber (8) for receiving the stent, and wherein the first chamber (5) for the fluid medium is separated from the second chamber (8) by at least one moveable and/or flexible wall (7). The invention also provides a method of processing a medical stent, comprising the steps of: holding a stent (S) with a holding device (2), and processing the stent with a processing device (3) while holding the stent with the holding device. The step of holding the stent comprises pressurizing a first chamber (5) for a fluid medium to exert pressure around the stent. The invention also provides a stent produced or manufactured according to this method.
B24B 31/116 - Machines ou dispositifs pour polir ou travailler par abrasion des surfaces "au tonneau", ou au moyen d'autres appareils, dans lesquels les pièces à travailler ou les produits abrasifs sont libresAccessoires à cet effet impliquant l'emploi d'autres moyens pour travailler les pièces par frottement utilisant un composé abrasif déformable plastiquement, mobile par rapport à la pièce sous l'action de la pression
A61F 2/91 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles fabriquée à partir de feuilles perforées ou de tubes perforés, p. ex. perforés par découpe au laser ou gravés
A vascular endoprosthesis (100, 200, 300, 400, 500, 600) includes a radially-expandable first segment and a radially expandable second segment. The vascular endoprosthesis further includes first and second coupling elements. The first coupling element extends from the proximal end of the first segment toward the distal end of the second segment, and the second coupling element extends from the distal end of the second segment toward the proximal end of the first segment. The first and second coupling elements cooperate one with another to couple the first and second segments together when the vascular endoprosthesis is in a delivery configuration and to decouple the first and second segments when the vascular endoprosthesis is in a deployed configuration.
A Stent-graft (10) comprising an inner stent (11) having a wall structure (12) including juxtaposed strut-patterns (13 - 17) with interconnected struts (18) and connectors (20 - 27) connecting the strut-patterns (13 - 17), the wall structure (12) of the inner stent (11) having a predetermined length (L1), an outer stent (28) coaxially arranged around the inner stent (11) and having a wall structure (34) including juxtaposed strut-patterns (29 - 33) with interconnected struts (35, 36) and connectors (37 - 44) connecting the strut-patterns (29 - 33), the wall structure (34) of the outer stent (12) having a predetermined length (L2) and a flexible stretchable material layer (45) arranged between the inner stent (11) and the outer stent (28), wherein the wall structure (12) of the inner stent (11) has a design differing from the design of the wall structure (34) of the outer stent (28) and wherein the length (L1) of the inner stent (11) is equal to the length (L2) of the outer stent (28).
A61F 2/91 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles fabriquée à partir de feuilles perforées ou de tubes perforés, p. ex. perforés par découpe au laser ou gravés
A61F 2/915 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles fabriquée à partir de feuilles perforées ou de tubes perforés, p. ex. perforés par découpe au laser ou gravés avec des bandes présentant une structure en méandre, des bandes adjacentes étant reliées l’une à l’autre
A61F 2/852 - Dispositifs maintenant le passage ou évitant l’affaissement de structures tubulaires du corps, p. ex. stents constitués d’au moins deux stents distincts se chevauchant
Stent delivery system (1) comprising a catheter (2) having an inner tube (3) and an outer tube (4) surrounding the inner tube (3); a balloon (5) having a proximal end (6) fixed to the outer tube (4) a distal end (7) fixed to the inner tube (3) and an interior (10) including a proximal portion (10A) and distal portion (10B), a stent (8) disposed on said balloon (5) and being expandable from a delivery position to a deployed position by a contrast medium (9) adapted to be supplied to the interior (10) of said balloon (5), and a contrast medium distribution means (11) disposed in the interior (10) of said balloon (5) adapted to equally distribute the contrast medium (9) to both the proximal portion (10A) and the distal portion (10B) of the interior (10) of the balloon (5).
A61F 2/95 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
A Balloon catheter (1) comprising a catheter tube (2), an inflatable and deflatable balloon (3) fixed to said catheter tube (2) and a refolding device (4) for folding the balloon (3) onto said catheter tube (2) during balloon deflation, wherein said refolding device (3) includes at least one flap arrangement (5) being fixed on said catheter tube (2) and being disposed within said balloon (3).
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
A device for preventing stent movement during delivery comprising a securement connector arranged to engage a catheter, at least one flexible connecting member, said flexible connecting member having a first end portion and a second end portion, the first end portion coupled to said securement connector, and a locking member located at said flexible connecting member second end portion arranged to engage a portion of a stent comprising struts defining gaps therebetween wherein said locking member takes the form of a clasp section snapping into one gap of said gaps between the struts.
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
A61F 2/95 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes
Balloon (1) of a balloon catheter comprising, in its folded state, a central, inflatable body portion (2) having an outer peripheral wall surface (3) and a plurality of hollow lobes (4, 5, 6, 7) being wrapped around the outer peripheral wall surface (3) and being in fluid communication with the inflatable body portion (2) said lobes (4, 5, 6, 7) including free end portions (4A, 4B, 5A, 5B, 6A, 6B, 7A, 7B) defining gaps (8, 9, 10, 11) therebetween.
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
The present invention refers to medical devices comprising cross-linked modified polyamides especially to stent carrying balloon catheters, for use in angioplasty and other procedures of vessel repair. In a preferred embodiment, a balloon catheter is made of Nylon 12, crosslinked using triallyl isocyanurate and electronic beam. (E-beam), but-2-ene.dioic acid and heating or 1,4-butylene diamine and UV radiation.
A61L 29/06 - Matériaux macromoléculaires obtenus autrement que par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carbone
34.
ENDOPROSTHESIS HAVING STRUTS LINKED BY FOOT EXTENSIONS
The present invention relates to an endoprosthesis having a plurality of web rings (30, 32) coupled by connectors (24), which include two or more essentially parallel struts (26, 28) and a foot extension (34) protruding from one of the struts. An endoprosthesis constructed according to the principles of the present invention provides an elevated degree of scaffolding to a body lumen while retaining an acceptable degree of flexibility.
A61F 2/90 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles
35.
ENDOPROSTHESIS HAVING A STABLE ARCHITECTURE AND FLEXIBLE CONNECTORS
The present invention relates to an endoprosthesis (10) that is expandable from a contracted configuration to an expanded configuration and that includes a plurality of longitudinally adjacent web rings (26, 30). Each of the web rings is defined by web elements (38) disposed circumferentially around a longitudinal axis, which are adjoined one to the other at junction bends. A first junction bend (24) in a first web ring (26) is coupled to a second junction bend (28) in a second web ring (30) by a connector (14) which includes three or more struts (16) of essentially equal length that extend circumferentially in essentially parallel directions. The struts of the connector are adjoined in sequence by coupling segments (18) that, in one embodiment of the invention, are arcuate in shape. In another configuration, the connector is a flexible connector that is structured to absorb at least some of the axial and torsional stresses applied to the endoprosthesis.
A61F 2/91 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles fabriquée à partir de feuilles perforées ou de tubes perforés, p. ex. perforés par découpe au laser ou gravés
A61F 2/915 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles fabriquée à partir de feuilles perforées ou de tubes perforés, p. ex. perforés par découpe au laser ou gravés avec des bandes présentant une structure en méandre, des bandes adjacentes étant reliées l’une à l’autre
The present invention refers to medical devices. Particularly it relates to stent devices and balloon catheter devices. In the most particular aspect of the invention it relates to balloon catheter devices carrying stents (2) with the medical balloon (3) comprising an inner layer (4) having a lower compliance rate and/or burst pressure than the outer layer (5) and an outer layer (5) having on the outer surface (6a) a higher adhesion strength than the inner layer (4), and its use in a variety of medical procedures to treat medical conditions in animal and human patients.
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
The present invention refers to medical devices. Particularly it relates to stent devices and balloon catheter devices. In the most particular aspect of the invention it relates to structures with at least two different lamellar sections used in such a medical device, especially in a balloon on a balloon catheter device carrying a stent comprising at least one layer with at least two lamellar sections different by their shore hardness and its use in a variety of medical procedures to treat medical conditions in animal and human patients.
A61L 29/12 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
The present invention refers to medical devices. Particularly it relates to stent devices and balloon catheter devices. In the most particular aspect of the invention it relates to the strengthening of the structure of such a medical device, especially of a balloon on a balloon catheter device and its use in a variety of medical procedures to treat medical conditions in animal and human patients.
A61L 27/00 - Matériaux pour prothèses ou pour revêtement de prothèses
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
The present invention refers to medical devices comprising co-extruded polymers of polyamide and poly-tetrafluoro-ethylene (PTFE), especially to tubings, used for constructing catheters like balloon catheters, especially like the inner member (forming the guide wire lumen) of catheters.
C08L 77/00 - Compositions contenant des polyamides obtenus par des réactions créant une liaison amide carboxylique dans la chaîne principaleCompositions contenant des dérivés de tels polymères
C08L 77/02 - Polyamides dérivés des acides oméga-aminocarboxyliques ou de leurs lactames
The present invention refers to medical devices comprising fluorinated polymers, especially to tubings, used for constructing catheters like balloon catheters, delivery catheters or guide catheters.
A61L 31/14 - Matériaux caractérisés par leur fonction ou leurs propriétés physiques
A61F 2/00 - Filtres implantables dans les vaisseaux sanguinsProthèses, c.-à-d. éléments de substitution ou de remplacement pour des parties du corpsAppareils pour les assujettir au corpsDispositifs maintenant le passage ou évitant l'affaissement de structures corporelles tubulaires, p. ex. stents
A61L 27/50 - Matériaux caractérisés par leur fonction ou leurs propriétés physiques
A61L 29/14 - Matériaux caractérisés par leur fonction ou leurs propriétés physiques
B05D 3/06 - Traitement préalable des surfaces sur lesquelles des liquides ou d'autres matériaux fluides doivent être appliquésTraitement ultérieur des revêtements appliqués, p. ex. traitement intermédiaire d'un revêtement déjà appliqué, pour préparer les applications ultérieures de liquides ou d'autres matériaux fluides par exposition à des rayonnements
The present invention refers to medical devices comprising non-linear block-co- polymers especially those selected form branched polyamides, branched or grafted Block-Co-Polymers as well as dendritic systems carrying polyamides, wherein the materials are having a high flexibility and a high stress resistance, especially tensile strength or tear resistance, allowing their use in medical devices, especially in balloons attached to a balloon catheter.
A61L 31/06 - Matériaux macromoléculaires obtenus autrement que par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carbone
A device (20) for crimping stents onto a catheter is described, comprising two opposing pressure walls (22, 22'). The walls are angled towards each other and provide surfaces that move in opposite directions so that a stent on a catheter placed between the surfaces is rotated while a force is applied to the stent. The stent is moved toward a narrower dimension between the pressure walls, to emerge from the walls fully crimped onto the catheter.
A system for controlled deployment of a prosthesis, in which a sheath is retracted from a prosthesis in a body vessel or duct. The system includes a handle (20) for deploying the prosthesis (34), the handle comprises a base member (40) fixed to a catheter (22), and a slide member (48) for sliding past the base member, the slide member being fixed to an end of a retraction member (24). The slide member includes a serrated gear rod (50), and the handle is configured such that, when activated, the gear rod moves in relation to the base member by no more nor less than the length of one serration on the gear rod.
The present invention concerns a stent with a highly flexible structure that is configured to provide an elevated degree of vessel scaffolding and to absorb torque applied on the stent. In one embodiment, the stent of the present invention includes an essentially tubular body formed by a web structure that is composed of a plurality of longitudinally adjacent web rings (46), each including a plurality of web elements that are disposed circumferentially around the longitudinal axis of the stent and that are adjoined one to the other by a junction bend (56). Each junction bend (56) in a first web ring is coupled to another junction bend (60) in a neighboring ring by a connector (58) having a step-wise configuration, in which a central segment of the connector is disposed essentially parallel to the longitudinal axis of the stent and may become twisted to absorb torque imposed on the stent.
A61F 2/90 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles
A system for controlled deployment of a prosthesis, in which a sheath is retracted from a prosthesis in a body vessel or duct. The system includes a handle for deploying the prosthesis, the handle comprises a base member fixed to a catheter, and a slide member for sliding past the base member, the slide member being attached to an end of a retraction member. The base member includes an opening having the general shape of a rectangular wave for interacting with the slide member, whereby, repeated manipulation of the slide member causes the sheath to be retracted.
The present invention concerns a stent including an essentially tubular body formed by a web structure that is configured to expand from a contracted delivery configuration to an expanded deployed configuration and that is composed of a plurality of longitudinally adjacent web rings (44, 46). Those web rings are formed by a plurality of web elements (32) disposed circumf erentially around the longitudinal axis of the stent and adjoined one to the other with a junction bend (40). Each junction bend in a first web ring is coupled to another junction bend in a neighboring ring with a s-shaped connector (42), and the coupled junction bends are not longitudinally aligned but are instead laterally offset. The s-shaped connectors may have a different cross-sectional area or may be biodegradable.
A61F 2/90 - Stents ayant une forme caractérisée par des éléments filiformesStents ayant une forme caractérisée par une structure de type filet ou de type à mailles caractérisés par une structure de type filet ou de type à mailles
47.
MEDICAL DEVICES COMPRISING A CO-POLYMER OF A POLYAMIDE AND A POLYCARBONATE DIAMINE
The present invention refers to medical devices comprising a modified Co-Polymer or to the modified Co-Polymer itself having high flexibility and high stress resistance, especially tensile strength or tear resistance, in addition to the good physical characteristics of a Block-Co-Polymers of a polyamide and a polycarbonate diamine.
C08G 81/02 - Composés macromoléculaires obtenus par l'interréaction de polymères en l'absence de monomères, p. ex. polymères séquencés au moins un des polymères étant obtenu par des réactions ne faisant intervenir que des liaisons non saturées carbone-carbone
48.
MEDICAL DEVICES COMPRISING A CO-POLYMER OF A MODIFIED POLYAMIDE AND A POLYCARBONATE
The present invention refers to medical devices comprising a modified Co-Polymer or to the modified Co-Polymer itself having high flexibility and high stress resistance, especially tensile strength or tear resistance, in addition to the good physical characteristics of a Block-Co-Polymers of a polyamide and a polycarbonate, either polycarbonate diol or polycarbonate diamine.
C08G 81/02 - Composés macromoléculaires obtenus par l'interréaction de polymères en l'absence de monomères, p. ex. polymères séquencés au moins un des polymères étant obtenu par des réactions ne faisant intervenir que des liaisons non saturées carbone-carbone
49.
MEDICAL DEVICES COMPRISING A CO-POLYMER OF A MODIFIED POLYAMIDE AND A POLYETHER
The present invention refers to medical devices comprising a modified Co-Polymer and the modified Co-Polymer itself having high flexibility and high stress resistance, especially tensile strength or tear resistance, in addition to the good physical characteristics of the known Block-Co-Polymers of a polyamide and a polyether, either polyether diol or polyether diamine.
C08G 69/48 - Polymères modifiés par post-traitement chimique
A61L 27/18 - Matériaux macromoléculaires obtenus par des réactions autres que celles faisant intervenir uniquement des liaisons non saturées carbone-carbone
The present invention refers to medical devices comprising a modified polyamide or to modified polyamides or modified polyamide elastomers with the polyamides having high flexibility and high stress resistance, especially tensile strength or tear resistance, in addition to the good physical characteristics of the known polyamide elastomers.
C08G 69/48 - Polymères modifiés par post-traitement chimique
C08J 11/26 - Récupération ou traitement des résidus des polymères par coupure des chaînes moléculaires des polymères ou rupture des liaisons de réticulation par voie chimique, p. ex. dévulcanisation par traitement avec une substance organique par traitement avec des composés organiques contenant de l'oxygène contenant des groupes acide carboxylique, leurs anhydrides ou esters
51.
Side by side lumen catheter and method of manufacture thereof
The present invention provides a dual lumen catheter shaft having a first dual lumen section and a second dual lumen section with a transition section therebetween. The present invention further provides a method of forming a dual lumen catheter shaft.
The present invention relates to a catheter comprising an outer tube; an inner tube; and a balloon fixed at its proximal sleeve to the outer tube and at its distal sleeve to the inner tube, wherein the inner tube comprises an elastic segment.
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
53.
METHOD OF THERMAL TREATMENT OF A THERMALLY RESPONSIVE MATERIAL OF MEDICAL DEVICES
The present invention relates to a method of thermal treatment of thermally responsive material wherein areas in or on the material to be thermally treated are defined and thermal energy is inputted on or into the defined areas in order to change/influence the material characteristics. The present invention further relates to medical devices or parts thereof manufactured at least in part from thermally responsive material by a process comprising at least one step of thermal treatment of this thermally responsive material.
Method of producing a balloon 1 of a balloon catheter comprising the following method steps: - preparing a balloon body 2 with a proximal sleeve 5 and a distal sleeve 6, with transitional sections 3, 4 extending between the balloon body 2 and the respective sleeve 5, 6; - creating folds 7 in at least the distal sleeve 6; and - fixing at least a distal section of the folds 7 of the distal sleeve 6.
Catheter 1, in particular PTCA catheter, comprising an outer tube 2; an inner guide wire tube 3 within the outer tube 2, said inner guide wire tube 3 having a tip 4; a first and a second marker 5, 6 fixed to the guide wire tube 3 at a fixed distance b to one another; and a balloon 7 having two sleeves 8, 9 fixed to the outer tube 2 and the inner tube 3, respectively, wherein that the distance b between the markers 5, 6 is set to be at least approximately equal to the distance a between the tip 4 and the marker 5 neighbouring the tip 4.
A61M 29/02 - Dilatateurs gonflablesDilatateurs faits de matériaux dilatables
A61F 2/958 - Instruments spécialement adaptés pour insérer ou retirer les stents ou les endoprothèses déployables couvertes ballons gonflables pour insérer les stents ou les endoprothèses déployables couvertes
Surgical and medical apparatus and instruments namely stents; catheters, balloon-catheters, diagnostic catheters, heart support systems; medical implants; suture materials; connections for conorary bypasses; guidewires for catheters.
