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    • 12. 发明授权
    • Deployment system for intraluminal devices
    • 管腔内装置的部署系统
    • US06899727B2
    • 2005-05-31
    • US09767314
    • 2001-01-22
    • Joseph P. ArmstrongEdward H. CullyEdward E. ShawMark J. UlmMichael J. Vonesh
    • Joseph P. ArmstrongEdward H. CullyEdward E. ShawMark J. UlmMichael J. Vonesh
    • A61F2/86A61F2/06
    • A61F2/97A61F2/86A61F2/95A61F2/958A61F2002/9511A61F2002/9522A61F2002/9583A61F2250/0071
    • A constraining sheath for use around an endoprosthesis (e.g., a stent device, with or without a graft covering), which may be a balloon expandable endoprosthesis but more preferably is a self-expanding prosthesis. The endoprosthesis is coaxially enclosed within the constraining sheath, which is an outer, disruptable, preferably implantable tubular sheath, preferably made of ePTFE. The constraining sheath and endoprosthesis are preferably mounted together as an assembly on an angioplasty balloon for delivery. Deployment of the endoprosthesis entails inflating the angioplasty balloon to a pressure sufficient to disrupt or break the constraining sheath in a prescribed fashion, thereby allowing a self-expanding endoprosthesis to spontaneously deploy. The constraining sheath of ePTFE may be attached to the endoprosthesis and implanted along with the device, or alternatively attached to the balloon catheter shaft and removed with the balloon catheter.
    • 用于内置假体周围使用的约束护套(例如,具有或不具有移植物覆盖物的支架装置),其可以是球囊可膨胀内置假体,但更优选是自膨胀假体。 内置假体同轴地封闭在约束护套内,约束鞘是外部的,可破坏的,优选可植入的管状护套,优选地由ePTFE制成。 约束鞘和内假体优选地作为组件安装在血管成形术气囊上用于递送。 内窥镜假体的部署需要将血管成形术气囊膨胀至足以以规定的方式破坏或打破约束鞘的压力,从而允许自膨胀内置假体自发部署。 ePTFE的约束鞘可以连接到内置假体并与装置一起植入,或者替代地附接到球囊导管轴并且用球囊导管去除。
    • 15. 发明申请
    • THERMOPLASTIC FLUOROPOLYMER-COATED MEDICAL DEVICES
    • 热塑性氟聚合物涂层医疗器械
    • US20120065721A1
    • 2012-03-15
    • US13282892
    • 2011-10-27
    • James W. ChangRobert L. CleekEdward H. CullyMichael J. Vonesh
    • James W. ChangRobert L. CleekEdward H. CullyMichael J. Vonesh
    • A61F2/82
    • A61L31/10A61L27/34C08L101/04
    • A medical device provided with at least a partial surface coating of a thermoplastic copolymer of tetrafluoroethylene and perfluoroalkylvinylether that is free of cross-linking monomers and curing agents. The fluoropolymer coating is preferably an amorphous thermoplastic, is highly inert and biocompatible, has elastomeric characteristics that provide desirable mechanical properties such as good flexibility and durability. These characteristics allow the coating to be considered “functionally transparent” because it withstands mechanical deformations required for the assembly, deployment, expansion, and placement of medical devices, without any adverse effect on the mechanical and biological functionality of the coated device. Further, its inertness, derived from the perfluorocarbon structure, contributes to its functionally transparent nature. The coating can be provided with various liquid or solid additives, can be loaded with large quantities of additives including a wide range of therapeutic agents, and has excellent drug elution characteristics when elutable additives are used.
    • 一种医疗装置,其具有不含交联单体和固化剂的四氟乙烯和全氟烷基乙烯基醚的热塑性共聚物的至少部分表面涂层。 含氟聚合物涂层优选为无定形热塑性塑料,具有高度惰性和生物相容性,具有提供所需机械性能(例如良好的柔韧性和耐久性)的弹性体特性。 这些特性使得涂层被认为是“功能上透明的”,因为它可以承受医疗装置的组装,展开,膨胀和放置所需的机械变形,而不会对涂覆装置的机械和生物功能产生任何不利影响。 此外,其衍生自全氟化碳结构的惰性有助于其功能上的透明性。 该涂层可以提供各种液体或固体添加剂,可以加载大量的添加剂,包括广泛的治疗剂,并且当使用可洗脱添加剂时具有优异的药物洗脱特性。
    • 16. 发明授权
    • Thermoplastic fluoropolymer-coated medical devices
    • 热塑性含氟聚合物涂层医疗器械
    • US08048440B2
    • 2011-11-01
    • US11378401
    • 2006-03-16
    • James W. ChangRobert L. CleekEdward H. CullyMichael J. Vonesh
    • James W. ChangRobert L. CleekEdward H. CullyMichael J. Vonesh
    • A61F2/82
    • A61L31/10A61L27/34C08L101/04
    • A medical device provided with at least a partial surface coating of a thermoplastic copolymer of tetrafluoroethylene and perfluoroalkylvinylether that is free of cross-linking monomers and curing agents. The fluoropolymer coating is preferably an amorphous thermoplastic, is highly inert and biocompatible, has elastomeric characteristics that provide desirable mechanical properties such as good flexibility and durability. These characteristics allow the coating to be considered “functionally transparent” because it withstands mechanical deformations required for the assembly, deployment, expansion, and placement of medical devices, without any adverse effect on the mechanical and biological functionality of the coated device. Further, its inertness, derived from the perfluorocarbon structure, contributes to its functionally transparent nature. The coating can be provided with various liquid or solid additives, can be loaded with large quantities of additives including a wide range of therapeutic agents, and has excellent drug elution characteristics when elutable additives are used. The desirable mechanical characteristics are surprising given the absence of cross-linking monomers and curing agents that would otherwise render such materials inadequately biocompatible. The perfluoroalkylvinylether may be perfluoromethylvinylether, perfluoroethylvinylether or perfluoropropylvinylether.
    • 一种医疗装置,其具有不含交联单体和固化剂的四氟乙烯和全氟烷基乙烯基醚的热塑性共聚物的至少部分表面涂层。 含氟聚合物涂层优选为无定形热塑性塑料,具有高度惰性和生物相容性,具有提供所需机械性能(例如良好的柔韧性和耐久性)的弹性体特性。 这些特性使得涂层被认为是“功能上透明的”,因为它可以承受医疗装置的组装,展开,膨胀和放置所需的机械变形,而不会对涂覆装置的机械和生物功能产生任何不利影响。 此外,其衍生自全氟化碳结构的惰性有助于其功能上的透明性。 该涂层可以提供各种液体或固体添加剂,可以加载大量的添加剂,包括广泛的治疗剂,并且当使用可洗脱添加剂时具有优异的药物洗脱特性。 鉴于不存在交联单体和固化剂,否则将使得这些材料生物相容性不足,理想的机械特性令人惊奇。 全氟烷基乙烯基醚可以是全氟甲基乙烯基醚,全氟乙基乙烯基醚或全氟丙基乙烯基醚。