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1. 发明申请

WO2017084725A1 VASCULAR GRAFT FOR INTERPOSITION AT A RESECTION OF VASCULAR STRUCTURES 审中-公开
标题翻译：在血管结构复位时植入血管移植物
公开(公告)号：WO2017084725A1
公开(公告)日：2017-05-26
申请号：PCT/EP2015/077284
申请日：2015-11-20
申请人： DOKTER PHILIPPE DE VLEESCHAUWER BV BVBA
发明人： DE VLEESCHAUWER, Philippe
IPC分类号： A61F2/06
CPC分类号： A61F2/06 , A61B2017/1132 , A61F2002/065 , A61F2210/0071 , A61F2210/0076 , A61F2230/0067 , A61F2230/0091 , A61F2240/002 , A61F2240/004 , A61F2250/0039 , A61F2250/0097 , A61L27/16 , A61L27/507 , B29C64/00 , B33Y80/00 , C08L27/18
摘要： The invention pertains to a vascular graft (1) for interposition at a resection of vascular structures, said vascular graft comprising a hollow body (2) elongated along a longitudinal axis (3) which includes a first end (4) defining a first opening (5) and a second end (6) defining a second opening (7), wherein said resection of vascular structures concerns a resection of the carotid bifurcation, and wherein said first end (4) is configured to be attached to the common carotid artery and said second end (6) is configured to be attached to the internal carotid artery or the external carotid artery, and wherein said vascular graft comprises polytetrafluoroethylene, and wherein said vascular graft comprises an inside diameter which decreases from said first end (4) towards said second end (6).
摘要翻译：本发明涉及用于在血管结构切除时插入的血管移植物（1），所述血管移植物包括沿着纵轴（3）延伸的中空主体（2），所述中空主体（2）包括第一端（4）限定限定第二开口（7）的第一开口（5）和第二端部（6），其中所述血管结构的切除涉及颈动脉分叉的切除，并且其中所述第一端部（4）被配置为被附接到颈总动脉并且所述第二端（6）被构造成附接到颈内动脉或颈外动脉，并且其中所述血管移植物包括聚四氟乙烯，并且其中所述血管移植物包括内直径，该内直径从所述第一端（4）朝向所述第二端（6）。

2. 发明申请

WO2015157176A3 KIT AND METHOD FOR MAKING A SPLINT 审中-公开
标题翻译：用于制作分支的套件和方法
公开(公告)号：WO2015157176A3
公开(公告)日：2015-12-10
申请号：PCT/US2015024519
申请日：2015-04-06
申请人： MAKEITMARKETUSA COM LLC
发明人： LIDDLE KATHERINE , MURDOCK MICHAEL , MEDINA WILLIAM
IPC分类号： A61F5/058
CPC分类号： A61F5/05841 , A61F2210/0071 , A61F2210/0076
摘要： A kit and method are presented for making a mending device, such as a splint, for immobilizing a body part, such as a limb. The kit includes a formable material and heating source. The heating source is used to selectively heat the formable material to an elevated material, molding the formable material into a required shape for the mending device and allowing the molded material to cool to room temperature and become hard again. The formable material may be molded on or around and in contact with the desired body part. The heating source may include a chemical composition that is selectively activated, for example by adding water to it.
摘要翻译：提出了用于制造诸如夹板的修补装置的用于固定身体部分（例如肢体）的工具箱和方法。该套件包括可成形材料和加热源。加热源用于将可成形材料选择性地加热到升高的材料，将可成形材料模制成用于修补装置的所需形状，并允许模制材料冷却至室温并再次变硬。可成型材料可以模制在所需身体部位上或周围并与其接触。加热源可以包括选择性地活化的化学组合物，例如通过向其中加入水。

3. 发明申请

WO2015179126A1 TETHER FOR PERSONAL PROTECTIVE DEVICE, SUCH AS A HEARING PROTECTION DEVICE 审中-公开
标题翻译：用于个人防护装置的耳塞，如听力保护装置
公开(公告)号：WO2015179126A1
公开(公告)日：2015-11-26
申请号：PCT/US2015/029349
申请日：2015-05-06
申请人： 3M INNOVATIVE PROPERTIES COMPANY
发明人： CAI, Feng
IPC分类号： A61F11/12
CPC分类号： A61F11/08 , A61F11/12 , A61F2210/0014 , A61F2210/0057 , A61F2210/0071
摘要： A tether for a personal protective device. The tether provides an initial length (L1). The tether is configured to self-retain a stretched length (L2) when stretched. The tether is further configured to self-transition or self-contract from the stretched length (L2) to a recovered length (L3) when heated. With this construction, the tether can be stretched by a user to the stretched state in which the stretched length (L2) approximates the length desired by the user; following use, the tether can be contracted to the recovered length (L3) for storage. Or, if the stretched length (L2) is longer than desired by the user, the tether can be contracted to a desired length in the recovered state (i.e., the recovered length (L3)) and then worn. The tether can be formed from a polymer blend of EVA and TPU.
摘要翻译：用于个人防护装置的系绳。系绳提供初始长度（L1）。系绳构造成在拉伸时自我保持拉伸长度（L2）。系绳进一步构造成在被加热时自动地从拉伸长度（L2）转变到自回收长度（L3）。利用这种结构，系绳可以被使用者拉伸到拉伸状态，拉伸长度（L2）接近用户期望的长度; 在使用后，系绳可以收缩到恢复的长度（L3）以便存储。或者，如果拉伸长度（L2）长于使用者所期望的长度（L2），则系绳可以在恢复状态（即，回收长度（L3））收缩到所需长度，然后磨损。系链可以由EVA和TPU的聚合物共混物形成。

4. 发明申请

WO2015040413A2 IMPLANTABLE MEDICAL DEVICES 审中-公开
标题翻译：可植入医疗器械
公开(公告)号：WO2015040413A2
公开(公告)日：2015-03-26
申请号：PCT/GB2014/052854
申请日：2014-09-19
申请人： RAINBOW MEDICAL ENGINEERING LIMITED
发明人： PROFIT, Alan Lynford , MARTINI, Luigi Gerard
IPC分类号： A61F2/915
CPC分类号： A61F2/91 , A61F2/915 , A61F2210/0014 , A61F2210/0071 , A61F2240/001 , A61F2250/0067 , A61L31/041 , A61L31/14 , B26D7/086 , B29C47/0066 , B29C71/02 , B29C2071/022
摘要： There is described a method of manufacturing a polymeric implantable medical device wherein the medical device comprises a tube with an opening said method comprising the simultaneous cutting and annealing of the opening; and polymeric implantable medical devices.
摘要翻译：描述了一种制造聚合物可植入医疗装置的方法，其中医疗装置包括具有开口的管，所述方法包括同时切割和退火开口; 和聚合物可植入医疗装置。

5. 发明申请

WO2014158580A8 METHODS AND APPARATUS FOR ASSEMBLING STENT-GRAFTS 审中-公开
标题翻译：组装装置的方法和装置
公开(公告)号：WO2014158580A8
公开(公告)日：2015-03-19
申请号：PCT/US2014018442
申请日：2014-02-25
申请人： GORE & ASS
发明人： ZUKOWSKI STANISLAW L
CPC分类号： A61F2/07 , A61F2/88 , A61F2/915 , A61F2002/075 , A61F2210/0071 , A61F2220/005 , A61F2240/001 , A61F2250/0097 , B29D23/001
摘要： The present disclosure describes methods and apparatus for forming medical devices comprising a stent member and a graft member. Such devices can include graft members that are bonded to the stent member in a selective manner. The selective bonding can allow for greater flexibility, curvature, and conformity of the device within the body of a patient.
摘要翻译：本公开描述了用于形成包括支架构件和移植构件的医疗装置的方法和装置。这样的装置可以包括以选择性方式结合到支架构件的移植物构件。选择性粘合可以允许装置在患者体内的更大的灵活性，曲率和一致性。

6. 发明申请

WO2013184010A2 FORMATION METHOD OF A MIDDLE EAR PROSTHESIS 审中-公开
标题翻译：中前期形成方法
公开(公告)号：WO2013184010A2
公开(公告)日：2013-12-12
申请号：PCT/PL2013/000069
申请日：2013-05-28
申请人： AKADEMIA GÓRNICZO-HUTNICZA
发明人： ZIĄBKA, Magdalena , CHŁOPEK, Jan , MERTAS, Anna , KRÓL, Wojciech , MENASZEK, Elżbieta , MORAWSKA, Agnieszka
IPC分类号： A61F2/18
CPC分类号： B29C33/72 , A61F2/18 , A61F2002/183 , A61F2210/0071 , A61F2240/001 , B29B9/06 , B29C45/00 , B29C45/0013 , B29C2033/725 , B29K2023/065 , B29L2031/7532
摘要： The process of preparing a middle ear prosthesis of polymeric material by injection moulding technology according to the presented invention is characterized by drying the thermoplastic polymer granules, preferably high density polyethylene or polyamide or polysulphone, at a temperature in the range of 60 to 150°C for a period of 2 to 8 hours. Subsequently granules are plasticized and then injected at a temperature between 180 and 400°C into the mold heated to a temperature between 60 and 150°C. Then obtained moulder is cooled and in the final stage it is hermetically packed in a vacuum and sterilized. In addition, the granules of the thermoplastic polymer composite are used, obtained by addition of bactericidal additive introduced into the thermoplastic polymer granules, preferably a silver powder with a particle size from 15 to 100 nm, in an amount of 0.1 - 3 wt %.
摘要翻译：通过根据本发明的注塑技术制备聚合物材料的中耳假体的过程的特征在于在60至150℃的温度范围内干燥热塑性聚合物颗粒，优选高密度聚乙烯或聚酰胺或聚砜为期2至8小时。随后将颗粒塑化，然后在180℃和400℃之间的温度下注入加热至60至150℃温度的模具中。然后将得到的模具冷却，并在最后阶段将其气密包装在真空中并进行灭菌。此外，使用热塑性聚合物复合材料的颗粒，其通过加入引入到热塑性聚合物颗粒中的杀菌添加剂，优选为0.1至3重量％的粒度为15至100nm的银粉末而获得。

7. 发明申请

WO2012021823A1 ADJUSTABLE PROSTHETIC LIMB SOCKET 审中-公开
标题翻译：可调节的前置轴承座
公开(公告)号：WO2012021823A1
公开(公告)日：2012-02-16
申请号：PCT/US2011/047614
申请日：2011-08-12
申请人： CJ SOCKET TECHNOLOGIES , CORNELL, Keith D.
发明人： CORNELL, Keith D.
IPC分类号： A61F2/80
CPC分类号： A61F2/80 , A61F2/76 , A61F2/78 , A61F2/7812 , A61F2002/5026 , A61F2002/5027 , A61F2002/5052 , A61F2002/5053 , A61F2002/5056 , A61F2002/7818 , A61F2002/7862 , A61F2002/7881 , A61F2002/7893 , A61F2002/802 , A61F2002/805 , A61F2210/0071 , Y10T29/4998
摘要： The present relates to an adjustable prosthetic limb socket system having a partial rigid support, a non-elastic, flexible support and adjustment means. The adjustable socket system of the present invention can be used for several types of amputations including transfemoral amputations, transtibial amputations, transhumeral amputations, transradial amputations, and other types of amputations. The present invention further includes kits having the adjustable prosthetic limb socket system, as well as methods of making the adjustable prosthetic limb socket system. Methods of using the socket system are further encompassed by the present invention.
摘要翻译：本发明涉及一种具有部分刚性支撑件，非弹性的柔性支撑件和调节装置的可调式假肢插座系统。本发明的可调插座系统可用于多种截肢，包括经股静脉截肢，腓骨截肢，经切除截肢，经桡动脉截肢和其他类型的截肢。本发明还包括具有可调式假肢插座系统的套件，以及制造可调式假肢插座系统的方法。使用插座系统的方法还包括在本发明中。

8. 发明申请

WO2011138646A1 INTEGRATED PROSTHETIC ELEMENT 审中-公开
标题翻译：综合优势元素
公开(公告)号：WO2011138646A1
公开(公告)日：2011-11-10
申请号：PCT/IB2011/000407
申请日：2011-02-25
申请人： LIMACORPORATE SPA , PRESSACCO, Michele
发明人： PRESSACCO, Michele
IPC分类号： A61F2/30
CPC分类号： A61F2/30 , A61F2/3094 , A61F2002/30065 , A61F2002/30772 , A61F2002/3092 , A61F2002/30971 , A61F2002/30985 , A61F2210/0071 , A61F2310/00023 , A61F2310/00029 , A61F2310/00131 , B33Y80/00
摘要： Integrated prosthetic element usable for bone implant operations or as a bone filler or replacement, comprising at least a metal support (30) and an insert (13) made of plastic material coupled with at least a first surface of said metal support (30) so as to define a wear surface, or insert, of adjustable thickness. The metal support (30) comprises, on the side opposite said first surface, a second surface intended to be coupled with the bone part on which the prosthesis or bone replacement is installed. The first surface comprises a layer (1 1) having cavities or holes (12) distributed in a substantially uniform manner and suitable for anchorage and solidarization of the plastic material that makes up the insert (13), while said second surface comprises a porous layer (16) suitable to optimize the bone anchorage. The first surface and the second surface are separated by a compact layer (14) that stops the plastic material in the step of forming the plastic insert (13). The cavities or holes (12) of the first surface have bigger shapes and sizes than, and in any case different from, the pores of the second surface.
摘要翻译：可用于骨植入操作或作为骨填料或替代物的集成假体元件，包括至少金属支撑件（30）和由与所述金属支撑件（30）的至少第一表面耦合的塑料材料制成的插入件（13），因此以限定可调节厚度的磨损表面或插入物。金属支撑件（30）在与所述第一表面相对的一侧包括旨在与其上安装有假体或骨置换物的骨部分联接的第二表面。第一表面包括具有以基本上均匀的方式分布并且适合于构成插入件（13）的塑料材料的固定和固化的空腔或孔（12）的层（11），而所述第二表面包括多孔层（16）适合于优化骨锚固。第一表面和第二表面由在形成塑料插入件（13）的步骤中使塑料材料停止的致密层（14）分开。第一表面的空腔或孔（12）具有比第二表面的孔更大的形状和尺寸，并且在任何情况下不同于孔的孔。

9. 发明申请

WO2011136929A1 METHODS FOR MOUNTING A SCAFFOLD TO A BALLOON CATHETER 审中-公开
标题翻译：将散热器安装到气瓶导管的方法
公开(公告)号：WO2011136929A1
公开(公告)日：2011-11-03
申请号：PCT/US2011/032283
申请日：2011-04-13
申请人： ABBOTT CARDIOVASCULAR SYSTEMS INC. , JOW, Kevin , WANG, Yunbing , Yang, Arlene Sucy , YAN, Kathleen W.
发明人： JOW, Kevin , WANG, Yunbing , Yang, Arlene Sucy , YAN, Kathleen W.
IPC分类号： A61F2/90 , A61F2/84
CPC分类号： A61F2/82 , A61F2/915 , A61F2/958 , A61F2002/91533 , A61F2002/91566 , A61F2002/9522 , A61F2210/0071 , Y10T29/49865 , Y10T29/49885 , Y10T29/49908 , Y10T29/49909 , Y10T29/49913 , Y10T29/49915 , Y10T29/49927 , Y10T29/53657
摘要： A medical device includes a polymer scaffold crimped to a catheter having an expansion balloon. The scaffold is crimped to the balloon by a process that includes heating the scaffold to a temperature below the polymer's glass transition temperature to improve scaffold retention without adversely affecting the mechanical characteristics of the scaffold when later deployed to support a body lumen. Additionally, before crimping begins the scaffold is placed on a support by an alignment carriage and deionized to remove any static charge buildup on the scaffold before placing the scaffold within the crimping mechanism.
摘要翻译：医疗装置包括压接到具有膨胀气囊的导管的聚合物构架。将支架通过包括将支架加热到低于聚合物玻璃化转变温度的温度的方法卷曲到球囊，以改善支架保留，而不会在稍后部署以支撑体腔时对支架的机械特性产生不利影响。另外，在卷曲开始之前，通过对准托架和去离子将支架放置在支撑件上，以在将支架放置在卷曲机构内之前去除脚手架上的任何静电荷。

10. 发明申请

WO2008106625A3 POROUS COMPOSITE BIOMATERIALS AND RELATED METHODS 审中-公开
标题翻译：多孔复合生物材料及相关方法
公开(公告)号：WO2008106625A3
公开(公告)日：2009-12-30
申请号：PCT/US2008055391
申请日：2008-02-28
申请人： UNIV NOTRE DAME DU LAC , ROEDER RYAN K , CONVERSE GABRIEL L , SMITH STEPHEN M
发明人： ROEDER RYAN K , CONVERSE GABRIEL L , SMITH STEPHEN M
IPC分类号： A61F2/28
CPC分类号： A61F2/4455 , A61F2/28 , A61F2/30965 , A61F2/4465 , A61F2002/2817 , A61F2002/2835 , A61F2002/30006 , A61F2002/30011 , A61F2002/30034 , A61F2002/30062 , A61F2002/30065 , A61F2002/30225 , A61F2002/30235 , A61F2002/30622 , A61F2002/30904 , A61F2002/3092 , A61F2002/30957 , A61F2210/0004 , A61F2210/0071 , A61F2230/0069 , A61F2250/0015 , A61F2250/0018 , A61F2250/0023 , A61F2250/0031 , A61L27/12 , A61L27/18 , A61L27/26 , A61L27/46 , A61L27/54 , A61L27/56 , B29C67/202 , C08J9/0066 , C08J9/28 , C08J9/36
摘要： Synthetic composite materials for use, for example, as orthopedic implants are described herein. In one example, a composite material for use as a scaffold includes a thermoplastic polymer forming a porous matrix that has continuous porosity and a plurality of pores. The porosity and the size of the pores are selectively formed during synthesis of the composite material. The example composite material also includes a plurality of a anisometric calcium phosphate particles integrally formed, embedded in, or exposed on a surface of the porous matrix. The calcium phosphate particles provide one or more of reinforcement, bioactivity, or bioresorption.
摘要翻译：本文描述了用作例如整形外科植入物的合成复合材料。在一个实例中，用作支架的复合材料包括形成具有连续孔隙率和多个孔的多孔基体的热塑性聚合物。在合成复合材料过程中选择性地形成孔隙率和孔径。该示例性复合材料还包括一体形成，嵌入或暴露于多孔基质的表面上的多个不等尺寸的磷酸钙颗粒。磷酸钙颗粒提供一种或多种增强，生物活性或生物再吸收。

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