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公开(公告)号:US20120330406A1
公开(公告)日:2012-12-27
申请号:US13554296
申请日:2012-07-20
CPC分类号: A61L31/16 , A61F2/82 , A61F2/848 , A61F2/89 , A61F2/91 , A61F2/915 , A61F2002/825 , A61F2002/91541 , A61F2002/91566 , A61F2210/0004 , A61F2210/0014 , A61F2220/0025 , A61F2230/0013 , A61F2240/001 , A61F2250/0023 , A61F2250/0025 , A61F2250/0026 , A61F2250/0036 , A61F2250/0037 , A61F2250/0051 , A61F2250/0067 , A61F2250/0068 , A61F2250/0096 , A61L31/022 , A61L31/10 , A61L2300/416 , A61L2300/606 , A61L2420/02
摘要: An improvement in drug-eluting stents, and method of their making, are disclosed. The surface of a metal stent is roughened to have a surface roughness of at least about 20 μin (0.5 μm) and a surface roughness range of between about 300-700 μin (7.5-17.5 μm). The roughened stent surface is covered with a polymer-free coating of a limus drug, to a coating thickness greater than the range of surface roughness of the roughened stent surface.
摘要翻译: 披露了药物洗脱支架的改进及其制作方法。 金属支架的表面被粗糙化以具有至少约20μin(0.5μm)的表面粗糙度和在约300-700μin(7.5-17.5μm)之间的表面粗糙度范围。 粗糙化的支架表面覆盖有无聚合物的斜肌药物涂层,涂层厚度大于粗糙化支架表面的表面粗糙度范围。
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公开(公告)号:US20090287294A1
公开(公告)日:2009-11-19
申请号:US12427620
申请日:2009-04-21
申请人: Arturo S. Rosqueta , Frank P. Becking , Maria G. Aboytes , Siddharth Loganathan , Chi Vu , Sepehr Fariabi
发明人: Arturo S. Rosqueta , Frank P. Becking , Maria G. Aboytes , Siddharth Loganathan , Chi Vu , Sepehr Fariabi
CPC分类号: A61B17/12159 , A61B17/12022 , A61B17/12031 , A61B17/12109 , A61B17/12113 , A61B17/12118 , A61B17/1215 , A61B17/12172 , A61B2017/00526 , A61B2017/00862 , A61B2017/00867 , A61B2017/1205 , A61B2017/12054 , A61B2017/12068 , A61B2018/00416 , A61B2090/3966 , A61M29/02 , Y10T156/1051
摘要: Embolic implants, delivery systems and methods of manufacture and delivery are disclosed. The devices can be used for aneurysm treatment and/or parent vessel occlusion. Implant designs offer low profile compressibility for delivery to neurovasculature, while maintaining other necessary features such as density for occlusion purposes and desirable radial strength characteristics.
摘要翻译: 公开了栓塞植入物,递送系统以及制造和递送方法。 该装置可用于动脉瘤治疗和/或母体血管闭塞。 植入物设计提供低调压缩性以递送至神经血管系统,同时保持其他必要特征,例如闭塞目的的密度和期望的径向强度特征。
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公开(公告)号:US07244319B2
公开(公告)日:2007-07-17
申请号:US10291930
申请日:2002-11-11
申请人: Robert M. Abrams , Sepehr Fariabi
发明人: Robert M. Abrams , Sepehr Fariabi
IPC分类号: A61F2/86
CPC分类号: A61L31/14 , A61L31/022 , A61L2400/16 , A61M25/09 , A61M2025/09008 , A61M2025/09083 , A61M2025/09141 , A61M2025/09175 , A61M2205/0266 , C22C14/00 , C22C30/00 , C22F1/006
摘要: An improved guiding member for use within a body lumen having a unique combination of superelastic characteristics. The superelastic alloy material has a composition consisting of about 30% to about 52% (atomic) titanium, and about 38% to 52% nickel and may have one or more elements selected from the group consisting of iron, cobalt, platinum, palladium, vanadium, copper, zirconium, hafnium and niobium. The alloy material is subjected to thermomechanical processing which includes a final cold working of about 10 to about 75% and then a heat treatment at a temperature between about 450° and about 600° C. and preferably about 475° to about 550° C. Before the heat treatment the cold worked alloy material is preferably subjected to mechanical straightening. The alloy material is preferably subjected to stresses equal to about 5 to about 50% of the room temperature ultimate yield stress of the material during the thermal treatment. The guiding member using such improved material exhibits a stress-induced austenite-to-martensite phase transformation at an exceptionally high constant yield strength of over 90 ksi for solid members and over 70 ksi for tubular members with a broad recoverable strain of at least about 4% during the phase transformation. An essentially whip free product is obtained.
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公开(公告)号:US06652472B2
公开(公告)日:2003-11-25
申请号:US10186858
申请日:2002-07-01
申请人: Mo Jafari , Sepehr Fariabi , Lawrence E. Brennan , Wayne E. Cornish , Marc M. Jalisi , David M. Anderson
发明人: Mo Jafari , Sepehr Fariabi , Lawrence E. Brennan , Wayne E. Cornish , Marc M. Jalisi , David M. Anderson
IPC分类号: A61B500
CPC分类号: A61M25/09 , A61M2025/09175
摘要: A guidewire for intraluminal advancement of a medical device within a patient which has an elongate core member with a flexible body member disposed on a distal section thereof. In one embodiment, the distal section of the elongate core member has at least one flexible segment with at least one pair of opposed tapered or parallel faces. Preferably the flexible segment with the tapered or parallel faces is disposed at the distal end of the elongate core and forms a shapable segment.
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公开(公告)号:US06592570B2
公开(公告)日:2003-07-15
申请号:US09884432
申请日:2001-06-18
申请人: Robert M. Abrams , Sepehr Fariabi
发明人: Robert M. Abrams , Sepehr Fariabi
IPC分类号: A61M2501
CPC分类号: A61M25/09 , A61L31/022 , A61L31/14 , A61L2400/16 , A61M2025/09008 , A61M2025/09083 , A61M2025/09141 , A61M2025/09175 , A61M2205/0266 , C22C14/00 , C22C30/00 , C22F1/006
摘要: An improved guiding member for use within a body lumen having a unique combination of superelastic characteristics. The superelastic alloy material has a composition consisting of about 30% to about 52% (atomic) titanium, and about 38% to 52% nickel and may have one or more elements selected from the group consisting of iron, cobalt, platinum, palladium, vanadium, copper, zirconium, hafnium and niobium. The alloy material is subjected to thermomechanical processing which includes a final cold working of about 10 to about 75% and then a heat treatment at a temperature between about 450° and about 600° C. and preferably about 475° to about 550° C. Before the heat treatment the cold worked alloy material is preferably subjected to mechanical straightening. The alloy material is preferably subjected to stresses equal to about 5 to about 50% of the room temperature ultimate yield stress of the material during the thermal treatment. The guiding member using such improved material exhibits a stress-induced austenite-to-martensite phase transformation at an exceptionally high constant yield strength of over 90 ksi for solid members and over 70 ksi for tubular members with a broad recoverable strain of at least about 4% during the phase transformation. An essentially whip free product is obtained.
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公开(公告)号:US5636641A
公开(公告)日:1997-06-10
申请号:US280209
申请日:1994-07-25
申请人: Sepehr Fariabi
发明人: Sepehr Fariabi
CPC分类号: A61M25/0012 , A61F2/958 , A61M25/0009 , A61M25/09 , A61F2210/0019 , A61M2025/09083
摘要: This invention is directed to an intracorporeal device formed of a high strength Co--Ni--Cr alloy and is particularly suitable for forming a composite product with a pseudoelastic member formed of NiTi alloy. Suitable intracorporeal products include guidewires and stents. The high strength alloy consists essentially of about 28 to about 65% cobalt, about 2 to about 40% nickel, about 5 to about 35% chromium, up to about 12% molybdenum, up to about 20% tungsten, up to about 20% iron and the balance inconsequential amounts of impurities and other alloying constituents, with a preferred alloy composition including about 30 to about 45% cobalt, about 25 to about 37% nickel, about 15 to about 25% chromium and about 5 to about 15% molybdenum. Intravascular devices such as guidewires, stents and the like can be formed of this high strength Co--Ni--Cr alloy.
摘要翻译: 本发明涉及由高强度Co-Ni-Cr合金形成的体内器件,特别适用于形成具有由NiTi合金形成的假弹性体的复合产品。 合适的体内产品包括导线和支架。 高强度合金主要由约28至约65%的钴,约2-约40%的镍,约5-35%的铬,至多约十二%的钼,至多约20%的钨,至多约20% 铁和余量是无关的量的杂质和其他合金成分,优选的合金组成包括约30至约45%的钴,约25至约37%的镍,约15至约25%的铬和约5至约15%的钼 。 诸如导线,支架等的血管内装置可以由这种高强度Co-Ni-Cr合金形成。
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公开(公告)号:US07806928B2
公开(公告)日:2010-10-05
申请号:US11689310
申请日:2007-03-21
申请人: Stanton J. Rowe , Henry Bourang , Sepehr Fariabi , Jan Otto Solem
发明人: Stanton J. Rowe , Henry Bourang , Sepehr Fariabi , Jan Otto Solem
IPC分类号: A61F2/24
CPC分类号: A61F2/2451 , A61B1/00082 , A61B5/064 , A61B8/06 , A61B8/12
摘要: A diagnostic device for determining the amount of change required in a coronary sinus to reduce valve regurgitation. The device includes a distal tube having a distal anchor at a distal end portion of the distal tube, a proximal tube having a proximal anchor at a distal end portion of the proximal tube, and an adjustor to move the distal tube relative to the proximal tube. The proximal tube and the distal tube together form a telescoping elongate body adapted to fit within the coronary sinus, and the device includes a scale to measure the movement of the distal anchor relative to the proximal anchor.
摘要翻译: 用于确定冠状窦所需的变化量以减少瓣膜反流的诊断装置。 该装置包括远端管,远侧管位于远端管的远端部分处,近端管具有位于近端管的远端部分处的近端锚固件,以及用于相对于近端管移动远侧管的调节器 。 近端管和远端管一起形成适于装配在冠状窦内的伸缩式细长体,并且该装置包括用于测量远端锚固体相对于近端锚的运动的标尺。
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公开(公告)号:US20080255581A1
公开(公告)日:2008-10-16
申请号:US12140900
申请日:2008-06-17
申请人: Henry Bourang , Gil M. Vardi , Eric Williams , Sepehr Fariabi , Udayan Patel , Javier Sagastegui
发明人: Henry Bourang , Gil M. Vardi , Eric Williams , Sepehr Fariabi , Udayan Patel , Javier Sagastegui
IPC分类号: A61F2/84
摘要: A stent delivery catheter comprises a catheter body having a proximal end, a distal end, and a guidewire lumen extending from the distal end to at least part way between the proximal end and the distal end. A balloon is disposed over the catheter body near the distal end, and a stent is positioned over the balloon. The stent has a proximal end, a distal end, and a side opening between the proximal end and the distal end. A side sheath is coupled to the catheter body and has a proximal end, a distal end, and a guidewire lumen extending between the proximal end and the distal end. The proximal end of the side sheath is located between the proximal end of the catheter body and the balloon, and the side sheath exits out of the side opening of the stent.
摘要翻译: 支架输送导管包括具有近端,远端和从远端延伸到近端和远端之间至少部分方向的导丝管的导管主体。 气囊在远端附近设置在导管主体上方,支架位于气囊上方。 支架具有近端,远端和在近端和远端之间的侧开口。 侧护套耦合到导管主体并且具有近端,远端和在近端和远端之间延伸的导丝管腔。 侧护套的近端位于导管主体的近端和气囊之间,侧鞘从支架的侧开口离开。
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公开(公告)号:US20080097591A1
公开(公告)日:2008-04-24
申请号:US11751268
申请日:2007-05-21
IPC分类号: A61F2/06
CPC分类号: A61L31/16 , A61F2/82 , A61F2/848 , A61F2/89 , A61F2/91 , A61F2/915 , A61F2002/825 , A61F2002/91541 , A61F2002/91566 , A61F2210/0004 , A61F2210/0014 , A61F2220/0025 , A61F2230/0013 , A61F2240/001 , A61F2250/0023 , A61F2250/0025 , A61F2250/0026 , A61F2250/0036 , A61F2250/0037 , A61F2250/0051 , A61F2250/0067 , A61F2250/0068 , A61F2250/0096 , A61L31/022 , A61L31/10 , A61L2300/416 , A61L2300/606 , A61L2420/02
摘要: An improvement in drug-eluting stents, and method of their making are disclosed. The surface of a metal stent is roughened to have a surface roughness of at least about 20 μin (0.5 μm) and a surface roughness range of between about 300-700 μin (7.5-17.5 μm). The roughened stent surface is covered with a polymer-free coating of a limus drug, to a coating thickness greater than the range of surface roughness of the roughened stent surface.
摘要翻译: 披露了药物洗脱支架的改进及其制作方法。 金属支架的表面被粗糙化以具有至少约20微米(0.5μm)的表面粗糙度和约300-700μ(7.5-17.5μm)之间的表面粗糙度范围。 粗糙化的支架表面覆盖有无聚合物的斜肌药物涂层,涂层厚度大于粗糙化支架表面的表面粗糙度范围。
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公开(公告)号:US07211110B2
公开(公告)日:2007-05-01
申请号:US11008055
申请日:2004-12-09
申请人: Stanton J. Rowe , Henry Bourang , Sepehr Fariabi , Jan Otto Solem
发明人: Stanton J. Rowe , Henry Bourang , Sepehr Fariabi , Jan Otto Solem
IPC分类号: A61F2/24
CPC分类号: A61F2/2451 , A61B1/00082 , A61B5/064 , A61B8/06 , A61B8/12
摘要: A diagnostic device for determining the amount of change required in a coronary sinus to reduce valve regurgitation. The device includes a distal tube having a distal anchor at a distal end portion of the distal tube, a proximal tube having a proximal anchor at a distal end portion of the proximal tube, and an adjustor to move the distal tube relative to the proximal tube. The proximal tube and the distal tube together form a telescoping elongate body adapted to fit within the coronary sinus, and the device includes a scale to measure the movement of the distal anchor relative to the proximal anchor.
摘要翻译: 用于确定冠状窦所需的变化量以减少瓣膜反流的诊断装置。 该装置包括远端管,远侧管位于远端管的远端部分处,近端管具有位于近端管的远端部分处的近端锚固件,以及用于相对于近端管移动远侧管的调节器 。 近端管和远端管一起形成适于装配在冠状窦内的伸缩式细长体,并且该装置包括用于测量远端锚固体相对于近端锚的运动的标尺。
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