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    • 2. 发明申请
    • EXPANDABLE STENT WITH CONSTRAINED END
    • 可扩展的支架,受限制的结束
    • WO2016109597A3
    • 2016-09-15
    • PCT/US2015067955
    • 2015-12-29
    • BARD INC C R
    • DIXON MATHEW
    • A61F2/07
    • A61F2/07A61F2/90A61F2/915A61F2/958A61F2002/072A61F2002/9522A61F2240/001A61F2250/0039
    • A stent graft having a tubular stent frame including a plurality of connected struts that form a wall extending along a longitudinal axis from a first end to a second end is described. The stent frame may have a substantially uniform expanded diameter from the first end to the second end, a first expanded polytetrafluoroethylene (ePTFE) covering positioned over an abluminal surface of the tubular stent frame, and a second ePTFE covering positioned over a luminal surface of the tubular stent frame. The second ePTFE covering may be joined to the first ePTFE covering through the tubular stent frame wall at the expanded diameter to form an encapsulated stent. The encapsulated stent may have a reduced diameter section at a first end of the encapsulated stent that is less than the expanded diameter.
    • 描述了具有管状支架框架的支架移植物,该支架框架包括多个连接的支柱,该支柱形成沿着纵轴从第一端延伸到第二端的壁。 支架框架可以具有从第一端至第二端的基本均匀的扩张直径,定位在管状支架框架的腔外表面上方的第一膨胀聚四氟乙烯(ePTFE)覆盖物和定位在管状支架框架的腔表面上方的第二ePTFE覆盖物 管状支架。 第二ePTFE覆盖物可以在膨胀直径处通过管状支架框架壁连接到第一ePTFE覆盖物以形成包封的支架。 封装的支架可在封装的支架的第一端具有小于扩张直径的减小直径的部分。
    • 6. 发明申请
    • IMPLANTABLE PROSTHESIS
    • 可植入的PROSTHESIS
    • WO0222047A9
    • 2010-09-02
    • PCT/US0128869
    • 2001-09-13
    • BARD INC C R
    • CHEROK DENNISDAROIS ROGERGREENE RONALD LCAPUZZIELLO THOMAS JMELLO JAMES D
    • A61L27/00A61F2/00A61F2/08
    • A61F2/02A61F2/0063A61F2002/009
    • An implantable prosthesis and a method of repairing an anatomical defect, such as a tissue or muscle wall defect, by promoting tissue growth thereto, while limiting the incidence of postoperative adhesions between a portion of the prosthesis and tissue or organs. The prothesis is formed of a biologically compatible, flexible layer of repair fabric suitable for reinforcing tissue or muscle and closing anatomical defects, and a barrier layer for physically isolating at least a portion of one side of the fabric from areas likely to form adhesions. A peripheral barrier extends about at least a portion of the outer peripheral edge of the repair fabric to inhibit adhesions between the outer peripheral edge and adjacent tissue and organs. The repair fabric may include an outer margin that has been melted and resolidified to render the outer peripheral edgte substantially impervious to tissue ingrowth. The barrier layer may be joined to the repair fabric with connecting stitches formed from PTFE to inhibit the formation of adhesions thereto.
    • 可植入假体和通过促进组织生长来修复诸如组织或肌肉壁缺陷的解剖缺陷的方法,同时限制假体的一部分与组织或器官之间的术后粘连的发生。 该假体由适于加强组织或肌肉并闭合解剖缺陷的生物相容性柔韧的修复织物层形成,以及用于物理隔离织物的一侧的至少一部分与可能形成粘连的区域的阻隔层。 周边障碍物围绕修复织物的外围边缘的至少一部分延伸,以抑制外围边缘和相邻组织和器官之间的粘连。 修复织物可以包括已经熔化并重新固化以使外周边缘基本上不可渗透组织向内生长的外边缘。 阻挡层可以用由PTFE形成的连接针迹连接到修复织物,以抑制其粘附的形成。
    • 8. 发明申请
    • LOW POWER ULTRASOUND SYSTEM
    • 低功率超声系统
    • WO2008124841A3
    • 2008-11-27
    • PCT/US2008059940
    • 2008-04-10
    • BARD INC C RCOHEN BENROBLES DYLAN KMESSERLY SHAYNEBURNSIDE EDDIE K
    • COHEN BENROBLES DYLAN KMESSERLY SHAYNEBURNSIDE EDDIE K
    • G01S7/52G01S15/89
    • A61B8/145A61B8/4472A61B8/4483A61B8/461A61B8/5207A61B8/56G01S7/003G01S7/52017G01S7/5208G01S7/52082G01S7/52085G01S7/52096G01S15/8909
    • A low power ultrasound system for use in sonography applications, including vascular imaging, is disclosed. In one embodiment, the low power ultrasound system comprises a base unit that includes an image processor and a display. An ultrasound probe is operably connected to the base unit. The probe includes a head portion including an array of crystal transducers. A plurality of pulser/receiver modules that cause the transducers to emit ultrasonic transmit pulses are also included in the probe. The pulser/receiver modules are further configured to receive analog signals relating to ultrasonic echo receive pulses detected by the transducers. The probe includes a singular low noise amplifier that amplifies the analog signals, and an analog-to-digital converter that converts the analog signals to a digital signal. A wireless interface is included for enabling the digital signal to be wirelessly transmitted from the probe to the image processor of the base unit.
    • 公开了用于超声波应用(包括血管成像)的低功率超声波系统。 在一个实施例中,低功率超声系统包括基座单元,该基座单元包括图像处理器和显示器。 超声探头可操作地连接到基座单元。 探针包括包含晶体换能器阵列的头部。 探头还包括使换能器发射超声波发射脉冲的多个脉冲发生器/接收器模块。 脉冲发生器/接收器模块进一步被配置为接收与由换能器检测到的超声回波接收脉冲有关的模拟信号。 该探头包括一个用于放大模拟信号的单个低噪声放大器,以及一个将模拟信号转换为数字信号的模数转换器。 包括一个无线接口,使数字信号能够从探头无线传输到基本单元的图像处理器。
    • 9. 发明申请
    • ACS THERAPY SYSTEM
    • ACS治疗系统
    • WO2008103625A3
    • 2008-10-30
    • PCT/US2008054199
    • 2008-02-18
    • BARD INC C RNISHTALA VASU
    • NISHTALA VASU
    • A61B5/00
    • A61M1/0023A61M1/0031A61M2210/1017
    • An ACS therapy system for continuously monitoring Intra-Abdominal Pressure (IAP) and preventing the onset of ACS. The automated ACS therapy system includes a urine withdrawal device, an IAP regulation circuit, an IAP monitor connected to the urine withdrawal device to supply an IAP value to the IAP regulation circuit, and an abdominal fluid removal device The abdominal fluid removal device may be connected to an active suction device, which withdraws fluid from the abdominal cavity through the abdominal fluid removal device when activated by the IAP regulation circuit. Based on the IAP value, the IAP regulation circuit may send a control signal that controls the active suction device to turn on and drain fluid from the abdominal cavity. When the IAP value reaches certain levels, the IAP regulation circuit may cause the active suction device to be turned off.
    • ACS治疗系统可持续监测腹腔内压(IAP)并预防ACS发作。 自动化ACS治疗系统包括尿液抽取装置,IAP调节回路,连接到尿液抽取装置以向IAP调节回路供应IAP值的IAP监控器,以及腹部流体去除装置。腹部流体去除装置可以连接 连接到主动抽吸装置,该主动抽吸装置在被IAP调节回路激活时通过腹腔流体去除装置从腹腔中抽出流体。 基于IAP值,IAP调节电路可以发送控制信号,该控制信号控制主动抽吸装置打开并从腹腔排出流体。 当IAP值达到一定水平时,IAP调节电路可能会导致主动吸入装置关闭。