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    • 1. 发明授权
    • Packaging for a sterilizable calibratable medical device
    • 可灭菌可校准医疗器械的包装
    • US4863016A
    • 1989-09-05
    • US224425
    • 1988-07-25
    • Conrad T. O. FongRichard W. GrabenkortScott P. Huntley
    • Conrad T. O. FongRichard W. GrabenkortScott P. Huntley
    • A61L2/20A61B19/02A61M25/00
    • A61M25/002A61B50/30
    • The present invention provides a package for and method of packaging a sterilizable calibratable medical device including a hydratable sensor component. The device is maintained in a sterile environment during storage and in a clean environment during the calibration procedure. The package includes a manifold connected to the sensor component by plumbing. The plumbing establishes fluid communication between the manifold and the sensor component and/or between the sensor component and the ambient environment of the plumbing. The manifold, plumbing and medical device are sealed in a wrap including a gas-permeable surface. The wrap and its contents, including the interior surfaces of the components, are sterilizable by exposing the wrap to a gaseous sterilization solution and appropriately adjusting the plumbing. The medical device is hydratable by directing the hydration solution to the sensor component by means of the plumbing. In order to store the package over an extended period of time, a gas-impermeable chamber is defined which includes the ambient environment of the plumbing. The gaseous environment of the medical device is thereby controllable. In this manner, the device is prepared for calibration and is storable in the sterile environment. By connecting a reservoir including calibration solution to the plumbing, the calibration solution is directed to the sensor component without removing the medical device from its clean enviroment. The temperatures of the sensor component and the solution are controlled throughout the calibration process in order to ensure that the device is calibrated in accordance with its intended use. The present invention further discloses a solution for preparing the medical device for use. The solution is chemically compatible with the intended use of the device.
    • 4. 发明授权
    • Method of packaging for a sterilizable calibratable medical device
    • 可灭菌可校准医疗器械的包装方法
    • US4941308A
    • 1990-07-17
    • US324181
    • 1989-03-16
    • Richard W. GrabenkortScott P. HuntleySheldon M. Wecker
    • Richard W. GrabenkortScott P. HuntleySheldon M. Wecker
    • A61B19/02A61M25/00
    • A61M25/002A61B50/30
    • The present invention provides a package for and method of packaging a sterilizable calibratable medical device including a hydratable sensor component. The device is maintained in a sterile environment during storage and in a clean environment during the calibration procedure. The package includes a manifold connected to the sensor component by plumbing. The plumbing establishes fluid communication between the manifold and the sensor component and/or between the sensor component and the ambient environment of the plumbing. The manifold, plumbing and medical device are sealed in a wrap including a gas-permeable surface. The wrap and its contents, including the interior surfaces of the components, are sterilizable by exposing the wrap to a gaseous sterilization solution and appropriately adjusting the plumbing. The medical device is hydratable by directing the hydration solution to the sensor component by means of the plumbing. In order to store the package over an extended period of time, a gas-impermeable chamber is defined which includes the ambient environment of the plumbing. The gaseous environment of the medical device is thereby controllable. In this manner, the device is prepared for calibration and is storable in the sterile environment. By connecting a reservoir including calibration solution to the plumbing, the calibration solution is directed to the sensor component without removing the medical device from its clean environment. The temperature of the sensor component and the solution are controlled throughout the calibration process in order to ensure that the device is calibrated in accordance with its intended use. The present invention further discloses a solution for preparing the medical device for use. The solution is chemically compatible with the intended use of the device.
    • 本发明提供了一种用于包装可消毒的可校准医疗装置的包装和方法,包括可水合的传感器部件。 在校准过程中,该装置在储存期间和在清洁的环境中保持在无菌环境中。 该包装包括通过管道连接到传感器部件的歧管。 管道在歧管和传感器部件之间和/或传感器部件与管道的周围环境之间建立流体连通。 歧管,管道和医疗设备被密封在包括透气表面的包裹中。 通过将包裹物暴露于气体杀菌溶液并适当地调节管道,包装及其内容物,包括组分的内表面可灭菌。 医疗设备可通过水管将水合溶液引导到传感器部件进行水合。 为了在长时间内存储包装,定义了气体不可渗透室,其包括管道的周围环境。 因此医疗装置的气体环境是可控的。 以这种方式,该装置被准备用于校准并且可存储在无菌环境中。 通过将包括校准溶液的储存器连接到管道上,校准溶液被引导到传感器部件,而不从其干净的环境中移除医疗装置。 在整个校准过程中控制传感器组件和溶液的温度,以确保根据其预期用途校准设备。 本发明还公开了一种用于制备用于使用的医疗装置的解决方案。 该解决方案与设备的预期用途化学兼容。
    • 5. 发明授权
    • Autoinjector with extendable needle protector shroud
    • 自动进样器带有可延长的针头保护罩
    • US06805686B1
    • 2004-10-19
    • US10430710
    • 2003-05-06
    • Marwan A. FathallahRichard W. Grabenkort
    • Marwan A. FathallahRichard W. Grabenkort
    • A61M520
    • A61M5/2033A61M5/3202A61M5/326A61M2005/206A61M2005/2073A61M2005/3109A61M2005/3247
    • The invention provides a syringe and a method for using the same. The syringe includes a housing having a reservoir disposed therein and a plunger to be received by the reservoir, the plunger being moveable between a first plunger position and a second plunger position. The syringe also includes a plunger spring to urge the plunger toward the second plunger position and an actuator to deploy the plunger spring. The syringe also includes a needle proximate the distal end of the housing displaceable from a first needle position to a second needle position, and a shroud coupled with the housing. The shroud is moveable between a retracted position and an extended position, the shroud surrounding at least a portion of the needle when in the extended position. The syringe also includes an interlocking assembly, a shroud spring, and a locking assembly configured to inhibit movement of the shroud.
    • 本发明提供一种注射器及其使用方法。 注射器包括具有设置在其中的储存器的壳体和由储存器容纳的柱塞,柱塞可在第一柱塞位置和第二柱塞位置之间移动。 注射器还包括柱塞弹簧,以将柱塞推向第二柱塞位置,以及致动器来展开柱塞弹簧。 注射器还包括靠近壳体的远端的针,其可从第一针位置移动到第二针位置,以及与壳体耦合的护罩。 护罩可在缩回位置和延伸位置之间移动,当延伸位置时护罩围绕针的至少一部分。 注射器还包括互锁组件,护罩弹簧和被配置为禁止护罩运动的锁定组件。
    • 9. 发明授权
    • Anesthetic vaporizer draining system
    • 麻醉蒸发器排水系统
    • US5915427A
    • 1999-06-29
    • US763914
    • 1996-12-11
    • Richard W. Grabenkort
    • Richard W. Grabenkort
    • A61M16/10A61M16/18B65B1/04
    • A61M16/183A61M2205/6045
    • A system is provided for draining an anesthetic agent from a reservoir of an anesthetic vaporizer. The system includes an anesthetic agent container having an inlet into which the agent can drain. The vaporizer has a draining station that defines an outlet and that defines a drain passage between the vaporizer reservoir and the outlet. A valve is operable to open and close the drain passage. A connector is provided with a receiving end for connecting to the draining station at the outlet. The connector has a discharge end for connecting to the container inlet. The connector holds the container below the draining station outlet and defines a transfer passage between the receiving end and the discharge end for draining the agent from the draining station into the container. Structural key configurations, uniquely associated with a specific anesthetic, are preferably provided at the connection of the container and connector and at the connection of the draining station and connector.
    • 提供一种用于从麻醉蒸发器的储存器排出麻醉剂的系统。 该系统包括具有入口的麻醉剂容器,药剂可以排出入口。 蒸发器具有限定出口并且在蒸发器储存器和出口之间限定排放通道的排水站。 阀可操作以打开和关闭排水通道。 连接器设置有用于连接到出口处的排水站的接收端。 连接器具有用于连接到容器入口的排放端。 连接器将容器保持在排水站出口下方,并且在接收端和排放端之间限定了一个传送通道,用于将试剂从排水站排出到容器中。 优选地,在容器和连接器的连接处以及在排水站和连接器的连接处提供与特定麻醉剂唯一相关联的结构关键构造。
    • 10. 发明授权
    • Pharmaceutical ampul
    • 药用安瓿
    • US5775506A
    • 1998-07-07
    • US719744
    • 1996-09-25
    • Richard W. Grabenkort
    • Richard W. Grabenkort
    • A61J1/06A61M5/24B65D85/00
    • A61J1/065A61M5/2429A61J1/062Y10S215/03
    • A pharmaceutical container having a body defining a chamber therein. The body includes a first end portion and a second end portion. A terminal end is included on the second end portion. A plug is positioned in the chamber defined by the body such that the plug is spaced from the terminal end. The plug and the body define a first chamber portion of the chamber between the plug and the first end portion of the body. The plug and the body define a second chamber portion of the chamber between the plug and the terminal end of the second end portion. The plug substantially fluidly seals the second chamber portion from the first chamber portion. The body is frangible at a position on the second end portion between the plug and the terminal end.
    • 一种药物容器,其具有在其中限定室的主体。 主体包括第一端部和第二端部。 末端包括在第二端部。 插头定位在由本体限定的室中,使得插头与终端间隔开。 塞子和主体在塞子和主体的第一端部之间限定腔室的第一腔室部分。 塞子和主体在塞子和第二端部的末端之间限定腔室的第二腔室部分。 插头基本上流体地密封第二室部分与第一室部分。 主体在插头和终端之间的第二端部的位置处是易碎的。