摘要:
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.
摘要:
An improved package for a medical device includes an inner wrap that envelopes the medical device, the inner wrap including a gas-permeable surface, and a chamber defined in the inner wrap to store a hydratable sensor of the medical device. Plumbing for the package controls fluid flow into and within the inner wrap, to selectively establish, without breaching a portion of the inner wrap surrounding the sensor, fluid communication between the gas-permeable surface and the sensor, to sterilize the sensor and the inner wrap with a gaseous sterilant, or to hydrate the sensor with hydration fluid obtained from a source of hydration fluid connected to the chamber, or to equilibrate the hydration fluid in the chamber with an external source of gas, to calibrate the sensor within the inner wrap.
摘要:
An improved site protector of simple one-piece construction includes a convex tapered bubble as the main body portion, and a plurality of aeration openings defined at step-down portions of the bubble, the step-down portions providing strength, stability and rigidity to the bubble. A locking member provided at one end of the site protector stabilizes the catheter at the insertion site.
摘要:
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.
摘要:
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.
摘要:
A suction drainage control system that reduces an operator's exposure to infectious waste by permitting waste-treating material to be dispersed into a sealed chamber in which the infectious waste is contained. The sealed chamber includes a cover with a flexible liner sealed to and suspended therefrom. A freely movable reservoir is provided inside the sealed chamber for storing the waste-treating material, which reservoir is opened by manipulating the flexible liner to open the reservoir.
摘要:
A filter for removing a liquid from a gas comprising a housing, a liquid absorbent material disposed in the housing to absorb the liquid from the gas passing through the filter, and a plurality of ribs disposed on an inner surface of the housing, the ribs spaced apart from each other and supporting the liquid absorbent material within the housing. The ribs define a plurality of open passages around the liquid absorbent material, and connecting an inlet of the housing in fluid communication with an outlet, so that the gas flowing between the inlet and the outlet experiences substantially no pressure drop, the liquid in the gas being absorbed by the liquid absorbent material in the filter, as the gas flows through the filter.
摘要:
A frangible element valve assembly including a housing having an inlet port and an outlet port connected by a fluid passage that extends through the housing; and an actuator selectively controlling fluid flow through the fluid passage being biased to a predetermined fluid flow control position by a spring member of the valve assembly. Frangible elements of the valve assembly oppose the spring member to temporarily prevent the actuator from assuming the predetermined fluid flow control position, and these elements include breakable members that are broken by an operator to allow the actuator to thereafter assume the predetermined fluid flow control position until selectively changed by the operator.
摘要:
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.
摘要:
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.