Abstract:
In one exemplary embodiment, an automated medication preparation system is provided and is in the form of an automated syringe preparation that includes reconstitution of the medication and delivery of the reconstituted medication to a syringe. The system includes an automated fluid delivery device that is movable in at least one direction and is adapted to perform at least one of the following operations: (1) receiving and discharging diluent from a diluent supply in a prescribed amount to reconstitute the medication in a drug vial; and (2) aspirating and later discharging reconstituted medication from the drug vial into the syringe. The system also includes a transfer device that includes a first section for piercing the septum of the drug vial and a second section for sealingly yet releasably mating with the fluid delivery device. The transfer device is constructed so that it remains within the drug vial for multiple uses without the need to pierce the septum more than one time and therefore, the disadvantages associated with the prior art are overcome. The transfer device has a first channel extending through the first and second sections for carrying diluent or reconstituted medication and a second channel that is in fluid communication with a vent that is formed as part of the transfer device to permit air to flow into the drug vial.
Abstract:
Medical needle shield apparatus for covering a needle after use. In embodiments of this invention a shield with two or more segments hingedly connected to each other is movable from a retracted position where the needle is exposed, to an extended position where the shield extends beyond the end of the needle. The needle is affixed in a hub of a medical needle device, and the shield is articulated to the hub. At least one of the two or more segments has an open orifice through which the needle passes to form an axis of intersection about the needle. The shield includes a channel for covering the needle when the shield is linearly extended. One or more locks associated with one or more of the segments secures one or more of the segments relative to the shield in the extended position.
Abstract:
A needle-free injection system, including an injection device and a vial adapter. The injection device is configured to be loaded with a dose of injectable fluid and forcibly inject such dose into an injection site. The vial adapter is configured to secure to and selectively seal a vial containing an external supply of injectable fluid. The vial adapter also includes a flexible adapter structure biased into a blocking position. The injection device includes a filling adapter configured to move the flexible adapter structure out of the blocking position to thereby permit the vial adapter and injection device to be secured together in an engaged configuration. In this engaged configuration, a dose of injectable fluid may be drawn from the external supply of injectable fluid into the injection device.
Abstract:
An inserter having a housing, a syringe carriage slidably mounted within the housing and a syringe socket defined within the syringe carriage. The syringe carriage is able to assume a cocked position and an extended position with the latter being the position for injection. A spring biases the syringe carriage to the extended position and a latch selectively retains the syringe carriage in the cocked position.
Abstract:
A fluid transfer system has a holder that is made of a cylindrical member having a closed end and an open end. The closed end has fitted thereto a luer and a cannula that extends into the interior of the holder. The holder has a distal portion that has a first cross section and a proximal portion that has a second cross section. The cross section of the distal portion is smaller than the cross section of the proximal portion. The distal and proximal portions are joined by a shoulder. The fluid transfer system also includes an adapter that is inserted to the holder from the open end of the holder. The adapter has a base having a central opening and a cylindrical tube that extends from the central opening. The diameter of the cylindrical tube is slightly smaller than the diameter of the distal portion and is configured to accept a first type of fluid collection store such as a vacuum tube. A non-continuous wall extends from the base of the adapter to surround the cylindrical tube. The cross section of the wall is slightly smaller than the diameter of the proximal portion. At each section of the non-continuous wall there is formed a protuberance. A groove is formed about the inner surface of the proximal portion. When the adapter is fully inserted to the holder, the protuberances would snap fit to the groove so that the adapter is prevented from being inadvertently removed from the holder. With the adapter removed, the holder can accept a differently dimensioned fluid collection store such as for example a blood culture collection bottle.
Abstract:
A tool for use with a medication vial and a syringe comprises a housing having a top side, a bottom side, and a surrounding edge, a slotted aperture defined in the housing and including a flange shaped to engage vial cap, a cylindrical aperture defined in the housing and sized to permit placement of a forward portion of the syringe including a cap into the cylindrical aperture, an actuator button mounted to the housing, and a gripper mounted within the housing and having a pair of opposed edges, with the gripper responsive to movement of the actuator button to permit movement of the edges between a retracted position in which the edges are disposed away from a central portion of the cylindrical aperture, and an extended position in which the edges are displaced toward the central portion of the cylindrical aperture.
Abstract:
A container assembly includes a container body having a port or aperture adapted for use with a luer end of a needleless syringe. The aperture is sealed to a closure top by a first frangible seal. An overcap has a cap base sealed to the container body and an upper cap connected to the cap base by a second frangible seal, providing a sterile barrier surrounding the first frangible seal. The second frangible seal is broken by depressing the upper cap toward the container body. Alternatively, the second frangible seal is a removable tear strip broken by tugging on the tear strip. The upper cap includes a detent portion frictionally securing the upper cap to the closure top when the upper cap is depressed toward the container body. The upper cap and secured closure top are removed from container body by twisting the upper cap to break the first frangible seal and open the port.
Abstract:
The present invention provides a connector device for establishing fluid communication between a first container and a second container. The device has a first sleeve member having a first and a second end, the first sleeve member having at the first end a first attaching member adapted to attach to the first container. The device further has a second sleeve member having a first end and a second end, the second sleeve member being associated with the first sleeve member and movable with respect thereto from an inactivated position to an activated position, the second sleeve member having at the second end a second attaching member adapted to attach the second sleeve member to the second container. First and second piercing members project from one of the first and second sleeve members for providing a fluid flow path from the first container to the second container, and the first and second piercing members are independently hermetically sealed.
Abstract:
A system for mixing four components (K1, K2, K3, K4) has a first syringe arrangement (10) and a second syringe arrangement (20). The first and second syringe arrangements (10, 20) each contain at least two chambers (11, 12; 21, 22) for holding one each of the components (K1, K2, K3, K4). It is possible to connect each chamber of one of the syringe arrangements (10) in a detachable fashion to a chamber (21, 22) of the other syringe arrangement (20). By transferring the components (K1, K2) from one of the syringe arrangements (10) into chambers (21, 22) of the other syringe arrangement (20), the transferred components (K1, K2) are mixed with components (K3, K4) which are contained in this chamber (21, 22).
Abstract:
A method and system for handling hazardous materials contained in a vial includes an isolation enclosure having an opening selectively sealable about the vial, a bag body portion, and a cap portion. A latching extraction element is attached to the cap portion and has a preceding engaging member to secure the vial to the isolation enclosure, an extraction member to be inserted into the vial and remove material therefrom, and a primary engaging member to secure the vial to the extraction member. A valve is mounted outside the isolation enclosure and controls the flow of fluid from the vial. An adaptor having a reseal member permits flow when coupled to the valve and restricts flow when uncoupled from the valve. Once uncoupled, the adaptor is removably associated with a second valve located remotely from the isolation enclosure, allowing fluid to pass into the second valve.