Abstract:
The invention relates to a dispense interface for use with a drug delivery device with an inner body and with a lockout element, wherein the lockout element is coupled to the inner body, wherein the lockout element is movable from a receptive condition to a locked condition, wherein in the receptive condition the dispense interface is attachable to the drug delivery device, wherein in the locked condition the dispense interface is not-attachable to the drug delivery device and wherein the lockout element is configured to move from the receptive condition to the locked condition when said dispense interface is attached to and detached from said drug delivery device. The invention solves the technical problem of reducing the risk of reuse of a dispense interface, after it has already been used with a drug delivery device.
Abstract:
Imaging systems, methods, sensor pods, and vehicles having imaging systems. An imaging system can be coupled to a vehicle and can comprise: a plurality of imaging sensors with multiple spectrums; and a processing unit configured to generate an image model in substantially real-time by: warping, fusing, and stitching images; and two or more displays coupled to the processing unit such that the two or more displays can simultaneously each show a different portion of the image model, and such that a user can manually calibrate via the processing unit at least one of the warping, fusing, or stitching. In some imaging systems, imaging sensors are coupled at different elevations relative to a ground vehicle. The present sensor pods can comprise a housing; two or more first imaging sensors having a first spectrum; and two or more second imaging sensors having a second spectrum that is different than the first spectrum.
Abstract:
The present invention relates to medical devices and particularly to a medication delivery device for self-injection of a medication, or for healthcare professionals to administer a medication. In one embodiment, a medication delivery device utilizes a source of gas pressure to deploy a needle, deliver a desired amount of medication through the needle, and retract the needle for disposal. Fluid flow paths from the source of gas pressure communicate the gas pressure to the needle and to the medication in order to accomplish these steps. In one embodiment, a valve is positioned to open and close the flow of the pressurized gas to the needle and the flow of the medication to the needle, so that the valve can be operated to deploy the needle and deliver the medication through the needle when the user is ready for the injection. The valve can also be operated to retract the needle when the dose is complete.
Abstract:
The present invention provides systems, methods, computer program products, and combinations and subcombinations thereof for filtering received messages. The invention includes a client system having filtering logic, a statistical classifier module, and a classifier database. The classifier module is automatically trained, without manual intervention, when the score generated by the classifier for a received message is inconsistent with a user-defined authoritative status indication. In addition, the classifier module is initialized using user-identified messages in a ratio representative of the ratio of non-spam to spam messages received by the user.
Abstract:
The present invention relates to medical devices and particularly to a medication delivery device for self-injection of a medication, or for healthcare professionals to administer a medication. In one embodiment, a medication delivery device utilizes a source of gas pressure to deploy a needle, deliver a desired amount of medication through the needle, and retract the needle for disposal. Fluid flow paths from the source of gas pressure communicate the gas pressure to the needle and to the medication in order to accomplish these steps. In one embodiment, a valve is positioned to open and close the flow of the pressurized gas to the needle and the flow of the medication to the needle, so that the valve can be operated to deploy the needle and deliver the medication through the needle when the user is ready for the injection. The valve can also be operated to retract the needle when the dose is complete.
Abstract:
A method of bonding an antimicrobial cationic polyelectrolyte to the surface of a substrate is described, wherein the antimicrobial thus attached to the substrate provides the substrate with antimicrobial properties, and at least a portion of the bonded antimicrobial is substantially non-leachable during normal conditions of use and storage. A method of manufacturing an antimicrobial material is described which comprises exposure of the substrate to a solution of antimicrobial cationic polyelectrolyte, followed by drying the exposed substrate thoroughly to impart a non-leaching property to at least a portion of the antimicrobial cationic polyelectrolytes.
Abstract:
The present invention provides a spring probe array for use in a semiconductor test fixture wherein the spring probes provide electrical continuity between a device under test and a test system. The array includes a spring probe retaining device with sockets for supporting spring probes. Fixed within the retaining device are a plurality of signal spring probes and a plurality of ground spring probes. A grounding board is fixed internal and captive to the spring probe retaining device and provides a common grounding connection between coaxial spring probes and adjacent non-coaxial spring probes in the spring probe retaining device.
Abstract:
Systems, devices and methods for treating internal tissue defects, such as septal defects, are provided. An exemplary method of treating an internal tissue defect, specifically a method of closing a patent foramen ovale (PFO), can include passing a closure element from a right atrium through a septal wall in a first location and into the left atrium. A capture device, which can be configured as a snare-like device, can be used to capture the closure element in the left atrium and pull the closure element back through the septal wall in a different, second location, such that the closure element is routed over the PFO. The closure element can then be anchored and/or locked against the septal wall such that the PFO is at least partially closed.
Abstract:
A sensor for measuring moisture content of a substrate, comprising: a coplanar waveguide; a directional coupler having a pair of generally parallel first and second strips defining a coupling gap therebetween; and a high frequency signal generator electrically coupled to said first strip and operable to couple power to said second strip with the substrate placed across said coupling gap to thereby generate a coupled power signal in said second strip having an amplitude related to moisture content of the substrate.
Abstract:
A ventilation system includes a ventilation tile. The ventilation tile has a substantially circular opening to allow air to flow through the ventilation tile and a collapsible damper operable to collapse and expand to alter the size of the substantially circular opening in the ventilation tile and thereby variably restrict air flow through the substantially circular opening.