Abstract: An electronic key may include a partial capacitor comprising a capacitive metal plate in communication with a processor. The capacitive metal plate of the partial capacitor is configured to form a capacitor with a corresponding capacitive metal plate of a lock when brought into proximity with the metal plate of the lock. Data may be transferred from the key to the lock using a capacitor formed by combining the two metal plates, wherein a common ground is established between the metal plate of the key and the metal plate of the lock through a parasitic capacitance present between the key and lock circuitry. Audit trail data may be recorded based on usage of the key.

Abstract: A wipe kit includes a pouch having a first compartment with a one-way valve coupled to an end thereof, a second compartment, and a frangible seal between the first and second compartments. The first compartment receives a liquid through the one-way valve and the second compartment contains a dry wipe. The frangible seal can be broken to permit liquid to flow from the first compartment onto the wipe in the second compartment. The deactivation wipe kit may be used in a clean room to deactivate most hazardous drugs on a work surface.

Abstract: An endoluminal device comprises a tubular member and a reinforcement member that is separable from, or together with, a wall of the tubular member, and removable in-situ.

Abstract: A method is provided for fabricating fiber reinforced plastic (FRP) panels filled with flame-retardant fillers. The method may include pre-treating fiber reinforcement with a polymer binder, spreading fillers of a selected size over the polymer binder, and forming a dry stack including the fiber reinforcement and the fillers. The method may also include infusing a polymer resin into the dry stack using a vacuum infusion process and forming a fiber reinforced plastic (FRP) laminate including the fiber reinforcement and substantially uniformly distributed fillers embedded within a polymer matrix formed from the polymer resin, the fillers having a filler loading of at least 70 parts per hundred parts of infused resin (phr).

Abstract: An implantable medical device deployment system is disclosed that employs both a sheath element and a constraint member to protect implantable medical devices during delivery in a body while providing simple, accurate, and reliable device deployment. The delivery system is configured so that loading and deployment forces are not directly related to device diameter, length, or design, thus allowing a more universal delivery system across various delivered device configurations and product lines. The deployment system can provide numerous benefits, include better protection for drug-coated implantable devices.

Abstract: Various aspects of the present disclosure are directed toward apparatuses, systems, and methods for example device delivery. The apparatuses, systems, and methods may include an actuation wire coupled to the expandable device at one or more locations thereon, the actuation wire being configured to steer the expandable device during delivery.

Abstract: A method for repairing an electric generator having a rotor that rotates about a vertical axis, the rotor including a spider having a number of spider arms extending radially away from the axis, and a rim surrounding the spider. The weight of the rim is normally carried at least in part by rim support ledges of the spider arms. The method for repair includes supporting the rim from the top of the spider and thereby relieving some or all of the weight of the rim being supported by the rim support ledges.

Abstract: A biocompatible membrane composite including a cell impermeable layer and a mitigation layer is provided. The cell impermeable layer is impervious to vascular ingrowth and prevents cellular contact from the host. Additionally, the mitigation layer includes solid features. In at least one embodiment, mitigation layer has therein bonded solid features. In some embodiments, the cell impermeable layer and the mitigation layer are intimately bonded or otherwise connected to each other to form a composite layer having a tight/open structure. A reinforcing component may optionally be positioned external to or within the biocompatible membrane composite to provide support to and prevent distortion. The biocompatible membrane composite may be used in or to form a device for encapsulating biological entities, including, but not limited to, pancreatic lineage type cells such as pancreatic progenitors.

Abstract: A gas separation device for use in combination with a liquid chromatography system is provided. The gas separation device includes a housing defining a fluid flow path between an outer surface and an inner surface. The fluid flow path includes an inlet portion, a diffuser portion, a recombination portion, and an outlet portion. Any gas bubbles contained within the fluid are trapped within the diffusor portion when fluid flow is in a forward direction. Fluid flow through the gas separation device is reversable so as to remove the trapped gas bubbles from within the gas separation device. In this operation state, the fluid is delivered from the gas separation device into the waste stream to ensure that gas bubbles leave the liquid chromatography system. The gas separation device may exhibit an air trapping effectiveness ratio (ATER) between 0.001 mb?1 and 0.51 mb?1 during forward direction fluid flow.

Abstract: Various aspects of the present disclosure are directed toward apparatuses, systems and methods that include an airflow conditioning device. The airflow conditioning device includes a channels defining airflow pathways through the airflow conditioning device. A heat and moisture exchanger is disposed in the airflow conditioning device with a plurality of air-permeable barriers separating the airflow pathways. The airflow conditioning device includes air-permeable barriers with a layer of a microporous film and a water vapor permeable resin layer adjoined to one or both of the surfaces of the microporous film as either a continuous microporous coating or a discontinuous coating.

Abstract: A wipe kit includes a pouch having a first compartment with a one-way valve coupled to an end thereof, a second compartment, and a frangible seal between the first and second compartments. The first compartment receives a liquid through the one-way valve and the second compartment contains a dry wipe. The frangible seal can be broken to permit liquid to flow from the first compartment onto the wipe in the second compartment. The deactivation wipe kit may be used in a clean room to deactivate most hazardous drugs on a work surface.

Abstract: The present disclosure includes an endoprosthesis delivery system comprising an elongate member, such as a catheter, an endoprosthesis, and an end cap having one or more protrusions extending therefrom. The protrusions may assist in retraction of end cap into an outer sheath, such as an introducer sheath. In some examples, the protrusion includes fins. In some embodiments, the endoprosthesis delivery system further includes a covering member disposed about the endoprosthesis. The protrusions may support the covering member, which may extend beyond the distal end of the endoprosthesis and onto the end cap. In some embodiments, the end cap comprises a tapered profile, which may assist in retraction of the catheter tip and end cap into an outer sheath.

Abstract: Some aspects of the disclosure relate to composite materials and cultivation systems with particular utility for use in aquaculture, for example cultivating various species of seaweed. The systems comprise at least one highly tortuous and often micro-fibrous material and at least one material having low tortuosity. These systems may be configured in a variety of shapes and associated with a number of different structures. Some of these composite materials and cultivation systems may be used in both direct and indirect seeding of macroalgae plants such as seaweed.

Abstract: A wire of a nickel-titanium alloy having a permanent set of less than 5% when 11% strain is applied to the wire is disclosed. The wire may be formed by applying a first heat treatment to the wire, the first heat treatment includes applying heat of a first temperature for a first period of time, applying a strain deformation to the wire to set a shape for the wire during the first heat treatment, and applying a second heat treatment to the wire. The second heat treatment includes applying heat of a second temperature different from the first temperature for a second period of time, and the second temperature is between 210° C. and 290° C. The wire may have a modulus of at least 53 GPa when 200 MPa of stress is applied to the wire, and the wire is bonded to a secondary component.

Abstract: Polyparaxylylene (PPX) polymers that can be expanded into porous articles that have a node and fibril microstructure are provided. The fibrils contain PPX polymer chains oriented with the fibril axis. The PPX polymer may contain one or more comonomer. PPX polymer articles may be formed by applying PPX to a substrate by vapor deposition. The nominal thickness of the PPX polymer film is less than about 50 microns. The PPX polymer film may be removed from the substrate to form a free-standing PPX polymer film, which may then be stretched into a porous article. Alternatively, a PPX polymer article can be formed by lubricating PPX polymer powder, heating the lubricated powder, and calendering or ram extruding to produce a preform that can subsequently be stretched into a porous article. The heating and expansion temperatures are from about 80° C. to about 220° C. or from about 220° C. to about 290° C. or from about 290° C. to about 450° C.

Abstract: Various examples relate to a transcatheter delivery system including a sheath, a delivery catheter, and an implantable device (e.g., a prosthetic valve, a stent, a stent graft, occluder, or vascular filter) maintained in a collapsed configuration by the delivery catheter. The delivery catheter includes a plurality of fiber guides separated by one or more reduced profile sections each having a smaller transverse outer profile than the transverse outer profiles of the fiber guides.

Abstract: The present disclosure describes endoluminal devices, such as stents and stent grafts capable of being bent smoothly, with various benefits resulting therefrom.

Abstract: An assembly includes an acoustic device. The acoustic device can include a polyethylene membrane. The polyethylene membrane can have first direction and a second direction, the second direction being orthogonal to the first direction. The polyethylene membrane can have a surface area per volume of at least 39×106/m. The polyethylene membrane can have a geometric mean tensile modulus of 250 to 750 MPa. The polyethylene membrane can have a maximum tensile modulus in the first direction of 440 to 915 MPa. The polyethylene membrane can have a maximum tensile modulus in the second direction of 275 to 515 MPa. The polyethylene membrane can be an expanded polyethylene membrane.

Abstract: This document provides implantable intraluminal stent graft medical devices. In some embodiments, the stent graft devices provided herein are implantable in bodily conduits that have side branches, and the stent graft devices are operable to allow the flow of fluids between the conduit and the side branches. In some embodiments, the walls of the stent graft devices provided herein include compliant channels which allow for fluid communication between the interior and the exterior of the stent graft devices. In some embodiments, the compliant channels are configured to inhibit or reduce tissue ingrowth, tissue bridging, and/or endothelialization.

Abstract: Some embodiments of the present disclosure relate to a method that includes disposing a vapor pump partially within an enclosure, such that the vapor pump is in fluid communication with the enclosure and an external environment, and where the enclosure comprises at least one vapor. In some embodiments, a portion of the at least one vapor is transferred with the vapor pump from the enclosure to the external environment. In some embodiments, a change in at least one parameter related to a mass of the at least one vapor within the enclosure is measured. In some embodiments, a rate of the portion of the at least one vapor transferred with the vapor pump from the enclosure to the external environment is calculated. In some embodiments, the rate of the portion of the at least one vapor transferred from the enclosure to the external environment with the vapor pump is calculated based on the change in the at least one parameter.