Abstract: Systems and methods for wayfinding in hazardous environments are disclosed. In one embodiment, a method for wayfinding in a hazardous environment may include: (1) receiving, at an emergency response computer program executed by an electronic device, a plurality of real time streams of data, each real time stream of data from a sensing device in an area; (2) detecting, by the emergency response computer program, an alarm condition in the area based on the real-time streams of data; (3) determining, by the emergency response computer program, that the alarm condition satisfies an alarm condition rule; (4) calculating, by the emergency response computer program, a plurality of routes to an egress point from the area; and (5) controlling, by the emergency response computer program, a digital signage in the area to display one of the plurality of routes the egress point.

Abstract: A system and method for determining whether a battery is operating in an anomalous condition can include or be configured to measure sensor data, estimate a local property of the battery using on the sensor data, and classify whether the battery is operating in the anomalous condition based on the local property.

Abstract: Methods and systems for maintaining and building an autonomous vehicle-related event blockchain are provided. One or more processors may receive indications of autonomous vehicle events. The autonomous vehicle events may include information relating to technology usage and/or operational events. The autonomous vehicle events may be compiled into a log of recorded autonomous vehicle events. Based upon the autonomous vehicle events, an action to implement may be determined. Additionally, the log may be distributed to a public or private network of distributed nodes to form a consensus on an update to the log of record autonomous vehicle events. As a result, the distributed nodes may maintain an up-to-date record of the shared ledger of autonomous vehicle events.

Abstract: A device for sealing an aperture in a tissue includes: a foot including a distal portion configured to be disposed distal to the tissue when the device is implanted in a position to seal the aperture; and a flexible wing positionable against a distal surface of the tissue adjacent the aperture such that the flexible wing is disposed between the distal portion of the foot and the distal surface adjacent the aperture.

Abstract: Features relating to vaporizer devices configured to allow for temperature adjustment are provided. User controlled actions with respect to removing a cartridge from a vaporizer body and inserting the cartridge into the vaporizer body provide for temperature adjustment, where the temperature refers to a setpoint temperature of operation of the vaporizer device. The temperature adjustment aspects of the current subject matter provide a user with a controlled, intuitive, and simple method to adjust the setpoint temperature of the vaporizer device by incrementing through a sequence of setpoint temperatures.

Abstract: Systems and methods are provided for splicing airframe components. One embodiment is a method for assembling an airframe of an aircraft. The method includes forming a first skin of a first circumferential section of fuselage, the first skin including a distal portion comprising a lip and a shoulder, aligning a second skin of a second circumferential section of fuselage with the shoulder such that the lip overlaps the second skin, and affixing the first skin and the second skin together via a circumferential splice.

Abstract: A sanitization system includes a plurality of light distribution hubs spaced along a longitudinal frame. Each hub includes a plurality of light emitting modules (e.g., LED chip-on-board) configured to deliver a predetermined type of light (e.g, UVC) to a target surface for a variable or predetermined amount of time at a variable or predetermined intensity to at least partially disinfect and/or sanitize the target surface. The target surface may be an interior surface of a medical imaging device, such as an inwardly facing bore surface and/or patient support surface of an MRI or CT scanner.

Abstract: Embodiments of the present invention provide systems, apparatus, methods and/or the like for generating a resource distribution hub using for fully electronic resource distribution by using mobile device application designed to interface with an embedded Near-Field Communication (NFC) tag in a resource distribution instrument that stores instructions for processing the resource distribution authorization information. The holder (i.e., resource provider) of the resource distribution instrument can use the resource distribution instrument to communicate to a mobile communication device having an NFC reader to read the instructions and process a resource distribution according to the parameters of the mobile device application. As such, the holder (i.e., resource provider) of the resource distribution request can process the resource distribution without having to issue a credentials, aliases, pin codes, and the like conventionally used to authorizes the distribution of resources to the resource requester.

Abstract: A method performs location-based multi-factor authentication. The method includes a mobile device that receives a first set of authentication credentials provided by a user, and transmits the first set of authentication credentials to an authentication server, which verifies the first set of authentication credentials. The authentication server transmits verified first factor authentication to the mobile device that sends a request for second factor authentication to an authentication system, which causes the mobile device to scan identifier information associated with a secure device, the secure device then sending a second set of authentication credentials to the authentication system. The authentication system verifies the second set of credentials system and transmits verified second factor authentication to the authentication server, which subsequently grants final authentication based on the verified first factor authentication and the verified second factor authentication.

Abstract: An apparatus for measuring pressure within a fluid path includes a housing defining the structure of the apparatus. The housing includes a fluid path that extends through the housing and allows a fluid to pass through the housing. The apparatus also includes a first volume chamber that is in fluid communication with the fluid path and has a first volume chamber opening, and a second volume chamber with a second volume chamber opening that is less than the first volume chamber opening. A diaphragm separates the first volume chamber from the second volume chamber and fluidly disconnects the second volume chamber from the fluid path. The diaphragm deforms based upon the pressure within the fluid path. The apparatus also includes an interface that is connectable to a pressure sensor, and the second volume chamber is in fluid communication with the interface.

Abstract: A continuous flow centrifuge bowl includes a rotatable outer body, and a top and bottom core that are rotatable with the outer body. The bottom core has a wall extending proximally from a bottom wall. The proximally extending wall is radially outward from at least a portion of the top core and, together with the top core, defines a primary separation region in which initial separation of the whole blood occurs. The bowl may also have a secondary separation region located between the top core and the outer body, and a rotary seal that couples an inlet port and two outlet ports to the outer body. The inlet port may be connected to an inlet tube that extends distally into a whole blood introduction region. Additionally, one of the outlet ports may be connected to an extraction tube that extends into a region below the bottom core.

Abstract: A continuous flow centrifuge bowl includes a rotatable outer body, and a top and bottom core that are rotatable with the outer body. The bottom core has a wall extending proximally from a bottom wall. The proximally extending wall is radially outward from at least a portion of the top core and, together with the top core, defines a primary separation region in which initial separation of the whole blood occurs. The bowl may also have a secondary separation region located between the top core and the outer body, and a rotary seal that couples an inlet port and two outlet ports to the outer body. The inlet port may be connected to an inlet tube that extends distally into a whole blood introduction region. Additionally, one of the outlet ports may be connected to an extraction tube that extends into a region below the bottom core.

Abstract: Systems and methods for wayfinding in hazardous environments are disclosed. In one embodiment, a method for wayfinding in a hazardous environment may include: (1) receiving, at an emergency response computer program executed by an electronic device, a plurality of real time streams of data, each real time stream of data from a sensing device in an area; (2) detecting, by the emergency response computer program, an alarm condition in the area based on the real-time streams of data; (3) determining, by the emergency response computer program, that the alarm condition satisfies an alarm condition rule; (4) calculating, by the emergency response computer program, a plurality of routes to an egress point from the area; and (5) controlling, by the emergency response computer program, a digital signage in the area to display one of the plurality of routes the egress point.

Abstract: Systems and methods for automatic redaction of sensitive information from video streams are disclosed. According to one embodiment, a method for automatic redaction of sensitive information from video streams may include: (1) receiving, by an image processing computer program executed by an electronic device, a video stream of an area; (2) identifying, by the image processing computer program, an object capable of having sensitive information thereon in the video stream of the area; and (3) redacting or obscuring, by the image processing computer program, the object in the video stream.

Abstract: A laminate sheet including a weldable margin is formed by laminating metal sheets having a core layer disposed therebetween. The core layer is formed of a core material which includes one or more of a viscoelastic, adhesive and acoustic material. The core layer is selectively distributed such that the laminate sheet includes an adhered region providing a laminate structure, and a non-adhered region including a weldable margin. The non-adhered region is adjacent an edge of the core layer and is characterized by a gap between the first and second metal sheets and by an absence of the core layer in the gap. The non-adhered region defines a weldable margin adjacent a core edge configured such that a weld is formable in the weldable margin without heat affecting the core layer. The laminate sheet can be joined by fasteners installed in the non-adhered region.

Abstract: A sanitization system includes a plurality of light distribution hubs spaced along a longitudinal frame. Each hub includes a plurality of light emitting modules (e.g., LED chip-on-board) configured to deliver a predetermined type of light (e.g, UVC) to a target surface for a variable or predetermined amount of time at a variable or predetermined intensity to at least partially disinfect and/or sanitize the target surface. The target surface may be an interior surface of a medical imaging device, such as an inwardly facing bore surface and/or patient support surface of an MRI or CT scanner.

Abstract: Embodiments of negative pressure wound therapy systems, apparatuses, and methods for operating the systems and apparatuses are disclosed. In some embodiments, the apparatus includes a negative pressure source, a connector port, at least one switch, and a controller. The negative pressure source is connected through the connector port to either (i) a wound dressing having a canister configured to store fluid aspirated from the wound or (ii) a wound dressing without a canister between the connector port and the wound dressing. The controller determines, based on a signal received from the at least one switch, whether the canister is positioned in the fluid flow path and adjusts one or more operational parameters of negative pressure wound therapy based on the determination. The switch is activated by the connection of either the canister or canisterless wound dressing to the apparatus.

Abstract: A method performs location-based multi-factor authentication. The method includes a mobile device that receives a first set of authentication credentials provided by a user, and transmits the first set of authentication credentials to an authentication server, which verifies the first set of authentication credentials. The authentication server transmits verified first factor authentication to the mobile device that sends a request for second factor authentication to an authentication system, which causes the mobile device to scan identifier information associated with a secure device, the secure device then sending a second set of authentication credentials to the authentication system. The authentication system verifies the second set of credentials system and transmits verified second factor authentication to the authentication server, which subsequently grants final authentication based on the verified first factor authentication and the verified second factor authentication.

Abstract: Embodiments disclosed herein provide for systems and methods for authenticating a mobile device. The systems and methods provide for a wireless, touchless multi-factor authentication process for the mobile device, wherein a first factor of authentication includes providing authentication credentials to the mobile device and a second factor of authentication includes scanning a physical identification at a secure device.

Abstract: Embodiments of negative pressure wound therapy systems, apparatuses, and methods for operating the systems and apparatuses are disclosed. In some embodiments, the apparatus includes a negative pressure source, a connector port, at least one switch, and a controller. The negative pressure source is connected through the connector port to either (i) a wound dressing having a canister configured to store fluid aspirated from the wound or (ii) a wound dressing without a canister between the connector port and the wound dressing. The controller determines, based on a signal received from the at least one switch, whether the canister is positioned in the fluid flow path and adjusts one or more operational parameters of negative pressure wound therapy based on the determination. The switch is activated by the connection of either the canister or canisterless wound dressing to the apparatus.