Abstract: To present augmented reality features without localizing a user, a client device receives a request for presenting augmented reality features in a camera view of a computing device of the user. Prior to localizing the user, the client device obtains sensor data indicative of a pose of the user, and determines the pose of the user based on the sensor data with a confidence level that exceeds a confidence threshold which indicates a low accuracy state. Then the client device presents one or more augmented reality features in the camera view in accordance with the determined pose of the user while in the low accuracy state.

Abstract: A battery pack includes a housing, at least one battery cell enclosed within the housing, a printed circuit board (PCBA) enclosed within the housing, a gauge electrically connected to the PCBA and including at least one light, and an actuator that, when actuated, activates the gauge to illuminate the at least one light to indicate a charge level of the at least one battery cell. The housing has a main body and a handle extending from the main body, and the handle defines an aperture sized and shaped to receive one or more of a user's fingers therein. The gauge is located on an outer surface of the handle.

Abstract: An intraluminal device includes a radially expandable body and a control member operable to expand and contract the radially expandable body. The radially expandable body comprises plural sets of first filaments spiraling in a first direction from a proximal end portion to a distal end portion of the radially expandable body and plural sets of second filaments spiraling in a second direction from the proximal end portion to the distal end portion. The plural sets of first filaments intersect the plural sets of second filaments, forming plural cross sections of the radially expandable body. At least one of the plural sets of first filaments comprises a filament constructed of a radiopaque material.

Abstract: Methods, computer program products, and systems are presented. The method computer program products, and systems can include, for instance: obtaining iteratively captured frames of image data representing a user interface screen, wherein one or more of the frames of image data represents an error screen indicating an error condition of one or more resource of a plurality of resources of a services system; performing recognition processing using image data of the captured frames of image data to determine an error classifier associated to the error screen: determining one or more action based on the error classifier; and performing the one or more action in response to the determining.

Abstract: A battery pack connection system includes a first battery pack, a second battery pack, and a battery receptacle. Each of the first and second battery packs includes a first guide slot, a second guide slot, and an electrical connector slot. The second battery pack has a power capacity and a width greater than the first battery pack. The battery receptacle defines an elongate passage sized and shaped to separately receive each of the first and second battery packs therein. The battery receptacle includes an electrical connector rail, a first guide rail sized and shaped to cooperatively engage the first guide slot of each of the first and second battery packs, and a second guide rail sized and shaped to cooperatively engage the second guide slot of each of the first and second battery packs.

Abstract: A battery pack includes a housing, at least one battery cell enclosed within the housing, a printed circuit board (PCBA) enclosed within the housing, a gauge electrically connected to the PCBA and including at least one light, and an actuator that, when actuated, activates the gauge to illuminate the at least one light to indicate a charge level of the at least one battery cell. The housing has a main body and a handle extending from the main body, and the handle defines an aperture sized and shaped to receive one or more of a user's fingers therein. The gauge is located on an outer surface of the handle.

Abstract: A medical device includes an inflatable balloon defining an interior surface and an exterior surface, and a coating including a therapeutic agent disposed on the exterior surface of the inflatable balloon. The coating has a release transition temperature within a range from about 25° C. to about 50° C. When the temperature of the coating is below the release transition temperature, the coating retains at least a portion of the therapeutic agent on the exterior of the inflatable balloon. When the temperature of the coating is above the release transition temperature, the coating releases at least a portion of the therapeutic agent from the exterior of the inflatable balloon.

Abstract: Embodiments herein describe techniques for binning integrated circuits (ICs) using an adaptive binning system that can re-bin the ICs in response to receiving a new or updated test specification. Unlike static binning systems, in one embodiment, the binning system receives measured test data from a testing system. Put differently, instead of a testing apparatus simply indicating whether an IC does (or does not) satisfy the criteria in the test specification, the testing apparatus provides measured test data to the binning system. The binning apparatus can then store the received test data. As such, if a new test specification is received or generated, the binning system can use the already saved test data to re-bin the ICs using the criteria in the new test specification without having to re-test the ICs. In this manner, the binning system can re-categorize the ICs as customer needs or customer demand changes.

Abstract: A tubular sheath for enclosing an expandable balloon attached to the distal portion of a catheter encloses and protects the expandable balloon. The tubular sheath is configured to be slidable and removable from the catheter. The tubular sheath may include a longitudinal splitting element that is removable as a result of a force applied to the longitudinal splitting element. The longitudinal splitting element is configured to split the wall of the tubular sheath in response to the force. Alternatively, the tubular sheath may include a gripping portion that has relatively poor cohesive strength to adjacent portions of the tubular sheath. The tubular sheath is configured to be removable in response to a force applied to the gripping portion.

Abstract: Methods, computer program products, and systems are presented. The method computer program products, and systems can include, for instance: obtaining iteratively captured frames of image data representing a user interface screen, wherein one or more of the frames of image data represents an error screen indicating an error condition of one or more resource of a plurality of resources of a services system; performing recognition processing using image data of the captured frames of image data to determine an error classifier associated to the error screen: determining one or more action based on the error classifier; and performing the one or more action in response to the determining.

Abstract: A tubular sheath for enclosing an expandable balloon attached to the distal portion of a catheter encloses and protects the expandable balloon. The tubular sheath is configured to be slidable and removable from the catheter. The tubular sheath may include a longitudinal splitting element that is removable as a result of a force applied to the longitudinal splitting element. The longitudinal splitting element is configured to split the wall of the tubular sheath in response to the force. Alternatively, the tubular sheath may include a gripping portion that has relatively poor cohesive strength to adjacent portions of the tubular sheath. The tubular sheath is configured to be removable in response to a force applied to the gripping portion.

Abstract: Methods, computer program products, and systems are presented. The method computer program products, and systems can include, for instance: obtaining iteratively captured frames of image data representing a user interface screen, wherein one or more of the frames of image data represents an error screen indicating an error condition of one or more resource of a plurality of resources of a services system; performing recognition processing using image data of the captured frames of image data to determine an error classifier associated to the error screen: determining one or more action based on the error classifier; and performing the one or more action in response to the determining.

Abstract: Disclosed are novel branched amphiphilic lipids, in particular novel branched amphiphilic lipids of general formula (II). Also disclosed is a method of synthesis for the compounds of formula (II), from unsaturated amphiphilic compounds of general formula (I). Further disclosed is the use of the compounds of general formula (II) and of the lipoplexes obtained by formulation of the compounds of general formula (II) for applications, particularly transfection, in which improved fusion properties are desired.

Abstract: Methods, computer program products, and systems are presented. The method computer program products, and systems can include, for instance: obtaining iteratively captured frames of image data representing a user interface screen, wherein one or more of the frames of image data represents an error screen indicating an error condition of one or more resource of a plurality of resources of a services system; performing recognition processing using image data of the captured frames of image data to determine an error classifier associated to the error screen: determining one or more action based on the error classifier; and performing the one or more action in response to the determining.

Abstract: A system for delivering an implantable medical device to a treatment site within a patient includes an implantable medical device including a rigid body, and a delivery device. The delivery device includes an elongated catheter shaft and an expandable balloon connected to the elongated catheter shaft adjacent a distal end of the elongated catheter shaft, where the expandable balloon includes a proximal region, a distal region, and an implant retaining portion disposed between the proximal region and the distal region. The delivery device also includes a compression element connected to the implant retaining portion of the expandable balloon, where the compression element is adapted to limit expansion of the implant retaining portion of the expandable balloon when the expandable balloon is at least partially inflated. At least a portion of the compression element and the implant retaining portion are disposed within a lumen of the implantable medical device.

Abstract: A tubular sheath for enclosing an expandable balloon attached to the distal portion of a catheter encloses and protects the expandable balloon. The tubular sheath is configured to be slidable and removable from the catheter. The tubular sheath may include a longitudinal splitting element that is removable as a result of a force applied to the longitudinal splitting element. The longitudinal splitting element is configured to split the wall of the tubular sheath in response to the force. Alternatively, the tubular sheath may include a gripping portion that has relatively poor cohesive strength to adjacent portions of the tubular sheath. The tubular sheath is configured to be removable in response to a force applied to the gripping portion.

Abstract: Disclosed are novel branched amphiphilic lipids, in particular novel branched amphiphilic lipids of general formula (II). Also disclosed is a method of synthesis for the compounds of formula (II), from unsaturated amphiphilic compounds of general formula (I). Further disclosed is the use of the compounds of general formula (II) and of the lipoplexes obtained by formulation of the compounds of general formula (II) for applications, particularly transfection, in which improved fusion properties are desired.

Abstract: A storage cabinet includes a base fixedly attached to a wall and a frame coupled to the base. The frame includes a first side, a second side, and a cavity. The storage cabinet also includes a storage bin having a first side and a second side. The storage bin is removably positionable within the cavity such that the first side of the storage bin is retained within the cavity by a flange of the frame extending from the first side of the frame toward the second side of the frame, and the second side of the storage bin is adjacent the second side of the frame. The storage cabinet further includes a lock coupled to the base adjacent the second side of the frame. The lock selectively engages the second side of the storage bin to secure the storage bin in the cavity.

Abstract: A medical device includes an inflatable balloon defining an interior surface and an exterior surface, and a coating including a therapeutic agent disposed on the exterior surface of the inflatable balloon. The coating has a release transition temperature within a range from about 25° C. to about 50° C. When the temperature of the coating is below the release transition temperature, the coating retains at least a portion of the therapeutic agent on the exterior of the inflatable balloon. When the temperature of the coating is above the release transition temperature, the coating releases at least a portion of the therapeutic agent from the exterior of the inflatable balloon.

Abstract: A system for delivering an implantable medical device to a treatment site within a patient includes an implantable medical device including a rigid body, and a delivery device. The delivery device includes an elongated catheter shaft and an expandable balloon connected to the elongated catheter shaft adjacent a distal end of the elongated catheter shaft, where the expandable balloon includes a proximal region, a distal region, and an implant retaining portion disposed between the proximal region and the distal region. The delivery device also includes a compression element connected to the implant retaining portion of the expandable balloon, where the compression element is adapted to limit expansion of the implant retaining portion of the expandable balloon when the expandable balloon is at least partially inflated. At least a portion of the compression element and the implant retaining portion are disposed within a lumen of the implantable medical device.