Abstract: A die-to-die serial data link may be dynamically configured to exclude lanes associated with data errors. In a test mode, data may be transmitted from a first die to a second die over lanes of the link. In the second die, data received on the link in the test mode may be compared with an expected data pattern to detect any bit mismatches. When there are no more than a threshold number of mismatched bits, a receive path in the second die may be configured to use all of the lanes. When there are more than the threshold number of mismatched bits, a sub-group of the lanes that are not associated with mismatched bits may be determined, and the receive path in the second die may be configured to use the sub-group of lanes. In the first die, a transmit path may be configured to use the sub-group of lanes.

Abstract: Techniques for analyzing audiovisual content, such as streaming content are disclosed. In one embodiment, a method is disclosed comprising obtaining a frame of audiovisual content, using a video decoder to decode compressed model weights of at least one trained model, using the at least one trained model with the decoded weights to analyze the frame and extract content based on the analysis, using the extracted content to make a determination that the audiovisual content comprises a category of content, and causing actionable information to be transmitted to a client device of a user in response to the determination that the audiovisual content comprises the category of content.

Abstract: A medical device includes a handle including a first slot, a first control device movable within the first slot in a proximal direction and a distal direction, and a sheath extending from the handle and having a longitudinal axis, the sheath defining a first lumen extending from the handle to a distal end of the sheath. A first tube extends within the first lumen, the first tube is connected to the first control device and moves between a first position, where a distalmost end of the first tube is flush with or proximal of a distalmost end of the sheath, and a second position, where the distalmost end of the first tube is positioned distal of the distalmost end of the sheath. The first slot extends parallel to the longitudinal direction of the sheath.

Abstract: A medical device includes a handle, a shaft extending from the handle, and an articulation member integral with or attached to a distal end of the shaft. The articulation member includes a first portion coupled to a second portion, the second portion is receivable in a slot defined by the first portion, and the handle is coupled to each of the first portion and the second portion and to articulate the first portion independently of articulating the second portion.

Abstract: A medical device that includes a handle, a shaft extending distally from the handle, an end effector extending distally from the shaft, a first actuator movably coupled to the handle, and a second actuator movably coupled to the handle. The first actuator is configured to (1) articulate the shaft in response to translating the first actuator in a first direction relative to the handle and the second actuator, and (2) actuate the end effector in response to translating the first actuator in a second direction relative to the handle and the second actuator. The second actuator is configured to (1) articulate the shaft in response to translating the second actuator in the first direction relative to the handle and the first actuator, and (2) actuate the end effector in response to translating the second actuator in the second direction relative to the handle and the first actuator.

Abstract: A method performed by a storage device for reducing latency of read operations performed on the storage device, includes: transmitting Host Memory Buffer (HMB) destination information to a host device. The HMB destination information relates to a read destination space reserved within a HMB of the host device. The method also includes receiving a read request from the host device for performing at least one data read operation on a memory of the storage device. The read request specifies data to be read from the memory of the storage device. The method further includes: performing the at least one data read operation on the memory for reading the data specified in the read request and transmitting the data read from the memory to the read destination space reserved within the HMB of the host device.

Abstract: In described examples, a test control circuit includes a subsystem and a transition control circuit. The subsystem outputs test signals to, and receives and measures response signals of, a device under test (DUT). The transition control circuit operates the test control circuit in response to a first operational state information indicating a first mode and a first set of configuration settings; receives a Transition Trigger signal and a second operational state information indicating a second mode and a second set of configuration settings; and, by performing allowed mode changes and in response to receiving the Transition Trigger signal, transitions the test control circuit to operating in response to the second operational state information. Allowed mode changes are restricted to: from a DUT driving mode to a DUT non-driving mode, from a DUT non-driving mode to another DUT non-driving mode, or from a DUT non-driving mode to a DUT driving mode.

Abstract: A biopsy forceps device includes a control member; a yoke coupled to the member; jaws coupled to the yoke; and a capsule. In an open configuration, the jaws are separated to receive target tissue. In a closed configuration, cutting edges of the jaws are moved toward one another to cut tissue. The capsule slidably receives the yoke and a portion of the jaws. The jaws are constrained to the closed configuration when withdrawn proximally to a first position within the capsule. When the jaws are moved to a second position, portions of the jaws are freed from the constraint capsule and spread apart. When the yoke and the jaws are moved distally and the jaws move to the open configuration, a tissue contacting structure of the yoke extends distally to engage tissue between the jaws to anchor the engaged tissue again lateral movement as the jaws contact the tissue.

Abstract: A delivery device comprises a tube having a proximal end, a distal end, and a lumen extending from the proximal to the distal end. The proximal end is mountable to a distal tip of a medical device via the lumen. The tube includes an inner wall defining the lumen, an outer wall coupled to the inner wall at the proximal and distal ends, a cavity formed from the coupled inner and outer walls and configured to hold a deliverable substance, and a plurality of openings connected to the cavity and positioned on a distal-facing surface of the distal end. At least a portion of the inner wall or the outer wall is a flexible wall that transitions between a first and a second configuration to cause delivery of the deliverable substance from the cavity to a treatment site through the openings when a force is applied to the flexible wall.

Abstract: Various embodiments are directed to processing conversions of digital assets to other digital assets. An example method includes determining a source exchange rate for a source digital asset and a fiat currency, determining a target exchange rate for a target digital asset and a fiat currency, and generating an aggregated conversion rate for the source digital asset and the target digital asset using the source exchange rate and the target exchange rate. The method further includes executing a digital asset conversion, which includes causing source digital asset units to be debited from a source digital asset user account and causing target digital asset units to be credited to a target digital asset user account, and subsequently executing fiat currency transactions (e.g., settlements) with a first digital asset exchange system associated with the source digital asset and a second digital asset exchange system associated with the target digital asset.

Abstract: A circuit includes a digital-to-analog converter and a gain stage. The gain stage includes: an operational amplifier; a variable gain network; and a leakage current control circuit. A first input of the operational amplifier is coupled to an input of the gain stage. An output of the operational amplifier is coupled to an output of the gain stage. A first terminal of the variable gain network is coupled to the second input of the operational amplifier. A second terminal of the variable gain network is coupled to the output of the operational amplifier. A first terminal of the leakage current control circuit is coupled to the output of the operational amplifier. A second terminal of the leakage current control circuit coupled to a third terminal of the variable gain network.

Abstract: A method and system for securing an anonymous discovery service may include receiving a request from a client device, the request being directed to an anonymous Autodiscover service, identifying a source from which the request originated from within the client device, and responsive to the source being of a first type of sources, transmitting a first response to the client and responsive to the source being of a second type of sources transmitting a second response to the client. The first response does not return a Uniform Resource Locator (URL) to a service endpoint, the second response returns a URL to a service endpoint. Furthermore, the anonymous discovery service may be a discovery service that requires no authentication.

Abstract: A first system may receive first data of a user associated with a first identifier and second data of the user associated with a second identifier that exclude user identifying information from a first and second data source, respectively. A key may be received from a second system that associates the first and second identifier with a common identifier generated to preserve user anonymity at the first system. The key may be used to generate aggregated data for the user that includes the first and second data and is associated with the common identifier. The aggregated data may be processed to determine the user as a candidate for an offer set. The common identifier for the user is included in a candidacy list for the offer set, and provided to the second system to facilitate request processing associated with the presentation of the offer set to candidate users.

Abstract: A medical device, for example a delivery catheter, may include a handle portion, a shaft portion extending distally from the handle portion, a deployment mechanism, and an actuation member positioned on the handle portion. The shaft portion may include a working channel and a distal tip portion having a payload chamber configured to receive a payload, such as a bio-absorbable foam. The distal tip portion may be operatively connected to the working channel. The deployment mechanism may be positioned in the working channel, and may be operable to deploy the payload out from the distal tip portion. The actuation member may be actuatable to operate the deployment mechanism.

Abstract: A medical device may include a handle including a fixed body and a movable body. The movable body may be movable relative to the fixed body. The medical device may include a shaft extending from the fixed body and an end effector at a distal end of the shaft. Rotation of the movable body relative to the fixed body may permit rotation of the end effector relative to the shaft, and rotation of the movable body with rotation of the fixed body may permit rotation of the end effector with the shaft. Deflection of the movable body relative to the fixed body may permit deflection of the end effector relative to the fixed body.

Abstract: An example system includes a turbine comprising an input port and mechanically coupled to a motor-generator and a compressor and control circuitry configured to determine whether a pressure of a fluid at the input port of the turbine is less than or equal to than a threshold pressure. In response to determining that the pressure of the fluid at the input port of the turbine is less than or equal to the threshold pressure, the control circuitry is configured to cause the motor-generator to operate in motor mode. The motor-generator is configured to be mechanically coupled to the compressor, and the motor-generator is configured to provide mechanical energy to drive the compressor when operating in motor mode.

Abstract: A medical device that includes a handle including a plurality of actuators. The handle defines a longitudinal axis extending through a distal end of the handle. The device includes a shaft extending from the handle and an end effector at a distal end of the shaft. A first actuator of the plurality of actuators is configured to actuate the end effector in response to translation of the first actuator relative to the handle along an axis parallel to the longitudinal axis. A second actuator of the plurality of actuators is configured to deflect the end effector relative to the shaft in response to pivoting the second actuator about an axis transverse to the longitudinal axis. A third actuator of the plurality of actuators is configured to rotate the end effector relative to the shaft in response to rotation of the third actuator relative to the handle about the longitudinal axis.

Abstract: A medical device comprising a handle including a handle body and an actuator, and a shaft extending distally from the handle body, wherein the shaft comprises of a shape memory material, wherein the shaft includes a proximal section and a distal section, the proximal section having a first austenitic finish temperature and the distal section having a second austenitic finish temperature, and wherein the first austenitic finish temperature is lower than the second austenitic finish temperature.

Abstract: A medical device that includes a handle, a shaft extending distally from the handle, an end effector extending distally from the shaft, a first actuator movably coupled to the handle, and a second actuator movably coupled to the handle. The first actuator is configured to (1) articulate the shaft in response to translating the first actuator in a first direction relative to the handle and the second actuator, and (2) actuate the end effector in response to translating the first actuator in a second direction relative to the handle and the second actuator. The second actuator is configured to (1) articulate the shaft in response to translating the second actuator in the first direction relative to the handle and the first actuator, and (2) actuate the end effector in response to translating the second actuator in the second direction relative to the handle and the first actuator.

Abstract: A clipping system includes an adapter configured to be mounted over an insertion device and a clip including first and second jaws movable between an insertion configuration and an initial deployed configuration. A first extending member is releasably coupled to the clip and movably connected to the adapter to permit a movement of the clip relative to the adapter from the insertion configuration to the initial deployed configuration. The first extending member is configured to permit withdrawal of the adapter away from the clip to place the system in a review configuration to enhance a visual observation of the clip. The first extending member is operable to retract the clip over the adapter so that the clip is forced open, freeing the clip from tissue on which it has been clipped. The first extending member is configured to release the clip therefrom in a final deployed configuration.