Abstract: Embodiments disclosed herein are directed to an insertion tool (100) for a catheter. The insertion tool (100) engages a proximal end of an introducer (10) and includes a guide channel (106) that aligns with a lumen of the introducer (10). The guide channel (106) supports the catheter (50) to maintain columnar integrity as the catheter (50) is urged distally, past a valve and into the lumen of the introducer (10). In an embodiment, the attachment structure can be inserted past the valve to define a pathway for the catheter. Embodiments also include an elongate opening to allow lateral ingress/egress of the catheter, a segmented cylindrical shape to provide a shortened elongate opening, and an offset elongate opening to allow a rolling introduction of the catheter to the guide channel to prevent abrasion of any coatings disposed on the catheter.

Abstract: A cannulator (100) can include a compound needle (104) and a compound cannula (102). The compound needle can include a needle (110), a dilator (108), and a needle hub (106). The dilator can be disposed over the needle with at least a tip of the needle extending beyond a distal end of the dilator. The needle hub can be around a proximal-end portion of the dilator. The compound cannula can include a cannula (140) and a cannula hub (142) around a proximal- end portion of the cannula. The cannulator can have a mated state of the compound needle and the compound cannula for at least cannulation with the cannulator. The mated state of the cannulator can include the dilator disposed in the cannula with a proximal-end portion of the cannula hub coupled to a distal-end portion of the needle hub.

Abstract: An error reporting system utilizes a parity checker to receive data results from execution of an original instruction and a parity bit for the data. A decoder receives an error correcting code (ECC) for data resulting from execution of a shadow instruction of the original instruction, and data error correction is initiated on the original instruction result on condition of a mismatch between the parity bit and the original instruction result, and the decoder asserting a correctable error in the original instruction result.

Abstract: An error reporting system utilizes a parity checker to receive data results from execution of an original instruction and a parity bit for the data. A decoder receives an error correcting code (ECC) for data resulting from execution of a shadow instruction of the original instruction, and data error correction is initiated on the original instruction result on condition of a mismatch between the parity bit and the original instruction result, and the decoder asserting a correctable error in the original instruction result.

Abstract: A family of software-hardware cooperative mechanisms to accelerate intra-thread duplication leverage the register file error detection hardware to implicitly check the data from duplicate instructions, avoiding the overheads of instruction checking and enforcing low-latency error detection with strict error containment guarantees.

Abstract: A family of software-hardware cooperative mechanisms to accelerate intra-thread duplication leverage the register file error detection hardware to implicitly check the data from duplicate instructions, avoiding the overheads of instruction checking and enforcing low-latency error detection with strict error containment guarantees.

Abstract: An 8-transistor SRAM (static random access memory) storage cell provides differential read bit lines that are precharged to a low voltage level for read operations. The 8-transistor storage cell provides separate ports for read and write operations, including differential read bit lines. Prior to each read operation, the differential read bit lines are precharged to the low voltage level. During read operations, one of the two differential read bit lines is pulled high towards a high voltage level while the complementary bit line remains at the low voltage level resulting from the precharge. The difference in voltage between the differential read bit lines is sensed to determine the value stored in each 8-transistor SRAM storage cell and complete the read operation.

Abstract: An 8-transistor SRAM (static random access memory) storage cell provides differential read bit lines that are precharged to a low voltage level for read operations. The 8-transistor storage cell provides separate ports for read and write operations, including differential read bit lines. Prior to each read operation, the differential read bit lines are precharged to the low voltage level. During read operations, one of the two differential read bit lines is pulled high towards a high voltage level while the complementary bit line remains at the low voltage level resulting from the precharge. The difference in voltage between the differential read bit lines is sensed to determine the value stored in each 8-transistor SRAM storage cell and complete the read operation.

Abstract: Various embodiments of a site marker are disclosed that comprise a body portion and a marker element. The body portion is constructed of a bioabsorbable material and defines at least one cavity therein. The marker element is captured within one of the cavities. The marker element is constructed of a material that may be imaged under at least one imaging modality.

Abstract: A site marker deployment device includes a housing defining a first portion, an outer cannula at least partially interposed within the first portion and having a proximal end and a distal end defined by an outer cannula aperture, an inner member at least partially interposed within the outer cannula, a first biasing portion, a second biasing portion, wherein the second biasing portion will selectively urge the outer cannula to move proximally relative to the inner member, and a site marker selectively disposed within the outer cannula adjacent the inner member, near the distal end of the outer cannula. The first biasing portion will selectively urge a site marker at least partially within the outer cannula.

Abstract: A site marker delivery system is provided that may be used in combination with a tissue cutting device for marking a biopsy site. The system includes a tube attached to a hub. A push-rod is slidably disposed within the lumen of the tube. The push-rod is advanced forward through the lumen of the tube causing a marker seated within the tube to be deployed at a biopsy site.

Abstract: A biopsy marker deployment device adapted to selectively deposit a marker in a target location, such as a biopsy site. In one embodiment, the device includes a deployment assembly comprising a cannula adapted to house at least one marker, an outlet aperture defined by a portion of the cannula, and an actuatable pushrod slidably disposed and movable within the cannula. The deployment assembly further comprises a selectively opening outlet door movable between an open position and a closed position. The outlet door is biased in the closed position and at least partially obstructs the aperture in the closed position to prevent a marker from reentering the cannula upon deployment.

Abstract: A biopsy marker deployment device adapted to selectively deposit a marker in a target location, such as a biopsy site. In one embodiment, the device includes a deployment assembly comprising a cannula adapted to house at least one marker, an outlet aperture defined by a portion of the cannula, and an actuatable pushrod slidably disposed and movable within the cannula. The deployment assembly further comprises a selectively opening outlet door movable between an open position and a closed position. The outlet door is biased in the closed position and at least partially obstructs the aperture in the closed position to prevent a marker from reentering the cannula upon deployment.

Abstract: A biopsy marker deployment device is provided herein. According to one exemplary embodiment, the deployment device includes a deployment assembly and an actuator configured to selectively actuate the deployment assembly. The deployment assembly is configured to selectively deposit a marker in a biopsy site through at least one aperture and to substantially reduce space between the aperture and the deployment assembly.

Abstract: A medical system includes a first medical device having a first engaging portion and a first cannula extending therefrom, a second medical device having a second engaging portion and a second cannula extending therefrom, an introducer having an introducer cannula and an axial distance adjustment system for providing an adjustable length between the introducer cannula distal end and at least a portion of one of the first engaging portion and the second engaging portion. The adjustment system includes at least one spacer having a side opening for permitting the at least one spacer to be interposed between the introducer and at least one of the first medical device and the second medical device. At least one of the first cannula and the second cannula may be selectively interposed within the side opening when at least a portion of the at least one of the first cannula and the second cannula is at least partially interposed within the introducer cannula.

Abstract: A medical system includes a first medical device having a first medical device engaging end, an introducer including an introducer cannula having a proximal end and a distal end, and an axial distance adjustment system for providing an adjustable distance between at least a portion of the first medical device end and the introducer cannula distal end. The adjustment system includes an inner member and an outer member. One of the inner member and the outer member includes a first interference surface. The other of the inner member and the outer member includes a second interference surface and a third interference surface. The inner member is at least partially interposed within the outer member and selectively axially moveable therebetween. The inner member and the outer member are selectively restrained from axial movement therebetween when the first interference surface contacts one of the second interference surface and the third interference surface.

Abstract: A site marker deployment device includes a housing defining a first portion, an outer cannula at least partially interposed within the first portion and having a proximal end and a distal end defined by an outer cannula aperture, an inner member at least partially interposed within the outer cannula, a first biasing portion, a second biasing portion, wherein the second biasing portion will selectively urge the outer cannula to move proximally relative to the inner member, and a site marker selectively disposed within the outer cannula adjacent the inner member, near the distal end of the outer cannula. The first biasing portion will selectively urge a site marker at least partially within the outer cannula.

Abstract: A marker deployment system is provided, including at least one cannula, a site marker and at least one wire. The cannula has a tubular side-wall and a distal opening. The cannula defines at least one aperture extending through the side-wall. The wire is selectively interposed within the cannula, and a distal wire end extends through the aperture. A portion of the wire is secured to an end portion of the site marker. The wire is pulled taut at the aperture, thereby at least partially aligning the end portion of the site marker with the distal opening of the cannula.

Abstract: Various embodiments of a site marker are disclosed that comprise a body portion and a marker element. The body portion is constructed of a bioabsorbable material and defines at least one cavity therein. The marker element is captured within one of the cavities. The marker element is constructed of a material that may be imaged under at least one imaging modality.