Abstract: A traction battery pack venting assembly includes an enclosure, at least one cell stack within the enclosure, a cross-member assembly within the enclosure, and a valve assembly that opens to provide a vent path from the at least one cell stack to a passageway of the cross-member assembly. A method of establishing a vent path within a traction battery pack includes, within a battery pack enclosure, using a valve assembly to block an opening to a passageway provided by a cross-member assembly; and in response to at least one battery cell within the battery pack enclosure venting, opening the valve assembly to permit flow through the opening to the passageway.

Abstract: A remote monitoring system for monitoring inventory, process, and product life-cycle data is disclosed. Data may be collected from the remote monitoring system. The data can include information on raw material components, source information, production or storage location and movement, production or storage temperature, production or storage barometric pressure, packaging, distribution, sales, or combinations thereof.

Abstract: Systems and methods for remotely monitoring liquids that are stored in containers are provided. Various aspects of the liquid can be monitored, such as volume level, pressure level, and temperature. Liquid monitoring systems can be installed into each container, with each liquid monitoring system collecting information and wirelessly providing it to a centralized monitoring system.

Abstract: Various aspects of the present disclosure are directed toward methods, apparatuses, and systems that include an implantable medical device comprising an implantable lead, a suture sleeve having an interior surface defining a lumen of the suture sleeve that receives the implantable lead, and an engagement feature configured to non-removeably secure the suture sleeve to the implantable lead.

Abstract: Apparatus and associated methods relate to a marker-buoy deployment system having a launching module that becomes armed by inserting a marker buoy, then laterally launches a loaded marker buoy in response to a user command. In an illustrative embodiment, launching module may be spring operated. In some embodiments, the release device may be foot operated. In an exemplary embodiment, a safety device may prevent an accidental launch, for example, from a trailered boat. In some embodiments, a visual indicator may indicate whether the safety is on, or the buoy has been loaded or launched. In some embodiments, a deployed-buoy location system may record the location coordinates of one or more deployed marker buoys. In an exemplary embodiment, marker buoys may be loaded automatically from a magazine each time a marker buoy is deployed. In some embodiments, marker-buoys may advantageously be deployed by a boater whose hands are otherwise occupied.

Abstract: Various aspects of the present disclosure are directed toward methods, apparatuses, and systems that include an implantable medical device comprising an implantable lead, a suture sleeve having an interior surface defining a lumen of the suture sleeve that receives the implantable lead, and an engagement feature configured to non-removeably secure the suture sleeve to the implantable lead.

Abstract: Described is a guide catheter for guiding other medical devices into or through a body lumen, comprising: a polymeric, tubular inner liner having a textured inner surface; and, a polymeric jacket bonded to an exterior of the inner liner; wherein the texture of the inner surface of the inner liner reduces the coefficient of friction between the inner liner and the other medical devices.

Abstract: Apparatus and associated methods relate to a marker-buoy deployment system having a launching module that becomes armed by inserting a marker buoy, then laterally launches a loaded marker buoy in response to a user command. In an illustrative embodiment, launching module may be spring operated. In some embodiments, the release device may be foot operated. In an exemplary embodiment, a safety device may prevent an accidental launch, for example, from a trailered boat. In some embodiments, a visual indicator may indicate whether the safety is on, or the buoy has been loaded or launched. In some embodiments, a deployed-buoy location system may record the location coordinates of one or more deployed marker buoys. In an exemplary embodiment, marker buoys may be loaded automatically from a magazine each time a marker buoy is deployed. In some embodiments, marker-buoys may advantageously be deployed by a boater whose hands are otherwise occupied.

Abstract: A method of manufacturing a medical electrical lead includes molding a lead body pre-form, stringing an electrode onto the pre-form and overmolding the pre-form with a polymer to form a lead body portion. The pre-form has a proximal end, a distal end and at least one lumen extending between the proximal and distal ends. At least one asymmetric region of the pre-form has a transverse cross-section that has a non-circular outer dimension. The overmolding causes the asymmetric region to become substantially circular.

Abstract: Described is a guide catheter for guiding other medical devices into or through a body lumen, comprising: a polymeric, tubular inner liner having a textured inner surface; and, a polymeric jacket bonded to an exterior of the inner liner; wherein the texture of the inner surface of the inner liner reduces the coefficient of friction between the inner liner and the other medical devices.

Abstract: An implantable medical system for anchoring a medical lead implanted in a patient includes a medical lead, an anchoring device received coaxially over the medical lead, and at least one fastener secured circumferentially about the anchoring device to cause compression of the anchoring device on the medical lead. The anchoring device includes an elastomeric sleeve having a substantially elongate, hollow, and tubular body and a compression governor coaxially secured about the elastomeric sleeve. The compression governor is adapted to limit compressive forces exerted on the lead by the anchoring device at a predetermined limit and provides a visual indicator that the predetermined limit has been reached.

Abstract: An implanted medical system includes a medical lead, an anchoring device and at least one suture secured circumferentially about the anchoring device to cause compression of the anchoring device on the medical lead. In particular, the anchoring device is received coaxially over the medical lead and includes an elastomeric sleeve and a compression governor. The elastomeric sleeve has a substantially elongate, hollow, and tubular body. The compression governor is substantially more rigid than the elastomeric sleeve and is coaxially secured to the elastomeric sleeve. The compression governor defines an inner bore having an effective diameter and is adapted to limit compression at a pre-selected minimum effective diameter to limit compressive forces exerted on the lead by the anchoring device.

Abstract: An implantable lead comprises a lead body extending from a lead proximal end portion to a lead distal end portion. The lead body includes one or more longitudinally extending lumens. A conductor is received in, and extends along, a lumen. In varying examples, the implantable lead further comprises a tubular electrode co-axial with, and overlying portions of, the lead body. In one example, a lumen wall is sized and shaped to urge an electrically conductive interposer coupled with the conductor toward an inner surface of the electrode. In another example, a ring member is disposed within a lumen and the conductor is drawn and coupled thereto. In yet another example, an electrically conductive connector couples a first and a second conductor via grooves or threads. In a further example, an axial support member couples a distal end electrode and the lead body. Methods associated with the foregoing are also discussed.

Abstract: A method of manufacturing a medical electrical lead includes molding a lead body pre-form, stringing an electrode onto the pre-form and overmolding the pre-form with a polymer to form a lead body portion. The pre-form has a proximal end, a distal end and at least one lumen extending between the proximal and distal ends. At least one asymmetric region of the pre-form has a transverse cross-section that has a non-circular outer dimension. The overmolding causes the asymmetric region to become substantially circular.

Abstract: An implantable lead comprises a lead body extending from a lead proximal end portion to a lead distal end portion. The lead body includes one or more longitudinally extending lumens. A conductor is received in, and extends along, a lumen. In varying examples, the implantable lead further comprises a tubular electrode co-axial with, and overlying portions of, the lead body. In one example, a lumen wall is sized and shaped to urge an electrically conductive interposer coupled with the conductor toward an inner surface of the electrode. In another example, a ring member is disposed within a lumen and the conductor is drawn and coupled thereto. In yet another example, an electrically conductive connector couples a first and a second conductor via grooves or threads. In a further example, an axial support member couples a distal end electrode and the lead body. Methods associated with the foregoing are also discussed.

Abstract: An implantable lead comprises a lead body extending from a lead proximal end portion to a lead distal end portion. The lead body includes one or more longitudinally extending lumens. A conductor is received in, and extends along, a lumen. In varying examples, the implantable lead further comprises a tubular electrode co-axial with, and overlying portions of, the lead body. In one example, a lumen wall is sized and shaped to urge an electrically conductive interposer coupled with the conductor toward an inner surface of the electrode. In another example, a ring member is disposed within a lumen and the conductor is drawn and coupled thereto. In yet another example, an electrically conductive connector couples a first and a second conductor via grooves or threads. In a further example, an axial support member couples a distal end electrode and the lead body. Methods associated with the foregoing are also discussed.

Abstract: An implanted medical system includes a medical lead, an anchoring device and at least one suture secured circumferentially about the anchoring device to cause compression of the anchoring device on the medical lead. In particular, the anchoring device is received coaxially over the medical lead and includes an elastomeric sleeve and a compression governor. The elastomeric sleeve has a substantially elongate, hollow, and tubular body. The compression governor is substantially more rigid than the elastomeric sleeve and is coaxially secured to the elastomeric sleeve. The compression governor defines an inner bore having an effective diameter and is adapted to limit compression at a pre-selected minimum effective diameter to limit compressive forces exerted on the lead by the anchoring device.

Abstract: An implantable medical system for anchoring a medical lead implanted in a patient includes a medical lead, an anchoring device received coaxially over the medical lead, and at least one fastener secured circumferentially about the anchoring device to cause compression of the anchoring device on the medical lead. The anchoring device includes an elastomeric sleeve having a substantially elongate, hollow, and tubular body and a compression governor coaxially secured about the elastomeric sleeve. The compression governor is adapted to limit compressive forces exerted on the lead by the anchoring device at a predetermined limit and provides a visual indicator that the predetermined limit has been reached.

Abstract: An implantable lead comprises a lead body extending from a lead proximal end portion to a lead distal end portion. In one example, the lead body may comprise a heat-formed bias portion. In another example, an outer insulator is fused to the lead body. In such an example, a lead body fusable plug may be disposed distal to at least one conductor. In another example, the lead comprises an inner boot and an outer boot fused to one another. In another example, the lead includes an atraumatic tip fused to the lead distal end portion. In another example, the lead body is reducable in size using heat shrink tubing. In yet another example, two or more lead sections may be interconnected using an outer insulator fused to the respective lead bodies. In a further example, a stiffener member is fused to the lead body adjacent a lead component.

Abstract: An implantable lead comprises a lead body extending from a lead proximal end portion to a lead distal end portion. The lead body includes one or more longitudinally extending lumens. A conductor is received in, and extends along, a lumen. In varying examples, the implantable lead further comprises a tubular electrode co-axial with, and overlying portions of, the lead body. In one example, a lumen wall is sized and shaped to urge an electrically conductive interposer coupled with the conductor toward an inner surface of the electrode. In another example, a ring member is disposed within a lumen and the conductor is drawn and coupled thereto. In yet another example, an electrically conductive connector couples a first and a second conductor via grooves or threads. In a further example, an axial support member couples a distal end electrode and the lead body. Methods associated with the foregoing are also discussed.