Abstract: An electrophysiology catheter includes a balloon that may be expanded with an irrigation liquid, and that can have the irrigation liquid removed more quickly therefrom than other catheter balloons having a similar volume and without damaging electrical componentry disposed on the balloon. The catheter includes a shaft assembly comprising a shaft-assembly lumen, a choke lumen, and ports that connect the shaft-assembly lumen to an interior of the balloon. A guidewire may be disposed in the choke lumen to divert irrigation liquid into the balloon via the ports, which expands the balloon. Upon removal of the guidewire from the choke lumen, irrigation liquid can exit the balloon through the ports and then exit the catheter via its distal tip.

Abstract: A medical device includes a sensor to observe a characteristic of an anatomy, and a sensor base coupled to the sensor. The medical device includes a coupling system to couple the sensor base to the anatomy. The coupling system includes a first adhesive member and a second adhesive member. The first adhesive member is coupled to the sensor base and the second adhesive member is to couple to the anatomy. The second adhesive member includes at least one cut-out to direct moisture to an ambient environment surrounding the medical device.

Abstract: A catheter balloon includes a membrane having a proximal end and a distal end. A plurality of substrates are bonded about the membrane. The ability of a bond's ability to withstand repeated stresses during use may be improved by using a reinforcement or a stress relief, while also minimizing the overall thickness of the balloon proximate to its distal end. The reinforcement may comprise a portion of an unassembled membrane. Alternatively, the reinforcement may comprise an adhesive-margin tip. The stress relief may be a serpentine portion of a distal tail of a substrate.

Abstract: A medical device includes a sensor to observe a characteristic of an anatomy, and a sensor base coupled to the sensor. The medical device includes a coupling system to couple the sensor base to the anatomy. The coupling system includes a first adhesive member and a second adhesive member. The first adhesive member is coupled to the sensor base and the second adhesive member is to couple to the anatomy. The second adhesive member includes at least one cut-out to direct moisture to an ambient environment surrounding the medical device.

Abstract: A catheter having an end effector with multiple spines forming a basket shape is disclosed herein. The end effector can include spine loops with overlapping extensions at a distal end of the end effector. The end effector can include one or more inflatable members that are deflated during delivery and inflate to prevent the distal end of the basket assembly from contacting tissue. The end effector can include a spine hub at a distal end of the basket assembly with spine loops that extend through openings of the spine hub. The end effector can include a spiral inductor at the distal end of the basket assembly. The end effector can include an atraumatic structure over a distal end of a frame of the basket assembly.

Abstract: The disclosed technology includes an expandable spine including a connecting portion that includes a first slit facing an interior space formed by the expandable spine when the expandable spine is in an expanded state, a first electrode attached to the expandable spine and disposed at a distal end of the first slit. a second electrode attached to the expandable spine and disposed proximal to the first electrode and at a proximal end of the first slit, and a wire configured to electrically connect the first and second electrodes and configured to be positioned within the first slit when the expandable spine is in a collapsed state and be positioned outside of the first slit such that the wire travels in a more direct path compared to the path of the connecting portion the first and second electrodes when in the expanded state.

Abstract: The disclosed technology includes a medical probe including a tubular shaft and an end effector. The tubular shaft can define a longitudinal axis and have a tubular shaft end. The end effector can be coupled to the tubular shaft end. The end effector can include a crown. The end effector can include at least one spine that extends along the longitudinal axis. The at least one spine can include a deployed position and delivery position relative to the longitudinal axis. The at least one spine can include a first material. The end effector can include at least one hinge coupling the at least one spine to the crown. The at least one hinge can include a second material different from the first material.

Abstract: An end effector of a medical probe, the end effector including a plurality of elongated support members extending along a longitudinal axis of the end effector and the plurality of elongated support members configured to expand from the longitudinal axis. Each of the plurality of elongated support members includes an electrode landing region. The electrode landing region of each of the plurality of elongated support members includes a first surface facing away from the longitudinal axis and at least one extension extending from the first surface and curving toward the longitudinal axis. The first surface of the electrode landing region includes an electrode coupled to the first surface.

Abstract: A catheter balloon includes a membrane having a proximal end and a distal end. A plurality of substrates are bonded about the membrane. The ability of a bond's ability to withstand repeated stresses during use may be improved by using a reinforcement or a stress relief, while also minimizing the overall thickness of the balloon proximate to its distal end. The reinforcement may comprise a portion of an unassembled membrane. Alternatively, the reinforcement may comprise an adhesive-margin tip. The stress relief may be a serpentine portion of a distal tail of a substrate.

Abstract: A medical device includes a sensor to observe a characteristic of an anatomy, and a sensor base coupled to the sensor. The medical device includes a coupling system to couple the sensor base to the anatomy. The coupling system includes a first adhesive member and a second adhesive member. The first adhesive member is coupled to the sensor base and the second adhesive member is to couple to the anatomy. The first adhesive member includes at least one cut-out to direct moisture to an ambient environment surrounding the medical device.

Abstract: The disclosed technology includes an expandable basket assembly of a medical probe that includes (i) a plurality of spines connected to the distal end of the hub and extending along the longitudinal axis and configured to bow radially outward from the longitudinal axis when the expandable basket assembly is transitioned from a collapsed form to an expanded form, (ii) a plurality of electrodes, each electrode of the plurality of electrodes may be attached to a spine of the plurality of spines, (iii) one or more struts respectively attached to at least one of the plurality of electrodes, and (iv) a force sensor attached to the distal end of the hub and at least one of the plurality of struts. The force sensor may be configured to detect a force applied to one or more of the plurality of electrodes via the one or more struts.

Abstract: The disclosed technology includes a medical end effector comprising one or more spines extending along a longitudinal axis. The spines further comprising a first surface being outward from the longitudinal axis; one or more contact pads affixed to a portion of the first surface of the spine; and one or more flexible circuits disposed over respective ones of the one or more contact pads, the one or more flexible circuits each comprising an electrode and an inductive coil as one unit.

Abstract: The disclosed technology includes a fluid evacuation device for a balloon catheter including at least one spine having a curved proximal portion and a straight distal portion extending along a longitudinal axis, a first coupler coupled to the curved proximal portion of the spine to constrain at least one spine to move along the longitudinal axis, and a second coupler attached to the distal portion of the at least one spine so that in a first operational mode, the curved proximal portion of the at least one spine is expanded to a first outer profile and in a second operational mode, the curved proximal portion of the at least one spine is compressed to a smaller outer profile than the first outer profile such that the at least one spine moves the second coupler along the longitudinal axis.

Abstract: A medical device includes a sensor to observe a characteristic of an anatomy, and a sensor base coupled to the sensor. The medical device includes a coupling system to couple the sensor base to the anatomy. The coupling system includes a first adhesive member and a second adhesive member. The first adhesive member is coupled to the sensor base and the second adhesive member is to couple to the anatomy. The first adhesive member includes at least one cut-out to direct moisture to an ambient environment surrounding the medical device.

Abstract: A system for a physiological characteristic sensor deployed with a sensor inserter includes an adhesive skin patch coupled to the physiological characteristic sensor. The adhesive patch is to couple the physiological characteristic sensor to an anatomy. The system also includes a gravity resistance system coupled to the adhesive patch and to be coupled to the sensor inserter. The gravity resistance system maintains the adhesive patch substantially perpendicular to a longitudinal axis of the sensor inserter prior to deployment of the physiological characteristic sensor and is removable from the adhesive patch by the sensor inserter upon deployment of the physiological characteristic sensor.

Abstract: A system for a physiological characteristic sensor deployed with a sensor inserter includes an adhesive skin patch coupled to the physiological characteristic sensor. The adhesive patch is to couple the physiological characteristic sensor to an anatomy. The system also includes a gravity resistance system coupled to the adhesive patch and to be coupled to the sensor inserter. The gravity resistance system maintains the adhesive patch substantially perpendicular to a longitudinal axis of the sensor inserter prior to deployment of the physiological characteristic sensor and is removable from the adhesive patch by the sensor inserter upon deployment of the physiological characteristic sensor.

Abstract: The disclosed technology includes couplers, nose pieces, and strain relief hubs for ablation catheter assemblies and methods of using the same. The disclosed technology can include a medical probe having a coupler having a first portion, a second portion, and a vent port. The second portion can slide between a first position and a second position. When in the first position, the vent port can be at least partially obstructed by the first portion and, when in the second position, the vent port can be unobstructed by the first portion. The medical probe can include a nose piece having an outer diameter of less than 0.14 inches and an aperture extending therethrough. The aperture can be sized to receive a catheter. The medical probe can include a strain relief hub having a first portion and a second portion and configured to be coupled to a handle of the medical probe.

Abstract: Flexible circuit strips of a catheter balloon may comprise a substrate and a contact electrode disposed on the substrate. A cover may be disposed over a peripheral portion of the contact electrode and an adjacent portion of the substrate The cover is intended to increase robustness of the contact electrode in response to fatigue that might arise from repeated expansion and contraction of the catheter balloon.

Abstract: A catheter balloon comprises an ellipsoidal membrane. A plurality of flexible circuit strips, each of which comprises a substrate and a contact electrode, are disposed about the membrane. A coating is disposed atop at least the outer surface of the membrane and may also be disposed atop a portion of each of the substrates. The coating may comprise a dielectric material, such as parylene. The coating may increase the smoothness of the balloon. When subject to internal pressures that expand the balloon, the coating may also increase the resilience of the balloon relative to a balloon that lacks the coating as determined by changes in the balloon's diameter before and after expansion.

Abstract: A catheter balloon includes a membrane having a proximal end and a distal end. A plurality of substrates are bonded about the membrane. The ability of a bond's ability to withstand repeated stresses during use may be improved by using a reinforcement or a stress relief, while also minimizing the overall thickness of the balloon proximate to its distal end. The reinforcement may comprise a portion of an unassembled membrane. Alternatively, the reinforcement may comprise an adhesive-margin tip. The stress relief may be a serpentine portion of a distal tail of a substrate.