A medical device includes an expansion body, an elongated shaft portion, and a plurality of electrode assemblies. The expansion body includes a recessed portion that is recessed radially inward. The recessed portion includes a radially innermost bottom portion including a proximal side curved portion and a distal side curved portion, a proximal side upright portion, and a distal side upright portion. Each of the plurality of electrode assemblies includes an electrode portion disposed along the expansion body from the proximal side upright portion or the distal side upright portion to the bottom portion so as to face a receiving space defined by the recessed portion. The proximal side curved portion and the distal side curved portion deform in response to expansion and contraction of the expansion body. The electrode portion is in a floating state with respect to the distal side curved portion and the proximal side curved portion.

A medical puncture device includes an elongate shaft having a proximal portion defining a proximal end and a distal portion defining a distal end. The distal portion tapers in outer diameter going towards the distal end to define a dilating tip. A lumen extends through the shaft from the proximal end to the distal end. The shaft includes a first electrical conductor that extends from the proximal portion to the distal portion and is electrically connectable to a radiofrequency generator. A radiofrequency puncture electrode is positioned proud of the distal end and is electrically connected to the first electrical conductor.

In one embodiment, a medical system includes a catheter configured to be inserted into a body part of a living subject, and including a deflectable element having a distal end, an expandable distal end assembly disposed at the distal end of the deflectable element, and comprising a plurality of electrodes, a distal portion, and a proximal portion, and configured to expand from a collapsed form to an expanded deployed form, and a stretchable irrigation tube disposed between the distal portion and the proximal portion, and comprising a plurality of irrigation holes, and configured to stretch longitudinally when the distal end assembly is collapsed from the expanded deployed form to the collapsed form.

Transducer-based systems can be configured to display a graphical representation of a transducer-based device, the graphical representation including graphical elements corresponding to transducers of the transducer-based device, and also including between graphical elements respectively associated with a set of the transducers and respectively associated with a region of space between the transducers of the transducer-based device. Selection of graphical elements and/or between graphical elements can cause activation of the set of transducers associated with the selected elements. Selection of a plurality of graphical elements and/or between graphical elements can cause visual display of a corresponding activation path in the graphical representation. Visual characteristics of graphical elements and between graphical elements can change based on an activation-status of the corresponding transducers. Activation requests for a set of transducers can be denied if it is determined that a transducer in the set of transducers is unacceptable for activation.

An integrated electrode structure can comprise a catheter shaft comprising a proximal end and a distal end, the catheter shaft defining a catheter shaft longitudinal axis. A flexible tip portion can be located adjacent to the distal end of the catheter shaft, the flexible tip portion comprising a flexible framework. A plurality of microelectrodes can be disposed on the flexible framework and can form a flexible array of microelectrodes adapted to conform to tissue. A plurality of conductive traces can be disposed on the flexible framework, each of the plurality of conductive traces can be electrically coupled with a respective one of the plurality of microelectrodes.

The devices and method described herein allow for therapeutic damage to increase volume in these hyperdynamic hearts to allow improved physiology and ventricular filling and to reduce diastolic filling pressure by making the ventricle less stiff.

A method for assembling a catheter is disclosed. The method includes printing conductive traces on at least one flexible substrate and encapsulating the at least one flexible substrate to provide for environmental protection. The at least one encapsulated flexible substrate is inserted into a shaft of a catheter. Then, connectors are attached to each end of the at least one encapsulated flexible substrate. One set of the connectors are further attached to sensors located at a distal end of the catheter and another set of the connectors are further attached to electronics in a handle of the catheter.

A system and method are provided for a navigational feedback to a catheter during an arrhythmia ablation procedure. A set of electrocardiogram (ECG) signals of a patient's arrhythmia is recorded that correspond to an unknown target location to be ablated by the catheter. During the ablation procedure, pacing locations and ECG signals corresponding to the pacing locations are collected to derive a mathematical operator that maps a 12-dimensional displacement vector in the ECG space to a 3-dimensional (3D) vector in a physical space. This 3D vector corresponds to a direction and a distance that the catheter needs to be moved in order to reach the target location of the arrhythmia.

Devices, systems, and methods of the present disclosure are directed to facilitating control of a graphical user interface associated with performing a medical procedure. Inputs can be received from a plurality of input devices interacting with respective sets of input options displayed on respective portions of the graphical user interface. One of the input devices can be operable by a physician, during a medical procedure, to navigate a set of input options to modify a graphical representation of at least one of a medical device and an anatomic structure displayed on the graphical user interface.

A partially-masked electrode includes a conductive material and an insulated coating having an outer surface. The insulated coating defines a contoured opening that exposes or reveals an area of the conductive material, wherein the contoured opening has an upper perimeter at the outer surface of the insulated coating. When the upper perimeter of the insulated surface coating is placed in contact with a tissue of interest, wherein the tissue of interest is proximate a blood pool, the insulated coating creates a seal between the blood pool and the contoured opening so that no blood in the blood pool can contact the conductive material. This seal reduces or eliminates the reception of far field effects in the blood pool by the electrode, making it easier to locate and diagnose unhealthy tissue.