A surgical instrument includes a housing, a shaft having a proximal end portion disposed within the housing, and an end effector assembly supported at a distal end portion of the shaft distally-spaced from the housing. A bobbin includes a body, a proximal rim, and a distal cylinder. The bobbin is disposed about the shaft such that at least one protrusion of the shaft is captured within a track defined within the distal cylinder. The bobbin is configured for positioning within the housing such that the body extends through a shaft aperture of a partition of the housing with the proximal rim disposed on a proximal side of the partition and the distal cylinder disposed within an interior cavity defined between the partition and a distal end of the housing on a distal side of the partition, thereby rotatably supporting the proximal end portion of the shaft within the housing.

Tumors in portions of a subject's body that have a longitudinal axis (e.g., the torso, head, and arm) can be treated with TTFields by affixing first and second sets of electrodes at respective positions that are longitudinally prior to and subsequent to a target region. An AC voltage with a frequency of 100-500 kHz is applied between these sets of electrodes. This imposes an AC electric field with field lines that run through the target region longitudinally. The field strength is at least 1 V/cm in at least a portion of the target region. In some embodiments, this approach is combined with the application of AC electric fields through the target region in a lateral direction (e.g., front to back and/or side to side) in order to apply AC electric fields with different orientations to the target region.

The electrosurgical instrument comprises a basic body configured as a hose or as a hollow rod on which an end piece is configured or into which an end piece is inserted. The end piece comprises a passage channel that comprises a narrowed section at its distal end. The electrode is held in a holder that comprises an extension surrounding the electrode. The extension is configured to extend through the narrowed section of passage channel up to the end surface such that it outcrops at the mouth opening of the narrowed section when the electrode is in the extended position. At this section of extension located at the mouth opening the electrode is connected with the extension.

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.

A catheter includes, a shaft for insertion into an organ, an expandable distal-end assembly coupled to the shaft and includes splines, at least one of the splines includes a flexible substrate, configured to conform to tissue of the organ, and a sensing electrode, configured: (a) to be coupled to the flexible substrate, and (b) when in contact with the tissue, to produce a electrically signal indicative of an electrocardiogram signal sensed in the tissue, the sensing electrode including: (i) a gold substrate, formed over the flexible substrate and configured to conduct the electrically signal, (ii) a first polymer layer, formed over a first section of the gold substrate and configured to electrically isolate between the tissue and the gold substrate, and (iii) a second polymer layer, formed over a second, different, section of the gold substrate, and configured to conduct the electrocardiogram signal between the tissue and the gold substrate.

An elongate medical device shaft may comprise an elongate body and an annular electrode disposed on the elongate body. The annular electrode may define a longitudinal axis and have an outer diameter. The outer diameter may be greater at an axial center of the electrode than at an axial end of the electrode. Additionally or alternatively, the elongate body may comprise three longitudinal sections having three wall thicknesses. The middle wall thickness may be less than the proximal and distal wall thicknesses and the distal wall thickness may be less than the proximal wall thickness. Additionally or alternatively, the shaft may comprise an inner cylindrical structure and an outer tube. The outer tube may comprise a first radial layer and a second radial layer that is radially-outward of the first radial layer, the first radial layer, second radial layer, and inner structure having different stiffnesses.

Example electrosurgical devices and systems are disclosed. An example electrosurgical device includes a body, an electrosurgical electrode secured to the body, the electrosurgical electrode including a distal tip. The electrosurgical device also includes a shroud translatable relative to the electrosurgical electrode between a first position and a second position, a first magnetic component which is operably connected to the body, and a second magnetic component which is operably connected to the shroud, wherein the first and second magnetic components magnetically interact to releasably maintain the shroud in the first position.

A medical device for cutting bone and soft tissue includes a shaft having a rotating component with a distal working end. A cutting member is carried on the working end of the rotating component and a motor rotates the rotating component. The cutting member has a ceramic body with cutting edges, and the ceramic body is formed of a ceramic composite including alumina and zirconia, wherein the alumina has a grain size ranging between 0.5-1.5 microns and the zirconia has a grain size ranging between 0.1-1.0 micron. The alumina grain shape and zirconia grain shape are non-elongated.

A controllable stiffness endoscope overtube includes an overtube shaft including an inner sheath defining an access lumen and an outer sheath surrounding the inner sheath from proximal to distal end of inner sheath to define an annulus therebetween having a proximal portion with a vacuum connection. The sheath distal ends are longitudinally fixed to one another and sized to receive an endoscope. The outer sheath has a constant outer diameter over at least a distal portion of the annulus proximate to the distal ends of the sheaths. A vacuum device is fluidically connected to the vacuum connection and applies vacuum to the annulus. Responsive thereto, annulus pressure is lowered, the sheaths are drawn together, and the overtube shaft is stiffened over at least the distal portion to stiffen and maintain a current shape of the overtube shaft over at least the distal portion of the annulus.

A hand piece for handling an optical fiber during a laser-surgical intervention comprises a handle body elongated along a main axis and having a through hole extending along the main axis. A guide tube having a tube lumen aligned and communicating with the through hole is attached to the handle body. A fixing device is provided in the handle body for fixing the optical fiber extending through the through hole and the tube lumen in direction of the main axis. The guide tube is made of a shaped memory alloy, which has a transition temperature between 50° C. and 120° C., and which has a straight base shape. Below the transition temperature, the guide tube is bendable by plastic deformation out of the straight base shape into a curved shape, and, when heated up above the transition temperature, the guide tube returns to its straight base shape.