A medical instrument sheath including an elongated hollow tube having a wall comprised of polymeric material; and at least one electrical lead embedded inside the wall, wherein the at least one electrical lead is configured to be connected with a respective electrode disposed in a member located inside the sheath and extending from a distal end of the sheath.

An arthroscopic tissue resecting probe includes an elongated shaft having outer and inner sleeves which are formed from an electrically conductive material extending about an axis to a working end. Outer and inner resecting windows are formed in the sleeves in the working end. The working end includes a ceramic body having a collar portion extending fully around a region of the outer sleeve proximal to outer resecting window. A radiofrequency (RF) electrode is disposed on an outer surface of the ceramic body and is spaced-apart from the outer resecting window.

A treatment tool includes: an insertion portion including a plurality of holes; a shaft that is arranged in the insertion portion; a plurality of needles that are connected to the shaft, each needle being configured to move between a first position and a second position; a plurality of first insulating materials, each insulating material being configured to cover the needle; and an energy supplier configured to supply electric power to the plurality of needles. The hole is configured to regulate a protruding direction of the needle to a direction intersecting with the longitudinal direction of the insertion portion. When an area that is positioned outside the insertion portion out of a whole area of the needle at the first position is sectioned into two areas that are a first area and a second area, the first insulating material is configured to cover the second area.

A catheter for focal cardiac ablation by irreversible electroporation includes a flexible catheter body, a plurality of tines disposed at a distal end of the catheter body, a flexible shaft, a return electrode, and an electrical conductor. The plurality of tines are formed of an electrically conductive material and configured to deploy from a lumen at the distal end of the catheter body. Each tine of the plurality of tines is configured to self-bias from a linear configuration within the lumen to a curved configuration when deployed from the lumen. The shaft is mechanically and electrically coupled to the plurality of tines. The shaft is configured to deploy the tines from the lumen when the shaft is moved toward the distal end of the catheter body. The return electrode is disposed on an outer surface of the catheter body. The electrical conductor is electrically coupled to the return electrode.

A catheter-based device tracks over a guidewire which has been placed from a first blood vessel into a second blood vessel. The distal tip of the catheter is advanced into the second vessel while a proximal member remains in the first vessel. Matching blunt tapered surfaces on each of the distal tip and the proximal member are clamped together, with adjacent walls of each vessel between them, after which a known, controlled pressure is applied between the two surfaces. Heat energy is then applied to the blunt surfaces for approximately 1-30 seconds to weld the walls of the two vessels together. After coaptation of the vessel walls, the heat is increased to then cut through the vessel walls to create a fistula of the desired size.

An electrosurgical forceps includes first and second shaft members each having a jaw member disposed at a distal end thereof and configured to rotate about a pivot to move the jaw members between an open position and a closed position, the first and second shaft members defining a longitudinal axis therebetween. A nerve monitoring probe is operably associated with one of the shaft members and is selectively movable relative to the longitudinal axis between a first, at rest position wherein the nerve monitoring probe is aligned with the longitudinal axis and a second, deployed position wherein the nerve monitoring probe is positioned at an angle relative to the longitudinal axis for nerve monitoring.

A method of applying RF energy includes using an RF energy applicator assembly to apply RF energy to a tissue. The RF energy applicator assembly includes a housing, and RF electrodes coupled to an RF energy source and movably mounted in the housing. The RF electrodes have a retracted position, in which the RF electrodes are retracted inside the housing, and deployed positions in which the RF electrodes protrude out of the housing at different protrusion lengths. An actuator is coupled to the RF electrodes and configured to move the RF electrodes from the retracted position to any one of the deployed positions.

An electrosurgical device is disclosed. The electrosurgical device includes a cartridge configured to be disposed within an elongate channel of an end effector. The cartridge includes an electrode having a plurality of electrode portions disposed along a longitudinal axis of the cartridge. The electrode is configured to electrically couple to a generator. Each electrode portion of the plurality of electrode portions is configured to deliver an amount of energy to a tissue placed proximate thereto. An amount of energy delivered by a first electrode portion of the plurality of electrode portions differs from an amount of energy delivered by a second electrode portion of the plurality of electrode portions.

An arthroscopic tissue resecting probe includes an elongated shaft having outer and inner sleeves which are formed from an electrically conductive material extending about an axis to a working end. Outer and inner resecting windows are formed in the sleeves in the working end. The working end includes a ceramic body having a collar portion extending fully around a region of the outer sleeve proximal to outer resecting window. A radiofrequency (RF) electrode is disposed on an outer surface of the ceramic body and is spaced-apart from the outer resecting window.

The present disclosure is directed towards a medical instrument. The medical instrument includes a housing and an end effector assembly operably connected to the housing. The end effector assembly includes first and second jaw members each having a tissue contacting surface, at least one of the first and second jaw members movable between a first, spaced-apart position and a second proximate position, wherein in the second position, the jaw members cooperate to define a cavity configured to receive tissue between the jaw members. The end effector also includes at least one light-emitting element coupled to at least one of the first and second jaw members, the at least one light-emitting element adapted to deliver light energy to tissue grasped between the first and second jaw members to treat the tissue.