An electrosurgical system including or connected to an output circuitry comprising an electrosurgical device and an electrical cable is modeled during a cable interrogation phase using a transfer matrix in order to determine a leakage capacitance in the electrosurgical system. After the leakage capacitance is assigned or set to a virtual capacitor in the transfer matrix, an output parameter of the electrosurgical system, such as output voltage, output current, output impedance or output electrical power, may be determined by applying an actual input voltage to the output circuitry and measuring a resulting input current, and multiplying the input voltage and measured current by the transfer matrix.

A surgical suturing system is disclosed. The surgical suturing system comprises a firing drive, an end effector, and a needle configured to be driven by said firing drive. The end effector comprises a track defined therein configured to guide the needle through a needle firing stroke. The surgical suturing system further comprises a needle driver configured to be driven by the firing drive and configured to drive the needle through the needle firing stroke.

Provided is a high frequency hyperthermia device which includes a main body (110) which includes a high frequency generator (114) which generates high frequency currents using drive power, a hand piece (120) which is connected to the main body (110) through a cable (140) and in which a handle (121) to be gripped by a user is disposed on an upper portion of the hand piece (120), and four or more contact electrodes (122), through which the high frequency currents being supplied are applied to skin (S) in contact with the contact electrodes (122) to generate deep heat in an internal body, are disposed on a lower surface of the hand piece (120), and an alternating switch (130) which is disposed between and connected to the high frequency generator (114) and the contact electrodes (122) in a circuit manner and which supplies the high frequency currents output from the high frequency generator (114) to the contact electrode (122), wherein the contact electrodes (122) are divided into pairs each having two contact electrodes (122), and the high frequency currents are alternately supplied to the pairs at a first speed.

Presented are an apparatus, method and electrosurgical device for surgical procedures. An exemplary apparatus includes a body comprising a longitudinal axis and an electrical wire maintained within the body extending along the longitudinal axis, and an electrode extending from a distal end of the body operably coupled to the electrical wire, the electrode with the electrical wire operable to conduct a flow of current at a plurality of levels. The apparatus further includes a first button arranged on an external surface of the body, the first button operable for selecting the flow of current at each one of the plurality of levels through the electrical wire and the electrode, and a second button arranged on the external surface of the body adjacent the first button, the second button operable activate and deactivate the flow of current to the electrode.

A method for controlling a user interface of a modular energy system. The modular energy system comprises a header module and a display screen on which the user interface is displayed. The modular energy system can detect attachment of a first module thereto, control the user interface to display one or more first user interface elements corresponding to the first module, detect attachment of a second module to the modular energy system, control the user interface to resize the one or more first user interface elements to accommodate display of one or more second user interface elements corresponding to the second module, and control the user interface to display the one or more second user interface elements. The various UI elements can correspond to the particular module type that is being connected to the modular energy system.

A medical device may include an elongated body, a balloon positioned at a distal portion of the elongated body, and one or more pressure-wave emitters positioned along a central longitudinal axis of the elongated body within the balloon. The one or more pressure-wave emitters may be configured to propagate pressure waves radially outward through the fluid to fragment a calcified lesion at the target treatment site. The at least one of the one or more pressure-wave emitters may include an electronic emitter comprising a first electrode and a second electrode. The first electrode and the second electrode may be arranged to define a spark gap between the first electrode and the second electrode, and the second electrode may comprise a portion of a hypotube.

An energy treatment device includes a sheath including a hollow portion, a fixed handle provided at a proximal end of the sheath, a probe provided in the hollow portion, a movable handle including a jaw having a recessed portion along a rotation axis of the movable handle extending in a direction orthogonal to the central axis, a metal member provided at a position including the rotation axis, and a preventing member which prevents the metal member from falling out from its position. The sheath extends along a central axis of the energy treatment device and includes an attaching portion by which the movable handle is attached to a position offset from the central axis, the metal member is provided around the rotation axis such that the jaw is rotatable with respect to the sheath, and the prevention member is fixed to the recessed portion.

Method and devices for delivering pulsed RF ablation energy to enable the creation of lesions in tissue are disclosed. The delivery of RF energy is controlled such that the generator power setting remains sufficiently high to form adequate lesions while mitigating against overheating of tissue. An ablation catheter tip having high-thermal-sensitivity comprises a thermally-insulative ablation tip insert supporting at least one temperature sensor and encapsulated, or essentially encapsulated, by a conductive shell. A system for delivering pulsed RF energy to a catheter during catheter ablation comprises an RF generator and a pulse control box operatively connected to the generator and configured to control delivery of pulsatile RF energy to an ablation catheter comprising at least one temperature sensor mounted in its tip. Also disclose is a method of controlling the temperature of an ablation catheter tip while creating a desired lesion using pulsatile delivery of RF energy.

A method for determining a switch-off time of a medical instrument includes measuring the duration for which the temperature of a tissue is above 85° Celsius, preferably above 95° Celsius, calculating, preferably online, the mean temperature from the first time when 85° Celsius, preferably 95° Celsius is reached, measuring and/or calculating the energy input until 85° Celsius, preferably 95° Celsius, and preferably below 110° Celsius, preferably below 100° Celsius is reached, calculating a parameter SP, which links the above mentioned results, and switches off at a predetermined value. The method can be practiced with a medical instrument as well as an application and a storage medium.

A method for measuring temperature includes emitting light with an illumination spectrum into a tissue with at least one illumination, receiving the remission of light with a remission spectrum from the tissue using at least one detector, converting the remission spectrum into a detector signal, sending the detector signal to a calculating unit, calculating a first theoretical remission spectrum based on a solution for describing the propagation of light in the tissue with the calculating unit, assuming estimated volume fractions of the individual tissue components, adapting the theoretical remission spectrum to the measured remission spectrum, and calculating at least one volume fraction of a tissue component from the remissions spectrum using a minimization algorithm, which is used by the calculating unit to adapt the theoretical remission spectrum to the measured remission spectrum using variations in the volume fractions of the individual tissue components which are present in the tissue.