An apparatus and method for sending test signals to an instrument, and checking the resultant and subsequently arriving echo signals in order to detect specific properties and changes of properties on the line, the instrument, the tissue or also on a fluid body, e.g., plasma body, present on an electrode of the instrument, and to control the operation of the supply arrangement accordingly.

A power supply device for a high frequency treatment instrument includes an active side detection circuit that acquires a first signal output from a treatment instrument-connecting terminal to the treatment instrument and a second signal returned from the treatment instrument to the treatment instrument-connecting terminal, a passive side detection circuit that acquires a third signal output from the treatment instrument-connecting terminal to the treatment instrument and passing through a return electrode to a return electrode-connecting terminal, and a processor that calculates a return loss as the second signal to the first signal and a first insertion loss as the third signal to the first signal and determines an abnormality occurrence location based thereon.

An injectate delivery device for expanding tissue is provided. The injectate delivery device comprises: at least one fluid delivery tube comprising a proximal end, a distal end and a lumen therebetween; at least one fluid delivery element in fluid communication with the at least one fluid delivery tube lumen; a radially expanding element comprising the at least one fluid delivery element; a supply of vacuum constructed and arranged to cause tissue to tend toward the at least one fluid delivery element; and at least one control constructed and arranged to perform a function. The at least one control can be constructed and arranged to expand the radially expandable element and activate the supply of vacuum. Systems and method of injectate delivery are also provided.

A surgical instrument includes a body extending along a longitudinal axis between opposite proximal and distal end surfaces. The distal end surface includes a first cavity and a second cavity. The first cavity includes a first light bulb disposed therein. The second cavity includes a second light bulb disposed therein. A shaft includes opposite proximal and distal ends. The proximal end is coupled to the body. A blade is coupled to the distal end. The first light bulb is an ultraviolet (UV) light bulb and the second light bulb is configured to emit visible light. Systems and methods of use are disclosed.

An electrosurgical device: (a) power cable comprising: (i) a primary lead that connects to a first pole of an AC power source and (ii) one or more auxiliary leads; wherein the power cable includes a dual core having the primary lead on a first side and the one or more auxiliary leads on a second side with a web being located between the first side and the second side.

A device for radio frequency (RF) skin treatment of skin of a user is provided. The device comprises an active electrode and a return electrode. The device further comprises an RF generator arranged to supply RF energy to the user's skin via the active electrode and the return electrode. The return electrode has a planar skin contact surface extending in a main plane. The active electrode has a skin contact surface with a maximum dimension in a range from 100 μm to 500 μm, and a surface area of the planar skin contact surface of the return electrode is at least 5 times larger than a surface area of the skin contact surface of the active electrode. The skin contact surface of the active electrode is arranged in a position at a distance from the main plane, seen in a direction perpendicular to the main plane. The device may be advantageously used, for example, to control the dimensions and shape of a thermal lesion in the user's skin generated by the RF energy.

In an example, an electrosurgical generator includes a power converter configured to convert a supply power received from a power source to an output power. The output power is suitable for delivering electrosurgical energy. The electrosurgical generator also includes a current sensor configured to sense a current of the output power and generate a logarithmic and analog representation of the current, and a voltage sensor configured to sense a voltage of the output power and generate a logarithmic and analog representation of the voltage. The electrosurgical generator further includes a controller configured to: (i) receive the logarithmic and analog representation of the current sensed by the current sensor, (ii) receive the logarithmic and analog representation of the voltage sensed by the voltage sensor, and (iii) adjust, based on the logarithmic and analog representation of the current and the voltage, a voltage

A flexible catheter has an ablation electrode disposed in its distal segment. The ablation electrode a cavity formed in its external surface, a microelectrode configured to fit into the cavity, a conductive wire lead connecting the microelectrode to receiving circuitry, and an electrical shield surrounding the wire lead. A power generator is connected to the ablation electrode and the electrical shield in a generator circuit. A back patch electrode adapted to contact with the subject is connected in the generator circuit. The microelectrodes can be active while energizing the ablation electrode.

Devices, systems and methods are provided for treating conditions of the heart, particularly the occurrence of arrhythmias. The devices, systems and methods deliver therapeutic energy to portions the heart to provide tissue modification, such as to the entrances to the pulmonary veins in the treatment of atrial fibrillation. Generally, the tissue modification systems include a specialized catheter, a high voltage waveform generator and at least one distinct energy delivery algorithm. Other embodiments include conventional ablation catheters and system components to enable use with a high voltage waveform generator. Example catheter designs include a variety of delivery types including focal delivery, “one-shot” delivery and various possible combinations. In some embodiments, energy is delivered in a monopolar fashion. However, it may be appreciated that a variety of other embodiments are also provided.

Embodiments described herein provide various examples of mitigating electrical burn risks when using a monopolar electrosurgery tool on a patient in an electrosurgery procedure. In one aspect, a process receives an electrode configuration of the monopolar electrosurgery tool which includes a location of an active electrode of the monopolar electrosurgery tool at a surgical site on the patient's body and a location of a return electrode of the monopolar electrosurgery tool elsewhere on the patient's body. The process further obtains information of a metal implant inside the patient's body. Next, the process computes a plurality of potential current paths between the locations of the active electrode and the return electrode. The process then determines if one or more current paths in the plurality of computed potential current paths flow through the metal implant. If so, the process informs a surgical staff of potential electrical burn injuries associated with the electrode configuration.