The invention relates to a device for producing a cold atmospheric pressure plasma for the treatment of human and/or animal surfaces, comprising a flexible, planar multilayer system with a side facing the surface to be treated and a side facing away from the surface to be treated, wherein the multilayer system comprises the following layers, namely a first electrode layer on the facing away side of the multilayer system, second electrode layer on the facing side of the multilayer system, wherein the electrode layer has a plurality of recesses or is formed in a grid-like or meander-shaped fashion, a dielectric layer arranged between the first electrode layer and the second electrode layer, and a spacer layer arranged adjacent the second electrode layer on the facing side of the multilayer system. In addition, the invention relates to a cable, a generator unit for providing a high voltage, and a system.

The present disclosure is directed to devices, systems, and methods for sensing and discerning whether a distal portion of a fat grafting cannula or probe is disposed in fat tissue or muscle tissue during fat grafting procedures. In one aspect of the present disclosure, a fat grafting cannula or probe is provided including first and second electrodes. Each electrode is coupled to a circuit, e.g., disposed in an electrosurgical generator. During a fat grafting procedure, the electrodes contact patient tissue. Based on signals received from each electrode, the circuit is configured to determine whether a distal portion of the fat grafting cannula is disposed in a fat tissue or muscle tissue. If the circuit determines that the fat grafting cannula is disposed in muscle tissue, the surgeon operating the fat grafting cannula is alerted to ensure that processed fat is not injected into the muscle tissue of the patient.

Methods, systems and devices for evaluating the integrity of a uterine cavity. A method comprises introducing transcervically a probe into a patient's uterine cavity, providing a flow of a fluid (e.g., CO.sub.2) through the probe into the uterine cavity and monitoring the rate of the flow to characterize the uterine cavity as perforated or non-perforated based on a change in the flow rate.

A prostate therapy system is provided that may include any of a number of features. One feature of the prostate therapy system is that it can access a prostate lobe transurethrally. Another feature of the prostate therapy system is that it can deliver condensable vapor into the prostate to ablate the prostate tissue. Methods associated with use of the prostate therapy system are also covered.

A prostate therapy system is provided that may include any of a number of features. One feature of the prostate therapy system is that it can access a prostate lobe transurethrally. Another feature of the prostate therapy system is that it can deliver condensable vapor into the prostate to ablate the prostate tissue. Methods associated with use of the prostate therapy system are also covered.

A method and system for artificial intelligence-based radiofrequency ablation parameter optimization and information synthesis are provided. The method is applied to a radiofrequency ablation controller including a processor and an artificial intelligence module. The processor of the radiofrequency ablation controller preprocesses sample data and sends the preprocessed sample data to the artificial intelligence module. The artificial intelligence module establishes an artificial neural network model according to the preprocessed sample data and a radiofrequency ablation control parameter for the sample data. The processor preprocesses signals collected by sensors on a plasma wand. The artificial intelligence module imports preprocessed sensor data into the artificial neural network model for analysis and fusion, to obtain the radiofrequency ablation control parameter.

A base member includes: a base member having a longitudinal direction; a first linear member extending in the longitudinal direction; and a second linear member extending in the longitudinal direction. The first linear member is fixed to the base member at a first position, and is movable with respect to the base member in the longitudinal direction, on one side of the first position in the longitudinal direction. The second linear member is fixed to the base member at a second position, and is movable with respect to the base member in the longitudinal direction, on the one side of the second position in the longitudinal direction. The base member is capable of detecting curvature of the base member between the first position and the second fixed position based on change in a relative position between the first linear member and the second linear member.

A balloon catheter includes: a balloon; an outside shaft connected to a proximal end of the balloon; an inside shaft extending inside the outside shaft and into the balloon to be connected to a distal end of the balloon; and a heating member disposed in the balloon for heating a liquid in the balloon. A distance between a distal end of the outside shaft and a proximal end of the heating member is 0 mm to 5 mm.

The present invention describes a method and kit for performing a prostate medical or surgical treatment.

A minimally invasive cosmetic procedure for de-bulking fat includes steps of: (a) injecting platelet rich plasma (PRP) into a subject area; followed by (b) heating fat cells in the subject area using radiofrequency; followed by (c) aspirating fat cells in the subject area using liposuction; followed by (d) injecting platelet rich plasma (PRP) into the subject area again. The PRP injecting step (a) may be performed two to seven weeks prior to the heating and liposuction steps (b) and (c); and the PRP injecting step (d) may be performed several days to four weeks after the heating and liposuction steps (b) and (c).