Abstract: The present application provides a massager for male genitalia. A user may insert his penis into a massage sleeve through an opening. A relative movement is generated between the massage sleeve and the penis to simulate a thrusting motion during sexual intercourse. The massage sleeve simulates a vaginal environment, and performs a massage to provide massaging stimulation, and a reciprocating movement to provide reciprocating stimulation, or the like. In addition, the massage of the user's penis is implemented during the simulation of a back-and-forth thrusting motion. Therefore, an all-around automatic massage of the penis is implemented, and the entire massage process is relaxing and pleasurable.

Abstract: A system and method for adaptive speech and biofeedback control of sexual stimulation devices. In an embodiment, the system and method involve receiving audio from a microphone, processing the audio through an automated speech detection engine to detect speech within the audio, matching the speech to a control command for a sexual stimulation device, generating a control signal for the sexual stimulation device based on the control command, receiving biometric data from a biometric sensor, and adjusting the control signals based on the biometric data before outputting the adjusted control signal for use in operating the sexual stimulation device. In some embodiments, the adjustment to the control signal is made automatically by a machine learning algorithm using the command and biometric data as inputs.

Abstract: The present disclosure relates to a tent-type mobile infectious disease clinic, and more particularly, to a mobile infectious disease clinic, which is a tent-type mobile infectious disease clinic that makes it possible to promptly install a large number of mobile infectious disease clinics due to having mobility and being easy to install and remove, that allows a test subject to be tested by a healthcare provider using an infectious disease test kit while the test subject is isolated in the tent-type mobile infectious disease clinic, the healthcare provider is outside the tent-type mobile infectious disease clinic, and exposure of the body parts is minimized, that performs sterilization of an infectious disease using an ultraviolet C (UV-C) lamp to reduce the time taken for disinfecting the clinic, and that allows the light radiation intensity of the UV-C lamp to be adaptively adjusted according to the body temperature of the test subject.

Abstract: An electromechanical stimulation system for treating tinnitus comprising a proximal unit (10), configured to be placed proximate to a user's ear (1), and an input interface (50) configured to be operated by the user. The proximal unit comprises an electromechanical device (30) configured to transmit mechanical vibrations (35) with predetermined frequency (f), intensity (A) and waveform, to tissues proximate to the user's ear; a control unit (20), configured to actuate the electromechanical device in such a way that the frequency, the intensity and the waveform of the mechanical vibrations can be modified; a transceiver element (40) adapted to receive control signals (45) for the control unit.

Abstract: A radiation treatment device is provided. The device includes an imaging unit and a single radiotherapy unit adjacent to a second end of the imaging unit. The imaging unit includes a first opening at a first end of the imaging unit adapted to receive a patient; at least one imaging source; and at least one imager arranged opposite the imaging source. The imaging source and the imager are rotatable about the rotational axis. The radiotherapy unit includes a source body carrying radioactive sources and a collimator having collimation channels. The collimation channels permit treatment beams emitted by the radioactive sources to be projected inside the imaging unit and focused at an intersection point located within an imaging beam of the imaging unit. The source body and the collimator are arranged concentric about the rotational axis and close a second opening at the second end.

Abstract: A microfluidic strain sensing device for monitoring intraocular pressure. The device has a contact lens and a closed microfluidic network embedded with the contact lens. The network has a volume that is sensitive to an applied strain. The network distinguishes: (i) a gas reservoir containing a gas, (ii) a liquid reservoir containing a liquid that changes volume when the strain is applied, and (iii) a sensing channel able to hold the liquid within the sensing channel. The sensing channel connects the gas reservoir on one end and connects the liquid reservoir on another end. The sensing channel establishes a liquid-gas equilibrium pressure interface and equilibrium within the sensing channel, which would fluidically change as a response to radius of curvature variations on a cornea, or as a response to mechanical stretching and release of the cornea. The liquid-gas equilibrium pressure interface and equilibrium are used for measuring the intraocular pressure.

Abstract: The present disclosure relates to systems and methods for reconstructing fluence map. The system may obtain a plurality of radiation tasks based on a radiotherapy plan. Each of the plurality of radiation tasks may include a radiation field corresponding to the radiation task. For each of the plurality of radiation tasks, the system may determine whether a shape change between a radiation field corresponding to the radiation task and a radiation field corresponding to a preceding radiation task exceeds a shape change threshold. The system may determine a fluence map corresponding to the radiation task based on a first determination result of whether the shape change between the radiation field corresponding to the radiation task and the radiation field corresponding to the preceding radiation task exceeds the shape change threshold.

Abstract: Devices, systems, and methods for providing remote traction to tissue may include a grasper and a control element. The grasper may have a first jaw, a second jaw, a main body, and a first magnetic element. The control element may include a second magnetic element. The first and second magnetic elements may attract the grasper to the control element such that the grasper is oriented parallel, perpendicularly, or at an angle between parallel and perpendicular with respect to the control element and/or a body. In some instances, the grasper may include first and second magnetic elements and the control element may include third and fourth magnetic elements.

Abstract: A portable and inflatable patient isolation chamber and stretcher system having an exoskeletal frame, which when inflated, forms a substantially tent contour enclosure when coupled to an inflatable flexible base. The exoskeletal frame has an apex section formed by a flexible apex conduit which is coupled to and in fluid communication with first and second flexible end conduits. The inflatable flexible base is connected to the exoskeletal frame and is in fluid communication with the exoskeletal frame for providing a flexible platform for the patient. A transparent envelope is secured to the exoskeletal frame and inflatable flexible base for forming a patient isolation chamber. When deflated, the flexible base can serve as a stretcher for transport of the patient.

Abstract: Disclosed is a transcranial magnetic stimulation (TMS) stimulation navigation method comprising the steps of: acquiring a stimulation target point in the brain of a subject to which an electrical stimulus is to be applied; acquiring data on the spatial distribution of a magnetic vector potential of a coil for a TMS procedure; acquiring, from the spatial distribution, at least one parameter for acquiring an optimal stimulation condition for the stimulation target point; and by using the acquired parameter, calculating a position and direction of the coil satisfying the optimal stimulation condition for the stimulation target point.

Abstract: The disclosure pertains to a strontium-90 sealed radiological or radioactive source, such as may be used with treatment of the eye or other medical or industrial processes. The sealed radiological source includes a toroidal shaped strontium radiological insert within an encapsulation. The encapsulation includes increased shielding in the center thereof.

Abstract: Systems and methods are provided for generating surface brachytherapy applicators in which catheter channel trajectories are generated laterally from both sides of a cut plane bisecting an initial model of the surface brachytherapy applicator model, thereby mitigating the effects of patient-surface-induced curvature. The catheter channels may be defined based on catheter channel trajectories that are spatially distributed, relative to the cut plane, on both sides of the cut plane, and spatially offset relative to a patient-facing surface of the surface brachytherapy applicator model. In some example embodiments, catheter channel trajectories are spaced relative to the cut plane such that neighbouring catheter channel trajectories are evenly spaced along a set of contours. Prior to fabrication, the local radius of curvature of catheter channels may be adjusted in a manual or automated manner to exceed a threshold.

Abstract: Featured is a robot and a needle delivery apparatus. Such a robot comprises a plurality of actuators coupled to control locating any of number of intervention specific medical devices such as intervention specific needle injectors. Such a robot is usable with image guided interventions using any of a number of types of medical imaging devices or apparatuses including MRI. The end-effector can include an automated low needle delivery apparatus that is configured for dose radiation seed brachytherapy injection. Also featured is an automated seed magazine for delivering seeds to such an needle delivery apparatus adapted for brachytherapy seed injection.

Abstract: A beam transport assembly conveys a particle beam from a particle source to an irradiation nozzle, which rotates about a swivel axis at the horizontal input of the nozzle. A support can move horizontally in a plane perpendicular to the swivel axis. The beam transport assembly can change a path length of the particle beam so as to follow a vertical location of the swivel axis of the irradiation nozzle with respect to the support. A controller can coordinate the path length change of the particle beam, rotation of the irradiation nozzle about the swivel axis, and/or horizontal motion of the support to provide irradiation of a supported object from various angles in the plane perpendicular to the swivel axis while maintaining the irradiation nozzle at a constant distance from the supported object.

Abstract: Medical systems and methods are provided in the present disclosure. The medical system may include a first medical device mounted on a first gantry. The first medical device may be configured to perform a first operation on a first region of an object. The medical system may also include a second medical device mounted on a second gantry. The second medical device may be configured to perform a second operation on a second region of the object. The second gantry may rotate relative to the first gantry. The first region may at least partially overlap the second region.

Abstract: A penis massager includes a housing, a massager member and a driving apparatus. The massager member includes a first massaging portion and a second massaging portion which are separately arranged. A space for inserting of the penis is defined between the first massaging portion and the second massaging portion. The driving apparatus is in transmission connection with the first massaging portion and the second massaging portion respectively for driving the first massaging portion and the second massaging portion to reciprocate in an axial direction of the housing. A movement direction of the first massaging portion is opposite to that of the second massaging portion.

Abstract: A penile prosthesis includes an inflatable cylinder implantable into a penis; a pump fluidically attachable to the inflatable cylinder through a first tube; and a reservoir attachable to the pump through a second tube that is fluidically attachable between the pump and the reservoir. Connectors are provided to couple the reservoir and the pump. A first connector includes a plurality of protrusions and a second connector includes an outer shell forming a plurality of openings. The protrusions mate with the openings to form a connection.

Abstract: Light weight, compact, battery powered, body-worn devices and systems are configured to allow automated, hands-free monitoring and care intervention, such as of an infant, by providing audio and/or physical stimulus when a negative comfort or health condition is detected by the body-worn device and system, and by monitoring the infant's temperature, pulse, and oxygen levels. The body-worn device preferably includes a flexible printed circuit board (“FPCB”) that allows the device to be conformed to the wearer's body, and has a plurality of linear resonant actuators affixed to the FPCB that are configured to impart soothing vibrations from the device to the wearer. A control program is provided and executable on a remote computing device, which control program is configured to enable users (such as a caregiver) to selectively control the actuators.

Abstract: A penis massager includes a housing and an sleeve. The housing is provided with an accommodating space, and a power source and a circuit board electrically connected to the power source are received in the accommodating space. The sleeve is removably mounted in the accommodating space, one end of the sleeve is concaved to form a interior volume for containing the penis. A vibrating apparatus is arranged in the sleeve and electrically connected to the circuit board for generating a mechanical vibration.

Abstract: Systems, kits and methods for preparing an injection system and/or treating target lesions with a selective internal radiation therapy which includes a double-barrel syringe loaded with a two-component tissue glue and radioisotope loaded microspheres. The microspheres are loaded into the syringe based on the size of the target location and are administered with a needle or dual-lumen catheter. Dosing regimens for treating breast cancer lesions or surgical beds up to 130 mm in diameter and hepatocellular carcinoma lesions up to 50 mm are included.