Abstract: A surgical instrument includes an end effector, a handle assembly, and a knife drive assembly. The end effector includes a first jaw, a second jaw, a knife, and an electrode assembly. The second jaw is pivotably coupled with the first jaw and is operable to move between an open position and a closed position. The knife is configured to actuate between a pre-fired position and a fired position. The electrode assembly is configured to apply RF energy to tissue. The handle assembly includes a housing associated with the first jaw and an arm associated with the second jaw. The arm is configured to pivot the second jaw between the open position and the closed position. The knife drive assembly includes an input assembly, an output assembly, and a threaded member rotatably disposed within the housing. The threaded member includes a first threaded portion and a second threaded portion. The first threaded portion is associated with the input assembly and includes a first pitch extending in a first pitch orientation.

Abstract: A surgical instrument includes an end effector, a handle assembly, and a knife drive assembly. The end effector includes a first jaw, a second jaw, a knife, and an electrode assembly. The handle assembly includes a housing, and an arm. The arm may pivot the second jaw between the open position and the closed position. The knife drive assembly includes an input assembly, and output assembly coupled with the knife, and a compound pulley assembly. The compound pulley assembly includes a pair of pulley wheels each having an input track, an output track, an input cable, and an output cable. The input assembly can drive the input cable a first proximal distance in order to rotate the pair of pulley wheels in a first angular direction, thereby driving the output cable a first distal direction to actuate the knife from the pre-fired position toward the fired position.

Abstract: A surgical instrument includes an end effector, a handle assembly, and an electrode activation assembly. The end effector includes a first jaw, a second jaw, a knife, and an electrode assembly. The handle assembly includes a housing, and an arm. The arm can pivot the second jaw between the open position and the closed position. The arm can pivot relative to the housing between a first position, a second position, and a third position. The electrode activation assembly includes an activation button associated with the handle assembly, a resilient body, and a detent associated with either the housing or the arm. The activation button can activate the electrode assembly in response to the arm pivoting to the third position. The resilient body includes a first cam feature. The detent can engage the first cam feature as the arm pivots between the first position and the second position.

Abstract: A surgical instrument includes an end effector, a handle assembly, and a latch assembly. The end effector includes a first jaw, a second jaw pivotably coupled with the first jaw, a knife, and an electrode assembly. The handle assembly includes a housing associated with the first jaw, and an arm associated with the second jaw. The arm can pivot the second jaw between an open position and a closed position. The latch assembly can transition between an unlatched configuration and a latched configuration. The latch assembly can prevent the arm from pivoting the second jaw from the closed position toward the open position in the latched configuration. The latch assembly can allow the arm to pivot the second jaw from the closed position toward the open position in the unlatched configuration.

Abstract: A surgical instrument includes an end effector, a handle assembly, a knife drive assembly, an electrode activation assembly, and a lockout assembly. The end effector includes a first jaw, a second jaw, a knife, and an electrode assembly. The handle assembly includes a housing associated with the first jaw and an arm associated with the second jaw, where the arm is configured to pivot the second jaw between an open position and a closed position. The lockout assembly is may transition between a locked configuration and an unlocked configuration. The lockout assembly may prevent activation of the electrode and prevent actuation of the knife drive assembly while in the locked configuration. The lockout assembly may allow activation of the electrode and allow actuation of the knife drive assembly while in the unlocked configuration.

Abstract: A treatment instrument including a heat transmitter that includes a treating surface and an installation surface, a substrate attached to the installation surface, and a heat generator formed on a surface of the substrate. The substrate surface and heat generator together form an uneven surface. First and second adhesion layers formed of a material having thermal conductivity and electrical insulation are provided between the installation surface and the substrate. The first adhesion layer is in close contact with the installation surface, and the second adhesion layer is in close contact with the heat generator and the substrate surface. The second adhesion layer is inserted into a recess in the uneven surface formed by the heat generator on substrate surface so as to increase the contact area between the second adhesion layer and the uneven surface.

Abstract: A device, a system and a method for applying radio frequency (RF) treatment to a tissue, the including: (a) contacting the tissue with an RF emission portion comprising: a first electrode, having a first contact surface and a second electrode having a second contact surface that is larger than the first contact surface and (b) emitting at least one RF current pulse from the first contact surface, through the treated tissue, to the second contact surface.

Abstract: Described embodiments include an apparatus that includes a flexible electrically-insulating substrate, including an inner surface and an outer surface, and shaped to define (i) multiple narrower channels passing between the inner surface and the outer surface, and (ii) one or more wider channels passing between the inner surface and the outer surface. The apparatus further includes an outer layer of an electrically-conducting metal covering at least part of the outer surface, an inner layer of the electrically-conducting metal covering at least part of the inner surface, a plating layer of the electrically-conducting metal that plates the wider channels such as to connect the outer layer to the inner layer, and respective columns of the electrically-conducting metal that fill the narrower channels such as to connect the outer layer to the inner layer. Other embodiments are also described.

Abstract: Described embodiments include a catheter tip that includes an outer layer of a thermally-conducting metal; an inner layer of a thermally-conducting metal; a polymer layer between the inner and outer layer; and a plurality of thermal bridges selectively positioned between the inner and outer layers and through the polymer layer thereby significantly increasing the heat transfer of the catheter tip through the polymer layer. Other embodiments are also described.

Abstract: The present invention provides a treatment apparatus for an endoscope, an endoscope, and an expandable frame. The treatment apparatus for an endoscope includes: a first electrode, including an electrical treatment part and an operating wire; a second electrode, provided inside the endoscope, and including a first electrically conductive part and a sliding contact part electrically connected to the first electrically conductive part, the first electrically conductive part being configured to contact a human body; and a sheath, provided on a surface thereof with a second electrically conductive part, where the operating wire is configured to be passed through the sheath, the sheath is configured to be passed through the endoscope, and when the sheath is located in a preset position, the sliding contact part contacts and is electrically connected to the second electrically conductive part and the sheath is in sliding fit with the sliding contact part.

Abstract: This invention provides a system and method that allows a therapeutic device, such as an atrial fibrillation microwave ablation catheter or ablation tip to be guided to a remote location within a body cavity and then accurately immobilized on the tissue, including that of a moving organ, such as the heart. In various embodiments, the system and method also enables accurate movement and steering along the tissue, while in engagement therewith. Such movement and engagement entails the use of vacuum or microneedle structures on at least two interconnected and articulated immobilizers that selectively engage to and release from the tissue to allow a crawling or traversing walking across the organ as the therapeutic catheter/tool tip applies treatment (AGE devices). In further embodiments that lack a movement capability (AID devices), the immobilizers allow a predetermined position for the introduced device to be maintained against the tissue while a treatment is applied to the location adjacent thereto.

Abstract: A hand-held device for providing a dermatological treatment by scanning laser beams to form a pattern of treatment spots on the skin includes a laser source configured to generate an input laser beam, an automated scanning system, and a treatment spot control system. The automated scanning system includes a rotating multi-sector scanning element configured to repeatedly scan the input laser beam, each scan of the input laser beam providing an array of output laser beams corresponding to the multiple sectors of the scanning element and forming a scanned row of treatment spots on the skin. The rotating multi-sector scanning element is configured such that the each sector provides a constant-angular-direction output laser beam as that sector rotates through the input laser beam. The treatment spots of each scanned row are spaced apart from each other by areas of non-irradiated skin.

Abstract: An ultrafast laser system and application thereof, relates to the technical field of laser, and the system comprises a control module, a laser, an optical path module, a movable platform, a visual locating module, and the control module is connected to the laser and controls an operation of the laser, and the control module is connected to the movable platform and controls a movement of the movable platform, and the optical path module is connected to the laser and is used for transmitting a laser light generated by the laser to the movable platform, and the control module is connected to the visual locating module and controls the visual locating module to position a laser emitting position at a position, and the laser is an ultrafast laser. The system is applied to equipment for removing mole, freckle, or tattoo, which has the advantages of fewer traumas and no pain.

Abstract: An apparatus and a system for performing thermotherapy on at least a portion of a tissue site is described. The apparatus and system comprise a heating probe comprising an emitting area. The heating probe is connectable to an energy source for heating the tissue by the emitting area. The apparatus and system comprise a sleeve. The heating probe is arrangable in the sleeve, and the sleeve is configured to be slid along the heating probe in a distal and/or proximal direction for positioning of the emitting area in said portion of tissue for controlling the thermotherapy.

Abstract: Described embodiments include a system that includes a current source generator and a processor. The processor is configured to drive the current source generator to supply, for application to tissue of a subject, an electric current having an amplitude that varies in accordance with a predefined function of time, such that the amplitude initially monotonically increases to a maximum value. Other embodiments are also described.

Abstract: A therapeutic method can include receiving an initial astigmatism condition of an eye; receiving a target final astigmatism condition of the eye; generating, based on the initial and target final astigmatism conditions, an eye incision pattern by iterating through a plurality of potential corrective combinations; and cutting the eye based on the eye incision pattern. Each of the potential corrective combinations can be defined by one or more of: an intraocular lens selected from a plurality of intraocular lens options, an access incision selected from a plurality of access incision options, and an arcuate incision selected from a plurality of arcuate incision options.

Abstract: A method and system for predicting a measure of hemodynamic compromise as a result of transcatheter cardiac treatment. The method includes providing a patient-specific anatomical model representing cardiac region and an implant model representing a three-dimensional representation of a cardiac implant. The method includes virtually deploying said implant model into said patient-specific anatomical model. A deformation of the patient-specific anatomical model is calculated as a result of implant model deployment A measure of hemodynamic compromise is determined from the virtually deployed implant model and the deformed patient-specific anatomical model.

Abstract: The present invention relates to a computer-implemented medical method of determining a spatial position of a medical optical observation device (1), the method comprising executing, on a processor of a computer (2), the steps of: —acquiring position data describing, for a plurality of points in time, the spatial position of the observation device (1) within a co-ordinate system of a medical tracking system (3); —determining, based on the position data, average position data describing an average value for the position of the observation device (1) within the co-ordinate system of the medical tracking system (2); —acquiring image data describing a plurality of images acquired at the plurality of points in time via a camera (4) assigned to the observation device (1) and detecting the field of view (5) of the observation device (1); —determining, based on the image data, optical flow data describing an optical flow for the plurality of images; —determining, based on the average position data and the optical flo

Abstract: A dynamic reference deviation detecting method is used for detecting a deviation of a dynamic reference coordinate system. A coordinate detecting step is for detecting and recording a first initial coordinate and a second initial coordinate. A first coordinate variation calculating step is for calculating a difference between a first instantaneous coordinate and the first initial coordinate to obtain a first difference value. A second coordinate variation calculating step is for calculating a difference between a second instantaneous coordinate and the second initial coordinate to obtain a second difference value. A relative coordinate variation calculating step is for obtaining a relative difference value. A dynamic reference deviation determining step is for determining whether or not the dynamic reference coordinate system is deviated according to the first difference value, the second difference value and the relative difference value.

Abstract: A location tracking system includes a location pad collar and a processor. The location pad collar is configured to be placed around a neck of a patient and includes one or more magnetic field generators configured to generate one or more magnetic fields within a head of the patient. The processor is configured to receive, in response to the one or more generated magnetic fields, one or more position signals that are indicative of a location of a distal end of a sheath of a probe inside a blood vessel in a brain of the patient. Based on the received position signals, the processor is configured to estimate the location of the distal end of the sheath in the brain relative to a clot in the brain.

Abstract: A robot for spinal surgery may include an open rectangular base designed to slide on a rail of a fixed support to reach to different parts of the spine. The robot may include a moving top platform that can accommodate a surgical instrument, and three legs to support the top platform on the base and move the top platform in 6-degree-of-freedom relative to the base. In one embodiment, each of the three legs may include a lower part and an upper part joined by an electric linear actuator for sliding the upper part linearly relative to the lower part. In one embodiment, the lower part of each leg may be joined to a shaft of a rotary actuator that is mounted to the base, and the upper part of each log can be joined to the top platform at a fixed point via a passive spherical joint.

Abstract: A navigation system is disclosed comprising a first and a second tracker support separately affixed to the same rigid object by a distance. A first and a second plurality of trackable elements are secured to the first and second tracker supports, respectively. The navigation system defines a tracking arrangement to be tracked based on a combination of the first and second plurality of trackable elements. A geometry of the tracking arrangement relative to the rigid object is registered. The navigation system has a localizer configured to track the rigid object by detecting the registered geometry of the tracking arrangement. The navigation system identifies a condition wherein at least one trackable element has been displaced relative to the registered geometry, and in response, generates a response to address the condition.

Abstract: The invention relates to a system for assisting in navigating a medical device (1) in a region of a patient body, such as a cardiac chamber. The system comprises a unit (5) for providing a three-dimensional model of the region and an ultrasound probe (2) for acquiring image signals of the region of the patient body. At least one an ultrasound sensor (6) is attached to the medical device (1) for sensing ultrasound signals emitted by the 5 ultrasound probe (2) and a tracking unit (7) determines a relative position of the at last one ultrasound sensor (6) with respect to the live images and/or the ultrasound probe (2) on the basis of the sensed ultrasound signals. Further, a mapping unit (8) maps the determined relative position of the at least one ultrasound sensor (6) onto the model to generate a visualization of region of the patient body.

Abstract: An instrument system includes an instrument, a drive system, and a controller operably connected to a first drive mechanism and a second drive mechanism of the drive system. The controller is configured to operate the first drive mechanism and the second drive mechanism drive a flexible tensioning member of the instrument to cause movement of an end effector of the instrument while maintaining a tension applied to the flexible tensioning member of the instrument in a tension range.

Abstract: Surgical assemblies and related methods are disclosed that provide for decoupling of instrument shaft roll and end effector actuation. A surgical assembly includes a base, an instrument shaft rotationally mounted to the base, an end effector supported at a distal end of the instrument shaft and including an actuation mechanism driven by a rotational motion, a drive shaft rotationally coupled with the actuation mechanism and configured to provide the rotational motion to the actuation mechanism, and a differential rotationally coupled to the drive shaft and receiving a first input motion and a second input motion. The differential combines the first and second input motions to generate an output motion that rotates the drive shaft. The first input motion is rotationally coupleable to an actuation source. The second input motion is coupled to rotation of the instrument shaft relative to the base.

Abstract: A method for positioning an input device of a workstation for use by a seated user in controlling a robotic surgery system is disclosed. The input device is operable to generate input signals representing a position of a hand controller moveable within an input device workspace. The method involves determining a vertical position of the hand controller within the input device workspace for an input signal received from the input device while a seated user's hand is grasping the hand controller in an initialization position defined with respect to the user's body. The method also involves determining a user ergonomic height of the input device based on the vertical position of the hand controller at the initialization position, and causing a platform of the workstation on which the input device is mounted to move vertically with respect to a base of the workstation to position the input device at the ergonomic height.

Abstract: An autoclavable handle (5) includes a handle housing (9) and with at least one switch element (11) mounted to the handle housing (9). The autoclavable handle (5) is permanently resistant to the effects of machine cleaning and of steam sterilization. The at least one switch element (11) is resiliently pressable into the handle housing (9). The switch element (11) is mounted in the handle housing (9) via at least one web (16) arranged on an underside of the switch element (11). The switch element (11) is sealed off from the handle housing (9) via a circumferential sealing element (12).

Abstract: An immobilization system, especially for use on the human head and neck area, is described in various embodiments. The system may include a bite block immobilization system having a bite block with a dental interface releasably engageable with a plurality of teeth of a patient, and a retention mask. The dental interface releasably engages the teeth of a patient and allows very highly accurate repositioning during multiple procedures. In some embodiments, the bite block may have an integral bite block airway passage, allowing a patient to have unobstructed breathing both during molding of the retention mask and during subsequent use of the system, and may include a tongue diverter, that may, by way of example only and not to limitation, be used to divert the tongue away from a therapeutic radiation beam. Steps for utilizing the system are further described.

Abstract: A holding device for human-medicine or veterinary-medicine applications having: a joint between a proximal holding segment and a distal holding segment; wherein one axially displaceable thrust element, in each case is arranged in the holding segments; wherein the joint has a tightening bolt, which defines the pivoting and tightening axis, and has deflection elements, by means of which a thrust force, acting relative to the axis, of the proximal thrust element is deflectable to lock the joint onto the tightening axis and to displace the distal thrust element; and wherein the deflection elements include at least one ramp system with a wedge body. A holding system including the specified holding device and a method for locking the joint of the specified holding device.

Abstract: A clamping device and method for human-medicine or veterinary-medicine applications for the frictionally engaged locking of at least two holding segments, the clamping device has a first holding segment, a second holding segment; a driveable spindle, via which a rotational movement can be converted into an axial longitudinal movement for spindle-locking the second holding segment, and a threaded plate. In this case, the threaded plate can be moved axially in the opposite direction during the spindle movement, wherein, by counter-movement of the threaded plate, at least one wedge body is moveable in a ramp system, in order to clamp the first holding segment.

Abstract: Systems and methods for providing a medical tool cleaning and/or lubrication system are provided. A cleaning system may include an attachment interface configured to receive one or more medical device tool modules. The attachment interface may include one or more input or output couplings which are configured to connect the attachment interface to a reservoir which provides one or more fluids in an input/output pathway for the circulation of the fluids into the one or more medical device tool modules. The cleaning system may also include one or more fluid reservoirs which contain fluid to be circulated through the one or more medical device tool modules. The cleaning system may further comprise a driver system configured to at least partially actuate components of connected medical device tool modules while the modules are being cleaned.

Abstract: The present disclosure provides a device having a circuit. The circuit includes at least one boost converter receiving power from an energy source, a square wave driver in series with the boost converter, an inductor in series with the square wave driver for converting a square wave to a sinusoidal wave, and a piezoelectric transducer in series with the inductor, the piezoelectric transducer connectable to a load. The device further includes a phase-locked loop coupled to the circuit to determine a resonance frequency of the piezoelectric transducer when the piezoelectric transducer is connected to the load.

Abstract: Provided herein are orthodontic systems and methods for automatically segmenting a person's teeth. Systems, methods and processes are provided to properly segment the teeth of a person's teeth from an image of the person's face showing at least some of the person's teeth (e.g., dental arch). Methods and systems are provided to automatically detect dental edges after a dental scan. Also described herein are methods and systems for generating a simulated image of the person's face from the final segmentation of the person's teeth in which the segmented teeth have been moved from their original position, including a new position based on an orthodontic treatment plan.

Abstract: A dental tools system with a plurality of guide tabs; a mold and a plurality of tissue punch heads. The mold has a plurality of mold holes, each mold hole having a top portion and a bottom portion. Each guide tab fits in the top portion of one of the mold holes and each tissue punch head fits in the top portion of one of the mold holes. A method of placing dental implants is also described.

Abstract: An implant fixture is disclosed. The implant fixture contains an elongated shaft section, and a head section, wherein the head section contains at least one concave area for bone growth therein.

Abstract: A dental tray appliance system including a maxillary tray appliance and optionally a mandibular tray appliance. The maxillary tray appliance includes a first base portion, a first premolar tooth form, optionally a first contacting portion, optionally a contralateral first premolar tooth form, and optionally a central incisor tooth form. Each premolar tooth form has no lingual cusp as part of improvements in occlusal registration components. The mandibular tray appliance includes a second base portion, optionally a second contacting portion; and optionally a second bite material accepting portion.

Abstract: A dental tray system includes a maxillary impression tray configured to be filled with an impression material and to take an impression of an upper jaw side of an oral cavity; a mandibular impression tray configured to be filled with the impression material and to take the impression of a lower jaw side of the oral cavity; and a support plate provided between the maxillary impression tray and the mandibular impression tray and configured to movably support the maxillary impression tray and the mandibular impression tray in a front-to-rear direction.

Abstract: Systems and methods are disclosed for processing and storing acquired data relating to one or more dental conditions. The methods can include acquiring a first oral feature in a first data acquisition using a data acquisition device, determining a first oral feature first reference point from the first data acquisition, diagnosing a first dental condition upon confirming that the first oral feature first reference point is associated with the first dental condition, acquiring the first oral feature in a second data acquisition using the data acquisition device, determining a first oral feature second reference point from the second data acquisition, and tracking the progression of the first dental condition by determining a discrepancy between the first oral feature first and second reference points.

Abstract: Computer-implemented method and an optimized implant site simulation system which performs a simulation of a damaged oral cavity of a patient and defines an implant site adapted to receive a dental implant to repair the damage observed. The invention further describes the optimized implant site simulated (SI) and a dental implant (ID) couplable to the optimized implant site (SI) simulated. The invention further describes a computer program to perform the steps of the method and an optimized implant site (SI) simulation system.

Abstract: A dental prosthesis having a prosthesis base and a set of teeth, namely a full set of teeth or a partial set of teeth, is provided, wherein the prosthesis base comprises at least one dental recess for receiving the set of teeth, and wherein the set of teeth is glued into the at least one dental recess by an adhesive. In the dental recess and/or in or at the set of teeth an adhesive channel is configured which extends along the at least one dental recess or the dental arch in its main direction of extension. It starts at an adhesive filling opening whose configuration is adapted to a filling element.

Abstract: A “Flossing Device with Spring-Type Head” is a device used to floss the teeth. A handle with a storage chamber in which the coiled floss thread is stored, is fixedly attached to a Spring-Type Head that includes a substantially U-shape flexible arm and two substantially cylindrical shape fixtures. Each piece of the floss thread is placed and secured between the said fixtures. Due to the flexibility of the said arm, a constant suitable tension of the floss thread is maintained at all times. Using the device, while flossing becomes possible with one hand, it gives the user a much more effective and easier flossing experience.

Abstract: An oral irrigator has a first liquid container, a nozzle outlet, a pump driven by a drive to pump liquid from the liquid container to the nozzle outlet so that a liquid jet is emitted via the nozzle outlet, a first switch arranged so that the drive is powered when the first switch is actuated once and the oral irrigator is switched into an ON state, and so that powering of the drive is stopped and the oral irrigator is switched into an OFF state when the first switch is actuated once again, and a second switch arranged so that the drive is powered only while the second switch is continuously actuated by the user and powering is stopped when the second switch is released.

Abstract: In one embodiment, the invention may be a teeth cleaning device including: a first support structure comprising a first dentature channel configured to receive at least a first portion of a dentature of a user; a plurality of teeth cleaning pads located within the first dentature channel; a plurality of air bladders operably coupled to the teeth cleaning pads; an air-flow subsystem operably coupled to the air bladders; and a control unit operably coupled to the air-flow subsystem, the control unit configured to: (1) pressurize the air bladders with external air in a pressurization mode; and (2) transfer air between select ones of the air bladders in a cleaning mode.

Abstract: The invention relates to tracking pieces (110) used in the context of tracking movements of hard tissue of a jaw. According to the invention, a tracking piece (110) to be used in such context is designed to be patient-specific by including in the design of the tracking piece (110) a surface model representing a part of a person's intraoral anatomy, which surface model is generated based on imaging results acquired by imaging the anatomy.

Abstract: The invention relates to an oral care device for teeth whitening or other purpose. The device is designed to provide a uniform light intensity distribution at the teeth. This is achieved by use of a light guide which at some surface parts is separated from surrounding parts of the mouthpiece of the oral care device by air-filled separation portions. The light guide mixes the injected light to improve the uniformity of the light intensity. In 5 order to couple light out from the light guide, the mouthpiece comprises an out-coupling structure located opposite to the buccal side of the teeth. The out-coupling structure may be shaped, e.g. by changing the area or density of parts of the out-coupling structure depending on the distance to a location of the light guide where light is injected.

Abstract: A doser including one or more cartridges for holding one or more products. The cartridge has a body defining a cavity for holding the products, a nozzle disposed on the body and connected to the cavity for dispensing the product from the cavity, and a piston arranged to move within the cavity to propel the product from the cavity into the nozzle. The cartridge also has a cap removably coupled to the cartridge for protecting the nozzle. Lastly, the doser has a dispenser for holding the cartridge or cartridges which actuates the piston, and removes the cap from the cartridge, so that the product is dispensed from the cartridge.

Abstract: The device (1) comprises an inlet element (28) comprising an interface (40) for connecting to an artificial vagina and delimiting an inlet opening (14), a filter delimiting with the inlet element (28) an inlet chamber (41) on the side of the filter turned towards the opening (14) and a collection bag (4) extending between a closed end (8) and an open end (7) in which said inlet element is engaged; said bag and said filter delimiting a collection chamber (42) on the side of the filter turned towards the end (8); by means of which the semen entering through the opening (14) passes through the filter and comes to the collection chamber (42); the filter being a perforated wall (30) having a tubular portion (22) and a bottom portion (15) closing said tubular portion, and having a surface density of orifices (24) that is greater on said bottom portion than on said tubular portion.

Abstract: The device (1) comprises an inlet element (28) comprising an interface (40) for connecting to an artificial vagina and delimiting an inlet opening (14), a filter associated with the inlet element (28) and delimiting therewith an inlet chamber (41) on the side of a first face of the filter turned towards the opening (14) and a collection bag (4) extending between a closed end (8) and an end (7) having an opening (6) in which said inlet element is engaged; said bag and said filter delimiting a collection chamber (42) on the side of the second face (18) of the filter turned towards the end (8); by means of which semen entering through the opening (14) passes through the filter and is collected in the collection chamber (42); characterized in that the filter is formed by a perforated wall (30) in one piece with the inlet element.

Abstract: An intra-pelvic fundus vesicae support disposed at the outer fundus vesicae position and fixing the front end to the pelvic pecten pubis position to lift internal organs. An injection channel is provided inside an intra-pelvic fundus vesicae support structure, and a screw hole is formed at an input hole, so that the support can be connected to an in-vitro device. According to the intra-pelvic fundus vesicae support, a tomoscan three-dimensional modeling technology is used to generate a model file which completely conforms to physiological shapes of the pelvic pecten pubis and the outer fundus vesicae and the spatial form of the abdominal cavity of a typical person, and the intra-pelvic fundus vesicae support of a frame structure and medical material quality is obtained using 3-D printing technologies. Before a surgery is conducted, a virtual reality technology is used to simulate and verify a surgical safety scheme.

Abstract: A device to prevent urinary leakage intended to be implanted in a patient includes a compressor to compress the patient's urethra, an electronic controller to actuate the compressor, and a measurer to measure the patient's activity. The measurer is coupled with the controller and the controller functions according to a predictive model of urinary leakage based on patient activity, so as to anticipate a possible urinary leak in relation to the measured activity of the patient.