Abstract: An X-ray imaging system includes a gantry with moving and stationary parts on moving and stationary sides, respectively, the parts communicatively coupled via a data communication system. The moving part includes an X-ray source to emit X-rays; an X-ray detector configured to generate detector data; and on-moving-gantry processing circuitry. The on-moving-gantry processing circuitry is configured to determine, for each of a number of partial data sets of the generated detector data, a metric value of at least one metric, the metric value being translatable into a type of data management for the partial data set among at least two different types of data management. The processing circuitry further configured to decide, for each partial data set, how it set is to be treated based on the determined metric value of the at least one metric and to selectively effectuate data management according to the corresponding type of data management.

Abstract: The present invention relates to a system (1010) for X-ray dark field, phase contrast and attenuation image acquisition, the system comprising: an X-ray source (1020); an interferometer arrangement (1030); an X-ray detector (1040); a control unit (1050); at least one vibration transducer (1080); a processing unit (1090); and an output unit (1060). An axis is defined extending from a centre of the X-ray source to a centre of the X-ray detector. An examination region is located between the X-ray source and the X-ray detector, wherein the axis extends through the examination region, and wherein the examination region is configured to enable location of an object to be examined. The interferometer arrangement is located between the X-ray source and the X-ray detector, and wherein the interferometer arrangement comprises a first grating (1032) and a second grating (1034).

Abstract: A quantitative analysis method for cardiac motion, and an ultrasonic system, said method comprising: emitting an ultrasonic wave to a target heart; receiving an ultrasonic echo returned from the target heart; determining an ultrasonic image of the target heart according to the ultrasonic echo; acquiring an area of interest in the ultrasonic image; and tracking the motion of the area of interest, so as to acquire torsion parameters of the target heart and the confidence of the torsion parameters. The present invention performs quantitative analysis on the torsion motion of the heart, and also provides the confidence of the analysis result, that is, quantitative evaluation is also performed on the analysis result, assisting the physician in making a more accurate cardiac function evaluation.

Abstract: An non-Doppler flow imaging system is disclosed that overlays a B-flow imaging sequence over B-mode ultrasound image data.

Abstract: The present invention relates to a system for indicating a position of an interventional device feature (11a) of an interventional device (11) respective an image plane (12) defined by an ultrasound imaging probe (18) of a beamforming ultrasound imaging system (15) in which the position of the interventional device feature (11a) is determined based on ultrasound signals transmitted between the ultrasound imaging probe (18) and an ultrasound transducer (16) attached to the interventional device at a predetermined distance (Lp) from the interventional device feature (11a). An icon providing unit (IPU) provides a first icon (Cde) indicative of a circular zone with a radius corresponding to the predetermined distance (Lp). The first icon (Cde) is displayed in a fused image that includes a reconstructed ultrasound image (RUI) from the beamforming ultrasound imaging system.

Abstract: Methods and systems are provided for evaluating a subject for a liver disease using ultrasound images. In one example, a method includes, in response to a request to evaluate the liver disease, determining, with a measurement model, that a selected medical image frame of the subject includes a target anatomical view and has an image quality above a threshold image quality, and in response, measuring, with the measurement model, a marker for the liver disease in the selected medical image, and outputting, for display on a display device, the measurement of the marker.

Abstract: The invention relates to a method of identifying, from a number of ultrasound images (34) acquired during an ultrasound examination of a subject (6), the ultrasound image best suited to analyze a pre-determined anatomical structure of the subject. The method comprises the steps of (a) Providing a number of ultrasound images (34) acquired during an ultrasound examination of the subject; (b) Deriving at least one biometric parameter (96) related to the anatomical structure from a physical examination of the subject, (c) Retrieving a reference image (38) showing a target view of the anatomical structure (35); (d) For each of the number of ultrasound images (34), calculating an image similarity index between the ultrasound image and the reference image, (e) For at least the ultrasound image(s) having the best image similarity index, determining (100) a biometric parameter from the ultrasound image, and calculating a biometric similarity index, i.e.

Abstract: The invention provides a handheld imaging device capable of performing biplane imaging, wherein a first image plane or a second imaging plane (having different orientations) may be selected for image capture based on a motion characteristic of the device as determined by a sensor.

Abstract: A spiral ultrasonic tomography imaging method and system are provided. The method is to use synchronous rotation of an ultrasonic probe or cyclic switching of emission array elements in the ultrasonic probe under the premise of a uniform displacement of the ultrasonic probe along the Z axis, so that the change trajectory of the positions of emission array elements over time in a three-dimensional space at each ultrasonic emission time is distributed along a spiral line or a curve. During the process of the uniform displacement of the ultrasonic probe along the Z axis, the ultrasonic probe emits ultrasonic waves and receives and collects echo data. The collected echo data is stored and post-processed to realize ultrasonic tomography imaging of an object. The spiral ultrasonic tomography three-dimensional scanning method and the corresponding system realize rapid continuous uninterrupted data acquisition to ensure that higher spatial resolution in the Z-axis direction.

Abstract: A device (100) and method for adhering by suction to a target surface (200). The device has a substrate (20) with a contact surface (20a) for contacting the device (100) to the target surface (200). A plurality of pocket (10) are formed by respective pocket surfaces (10a) concavely extending into the contact surface (20a). The pockets (10) have an open side (10b) facing and being closed off by the target surface (200). A flexible membrane (15) forms at least part of the pocket surface (10a). An actuator (40) is configured to actuate the flexible membrane (15). A one-way valve (30) through the pocket surface (10a) is configured to direct a contents of the pocket (10) via the one-way valve (30) to an environment (300).

Abstract: Methods may be provided to operate an imaging system using a contact imaging probe to generate imaging of a body. A robotic actuator may be controlled to position the contact imaging probe at a first location on a surface of the body such that the contact imaging probe is in a first radial alignment with an imaging isocenter. The robotic actuator may then be controlled to position the contact imaging probe at a second location on the surface of the body such that the contact imaging probe is in a second radial alignment with the imaging isocenter. Moreover, the first and second radial alignments may be different.

Abstract: Systems, apparatuses, methods, and non-transitory computer-readable media for mapping a section of a vasculature of a subject are described herein, including moving a probe to a first position at a body of the subject adjacent the section of the vasculature; transmitting, by the probe, a first ultrasound beam into a first portion of the section of the vasculature through the body of the subject; receiving first ultrasound data including at least one imaging parameter of the first portion based on the first ultrasound beam; moving the probe to a second position at the body of the subject adjacent the section of the vasculature and different from the first position; transmitting, by the probe, a second ultrasound beam into a second portion of the section of the vasculature through the body of the subject; receiving second ultrasound data including the at least one imaging parameter of the second portion based on the second ultrasound beam; and constructing a map of the section of the vasculature based on the fi

Abstract: A system for detecting/quantifying the conductance of a right-to-left cardiac shunt includes a mouthpiece assembly, a solenoid-driven vacuum/pressurization assembly; a controller for operating the solenoid-driven vacuum/pressurization assembly; and a monitor for displaying the instructions from the controller. A microbubble counting cell and digital image sensor are combined with software-based image analysis to determine a number of microbubbles contained in a microbubble counting zone. A monitor enables operator specification of total volume of contrast agent to be injected into the patient. One or more first Doppler ultrasound transducer arrays are positioned adjacent to targeted intracranial arteries at one side of the skull or a pair of first Doppler ultrasound transducer arrays positioned adjacent to targeted intracranial arteries at both sides of the skull.

Abstract: An ultrasound imaging system transmits two beams in succession in the same beam direction, the waveform of the second beam being a phase inverted form of the first waveform, and each waveform containing first and second major frequency components. Echoes are received from along the beam direction in response to each beam transmission, and are processed by additively and subtractively combining the two echo sequences on a common depth basis. The echo components resulting from this processing extend from high frequencies for good near field resolution to low frequencies for good depth penetration, and include fundamental, harmonic, and sum or difference frequency components. The linear and nonlinear echo signal components may be frequency compounded for speckle reduction.

Abstract: A brace for retaining an organ in an expanded state configured to adhere and substantially conform to an external surface of the organ includes an inner layer, an outer layer, and at least one sheet of thin malleable material forming a middle layer between the inner layer and outer layer, the at least one sheet being enclosed and configured to rigidify and maintain the organ in an expanded state upon application of a vacuum. The brace can be incorporated into a brassiere.

Abstract: A spinal construct includes a first member having a first thread form and an implant cavity configured for disposal of the spinal implant. A second member is engageable with a spinal implant and includes a second thread form configured for engagement with the first thread form. A gauge is coupled to the second member. The gauge is configured to measure a force between the second member and the spinal implant when the second member is engaged with the first member. The second thread form is timed with the first thread form to position the gauge in a selected orientation relative to the spinal implant. Systems and methods are disclosed.

Abstract: A biopsy site marker includes a carrier and a marker element. The marker element is disposed within the carrier. The carrier including a first marker material and a second marker material. The first marker material and the second marker material are each configured to expand in the presence of moisture. The first marker material is configured to expand at a rapid rate relative to the second marker material in the presence of moisture.

Abstract: A medical device system includes: an auxiliary rail including a frame and a flange extending from the frame; and a surgical arm mounting device including a coupler and a surgical arm interface. The frame is configured to be mounted on a side rail of an operating table. The coupler includes a clamp for the flange of the auxiliary table rail. The clamp of the coupler has a first mechanical state in which the mounting device is fixed to the auxiliary rail and a second mechanical state in which the mounting device is translatable along the auxiliary rail. The surgical arm interface receives a mating mounting device interface of a surgical arm.

Abstract: A method of reprocessing a surgical instrument that includes a handpiece having opposed shells secured together with a fastener, a shroud secured to the handpiece and overlaying the fastener and a portion of the handpiece, an outer shaft extending from the shroud and defining a cutting window, and a cutting shaft movable within the outer shaft and including a cutting tip for resecting tissue within the cutting window is disclosed. The method includes mutilating the shroud so as to remove the shroud from the handpiece, removing the fastener, separating the opposed shells to access an interior of the handpiece, servicing or replacing at least one component within the interior of the handpiece, securing the opposed shells to one another with the fastener or another fastener, and securing a replacement shroud to the handpiece.

Abstract: A customized resorbable three-dimensional scaffold for oral and maxillofacial bone grafting involves merging two sets of three-dimensional information obtained from a patient, the first set includes three-dimensional bone information and the second set includes three-dimensional teeth and tissue information. The merged information is used to generate a three-dimensional shape of the bone to be regenerated, a three-dimensional position of the missing tooth/teeth, and a three-dimensional model of the customized resorbable three-dimensional scaffold for oral and maxillofacial bone grafting. The three-dimensional model is used to generate the customized resorbable three-dimensional scaffold and resorbable connectors for the customized resorbable three-dimensional scaffold.

Abstract: Removable denture data of a removable denture is produced, and disk frame data of a disk frame in which the removable denture is accommodated is produced, thereby building the disk frame based on the disk frame data. Next, a resin disk in which artificial teeth are embedded is produced by arranging the artificial teeth in the disk frame and curing a base resin, and a denture base is milled by milling the resin disk based on the removable denture data, thereby manufacturing the removable denture in which a base side of the artificial teeth is embedded in the denture base. As a result, artificial teeth having an excellent aesthetics may be used, it is possible to firmly join the artificial teeth and the denture base to each other, and it is possible to manufacture a removable denture with a favorable restoration accuracy of the artificial teeth.

Abstract: An apparatus includes a toothbrush head configured to brush teeth, an appliance brush configured to brush a dental appliance, and a body configured to be releasably coupled with either one of the toothbrush head and the appliance brush such that the appliance brush and the toothbrush head are interchangeable. The body includes a vibration component configured to vibrate the toothbrush head or the appliance brush head when coupled with the body. When the appliance brush is coupled with the body, a greater portion of the body is exposed than when the toothbrush head is coupled with the body.

Abstract: A system and method for sealing and isolating an area of an intra-oral cavity using a rubber dental dam is provided. The rubber dental dam is sized to isolate and seal a partial area of the intraoral cavity, such as a lower half or an upper rear quadrant of the intraoral cavity. The rubber dental dam includes a saliva ejector port for allowing suction to remove fluids from the area.

Abstract: A dental matrix system enabling back-to-back tooth cavity fillings to be less tedious and more efficient. A wedge attached to a matrix band that is designed to be inserted between two teeth and then expanded into position on opposing sides of a tooth so a ring can be placed. The device is inserted perpendicular to the biting/occlusal surface of the tooth or teeth identified for repair. The folded/bonded band is dropped down between the teeth. The matrix consisting of the matrix band and the end tail section of the wedge is pushed between the teeth. The bond between the two halves of matrix band is broken. The matrix band is folded into an open position. A ring is then placed over the device with the tips of the ring aligned inside the open geometry of the folded matrix band or outside of the matrix band after being folded in.

Abstract: Dental attachment placement templates and dental appliance systems. The dental attachment placement templates may include a body configured to position a dental attachment over an attachment site on a surface of a tooth. The body may include an aperture, supports that extend from the body within the aperture, a connection member that connects the dental attachment to the supports, and a contoured surface shaped to register with one or more teeth. The connection member may be integrally formed with the dental attachment to provide a unitary structure. The connection member may be joined to the dental attachment at a breakable single point of connection and being further joined to the supports such that when the single point of connection is broken, the dental attachment is detached from the supports.

Abstract: A zygomatic dental implant includes a generally cylindrical body, an interior threaded bore, and an asymmetrical external feature. The generally cylindrical body has a coronal portion and an apical portion. The generally cylindrical body has a main-central axis. The interior threaded bore is formed in the coronal portion of the generally cylindrical body for receiving a screw configured to removably hold an abutment in engagement with the zygomatic dental implant. The interior threaded bore has a bore-central axis. The asymmetrical external feature is on at least a portion of a first side of the generally cylindrical body such that the asymmetrical external feature is configured to directly engage alveolar bone of the patient. The asymmetrical external feature includes a plurality of circumferentially extending grooves.

Abstract: Disclosed are a scan guide providing method and an image processing device therefor. A scan guide providing method according to an embodiment comprises the steps of: displaying, on a scan screen, a guide scan path for providing a scanning strategy of an intraoral scanner; tracking a user scan path actually scanned, along the guide scan path, by the intraoral scanner; and displaying the tracked user scan path together with the guide scan path.

Abstract: A dog toothbrush assembly has two plastic end caps with blind cavities that face one another and receive an elongated generally cylindrical chew element which is attractive to dogs such as an edible treat or other chewable material. The end caps are connected by screw fasteners to the support member of a brush, and an array of tufts of bristles project upwardly from the support member to engage the elongated chew element. The chew element is supported with respect to the bristles such that when a dog chews on the chew element the dog's teeth also encounter and are brushed by the bristles. When the chew element is worn or consumed, an end cap is removed by releasing one of the screw fasteners, thereby giving access for insertion of a replacement chew element.

Abstract: Systems and methods for occluding a duct and attenuating sound may be provided. In some embodiments, a device for attenuating sound passing through a duct or orifice may include a body sized and shaped to be inserted, at least partially, into a duct or orifice. The body may have an interior volume that contains a fluid suspension. In some embodiments, the fluid suspension may include a plurality of gas-filled spheres dispersed in an interstitial fluid. The gas-filled spheres may increase an acoustic attenuation of the fluid suspension relative to the interstitial fluid alone.

Abstract: Earmuffs include a bowl-shaped housing base having a first engagement portion, an annular plate-shaped base plate having a second engagement portion on one side and a third engagement portion on the other side, and is integrated with the housing base by causing the second engagement portion to be engaged with the first engagement portion, and a pad portion that includes a pad fixed on one side and a pad base having a fourth engagement portion on the other side, and is integrated with the base plate by causing the fourth engagement portion to be engaged with the third engagement portion. The base plate has a groove portion adjacent to the third engagement portion and the pad base has a rib that enters the groove portion. The rib enters the groove portion and restricts an inclination of the third engagement portion involved with an engagement with the fourth engagement portion.

Abstract: Some embodiments of the present disclosure relate to a wound packing material, suitable for use in negative pressure wound therapy, comprising a body of a porous material, the body comprising frangible regions defining a plurality of portions, the frangible regions allowing the portions to be selectively removed from the body. The wound packing material can be shaped to partially or fully surround a secondary wound packing member, such as a stabilizing structure. Some embodiments further relate to methods of manufacturing the wound packing material, and to methods of its use.

Abstract: This disclosure includes wound dressings and systems with remote oxygen generation for topical wound therapy and related methods.

Abstract: Ultrasonic welding is performed by passing a first sheet layer, a second sheet layer, and an elastic film interposed therebetween in a stretched state in a machine direction between an anvil roll having a large number of protrusions and an ultrasonic horn. The anvil roll includes a region having the protrusions and in the region. A site, in which welding is performed by one ultrasonic horn, has a portion in which an area rate of the protrusions changes in a roll circumferential direction and a roll length direction. A difference between a maximum value and a minimum value in a change of the area rate of the protrusions in the roll circumferential direction is 4.5% or less, and a difference between a maximum value and a minimum value in a change of the area rate of the protrusions in the roll length direction is 1.5% or less.

Abstract: A folding device for a disposable hygiene article includes: a first conveying portion along a first path; a second conveying portion along a second path extending in a direction intersecting with the first path; a folding mechanism to fold the disposable hygiene article between the first and second conveying portions; a driving mechanism connected to the folding component, to drive the folding component by performing reciprocating linear motion along the direction of the second path between a folding and retracted positions; and a guiding mechanism in an extension direction of the first path or by using the first path as a reference, a front end portion of the article to an opposite side of the second conveying portion. The driving mechanism includes at least one pulley directly connected to a servo motor and a synchronous belt wrapped around the outer circumference of the pulleys in a looping path.

Abstract: A tampon applicator assembly is disclosed. The applicator assembly may include a barrel portion, a grip portion and an ejection plunger configured to slide coaxially within one or both the barrel portion and the grip portion. One or more of the barrel portion, grip portion and ejection plunger may be molded from a molding composite comprising cellulose fibers.

Abstract: The diaper of the present invention is a fixed flat cloth diaper. The diaper is ‘fixed’, because an outer layer of the diaper resembles the final format of a flat, rectangular cloth diaper having been folded origami style into a shape suitable for donning on a wearer by a user. The outer layer functions primarily to retain the diaper upon the wearer and has a stomach panel for obtaining a good closure of the diaper on the wearer. The diaper is ‘flat’, because an inner layer of the diaper is attached to the outer layer, and the inner layer is a flat, rectangular shape which is customizable for absorbency and can be folded into a flat insert configuration of the user's choice prior to donning the diaper on the wearer. The inner layer functions primarily to absorb waste (urine and feces) excreted by the wearer.

Abstract: A disposable absorbent pant having a front belt portion and a rear belt portion is disclosed. The front and rear belt portions are joined at side seams and the rear belt portion has a greater length than the front belt portion. A lower edge of the rear belt portion forms at least in part edges of left and right leg openings to the rear of the side seams. The rear belt portion includes first and second layers of nonwoven web material sandwiching a plurality of laterally extending and laterally pre-strained elastic strands, disposed below the side seams. A first of the plurality of elastic strands differs from a second of the plurality of elastic strands by one or more of amount of pre-strain, tensile modulus, decitex, and combinations thereof.

Abstract: An apertured nonwoven web is provided. The apertured nonwoven web comprises carded fibers, a first side, and a second side. The apertured nonwoven web defines a plurality of apertures therein. The apertures may each have a first side aperture size and a second side aperture size, and a ratio of the first side aperture size to the second side aperture size may be between about 1.15:1 to about 1:1.15. The plurality of apertures may have an aperture size regularity of about 1% to about 15%. The plurality of apertures may have an aperture shape regularity between about 1% to about 12%.

Abstract: The present disclosure relates to a nonwoven substrate comprising a plurality of apertures that form a pattern and define a plurality of discrete non-aperture zones. Each of the plurality of discrete non-aperture zones has a periphery formed by a continuous line of apertures, with adjacent apertures being spaced apart by an edge-to-edge distance of no more than 3 mm, while each of the plurality of discrete non-aperture zones is substantially free of apertures within the periphery. Particularly, the area ratio of such plurality of discrete non-aperture zones over the nonwoven substrate ranges from 60% to 90%, and at least some of said plurality of discrete non-aperture zones have an area of 100 mm2 or more.

Abstract: An absorbent article comprising a liquid permeable topsheet, a backsheet, an absorbent core comprising an absorbent material and a core wrap is provided. The core comprises at least one channel-forming area that is substantially free of absorbent material. The absorbent article comprises a masking layer between the bottom side of the core wrap and the backsheet. The masking layer and the bottom side of the core wrap are only partially bonded to each other at their interface, the interface thus comprising a bonded portion and an unbonded portion, wherein the channel-forming area at least partially corresponds to the unbonded portion of the interface, so that when the absorbent material swells, the masking layer can decouple from the three-dimensional channels.

Abstract: A garment having a fabric body and an absorbent pad attached to the fabric body is disclosed. The absorbent pad includes a liquid impermeable barrier layer and a functional layer attached to the barrier layer. The functional layer has a wicking component and a liquid absorbent component. The liquid absorbent component is disposed between the wicking component and the barrier layer. The absorbent pad is washable and reusable.

Abstract: An incontinence clamping device has been presented herein. The incontinence clamping device comprises an upper clamp arm having a stopper and a bottom clamp arm having a locking component with a plurality of interlocking gaps. The incontinence clamping device further comprises a top and a bottom stabilizer having a plurality of zig-zag portion including at least one or more elevated and one or more non-elevated portions. The incontinence clamping device further comprises an upper silicone fitting that is used for accommodating the top stabilizer and a bottom silicone fitting that is used for accommodating the bottom stabilizer. The incontinence clamping device in its closed state allows for delivery of different pressures to urethra and corpus spongiosum as a function of various sizes of penises in a flaccid state.

Abstract: Apparatus for delivering a surgical mesh, the apparatus comprising: a hollow outer tube having a distal end and a proximal end; a distal housing mounted to the distal end of the hollow outer tube; a hollow inner tube having a distal end and a proximal end, wherein the hollow inner tube is slidably disposed within the hollow outer tube; a central rod having a distal end and a proximal end, wherein the central rod is slidably disposed within the hollow inner tube; an actuation element mounted to the proximal end of the central rod; and a surgical mesh carriage comprising a plurality of legs, wherein each of the plurality of legs comprises a first hinged end mounted to the distal end of the hollow inner tube and a second hinged end mounted to the distal end of the central rod.

Abstract: Described herein are devices, systems, and methods for modifying blood flow and improving tissue oxygenation in an individual. More specifically, described herein are flow modifying implants, delivery systems, and methods of treatment using flow modifying implants. Also described herein are methods for preventing reperfusion injury in an individual using a flow modifying implant to prevent the reperfusion injury.

Abstract: A transcatheter growth device for treating congenital illnesses in infantile and other pediatric heart disease patients and methods for making and using the same. The growth device includes an elongated device frame with alternating annular growth cell members and spacing members that axially span proximal and distal end regions of the device frame. The growth cell members and spacing members define a radial periphery for the growth device. Each growth cell member can comprise a scaffolded growth cell member with first and second annular strut arrangements coupled via a growth cell junction to provide device frame flexibility. A retention member for engaging a selected lumen within a patient and a covering member for sealing the growth device, when deployed, are disposed at the device periphery. The growth device advantageously can be deployed for treating heart disease alone or in combination with one or more additional growth devices.

Abstract: A system for treating aortic dissection includes a sinotubular junction magnetic array having a first plurality of magnetic elements, a counter-magnetic array having a second plurality of magnetic elements, and an ascending aortic stent graft comprising a third plurality of magnetic elements. A method for treating aortic dissection includes the steps of positioning a sinotubular junction magnetic array at the sinotubular junction, advancing counter magnetic constructs from the femoral vein and positioning them in the right atrium, expanding the sinotubular junction ring at a target position, advancing the counter magnetic array to form an at least partial circumferential seal, and advancing and positioning an ascending magnetic graft within an interior of the sinotubular junction magnetic array. A system for treating aortic dissection, a fixation device for anchoring an ascending aortic stent graft, and a transcatheter device for treating aortic dissection are also described.

Abstract: A stent-graft comprises: a graft defining an elongate lumen having a longitudinal axis; an external stent having a plurality of struts and apices between the struts, the apices including proximal apices and distal apices; a set of proximal sutured knots, the proximal sutured knots securing the proximal apices of the stent to the graft; a set of distal sutured knots, the distal sutured knots securing the distal apices of the stent to the graft; and a plurality of intermediate sutured knots, formed along a continuous suture, the continuous suture including a plurality of bridging portions, the bridging portions bridging between neighbouring struts of the stent, the intermediate sutured knots securing struts of the stent to the graft.

Abstract: The present invention relates to a mesh or membrane covering (2) based on biological material, for example collagen, or biosynthetic material for prostheses (1), in particular for a breast prosthesis (1), said prosthesis (1) having a rear surface that, when applied, is faced towards the person on whom (1) is applied, said covering (2) being characterized in that it provides a fixing system (4; 3) for fixing to said prosthesis (1), said fixing system providing a plurality of teeth or petals (4) or outer perimeter edge foldable on said rear surface of the prosthesis (1) by means (5). The invention further relates to a method for fixing said covering to a prosthesis, a prosthesis comprising said covering and a process for making said covering.

Abstract: In some embodiments, a method for controlling an artificial iris may include receiving a measurement of light intensity detected by a sensor on or adjacent to the artificial iris. The method may include accessing a user-specific profile based on user calibration for determining one or more user-specific thresholds of light intensity of the user-specific profile. The one or more user-specific thresholds are associated with light intensities for triggering a change of light transmittance through the artificial iris. The method may include comparing the received measurement of light intensity to the one or more thresholds in the user-specific profile. The method may include determining, based on the comparing, whether to turn on or turn off one or more concentric rings of liquid crystals of the artificial iris for controlling an amount of light transmitted through the artificial iris.

Abstract: There is disclosed a surgical device comprising a handle (14) for releasable attachment to a cartridge (1) adapted to hold an endothelial corneal implant in a scrolled or double coiled configuration. The handle has a forward end for releasable attachment to the cartridge, a rearward end and a gripping portion (60) between said forward and rearward ends. The gripping portion is substantially planar so as to facilitate being gripped between finger and thumb. The handle incorporates a first flexible fluid conduit (61) for releasable fluid connection to the cartridge at the forward end of the handle. There is further disclosed a surgical device comprising a handle having a forward end and a rearward end and a gripping portion between said forward and rearward ends. The gripping portion is substantially planar so as to facilitate being gripped between finger and thumb.