Abstract: An ostomy appliance (20) including a sealing wafer (22) with a first adhesive (32) having a first opening (34) configured to be attached to a skin surface around an ostomy of a user, and a bag (36) for collecting stomal output that includes a second adhesive (44) configured to engage with the skin surface radially outside of the sealing wafer. The sealing wafer and the bag are configured to be connectible to each other either in direct connection or by a coupling interface. One kind of coupling interface includes one or more pipe sections (50). The ostomy appliance allows for differentiation of adhesive types for different purposes, such as sealing and load carrying.

Abstract: Disclosed is a base plate for an ostomy appliance and a method for manufacturing a base plate. The base plate comprising: a top layer; a first adhesive layer; an electrode assembly comprising a plurality of electrodes, the electrode assembly having a first part and a second part, the first part comprising connection parts of the plurality of electrodes, the second part being arranged between the first adhesive layer and the top layer; and a monitor interface configured for connecting the base plate to a monitor device, the monitor interface comprising a plurality of terminals configured to form electrical connections with respective terminals of the monitor device. The top layer comprises a top layer opening configured to allow for connection between the plurality of electrodes of the electrode assembly and terminals of the monitor device.

Abstract: A base plate and/or a sensor assembly part for an ostomy appliance is disclosed, the base plate and/or the sensor assembly part comprising a first adhesive layer with a proximal side configured for attachment of the base plate and/or the sensor assembly part to the skin surface of a user, the first adhesive layer having a stomal opening with a center point; and a plurality of electrodes including a ground electrode, a first electrode, and a second electrode, the ground electrode comprising a ground connection part, the first electrode comprising a first connection part, and the second electrode comprising a second connection part; wherein the ground electrode forms a ground for the first electrode and the second electrode.

Abstract: An ostomy system configured to detect moisture content in a base plate or a sensor assembly part of the ostomy system, the ostomy system comprising the base plate and/or a sensor assembly part and a monitor device. The base plate or the sensor assembly part includes a first adhesive layer, a plurality of electrodes, and one or more sensing zones each covering one of one or more regions of the first adhesive layer, each of the one or more sensing zones including at least two of the plurality of electrodes. The monitor device is electrically coupled to the plurality of electrodes of the base plate or the sensor assembly part and configured to measure one or more resistances in the one or more sensing zones between the plurality of electrodes, each of the one or more resistances measured by two of the plurality of electrodes at one of the one or more sensing zones, and determine moisture content of the first adhesive layer at each of the one or more sensing zones based on the measured one or more resistances.

Abstract: The disclosure relates to a system for determining and signalling moisture propagation in an adhesive material layer of a base plate and/or a sensor assembly part for an ostomy appliance. The disclosure further relates to aspects of a base plate and/or a sensor assembly part for an ostomy appliance and its use in such a system.

Abstract: The present hernia belt ostomy support system is designed to provide support to a hernia and house a medical device (e.g., an ostomy appliance) within a compartment, wherein the device is comfortable, supportive, inconspicuous, and aesthetically pleasing.

Abstract: A method of therapy for a tumor or other pathology by administering thermotherapy or a combination of thermotherapy and immunotherapy optionally combined with gene delivery. The combination therapy beneficially treats the tumor and prevents tumor recurrence, either locally or at a different site, by boosting the patient's immune response both at the time of original therapy and/or for later therapy. The therapy may further include the administration of a vaccine.

Abstract: Systems for maintaining normothermia in a patient via compression and warming are disclosed and include a first warming element configured to apply warming to the popliteal fossa, a second warming element configured to apply warming to the sole of the foot, and a compression element configured to apply compression to the calf.

Abstract: A contact lens (318,400,500,600) may include a contact lens body (402), an exterior contact surface (322,404), and an annular bifocal surface (326,408). The contact lens (318,400,500,600) may be configured for use in a contact lens assembly (300) for laser-based ophthalmological surgical treatments. The exterior contact surface (322,404) may be on a first end of the contact lens body (402). The exterior contact surface (322,404) may be configured for direct physical contact with a cornea (102) of an eye (100) of a patient. The annular bifocal surface (326,408) may be on a second end of the contact lens body (402). The second end may be opposite the exterior contact surface (322,404). The annular bifocal surface (326,408) may include a central portion (347,412,502,602). The central portion (347,412,502,602) may include a first focal distance. The annular bifocal surface (326,408) may include an outer portion (349,414,504,604) that surrounds at least a portion of the central portion (347,412,502,602).

Abstract: Micro-droplet delivery devices and methods are described where the device may comprise a piezoelectric actuator having a piezoelectric chip that is operatively coupled to a drug package under a preloading force. The actuator is configured to generate an acoustic pressure within the drug package to dispense droplets of an agent from an aperture, e.g., to the corneal surface of the eye. The piezoelectric actuator can be coupled or decoupled from the drug package.

Abstract: The present disclosure provides a system and method for maintaining the position of a suction cone on an eye during laser ophthalmic surgery that includes determining a distance and direction the suction cone or a support must be adjusted to maintain the position of the suction cone within an optimal working range, based on a detected position of the suction cone. The disclosure further provides a method for maintaining the position of a suction cone by determining a distance and direction the suction cone or a support must be adjusted to maintain the position of the suction cone within an optimal working range, based on a detected position of the suction cone. In the system and the method, a control signal is generated to adjust the position of the suction cone and/or the support to maintain the suction cone within the optimal working range.

Abstract: An ophthalmological patient interface apparatus, having a coupling apparatus for mechanically coupling to an application head of an ophthalmological laser system, comprises a lens-element system which is arranged between the eye and the application head in the state coupled to the application head during the treatment of an eye, said lens-element system being coupled into the beam path from the projection lens to the eye. The lens-element system is configured to image a first focal area of the projection lens disposed upstream of the lens-element system in the beam path onto a second focal area in the eye disposed downstream of the lens-element system in the beam path, in such a way that a laser beam focused onto the first focal area by the projection lens causes tissue processing in the second focal area in the eye.

Abstract: An eye drop alignment assembly includes a ring that has a bottle of eye drops being extendable therethrough. The ring has a plurality of engagements thereon and the engagements are spaced apart from each other and are positioned at strategic points around the ring. A plurality of legs is each movably coupled to a respective one of the engagements. A plurality of extensions is each pivotally coupled to a respective one of the legs. Each of the extensions is positionable at a selected angle with respect to the respective leg for aligning with a respective top and bottom eyelid. Additionally, each of the extensions spaces the ring away from the eyeball associated with a top and bottom eyelids. In this way the ring aligns the bottle of eye drops with the eyeball for successfully dispensing eye drops onto the eyeball.

Abstract: The present disclosure is directed to medical devices and methods of manufacturing medical devices, such as an ophthalmologic medical device.

Abstract: Systems and methods are disclosed comprising an ultrasonic handpiece having a housing, a working tip extending from the distal end of the housing, and a crystal and horn assembly positioned within the housing. The proximal end of the ultrasonic horn is free to move relative to the housing. In embodiments, the ultrasonic horn is resiliently suspended within the housing, with no rigid fixation points. The ultrasonic horn may be resiliently suspended by one or more resilient rings at the proximal end of the ultrasonic horn and by one or more resilient rings at the single nodal region of the ultrasonic horn. The ultrasonic handpiece may include a pumping module located at the proximal end of the handpiece.

Abstract: An inserter for treating glaucoma can comprise a housing, a needle, a plunger, a slider component, and a drive component. The drive component is disposed within a cavity of the housing and rotatable within the cavity to result in movement along a longitudinal axis of the inserter to the needle and the plunger upon rotation of the drive component. The slider component is coupled to the housing and slidable along an elongate groove of the drive component such that movement of the slider component along the axis rotates the drive component within the housing.

Abstract: A hearing protector having an ear cup forming a space for a wearer's ear. The ear cup has a shell with an ear facing inner side and a passageway extending through the shell between the ear facing inner side and an outer side of the shell. The ear cup further has a loudspeaker assembly which seals the passageway from the outer side. The loud speaker assembly further has a seal member and a loudspeaker module. A portion of the seal member is arranged between the shell and a fastener, and the fastener retains the loudspeaker assembly at the shell. The hearing protector facilitates manufacturing and maintenance and provides for maximize wearing comfort and technical reliability.

Abstract: A dressing for treating a tissue site with negative pressure, a sealing tape, methods of use and methods of manufacturing the sealing tape are described. The dressing includes a tissue interface configured to be positioned adjacent to the tissue site and a sealing member configured to be positioned over the tissue interface and the tissue site to form a sealed environment. The dressing also includes a sealing tape having a carrier layer having a first side and a second side, a silicone adhesive layer bonded to the first side of the carrier layer, and an acrylic adhesive layer bonded to the second side of the carrier layer. A plurality of holes extend through the silicone adhesive layer, the acrylic adhesive layer, and the carrier layer. A first release liner is coupled to silicone adhesive layer, and a second release liner is coupled to the acrylic adhesive layer.

Abstract: The present application provides a negative pressure wound dressing, including foam and a bio-cellulose film with a three-dimensional reticular structure formed on a surface of the foam, wherein a projected area of the bio-cellulose film on a bonding surface of the foam and the bio-cellulose film is greater than or equal to that of the foam. The presence of the bio-cellulose film between the foam and a wound avoids the foam from sticking to the wound and the growth of new tissue into the foam when performing a negative pressure wound therapy. Also, when replacing the foam, a secondary damage to the wound is reduced, so as to relieve pain that the patient suffers.

Abstract: The present invention relates to wound dressings for use in cases of a patient suffering a penetrating chest trauma. The wound dressing comprises a base layer having a lower surface facing the wound and an upper surface facing away from the wound, and an aperture therethrough for locating over the wound, and a top layer extending over the aperture and at least a part of the upper surface. The base layer is connected to the top layer such that the wound dressing can transition from an open configuration in which the aperture and an area external to the wound dressing are in fluid communication via at least one opening at a perimeter between the base layer and the top layer, to a closed configuration in which the top layer forms a seal over the aperture.

Abstract: A conformable adhesive bandage is disclosed including a central body, a plurality of bandage limbs including an adhesive coating disposed on a first side of the conformable adhesive bandage, and a plurality of flexion sites, each of the plurality of flexion sites inflecting inward into the central body or the plurality of bandage limbs. In one embodiment, the plurality of flexion sites is disposed at a plurality of vertices along the central body between adjacent bandage limbs of the plurality of bandage limbs, the plurality of flexion sites inflecting radially inward at the plurality of vertices into the central body. In another embodiment, is the plurality of flexion sites includes a plurality of central body flexion sites disposed at a plurality of vertices along the central body between adjacent bandage limbs, and a plurality of bandage limb flexion sites disposed along at least one of the plurality of bandage limbs.

Abstract: A wound therapy system includes a dressing sealable over a wound and defining a wound space between the dressing and the wound, tubing fluidly communicable with the wound space, and a canister fluidly communicable with the tubing. The canister, the tubing, and the dressing define a sealed space that includes the wound space. The wound therapy system also includes a therapy unit coupled to the canister. The therapy unit includes a sensor configured to measure a pressure in the sealed space, a valve positioned between the sealed space and a surrounding environment and controllable between an open position and a closed position, and a control circuit. The control circuit is configured to control the valve to alternate between the open position and the closed position to allow airflow through the valve, receive measurements from the sensor, and determine a volume of the wound space based on the measurements.

Abstract: Methods of debriding a wound include applying a wound debridement material in frictional contact across at least a portion of a wound surface of a patient and removing tissue from the wound surface via adherence of the tissue to the wound debridement material without leaving solid debris of the wound debridement material on the wound surface after the application of the wound debridement material. A wound debridement material comprising a solid porous foam soaked by a fluid suitable for use in such methods is also provided.

Abstract: An applicator for a tampon is provided. The applicator has an inner tube and an outer tube and the inner tube is slideable within the outer tube. The applicator has a forward end, and the inner surface of the outer tube has an annular protrusion near to the rear end of the outer tube. The internal diameter of the outer tube is smaller rearward of the annular protrusion than forward of the annular protrusion.

Abstract: An applicator for a tampon comprising an inner tube and an outer tube is provided. The inner tube is slideable within the outer tube and the applicator has a forward end. A plurality of petals are provided at the forward end of the inner tube and at least one protrusion is provided at the base of each petal. Each protrusion extends in a radially outward direction from the outer surface of the inner tube.

Abstract: Cleaning and disinfection stick is designed in the manner of a nylon toothpick. In contrast to a toothpick, it is arcuate over its length, wherein straight embodiments are also possible. It tapers from its remaining diameter into a fine tip in at least one of its ends regions. Adjacent to the fine tip, the stick can include a round brush. Alternatively, it can also include a felt-like, textile or fluffy surface or be provided with a rod-like paper or plastic attachment. After removing a piercing, it can be inserted, leading with the fine tip into the skin hole and subsequently be pushed further into the skin hole until its cleaning body is inserted therein. It is then gently moved to and fro or rolled to and fro about its axis and pulled out again.

Abstract: A patterned apertured web is disclosed. The patterned apertured web includes a plurality of land areas in the patterned apertured web and a plurality of apertures defined in the patterned apertured web. At least some land areas of the plurality of land areas surround at least some apertures of the plurality of apertures. The patterned apertured web has an Effective Open Area in the range of about 3% to about 30%, according to the Aperture Test herein. The plurality of apertures include a first set of apertures defining a first shape and a second set of apertures defining a second shape. The first shape is positioned within the second shape.

Abstract: On a skin side surface of a liquid permeable top sheet (3), embossed portions (10, 10, . . . ) depressed toward a non-skin side are arranged at intervals. Each embossed portion (10) is formed in a planar shape passing through each corner (12) of an original shape (11) and having concave shaped outlines (14) each formed by a curve bulging each side (13) of the original shape toward the center. A quadrangle having four or more sides is defined as the original shape (11). Because liquid intensive regions (15) formed along a periphery of the embossed portion (10) are separated at a central portion, the liquid intensive regions (15) become less noticeable. Also, a perimeter is increased by the concave shaped outlines (14) while a compressed area is reduced, the body fluid is dispersed and a color of the body fluid becomes less noticeable without deteriorating the touch feeling.

Abstract: An absorbent article having a pair of longitudinal edges, front and rear transverse edges, a front end region, a rear end region, and a central region disposed between the front and rear end regions. The absorbent article has a liquid pervious topsheet, a liquid impervious backsheet, an absorbent core disposed between the topsheet and the backsheet, a pair of outwardly convex longitudinal central channels formed at least in the central region. The traversal distance of the pair of outwardly convex longitudinal central channels decreases towards both ends of the channels to define a central closed area. The absorbent article has a rear channel defining a rear closed area in the rear end region.

Abstract: An elastic panel for use in an absorbent article including a first nonwoven web layer, a second nonwoven web layer and an elastomeric film layer disposed between the first and second nonwoven layers. At least one of the first and second nonwoven web layers includes at least one group of folded portions. Each folded portion includes a first fold line and a second fold line so that the folded portion is divided into a proximal section, a distal section and a medial section disposed between the proximal and distal sections. The proximal section is directly attached to the elastomeric film layer and the medial and distal sections are not directly attached to the elastomeric film layer so that the folded portions extend to allow the web panel to stretch elastically.

Abstract: An undergarment article has a fabric a fabric layer for wearing about a pelvic region of a person, a water-repellent layer coupled to a crotch portion of the fabric layer to form an inner chamber, and an inner pad disposed within the inner chamber between the water-repellent layer and the fabric layer. The inner pad is resistant to heat and includes a liquid-absorbent layer and a waterproof layer. The liquid-absorbent layer contacts the water-repellent layer and is effective for absorbing a volume of liquid greater than 2 fluid ounces. The waterproof layer is effective for restricting liquid from reaching the fabric layer. The crotch portion of the fabric layer and the water-repellent layer can be substantially elastic in at least one of a lateral direction and a longitudinal direction of the crotch portion. Methods for using the undergarment, kits and uses of the undergarment are also disclosed.

Abstract: A mobile object of the invention includes: a moving base including a front wheel and a rear wheel; a seat having a seating surface; and an armrest located outward of the seating surface in a width direction of the mobile object. The armrest includes: a supporting part supported on the moving base; a body part supported by the supporting part; and a grip protruding from the body part. The armrest is configured so as to be changeable between the position of use in which a user seated on the seating surface can hold the grip with the arm positioned upward of the armrest, and the lift-up position in which the grip is positioned upward of the position of use. The grip in the lift-up position is located outward in the width direction of the mobile object with respect to the grip in the position of use.

Abstract: A wheel structure includes a rim and a tire. The rim includes a body, hub and spokes. The body has two edges which first and second flanges are annularly disposed at, respectively, to form a tire holder. First and second walls are annularly disposed at the edges of the body in such a manner to face the first and second flanges, respectively, allowing a first engaging slot to be formed between the first flange and the first wall and a second engaging slot to be formed between the second flange and the second wall. The tire is coupled to the tire holder. First and second coupling portions are disposed at two inner edges of the tire and coupled to the first and second engaging slots, respectively. A hollow core portion is formed between the first and second coupling portions.

Abstract: Devices described in this disclosure can interconnect a wheelchair with another wheeled apparatus. For example, this document describes interfacing devices that releasably receive the front wheels of a wheelchair and the rear wheels of another wheeled apparatus in such a way that a user of the wheelchair can conveniently maneuver the wheeled apparatus in conjunction with the operation of the wheelchair.

Abstract: An adjustable seat comfort wheelchair for maximizing comfort and convenience includes a chair base, a chair seat with a chair back, a headrest, a pair of armrests, a seat bottom, and a footrest. An electric drive train is coupled to the chair base and comprises: a battery compartment housing a rechargeable battery, a motor that is in operational communication with the rechargeable battery, a drive chain coupled to the motor, a pair of rear wheels that are driven by the motor coupled to the drive chain, a steering linkage, a pair of front wheels, a steering actuator, a control module, a lift piston, and a control stick that is in operational communication with the control module to operate the motor, the steering actuator, and the lift piston. The lift piston lifts the seat bottom to a lifted position to assist the user in standing.

Abstract: A flexible rapid deployable system that may be used create an isolated space within a medical transport vehicle for use when transporting infected or contaminated patients, including a flexible tent-like liner creates a room inside the vehicle where both the patient and medical personnel can be isolated and contain contaminants within and a filtration system capable of producing the required air flow to maintain a negative pressurized isolated environment, sized to effectively accomplish this for the isolated cubic space.

Abstract: Apparatus (1) for rehabilitation of an upper limb of a person comprising a base frame (10) and a kinematic chain (100) connected to each other. The kinematic chain (100) comprises a plurality of rigid links (21-25) connected in series one after the other through a plurality of rotational joints (31-34), each of which having a respective rotation axis (131-134) and arranged to rotatably connect two successive rigid links of the series. The apparatus (1) comprises a plurality of actuation groups (70), each of which associated to a respective rotational joint and configured to generate and transmit a predetermined driving power to the rotational joint associated to it.

Abstract: Disclosed herein are self-adjusting devices and systems for assistive ambulation and traversing of stairs. In one aspect, a disclosed assistive device encompasses a frame assembly including a first side frame connected with a second side frame, each side frame with first and second legs each having first and second opposed ends, and a gripping member connecting first ends of the first and second legs, the second ends of first and second legs having an extendable portion configured to allow selective adjustment of a leg length; and a leg adjustment system contained within a portion of each side frame configured to correspondingly lengthen one leg at a leg length adjustment ratio in response to shortening of another leg. In further aspects, the legs can releasably attach to a stabilizing component for stabilizing the device. Also disclosed herein are kits and methods for using the disclosed devices and systems.

Abstract: A method of performing a fit test on an actuator unit coupled to a user. The method includes determining a first configuration of the actuator unit generated in response to actuating the actuator unit while the user is performing one or more movements for the fit test; determining a change from the first configuration of the actuator unit while the user is performing the one or more movements for the fit test; determining that the change from the first configuration corresponds to an improper fit of the actuator unit coupled the user; and generating an improper fit indication that indicates improper fit of at least leg actuator units coupled the user.

Abstract: The present invention relates to an electronic device to be worn on a user body, the electronic device comprising: a sensor configured to sense the user body and generate body condition information; an operation implementator configured to perform a health care operation having one state among a plurality of operation states; a communicator configured to communicate with an external device; and a controller configured to: control the operation implementator to perform a health care operation of one state among the plurality of operation states with regard to the user body, control the communicator to transmit the body condition information and information about the operation state of the operation implementator to the external device, and control the operation implementator to perform the health care operation of the operation state corresponding to user control information received from the external device through the communicator among the plurality of operation states of the operation implementator.

Abstract: A device for treating edema and other skin and tissue ailments is provided. The device includes a section of flexible material, a first handle carried at a first end of the section of material, and a second handle carried at a second end of the section of material. The flexible material extends through opening of each of an array of roller wheels. Each wheel defines a patient engaging outer surface formed from foam or cushion material.

Abstract: An adjustably tensioned roller massage system provides a pair of roller massage assemblies in opposed adjustable tensioned or spaced relation to allow engagement of each one of a pair of roller massage assemblies on a corresponding massageable portion of a body.

Abstract: A sexual toy is provided that is made from a composite material formed from joining, at least, two components, where a first component is an elastomer, and a second component is a granulated element. The sexual toy can include a sheath of silicone and a rigid core.

Abstract: A vibrating ingestible capsule includes a housing having a longitudinal axis, and having a vibrating agitator adapted such that, in a first vibrating mode of operation, the housing exerts vibrations on an environment surrounding the capsule. A power supply disposed within the housing is adapted to power the vibrating agitator. A temperature sensor provides temperature information signals with respect to a temperature in an environment surrounding the vibrating ingestible capsule over a period of time.

Abstract: A system for managing treatment of a person in need of emergency assistance is provided. The system includes at least one camera configured to be mounted to a person in need of medical assistance. The system also includes an image processing device, which can be configured to receive images captured by the at least one camera and to process the images to generate a representation of a rescue scene surrounding the person. The system further includes an analysis device. The analysis device can be configured to determine a characteristic associated with a resuscitation activity based on analysis of the representation of the rescue scene generated by the image processing device. A computer-implemented method for managing treatment of a person in need of emergency assistance is also provided.

Abstract: In embodiments, a Cardio-Pulmonary Resuscitation (CPR) system includes a retention structure, a compression mechanism coupled to the retention structure and a backboard. The retention structure and the backboard can be assembled together so as to form a closed loop that surrounds the patient's torso, and a piston of the compression mechanism is movable towards and away from a chest of a patient. In addition, the CPR system has a stabilizing member, and a coupler configured to couple the stabilizing member to the backboard. The stabilizing member can prevent the retention structure from tilting while the CPR system delivers chest compressions to the patient.

Abstract: This needle puncture detection sheet 100 has a whitening resin layer 10 that, when punctured by an RB type injection needle having a diameter of 0.80 mm to form a puncture hole 50, whitens and forms a whitened region 60 having a width of at least 0.2 mm around the puncture hole 40.

Abstract: A double-layer medical fluid bag includes an inner wall, an outer wall, clean air filled between the inner and outer walls, and a piercing device installed between the inner and outer walls. When it is necessary to use a liquid medicine contained in the medical fluid bag, the piercing device is moved forward to pierce a plate to be pierced, so that the clean air can enter into the inner wall slowly to push the liquid medicine to flow downwardly to the outside. During the operation and use processes, the liquid medicine is completely isolated from outside air, so as to avoid the danger of having unknown outside air to enter into the medical fluid bag and endure the safety of using the medical fluid bag.

Abstract: A closure system for a screw top container intended to contain a pharmaceutical or surgical medium comprises: a screw cap including a main body comprised of an annular wall with an internal thread for cooperating with an external thread adjacent an open end of the container, the body having a first open end for receiving the open end of the container and a second end closed by an end disc; a sealing formation within the main body for forming a seal with the open end of the container; and a tamper-evident band connected to the screw cap at the open end of the main body by at least one severable linkage, wherein the screw cap, sealing formation and tamper-evident band are integrally formed as a single unit for maintaining a hermetic seal with the container throughout a terminal sterilisation process.

Abstract: Systems and methods for removing a preservative from a solution, emulsion, or suspension may include an ophthalmic agent, a complexing agent, and a matrix. A method for administering an ophthalmic agent may include: providing a solution, emulsion, or suspension comprising a hydrophobic ophthalmic agent, a preservative, and a complexing agent, wherein the complexing agent is configured to host the hydrophobic ophthalmic agent; and providing a polymeric matrix, wherein the complexing agent is configured to reduce an affinity of the ophthalmic agent for the polymeric matrix and wherein the polymeric matrix is configured to selectively absorb the preservative when the solution, emulsion, or suspension is passed therethrough.