Abstract: A package of one or more absorbent articles is disclosed. The package has a package material including natural fibers. The package has a plurality of panels, including a consumer-facing panel, and wherein the package is sealed such that the one or more absorbent articles are completely enclosed therein. The package material has a basis weight of between 50 gsm to 120 gsm, between 60 gsm to 105 gsm or between 70 gsm to 90 gsm, as determined via ISO 536 as modified herein. The package material is recyclable.

Abstract: Medical device kits for use in placing, maintaining, altering, and/or removing medical devices in, on, and/or from the body of a patient can include one or more wrap assemblies for use in the placement/maintenance procedure. The one or more wrap assemblies of the medical device kit can include various features to assist the clinician performing the particular procedure, such as a urinary catheterization procedure. A wrap assembly can include a wrap body including a front surface defining an aseptic field for the urinary catheterization procedure, a plurality of pockets on the front surface, and urinary catheterization components disposed in the plurality of pockets, the urinary catheterization components arranged in a predetermined order of use for the urinary catheterization procedure. The wrap assembly can be in a rolled configuration. A method of using the wrap assembly includes unrolling the wrap assembly and removing the urinary catheterization components to perform the procedure.

Abstract: The present disclosure discloses arrays (retail store shelves and digital retail) of disposable, fibrous, rolled products comprising Traditional Diameter Rolls and Packages and Larger Diameter Rolls and Packages.

Abstract: The present disclosure provides a composition. In an embodiment, the composition includes an olefin-based polymer and from 0.15 wt % to 15 wt % of an odor suppressant. The odor suppressant includes (i) from 0.05 wt % to 2 wt % of a metal oxide having a band gap greater than 5.0 electron volts (eV), and (ii) from 0.1 wt % to 13 wt % of an acid copolymer. The ratio of metal oxide to acid copolymer is from 1:20 to 1:1. Weight percents are based on the total weight of the composition.

Abstract: A hygienic receptacle for storing and transporting soiled articles, the hygienic receptacle including odor-neutralizing and/or absorbing material and sealable opening.

Abstract: Herein is disclosed a composition for application to a wound comprising: a first layer comprising a skin adhesive, wherein the first layer has a wound-facing side and a non-wound-facing side and, in a first area, apertures extend through the first layer from the wound-facing side to the non-wound-facing side; and a second layer disposed on a non-wound-facing side of the first layer, the second layer comprising a polymeric film that is continuous in that it extends over and covers each of the apertures of the first layer, the second layer having a moisture vapour transmission rate (MVTR) of at least 500 g/m2/24 hours, measured in accordance with BS EN 13726-2:2002, wherein the composition further comprises a third layer disposed between the first layer and second layer, the third layer being a supporting layer for the first layer, the third layer having apertures therethrough, substantially corresponding to the apertures in the first layer. A method of making such a composition is also disclosed.

Abstract: A dressing is described having a backing layer, an (absorbent) pad, an adhesive coating and a release liner. The release liner is releasably attached to the adhesive coating. The release liner is configured to stiffen up and protect protrusions and/or border portions of the dressing that may otherwise be wrinkled, folded, kinked or otherwise damaged or impaired prior to (transportation or storage) or during application at the point-of-use. The dressing can be used for wound treatment. The dressing can prevent shearing and/or friction from causing (deep tissue) skin damage.

Abstract: The present application relates to a method for desensitization of allergic patients. More specifically it relates to an epicutaneous desensitization method, applicable to any type of allergens and of patients. The method of the invention is essentially non-invasive and does not require the use of adjuvants. Further, it may be easily applied and monitored by the actual patient.

Abstract: A novel device and method for delivering a liquid containing an active ingredient to a treatment site on the skin is disclosed. The device is useful for treating lesions or abnormal skin features such as corns, warts, calluses, bunions, actinic keratoses and hard hyperkeratotic skin as is often found on the face, arms, legs or feet.

Abstract: A CPAP system for respiratory therapy includes an RPT device configured to supply a flow of gas at a therapeutic pressure, a patient interface, an air delivery conduit configured to pass the flow of gas from the RPT device to the patient interface, and a vent assembly configured to provide a vent flow of gas to discharge gas exhaled by the patient from a pressurized volume to ambient. The vent assembly includes a base including at least one first orifice to allow gas to be discharged along a primary vent flow path and at least one second orifice to allow gas to be discharged along a secondary vent flow path, a diffusing member provided to the base, and a membrane provided to the base. The membrane is configured to apportion the vent flow of gas along the primary vent flow path and the secondary vent flow path throughout respiratory therapy.

Abstract: A dressing configured to be positioned adjacent to a tissue site is disclosed herein. The dressing may include oxidized regenerated cellulose (ORC), collagen, and at least one nutrient including glutamine. Methods of treating a tissue site are also disclosed herein.

Abstract: A compression sock or bandage made of a base textile includes a tubular leg having a collar, on which compression elements are arranged over the length of the tubular leg, which have a structure, yarn thickness, or yarn material differing from a structure, yarn thickness, or yarn material of the base textile. The compression elements include at least two opposing helices, which extend circumferentially around the tubular leg from the ankle region in the direction of the collar, and which cross at least once and are connected to the base textile in that the knitting pattern or the yarn of the helices is fastened to the base textile to provide stabilizing support. At least one cushion is formed on the base textile on the front side of the compression sock or bandage along a shin region, which protrudes from the collar to the ankle region and at least partially overlaps the crossing helices.

Abstract: A drape (600) suitable for covering non-planar surfaces of equipment (1201) is provided. The drape (600) facilitates quick and efficient deployment while ensuring that a sterile field established by a drape portion (601) is not compromised. The drape (600) can include a drape wrapping layer (209) wrapped about a drape portion (601) that is formed initially with two abutting elongated accordion fold stacks (604,605). Non-sterile personnel (801) can handle the drape wrapping layer (209) to position the drape (600) along surfaces of the equipment (1201) without touching the sterile drape portion (601). Sterile personnel can then expand the abutting elongated accordion fold stacks (604,605) to drape the surfaces of the equipment (1201).

Abstract: A product including a feminine hygiene pad in a folded configuration provided within an individualized envelope package is disclosed. The pad is folded separately of the envelope package and is entirely contained within the package. The package has a rectangular shape and includes a section of polymeric film, a pair of side seams, and a closure flap overlapping an opening edge, wherein the package is configured to create an access opening upon lifting of the closure flap, while allowing material along the side seams to remain unseparated.

Abstract: A breathable medical gauze patch includes at least one bandage body coupled with at least one ply of gauze or similar to, which not only helps wounds heal fast, but also prevent infections and potential complications. The at least one bandage body includes an adhesive on the underside that permits mounting about the wound site of a user/recipient. The at least one ply is disposed about a bandage aperture of the at least one bandage body. The at least one ply permits aeration therethrough to the wound site and facilitates absorption of any seepage of the wound while protecting the wound from the exterior environment. Further, the at least one ply may include multiple layers of sterilized medical grade gauze, a gel and an adhesive that allow the present invention to be efficiently and effectively applied to various deep or shallow wounds for facilitating speedy healing of the wounds.

Abstract: Disclosed is a wound dressing material comprising a substrate, about 2.5% to about 8% by weight of a bicarbonate, and a film-forming agent, the film-forming agent serving as a binder for said bicarbonate to said substrate, the film-forming agent and the bicarbonate being present in a ratio of between 1:2 and 2:1 with respect to one another. Also disclosed are a method for preparing a wound dressing material and a method for treating a wound.

Abstract: A novel device and method for delivering a liquid containing an active ingredient to a treatment site on the skin is disclosed. The device is useful for treating lesions or abnormal skin features such as corns, warts, calluses, bunions, actinic keratoses and hard hyperkeratotic skin as is often found on the face, arms, legs or feet.

Abstract: A feminine hygiene product assembly for fulfilling feminine hygiene requirements away from a home of a user includes a master kit, which in turn comprises a plurality of subkits. Each subkit comprises a plurality of hygienic products, such as tampons, compact tampons, sanitary napkins, panty liners, sanitary wipes, analgesic capsules, and analgesic tablets. Each hygienic product is positioned in an associated bag and has a respective function so that each subkit comprises hygienic products that have a variety of functions. The master kit is configured to provide a user a respective subkit to address associated hygienic requirements of the user.

Abstract: A CPAP system for respiratory therapy includes an RPT device configured to supply a flow of gas at a therapeutic pressure, a patient interface, an air delivery conduit configured to pass the flow of gas from the RPT device to the patient interface, and a vent assembly configured to provide a vent flow of gas to discharge gas exhaled by the patient from a pressurized volume to ambient. The vent assembly includes a base including at least one first orifice to allow gas to be discharged along a primary vent flow path and at least one second orifice to allow gas to be discharged along a secondary vent flow path, a diffusing member provided to the base, and a membrane provided to the base. The membrane is configured to apportion the vent flow of gas along the primary vent flow path and the secondary vent flow path throughout respiratory therapy.

Abstract: The invention comprises a package for reactive materials comprising a panel defining a first end, a second end opposite the first end, and at least two side edges. The panel comprises at least one film layer, an adhesive adjacent the film layer, wherein the adhesive is pattern applied such that it is disposed within an interior region of the film layer and wherein a perimeter of the film layer is adhesive-free adjacent each of the first end, second end, and side edges, and a release liner comprising a substrate layer and a cured silicone layer. The release liner is adhered to the film layer via the adhesive, the substrate layer of the release liner is disposed adjacent the film layer, and a perimeter of the release liner is smaller than the perimeter of the film structure. In an embodiment, the panel comprises a tubular body and the side edges are sealed together to form a fin seal, the first end is sealed closed to form an end seal, and the second end is sealed closed to form an end seal.

Abstract: A kit for dispensing disposable stethoscope covers and other instrument covers is provided. The kit may include a cartridge and a dispenser for automatic touch-free dispensing of disposable stethoscope covers. The kit further includes a first spool having a roll of backing member with disposable stethoscope covers disposed thereon and a second spool for receiving the spent backing member after a disposable stethoscope cover has been removed, self-contained within the cartridge. The cartridge is inserted within the dispenser so that a user may insert a stethoscope head through a window of the dispenser to attach to a disposable stethoscope cover. Alternatively, the cartridge or cassette may be comprised of disposable instrument covers so that a user may insert the instrument near or through the window of the dispenser for application of the instrument cover directly to the instrument. The kit may further include a proximity sensor for detecting a user.

Abstract: A package containing a plurality of disposable absorbent articles, the package being formed of flexible polymeric film, and having a path defining a hood opening structure is disclosed. The hood may be configured so as to serve as an effective package reclosure device whereby the package may be used to store the unused supply of articles following opening.

Abstract: A urinary catheter assembly (1) for relieving urinary retention is provided, which comprises a package (3) housing a protective sleeve (5) and a catheter (7), the protective sleeve protecting the catheter. To allow a catheter to be removed from the package with or without a protective sleeve, the catheter assembly forms a removal structure configured for at least a first removal procedure and a second removal procedure. The first removal procedure provides simultaneous removal of the catheter and the protective sleeve from the package with the protective sleeve protecting the catheter, and the second removal procedure provides removal of the catheter from the package and retains the protective sleeve in the package.

Abstract: A package and method for opening the package are disclosed. The package includes a first film and a second film forming an enclosure and at least one tab area and defining a package periphery, the enclosure defining an interior volume configured to receive a product. The package further includes first and second breachable bubbles formed within first and second tab portions of the at least one tab area. Upon application of pressure by a user, the first and second breachable bubbles breach. The package may be alternated between a first position, wherein the first tab portion and the second tab portion are substantially sealed from each other to facilitate breaching, and a second position, wherein the first tab portion and the second tab portion are in fluid communication with each other.

Abstract: The package (1) for a surgical mesh (100) comprises: a receiving member (2) configured and dimensioned to receive at least one surgical mesh (100), and a covering member (3) configured and dimensioned to cover the said at least one surgical mesh (100) maintaining with the receiving member (2) the surgical mesh (100) in a substantially flat position, and a gas channelling network interposed between the said receiving member (2) and the said covering member (3) configured to channel a sterilization gas within the at least one surgical mesh (100).

Abstract: A viscous liquid vessel system for presenting a gift is described herein. In some embodiments, the viscous liquid vessel system comprises a vessel containing a viscous liquid in which a gift is disposed. The vessel comprises a lid for enclosing the viscous liquid and the gift. The viscous liquid vessel system may be presented to a gift recipient and the gift recipient may remove the gift from the vessel and the viscous liquid creating a heightened emotion upon receipt and extraction of the gift.

Abstract: Systems and methods are provided for dispensing sheets of material (e.g. tissues, wipes, towels, etc.) from a container or other suitable receptacle for storing the sheets of material for dispensing therefrom. The dispenser systems are integrated with storage and/or organizer, which are configured to be above, below, behind, or in front of a dispenser without affecting the dispensing function of the system. The dispensers can be used in a vertical position, capable of dispensing a sheet in a downward or upward direction when mounted on a wall, for example, or in a horizontal position, capable of dispensing a sheet sideways and/or popup direction. One of the advantages of these dispensers is that it allows a prior art flat top tissue box for use in a vertical position, i.e., standing up on its end, thereby taking even less horizontal space than the cubic tissue box.

Abstract: A compacted feminine hygiene kit comprising basic items such as at least underwear, at least a feminine wipes and at least a feminine sanitary towel. Further the compacted feminine hygiene kit comprises a shaped base for keeping the feminine hygiene kit assembly rigid body while providing a kit, easy to carry, that offers a greater degree of discretion, convenience, and portability to females.

Abstract: A kit for dispensing disposable stethoscope covers is provided. The kit may include a cartridge and a dispenser for automatic touch-free dispensing of disposable stethoscope covers. The kit further includes a first spool having a roll of backing member with disposable stethoscope covers disposed thereon and a second spool for receiving the spent backing member after a disposable stethoscope cover has been removed, self-contained within the cartridge. The cartridge is inserted within the dispenser so that a user may insert a stethoscope head through a window of the dispenser to attach to a disposable stethoscope cover. The kit may further include a proximity sensor for detecting a user. Upon detection of the user, the first and second spools rotate to align a disposable stethoscope cover with the window of the dispenser in a ready-to dispense position.

Abstract: A package includes a first pouch and either a second pouch or a cover, where the pouches are configured to contain a product, such as a food product, and attached relative to each other about a hinge. The package includes at least one closure flap. The first and second pouches or first pouch and cover are movable about the hinge from a closed position where access is at least partially blocked by the closure flap toward an open position where the closure flap is separated to allow greater access. Methods of manufacturing such packages are also provided.

Abstract: In one embodiment, taped and pant articles of the present disclosure may comprise first and second chassis and first and second belt flaps that are at least substantially identical.

Abstract: A method for manufacturing a touch panel and a conductive strippable adhesive are provided. The method for manufacturing the touch panel including forming a touch electrode and forming a conductive strippable adhesive layer on the touch electrode, wherein the conductive strippable adhesive layer is electrically connected with the touch electrode. The conductive strippable adhesive layer enables charges to flow freely in the touch electrodes, so as to balance the electric potential in the touch electrodes, and improve the ability of resisting electrostatic breakdown of touch panel products in the production process, and effectively eliminate risk of ESD in a manufacturing process of a touch panel, and hence improve the product yield, and reduce the cost.

Abstract: A kit for assembling a device designed to prevent flexing of a joint to reduce joint pain or to prevent reopening of a wound over said joint. The kit allows a user to assemble a device of any desired size or shape.

Abstract: An automatic dispensing device for volatile fluid operable to apply one or more agent to a local environment for more than 14 days. Preferred devices dispense a first agent for air freshening, and may optionally dispense a second agent, such as a drain cleaner. A workable drain cleaner is structured to permit a slow release of drain cleaning agent. A dispensing device may nonexclusively operate by evaporation of volatile fluid from a polymer or rubber-like carrier material that is infused with the volatile fluid; gravity-induced drip from a bulk supply of volatile fluid through a small orifice onto an emanator; osmotic transfer of volatile fluid from a bulk supply; gas-pump drive of volatile fluid at controlled pressure; or diffusion of volatile fluid through a wall of a container of bulk volatile fluid; and combinations thereof.

Abstract: The present application relates to a method for desensitization of allergic patients. More specifically it relates to an epicutaneous desensitization method, applicable to any type of allergens and of patients. The method of the invention is essentially non-invasive and does not require the use of adjuvants. Further, it may be easily applied and monitored by the actual patient.

Abstract: The present invention relates to a method and system for aseptically filling of flexible packages containing dry cloth. Such a method may include a first stage that is performed in a non-sterile environment. The first stage may include cutting a first substantially dry cloth to a predetermined size; inserting the first cloth into a flexible package; sealing a first end of the flexible package; and sterilizing the flexible package. The method may also include a second stage performed in a sterile environment. The second stage may include filling the flexible package with a medical solution such that the substantially dry cloth absorbs at least a portion of the medical solution; and sealing the an open end of the flexible package.

Abstract: A drape (600) suitable for covering non-planar surfaces of equipment (1201) is provided. The drape (600) facilitates quick and efficient deployment while ensuring that a sterile field established by a drape portion (601) is not compromised. The drape (600) can include a drape wrapping layer (209) wrapped about a drape portion (601) that is formed initially with two abutting elongated accordion fold stacks (604,605). Non-sterile personnel (801) can handle the drape wrapping layer (209) to position the drape (600) along surfaces of the equipment (1201) without touching the sterile drape portion (601). Sterile personnel can then expand the abutting elongated accordion fold stacks (604,605) to drape the surfaces of the equipment (1201).

Abstract: A resealable flexible package is provided comprising polymeric wall panels and a peel-reseal feature sealed therebetween. A peel-off portion is removed to transition the package from a closed position to an open position, removal of the peel-off portion both opening the package and exposing a pressure sensitive adhesive of the peel-reseal feature. The exposed pressure sensitive adhesive is coupled to one of the wall panels and moved into adhesive engagement with an exterior surface of another wall panel to transition the package to a reseated position.

Abstract: Adjustable covers, systems, and methods are presented that include an adjustable cover that may be adjusted to an appropriate size by hand without requiring cutting tools and without substantial leaks. In one instance, the adjustable covering includes a drape member with a plurality of non-leaking tear paths. Each non-leaking tear path includes a weakened path of the drape member that may be torn. The adjustable covering may further include a first plurality of tear starters formed on a first initiation edge of the drape member. Each tear starter of the first plurality of tear starters is aligned with one of the plurality of tear paths. Each of the first plurality of tear starters is adapted to facilitate the initiation of a tear along a tear path. The grains of the drape member, a backing layer, and support layer may also be in the same direction. Other adjustable covers, systems, and methods are presented.

Abstract: An individual package for an absorbent article is provided with the absorbent article and a wrapping body containing the absorbent article. The absorbent article has a main body extending in a longitudinal direction and a pair of flaps extending from the main body in opposite directions along the longitudinal direction. Each of the main body and the pair of flaps has a fixing section and the main body and the pair of flaps are fixed to the same face of the wrapping body with the fixing sections interposed therebetween. The wrapping body is provided with a pair of bonding regions bonding the wrapping body, the bonding regions being located outward in the widthwise direction and each having a bonding section and a non-bonding section. The fixing sections of the pair of flaps and the non-bonding sections overlap in the widthwise direction.

Abstract: Methods and products for protecting tissue of a patient during a surgical procedure that involve making an incision in the tissue and retracting the tissue to make a larger opening, wherein the methods and products use a water-resistant stress-distributing layer.

Abstract: An array of disposable absorbent articles comprising a sequence of graphic designs corresponding to a wearer's stage of development.

Abstract: A variable flexibility adhesive system may adhere a surface of a medical infusion device to the skin of a user. The system may be configured to hold a location on the surface stationary with respect to a site on the user's skin. The system may include an adhesive substrate for adhering to the user and an interface where the substrate is held to the surface of the device. The interface may totally and/or partially surround the stationary location. A skirt of the substrate may totally and/or partially surround the interface. Parts of the skirt may be stiffened. Optional features may include tabs for activation of the adhesive and/or a location for peeling the infuser away from the skin. Additionally or alternatively, the interface may have variable flexibility. Additionally or alternatively, the stiffener may include a plastic layer.

Abstract: A wound care product is provided. It comprises a sealed chamber in which a wound care article is arranged around a support member in such a manner that a curved portion of the wound care article is in contact with the support member. The curved portion interconnects two other portions on opposite sides of the support member.

Abstract: The present application relates to a method for desensitization of allergic patients. More specifically it relates to an epicutaneous desensitization method, applicable to any type of allergens and of patients. The method of the invention is essentially non-invasive and does not require the use of adjuvants. Further, it may be easily applied and monitored by the actual patient.

Abstract: A method for collecting a compound from a surface, the method comprising providing a silicone adhesive collector comprising a silicone adhesive layer on a backing; contacting the silicone adhesives collector and a first solvent to provide a wetted collector; contacting the silicone adhesive layer of the silicone adhesive collector and a surface to be analyzed to provide a loaded collector; and removing the loaded collector from the surface to collect the compound. The disclosure also relates to a system for collecting a chemical compound from surfaces, the system comprising a silicone adhesive collector comprising a backing, and a silicone adhesive layer disposed on the backing; a first solvent; and instructions to dispose the first solvent on the silicone adhesive collector, the surface, or a combination thereof.

Abstract: A packaging unit for hygiene articles that is formed from a sheet of material having an inner surface comprises an edge zone comprising an inner edge portion and an outer edge portion. At least one of the outer and inner edge portions comprises at least one region provided with a resealable adhesive. The sheet has at least one folding axis dividing said sheet into a first and second regions region. The sheet is folded about said at least one folding axis with said first and second regions in an overlapping configuration, thereby providing a packaging unit. Overlapping outer edge portions of the sheet layers are at least partly adhesive-free and are at least partially connected to each other by a mechanical interaction providing a sealing strength of 0.2 to 1.5 N. A method for forming the packaging unit is provided.

Abstract: Packages containing a plurality of individually wrapped articles are described. The wrappers comprise at least two different printed elements, and the appearance of the individually wrapped articles can vary within a single package. Methods for individually wrapping a plurality of articles are also described.

Abstract: A microneedle-sheet packaging body includes a microneedle sheet, a forming sheet, and a support body. The microneedle sheet includes a substrate, and a plurality of microneedles formed on a lower surface of the substrate. The forming sheet is tightly adhered to the lower surface of the substrate. The forming sheet includes a plurality of micro-recess parts in which the plurality of microneedles are housed. The support body is fixed to an upper surface of the substrate of the microneedle sheet and is further fixed to the forming sheet around the substrate. Thus, the microneedle-sheet packaging body protects a plurality of microneedles on the microneedle sheet.

Abstract: Packaging including a line of weakness (10, 11) that is broken to obtain access to an article within said packaging is disclosed. A varnish or lacquer coating is applied to spaced regions (12) along the length of the line of weakness.