Abstract: A respirator mask dispensing system is provided. It includes a carrier material and a plurality of respirator masks mounted in parallel on the carrier material by an adhesive. The carrier material is deformed between adjacent ones of the plurality of respirator masks, the deformation being configured to assist in the tearing of the carrier material at points of deformation. The carrier material with the plurality of respirator masks as mounted therein is wound on the central core member to provide a continuous roll The adhesive bonds more strongly with the respirator masks than the carrier material such that when an individual respirator mask is removed from the carrier material the adhesive will separate from the carrier material and remain attached to the individual respirator mask.

Abstract: A wrapper that opens relatively quietly and wraps a sheetlike hygiene product provided on one side with an adhesive, said wrapper being based on a packaging material in web form and composed of a polymeric film comprising a) at least one heat-sealable layer based on a mixture of at least one C2 or C3 olefin homopolymer or copolymer and not more than 30% by weight, based on the total weight of the layer a), of polybutylene and b) optionally a layer of polyethylene having a density of 0.88-0.94 g/cm3; the layer a), at least in those sections which face the regions of the hygiene product that are provided with the adhesive, has a release coating, and otherwise, at least in the sub-regions which are joined to form edge closures in the form of stripes or lines, has no release coating.

Abstract: An orthopedic fixation system includes a sterile packaged implant kit and a sterile packaged instrument kit. The sterile packaged implant kit includes at least one surgical implant, an insertion device, and an implant package adapted to receive the at least one surgical implant and the insertion device therein. The implant package maintains the at least one surgical implant and the insertion device sterile after sterilization of the sterile packaged implant kit. The sterile packaged instrument kit includes one or more instruments necessary to use the sterile packaged implant kit and an instrument package adapted to receive the one or more instruments therein. The instrument package maintains the one or more instruments sterile after sterilization of the sterile packaged instrument kit.

Abstract: A drug storage container includes: a first container; a second container that is disposed on the lower end side of the first container; a needle tube for making an internal space of the first container and an internal space of the second container communicate with each other; operating means for performing an operation of bringing the first container closer to the second container; a drug stored in the internal space; and a liquid stored in the internal space. In the drug storage container, with the first container and the second container brought closer to each other by the operating means, the internal space of the first container and the internal space of the second container are made to communicate with each other through the needle tube, and the volume of the internal space of the second container is reduced.

Abstract: Disclosed are methods for improvement of beta cell function in a subject using an anti-IL-1? antibody or fragment thereof.

Abstract: A sterile container having a lower container part and an upper container part for closing the lower container part is provided. The lower and upper container parts define, in a closed position, a container interior. A sealing device is provided for gastight sealing of the sterile container in the closed position. The sealing device comprises a circumferential sealing element bearing against both the lower and upper container parts in the closed position. The sealing element comprises an upper container part sealing section with an upper container part sealing surface region bearing against the upper container part, and a lower container part sealing section with a lower container part sealing surface region bearing against the lower container part. The sealing device further comprises a pretensioning device for exerting a pretensioning force on at least the lower container part sealing section or on the upper container part sealing section.

Abstract: The present invention relates to a syringe, particularly to a small volume syringe such as a syringe suitable for ophthalmic injections.

Abstract: Containers and components thereof for use in the medical industry and methods to manufacture the same are described. An example tab for use with a medical container includes opposing sheets sealed to define an open ended chamber into which a port is to be at least partially positioned. The port is to enable access to the medical container. The tab includes a tear seal defined by each of the opposing sheets and a first guide positioned on a first side of each of the tear seals. The tab includes a second guide positioned on a second side of each of the tear seals, wherein the first and second guides are to enable a tear to propagate substantially between the guides and adjacent the tear seals.

Abstract: The present invention relates to a novel device for the collection, storage, shipping and retrieval of hair follicles from animals for the purpose of isolating DNA or other genetic material from the follicles for analysis. The device has outer flaps for the protection as well as identification of the samples and an inner part where samples are placed. The inner device has thicker base and a clear plastic cover, the easy peel back of which is facilitated by a) low tack adhesives that hold the two together and b) a touch cut on one end, through the base sheet which creates a grip. This makes the device convenient and easy to use, and yet a robust collection device for hair follicles from animals in a farm or real-life situation. Hair follicles can be punched out through the inner device for direct DNA isolation and analysis.

Abstract: The present is an alternative nutrition and/or intravenous bag concealing sack fabricated from a series of fabric, plastic and/or paper components, a zipper, Velcro or snaps providing a means of easy access to the bags and an elastic band, positioned in the bottom seam of the sack, providing a means which permit the sack free movement horizontally in and out covering adjacent surfaces.

Abstract: The invention relates to an emergency tubing set, including an oxygen mask adapted to cover a users mouth and nose, a tubing connected at a first end to said tubing set to provide oxygen to said oxygen mask, and a connect or connected to said tubing at a second end opposed to said first end, the connector being adapted to be connected to an oxygen source for supplying oxygen to said tubing. According to the invention the tubing includes an excess tubing section and a connecting tubing section wherein the excess tubing section is stored in a bottom pouch and a first part of an intermediate tubing section is arranged inside the bottom pouch and a second part of said intermediate tubing section is arranged outside said bottom pouch, wherein the intermediate tubing interconnects the excess tubing section and the connecting tubing section.

Abstract: A container holds at least one surgical implement, has a lock mechanism, and has a signature label that impedes access to the surgical implement until the correct surgical site is confirmed. A method of using the container includes the steps of confirming the correct surgical site, signing the label and removing it from the container, placing the label in the medical record, unlocking the container, removing the implement, and beginning the surgery, wherein the surgical team is forced to pause to confirm the correct surgical site before starting the surgery. Preferably, the container top may be removed and placed between the surgeon and surgical technician to define a no-hands “neutral zone” to avoid being stuck by the sharps. Also, the container preferably includes compartments for storing used sharps and/or a local anesthetic-loaded syringe, and the top may be replaced and secured for safely disposing of the sharps after the surgery.

Abstract: A method for preparing placenta membrane tissue grafts for medical use, includes obtaining a placenta from a subject, cleaning the placenta, separating the chorion tissue from the amniotic membrane, mounting a selected layer of either the chorion tissue or the amniotic membrane onto a drying fixture, dehydrating the selected layer on the drying fixture, and cutting the selected layer into a plurality of tissue grafts. Preferably, the drying fixture includes grooves or raised edges that define the outer contours of each desired tissue graft, after they are cut, and further includes raised or indented logos that emboss the middle area of the tissue grafts during dehydration and that enables an end user to distinguish the top from the bottom side of the graft. The grafts are comprised of single layers of amnion or chorion, multiple layers of amnion or chorion, or multiple layers of a combination of amnion and chorion.

Abstract: Compounds and their pharmaceutically acceptable salts for treatment of synucleinopathies, such as Parkinson's disease and tauopathies.

Abstract: The present invention relates to the use of a container, made of an inorganic additive containing plastic material, for reducing physical/chemical interaction between the container and an oil, fat and/or wax containing formulation contained therein.

Abstract: A container storing an anesthetic is disclosed. The container is sealed by a closure and stores a liquid anesthetic solution. The anesthetic is from 0.1% to 10% by weight of the liquid anesthetic solution. The container is made of a material that is inert to the anesthetic and the closure is made of siliconized rubber or a metal. A concentration of the anesthetic in a liquid anesthetic solution stored in the container following a predetermined time period is at least 93% of a concentration of the anesthetic in a liquid anesthetic solution before the liquid anesthetic solution is stored in the container.

Abstract: An housing for a medical device includes an insert configured for removable insertion into the housing, outer dimensions of the insert conforming to inner dimensions of the housing to prevent movement thereof within the housing. The insert includes first and second planar walls connected to one another and having first and second openings extending therethrough. The first and second walls are movable between an open configuration in which the first and second walls are separated from one another and a closed configuration in which the first and second walls are folded to contact one another such that the first and second openings are aligned to define a medical device receiving cavity configured to house a medical device. In the closed configuration, the first and second walls apply a frictional clamping force to a packet containing the medical device to prevent movement of the medical device relative to the inlay.

Abstract: A method and a receptacle for storing and supplying a liquid, especially a liquid medical preparation. It is an object of the invention to provide a suitable receptacle and method for storing and supplying a desired liquid quantity. It is solved by a liquid tight and preferably gas-tight receptacle, comprising a compressible tube (7) or foil bag. A rigid opening portion (6) is sealingly mounted to one end of the tube (7). The diameter of the opening portion (6) is the same as the diameter of the tube (7). The tube (7) diameter is not more than 10 mm The liquid has a volume of not more than 1.5 ml, preferably of not more than 1.3 ml. The tube (7) contains additionally a gas having a volume of 10 to 15% of the liquid volume. The tube (7) or foil bag comprises a flat portion having an inscription.

Abstract: Topical compositions, such as lip balms and other products for lip care, include combinations of ingredients that condition and heal the lips and skin. The topical compositions may be configured to remain in place on the lips or skin for relatively long periods of time. Methods of making topical compositions are also disclosed.

Abstract: Described herein are tissue grafts derived from the placenta. The grafts are composed of at least one layer of amnion tissue where the epithelium layer has been substantially removed in order to expose the basement layer to host cells. By removing the epithelium layer, cells from the host can more readily interact with the cell-adhesion bio-active factors located onto top and within of the basement membrane. Also described herein are methods for making and using the tissue grafts. The laminin structure of amnion tissue is nearly identical to that of native human tissue such as, for example, oral mucosa tissue. This includes high level of laminin-5, a cell adhesion bio-active factor show to bind gingival epithelia-cells, found throughout upper portions of the basement membrane.

Abstract: A bag having two accesses, an inlet and an outlet, both containing closing devices for releasing or stopping the flow of a liquid that flows into or out of the bag. The inlet has a filtering element for retaining particles possibly produced by the coring phenomenon which can occur when the spike of the inlet ruptures the plug of the bottle. Also provided is a safety device used for permanently attaching the bottle to the inlet.

Abstract: An embodiment of the present invention includes a tray and a method for loading a medical device on a catheter assembly. The tray can include a tray body defining a first receptacle for seating the handle assembly of the catheter assembly, an elongate receptacle for seating a delivery shaft of the catheter assembly, and a reservoir for holding a fluid. A portion of the elongate receptacle slopes downward towards the reservoir. The reservoir has a bottom surface that is below a portion of the elongate receptacle that is contiguous with the reservoir. Accordingly, when the reservoir is filled with a fluid and the catheter assembly is seated in the first receptacle and the elongate receptacle, the distal tip of the catheter assembly is submerged in the fluid in the reservoir. The tray body is also configured to prevent movement of a catheter assembly seated therein.

Abstract: The system according to the present disclosure includes a metal stent (3) as a medical implant for treating lesions in blood vessels and a packaging (1) having an inside volume, in which the stent (3) is arranged in a protected manner. The stent (3) has a plurality of webs (33), which produce a tubular shape with each other, and a proximal end (31) and a distal end (32), between which a stent lumen (34) extends. The stent surface (35) has a hydrophilic property. The molecular chemical impurities originating in the atmosphere, primarily hydrocarbon compounds, are significantly reduced on the surface by a treatment, whereby the contact angle as a measure of the hydrophilicity of a water drop present on the surface (35) is reduced in proportion to the contact angle prior to said treatment. The stent (3) is stored in an inert manner in the packaging (1).

Abstract: The present invention provides a medical device containing a cake composition comprising aripiprazole as an active ingredient and capable of suppressing agglomeration of aripiprazole in a suspension obtained by resuspending a freeze-dried substance; and a cake composition comprising aripiprazole as an active ingredient. The present invention relates to a medical device containing, in a storage container whose inner wall is treated with silicone, a freeze-dried cake composition comprising separately prepared aripiprazole as an active ingredient, wherein there is a space between the inner wall and the cake composition; and a cake composition comprising aripiprazole as an active ingredient and having a strength of 5 to 100 N.

Abstract: Package for a catheter, with a catheter having catheter tube with a distal end and a proximal end, the proximal end being provided with a catheter connector. A main body is provided for holding the catheter, and a cap for closing off the main body. A gel container is positioned inside the main body, the gel container being provided with a cavity for holding an amount of gel-like lubricating agent. The gel container comprises a first opening at a distal end, and a second opening at a proximal end. The catheter tube is disposed through the first opening and second opening when stored in the package. The main body is made of a rigid material to allow easy and reliable storage.

Abstract: A portable cosmetic container is disclosed. The portable cosmetic container includes a tube that has a receiving space with an opening at one end, and a crease is located at a bottom portion of the receiving space, so that a user can easily break the tube from the crease to form the opening of the receiving space. Substance is partially filled in the receiving space, and air therein is extracted to form a negative pressure status. It is advantageous that when a user breaks the tube from the crease, the substance will not randomly spray out since the air pressure moves towards the opening to keep the substance in the receiving space.

Abstract: The present disclosure is concerned with packaging which can accommodate a series of femoral stem components for prosthetic hip joints which have a dimension which varies minimally across the series but which vary considerably in overall size. The packaging is designed to minimize the travel of any member of the series packaged therein such that all the packaged components in the series can pass the standard handling and shipping tests typically used by the manufacturers of medical implants. The packaging comprises two thermoformed tray components which each carry three types of cavities which are interconnected. The tray components are designed to be assembled with their cavities facing each other. The cavities are designed to contain the lower stem, body and angled shaft of the stem component, respectively. The cavities for the lower stem and the body cooperate to capture the minimally varying dimension of the series.

Abstract: An elongate member housing tool assembly includes a distal end side tubular member disposed on the distal end side and a proximal end side tubular member disposed on the proximal end side, which accommodate an elongate member, and a liquid inlet port to which a liquid supplying tool for supplying liquid into the distal end side tubular member is removably connected and which is provided on the distal end side tubular member. The distal end side tubular member and the proximal end side tubular member are wound spirally, and the proximal end of the distal end side tubular member and the distal end of the proximal end side tubular member are disposed in a spaced relationship from each other. A distal portion of the guide wire is accommodated in the distal end side tubular member, except possibly the most distal portion of the elongate member.

Abstract: A system for packaging a medical implant may include a sleeve for housing the implant within a cavity in the sleeve, with at least a portion of the cavity conforming to the shape of the implant. A flexible material film may cover and substantially conform to the shape of the sleeve so as to aid in stabilizing the sleeve and implant within an outer package. An insertion instrument for inserting the implant within the body of a patient may also be provided with the system. In some embodiments, the sleeve, with the implant inserted in the cavity of the sleeve, is configured for manipulation by a user without contacting the implant, and the implant is connectable to the insertion instrument while in the sleeve.

Abstract: The present disclosure relates to a dynamic bioactive bone graft material and a method of handling the material to prepare an implant. In one embodiment, a method of preparing a dynamic bioactive bone graft implant is provided. The method includes the step of providing a porous, fibrous composition of bioactive glass fibers, wherein the fibers are characterized by fiber diameters ranging from about 5 nanometers to about 100 micrometers, and wherein the porosity of the matrix ranges from about 100 nanometers to about 1 millimeter. The porous, fibrous composition is introduced into a mold tray, and a shaped implant is created using the mold tray. The composition may be wetted with a fluid such as saline or a naturally occurring body fluid like blood prior to creating the shaped implant. In another embodiment, the porous, fibrous composition is provided with the mold tray as a kit.

Abstract: The present disclosure concerns packaging adapted to accommodate a series of femoral components for artificial knee joints which vary in size but have a common thickness dimension. The packaging is designed to provide a clearance between its internal parts which approximates this common thickness dimension but is also able to accommodate variations in the other dimensions of the femoral components. In a convenient approach, a base portion is provided which has a vertical projection with a top surface adapted to support a portion of the inner surface of the major arch of the femoral components of said series. It is mated with a second structural member which has an arcurate surface whose contour approximates a portion of the outside surface of the major arch of the femoral components in this series. Means are provided for holding it in a fixed special relationship with said base portion.

Abstract: A medication carrying case is provided having a first and second half hingedly attached and removably securable to one another along a removable line of connection. Within the interior of the carrying case halves is a removable medication support member having a plurality of surface depressions along its upper surface and a case connection means along its underside surface. Each support member secures to an inner surface of the case halves and is designed to fit therewithin. The depressions are adapted to form-fittingly secure pill bottles, medication vials, syringes, and other medical supplies therein. Further provided over each depression is a strap securement means, which is connected to the member upper surface along one end and is removably attachable across the depression along its second end. In this way, the carrying case provides a medication transport means and support that securely holds medication and accessories on the go.

Abstract: Certain aspects of the invention are generally directed to devices for withdrawing a substance from the skin and/or from beneath the skin of a subject, and/or for delivering a substance to the skin and/or to a location beneath the skin of a subject. In some embodiments, the devices may comprise one or more skin insertion objects, such as needles or microneedles. In some cases, the device also may comprise one or more vacuum chambers. In some aspects, the device may be contained within an environment able to assist with maintenance of such pressures. For example, a package containing such an environment may also have a pressure less than atmospheric pressure, and/or the package may be molded to the device or otherwise have a shape that does not contain substantial gases that can “leak” into the device and alter the pressure of any vacuum chambers that may be contained therein.

Abstract: A tag for tracking inventory levels and uses of an implant. The tag has a first component having a proximal portion and a distal portion and a second component having a proximal portion and distal portion. Additionally, the tag has an implant receiving cavity formed by the distal portion of the first component and the distal portion of the second component, in which the implant receiving cavity includes an encapsulating extension to substantially encapsulate an implant. Furthermore, the tag has a planar surface formed by the proximal portion of the first component and the proximal portion of the second component. The planar surface extending from the implant receiving cavity is substantially transverse to a longitudinal axis of the implant received within the implant receiving cavity. In addition, the tag has a tamper evident locking mechanism configured for locking the first component to the second component.

Abstract: A urinary catheter assembly (1) is provided. The catheter assembly has an intermittent urinary catheter (2) with low-friction surface and a tubular elongated package (3) with a side-opening (15). The catheter may be provided with a hydrophilic surface and the package may include a liquid swelling medium. The user may grab the connector (4) through the side-opening and pull out the catheter of the package through there. Spillage of the liquid swelling medium or lubricant is avoided. The side-opening may be configured so that it has two stable configurations, a storing and a folded configuration.

Abstract: In order to achieve both ease of removal and an increase in the rate of impregnation by a predetermined chemical, in this packaging structure of a package of wet wipes, a convex region is formed at a position containing a region that faces the opening of a main package body and that is on the upper surface of a stacked body of wet wipes. The convex region is formed protruding towards the main package body. A space is formed between the region (corresponding to the ends) aside from the convex region formed on the wet wipes and the upper surface to which the opening of the main package body is provided.

Abstract: This invention relates to compositions for combating parasites in animals, comprising 1-arylpyrazole compounds alone or in combination with formamidine compounds. This invention also provides for an improved methods for eradicating, controlling, and preventing parasite infestation in an animal comprising administering the compositions of the invention to the animal in need thereof.

Abstract: A device for supporting at least one vessel containing a target material to be lyophilized generally includes a support panel, a central region, a perimeter region, a thermal shield, and at least one shielding cavity. The support panel has a support surface. The central region is defined by the support panel for supporting the at least one vessel. The perimeter region is also defined by the support panel and surrounding the central region. The thermal shield is positioned about the perimeter region and extends transverse to the support surface of the support panel such that the thermal shield and the support panel define a storage space for accommodating the at least one vessel. The at least one shielding cavity is defined by the thermal shield and contains a shielding material during a lyophilization process. The shielding material is distinct from the target material.

Abstract: The medical safety box is a system using RFID (Radio Frequency Identification) technology to ensure that correct delivery of the correct treatment in the form of medication or injection to in-hospital patients is consistently carried out. The system includes a medical box containing whatever medication or injection that needs to be administered to a specific patient. The box has a locking mechanism that can only be opened by an RFID wristband, which is worn by that same specific patient, thus assuring that the medicine in the box is administered to the correct patient.

Abstract: An array of disposable absorbent articles comprising a sequence of graphic designs corresponding to a wearer's stage of development. For a disposable diaper, the array of disposable absorbent article graphic designs may comprise a first absorbent article graphic design for newborns and infants, a second absorbent article graphic design for toddlers, and a third absorbent article graphic design for older wearers, and other absorbent article graphic designs.

Abstract: The present invention provides a pharmaceutical composition comprising an aqueous solution of an ibuprofen solubilizing agent and ibuprofen, the ibuprofen solubilizing agent being in an effective amount such that the ibuprofen in the solution remains soluble at concentrations from 100 mg/mL to 5 mg/mL without undergoing a phase transition. The invention further provides a method of treating a condition chosen from pain, inflammation, fever, and/or patent ductus arteriosis, comprising administering to a patient in need thereof an effective amount of an aqueous solution a ibuprofen solubilizing agent and ibuprofen, the ibuprofen solubilizing agent being in an effective amount such that the ibuprofen in the solution remains soluble at concentrations from 100 mg/mL to 5 mg/mL without undergoing a phase transition, as well as a method for manufacturing the composition.

Abstract: An apparatus for safely retaining an eye implant lens for transport and access for inspection and use in which a holding apparatus has a chamber for holding a lens. In one embodiment the chamber has a pin on which a lens can be placed and a ramp leading to the pin so that a gripping member can slide up the ramp into proper placement to grip the lens and remove it. The gripper can be configured so that after removing the lens from the holding apparatus, it can be used to implant the lens. Also, a system including the apparatus and a bottle assembly that will hold the apparatus in the bottle. A method for holding an eye implant lens in which a lens is placed in the apparatus which can then be placed in a bottle assembly.

Abstract: A protective packaging with one or more product preparation features is provided.

Abstract: An array of absorbent article packages for multiple baby stages of development displayed via a merchandise display system may comprise multiple packages. Each package may comprise articles having absorbent article configurations appropriate for the stage of development of an infant, newborn, or toddler. Each package may also comprise indicia representative of the appropriate stage of development of the infant, newborn, or toddler. And, absorbent article configurations may differ between packages having overlapping size ranges.

Abstract: The potential for substance abuse involving residual amounts of abusable substances remaining in used skin-worn patches is reduced by the provision of a system and method for combining the abusable substance with a separate anti-abuse substance agent as part of a removal or disposal procedure.

Abstract: A substantially rigid defibrillator carrying case having a hinged side, a latch disposed on a latch side opposite the hinged side, and a handle disposed on a handle side disposed between the hinged side and the latch side. The carrying case is constructed without protrusions and with a rigid handle, which combine to allow easy removal and deployment of the contents from a vehicle storage location to a cardiac arrest patient. The carrying case latch is further constructed for greater ease of case opening and closing, and for greater latch hold strength.

Abstract: An implant container for accommodating one or more bone plate implants has a base having a receiving structure configured to receive at least one bone plate implant so that the bone plate implant is held in a defined relationship relative to the base. A lid of the implant container has an opening and is movable relative to the base from a first position to at least a second position. In the first position the lid covers the receiving structure at least partially so as to prevent implant removal, whereas in the second position the lid provides access to the receiving structure via the opening so as to permit implant removal.

Abstract: A package for a flat medical implant includes a flexible outer component, such as Tyvek®, including a first panel and a second panel foldable over said first panel for closing the package, and an inner component, such as paper, mechanically interlocked with the flexible outer component. A flat medical implant is held by the inner component. While the outer and inner components remains mechanically interconnected to one another, the upper ends of the first and second panels of the outer component are peelable away from one another for opening the package and accessing the flat medical implant at an upper end of the package.

Abstract: A disposable absorbent article is provided. The article comprises one or more disposable absorbent articles having a configuration corresponding to a wearer's stage of development, the disposable absorbent articles being enclosed in a package; a brand indicator disposed on the package and a line-up indicator disposed on the package, the line-up indicator including visual indicia and narrative indicia. The line-up indicator associates the absorbent article configuration with a corresponding stage of development, the association enabling a consumer to identify the appropriate absorbent article configuration for a wearer. An array of disposable absorbent article configurations is also provided.

Abstract: An orthopedic fixation system includes a sterile packaged implant kit and a sterile packaged instrument kit. The sterile packaged implant kit includes at least one surgical implant, an insertion device, and an implant package adapted to receive the at least one surgical implant and the insertion device therein. The implant package maintains the at least one surgical implant and the insertion device sterile after sterilization of the sterile packaged implant kit. The sterile packaged instrument kit includes one or more instruments necessary to use the sterile packaged implant kit and an instrument package adapted to receive the one or more instruments therein. The instrument package maintains the one or more instruments sterile after sterilization of the sterile packaged instrument kit.