Abstract: A wire organizer includes a basin having an inner surface that defines a reservoir. The reservoir has a liquid therein. A hub is positioned within the reservoir. A plurality of spools are positioned on the hub such that the spools are spaced apart from the inner surface and are rotatable relative to the basin. The spools each have a wire wrapped around each of the spools. At least a portion of each of the wires extends through the liquid. Systems and methods are disclosed.

Abstract: A container for separating, storing, and dispensing dental picks includes a container to receive a sheet of dental picks, wherein the sheet of dental picks includes multiple interconnected dental picks, a separating device to separate the sheet of dental picks into singular dental picks, and a dispensing device to dispense the singular dental picks, one at a time. A method for separating and dispensing dental picks includes obtaining a sheet of dental picks, wherein the sheet of dental picks includes multiple interconnected dental picks, loading the sheet of dental picks into a container, separating the sheet of dental picks into singular dental picks, and dispensing the singular dental picks one at a time.

Abstract: A recloseable container comprising a substantially rectilinear, paperboard-based carton and a plastic recloseable device is provided. The carton defines a container interior and has a face panel defining an opening. The opening has a perimeter sized to receive the recloseable device. The recloseable device may be a plastic unitary structure similar to a clamshell type blister pack and may comprise a frame attached to the carton and a door hingedly attached to the frame.

Abstract: An irrigating device including a massage mode module in communication with a motor driving a pump. During a normal mode the pump has a first pulse rate and during massage mode the massage mode module provides a massage control signal to the motor to cause the pump to have a second pulse rate. In other embodiments, the disclosure includes an oral irrigator including a base and a reservoir removably connected to the base. The oral irrigator further includes a prow operably connected to the base and extending vertically upwards from the base. The prow may extend in a similar direction as sidewalls of the reservoir. The oral irrigator further includes a lid rotatably connected to the prow. The lid rotates between a first position where a fluid cavity of the reservoir is exposed to a second position where the lid covers at least a portion of the fluid cavity.

Abstract: The invention relates to a catheter kit comprising a catheter and a urine bag stored in a package wherein flow is prevented between the catheter and urine bag when stored but enabled when the kit is used.

Abstract: The disclosure relates to a container for shipping, storing, dispensing, and receiving units for storing, dispensing, and receiving medical sharps, wherein the container includes a plurality of compartments, said compartments each being capable of containing one unit for storing, dispensing, and receiving medical sharps and to a method of using said container to store, dispense, receive, and ship said units.

Abstract: A heating system comprising a pouch, into which one or more single-use packettes are placed for heating. In preferred embodiments, the pouch comprises printed heating elements, printed circuit elements and a means of connecting to a power source. Power may be supplied through a USB-type connector or a handheld power supply that is custom designed to work with the heating pouch.

Abstract: A heating system comprising a packette for heating a mask, wipe or towelette. In preferred embodiments, the packette comprises printed heating elements, printed circuit elements and a means of connecting to a power source. Power may be supplied through a USB-type connector or a handheld power supply that is custom designed to work with the heating packette.

Abstract: A system and method for protecting biological or other material from contamination through the steps of filling, freeze-drying, packaging, storing and use are disclosed. A system can include a flexible container, a membrane configured to transmit air or solvent vapor out of the flexible container, and a membrane frame supporting the membrane and engaged with at least one column member. The at least one column member can be configured to maintain the membrane and the membrane frame a spaced distance from one or more contents received within the flexible container. Upon application of a downward force, the at least one column member can assume a collapsed configuration. A method can include inserting a biological material, for example, into a flexible container, freeze-drying the biological material, moving the freeze-dried biological material to a portion of the flexible container that includes at least one port, and sealing the biological material within the portion.

Abstract: A catheter assembly includes a catheter attached to a connector and a package. The catheter has a proximal end sized for insertion into a bladder though a urethra and a distal end opposite of the proximal end. The connector is attached to the distal end of the catheter. The package is sized to receive the catheter and the connector, with the package including an opening sized for removal of the catheter and the connector from the package. A tab is placed over the opening of the package to seal the catheter and the connector inside of the package. An extractor has a first portion connected to the tab and a second portion coupled to the catheter proximal of the connector.

Abstract: A plastic package for hydrophilic articles, in particular for hydrophilically coated medical instruments, is intended to ensure the hydrophilic nature of the enclosed instrument over a long period of time. The package includes at least one receiving compartment with a medical instrument for insertion into body tissue and is characterized in that, after sterilization by radiation, it has a proportion of volatile constituents of ?0.1 ?g/cm2.

Abstract: The present invention provides a urinary catheter assembly which comprises at least one urinary catheter for collecting urine from a body opening and a collecting bag connected to the catheter, in a way that a urinary flow can be established in a flow path from the catheter into the bag. The assembly further comprises a catheter package with a container and a cover. The container forms an accommodation for an insertable part of the catheter, and the cover forms a cavity for the collecting bag. The cover is releasably fixed to the container. Furthermore, the package forms an overlap in which the cavity partly covers the accommodation.

Abstract: An aqueous emulsion composition of organic peroxide, including from 10 to 65% by weight of one or a plurality of organic peroxides, from 2 to 25% by weight of at least one antifreeze agent, from 0.01 to 10% by weight of at least one emulsifying agent, optionally at least one additive, water, of which the quantity is defined in order to form the remainder of the total composition (100%), wherein the emulsifying agent is a colloid agent of a polyvinyl acetate having a degree of hydrolysis greater than 80% and a viscosity, measured in solution in water at 4% by weight at 20° C., less than or equal to 5 mPa·s, said viscosity being measured with a Brookfield RVT viscometer, needle no. 3, 20 rpm, in accordance with the ISO 2555 standard. Also, to the method of preparing same and the use thereof.

Abstract: A syringe assembly including a plunger rod separate and detached from a syringe barrel and a packaging member, the plunger rod having a sealing member and the packaging member having a first compartment and a second compartment is disclosed. With the syringe barrel received within the first compartment and the plunger rod received within the second compartment, the sealing member of the plunger rod seals the syringe barrel and the plunger rod within the packaging member. In this manner, the syringe assembly is placed in the packaging member in a manner that allows for reduced storage space of the syringe assembly.

Abstract: A multifunctional enclosure is described having an elongated sleeve configured with an enlarged opening for the insertion of an elongated member of a medical probe. The multifunctional enclosure is configured to prevent the elongated member of the medical probe from swinging and becoming damaged during transport. The multifunctional enclosure may further comprise at attachment component for securing the medical probe to the multifunctional enclosure. Furthermore, at least one vent may be configured onto the multifunctional enclosure, such as on a first end closure portion. The vent may allow for adequate flow for sterilization and/or drying.

Abstract: A flip-open multi-pack assembly is provided which can contain a plurality of new pen needles, such as through the provision of a rectangular or tube-shaped shaped, hinged shell housing, wherein new pen needles can be stored in a plurality of user accessible openings each having a sterility barrier formed, for example, by covers that cover the non-patient end of the openings in which the new pen needles are contained. Used pen needles can be returned and stored in openings accessible by rotatably opening the shell housing. One or more of the openings within first and second opposite ends of the housing shell can be provided with a slidable internal holder within the device and are configured to releasably secure the inner shield of the new pen needle, and to then be pulled forward when the new pen needle is removed and lock at a forward position, and thereby create an interior space, accessible from an opposite end when the hinged housing is opened, for a used pen needle to be inserted and stored.

Abstract: A catheter assembly (1) comprising a catheter (8) having a proximal end (10) adapted to be inserted into a bodily cavity and a distal end (11) having a drainage outlet (13), a catheter package (2) having a cavity for accommodating the catheter and an opening for withdrawing the catheter from the package, and extracting means (17) that are coupled to the catheter for extracting the distal end of the catheter out of the package.

Abstract: Charcoal barbecue grills have a grate (coarse screen) for grilling foods which has generally a size of 430 mm×250 mm or a diameter of 550 mm (in kettle barbecue grills). With these dimensions it is not possible to soak the grate (coarse screen) in the sink of any household kitchen in order to remove residues which accumulate during barbecuing (grease and food remains) because without soaking the grate (coarse screen), it is impossible to completely remove the waste. With the cleaning basin it is possible to clean the dirty grate easily on the barbecue grill. In addition, the residual heat of the grilling coals is used to heat up the wash basin to thus be better able to loosen the impurities. Another advantage of this invention is that the cleaning basin is stored in or on the barbecue grill, thus requiring no separate place. The cleaning basin for rectangular barbecue grills is represented in FIG. 6. The cleaning basin for the round (kettle grill) barbecue grill is represented in FIG. 2.

Abstract: Medical device packaging, medical device packaging assemblies, and methods for preparing and packaging medical devices. An example medical device packaging assembly may include a packaging pouch including a front pouch portion and a back pouch portion. The front pouch portion may include a first sheet of material having a plurality of layers. The back pouch portion may include a second sheet of material having a plurality of layers. A medical device may be disposed in the pouch. At least one of the plurality of layers of first sheet of material and the plurality of layers of second sheet of material may include a moisture scavenging layer. In addition, at least one of the plurality of layers of first sheet of material and the plurality of layers of second sheet of material includes an oxygen scavenging layer.

Abstract: A catheter assembly including an elongate member having a proximal end and a distal end. The distal end has at least one drainage opening. A hydrophilic coating is provided on at least a portion of the elongate end of the catheter. A fluid containing member is provided and is either arranged on the elongate member or within a separate area of the container. The fluid containing member contains sufficient hydrating fluid to hydrate the coating of the catheter. A container contains the elongate member and the fluid containing member and incorporates at least one foil layer to prevent evaporation of the hydrating fluid. A method of using the catheter includes inserting a catheter into a user's body and draining fluid from the user's body.

Abstract: A toilet training device includes an odor remediation system for absorbing or masking odors that may be created during toilet training. The odor remediation system may include a modular odor remediating insert that may be releasably positioned within a recess that is provided within the toilet training device. The odor remediating insert may include an odor absorbing substance such as sodium bicarbonate, an odor masking substance such as a fragrance or a combination of an odor absorbing substance and an odor masking substance. The toilet training device also includes a system for dispensing wipes that may utilize a recess that is defined in a side wall of the main body portion of the toilet training device. A wipes cartridge is designed so that it can be used to conveniently dispense wipes regardless of whether it is separated from the toilet training device or mounted within the recess of the toilet training device.

Abstract: A receptacle for consistently orienting a sterilized surgical instrument for natural grasping by a physician without removing his or her vision from the operational field, wherein the receptacle may also comprise a reservoir and desiccant for maintaining sanitized or sterilized instruments.

Abstract: A disposable sterile breakable vial includes a handle section and a vial section which are completely separable in response to a manually applied separation force. The vial section includes a sterile void dimensioned to contain a unit dose of a sterile therapeutic topical agent. An elongated member comprises a proximal portion supported by the handle section and a distal portion provided with a sterile applicator element, such as a brush. At least the applicator element is completely enclosed within the vial section with the applicator element immersed within the therapeutic topical agent. A hermetic seal between the handle and vial sections maintains sterility of at least the vial section prior to handle and vial section separation. Complete separation of the handle section and the vial section exposes the elongated member and the applicator element for topical application of the therapeutic agent saturating the applicator element.

Abstract: A protective cover for a nasal cannula completely encloses the two prongs of the nasal cannula when properly installed. This protective cover will keep the nasal cannula from contacting potentially unclean surfaces when the nasal cannula is not in use. An optional UV light may be present in the protective cover to provide UV cleaning of the nasal cannula prongs when the cover is closed.

Abstract: A method of making a ready-to-use catheter assembly and a ready-to-use catheter are provided, which avoids any degradation of the catheter during sterilization. The method comprises: placing a catheter with a hydrophilic coating and a wetting fluid in a catheter package made of low moisture transmission material while the package is in a first condition wherein an insertable length of the hydrophilic coating of the catheter is not in contact with the wetting fluid, sterilizing the catheter package with the catheter and the wetting fluid by radiation sterilization while the catheter package is kept in a condition in which the insertable length is not in contact with the wetting fluid, transferring the catheter package with the catheter and the wetting fluid into a second condition, bringing the wetting fluid into contact with at least the insertable length and activating the insertable length via gravity and/or via inertia.

Abstract: A method of making a packaged antimicrobial suture. The method includes the steps of providing a containment compartment molded from a polymeric resin comprising a polymeric material and an antimicrobial agent, positioning a suture within the containment compartment, the suture comprising one or more surfaces; covering the containment compartment having the suture in an outer package cover having an inner surface, and subjecting the outer package, the containment compartment and the suture to time, temperature and pressure conditions sufficient to vapor transfer an effective amount of the antimicrobial agent from the containment compartment to the suture, while retaining an effective amount of the antimicrobial agent on the containment compartment, thereby substantially inhibiting bacterial colonization on the suture and the containment compartment. A packaged antimicrobial suture is also provided.

Abstract: A container for storing personal care articles comprising a lid structure attached to the container is disclosed. The lid structure has a top lid portion connected to a base lid portion. The base lid portion includes a rigid port surrounding a unitary dispensing partition extending in an x and z direction to the rigid port, the unitary dispensing partition having a dispensing slit formed therethrough. The unitary dispensing partition forms an arc extending a first depth into the interior of the container in a z-direction. The depth of the dispensing partition allows for the personal care article to be stored in a pop-up dispensing position with a larger portion of the personal care article extending from the dispensing slit. This allows for easier retrieval of the product by a consumer and less dispensing failures.

Abstract: A medical device assembly is disclosed, comprising a medical device, preferably having a hydrophilic surface coating, and a package accommodating said medical device. The package if formed of two sheets of foil material, a first foil of which has been deep drawn into a trough shape, the package further comprising a resealable opening arranged within the bounds of the second foil. The medical device may e.g. be a urinary catheter.

Abstract: A moist wipes dispenser has a top attached to a bottom along a hinge. The top is adapted to pivot about the hinge's axis of rotation. The top is adapted to assume a closed position and a dispensing position. In one embodiment, the top can assume a warning position adapted to warn a user that the top is not shut. The top is urged to the warning position if the top is angularly disposed in a red zone that extends between the closed position and the warning position. The warning position is angularly displaced from the closed position by at least five degrees. In another embodiment, the hinge includes a pin integrally molded with the top or bottom, and an open knuckle integrally molded with the other of the top and bottom. The hinge is adapted to urge the top into closed and dispensing positions in selected angular ranges.

Abstract: A package for a catheter is provided. The package includes a container with a first cavity and a second cavity. The cavities are configured so as to prevent liquid swelling medium stored in the container from travelling from the second cavity into the first cavity and out through an opening into the container. Thus, the position of the cavities with respect to each other allows them to function as a water-lock.

Abstract: A CPAP mask storage apparatus having a first storage compartment that is hermetically sealed so as to substantially isolate the CPAP mask stored therein from airborne particles. The CPAP mask storage device includes a first panel and a second panel operable to provide access to the interior volume of the first compartment. The first panel and the second panel are configured to have adjacent longitudinal edges having semi-annular cutouts forming an aperture to accept an oxygen supply tube therethrough when the first panel and the second panel are in a closed position. The CPAP mask storage apparatus further includes a second container having a disinfecting liquid stored therein operable to disinfect the CPAP mask. A third compartment is contiguously formed with the first compartment and is operable to receive and store CPAP mask accessories.

Abstract: Packaging for prosthetic heart valves including an assembly for securely retaining a heart valve within a jar and facilitating retrieval therefrom. The assembly includes a packaging sleeve that fits closely within the jar and has a clip structure for securing a valve holder. Contrary to previous designs, in one embodiment the valve holder is directed downward into the jar, and the valve is retained with an inflow end upward. The valve may have flexible leaflets, and a leaflet parting member on the end of the shaft extends through the leaflets and couples with the valve holder. The assembly of the packaging sleeve, valve, and holder can then be removed from the jar and a valve delivery tube connected with the holder, or to the leaflet parting member. The packaging sleeve may be bifurcated into two halves connected at a living hinge to facilitate removal from around the valve/holder subassembly.

Abstract: The present invention provides a urinary catheter assembly which comprises at least one urinary catheter for collecting urine from a body opening and a collecting bag connected to the catheter, in a way that a urinary flow can be established in a flow path from the catheter into the bag. The assembly further comprises a catheter package with a container and a cover. The container forms an accommodation for an insertable part of the catheter, and the cover forms a cavity for the collecting bag. The cover is releasably fixed to the container. Furthermore, the package forms an overlap in which the cavity partly covers the accommodation.

Abstract: The present disclosure relates to a packaged urinary catheter. The catheter includes a conduit having a proximal end and a distal end. The distal end includes at least one aperture for receiving urine from the bladder. The catheter is contained within a sleeve having a length, a width, and a size configured to receive the catheter. According to one embodiment, the catheter and the sleeve may be arranged in a helical coil. The outer surface of the catheter may have a lubricious and/or an antimicrobial coating.

Abstract: An assembly comprising a catheter package (1), a catheter (7) and a collecting bag (3) is provided. The assembly has means for preventing flow of liquid through the catheter during storage. A sealing element (11) closing the eyelets is provided. An extended cone-lock (23) in a telescopic catheter is also provided.

Abstract: A vapor hydrated packaged catheter assembly and method of manufacturing and distributing same includes a gas impermeable package housing a catheter within a catheter-receiving cavity. The catheter assembly has a hydrophilic coating applied to at least a portion of the outer surface of a catheter tube or shaft which may be surrounded by a sleeve to provide a no-touch, sure grip feature. The catheter assembly is disposed within the catheter receiving cavity of the package together with a limited amount of a vapor donating liquid provided as a source of vapor to activate the hydrophilic coating. The amount of vapor donating liquid is less than the amount that would otherwise be sufficient to cause a spill hazard. It may be loose liquid as a desired percentage of the volume of a tube-receiving portion of the catheter receiving cavity of the package, or it may be contained in a liquid sequestering element.

Abstract: A disposable sterile breakable vial includes a handle section and a vial section which are completely separable in response to a manually applied separation force. The vial section includes a sterile void dimensioned to contain a unit dose of a sterile therapeutic topical agent. An elongated member comprises a proximal portion supported by the handle section and a distal portion provided with a sterile applicator element, such as a brush. At least the applicator element is completely enclosed within the vial section with the applicator element immersed within the therapeutic topical agent. A hermetic seal between the handle and vial sections maintains sterility of at least the vial section prior to handle and vial section separation. Complete separation of the handle section and the vial section exposes the elongated member and the applicator element for topical application of the therapeutic agent saturating the applicator element.

Abstract: A wipes container adapted to be set on a flat surface includes a dispenser housing defining a top and bottom walls, first and second side walls, and first and second end walls. The top wall includes a dispensing orifice. A plurality of wipes is disposed within an interior space. The first end wall has a first slip-resistant periphery and the second end wall has a second slip-resistant periphery. Each slip-resistant periphery includes thermoplastic elastomer material. The thermoplastic elastomer material is disposed along each periphery such that thermoplastic elastomer material contacts an underlying flat surface whether the container is position on its bottom, on a side, or on an end.

Abstract: A receptacle for consistently orienting a sterilized surgical instrument for natural grasping by a physician without removing his or her vision from the operational field, wherein the receptacle may also comprise a reservoir and desiccant for maintaining sanitized or sterilized instruments.

Abstract: With the subject invention, a container for an injection device with an injection needle is provided. The container includes a body having a compartment formed therein to accommodate the injection device in both a pre-use and a post-use condition. The body defines a first opening through which the injection device in its pre-use condition may be accessed, and the body defines a second opening into which the injection device may be directed in its post-use condition. A closure is provided for closing the first opening. The container also includes a retainer proximate the second opening for retaining the injection device in the container in its post-use condition preventing access to the injection needle after the injection device has been used to administer an injection.

Abstract: A vapor hydrated packaged catheter assembly and method of manufacturing and distributing same includes a gas impermeable package housing a catheter within a catheter-receiving cavity. The catheter assembly has a hydrophilic coating applied to at least a portion of the outer surface of a catheter tube or shaft which may be surrounded by a sleeve to provide a no-touch, sure grip feature. The catheter assembly is disposed within the catheter receiving cavity of the package together with a limited amount of a vapor donating liquid provided as a source of vapor to activate the hydrophilic coating. The amount of vapor donating liquid is less than the amount that would otherwise be sufficient to cause a spill hazard. It may be loose liquid as a desired percentage of the volume of a tube-receiving portion of the catheter receiving cavity of the package, or it may be contained in a liquid sequestering element.

Abstract: An arrangement having a plurality of moistened cosmetic pads based on nonwovens which are piled into a closable packaging container in order to distribute to the final consumer and to prevent evaporation. The pads have, on average, a moisture content of at least 200% of the dry weight thereof in the arrangement, the pads have a fiber structure made of staple fibers, are individually moistened and have a homogeneous moisture content such that the difference of the average moisture content of the pads which are arranged in the upper and in the lower quarter of the stack is, at a maximum, 30% of the average moisture content of all of the pads.

Abstract: The present invention provides an insertion device and method for implanting a biosensor into a patient subject. In one embodiment, a biosensor is stored in the instrument's hydration chamber which enables the biosensor to maintain proper hydration and sterilization prior to insertion. The instrument further includes a plunger that travels along a channel within the support device. After the biosensor is placed into the channel, the user pushes the plunger causing the biosensor to move through the channel and a hollow tube and into the patient subject. The present invention also provides for packaging and storing a biosensor and insertion device so that the biosensor is hydrated and sterile prior to insertion.

Abstract: A package in which a medical device is stored, the package comprising an outer shell providing a vapor barrier, a medical device positioned in the interior space inside the outer shell, the medical device including a liquid-containing element that is subject to drying out, a condition sensor comprising two metallic elements and a conductive water-containing element, each of the two metallic elements being composed of different metals, with each of the different metals selected so that the two metallic elements form an anode and a cathode of an electrochemical cell, so that the water-containing element forms the electrolyte of the electrochemical cell, and the voltage of the cell provides an indication the conductive water-containing element of the medical device has dried out.

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 catheter assembly includes a catheter, preferably having a hydrophilic surface coating; and a package accommodating said catheter. The package preferably also accommodates a wetting fluid. The package includes a first and a second sheet material connected around the edges; a perforation line extending along a non-closed loop in one of said sheet materials, which defines a flap opening; a third sheet material connected by means of an adhesive over said flap opening. The third sheet material with a margin covers the entire flap opening. The adhesive is adapted to maintain a sterile closure of the package before use, and to be resealable after use. The third sheet material forms a tab not provided with adhesive and the tab provides a grip portion for peel opening of the package.

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

Abstract: An IOL (intraocular lens) injector system comprises an IOL injector (2); an IOL holder (3) for holding an IOL (4); and an IOL holder container (100) for holding said IOL holder holding said IOL.

Abstract: This disclosure describes example portable medical device protectors that may be used in combination with various antimicrobial and/or antiseptic agents to reduce contaminants on a portable medical device. According to some embodiments, the disclosure describes that the protectors may comprise an impermeable container to store a permeable applicator impregnated with an antimicrobial or antiseptic agent.

Abstract: A body washing system provides an integrated single-use package co-locating a moist towelette and a dry towelette, the latter sized and design to permit drying of an individual after applying the moist towelette to his or her body in a washing process. The compact size and availability of the dry towelette substantially increases at the availability of bathing systems to individuals to whom conventional bathing or showering is inaccessible.