Abstract: Embodiments of the invention provide a bone screw device including a bone screw with a temporary encasement. In some embodiments, the temporary encasement comprises a biocompatible material that may be an osteoinductive, a hemostatic and or a bacteriocide. Some embodiments include a temporary encasement including a therapeutic. In some embodiments, the temporary encasement comprises a wax. In some embodiments, the screw head is substantially U-shaped. In some embodiments, the screw includes an extension tip extending from the screw shaft. Some embodiments of the invention include a system for percutaneous implantation of a bone screw including a screwdriver shaft rotatably coupled to a screw that includes a temporary encasement. In some embodiments, the screw shaft can be at least partially rotated by the screwdriver shaft. Some further embodiments further include a retractable sleeve at least partially surrounding the screwdriver shaft and the bone screw.

Abstract: Disclosed is a method for processing cut edges of a blank member, so called “package sleeve”, made from packaging material, in particular paper/plastics composite material, the cut edges of which are open from above and/or below, by applying a processing medium. In order to develop a simple and cost-effective method, in which the risk of contamination of the packaging and the aseptic region of a filling installation when the package sleeves are filled and closed is reduced, the processing medium contains at least one sterilizing medium and the sterilizing medium remains after being applied to the cut edges and is introduced into the packaging material.

Abstract: Embodiments of the invention provide a bone screw device including a bone screw with a temporary encasement. In some embodiments, the temporary encasement comprises a biocompatible material that may be an osteoinductive, a hemostatic and or a bacteriocide. Some embodiments include a temporary encasement including a therapeutic. In some embodiments, the temporary encasement comprises a wax. In some embodiments, the screw head is substantially U-shaped. In some embodiments, the screw includes an extension tip extending from the screw shaft. Some embodiments of the invention include a system for percutaneous implantation of a bone screw including a screwdriver shaft rotatably coupled to a screw that includes a temporary encasement. In some embodiments, the screw shaft can be at least partially rotated by the screwdriver shaft. Some further embodiments further include a retractable sleeve at least partially surrounding the screwdriver shaft and the bone screw.

Abstract: A woven laminated plastic bag having an easy open feature is provided. The easy open feature is generally defined by a weakened portion in the bag. In various aspects the bag can be fabricated from woven polypropylene and/or polyethylene layer which can be laminated with a film layer, can form a pinch bottom bag, and can have one or both sides include graphics and/or printing. The bag can also provide a top end and/or a bottom end either or both of which provide a discrete area which may contain discrete graphics and/or printing.

Abstract: A plurality of integrally arranged panels include a first panel and a second panel with a fold line therebetween. A compression reinforcement feature has a planar edge oriented orthogonal to a first planar surface of the first panel and perpendicular to a z-axis that defines a stacking load direction, the planar edge being disposed at a distance away from the fold line of half a thickness of the first panel, the first panel having a void between the fold line and the planar edge. The compression reinforcement feature is formed by at least four cut lines that define at least a portion of a closed perimeter of a cutout. One of the cut lines defines a location of the planar edge of the compression reinforcement feature.

Abstract: Provided is a multi-compartment pouch with a breakable or openable inner compartment used for mixing of two or more ingredients contained within the compartments without opening the pouch to the atmosphere. In one form, a two-compartment pouch includes a top compartment and a bottom compartment and an inner gusset separating the top compartment from the bottom compartment. The inner gusset includes an openable region and a fold line, and means for grasping and pulling apart the front and rear panels of the pouch to cause the openable region to open to allow for the combining of contents of the top compartment with contents of the bottom compartment without opening the pouch. Also provided are methods for making the multi-compartment pouch.

Abstract: The invention relates to a method and a device for packaging a flexible hydrophilic intraocular lens (1) placed flat on an injection support (4) which is adapted to carry out folding of the lens (1) during its implantation. The lens is immersed in a bath of liquid conserving solution contained in a sealed flask (30) which is itself enclosed in a packaging envelope (48), the assembly being steam-sterilized.

Abstract: A sterilization cabinet for use in an autoclave. The sterilization cabinet includes one or more filtered vents permitting sterilization agent to enter and exit the interior space of the cabinet during a sterilization cycle. Each vent is occluded by a cover plate. The cover plate contains a latch configured to accept a rod extending from the center of the vent and engage a notch disposed thereon. The floor of the cabinet is shaped to direct the liquid contained within the cabinet to flow into the drain port disposed within the floor. The drain assembly is used to expel the liquid from the cabinet while preventing microbes and contaminants from entering the cabinet. The hinges connecting the door to the cabinet can be used to adjust an angle of inclination, a horizontal position, and a vertical position of the door.

Abstract: A method of using a sterilization wrap system including a permeable material having barrier properties and having a first surface and a second opposing surface, the exterior panel being substantially opaque or having a first level of translucence, and an interior panel including a permeable material having barrier properties and having a first surface and a second opposing surface, the interior panel having a level of translucence that is higher than the translucence of the exterior panel, the panels being joined together over at least a portion of their surfaces. Also disclosed is inspection of the sterilization wrap system for exterior panel breaches by looking for light passing through a panel facing the viewer.

Abstract: Methods and apparatus for sterilization are presented. An exemplary embodiment includes a sterilizing cabinet assembly. The sterilizing cabinet includes a cabinet having an access port, a door connected to the cabinet, the door moveable between an open position permitting passage through the access port to an interior of the cabinet and a closed position precluding passage through the access port. The sterilizing cabinet assembly also includes at least one of the cabinet and the door having a vent port. The sterilizing cabinet has a primary filter overlying the vent port and forming a sealed interface with an adjacent portion of the one of the cabinet and the door and a secondary filter overlying at least a portion of the primary filter.

Abstract: Instrument containers for use in sterilizing, storing, transporting, and/or presenting medical instruments, such as dental and surgical instruments, are disclosed. The instrument containers may include, an instrument tray; a cover; and a plurality of openings formed in the instrument tray and cover. The instrument containers may be flexible containers, wherein the cover can be snap-fitted onto the instrument tray.

Abstract: Embodiments of the invention provide a bone screw device including a bone screw with a temporary encasement. In some embodiments, the temporary encasement comprises a biocompatible material that may be an osteoinductive, a hemostatic and or a bacteriocide. Some embodiments include a temporary encasement including a therapeutic. In some embodiments, the temporary encasement comprises a wax. In some embodiments, the screw head is substantially U-shaped. In some embodiments, the screw includes an extension tip extending from the screw shaft. Some embodiments of the invention include a system for percutaneous implantation of a bone screw including a screwdriver shaft rotatably coupled to a screw that includes a temporary encasement. In some embodiments, the screw shaft can be at least partially rotated by the screwdriver shaft. Some further embodiments further include a retractable sleeve at least partially surrounding the screwdriver shaft and the bone screw.

Abstract: Embodiments of the invention provide a bone screw device including a bone screw with a temporary encasement. In some embodiments, the temporary encasement comprises a biocompatible material that may be an osteoinductive, a hemostatic and or a bacteriocide. Some embodiments include a temporary encasement including a therapeutic. In some embodiments, the temporary encasement comprises a wax. In some embodiments, the screw head is substantially U-shaped. In some embodiments, the screw includes an extension tip extending from the screw shaft. Some embodiments of the invention include a system for percutaneous implantation of a bone screw including a screwdriver shaft rotatably coupled to a screw that includes a temporary encasement. In some embodiments, the screw shaft can be at least partially rotated by the screwdriver shaft. Some further embodiments further include a retractable sleeve at least partially surrounding the screwdriver shaft and the bone screw.

Abstract: Described are gas-permeable bags for storing respiring materials. The bags can be formed using a single sheet of a sturdy, transparent, gas-impermeable material to facilitate the viewing of bag contents. The bags can also include two or more gas-permeable walls with respective and different gas-transmission rates that are selected so that the overall gas-transmission rates for the bags are tailored for their contents. The types of films and laminates used for the gas-permeable walls exhibit gas-transmission rates for oxygen, carbon dioxide, and water that are favorable for different types of respiring materials.

Abstract: A sterilization cabinet for use in an autoclave. The sterilization cabinet includes one or more filtered vents permitting sterilization agent to enter and exit the interior space of the cabinet during a sterilization cycle. Each vent is occluded by a cover plate. The cover plate contains a latch configured to accept a rod extending from the center of the vent and engage a notch disposed thereon. The floor of the cabinet is shaped to direct the liquid contained within the cabinet to flow into the drain port disposed within the floor. The drain assembly is used to expel the liquid from the cabinet while preventing microbes and contaminants from entering the cabinet. The hinges connecting the door to the cabinet can be used to adjust an angle of inclination, a horizontal position, and a vertical position of the door.

Abstract: A package providing a storage space with features capable of affecting atmospheric conditions therein, comprising a body having a first and at least one second storage space adjacent thereto, wherein the first storage space is defined by sidewalls, and the at least one second storage space is defined by sidewalls including at least a portion thereof which further defines the first storage space, the second storage space providing a reservoir for containing an antimicrobial agent therein, wherein the antimicrobial agent includes a precursor to chlorine dioxide gas and the portion of the sidewall which further defines the first storage space is configured to allow for the delivery of the chlorine dioxide gas from the second storage space into the first storage space.

Abstract: A glucose sensor product is manufactured by a process that maintains the sterility of the glucose sensor while allowing gaseous manufacturing by-products to be vented from the inside of the glucose sensor package. The method begins by placing a glucose sensor assembly into a plastic package tray having a sealing surface surrounding an opening. The method continues by covering the opening with a microbial barrier material such that the microbial barrier material overlies the sealing surface, forming a seal between the sealing surface and the microbial barrier material, resulting in a sealed package tray containing the glucose sensor assembly, and sterilizing the glucose sensor assembly inside the sealed package tray. The microbial barrier material maintains sterility of the glucose sensor assembly while allowing volatile by-products outgassed from the glucose sensor assembly and the plastic package tray to pass therethrough.

Abstract: A sterilizable pouch for surgical instruments includes a sterilant permeable sheet with a first sealing strip and a sterilant impermeable sheet with a second sealing strip. The sealing strips are sealed together to define the pouch. At least one sealable open portion is for sealing the pouch after surgical instruments are located inside the pouch. An indicator material for indicating sterile processing conditions inside the pouch is located on an inner surface of the sterilant impermeable sheet inside the pouch.

Abstract: The present invention provides a gas permeable sterilization and shipping package system for medical products. The system includes a gas permeable sterilization package composed of an upper panel and a lower panel. Each panel has a main panel element, panel edges, and panel margins at or near the panel edges. The upper panel and the lower panel are joined at their respective panel margins so the respective main panel elements define a compartment for holding one or more articles to be sterilized. At least a portion of at least one panel is permeable to sterilant gas. The system includes at least one reinforcement strip joined to a panel at least at one location on its main panel element between its panel margins. Also disclosed is a method of sterilizing and shipping one or more items used in a medical procedure by utilizing the gas permeable sterilization and shipping package system.

Abstract: The present invention relates to bags made from medical-grade paper for sterilization, with sterilization-process indicators and pigmented-adhesive-based safety features, which is easy to handle and use and can be used to store materials, more particularly surgical medical material, for sterilization. Such bags are produced using medical-grade paper that is treated on the surface thereof with a microbiocide for sterilization, and, owing to the structure and design thereof, allow safe, rapid handling of the sterilized material placed within, since there are visual indicators that guarantee the hermetic closure and sealing thereof. Furthermore, generally, the invention has printed indicators that change color depending on the sterilization process carried out on the bags and on whether said process was carried out correctly.

Abstract: A packaging including a grouping nest for receiving syringes, a packaging tub, and a sealing cover for sealing the packaging tub. The packaging includes a plate intended to be positioned close to the flanges of the syringes before sealing of the tub; this plate includes a plurality of first surfaces intended to be placed in contact with the flanges and a plurality of second surfaces located on the side of the cover plate opposite this plurality of first surfaces, the distance between the plurality of first surfaces and the plurality of second surfaces being chosen in such a way that, when the plurality of first surfaces lies against the flanges, the plurality of second surfaces is in contact or in close proximity to the sealing cover.

Abstract: A preferably disposable item protector having a first and second layer, sealed peripheral edges, and an opening to provide access to the interior, formed of material substantially permeable to vapor and substantially impermeable to liquid and microbial contaminants. A method of producing such item protectors comprising the steps of folding a continuous strip of material, bonding the peripheral edges with adhesives, sonic bonding, heat bonding, or other techniques, and cutting the material proximate to the bonded edges to release the item protectors.

Abstract: A gas sterilization package component having (a) a gas diversion wall stock for at least a portion of a container, the wall stock having an opening therethrough; (b) a gas diversion layer; (c) a filter sheet disposed between (a) and (b), the filter sheet having a first surface and an opposing second surface circumscribed by a perimeter edge; and wherein the first surface of the filter sheet is attached to a surface of said gas diversion layer and the second surface of the filter sheet is sealed to a surface of the wall stock whereby an opening in the wall stock is covered by the filter sheet and a gas passageway is defined from the opening through a portion of the second surface of the filter sheet and extending through said filter perimeter edge.

Abstract: A pouch for retaining an endoscope during and after a decontamination process includes a first pouch side, a second pouch side attached to the first pouch side to form the pouch that is configured to retain the endoscope, and a port member coupled to the second pouch side. The second pouch side is securable to the first pouch side to seal the endoscope within the pouch. The second pouch side is configured to permit passage of a decontaminating substance. The port member is coupled to the second pouch side and includes an external interface configured to be connected to a device that provides the decontaminating substance for passage through the port member into an interior of the pouch.

Abstract: Packaging for prosthetic heart valves including an assembly for stabilizing dry prosthetic tissue implants such as heart valves during storage. The packaging assembly includes a primary sterile barrier that permits gas sterilization of the tissue implant, and a secondary sterile barrier that prevents oxidation of the implant during storage. Tissue heart valves are placed inside an inner tray and sealed with a gas-permeable lid. The inner tray is placed within an outer sterile barrier and the assembly is sterilized. The outer sterile barrier may include a double seal so that a first gas-permeable seal can be closed for sterilization, after which a second gas-impermeable seal is closed to seal out any further oxygen contact with the tissue implant. Alternatively, the inner tray is placed within a sterile pouch and the assembly gas-sterilized, and then the entire assembly is placed within another pouch that provides an impermeable barrier.

Abstract: A packaged, sterilized intraocular lens prepared by a process comprising providing a hydrophobic acrylic, or low water acrylic, intraocular lens and positioning the acrylic lens in a lens enclosure with an aqueous solution to provide a lens package. The lens package is then heated to a temperature sufficient for sterilization, however, the heating of the lens package must begin before the acrylic lens reaches an equilibrated, hydrated state following contact of the lens with the aqueous solution. The resulting sterilized acrylic intraocular lens will have less than sixty percent of total volume of disc-like features, or less than forty percent of total volume of water vacuoles, after 60 days following sterilization compared to an acrylic lens of the same composition, which was sterilized under the same conditions, but in an equilibrated, hydrated state.

Abstract: The present invention relates to novel smart packaging, designed using a novel material comprising a partially polar adsorbent solid base impregnated with a solution of vanillin, which allows the growth of microorganisms in different types of products to be detected visually without having to be in direct contact with the microorganism or with the medium containing same.

Abstract: A sampling system and method may use a kit that has a package enclosing a swab and a receptacle. The swab may have a shaft and a tip. The tip may be substantially made of calcium alginate. The receptacle may contain a diluent, such as sodium citrate, and glass beads. The swab may be used in an environment to sample microorganisms present on surfaces or in equipment. The kit may be used in a method of sampling and the resulting sample may be used in a method of quantitative testing.

Abstract: Packaging for prosthetic heart valves including an assembly for stabilizing dry prosthetic tissue implants such as heart valves during storage. The packaging assembly includes a primary sterile barrier that permits gas sterilization of the tissue implant, and a secondary sterile barrier that also prevents oxidation of the implant during long-term storage. Tissue heart valves may be placed or suspended within a cavity of an inner rigid tray with a gas-permeable lid sealed thereon, and a cap placed over the cavity to limit movement of the valve therein. The inner tray is placed within an outer sterile barrier, such as another rigid tray or a flexible pouch, and the assembly is then sterilized. The outer sterile barrier may include a double seal so that a first gas-permeable seal can be closed for sterilization, after which a second gas-impermeable seal can be closed to seal out any further oxygen contact with the tissue implant.

Abstract: The invention provides a syringe or autoinjector for dispensing a drug comprising a rigid syringe body containing the drug, an oxygen absorbing material, a separating element between the drug and oxygen absorbing material to prevent the drug from contacting the oxygen absorbing material but which allows oxygen to pass from the drug to the oxygen absorbing material, and an oxygen impermeable container enclosing both the drug and the oxygen absorbing material, wherein the oxygen impermeable container partially or fully forms the rigid syringe body or is held within the rigid syringe body.

Abstract: A non-reusable, locking container for sterilizing and storing surgical materials and presenting surgical materials in a sterilized condition. The non-reusable, locking sterilization container includes a tray, a lid, a permeable filter, a non-reusable lock and a frangible release that limit the container to only a single sterilization cycle or single use.

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: 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: The disclosed invention relates to an indicator composition comprising at least one iodide salt, at least one binder, at least one carbonate salt and/or at least one sulfate salt, and at least one antioxidant. The indicator composition may contain at least one dye, complexing agent, inhibitor, and/or solvent. A sterilization indicator comprising the foregoing indicator composition is disclosed. The sterilization indicator may be used for monitoring sterilization processes involving oxidative chemistries.

Abstract: A package (1) for an object such as a preferably-sterile medical component, includes: a support element (2) provided with elements (21) for coupling the object (5); a stopper (3) that can be coupled to the support element (2) in such a manner as to define a first chamber (7) for containing the object (5), and such that a grip portion (20) of the support element (2) projects from the stopper (3); and a cover (4) that can be coupled to the stopper (3) in such a manner as to define a second chamber (8) inside which the grip portion (20) of the support element (2) extends, and such that a portion (30) of the stopper (3) coupled to the support element (2) projects from the cover (4).

Abstract: A package is provided to include first and second sheets being releasably sealed together in a manner to define multiple compartments, each having one or more medical implements. A perimeter sealed region can have a seal width greater than an intermediate sealed region. A longitudinal intermediate sealed region and a transverse intermediate sealed region can be arranged within the perimeter sealed region. Formation of the perimeter sealed region along first and second ends of the package can be subsequent to the perimeter sealed region along third and fourth ends of the package. Before the formation, compartments having an opening facing the first end can receive medical implements, and compartments having an opening facing the second end can receive medical implements. The medical implements can remain uncovered by individual pouches when inserted into the respective compartments, thereby reducing manufacturing costs and environmental wastes.

Abstract: The present invention relates to a method of packaging and a packaging system for treated stents which minimize the level of exposure of the stents to oxygen, moisture and light. The package comprises two compartments, the compartments being in communication with each other via a breathable membrane.

Abstract: A package is provided to include first and second sheets being releasably sealed together in a manner to define multiple compartments, each having one or more medical implements. A perimeter sealed region can have a seal width greater than an intermediate sealed region. A longitudinal intermediate sealed region and a transverse intermediate sealed region can be arranged within the perimeter sealed region. Formation of the perimeter sealed region along first and second ends of the package can be subsequent to the perimeter sealed region along third and fourth ends of the package. Before the formation, compartments having an opening facing the first end can receive medical implements, and compartments having an opening facing the second end can receive medical implements. The medical implements can remain uncovered by individual pouches when inserted into the respective compartments, thereby reducing manufacturing costs and environmental wastes.

Abstract: A syringe assembly carrier includes a syringe-well holding fixture, a plurality of openings defined in the syringe-well holding fixture, and a plurality of syringe wells. Each of the syringe wells is configured to removeably receive a syringe assembly. The syringe-well holding fixture includes an upper surface and a plurality of mounting flanges coupled to the upper surface. Each of the plurality of mounting flanges is individually associated with a different opening in the syringe-well holding fixture and configured to receive a syringe well.

Abstract: A package for household articles provided with a holistic coding system. The coding system allows consumers to select the articles required for their needs without confusion. The coding system includes first coding elements on the dispensing means of package and second coding elements on the articles contained in the package.

Abstract: A system for organizing, protecting, sterilizing, storing and delivery of surgical instruments, implants and related devices. Post and button fasteners are removably mounted to a tray and hold rigid and flexible bracketry for securing devices within the assembly. Silicone holders are mounted to upstanding pegs secured to the tray wall by nuts limiting movement of the holders relative to the tray wall.

Abstract: A collapsible single-use sterilization container for use in the sterilization of medical instruments is provided. The sterilization container includes a lid having central portion defined by a frangible region. Upon activation of the frangible region, the central portion may be removed rendering the sterilization container inoperable for future use.

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 pouch having a pocket formed therein. A carrier tube may be disposed in the pocket. The carrier tube may have a plurality of apertures formed therein. A medical device may be disposed within the carrier tube.

Abstract: The invention relates to protected filter units for safety filtration, in which the filter units are at least double-packed with different packaging materials and to a method for producing the protected filter units. In this case, the first packaging material is permeable to gases but impermeable to microorganisms and the at least second packaging material is impermeable to gases. The first packaging material fixes the at least one filter unit, and so no abrasion can take place during transport and handling. The filter units according to the invention are suitable for sterile filtration processes and for filtration processes under clean-mom conditions.

Abstract: The system contains a base with a plurality of base ventilation holes and a plurality of side walls. The base includes a base instrument holder fixed to the base. At least one stage with a plurality of stage ventilation holes is positioned within the base. The stage includes at least two legs fixed to the stage, at least one stage instrument holder fixed to the stage, and a stage notched member fixed to the stage and positioned to engage a medical instrument beneath the stage. A fixed or removable cover having a plurality of cover ventilation holes is included to surround the base.

Abstract: The invention concerns a package (2) for sterilized products or products to be sterilized comprising a plastic box (4) and a lid (16) fixed on the box (4) to seal the latter with a tight sealing zone. The invention is characterized in that the lid (16) comprises: a plastic cover sheet (20) transparent for electronic irradiation and for light radiation; at least a window (22) provided in the cover sheet (20); at least a sheet of selectively sealing material (24) integral with said cover sheet (20) and closing the window (22); and an opaque screen (26, 126) for at least an electronic irradiation passing through the cover sheet or the selectively sealing material, said screen extending inside the package (2), proximate to the cover sheet (20), so as to allow through a sterilizing gas, for example ethylene oxide (ETO) or water vapor, through the selectively sealing material (24).

Abstract: A catheter assembly is disclosed comprising a catheter and a receptacle enclosing said catheter. The receptacle has a first part and a second part, which parts are foldable over each other. Further, at least one sticky adhesive area is arranged on the surface of one of the parts of the receptacle in such a way that the sticky adhesive area is covered by the other part when the receptacle is in a folded disposition, and exposed to the environment when the receptacle is in an unfolded disposition.

Abstract: The tampon applicator assembly includes a tampon applicator section, an outer housing section, and a plunger section. The combined tampon applicator section and plunger section function as a conventional plunger-type tampon applicator. The outer housing section includes a sleeve with a proximal portion and a distal portion. The (distal) insertion end of the tampon applicator section essentially fits inside the proximal portion of the sleeve, and the distal portion of the sleeve is designed to accommodate a feminine hygiene product, such as a pad, a disposable wipe, a towelette disposal mitt, a simple disposal bag, and other products associated with menstruation.

Abstract: A single-use sterilization container for use in the sterilization of medical instruments is provided. The sterilization container includes a lid having central portion defined by a frangible region. Upon activation of the frangible region, the central portion may be removed rendering the sterilization container inoperable for future use.

Abstract: A package (599) with three layers allows sterilization of the package contents, provides a separate area for a scavenger and minimizes the oxygen transmission rate for the package and has, in one embodiment, a third layer (330) with a first section (336) of breathable polymeric material, a second section (334) of substantially non-breathable polymeric material and a third section (332) of breathable polymeric material which is positioned between a first layer (512) of substantially non-breathable polymeric material and a second layer (514) of substantially non-breathable polymeric material. The first layer (512) and the second layer (514) are fixed together to define a non-breathable pouch (516); and the third layer (330) is fixed to the first layer (512) and the second layer (514) and divides the non-breathable pouch (516) into a first compartment (592) and a second compartment (594).