Sterilizable multilayer material (1), in particular for packaging at least one device for medical use, comprising a non-thermofusible sheet (2) sandwiched between two lower and upper thicknesses (3, 4) of thermofusible material of at least one thermofusible sheet (F), these thicknesses of thermofusible material being welded together across the non-thermofusible sheet.

Packaging for the sterile storage and transport of objects for medical, pharmaceutical or cosmetic applications and a packaging process are provided. The packaging includes at least one bag made of a first and a second web, bonded to one another, a feature thereof being that the first web consists of a selectively permeable nonwoven fabric and that the second web consists of a laminated film with at least three layers, where the first layer is a polymer film arranged on the external side of the bag, the second layer is a lamination adhesive and the third layer is a polymer film arranged on the internal side of the bag. At least one of the layers of the second web includes one or more pigments. In an 8-bit greyscale image, the seal seam, imaged in transmitted light and contrast-standardized, is depicted within a greyscale value range of 50-200.

A package system suitable for sterilizing cyanoacrylate compositions and providing the sterile cyanoacrylate compositions a shelf life of at least 24 months, wherein the package system comprises: an ampoule comprising a chamber comprising a cyanoacrylate monomer, wherein the chamber is defined by an opening and sidewalls, wherein the ampoule comprises a material comprising a cyclic olefin copolymer; a multilayer foil seal sealing the opening of the ampoule; and a secondary package housing the ampoule.

A preheating device for endoscopy includes a flexible bag, a plurality of first welded joint, and a mark member. The flexible bag is disposed with a saturated sodium acetate solution and a trigger. The flexible bag includes a closed circumference around the outer periphery thereof. The closed circumference includes a longer side and a shorter side next to each other. The plurality of the first welded joint is arranged into a folding line along a longitudinal direction, wherein every two adjacent first welded joints of the folding line forms a flowing space. The folding line is substantially parallel to the longer side. The first welded joint nearest to the shorter side is the last first welded joint, and the mark member is disposed on the flexible bag between the last first welded joint and the shorter side. The mark member is used for indicating a placement of an endoscopy.

A flexible, sterilizable pouch includes a first wall coupled to a second wall and a cavity defined between the first wall and the second wall. The cavity is configured to receive a medical device, and the pouch is configured to seal the medical device within the cavity. At least one of the first wall and the second wall of the pouch includes two layers. Each layer is coupled to the adjacent layer such that a breach in any one layer of the multi-layered wall will not breach the seal of the pouch. A pocket may be formed between the layers of the multi-layered wall and may include a gas under pressure to inflate the corresponding wall to an inflated state.

A package for a medical device includes a blister having a base and a plurality of walls extending from the base with the base and the walls defining a cavity for receiving the medical device. The blister includes a first thermoplastic polyurethane or a combination of the first thermoplastic polyurethane and polyethylene terephthalate glycol. The package also includes a lid disposed on the blister and at least partially covering the cavity. The lid has outer and inner surfaces and includes a high density polyethylene. The package further includes an insert disposed on and in direct contact with the inner surface of the lid and facing the cavity. The insert includes a second thermoplastic polyurethane for increasing puncture resistance of the lid from the medical device.

A package comprises a sterilized, reusable textile item comprising a textile material; a reusable bag comprising a sterilized textile material defining an interior cargo space in which the sterilized textile item is contained; a reusable envelope comprising a folded, sheet of sterilized textile material by which the bag containing the sterilized textile item is entirely enveloped; and a reusable tie comprising an elongate length of a sterilized textile material extending around and securing the envelope onto the bag. A method comprises inserting the textile item into the bag; folding the sheet about the bag; and securing the folded sheet enveloping the bag using the tie. All four components are reusable of the packaging including the textile item. The package preferably constitutes mono material packaging.

A sterile barrier system for medical device packaging. The sterile barrier system includes a layer forming a breathable sterile barrier. The layer includes a plurality of fibers. Each of the fibers includes a hollow fiber body and an agent contained within the hollow fiber body. The fibers are configured such that the agent flows from the corresponding hollow fiber body when the hollow fiber body is severed. When the sterile barrier system is subjected to damage, the agent is released from any hollow fiber body severed by the damage and imparts one or both of repair or visual indication of a possible integrity breach. In some embodiments, the agent is a self-healing agent. In other embodiments, the agent is a dye. In some embodiments, the layer is an electrospun web. A medical device packaged in a sterile barrier system is also provided.

A biological containment and transport carrier apparatus for use with an equipment table in an operating room, including a base layer having an inner surface and an opposing outer surface, a top layer having an inner surface and an opposing outer surface, a perimeter of the top layer being coupled to a perimeter of the base layer to form a sealed bag, an inner seam portion formed between the base layer and the top layer, the inner seam portion having a length and width dimension configured to respectively match a length and a width dimension of a top surface of an equipment table in an operating room, and a zipper formed within the top layer to open and close an insertion flap of the top layer so as to provide access to the inner seam portion such that when the zipper is open, at least a portion of the inner seam portion is configured to fold inside out over a top surface of the table and wrap around one or more outer edges of the table and extend a predetermined distance below the bottom surface of the table to secure the base layer to the table and to provide a sterile margin, or drape portion, around the table, and to provide a custom fit for the table to allow for sterile use in procedure of setup packs with reduced exposure of contaminated surfaces.

There is disclosed a system for cleaning and disinfecting allograft material. In an embodiment, the system includes a sterile bag and a motorized paddle blender. The sterile bag having an outer wall configured to withstand blending forces, at least one paddle contact section, and an allograft retaining section separate from the at least one paddle contact section. The motorized paddle blender having at least one paddle configured to apply blending forces on the sterile bag on the at least one paddle contact area, a motorized portion to actuate the at least one paddle, and a door component configured to hold the sterile bag adjacent the at least one paddle. The at least one paddle and the allograft retaining section are configured to prevent the paddle from contacting the allograft material when the blending forces are applied on the sterile bag on the at least one paddle contact area.