A multi-layer bag comprising a porous portion configured to allow a sterilizing gas to penetrate into the bag and a gas-impervious portion, characterized in that the gas-impervious portion comprises an outer layer, an inner layer and an intermediate layer integrally formed together so that the intermediate layer is sealingly enclosed between the outer layer and the inner layer so as to be physically isolated from inner and outer environment of the bag, and the intermediate layer comprises a matrix and at least one pigment distributed within the matrix, the pigment being configured to change at least one optical property in reaction to an environment change resulting from a damage of the outer and/or inner layer.

The present invention relates to a method and apparatus for preventing bacterial cross-contamination between a user's personal item and a bacterially sensitive environment. More particularly, the present invention is directed to a method and apparatus for sanitizing a user's hands and cell phone prior to the user entering into a sterile operating room, thereby minimizing the introduction of contaminants via the cell phone.

Provided among other things is a sampling system for determining an amount or type of contamination a narrow, elongated passageway in a medical device, said sampling system comprising: (a) a fluid supply system that supplies to said passageway a sampling liquid for flowing through said passageway and a gas for flowing through said passageway; and (b) a receiving container that receives liquid from said passageway, wherein said sampling liquid is sterile, wherein said sampling liquid is configured to allow recovery of viable pathogens from the passageway, and wherein said sampling liquid comprises an amount and selection of surfactant effective to enhance the dislodgement of Enterococcus faecalis and Pseudomonas aeruginosa bacteria from the narrow passageways.

The present disclosure includes and provides for methods of packaging medical devices that are to be treated with a fluorinated liquid to alter their surface properties, packaging systems for such medical devices, and methods of utilizing the packaging systems to treat the medical devices. The packaging systems permit effective storage and distribution of medical devices that upon contact with mammalian blood have limited thrombogenicity or are non-thrombogenic and/or are resistant to adhesion of blood cells or clots.

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.

To provide an endoscope cap with a raising base or the like which is easily attached and detached to and from a distal end of an endoscope.

The endoscope cap includes: a cover that is attachable and detachable to and from a distal end of an insertion portion of an endoscope including a lever which is rotatably provided at the distal end of the insertion portion of the endoscope and a rotating portion which rotates the lever; and a raising base that has a lever connection portion connected to the lever and is rotatably provided inside the cover, and the endoscope cap is supplied in the state of being enclosed in an individual packaging member.

Single-use devices configured to sanitize accessible surfaces of luer access devices (e.g., needleless medical valves) at risk of contamination with infectious agents are described, as are methods for making and using such devices. In particularly preferred embodiments, such devices include a container (e.g., laminated foil pouches or packets) that contain a sanitizing component that includes a substrate with a cleaning port or recess, a cleansing matrix associated with the substrate, and a sanitizing reagent dispersed in the cleansing matrix.

Systems and methods that provide enhanced capability for toilets and bathrooms in general by adding feature sets such as user weighing, leak detection, enhanced toilet cleaning/deodorizing and other features, connected over networks to user devices and servers, creating a complete bathroom ecology where users have direct and remote control and access to system functions and data, and server based bathroom support applications provide a wide range of capabilities including user control and readout of toilet systems functions, bathroom condition, supply levels, and health data.

A hydrogen peroxide sterilization device for sterilizing a medical device, the hydrogen peroxide sterilization device including a hermetic outer container, a hydrogen peroxide pouch, and a hydrogen peroxide solution in the solution chamber. The hermetic outer container includes a sterilization enclosure configured to receive the medical device. The hydrogen peroxide pouch includes a permeable membrane enclosing a solution chamber and is configured to be positioned in the sterilization enclosure of the outer container. The permeable membrane is configured to allow hydrogen peroxide vapor to diffuse from the solution chamber through the permeable membrane into the sterilization enclosure.

A cleaning kit. The cleaning kit including a first liquid-tight container including a solute and a second liquid-tight container including a solvent adapted to be received within the first container to be ruptured by the application of pressure to the container by a user. The second container includes a sealable liquid-tight pouch; and a frangible seal along at least a portion of an outer edge of the pouch, wherein the frangible seal is broken by the application of pressure to the second container by a user greater than about 30 inches of water when tested according to ASTM Test F1140-07 (2007), wherein the second container is adapted to be openable while it is located in the first container to release the solvent from the second container into the first container, whereby the solute and the solvent are combined to form a cleaning liquid.