An assembly for removing odors from items having a first container formed from a material that is at least partially ozone impervious and that defines a first interior that is accessible via a selectively closeable opening, an ozone generator that is adapted to generate and expel ozone gas from the ozone generator into the first interior of the first container, and a fastening mechanism for selectively maintaining the selectively closeable opening in a closed orientation in which the fastening mechanism prevents access to the first interior. In various embodiments, when the selectively closeable opening is in the closed orientation and the ozone generator expels ozone into the first interior of the first container, the ozone concentration in the first interior is at a concentration of between 1 ppm and 2000 ppm and the ozone leakage from the first container is between 0.01 ppm and 0.03 ppm of ozone.

Apparatus, system, and methods are provided for reducing infectious agents at a sterile site by preventing infectious agents from coming into contact with the sterile site. A barrier is produced for infectious agents that may come in proximity or otherwise communicate with the site. The apparatus is configured to create a void-free barrier in which infectious agents are reduced with minimal exposure of potentially harmful effects of the barrier to the sterile site, objects, or users of the apparatus.

Systems and methods for detection, treatment, prevention and protection are shown and described. UVC may be used in such applications.

A system and method for systematic, controlled removal of sterile products from blister packs for use during surgery is disclosed.

The disclosure relates to a microbicidal composition with excellent action of limiting a decrease in durability of synthetic adhesives as well as high microbicidal action. The microbicidal composition contains 0.03 to less than 1.0 mass % of peracetic acid, 0.045 to less than 1.5 mass % of hydrogen peroxide, and 0.036 mass % or more of glycine.

A system and method for systematic, controlled removal of sterile products from blister packs for use during surgery is disclosed.