Aspects of the present disclosure relate to an electronic device having a housing that includes a major side portion having a curved major surface and an inside major surface, the major side portion comprises a first section and a second section each having different opacities. An aspect of the present disclosure is that the housing is not powder coated, or painted. The electronic device can have a display comprising an array of display elements surface mounted on a rigid printed circuit board such that the array of display elements are planar, a display element from the array of display elements is aligned with the second section such that light is transmitted through the second section and projected onto the curved major surface.

Methods, devices and program products are provided for a medical instrumentation storage cabinet. First and second instrumentation retention trays are configured to receive surgical instruments. The housing includes a top plate, a bottom shelf and at least one intermediate shelf there between. The bottom and intermediate shelfs and the first and second instrumentation retention trays include a plurality of holes there through to allow passage of a sterilization medium during a sterilization process. Standoffs are distributed about a perimeter of the housing. The standoffs separate the intermediate shelf from the top plate and bottom shelf to define first and second tray storage areas there between. The first and second tray storage areas have a shape and dimension to receive the first and second instrumentation retention trays. The standoffs are spaced apart from one another to define tray passages there between. The tray passages re sized and located to allow both of the first and second instrumentation retention trays to be inserted into the housing and opened to an open position relative to the housing in at least three directions.

Methods, devices and program products are provided for a medical instrumentation storage cabinet. First and second instrumentation retention trays are configured to receive surgical instruments. The housing includes a top plate, a bottom shelf and at least one intermediate shelf there between. The bottom and intermediate shelfs and the first and second instrumentation retention trays include a plurality of holes there through to allow passage of a sterilization medium during a sterilization process. Standoffs are distributed about a perimeter of the housing. The standoffs separate the intermediate shelf from the top plate and bottom shelf to define first and second tray storage areas there between. The first and second tray storage areas have a shape and dimension to receive the first and second instrumentation retention trays. The standoffs are spaced apart from one another to define tray passages there between. The tray passages re sized and located to allow both of the first and second instrumentation retention trays to be inserted into the housing and opened to an open position relative to the housing in at least three directions.

A method for sterilizing and decontaminating post-consumer absorbent sanitary products contaminated by organic compounds deriving from human metabolism and comprising drug residue, said post-consumer absorbent sanitary products comprising fractions of plastic, super-absorbent polymers (SAPs), and optionally cellulose, the method comprising at least the steps of: i) sterilizing (SR) said post-consumer absorbent sanitary products by heating to a temperature equal to or lower than 140° C. and at a pressure comprised between 1 bar and 3.6 bar to obtain sterilized post-consumer absorbent sanitary products; and ii) decontaminating (DC) from organic compounds said sterilized post-consumer absorbent sanitary products by means of an oxidizing treatment. The oxidizing treatment is carried out by putting the sterilized post-consumer absorbent sanitary products in contact with a gas containing ozone preferably at a temperature equal to or higher than 60° C., more preferably comprised between 60° C. and 80° C. The sterilized post-consumer absorbent sanitary products subjected to the decontaminating step have a humidity of less than 80%, preferably comprised between 60% and 75%.

A method for sterilizing and decontaminating post-consumer absorbent sanitary products contaminated by organic compounds deriving from human metabolism and comprising drug residue, said post-consumer absorbent sanitary products comprising fractions of plastic, super-absorbent polymers (SAPs), and optionally cellulose, the method comprising at least the steps of: i) sterilizing (SR) said post-consumer absorbent sanitary products by heating to a temperature equal to or lower than 140° C. and at a pressure comprised between 1 bar and 3.6 bar to obtain sterilized post-consumer absorbent sanitary products; and ii) decontaminating (DC) from organic compounds said sterilized post-consumer absorbent sanitary products by means of an oxidizing treatment. The oxidizing treatment is carried out by putting the sterilized post-consumer absorbent sanitary products in contact with a gas containing ozone preferably at a temperature equal to or higher than 60° C., more preferably comprised between 60° C. and 80° C. The sterilized post-consumer absorbent sanitary products subjected to the decontaminating step have a humidity of less than 80%, preferably comprised between 60% and 75%.

Methods, devices and program products are provided for a medical instrumentation storage cabinet. First and second instrumentation retention trays are configured to receive surgical instruments. The housing includes a top plate, a bottom shelf and at least one intermediate shelf there between. The bottom and intermediate shelfs and the first and second instrumentation retention trays include a plurality of holes there through to allow passage of a sterilization medium during a sterilization process. Standoffs are distributed about a perimeter of the housing. The standoffs separate the intermediate shelf from the top plate and bottom shelf to define first and second tray storage areas there between. The first and second tray storage areas have a shape and dimension to receive the first and second instrumentation retention trays. The standoffs are spaced apart from one another to define tray passages there between. The tray passages re sized and located to allow both of the first and second instrumentation retention trays to be inserted into the housing and opened to an open position relative to the housing in at least three directions.

Methods, devices and program products are provided for a medical instrumentation storage cabinet. First and second instrumentation retention trays are configured to receive surgical instruments. The housing includes a top plate, a bottom shelf and at least one intermediate shelf there between. The bottom and intermediate shelfs and the first and second instrumentation retention trays include a plurality of holes there through to allow passage of a sterilization medium during a sterilization process. Standoffs are distributed about a perimeter of the housing. The standoffs separate the intermediate shelf from the top plate and bottom shelf to define first and second tray storage areas there between. The first and second tray storage areas have a shape and dimension to receive the first and second instrumentation retention trays. The standoffs are spaced apart from one another to define tray passages there between. The tray passages re sized and located to allow both of the first and second instrumentation retention trays to be inserted into the housing and opened to an open position relative to the housing in at least three directions.

A step of letting a preform made of resin adsorb a sterilizer, a step of sterilizing the preform by heating the preform having adsorbed the sterilizer to a temperature suitable for a blow-molding treatment to activate the sterilizer adsorbed by the preform and a step of shaping the preform into a bottle by blowing aseptic air into the preform in a mold are performed sequentially. According to the above-mentioned steps, the sterilizer does not enter a blow-molding machine.

A step of letting a preform made of resin adsorb a sterilizer, a step of sterilizing the preform by heating the preform having adsorbed the sterilizer to a temperature suitable for a blow-molding treatment to activate the sterilizer adsorbed by the preform and a step of shaping the preform into a bottle by blowing aseptic air into the preform in a mold are performed sequentially. According to the above-mentioned steps, the sterilizer does not enter a blow-molding machine.

A step of letting a preform made of resin adsorb a sterilizer, a step of sterilizing the preform by heating the preform having adsorbed the sterilizer to a temperature suitable for a blow-molding treatment to activate the sterilizer adsorbed by the preform and a step of shaping the preform into a bottle by blowing aseptic air into the preform in a mold are performed sequentially. According to the above-mentioned steps, the sterilizer does not enter a blow-molding machine.