Patent classifications
A61L2/208
METHOD AND APPARATUS FOR STERILIZATION OF RESPIRATORY MASKS
A sterilization apparatus for sterilizing a respiratory mask is described. The sterilization apparatus comprises a sterilization chamber, an articulating mask support disposed inside the sterilization chamber, a bi-directional fan system disposed inside the sterilization chamber and configured to move air through an air passage to simulate human breathing, and a sterilization agent generator coupled to the sterilization chamber. The bi-directional fan system pumps air that includes the sterilization agent back and forth through the oxygen mask via the air passage, to mimic normal breathing of an individual using the mask.
CATALYST FOR GENERATING HYDROGEN PEROXIDE INDUCED BY TEMPERATURE DIFFERENCE AND METHOD FOR ENVIRONMENTAL DISINFECTION USING SAME
A catalyst adapted for generating hydrogen peroxide induced by a temperature difference and a method for environmental disinfection using the same are provided. The catalyst includes a thermoelectric material distributed on a substrate. The thermoelectric material induces a reaction between water vapor and oxygen contained in the air through a temperature difference to generate hydrogen peroxide, to serve a sterilization function through the hydrogen peroxide generated. The method for environmental disinfection using the catalyst includes the following. The catalyst is placed in an environment with a temperature difference. The catalyst is caused to induce a reaction between water vapor and oxygen contained in air through the temperature difference to generate hydrogen peroxide without applying power, and serve a sterilization function through the hydrogen peroxide generated.
Device for treating container closures
A device for treating container closures, for example for disinfecting container closures in a beverage bottling plant, includes a transport disk, rotatable about a vertical rotational axis, for transporting the container closures, and a helical closure guide, arranged above the transport disk, for laterally guiding the container closures, wherein the closure guide has a ceiling guide for guiding the container closures from above.
HYDROGEN PEROXIDE VAPOR GENERATION DEVICE, SPACE STERILIZATION APPARATUS INCLUDING SAME, AND SPACE STERILIZATION METHOD
The present invention relates to a hydrogen peroxide vapor generation device, a space sterilization apparatus including same, and a space sterilization method, including: an evaporation chamber which has a space formed therein, and includes a nozzle unit and a discharge port which are formed in an upper portion thereof; an evaporation unit which is formed in a lower inner portion of the evaporation chamber and equipped with a plurality of heating units and a hydrogen peroxide transfer pipe which are arranged in stack; and an air supply unit which is formed in a lower portion of the evaporation chamber and through which outside air is suctioned, discharged, and fed to the evaporation unit.
Nanocarriers for the delivery of active ingredients
Various embodiments of the present invention relate to, among other things, a nano carrier platform for generating enhanced engineered water nanostructures (iEWNS) encapsulating and delivering reactive oxygen species (ROS) and, in some instances, other active ingredients, methods for inactivating at least one of viruses, bacteria, bacterial spores, and fungi on a substrate by applying iEWNS to the substrate.
BLOW-MOLDING MACHINE AND METHOD OF STERILIZING THE SAME
To simply sterilize a blow-molding machine.
A mist or gas of hydrogen peroxide or a mixture thereof is introduced through a valve block (14) disposed adjacent to a molding die (13), thereby sterilizing at least the molding die (13) and an extension rod (15) that extends into the molding die (13) through the valve block (14).
APPARATUS AND METHOD FOR STERILIZING ENDOSCOPE
A method of sterilizing an article such as a flexible endoscope is performed in a sterilization chamber. A vacuum is applied in the sterilization chamber while the article is contained in the sterilization chamber. A sterilant is then introduced into the sterilization chamber. The pressure within the sterilization chamber is incrementally increased to provide a step-wise transition from a high vacuum state to atmospheric pressure. The article is thereby sterilized.
BARRIER LAYER
A barrier layer and corresponding method of making provide anti-inflammatory, non-inflammatory, and anti-adhesion functionality for a medical device implantable in a patient. The barrier layer can be combined with a medical device structure to provide anti-adhesion characteristics, in addition to improved healing, non-inflammatory, and anti-inflammatory response. The barrier layer is generally formed of a naturally occurring oil, or an oil composition formed in part of a naturally occurring oil, that is at least partially cured forming a cross-linked gel. In addition, the oil composition can include a therapeutic agent component, such as a drug or other bioactive agent.
METHOD FOR STERILIZING BLOW MOLDING MACHINE, AND BLOW MOLDING MACHINE
A blow molding machine is subjected to a sterilizing treatment in a simple manner. A liquid sterilizer is filled into preforms of at least the same number as the number of spindles. In a heating unit that heats the preforms to a molding temperature, some of the liquid sterilizer is caused to diffuse, and blow air is blasted into preforms in which the liquid sterilizer remains to cause the liquid sterilizer to diffuse in a molding unit, and molded bottles are discharged.
Biological indicator with variable resistance
A biological indicator with variable resistance may be controlled by moving a cap or housing of the biological indicator to cause the size of vents that allow flow of sterilant through the housing to decrease or increase in effective size. An indicator window may show a user the current resistance of the biological indicator, and may also show a readable indicator that may be captured by a scanner to allow a sterilizing cabinet to identify the current resistance. When the level of resistance shown by the readable indicator is not compatible with a sterilization cycle selected by a user, the procedure may be delayed and a notification provided to the user that a problem exists. The readable indicator may be a passive tag with a memory that allows information to be read and written, so that the biological indicator may carry data from one device to another.