Abstract: A method for sterilizing the interior of a diffusion restricted area by introducing a sterilant in a chamber, condensing the vapor, reducing the pressure in the chamber to revaporize the condensed vapor, and maintaining the device in the chamber until the device is sterilized. The sterilant has a vapor pressure less than the vapor pressure of water and is preferably hydrogen peroxide. The pressure in the chamber while maintaining the device in the chamber may be held constant, varied, or increased. Plasma may additionally be introduced into the chamber to improve the rate of sterilization.

Abstract: An apparatus and method for monitoring a cleaning process for a medical device. The apparatus comprises a soil detector. The soil detector is capable of detecting inorganic and/or organic soil on a medical device or in a liquid utilized in a cleaning or cleaning monitoring process or on a soil-covered standard which can serve as a surrogate indicator of cleanliness for the medical device. The method of the invention for monitoring a cleaning process for a medical device comprises the step of measuring the soil removed from a medical device with the apparatus of the invention comprising a soil detector. Preferably, the method further comprises the step of determining when the device is sufficiently cleaned so that it can be sterilized.

Abstract: A method for determining and sterilizing a load in a sterilization chamber. A small amount of sterilant is introduced into the sterilization chamber and the concentration of sterilant is measured. The load of equipment to be sterilized is determined from the concentration of sterilant, and more sterilant is added, if necessary, based on the load. The process is repeated, if necessary, until the load is sterilized. The sterilant is preferably hydrogen peroxide, and the concentration of hydrogen peroxide is preferably determined by a spectrophotometric method in the infrared or ultraviolet regions. By monitoring the sterilant concentration and adding more as needed, the equipment in the chamber can be sterilized efficiently without exposing it to high concentrations of sterilant which could damage the equipment or leave too much residual on the equipment.

Abstract: A connector for use with a lumen device during the cleaning and sterilization of devices is provided. The connector provides fluid communication between a fluid source and the device. In particular, during the cleaning and sterilization cycle, the connection between the connector and the device does not produce occluded areas at the point of connection where the connector is sealably attached to the device.

Abstract: A method for determining and sterilizing a load in a sterilization chamber. A small amount of sterilant is introduced into the sterilization chamber and the concentration of sterilant is measured. The load of equipment to be sterilized is determined from the concentration of sterilant, and more sterilant is added, if necessary, based on the load. The process is repeated, if necessary, until the load is sterilized. The sterilant is preferably hydrogen peroxide, and the concentration of hydrogen peroxide is preferably determined by a spectrophotometric method in the infrared or ultraviolet regions. By monitoring the sterilant concentration and adding more as needed, the equipment in the chamber can be sterilized efficiently without exposing it to high concentrations of sterilant which could damage the equipment or leave too much residual on the equipment.

Abstract: A method for monitoring a cleaning process for a soiled medical device. The method involves cleaning the soiled device with a cleaning liquid in a cleaning chamber, exposing a detector to the cleaning liquid to measure the amount of soil removed, determining whether a sufficient amount of the soil has been removed from the soiled device so that the soiled device can be sterilized, and sterilizing the soiled device. One method of determining the amount of soil is by detecting the signal generated from the reaction between a chemical and the soil. Another method is to provide a soiled standard and measure the amount of soil removed from the soiled standard to determine whether enough soil has been removed from the soiled standard so that the soiled device can be sterilized. Another method involves measuring the amount of soil removed from the soiled device with at least two detectors.

Abstract: A connector for use with a lumen device during the cleaning and sterilization of devices is provided. The connector provides fluid communication between a fluid source and the device. In particular, during the cleaning and sterilization cycle, the connection between the connector and the device does not produce occluded areas at the point of connection where the connector is sealably attached to the device.

Abstract: A method and device for enhancing the vapor sterilization of the lumen of medical instruments and like articles under reduced pressure. A vessel containing a small amount of a vaporizable liquid sterilant solution is attached to the lumen. The sterilant vaporizes and flows directly into the lumen of the article as the pressure is reduced for the sterilization cycle.

Abstract: A glutaraldehyde sterilizing and disinfecting solution which is hard water compatible and which contains a nitrilo tris (ethyl phosphoric acid) salt as a buffering agent.

Abstract: A sterilization process wherein articles contacted with hydrogen peroxide and containing trace amounts of residual hydrogen peroxide are subjected to plasma treatment to generate an active species from the residual hydrogen peroxide which effects sterilization of the article and concurrently removes the residual hydrogen peroxide by converting it into non-toxic decomposition products.

Abstract: A plasma sterilization process which employs hydrogen peroxide vapor as the precursor for the active species generated during the plasma generation cycle and employs a pre-treatment cycle prior to the plasma generation cycle.

Abstract: An improved disinfecting and sterilizing composition having low odor and irritation potential is disclosed. The composition is an aqueous solution containing a 2 to 6 carbon atom dialdehyde and may also contain formaldehyde and a diol or monosubstituted diol of the formula RO(CH.sub.2 CH.sub.2 O).sub.n CH.sub.2 CH.sub.2 OH; where R is H or CH.sub.3 and n is an integer from 1 to about 22. Such compositions may be employed at a wide range of pH, from pH2 to pH9.