Ethylenoxid (EO) Sterilization Glossary
Understanding the technical terminology is essential for maintaining compliance with FDA and ISO 11135 Standards. Below is an alphabetical guide to terms frequently used in Ethylenoxid (EO) Sterilisation discussions among medical device manufacturers.
The process of removing Gas-EO from a sterilized product by exposing it to air to reduce residual EO levels.
The number and type of microorganisms present on a product prior to the EO sterilization process.
The sealed vacuum container where the Sterilisationsprozess takes place under controlled parameters.
A colorless gas used as a potent Sterilisationsmittel due to its ability to penetrate packaging and reach complex device areas.
The movement of Gas-EO molecules from areas of high concentration to areas of low concentration within the load.
The measured ability of the Sterilisationsprozess to effectively kill specific microorganisms.
Preparing a product by exposing it to controlled humidity and temperature prior to EO gas injection.
The documented process of verifying that the sterilization cycle consistently achieves the desired sterility level.
Critical Technical Metrics: D-Value
In Ethylenoxid-Sterilisationstechnologie, Die D-Wert is one of the most vital metrics for quality control. It represents the specific time required to achieve a one-log (90%) reduction in the number of viable microorganisms at a set temperature and gas concentration.
BOCON: Your Expert in EO Sterilization Compliance
BOCONs ETO-Sterilisatoren der BCS-Serie are designed to meet all FDA sterilization Und ISO 11135 requirements. Our equipment provides precise control over Gaskonzentration, Expositionszeit, Und aeration, ensuring your products achieve the highest standards of safety and low residual EO levels.
