SteriVIT STERILIZATION
Our SteriVIT Process
Ethylene oxide gas penetrates material even at lowest temperatures and inactivates bacteria, viruses and funghi. Therefore, it is the method of choice for the sterilization of thermo-labile products. By means of the overpressure method and by using low ethylene oxide concentrations, we are able to sterilize in a reliable, efficient and reproducible way even narrow-lumened products and geometries which are hard to penetrate. A low agent concentration ensures the integrity of your products equipped with drugs, whereas other sterilization methods reach their performance limits here. Conditioning, sterilization and desorption are done in a fully-automatic process and guarantee procedurally safe and easy handling. The processes required for your products are checked in the framework of a validation. Here, it is proved that all valid standards have been met with regard to microbiology and EtO residues. The data recorded during the sterilization allows a reliable parametric release of the sterilization process. Thus, no laboratory analytics are required, which saves time and money.
The SteriVIT process is synonymous with a modern, up-to-date sterilization of your medical devices. Latest findings in the field of process engineering support our future-oriented and environmentally friendly technology
Parameters of parametric release:
- Pressure
- Humidity
- Temperature
- Agent
- Time
Contact
DMB Apparatebau GmbH
Spiesheimer Weg 25a
D-55286 Wörrstadt
Deutschland
© 2017 DMB