Sterilizer For The Pharmaceutical Industry

Chamber for preconditioning

Preconditioning chambers guarantee that the sterilization load attains a uniform temperature and humidity, as stipulated by ISO 11135:2014. This establishes the optimal conditions for a sterilization process that is effective.input:
output:Chamber for degassing

Residual gas emissions remain on the devices following vacuum sterilization with ethylene oxide (EO). The purpose of these post-conditioning chambers is to achieve the device’s permissible EO residue value. The gas residue value is reduced below the limit specified by ISO EN 10993-7 through the circulation of fresh air and the supply of air to degassing chambers. This procedure is implemented in compliance with EN 11135:2014.input:
output:Features of the system

Consultations with an individual

We are pleased to provide you with guidance on the necessity and design of your preconditioning and degassing chambers.input:
output:Reliability

The preconditioning and degassing chambers can be precisely parameterized, allowing for the reliable repetition of the corresponding cycles for each product load.input:
output:The optimization of cyclesThe optimization of cycle times is facilitated by the controlled preconditioning and degassing of medical devices.