Introducing Our New EO Degassing Chamber – The Next Step in Safe & Compliant Medical Device Processing
At SUPHATEC, innovation has always been driven by one objective: helping our customers stay ahead of market demands, regulatory requirements, and operational challenges.
For more than 35 years, we have been developing advanced sterilization technologies for the Medical Device and Pharmaceutical industries, continuously improving our solutions to deliver higher efficiency, greater safety, and full process traceability.
Today, we are pleased to introduce our latest innovation:
NEW SUPHATEC EO DEGASSING CHAMBER
Designed specifically for medical devices sterilized with Ethylene Oxide (EO), our new Degassing Chamber provides a reliable, automated, and fully controlled solution for the removal of residual EO after sterilization.
Key Benefits
- Safe and efficient removal of residual Ethylene Oxide
- Optimized aeration cycles to reduce processing time
- Advanced SCADA software with complete process control
- Full traceability, Audit Trail and electronic records
- Ready for FDA 21 CFR Part 11 compliance
- Designed according to the latest international standards
- Flexible configurations to suit different production capacities
Whether you operate an existing EO sterilization facility or are planning a new installation, our new Degassing Chamber has been engineered to improve productivity while ensuring the highest levels of product safety and regulatory compliance.
At SUPHATEC, we don’t simply manufacture equipment—we develop complete process solutions tailored to our customers’ needs.
For further information or to discuss your project, our engineering team will be pleased to assist you.
Contact us:
