The temperature setting range of the ETO Sterilization Chamber should be between 30-60°C. It is recommended to perform temperature distribution testing of the sterilizer’s internal surface and temperature and humidity distribution testing inside the sterilization chamber to ensure the effectiveness of the heating and humidifying systems.

Routine Monitoring and Control The purpose of routine monitoring and control of EO (Ethylene Oxide) sterilization is to demonstrate that

3.4.1.1 Production of Process Challenge Devices (PCD) A Process Challenge Device (PCD) is a microbiological challenge system used to evaluate

Industry Eto Sterilizer Installation Verification The installation of Industry Eto Sterilizer and all associated services should comply with the requirements

The humidification water used in the ETO Sterilization Equipment should be free from contaminants, should not weaken the ETO sterilization process, and should not damage the sterilizer, sterilized products, or the load. Humidification should be done by injecting steam, not by directly injecting atomized water.

杭州博康機電設備有限公司，俗稱HZBOCON，是一家專業的環氧乙烷（EO/ETO）滅菌器製造商。 HZBOCON成立於2006年，致力於環氧乙烷滅菌設備的設計、開發與製造，滿足各產業需要有效熱敏產品滅菌解決方案的需求。

PQ is the stage of validation that uses Ethylene oxide sterilization chamber to demonstrate that the Ethylene oxide sterilization equipment consistently operates in accordance with predetermined acceptance criteria and the process yields a product that is sterile and meets the specified requirements.

OQ is undertaken to demonstrate the ability of the ETO STERILIZATION MACHINE to meet the performance requirements of its design

Iq in eto sterilization process is undertaken to demonstrate that the sterilization equipment and any ancillary items have been supplied

Low-Temperature Sterilization: Ethylene oxide sterilizer operate at low temperatures, making them ideal for sterilizing heat-sensitive medical devices and instruments. This