ETO Sterilizer

Start cycle phase(Select parameters/sterilization recipe) Serial number Potentially risky content Risk assessment under existing process conditions Risk assessment of the

9.1 During ETO Sterilization, operators are not allowed to leave the operating area and must continuously observe the ETO Sterilization process. If any abnormal phenomena occur, the machine must be immediately shut down, and the power supply should be cut off for inspection.

For the purposes of this document, the following terms and definitions apply in ethylene oxide sterilization 3.1 Aeration part of

Appearance Inspection: Check for any damage on the surfaces of the main machine, control rack, and electrical control cabinet.
Power Supply Check: Ensure the power supply meets the requirements and check the rotation direction of the water pump and vacuum pump.
Qhib lub hwj chim thiab saib seb qhov ntsuas qhov ntsuas qhov ntsuas puas zoo li qub; txwv tsis pub, txiav tawm lub hwj chim, tshuaj xyuas thiab kho ua ntej rov pib dua.
Pipeline Inspection: Check for leaks in the water supply, vacuum, and medication delivery pipelines, and ensure all valves are in standby mode; adjust if necessary.

2.1.1 The overall shape should be precise, with smooth, clean surfaces and uniform color. There should be no burrs, sharp edges, cracks, visible scratches, or unevenness.
2.1.2 All external text, graphics, and symbols must be printed clearly, with precise and durable markings.
2.1.3 Fasteners must be securely installed. All control switches and adjustment knobs (or buttons) should operate smoothly and reliably without obstructions.

Within a certain range of gas concentration, the higher the concentration, the better theEO Gas Sterilization effect; beyond 1000 mg/L, the improvement in sterilization effect is not significant.

eto sterilization technologies vs others: Advantages and Disadvantages Sterilization is a critical process in infection control, ensuring that medical instruments

Qhov ntsuas kub teeb tau tshwm sim ntau ntawm cov eto sterilization chamber yuav tsum yog ntawm 30-60 ° C. Nws raug nquahu kom ua qhov ntsuas kub thiab kub thiab kub thiab kub thiab kub thiab kub thiab kub thiab sov thiab sov thiab huab cua sov thiab huab cua sov thiab huab cua sov thiab huab cua sov thiab huab cua sov thiab huab cua sov thiab av sov.

The purpose of routine monitoring and control of EO (Ethylene Oxide) sterilization is to demonstrate that the confirmed and specified sterilization process has been applied to the product. Data from each sterilization cycle should be recorded and retained to prove that the confirmed sterilization process specifications have been met. This should include at least the following content: