Author name: Bocon Technical Team

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

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.

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:

A Process Challenge Device (PCD) is a microbiological challenge system used to evaluate the kill rate of selected process parameters. It is typically a device or test package containing biological indicators (e.g., Bacillus atrophaeus spores with known spore count). The resistance of the PCD to the sterilization process should be greater than or equal to the resistance of the natural microbial load in the most difficult-to-sterilize area of the product. The quantity of PCDs should meet the requirements outlined in Table C.3 of Appendix C in GB18279.1-2015. PCDs are classified into Internal PCDs (IPCD) and External PCDs (EPCD).

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

Die bevogtigingswater wat in die ETO-sterilisasietoerusting gebruik word, moet vry wees van kontaminante, moet nie die ETO-sterilisasieproses verswak nie, en moet nie die sterilisator, gesteriliseerde produkte of die vrag beskadig nie. Bevogtiging moet gedoen word deur stoom in te spuit, nie deur direk vernevelde water in te spuit nie.

Hangzhou Bocon Mechanical and Electrical Equipment Co., Ltd., wat algemeen na verwys word as HZBOCON, staan ​​uit as 'n toegewyde Etileenoksied (EO/ETO) steriliseerder vervaardiger. HZBOCON, wat in 2006 gestig is, het hom verbind tot die ontwerp, ontwikkeling en vervaardiging van EO-sterilisasietoerusting, wat voorsiening maak vir 'n wye verskeidenheid nywerhede wat effektiewe sterilisasie-oplossings vir termosensitiewe produkte benodig.

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.