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

ETO стеро-сасизмын температурын хүрээ нь 30-60 ° C-ийн хооронд байх ёстой. Ариум садан нь халаалт, чийгшүүлэх системийн температур, чийгшлийн дотоод талыг арилгахыг баталгаажуулахыг зөвлөж байна.

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:

Процесс сорилтын төхөөрөмж (PCD) нь сонгосон процессын параметрүүдийг устгах хурдыг үнэлэхэд ашигладаг микробиологийн сорилтын систем юм. Энэ нь ихэвчлэн биологийн үзүүлэлтүүдийг (жишээлбэл, спорын тоо нь мэдэгдэж байгаа Bacillus atrophaeus спор) агуулсан төхөөрөмж эсвэл туршилтын багц юм. Ариутгалын процесст PCD-ийн эсэргүүцэл нь бүтээгдэхүүний ариутгахад хамгийн хэцүү хэсгийн байгалийн бичил биетний ачааллын эсэргүүцэлтэй тэнцүү буюу их байх ёстой. PCD-ийн тоо хэмжээ нь GB18279.1-2015 хавсралт С-ийн Хүснэгт С.3-т заасан шаардлагыг хангасан байх ёстой. PCD-ийг дотоод PCD (IPCD) болон гадаад PCD (EPCD) гэж ангилдаг.

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.

Hangzhou Bocon Mechanical and Electrical Equipment Co., Ltd., commonly referred to as HZBOCON, stands out as a dedicated Ethylene Oxide (EO/ETO) sterilizer manufacturer. Established in 2006, HZBOCON has committed itself to the design, development, and manufacturing of EO sterilization equipment, catering to a wide array of industries that require effective sterilization solutions for thermosensitive products.

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.