Terms and definitions of eto gas sterilization
For the purposes of this document, the following terms and definitions apply in ethylene oxide sterilization 3.1 Aeration part of […]
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November 2024
Preparation Work Before eo Sterilization
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.
Turn on the power and observe whether the instrument display values are normal; otherwise, cut off the power, inspect and repair before restarting.
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.
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Request For Eto Gas Sterilizer Manufacturer
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.
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Factors Affecting the EO Gas Sterilization Process
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.
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Comparing ETO Sterilization to Other Methods
eto sterilization technologies vs others: Advantages and Disadvantages Sterilization is a critical process in infection control, ensuring that medical instruments
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ETO Sterilization Chamber Testing
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.
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Routinemäßige Überwachung, Kontrolle und Freisetzung der Ethylenoxid-Sterilisation
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:
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Production of Process Challenge Devices in eo sterilization
Ein Process Challenge Device (PCD) ist ein mikrobiologisches Challenge-System, das zur Bewertung der Abtötungsrate ausgewählter Prozessparameter verwendet wird. Typischerweise handelt es sich um ein Gerät oder eine Testpackung, die biologische Indikatoren enthält (z. B. Bacillus atrophaeus-Sporen mit bekannter Sporenzahl). Die Beständigkeit des PCD gegenüber dem Sterilisationsprozess sollte größer oder gleich der Beständigkeit der natürlichen mikrobiellen Belastung im am schwierigsten zu sterilisierenden Bereich des Produkts sein. Die Menge an PCDs sollte den in Tabelle C.3 von Anhang C in GB18279.1-2015 aufgeführten Anforderungen entsprechen. PCDs werden in interne PCDs (IPCD) und externe PCDs (EPCD) unterteilt.
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Installationsüberprüfung des Industrie-Eto-Sterilisators
Industry Eto Sterilizer Installation Verification The installation of Industry Eto Sterilizer and all associated services should comply with the requirements
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Purified Water Requirements for ETO Sterilization
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.
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