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EO नसबंदी उपकरण र प्रक्रिया विशेषता ढाँचा र प्रभाव विश्लेषण

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

EO नसबंदी उपकरण र प्रक्रिया विशेषता ढाँचा र प्रभाव विश्लेषण Read more

ETO स्टेरिलाइजरहरूको लागि मर्मत गाइड

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.

ETO स्टेरिलाइजरहरूको लागि मर्मत गाइड Read more

ईओ नसबंदी गर्नु अघि तयारी कार्य

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.

ईओ नसबंदी गर्नु अघि तयारी कार्य Read more

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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Routine Monitoring, Control, and Release of Ethylene Oxide Sterilization

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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