Environmental pretreatment At present, most of the EO sterilization process starts from the requirements of products outside the sterilization room, such as masks and medical masks. Pretreatment is generally carried out in a specially designed room t...
Read MoreTechnical characteristics of ethylene oxide sterilizer Ethylene oxide sterilizer is a kind of anti-virus and sterilization product. It is a kind of equipment using ethylene oxide for sterilization, so it has strict requirements for application and ma...
Read MoreIn order to perform the EO process 100% safely, at least 97% of the air must be removed from the chamber. Today, the two most common ways to meet this requirement are (1) a deep vacuum, or (2) a series of partial vacuums, followed by a series of nitr...
Read MoreInstallation area of ethylene oxide sterilizer requirements site 1. the sterilizer should be placed in a separate room. 2. ethylene oxide sterilization site should stay away from the crowd, scene within 50 meters prohibited open flame fire operation...
Read MoreLE Series EO sterilizer The brand, quantity of parts , function, control system , overall standard of BE, LE and GE series are different, so are the costs. These three series are different. Customers can choose one series according to functional requ...
Read MoreEO sensor.This can be achieved by using independent control and monitoring systems, or by cross checking between control and monitoring to identify any differences or indicate faults. If there is no detected fault in the control or monitoring functio...
Read MorePresumably, people all know that there are a lot of germs in todays environment. Officially, because of this, the sterilizer industry is expanding from time to time. There are many kinds of sterilizers, including ethylene oxide sterilizers. ETO is ab...
Read MoreSterilization equipment shall comply with the applicable safety standards. Validation,IQ,OQ,PQ, The purpose of validation is to demonstrate that the sterilization process established in the process definition (see Clause 8) can be delivered effective...
Read MoreDedicated partners The latest designs, secure process configurations, intuitive interfaces, and a global service network are some of the reasons to eliminate unplanned outages. From the beginning, he has been a loyal partner throughout the product li...
Read MoreIn practical applications, the rate can be determined as the time (with tolerance) required to achieve a specified pressure change. a) The minimum temperature at which the product enters the sterilization process and / or the specified conditions req...
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