Ethylene Oxide Ethylene Oxide (EtO) Sterilization Process 环氧乙烷（EtO）灭菌主要用于对不适应采用常规高温蒸汽灭菌的医药产品进行灭菌，例如带有电子元器件的设备、塑料包装或者塑料容器。 EtO 气体渗透到外包装及产品内杀死生产或包装过程中残存的微生物。该气体和空气混合，当 EtO 气体的比率达到至少3%时，形成爆炸...
What is Ethylene Oxide Sterilization Process? Eto Sterilizer is used to sterilize hospital instruments. Ethylene Oxide sterilization process ensures that a safe product is delivered each time. The time taken by the process varies as per the product which needs to be sterilized. Usually, the time ...
Ethylene oxide sterilization process indicator inks
Second, inanethylene oxide(EO)sterilization process, water is introduced as a vapor because moisture enhances the effectiveness of EO as a sterilant. www2.dupont.com www2.dupont.com 第二,在环氧乙烷(EO)灭菌过程中,水作 为蒸汽引入,因为水分会增强环氧乙烷作为灭菌剂 的有效性。
Google Share on Facebook ethylene (redirected fromethylene oxide sterilization) Thesaurus Medical Encyclopedia eth·yl·ene (ĕth′ə-lēn′) n. A colorless flammable gas, C2H4, derived from natural gas and petroleum and also occurring as a natural plant hormone, used as a source of many org...
Sterilize medical and pharmaceutical products Ethylene Oxide (EtO) sterilization is mainly used to sterilize medical and pharmaceutical products tha
ETHYLENE OXIDE STERILIZATION 01 COST AND TIME SAVING We have reduced the entire sterilization process, the batch load release time is less than 1 day, compared to 7 days. Reducing your cost of on-hands inventory. 02 ECO-EFFICIENT Our EtO sterilization virtually eliminates the presence of ethylen...
Sterilize medical and pharmaceutical products Ethylene Oxide (EtO) sterilization is mainly used to sterilize medical and pharmaceutical products tha
【英语版】国际标准 ISO 11138-2:2017 EN 医疗保健产品的灭菌 生物指标 第2部分:环氧乙烷灭菌工艺的生物指标 Sterilization of health care products — Biological indicators — Part 2: Biological indicators for ethylene oxide sterilization processes.pdf 关闭预览 想预览更多内容,点击免费在线预览全文 免费在线...
英文名称:Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals 标准状态:废止 发布日期:1995-10-12 文档简介 ISO10993系列标准是医疗器械生物学评价标准,用于评估医疗器械在生产、处理、储存和植入过程中可能对生物系统产生的影响。该系列标准中的每一部分都关注特定的主题,如灭菌...