{"id":2453,"date":"2024-12-20T11:08:14","date_gmt":"2024-12-20T03:08:14","guid":{"rendered":"https:\/\/zjbocon.com\/?p=2453"},"modified":"2025-10-01T19:14:06","modified_gmt":"2025-10-01T11:14:06","slug":"microbial-killing-performance-of-ethylene-oxide-sterilizers","status":"publish","type":"post","link":"https:\/\/zjbocon.com\/microbial-killing-performance-of-ethylene-oxide-sterilizers\/","title":{"rendered":"Microbial Killing Performance of Ethylene Oxide Sterilizers"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\"><strong>Примітка 1:<\/strong> Умови стерилізації оксидом етилену повинні бути отримані шляхом підтвердження валідації та перевірені моніторингом і регулярним контролем під час кожного циклу стерилізації. Вимоги до валідації та регулярного контролю викладені в GB 18279.<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong>Примітка 2:<\/strong> Цей метод тестування також застосовний до стерилізаторів етиленоксиду класу А, обладнаних попередньою настройкою <a href=\"https:\/\/zjbocon.com\/product\/hospital-laboratory-eto-sterilizer\/\">Стерилізація етиленоксидом<\/a> програми.<\/p>\n\n\n\n<div class=\"wp-block-uagb-image uagb-block-f1766043 wp-block-uagb-image--layout-default wp-block-uagb-image--effect-static wp-block-uagb-image--align-none\"><figure class=\"wp-block-uagb-image__figure\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/zjbocon.com\/wp-content\/uploads\/2024\/10\/banner__.webp\" alt=\"Microbial Killing Performance of Ethylene Oxide Sterilizers\" class=\"uag-image-1243\" width=\"731\" height=\"359\" title=\"Microbial role =\"img\" \><\/figure><\/div>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-e-1-equipment\">E.1 Обладнання<\/h2>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-1-1\">E.1.1<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Потрібні чотири пристрої виклику процесу, а саме:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Пристрій для перевірки процесу складається з труби з нержавіючої сталі та напівзакритої камери, заповненої забрудненими носіями. Сталева труба та камера з’єднані за допомогою кільцевих ущільнень і різьбових з’єднань. Єдиний шлях у камеру пролягає через довжину труби.<\/li>\n\n\n\n<li>Довжина труби становить 4,55 м (номінальна), з внутрішнім діаметром 3,0 мм (номінальна), що дає співвідношення довжини до діаметра 1500:1. Загальний внутрішній об’єм становить приблизно 32 мл, з яких 0,85 мл становить об’єм камери.<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-1-2\">E.1.2<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Eight paper-plastic packaging bags that comply with GB\/T19633, YY\/T0698.4, and YY\/T0698.5.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-1-3\">E.1.3<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Забруднені носії, які відповідають GB18281.1 і GB18281.2.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-1-4\">E.1.4<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Відповідні культуральні середовища відновлення для забруднених носіїв.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-1-5\">E.1.5<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Горщик для вирощування.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-e-2-testing-steps\">E.2 Етапи тестування<\/h2>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-2-1\">E.2.1<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Виберіть програму стерилізації окисом етилену для перевірки.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-2-2\">E.2.2<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Помістіть один забруднений носій у випробувальну камеру кожного технологічного пристрою. Оберніть кожен пристрій для перевірки процесу двома паперово-пластиковими пакувальними пакетами, запечатавши кожен пакет за допомогою запаювальної машини.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-2-3\">E.2.3<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">The process challenge device does not need initialization but should be maintained at 20\u00b0C \u00b1 5\u00b0C for at least one hour before testing.<br><strong>Примітка:<\/strong> Це імітує найгірші умови.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-2-4\">E.2.4<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Підніміть стерилізатор з оксидом етилену до температури стерилізації, завантажте чотири загорнуті контрольні пристрої в камеру стерилізатора з оксидом етилену та почніть цикл тестування протягом 15 хвилин після завантаження. Час витримки стерилізатора під час циклу випробування має становити половину часу, зазначеного для цього циклу стерилізації оксидом етилену.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-2-5\">E.2.5<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Після завершення циклу тестування вийміть контрольні пристрої зі стерилізатора етиленоксиду.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-2-6\">E.2.6<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Вийміть забруднені носії з випробувальної камери, посівіть їх відповідно до інструкцій виробника та перевірте відповідність вимогам розділу 2.13.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-2-7\">E.2.7<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Культивуйте один неекспонований забруднений носій з тієї ж партії відповідно до інструкцій виробника; він повинен показати наявність життєздатних мікроорганізмів. Якщо ні, тест вважається недійсним і має бути проведено повторне тестування.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"h-e-2-8\">E.2.8<\/h3>\n\n\n\n<p class=\"wp-block-paragraph\">Повторіть тест ще два рази.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"h-if-you-want-to-know-more-about-ethylene-oxide-sterilization\">ЯКЩО ВИ ХОЧЕТЕ ДІЗНАТИСЯ БІЛЬШЕ про стерилізацію етиленоксидом<\/h2>\n\n\n\n<p class=\"wp-block-paragraph\">телефон:<a href=\"https:\/\/wa.me\/8619975258603\">+8619975258603<\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Електронна пошта:<a href=\"mailto:hayley@hzbocon.com\">hayley@hzbocon.com<\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">Місцевий сайт: кімната 1202, Caitong Zhongxin, Xiasha District, Hangzhou City, Zhejiang Province, China<\/p>\n\n\n\n<p class=\"wp-block-paragraph\">сайт:<a href=\"https:\/\/www.hzbocon.com\/\">hzbocon.com<\/a><a href=\"https:\/\/zjbocon.com\/\">&nbsp;zjbocon.com<\/a><\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Note 1: The Ethylene Oxide sterilization conditions must be obtained through validation confirmation and should be verified with monitoring and [&hellip;]<\/p>\n","protected":false},"author":234312599,"featured_media":1243,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_uag_custom_page_level_css":"","site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"default","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","ast-disable-related-posts":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"set","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center 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