现行

YY/T 0679-2016

医用低温蒸汽甲醛灭菌器
Low temperature steam and formaldehyde sterilizers for medical purposes

2016-07-29

现行

DIN EN 15424

Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices
医疗器械灭菌-低温蒸汽和甲醛-医疗器械灭菌过程的开发、验证和常规控制要求；德文版EN 15424:2007

2007-08-01

现行

GOST R ISO 25424-2013

Стерилизация медицинских изделий. Стерилизация низкотемпературная пароформальдегидная. Требования к разработке, валидации и рутинному контролю процесса стерилизации
医疗器械灭菌低温蒸汽和甲醛 对医疗器械灭菌过程的开发 验证和常规控制的要求

现行

BS EN 14180-2014

Sterilizers for medical purposes. Low temperature steam and formaldehyde sterilizers. Requirements and testing
医用消毒器 低温蒸汽和甲醛灭菌器 要求和测试

2014-05-31

现行

UNE-EN 14180-2004+A2-2010

Sterilizers for medical purposes - Low temperature steam and formaldehyde sterilizers - Requirements and testing
医用消毒器.低温蒸汽和甲醛消毒器.要求和试验

2010-01-13

现行

UNE-EN 14180-2004

Sterilizers for medical purposes - Low temperature steam and formaldehyde sterilizers - Requirements and testing
医用消毒器.低温蒸汽和甲醛消毒器.要求和试验

2004-03-18

现行

GOST EN 14180-2011

Стерилизаторы медицинского назначения. Стерилизаторы низкотемпературные пароформальдегидные. Технические требования и методы испытаний
杀菌剂用于医疗用途 低温蒸汽和甲醛灭菌器 要求和测试

2011-11-29

现行

BS 05/30066638 DC

EN 15424. Sterilization of medical devices. Development, validation and routine control of sterilization processes. Low temperature steam and formaldehyde
EN 15424 医疗器械的消毒 灭菌过程的开发、验证和常规控制 低温蒸汽和甲醛

2005-10-26

现行

BS 3970-6-1993

Sterilizing and disinfecting equipment for medical products-Specification for sterilizers using low-temperature steam with formaldehyde
医疗产品的消毒设备 甲醛低温蒸汽灭菌器规范

1993-04-15

现行

BS 3970-5-1990

Sterilizing and disinfecting equipment for medical products-Specification for low temperature steam disinfectors
医疗产品的消毒设备 低温蒸汽消毒器规范

1990-09-28

现行

BS EN ISO 25424-2019+A1-2022

Sterilization of health care products. Low temperature steam and formaldehyde. Requirements for development, validation and routine control of a sterilization process for medical devices
医疗保健产品的灭菌 低温蒸汽和甲醛 医疗器械灭菌过程的开发、验证和常规控制要求

2022-06-24

现行

YY/T 1464-2022

医疗保健产品灭菌　低温蒸汽甲醛　医疗器械灭菌过程的开发、确认和常规控制要求
Sterilization of health care products—Low temperature steam and formaldehyde—Requirements for development,validation and routine control of a sterilization process for medical devices

2022-10-17

现行

KS P ISO 25424

의료제품의 멸균 — 저온 증기 및 포름알데히드 — 의료기기 멸균 공정 개발, 유효성 확인, 일상 관리 요구사항
医疗保健产品的灭菌.低温蒸汽和甲醛.医疗器械灭菌过程的开发、验证和常规控制要求

2020-12-30

现行

ISO 25424-2018

Sterilization of health care products — Low temperature steam and formaldehyde — Requirements for development, validation and routine control of a sterilization process for medical devices
医疗保健产品的灭菌.低温蒸汽和甲醛.医疗器械灭菌过程的开发、验证和常规控制要求

2018-10-19

现行

ISO 25424-2018/Amd 1-2022

Sterilization of health care products — Low temperature steam and formaldehyde — Requirements for development, validation and routine control of a sterilization process for medical devices — Amendment 1
医疗保健产品的灭菌.低温蒸汽和甲醛.医疗器械灭菌过程的开发、验证和常规控制要求.修改件1

2022-01-12

现行

BS EN 868-6-2017

Packaging for terminally sterilized medical devices-Paper for low temperature sterilization processes. Requirements and test methods
最终灭菌医疗器械的包装

2017-02-28

现行

BS EN 868-7-2017

Packaging for terminally sterilized medical devices-Adhesive coated paper for low temperature sterilization processes. Requirements and test methods
最终灭菌医疗器械的包装

2017-02-28

现行

UNE-EN 868-6-2009

Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods
最终灭菌医疗器械的包装第6部分:低温灭菌用纸要求和试验方法

2009-12-02

现行

UNE-EN 868-7-2009

Packaging for terminally sterilized medical devices - Part 7: Adhesive coated paper for low temperature sterilization processes - Requirements and test methods
最终灭菌医疗器械的包装.第7部分:低温灭菌过程用胶粘剂涂布纸.要求和试验方法

2009-12-02

现行

ISO 22441-2022

Sterilization of health care products — Low temperature vaporized hydrogen peroxide — Requirements for the development, validation and routine control of a sterilization process for medical devices
保健产品灭菌.低温汽化过氧化氢.医疗器械灭菌过程的开发、验证和常规控制要求

2022-08-26