BS EN 868-2:2017-最终灭菌医疗器械的包装-国家数字标准馆

现行 BS EN 868-2:2017

到馆阅读

收藏跟踪

购买正版

Packaging for terminally sterilized medical devices-Sterilization wrap. Requirements and test methods 最终灭菌医疗器械的包装

发布日期： 2017-02-28

参考参考文献:EN 20187 ISO 187ISO 187ISO 187ISO 187ISO 187ISO 187EN 20811 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 12 ISO 6588-2:2012 ISO 8601 ISO 9197ISO 9198EN 1041EN 1149-1EN13795EN ISO 9073-9ISO 9073-9EN ISO 11607-2ISO 11607-2EN ISO 15223-1ISO 15223-1ISO 5725-293/42/EECAll购买本文件时提供的当前修订包括在购买时。

Cross References:EN 20187ISO 187EN 20811ISO 811EN 29073-3ISO 9073-3EN ISO 535ISO 535EN ISO 536ISO 536EN ISO 1924-2ISO 1924-2EN ISO 1974ISO 1974EN ISO 2758ISO 2758EN ISO 9237ISO 9237EN ISO 11607-1:2009+A1:2014ISO 11607-1:2006ISO 11607-1:2006/A1:2014EN ISO 13937-1ISO 13937-1EN ISO 13938-1ISO 13938-1ISO 2470-2ISO 3689ISO 3781ISO 5636-3ISO 6588-2:2012ISO 8601ISO 9197ISO 9198EN 1041EN 11491EN 13795EN ISO 9073-9ISO 9073-9EN ISO 11607-2ISO 11607-2EN ISO 15223-1ISO 15223-1ISO 5725-293/42/EECAll current amendments available at time of purchase are included with the purchase of this document.

分类信息

发布单位或类别：英国-英国标准学会

关联关系

研制信息

相似标准/计划/法规

UNE-EN 868-2-2009

Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
最终灭菌医疗器械的包装第2部分:灭菌包装要求和试验方法

YY/T 0698.2-2022

最终灭菌医疗器械包装材料　第2部分：灭菌包裹材料　要求和试验方法
Packaging materials for terminal sterilized medical devices—Part 2:Sterilization wrap—Requirements and test methods

SN/T 3062.4-2011

进口医疗器械灭菌包装第4部分：材料和预成型无菌屏障系统要求
Packaging materials for terminally sterilized medical devices for import-Part 4:Requirements for materials and sterile barrier systems of importing medical device sterilization packaging

UNE-EN 556-1-2002

Sterilization of medical devices. Requirements for medical devices to be designated "STERILE". Part 1: Requirements for terminally sterilized medical devices.
医疗器械的消毒医疗器械被指定为“无菌”的要求第1部分:最终灭菌医疗器械的要求

GOST EN 556-1-2011

Стерилизация медицинских изделий. Требования к медицинским изделиям категории «стерильные». Часть 1. Требования к медицинским изделиям, подлежащим финишной стерилизации
医疗器械灭菌医疗器械要求被指定为“无菌” 第一部分终末消毒医疗器械的要求

进口医疗器械灭菌包装检验操作规程
Rules of the inspection of packaging for import terminally sterilized medical devices

KS P ISO 11607-1

최종 멸균 처리한 의료기기의 포장 — 제1부: 재료, 무균 장벽 시스템 및포장 시스템에 대한 요구사항
用于终端灭菌医疗器械的包装 - 第1部分:材料无菌屏障系统和包装系统的要求

KS P ISO 11607-1

최종 멸균 처리한 의료기기의 포장 — 제1부: 재료, 무균 장벽 시스템 및 포장 시스템에 대한 요구사항
最终灭菌医疗器械的包装.第1部分:材料、无菌屏障系统和包装系统的要求

GB/T 19633.1-2015

最终灭菌医疗器械包装第1部分：材料、无菌屏障系统和包装系统的要求
Packaging for terminally sterilized medical devices—Part 1: Requirements for materials, sterile barrier systems and packaging systems

ISO 11607-1-2019

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems
用于终端灭菌医疗器械的包装 - 第1部分:材料无菌屏障系统和包装系统的要求

AAMI/ISO 11607-1-2019

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems
最终灭菌医疗器械的包装第1部分:材料、无菌屏障系统和包装系统的要求

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

YY/T 0615.1-2007

标示"无菌"医疗器械的要求　第1部分:最终灭菌医疗器械的要求
Requirements for medical devices to be designated "STERILE"—Part 1:Requirements for terminally sterilized medical devices

BS EN 868-8-2018

Packaging for terminally sterilized medical devices-Re-usable sterilization containers for steam sterilizers conforming to EN 285. Requirements and test methods
最终灭菌医疗器械的包装符合EN 285的蒸汽灭菌器用可重复使用的灭菌容器要求和试验方法

YY/T 0698.8-2009

最终灭菌医疗器械包装材料　第8部分：蒸汽灭菌器用重复性使用灭菌容器　要求和试验方法
Packaging materials for terminally sterilized medical devices—Part 8:Re-usable sterilization containers for steam sterilizers—Requirements and test methods

BS EN 868-4-2017

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

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

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

Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices; English version of DIN EN 556-1
医疗器械的灭菌.指定为“无菌”的医疗器械的要求.第1部分:最终灭菌医疗器械的要求；德文版EN 556-1:2001

UNE-EN 868-8-2009

Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods
最终灭菌医疗器械的包装.第8部分:符合EN 285的蒸汽灭菌器用可重复使用的灭菌容器.要求和试验方法

《国家标准化发展纲要》提出建设国家数字标准馆，推动标准化工作向数字化、网络化、智能化转型。中国标准化研究院正在全力推进国家数字标准馆建设，力争在2026年底建成“一个中心”和“一个平台”，即全球领先的标准数据资源中心，涵盖标准全生命周期的数字化、网络化、智能化研究与服务平台。

专题数据库

标准管理系统

大数据分析系统

标准智能研制系统