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
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
2018-11-05
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
2021-06-28
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
2015-12-10
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
2019-01-31
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
Pachaking materials for terminally sterilized medical devices for import--Part 4:Requirements for materials and sterile barrier systems of importing medical device sterilization packaging
2011-09-09
UNE-EN ISO 11607-1-2009
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006)
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（ISO 11607-1-2006）
2009-10-14
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
2022-10-17
ISO 11607-1-2019/Amd 1-2023
Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1: Application of risk management
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修改件1:风险管理的应用
2023-09-13
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
2002-02-28
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
2011-11-29
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
2007-07-02
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
2009-06-16
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
2009-12-02
YY/T 0698.4-2009
最终灭菌医疗器械包装材料 第4部分：纸袋 要求和试验方法
Packaging materials for terminal sterilized medical devices—Part 4:Paper bags—Requirements and test methods
2009-06-16
BS EN 868-9-2018
Packaging for terminally sterilized medical devices-Uncoated nonwoven materials of polyolefines. Requirements and test methods
最终灭菌医疗器械的包装 聚烯烃无涂层非织造材料 要求和试验方法
2019-01-09
DIN EN 556-1
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
2002-03-01
UNE-EN 868-9-2009
Packaging for terminally sterilized medical devices - Part 9: Uncoated nonwoven materials of polyolefines - Requirements and test methods
最终灭菌医疗器械的包装.第9部分:聚烯烃的无涂层非织造材料.要求和试验方法
2009-12-02
BS EN 868-10-2018
Packaging for terminally sterilized medical devices-Adhesive coated nonwoven materials of polyolefines. Requirements and test methods
最终灭菌医疗器械的包装 聚烯烃粘合剂涂层非织造材料 要求和试验方法
2019-01-09
UNE-EN 868-10-2009
Packaging for terminally sterilized medical devices - Part 10: Adhesive coated nonwoven materials of polyolefines - Requirements and test methods
最终灭菌医疗器械的包装.第10部分:聚烯烃粘合剂涂层非织造材料.要求和试验方法
2009-12-02