YY/T 0681.16-2019 菌医疗器械包装试验方法 第16部分:包装系统气候应变能力试验
Sterile medical device packaging test methods Part 16: Packaging system climate adaptability test
GB/T 19633.1-2015 最终灭菌医疗器械包装 第1部分:材料、菌屏障系统和包装系统的要求
GB/T19633 的本部分规定了材料、预成形菌屏障系统、菌屏麻系统和预期在使用前保持最终灭菌医疗器械菌的包装系统的要求和试验方法。 本部分适用于工业、医疗机构以及任何将医疗器械装和菌屏障系统后灭菌的情况。 本部分未包括菌制造医疗器械的菌屏障系统和包装系统的全部要求。 对药物与器械组合的
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems
BS EN ISO 11607-1:2020+A1:2023 最终灭菌医疗器械的包装 材料、菌屏障系统和包装系统的要求
Packaging for terminally sterilized medical devices - Requirements for materials, sterile barrier systems and packaging systems
TCVN 7394-1-2008 最终灭菌医疗器械的包装.第1部分:材料,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
DS/EN ISO 11607-1:2009 最终灭菌医疗器械的包装 第1部分：材料、菌屏障系统和包装系统的要求
This part of ISO 11607 specifies the requirements and test methods for materials, preformed sterile barrier systems, sterile barrier systems
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems
NF S98-052-1*NF EN ISO 11607-1:2020 最终灭菌医疗器械的包装 第1部分：材料、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
GOST ISO 11607-1-2018 最终灭菌医疗器械的包装 第1部分：材料、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
KS P ISO 11607-1:2021 最终灭菌医疗器械的包装.第1部分:材料、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
KS P ISO 11607-1-2021 最终灭菌医疗器械的包装.第1部分:材料、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
NF EN ISO 11607-1:2020 最终灭菌医疗器械的包装 第1部分：材料、菌屏障系统和包装系统的要求
Emballages des dispositifs médicaux stérilisés au stade terminal - Partie 1 : exigences relatives aux matériaux, aux systèmes de barrière stérile et aux systèmes d'emballage
UNE-EN ISO 11607-1:2020 最终灭菌医疗器械的包装 第1部分：材料、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)
DIN EN ISO 11607-1/A11:2022-08 最终灭菌医疗器械的包装 第1部分：材料、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); German version EN ISO 11607-1:2020/A11:2022
DIN EN ISO 11607-1:2020-05 最终灭菌医疗器械的包装 第1部分：材料、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); German version EN ISO 11607-1:2020 / Note: To be amended by DIN EN ISO 11607-1/A1 (2022-08).
UNE-EN ISO 11607-1:2020/A11:2022 最终灭菌医疗器械的包装 第1部分：材料、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)
DIN EN ISO 11607-1 Berichtigung 1:2016 最终灭菌医疗器械的包装 第1部分：材料、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
YY/T 0681.16-2019 菌医疗器械包装试验方法 第16部分:包装系统气候应变能力试验
Sterile medical device packaging test methods Part 16: Packaging system climate adaptability test
GB/T 19633.1-2015 最终灭菌医疗器械包装 第1部分:材料、菌屏障系统和包装系统的要求
GB/T19633 的本部分规定了材料、预成形菌屏障系统、菌屏麻系统和预期在使用前保持最终灭菌医疗器械菌的包装系统的要求和试验方法。 本部分适用于工业、医疗机构以及任何将医疗器械装和菌屏障系统后灭菌的情况。 本部分未包括菌制造医疗器械的菌屏障系统和包装系统的全部要求。 对药物与器械组合的
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems
BS EN ISO 11607-1:2020+A1:2023 最终灭菌医疗器械的包装 材料、菌屏障系统和包装系统的要求
Packaging for terminally sterilized medical devices - Requirements for materials, sterile barrier systems and packaging systems
TCVN 7394-1-2008 最终灭菌医疗器械的包装.第1部分:材料,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
DS/EN ISO 11607-1:2009 最终灭菌医疗器械的包装 第1部分：材料、菌屏障系统和包装系统的要求
This part of ISO 11607 specifies the requirements and test methods for materials, preformed sterile barrier systems, sterile barrier systems
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems
NF S98-052-1*NF EN ISO 11607-1:2020 最终灭菌医疗器械的包装 第1部分：材料、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
GOST ISO 11607-1-2018 最终灭菌医疗器械的包装 第1部分：材料、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
KS P ISO 11607-1:2021 最终灭菌医疗器械的包装.第1部分:材料、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
KS P ISO 11607-1-2021 最终灭菌医疗器械的包装.第1部分:材料、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
DIN EN ISO 11607-1/A11:2022-08 最终灭菌医疗器械的包装 第1部分：材料、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); German version EN ISO 11607-1:2020/A11:2022
DIN EN ISO 11607-1:2020-05 最终灭菌医疗器械的包装 第1部分：材料、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); German version EN ISO 11607-1:2020 / Note: To be amended by DIN EN ISO 11607-1/A1 (2022-08).
UNE-EN ISO 11607-1:2020/A11:2022 最终灭菌医疗器械的包装 第1部分：材料、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)
UNE-EN ISO 11607-1:2020 最终灭菌医疗器械的包装 第1部分：材料、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)
NF EN ISO 11607-1:2020 最终灭菌医疗器械的包装 第1部分：材料、菌屏障系统和包装系统的要求
Emballages des dispositifs médicaux stérilisés au stade terminal - Partie 1 : exigences relatives aux matériaux, aux systèmes de barrière stérile et aux systèmes d'emballage
DIN EN ISO 11607-1 Berichtigung 1:2016 最终灭菌医疗器械的包装 第1部分：材料、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
编辑：北检院编辑部
