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材料、无菌屏障系统、和包装系统检测

发布时间:2023-06-28 07:40:49

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军工检测 其他检测

BS EN ISO 11607-1:2009 终端医学设备的.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 - Requirements for materials, sterile barrier systems and packaging systems

GB/T 19633.1-2015 最终灭医疗器械 第1部分:的要求

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems

TCVN 7394-1-2008 最终灭医疗器械的.第1部分:,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 最终灭医疗器械的 第1部分: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 最终灭医疗器械的 第1部分: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 最终灭医疗器械的 第1部分: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 最终灭医疗器械的.第1部分: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 最终灭医疗器械的.第1部分:的要求

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems

KS P ISO 11607-1:2018 用于终端灭医疗器械的 - 第1部分: 的要求

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems

KS P ISO 11607-1-2018 用于终端灭医疗器械的 - 第1部分: 的要求

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems

NF S98-052-1/A1:2014 终端医疗器械的. 第1部分: , 要求. 修改件1

Le présent amendement porte principalement sur la refonte de l'Annexe B (nouvelle table des Méthodes d'essai et modes opératoires normalisés pouvant

Packaging for terminally sterilized medical devices - Part 1 : requirements for materials, sterile barrier systems and packaging systems - Amendment 1

ISO 11607-1:2006/Amd 1:2014 终端医疗器械的. 第1部分: , 要求; 修改件1

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems; Amendment 1

ISO 11607-1:2019 最终灭医疗器械的第1部分:的要求修改1

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1

ISO 11607-1:2019/FDAmd 1 最终灭医疗器械 第1部分:的要求 修正案1

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1

LST EN ISO 11607-1:2009 最终灭医疗器械的 第1部分:的要求(ISO 11607-1:2006)

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006)

BS EN ISO 11607-1:2009 终端医学设备的.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 - Requirements for materials, sterile barrier systems and packaging systems

GB/T 19633.1-2015 最终灭医疗器械 第1部分:的要求

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems

TCVN 7394-1-2008 最终灭医疗器械的.第1部分:,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 最终灭医疗器械的 第1部分: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 最终灭医疗器械的 第1部分: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 最终灭医疗器械的 第1部分: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 最终灭医疗器械的.第1部分: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 最终灭医疗器械的.第1部分:的要求

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems

KS P ISO 11607-1:2018 用于终端灭医疗器械的 - 第1部分: 的要求

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems

KS P ISO 11607-1-2018 用于终端灭医疗器械的 - 第1部分: 的要求

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems

NF S98-052-1/A1:2014 终端医疗器械的. 第1部分: , 要求. 修改件1

Le présent amendement porte principalement sur la refonte de l'Annexe B (nouvelle table des Méthodes d'essai et modes opératoires normalisés pouvant

Packaging for terminally sterilized medical devices - Part 1 : requirements for materials, sterile barrier systems and packaging systems - Amendment 1

ISO 11607-1:2006/Amd 1:2014 终端医疗器械的. 第1部分: , 要求; 修改件1

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems; Amendment 1

ISO 11607-1:2019 最终灭医疗器械的第1部分:的要求修改1

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1

ISO 11607-1:2019/FDAmd 1 最终灭医疗器械 第1部分:的要求 修正案1

Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems — Amendment 1

LST EN ISO 11607-1:2009 最终灭医疗器械的 第1部分:的要求(ISO 11607-1:2006)

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006)

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