ISO 11607-2:2020/A1 标准查询与下载

EN ISO 11607-2:2020/A1:2023 最终灭菌医疗器械的包装 第 2 部分：成型、密封和组装工艺的验证要求 修正案 1：风险管理的应用 (ISO 11607-2:2019/Amd 1:2023)

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes - Amendment 1: Application of risk management (ISO 11607-2:2019/Amd 1:2023)

DANSK DS/EN ISO 11607-2/A1:2020 最终灭菌医疗器械的包装 第2部分：成型、密封和组装过程的验证要求 (ISO 11607-2:2019)

Packaging for terminally sterilized medical devices – Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)

DIN EN ISO 11607-2 A1 E:2022-08 DIN EN ISO 11607-2 A1 E:2022-08

DIN EN ISO 11607-2 A1 E:2013-04 DIN EN ISO 11607-2 A1 E:2013-04

DIN EN ISO 11607-2:2014 最后灭菌的医疗器械的包装.第2部分:组成、密封和装配过程的确认和要求(ISO 11607-2-2006+Amd 1-2014);德文版本EN ISO 11607-2-2006+A1-2014

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006 + Amd 1:2014); German version EN ISO 11607-2:2006 + A1:2014

DIN EN ISO 11607-2 A11:2022 最终包装中待灭菌医疗器械的包装 第2部分：成型、密封和组装过程的验证要求（ISO 11607-2:2019）；德文版 EN ISO 11607-2:2020/A11:2022

Packaging for medical devices to be sterilized in final packaging – Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019); German version EN ISO 11607-2:2020/A11:2022

DIN EN ISO 11607-2:2020 最终灭菌医疗器械的包装 第2部分：成型、密封和组装过程的验证要求（ISO 11607-2:2019）

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)

DIN EN ISO 11607-1 A1 E:2022-08 DIN EN ISO 11607-1 A1 E:2022-08

DIN EN ISO 11607-2:2024 终末灭菌医疗器械包装 第2部分:成型、密封和组装过程的验证要求 (ISO 11607-2:2019 + Amd 1:2023)（包括修订 A1:2023）

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019 + Amd 1:2023) (includes Amendment A1:2023)

DIN EN ISO 11607-1 A1 E:2013-04 DIN EN ISO 11607-1 A1 E:2013-04

EN ISO 11607-2:2006 终端无菌医学设备的包装.第2部分:组成,密封和装配过程的确认要求 ISO 11607-2-2006

This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006)

NS-EN ISO 11607-2:2020 最终灭菌医疗器械的包装 第2部分：成型、密封和组装过程的验证要求 (ISO 11607-2:2019)

  Full Description ADOPTED_FROM:EN ISO 11607-2:2020 This document specifies requirements for the development and validation

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)

DIN EN ISO 11607-2/A1 E:2013 最终灭菌医疗器械包装 第2部分：成型、密封和组装工艺的验证要求 (ISO 11607-2:2006/DAM 1:2013) 草案

Draft Document - Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006/DAM 1:2013); German version EN ISO 11607-2:2006/prA1:2013

EN ISO 11607-2:2020/prA1 最终灭菌医疗器械的包装 第2部分：成型、密封和组装过程的验证要求 修正案 1（ISO 11607-2:2019/DAM 1:2022）

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes - Amendment 1 (ISO 11607-2:2019/DAM 1:2022)

AENOR UNE-EN ISO 11607-2/A1:2007 最终灭菌的医疗保健产品的包装 第2部分：成型、密封和装配工艺的要求 (ISO 11607-2:2006)

  Full Description SPANISH

Packaging for terminally sterilized healthcare products. Part 2: Requirements for forming, sealing and assembly processes (ISO 11607-2:2006)