EN ISO 11607-2:2020/prA1
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)

Standard No.

EN ISO 11607-2:2020/prA1

Published By

European Committee for Standardization (CEN)

Status

Be replaced 2022-09

Replace By

EN ISO 11607-2:2020/A11:2022

Latest

EN ISO 11607-2:2020/A1:2023

EN ISO 11607-2:2020/prA1 history

• 2023 EN ISO 11607-2:2020/A1:2023 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)
• 2022 EN ISO 11607-2:2020/A11:2022 Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
• 2020 EN ISO 11607-2:2020 Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
• 2017 EN ISO 11607-2:2017 Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming@ sealing and assembly processes
• 2014 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)
• 2006 EN ISO 11607-2:2006 Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006)