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DIN 58953-9

Sterilization - Sterile supply - Part 9: Use of sterilization container

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Organization: DIN
Publication Date: 1 May 2010
Status: active
Page Count: 9
ICS Code (Sterilized packaging): 11.080.30

Document History

DIN 58953-9
May 1, 2010
Sterilization - Sterile supply - Part 9: Use of sterilization container
A description is not available for this item.
DIN 58953-9
October 1, 2008
Sterilization - Sterile supply - Part 9: Use of sterilization container
A description is not available for this item.
DIN 58953 P9
October 1, 2002
Sterilisation - Sterilgutversorgung - Teil 9: Anwendungstechnik von Sterilisierbehaeltern
A description is not available for this item.
DIN 58953 P9
September 1, 2000
Sterilisation - Sterilgutversorgung - Teil 9: Anwendungstechnik von Sterilisierbehaeltern
A description is not available for this item.
DIN 58953 P9
November 1, 1996
Sterilisation - Sterilgutversorgung - Teil 9: Anwendungstechnik von Sterilisierbehaeltern
A description is not available for this item.
DIN 58953 P9
May 1, 1987
Sterilisation; Sterilgutversorgung; Anwendungstechnik von Sterilisierbehaeltern
A description is not available for this item.
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References

This document is referenced by:
EN ISO 11607-2 - Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes
Published by CEN on January 1, 2020
This document specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing and...
This document is referenced by:
AAMI 11607-2 - Packaging for terminally sterilized medical devices – Part 2: Validation requirements for forming, sealing, and assembly processes
Published by AAMI on January 1, 2019
This document specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing and...
This document is referenced by:
DIN EN ISO 11607-2 - Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
Published by DIN on May 1, 2020
A description is not available for this item.
This document is referenced by:
CSA ISO 11607-2 - Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes
Published by CSA on January 1, 2016
This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing,...
This document is referenced by:
BS EN ISO 11607-2 - Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes
Published by BSI on January 31, 2020
A description is not available for this item.
This document is referenced by:
DIN EN ISO 11607-2 - Verpackungen fuer in der Endverpackung zu sterilisierende Medizinprodukte - Teil 2: Validierungsanforderungen an Prozesse der Formgebung, Siegelung und des Zusammenstellens (ISO 11607-2:2019); Deutsche Fassung EN ISO 11607-2:2020
Published by DIN on May 1, 2020
A description is not available for this item.
This document is referenced by:
ISO 11607-2 - Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
Published by ISO on February 1, 2019
This document specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing and...
This document is referenced by:
BS EN ISO 11607-2 - TC - Tracked Changes (Redline) - Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes
Published by BSI on November 12, 2020
A description is not available for this item.
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