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DIN 58953-7

Sterilisation - Sterilgutversorgung - Teil 7: Anwendungstechnik von Sterilisationspapier, Vliesstoffen, Papierbeuteln und siegelfaehigen Klarsichtbeuteln und -schlaeuchen

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Organization: DIN
Publication Date: 1 November 2020
Status: active
Page Count: 14
ICS Code (Sterilized packaging): 11.080.30

Document History

DIN 58953-7
November 1, 2020
Sterilisation - Sterilgutversorgung - Teil 7: Anwendungstechnik von Sterilisationspapier, Vliesstoffen, Papierbeuteln und siegelfaehigen Klarsichtbeuteln und -schlaeuchen
A description is not available for this item.
DIN 58953-7
December 1, 2019
Sterilization - Sterile supply - Part 7: Use of sterilization paper, nonwoven wrapping material, paper bags and sealable pouches and reels
A description is not available for this item.
DIN 58953-7
May 1, 2010
Sterilization - Sterile supply - Part 7: Use of sterilization paper, nonwoven wrapping material, textile materials, paper bags and sealable pouches and reels
A description is not available for this item.
DIN 58953-7
June 1, 2008
Sterilization - Sterile supply - Part 7: Use of sterilization paper, nonwoven wrapping material, textile materials, paper bags and sealable pouches and reels
A description is not available for this item.
DIN 58953-7
October 1, 2003
Sterilization - Sterile supply - Part 7: Use of sterilization paper, nonwoven wrapping material, paper bags and heat and self-sealable pouches and reels
A description is not available for this item.
DIN 58953-7
March 1, 2002
Sterilization - Sterile supply - Part 7: Use of sterilization paper, paper bags and heat and self-sealable pouches and reels
A description is not available for this item.
DIN 58953-7
August 1, 1999
Sterilization - Sterile supply - Part 7: Use of paper bags and heat and self-sealable pouches and reels of paper and plastic film construction
A description is not available for this item.
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References

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.
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:
TS 16775 - Packaging for terminally sterilized medical devices — Guidance on the application of ISO 11607-1 and ISO 11607-2
Published by ISO on November 1, 2021
This document provides guidance for the application of the requirements contained in ISO 11607-1 and ISO 11607-2. It does not add to, or otherwise change, the requirements of ISO 11607-1 and ISO...
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:
PD CEN ISO/TS 16775 - Packaging for terminally sterilized medical devices — Guidance on the application of ISO 11607-1 and ISO 11607-2
Published by BSI on November 30, 2021
A description is not available for this item.
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