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BSI - BS EN ISO 11607-2

Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes

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Organization: BSI
Publication Date: 31 May 2006
Status: inactive
Page Count: 24
ICS Code (Sterilized packaging): 11.080.30

Document History

BS EN ISO 11607-2 + A1
January 31, 2020
Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes
A description is not available for this item.
BS EN ISO 11607-2
January 31, 2020
Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes
A description is not available for this item.
BS EN ISO 11607-2 + A11
January 31, 2020
Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes
A description is not available for this item.
BS EN ISO 11607-2
May 31, 2018
Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes
A description is not available for this item.
BS EN ISO 11607-2
May 31, 2006
Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes
A description is not available for this item.
BS EN ISO 11607-2
May 31, 2006
Packaging for terminally sterilized medical devices — Part 2: Validation requirements for forming, sealing and assembly processes
A description is not available for this item.
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References

This document references:
AAMI ST65 - Processing of reusable Surgical textiles for use in health care facilities
Published by AAMI on January 1, 2008
General This recommended practice provides guidelines for properly handling, processing, and preparing reusable surgical textiles for use in health care facilities. These guidelines describe a...
This document references:
BS EN ISO 13485 + A11 - Medical devices - Quality management systems - Requirements for regulatory purposes
Published by BSI on March 31, 2016
A description is not available for this item.
This document references:
ISO 2859-1 - Sampling procedures for inspection by attributes — Part 1: Sampling schemes indexed by acceptance quality limit (AQL) for lot-by-lot inspection AMENDMENT 1
Published by ISO on June 15, 2011
This part of ISO 2859 specifies an acceptance sampling system for inspection by attributes. It is indexed in terms of the acceptance quality limit (AQL). Its purpose is to induce a supplier through...
This document references:
BS EN ISO 9000 - Quality management systems - Fundamentals and vocabulary
Published by BSI on September 30, 2015
A description is not available for this item.
This document is referenced by:
BS EN ISO 14937 - Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices
Published by BSI on March 31, 2010
A description is not available for this item.
This document is referenced by:
BS EN 868-10 - Packaging for terminally sterilized medical devices Part 10: Adhesive coated nonwoven materials of polyolefines – Requirements and test methods
Published by BSI on January 31, 2019
A description is not available for this item.
This document is referenced by:
BS EN ISO 10451 - Dentistry - Contents of technical file for dental implant systems
Published by BSI on July 31, 2010
A description is not available for this item.
This document is referenced by:
BS EN ISO 8836 - Suction catheters for use in the respiratory tract
Published by BSI on October 31, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 17665-1 - Sterilization of health care products Moist heat Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by BSI on September 29, 2006
A description is not available for this item.
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