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DIN EN ISO 18472

Sterilization of health care products - Biological and chemical indicators - Test equipment (ISO 18472:2006)

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Organization: DIN
Publication Date: 1 October 2006
Status: inactive
Page Count: 34
ICS Code (Disinfectants and antiseptics): 11.080.20

Document History

DIN EN ISO 18472
November 1, 2018
Sterilization of health care products - Biological and chemical indicators - Test equipment (ISO 18472:2018)
This document specifies the requirements for test equipment to be used to: — test biological indicators for steam, ethylene oxide gas and dry heat sterilization processes for conformity to the...
DIN EN ISO 18472
December 1, 2016
Sterilization of health care products - Biological and chemical indicators - Test equipment (ISO/DIS 18472:2016); German and English version prEN ISO 18472:2016
A description is not available for this item.
DIN EN ISO 18472
October 1, 2006
Sterilization of health care products - Biological and chemical indicators - Test equipment (ISO 18472:2006)
A description is not available for this item.

References

This document is referenced by:
DIN EN ISO 11140-1 - Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO 11140-1:2014)
Published by DIN on March 1, 2015
This part of ISO 11140 specifies general requirements and test methods for indicators that show exposure to sterilization processes by means of physical and/or chemical change of substances, and...
This document is referenced by:
DIN EN ISO 14534 - Ophthalmic optics - Contact lenses and contact lens care products - Fundamental requirements (ISO 14534:2011)
Published by DIN on August 1, 2015
This International Standard specifies safety and performance requirements for contact lenses, contact lens care products, and other accessories for contact lenses. This International Standard does...
This document is referenced by:
DIN EN ISO 20857 - Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010)
Published by DIN on August 1, 2013
Inclusions This International Standard specifies requirements for the development, validation and routine control of a dry heat sterilization process for medical devices. NOTE Although the scope of...
This document is referenced by:
DIN EN ISO 11138-3 - Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2017)
Published by DIN on July 1, 2017
This document specifies requirements for test organisms, suspensions, inoculated carriers, biological indicators and test methods intended for use in assessing the performance of sterilization...
This document is referenced by:
DIN EN ISO 11138-4 - Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2017)
Published by DIN on July 1, 2017
This document specifies requirements for test organisms, suspensions, inoculated carriers, biological indicators and test methods intended for use in assessing the performance of sterilization...
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