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BSI - BS EN ISO 11138-3

Sterilization of health care products - Biological indicators Part 3: Biological indicators for moist heat sterilization processes

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Organization: BSI
Publication Date: 30 April 2017
Status: active
Page Count: 20
ICS Code (Sterilization and disinfection in general): 11.080.01
ICS Code (Disinfectants and antiseptics): 11.080.20

Document History

BS EN ISO 11138-3
April 30, 2017
Sterilization of health care products - Biological indicators Part 3: Biological indicators for moist heat sterilization processes
A description is not available for this item.
BS EN ISO 11138-3
November 30, 2009
Sterilization of health care products - Biological indicators Part 3: Biological indicators for moist heat sterilization processes
A description is not available for this item.
BS EN ISO 11138-3
August 31, 2006
Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes
A description is not available for this item.

References

This document references:
ISO 18472 - Sterilization of health care products - Biological and chemical indicators - Test equipment
Published by ISO on August 1, 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...
This document references:
ISO 11138-1 - Sterilization of health care products - Biological indicators - Part 1: General requirements
Published by ISO on March 1, 2017
This document specifies general requirements for production, labelling, test methods and performance characteristics of biological indicators, including inoculated carriers and suspensions, and their...
This document references:
BS EN ISO 18472 - Sterilization of health care products - Biological and chemical indicators - Test equipment
Published by BSI on September 30, 2018
A description is not available for this item.
This document is referenced by:
BS EN ISO 7197 - Neurosurgical implants - Sterile, single-use hydrocephalus shunts and components
Published by BSI on October 31, 2009
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.
This document is referenced by:
BS EN ISO 14534 - Ophthalmic optics - Contact lenses and contact lens care products - Fundamental requirements
Published by BSI on February 28, 2015
A description is not available for this item.
This document is referenced by:
BS EN ISO 15882 - Sterilization of health care products — Chemical indicators — Guidance for selection, use and interpretation of results
Published by BSI on January 31, 2009
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.
This document is referenced by:
BS EN ISO 16061 - Instruments for use in association with non-active surgical implants — General requirements
Published by BSI on April 30, 2021
A description is not available for this item.
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