BS EN ISO 14937:2009

Cross References:
ISO 10012
ISO 10993-1
ISO 10993-17
ISO 11138-1:2006
ISO 11140-1
ISO 11737-1
ISO 11737-2
ISO 13485:2003
IEC 61010-2-040
ISO 9000:2005, Quality
ISO 9001
ISO 9004
ISO 11135-1
ISO 11137-1
ISO 11137-2
ISO/TS 11139:2006
ISO 11607-1
ISO 11607-2
ISO 14001
ISO 14040
ISO 14160
ISO 14161
ISO 14971
ISO 15883
ISO/IEC 17025
ISO 17664
ISO 17665-1
ISO 20857
ISO 22442-1
ISO 22442-2
ISO 22442-3
ISO 90003
EN 556-1
AAMI ST67
90/385/EEC
93/42/EEC
98/79/EC


All current amendments available at time of purchase are included with the purchase of this document.



Keywords: Sterilization (hygiene); Sterile equipment; Sterilizers; Medical equipment; Medical instruments; Process control; Quality control; Verification

Product Code(s): 30157762,30157762

This product references:ISO 11138-1:2006 - Sterilization of health care products - Biological indicators - Part 1: General requirements
ISO 13485:2003 - Medical devices - Quality management systems - Requirements for regulatory purposes
ISO 9000:2005 - Quality management systems - Fundamentals and vocabulary
This product replaces:BS EN ISO 14937:2001 - 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
This product same asISO 14937:2009 - 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

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BS EN ISO 14937:2009
BS EN ISO 14937:2001

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