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About This Item

 

Full Description

This part of ISO 17665 specifies requirements for the development, validation and routine control of a moist heat sterilization process for medical devices. NOTE: Although the scope of this part of ISO 17665 is limited to medical devices, it specifies requirements and provides guidance that may be applicable to other health care products.

Moist heat sterilization processes covered by this part of ISO 17665 include but are not limited to:
a) saturated steam venting systems;
b) saturated steam active air removal systems;
c) air steam mixtures;
d) water spray;
e) water immersion.
 

Document History

  1. CAN/CSA Z17665-1-09 (R2023)

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    Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (Adopted ISO 17665-1:2006, first edition, 2006-08-15)

    • Most Recent
  2. CAN/CSA-ISO 11134-98 (R2003)


    Sterilization of Health Care Products - Requirements for Validation and Routine Control - Industrial Moist Heat Sterilization (Adopted ISO 11134:1994)

    • Historical Version