SS-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)
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ISO 20857:2010 specifies requirements for the development, validation and routine control of a dry heat sterilization process for medical devices. Although ISO 20857:2010 primarily addresses dry heat sterilization, it also specifies requirements and provides guidance in relation to depyrogenation processes using dry heat.
To find similar documents by classification:
Active implantable medical devices. Medical devices. In vitro diagnostic medical devices
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SS-EN ISO 20857:2013
April 22, 2013
EN ISO 20857:2013(IDT); ISO 20857:2010(IDT)