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)

SS-EN-ISO-20857 - 2013 EDITION - CURRENT


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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:

11.080.01 (Sterilization and disinfection in general Including sterilization methods, air quality of surgery rooms, etc.)


Active implantable medical devices. Medical devices. In vitro diagnostic medical devices

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Designation Name

SS-EN ISO 20857:2013

Revision Level

2013 EDITION

Status

Current

Publication Date

April 22, 2013

Language(s)

English

Page Count

80

International Equivalent

EN ISO 20857:2013(IDT); ISO 20857:2010(IDT)