Sterilization of health care products -- Dry heat -- Requirements for the development, validation and routine control of a sterilization process for medical devices
This standard was last reviewed and confirmed* in 2016.
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.
Document published on: 2010-08 Edition: 1 (Monolingual) ICS: 11.080.01 Status: Published Stage: 90.93 (2016-01-27) TC/SC: ISO/TC 198 Number of Pages: 58
This standard has not been revised
No corrigenda or amendments available