SS ISO 20857:2018

Sterilisation of health care products — Dry heat — Requirements for the development, validation and routine control of a sterilisation process for medical devices

OVERVIEW

Specifies requirements for the development, validation and routine control of a dry heat sterilisation process for medical devices.

Also specifies requirements and provides guidance in relation to depyrogenation processes using dry heat.

COMMENTS

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PRODUCT DETAILS

Status Current
Edition 2018
No. of Pages 77
ICS Classification 11.080.01 Sterilization and disinfection in general
Committee Biomedical and Health Standards Committee
Available for Purchase Global
Adoption ISO 20857 : 2010 IDT