
Sterilization of Health Care Products - Ethylene Oxide Part 1: Requirements for Development, Validation and Routine Control of a Sterilization Process for Medical Devices
出版:National Standards Authority of Ireland

专家解读视频
Describes requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices.
UNE EN ISO 11135-1:2007 - Identical
NS EN ISO 11135-1 Ed. 1 (2007) - Identical
NBN EN ISO 11135-1:2007 - Identical
NF EN ISO 11135-1:2007 - Identical
DIN EN ISO 11135-1 (2007-08) - Identical
SN EN ISO 11135-1:2007 - Identical
BS EN ISO 11135-1:2007 - Identical
SS EN ISO 11135-1 Ed. 1 (2007) - Identical
ISO 11135-1:2007 - Identical
UNI EN ISO 11135-1:2008 - Identical
NEN EN ISO 11135-1:2007 - Identical
ONORM EN ISO 11135-1:2007 - Identical