YY/T 1302.1-2015
Physical requirements and microbiological performance of ethylene oxide sterilization—Part 1: Physical aspects
GB 18279.1-2015
Sterilization of health care products—Ethylene oxide—Part 1:Requirements for development,validation and routine control of a sterilization process for medical devices
T/SDSCCE 031-2022
BS DD CEN/ISO TS 11135-2:2008
Sterilization of health care products. Ethylene oxide. Guidance on the application of ISO 11135-1
SAE AMST81533A
Trichloroethane 1, 1, 1, (Methyl Chloroform) Inhibited, Vapor Degreasing
AAMI TIR14:1997/A1:2004
Contract Sterilization for Ethylene Oxide, Includes Amendment 1
EN ISO 11135:2014/A1:2019
EN ISO 10993-7:2008/A1:2022
32018D1463
UNE-CEN ISO/TS 11135-2:2009 EX
Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1 (ISO/TS 11135-2:2008)
CSA Z314.2-09
Effective sterilization in health care facilities by the ethylene oxide process, Includes Update No. 1 (2010), Update No. 2 (2010)
EN ISO 10993-7:2008/AC:2009
KS P ISO TS 11135-2-2014
Sterilization of health care products — Ethylene oxide — Part 2: Guidance on the application of ISO 11135-1
MIL MIL-T-81533A Notice 2-Cancellation
Trichloroethane 1, 1, 1, (Methyl Chloroform) Inhibited, Vapor Degreasing (No S/S Document)
UNE-EN ISO 11135-1:2007
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007)
SAE AMST81533
Trichloroethane 1, 1, 1, (Methyl Chloroform) Inhibited, Vapor Degreasing
BS ISO 17280:2015
Surface active agents. Determination of 1,4-dioxan residues in surfactants obtained from epoxyethane by gas chromatography
ISO 17280:2015
Surface active agents — Determination of 1,4-dioxan residues in surfactants obtained from epoxyethane by gas chromatography
CSA Z314.9-09(R2013)
Installation, ventilation, and safe use of ethylene oxide sterilizers in health care facilities, Includes Update No. 1 (2010)
DIN EN ISO 11135-1
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007)