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ASSE/SAFE - ANSI ASSE Z9.9 - PORTABLE VENTILATION SYSTEMS Organization: ASSE/SAFE
Date: 2010-01-01
Description: This Standard covers components of portable ventilation systems, including: — air movers and their modes of power — other components of portable ventilation systems including entry hoods; duct, hose, and other conveying structures; air-cleaning equipment including filters and sorbent air-purifying devices; and air coolers and heaters.
SAE J2554 - (R) ENGINE INTAKE AIR WATER SEPARATION TEST PROCEDURE Organization: SAE
Date: 2017-02-01
Description: This water separation section has been established to cover heavy-duty engine intake filter systems. It may also be applicable to some automotive and industrial air inlet systems where water separation is an issue Purpose The purpose of this document is to establish and specify a uniform test method to permit a general evaluation of the water separation performance of engine intake systems The performance and reliability of internal combustion engines and other equipment employing intake air filtration or separation systems, is affected by the performance of the intake system in removing contaminants including water from the intake airflow.
DIN EN ISO 11135 - STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 11135:2014) Organization: DIN
Date: 2014-10-01
Description: National and/or regional regulations for the provision of medical devices might require the implementation of a full quality management system and the assessment of that system by a third party. This International Standard does not specify requirements for occupational safety associated with the design and operation of EO sterilization facilities.
CEN - EN ISO 11135 - STERILIZATION OF HEALTH-CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES Organization: CEN
Date: 2014-07-01
Description: National and/or regional regulations for the provision of medical devices might require the implementation of a full quality management system and the assessment of that system by a third party. This International Standard does not specify requirements for occupational safety associated with the design and operation of EO sterilization facilities.
SNV - SN EN ISO 11135 - STERILIZATION OF HEALTH-CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES Organization: SNV
Date: 2014-10-01
Description: National and/or regional regulations for the provision of medical devices might require the implementation of a full quality management system and the assessment of that system by a third party. This International Standard does not specify requirements for occupational safety associated with the design and operation of EO sterilization facilities.
AAMI 11135 - STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES Organization: AAMI
Date: 2014-01-01
Description: National and/or regional regulations for the provision of medical devices might require the implementation of a full quality management system and the assessment of that system by a third party. This International Standard does not specify requirements for occupational safety associated with the design and operation of EO sterilization facilities.
ASTM MNL20 - CORROSION TESTS AND STANDARDS: APPLICATION AND INTERPRETATION - 2ND EDITION Organization: ASTM
Date: 2005-01-01
Description: Hack, Section Editor) includes chapters on outdoor and indoor atmospheres, seawater, flesh water, soils, concrete, industrial waters, industrial chemical, petroleum, high-temperature gases, organic liquids, molten salts, liquid metals, corrosion inhibitors, in-vivo, and microbiological effects.

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