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IEC 60522 - DETERMINATION OF THE PERMANENT FILTRATION OF X-RAY TUBE ASSEMBLIES - EDITION 2.0 Organization: IEC
Date: 1999-02-01
Description: NOTE 1 This standard does not contain requirements for any specific values of PERMANENT FILTRATION or TOTAL FILTRATION to be provided. For X-RAY TUBE ASSEMBLIES and X-RAY EQUIPMENT used for diagnostic purposes, appropriate requirements are given in IEC 60601-1-3.
SNV - SN EN ISO 10524-3/A1 - PRESSURE REGULATORS FOR USE WITH MEDICAL GASES - PART 3: PRESSURE REGULATORS INTEGRATED WITH CYLINDER VALVES - AMENDMENT 1: FILTRATION AND INFORMATION TO BE SUPPLIED BY THE MANUFACTURER; AMENDMENT A1 Organization: SNV
Date: 2014-04-01
Description: Amendment 1 to ISO 10524-3:2005 was prepared by Technical Committee ISO/TC 121, Anaesthetic and respiratory equipment, Subcommittee SC 6, Medical gas systems.
AAMI 14937 - STERILIZATION OF HEALTH CARE PRODUCTS - GENERAL REQUIREMENTS FOR CHARACTERIZATION OF A STERILIZING AGENT AND THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES Organization: AAMI
Date: 2009-01-01
Description: This International Standard is intended to be applied by process developers, manufacturers of sterilization equipment, manufacturers of medical devices to be sterilized, and organizations responsible for sterilizing medical devices.
SNV - SN EN ISO 14937 - STERILIZATION OF HEALTH CARE PRODUCTS - GENERAL REQUIREMENTS FOR CHARACTERIZATION OF A STERILIZING AGENT AND THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES Organization: SNV
Date: 2010-03-01
Description: This International Standard is intended to be applied by process developers, manufacturers of sterilization equipment, manufacturers of medical devices to be sterilized, and organizations responsible for sterilizing medical devices.
ISO 14937 - STERILIZATION OF HEALTH CARE PRODUCTS - GENERAL REQUIREMENTS FOR CHARACTERIZATION OF A STERILIZING AGENT AND THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES - SECOND EDITION Organization: ISO
Date: 2009-10-15
Description: This International Standard is intended to be applied by process developers, manufacturers of sterilization equipment, manufacturers of medical devices to be sterilized, and organizations responsible for sterilizing medical devices.
CSA ISO 14937 - STERILIZATION OF HEALTH CARE PRODUCTS - GENERAL REQUIREMENTS FOR CHARACTERIZATION OF A STERILIZING AGENT AND THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES - SECOND EDITION Organization: CSA
Date: 2011-01-01
Description: This International Standard is intended to be applied by process developers, manufacturers of sterilization equipment, manufacturers of medical devices to be sterilized, and organizations responsible for sterilizing medical devices.
ASTM F3021 - STANDARD TEST METHOD FOR USING AEROSOL FILTRATION FOR MEASURING THE PERFORMANCE OF POROUS PACKAGING MATERIALS AS A SURROGATE MICROBIAL BARRIER Organization: ASTM
Date: 2016-10-01
Description: Products designed to meet this specification must not be automatically classified as fit for medical or rehabilitation fitness purposes. Products intended for medical use should comply with any applicable international or national standards.

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