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MANEY - X-RAY AND ELECTRON DIFFRA - X-RAY AND ELECTRON DIFFRACTION STUDIES IN MATERIALS SCIENCE Organization: MANEY
Date: 2004-01-01
Description: X-ray diffraction was first applied almost a century ago. The subsequent development of the technique and its application across industry and academia to physical, chemical and biological problems has made it an important tool in the armoury of the analyst.
ASTM ISO/ASTM 51431 - STANDARD PRACTICE FOR DOSIMETRY IN ELECTRON BEAM AND X-RAY (BREMSSTRAHLUNG) IRRADIATION FACILITIES FOR FOOD PROCESSING Organization: ASTM
Date: 2005-01-01
Description: For information concerning electron beam irradiation technology and dosimetry, see ISO/ASTM Practice 51649. For information concerning X-ray irradiation technology and dosimetry, see ISO/ASTM Practice 51608.
IEC 62220-1 - MEDICAL ELECTRICAL EQUIPMENT CHARACTERISTICS OF DIGITAL X-RAY IMAGING DEVICES PART 1: DETERMINATION OF THE DETECTIVE QUANTUM EFFICIENCY - EDITION 1.0 Organization: IEC
Date: 2003-10-01
Description: It is restricted to DIGITAL X-RAY IMAGING DEVICES that are used for radiographic imaging, such as CR systems, selenium-based systems, flat panel detectors, optically coupled CCD detectors, and digital X-RAY IMAGE INTENSIFIERS used for single exposures.
DS/EN 61223-3-2 - EVALUATION AND ROUTINE TESTING IN MEDICAL IMAGING DEPARTMENTS - PART 3-2: ACCEPTANCE TESTS - IMAGING PERFORMANCE OF MAMMOGRAPHIC X-RAY EQUIPMENT Organization: DS
Date: 2008-10-03
Description: This part of IEC 61223 applies to the effectiveness of mammographic X-RAY EQUIPMENT, with respect to image quality and dose, in combination with aspects of EQUIPMENT safety.
IEC 61223-3-2 - EVALUATION AND ROUTINE TESTING IN MEDICAL IMAGING DEPARTMENTS – PART 3-2: ACCEPTANCE TESTS – IMAGING PERFORMANCE OF MAMMOGRAPHIC X-RAY EQUIPMENT - EDITION 2.0 Organization: IEC
Date: 2007-07-01
Description: This part of IEC 61223 applies to the effectiveness of mammographic X-RAY EQUIPMENT, with respect to image quality and dose, in combination with aspects of EQUIPMENT safety.
DS/EN 62220-1-2 - MEDICAL ELECTRICAL EQUIPMENT - CHARACTERISTICS OF DIGITAL X-RAY IMAGING DEVICES - PART 1-2: DETERMINATION OF THE DETECTIVE QUANTUM EFFICIENCY - DETECTORS USED IN MAMMOGRAPHY Organization: DS
Date: 2007-10-29
Description: This part of IEC 62220 specifies the method for the determination of the DETECTIVE QUANTUMEFFICIENCY (DQE) of DIGITAL X-RAY IMAGING DEVICES as a function of AIR KERMA and of SPATIAL FREQUENCY for the working conditions in the range of the medical application as specified by the MANUFACTURER.
IEC 62220-1-2 - MEDICAL ELECTRICAL EQUIPMENT – CHARACTERISTICS OF DIGITAL X-RAY IMAGING DEVICES – PART 1-2: DETERMINATION OF THE DETECTIVE QUANTUM EFFICIENCY – DETECTORS USED IN MAMMOGRAPHY - EDITION 1.0 Organization: IEC
Date: 2007-06-01
Description: This part of IEC 62220 specifies the method for the determination of the DETECTIVE QUANTUM EFFICIENCY (DQE) of DIGITAL X-RAY IMAGING DEVICES as a function of AIR KERMA and of SPATIAL FREQUENCY for the working conditions in the range of the medical application as specified by the MANUFACTURER.
DS/EN ISO 11137-1 - STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 11137-1:2006, INCLUDING AMD 1:2013) Organization: DS
Date: 2015-07-06
Description: ISO 11137-1:2006 covers radiation processes employing irradiators using the radionuclide 60Co or 137Cs, a beam from an electron generator or a beam from an X-ray generator. ISO 11137-1:2006 does not: specify requirements for development, validation and routine control of a process for inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeldt-Jakob disease; detail specified requirements for designating a medical device as sterile; specify a quality management system for the control of all stages of production of medical devices; specify requirements for occupational safety associated with the design and operation of irradiation facilities; specify requirements for the sterilization of used or reprocessed devices.
NBN EN ISO 11137-1 FR - STÉRILISATION DES PRODUITS DE SANTÉ - IRRADIATION - PARTIE 1: EXIGENCES RELATIVES À LA MISE AU POINT, À LA VALIDATION ET AU CONTRÔLE DE ROUTINE D'UN PROCÉDÉ DE STÉRILISATION POUR LES DISPOSITIFS MÉDICAUX (ISO 11137-1:2006, Y COMPRIS AMD 1:2013) Organization: NBN
Date: 2015-07-24
Description: ISO 11137-1:2006 covers radiation processes employing irradiators using the radionuclide 60Co or 137Cs, a beam from an electron generator or a beam from an X-ray generator.ISO 11137-1:2006 does not:specify requirements for development, validation and routine control of a process for inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeldt-Jakob disease;detail specified requirements for designating a medical device as sterile;specify a quality management system for the control of all stages of production of medical devices;specify requirements for occupational safety associated with the design and operation of irradiation facilities;specify requirements for the sterilization of used or reprocessed devices.
NBN - EN ISO 11137-1 - STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 11137-1:2006, INCLUDING AMD 1:2013) Organization: NBN
Date: 2015-07-24
Description: ISO 11137-1:2006 covers radiation processes employing irradiators using the radionuclide 60Co or 137Cs, a beam from an electron generator or a beam from an X-ray generator.ISO 11137-1:2006 does not:specify requirements for development, validation and routine control of a process for inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeldt-Jakob disease;detail specified requirements for designating a medical device as sterile;specify a quality management system for the control of all stages of production of medical devices;specify requirements for occupational safety associated with the design and operation of irradiation facilities;specify requirements for the sterilization of used or reprocessed devices.
NBN - EN ISO 11137-1 - STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 11137-1:2006, INCLUDING AMD 1:2013) Organization: NBN
Date: 2015-07-24
Description: ISO 11137-1:2006 covers radiation processes employing irradiators using the radionuclide 60Co or 137Cs, a beam from an electron generator or a beam from an X-ray generator.ISO 11137-1:2006 does not:specify requirements for development, validation and routine control of a process for inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeldt-Jakob disease;detail specified requirements for designating a medical device as sterile;specify a quality management system for the control of all stages of production of medical devices;specify requirements for occupational safety associated with the design and operation of irradiation facilities;specify requirements for the sterilization of used or reprocessed devices.
DIN EN ISO 11137-1 - STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 11137-1:2006, INCLUDING AMD 1:2013) Organization: DIN
Date: 2015-11-01
Description: This part of ISO 11137 covers radiation processes employing irradiators using, a) the radionuclide 60Co or 137Cs, b) a beam from an electron generator or c) a beam from an X-ray generator. This part of ISO 11137 does not specify requirements for development, validation and routine control of a process for inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeld-Jakob disease.
ASTM ISO/ASTM 51204 - STANDARD PRACTICE FOR DOSIMETRY IN GAMMA IRRADIATION FACILITIES FOR FOOD PROCESSING Organization: ASTM
Date: 2004-06-30
Description: NOTE 2 - ISO/ASTM Practice 51431 describes dosimetric procedures for electron beam and X-ray (bremsstrahlung) irradiation facilities for food processing.
ISO - ISO/ASTM 52303 - GUIDE FOR ABSORBED-DOSE MAPPING IN RADIATION PROCESSING FACILITIES - FIRST EDITION Organization: ISO
Date: 2015-07-15
Description: This document provides guidance in determining absorbed-dose distributions (mapping) in products, materials or substances irradiated in gamma, X-ray (bremsstrahlung) and electron beam facilities. NOTE 1-For irradiation of food and the radiation sterilization of health care products, specific ISO and ISO/ASTM standards containing dose mapping requirements exist.
ASTM ISO/ASTM 52303 - STANDARD GUIDE FOR ABSORBED-DOSE MAPPING IN RADIATION PROCESSING FACILITIES Organization: ASTM
Date: 2015-02-09
Description: This document provides guidance in determining absorbed-dose distributions (mapping) in products, materials or substances irradiated in gamma, X-ray (bremsstrahlung) and electron beam facilities. NOTE 1—For irradiation of food and the radiation sterilization of health care products, specific ISO and ISO/ASTM standards containing dose mapping requirements exist.
ASTM E2303 - STANDARD GUIDE FOR ABSORBED-DOSE MAPPING IN RADIATION PROCESSING FACILITIES Organization: ASTM
Date: 2011-07-01
Description: This document provides guidance in determining absorbed-dose distributions (mapping) in products, materials or substances irradiated in gamma, X-ray (bremsstrahlung) and electron beam facilities. NOTE 1—For irradiation of food and the radiation sterilization of health care products, specific ISO and ISO/ASTM standards containing dose mapping requirements exist.
CEN - EN ISO 11137-1 - STERILIZATION OF HEALTH CARE PRODUCTS - RADIATION - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES Organization: CEN
Date: 2015-06-01
Description: This part of ISO 11137 covers radiation processes employing irradiators using, a) the radionuclide 60Co or 137Cs, b) a beam from an electron generator or c) a beam from an X-ray generator. This part of ISO 11137 does not specify requirements for development, validation and routine control of a process for inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeld-Jakob disease.
AAMI - 11137-1 - STERILIZATION OF HEALTH CARE PRODUCTS—RADIATION—PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION, AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES - INCORPORATES AMENDMENT 1: 2013 Organization: AAMI
Date: 2006-01-01
Description: This part of ISO 11137 covers radiation processes employing irradiators using, a) the radionuclide 60Co or 137Cs, b) a beam from an electron generator or c) a beam from an X-ray generat or. This part of ISO 11137 does not specify requirements for development, validation and routine control of a process for inactivating the causative agents of spongiform encephalopathies such as scrapie, bovine spongiform encephalopathy and Creutzfeld-Jakob disease.
ISO - ISO 14470 - FOOD IRRADIATION — REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF THE PROCESS OF IRRADIATION USING IONIZING RADIATION FOR THE TREATMENT OF FOOD - FIRST EDITION Organization: ISO
Date: 2011-12-01
Description: This International Standard covers irradiation processes using the radionuclides 60Co or 137Cs, electron beams or X-ray generators. The requirements given in this International Standard are the minimum necessary to control the food irradiation process.

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