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ASTM E1894 - STANDARD GUIDE FOR SELECTING DOSIMETRY SYSTEMS FOR APPLICATION IN PULSED X-RAY SOURCES Organization: ASTM
Date: 2013-08-01
Description: Both dose and dose-rate techniques are described. Operating characteristics of flash X-ray sources are given, with emphasis on the spectrum of the photon output.
CSA C22.2 NO 60601-2-43 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-43: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF X-RAY EQUIPMENT FOR INTERVENTIONAL PROCEDURES - SECOND EDITION Organization: CSA
Date: 2011-01-01
Description: NOTE 2 Specific requirements for magnetic navigation devices, and for the use of INTERVENTIONAL X-RAY EQUIPMENT in an operating room environment were not considered in this particular standard; therefore no specific requirements have been developed for these devices or uses.
CENELEC - EN 60601-2-43 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-43: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF X-RAY EQUIPMENT FOR INTERVENTIONAL PROCEDURES - INCORPORATING CORRIGENDAM JULY 2014 Organization: CENELEC
Date: 2010-06-01
Description: NOTE 2 Specific requirements for magnetic navigation devices, and for the use of INTERVENTIONAL X-RAY EQUIPMENT in an operating room environment were not considered in this particular standard; therefore no specific requirements have been developed for these devices or uses.
CSA C22.2 NO 60601-2-68 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-68: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF X-RAY-BASED IMAGE-GUIDED RADIOTHERAPY EQUIPMENT FOR USE WITH ELECTRON ACCELERATORS, LIGHT ION BEAM THERAPY EQUIPMENT AND RADIONUCLIDE BEAM THERAPY EQUIPMENT - FIRST EDITION Organization: CSA
Date: 2015-01-01
Description: This particular standard, with the inclusion of TYPE TESTS and SITE TESTS, applies respectively to the MANUFACTURER and some installation aspects of X-IGRT EBE SYSTEMS intended to be • for NORMAL USE, operated under the authority of appropriately licensed or QUALIFIED PERSONS by OPERATORS having the required skills for a particular medical application, for particular specified clinical purposes, e.g.
CEI - EN 60601-2-68 - ELECTRICAL MEDICAL EQUIPMENT PART 2: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF X-RAY-BASED IMAGE-GUIDED RADIOTHERAPY EQUIPMENT FOR USE WITH ELECTRON ACCELERATORS, LIGHT ION BEAM THERAPY EQUIPMENT AND RADIONUCLIDE BEAM THERAPY EQUIPMENT Organization: CEI
Date: 2016-06-01
Description: This particular standard, with the inclusion of TYPE TESTS and SITE TESTS, applies respectively to the MANUFACTURER and some installation aspects of X-IGRT EBE SYSTEMS intended to be • for NORMAL USE, operated under the authority of appropriately licensed or QUALIFIED PERSONS by OPERATORS having the required skills for a particular medical application, for particular specified clinical purposes, e.g.
IEC 60601-2-68 - MEDICAL ELECTRICAL EQUIPMENT – PART 2-68: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF X-RAY-BASED IMAGE-GUIDED RADIOTHERAPY EQUIPMENT FOR USE WITH ELECTRON ACCELERATORS, LIGHT ION BEAM THERAPY EQUIPMENT AND RADIONUCLIDE BEAM THERAPY EQUIPMENT - EDITION 1.0 Organization: IEC
Date: 2014-09-01
Description: If that is not the case, the clause or subclause applies only to X-IGRT EQUIPMENT This particular standard, with the inclusion of TYPE TESTS and SITE TESTS, applies respectively to the MANUFACTURER and some installation aspects of X-IGRT EBE SYSTEMS intended to be for NORMAL USE, operated under the authority of appropriately licensed or QUALIFIED PERSONS by OPERATORS having the required skills for a particular medical application, for particular specified clinical purposes, e.g.
CENELEC - EN 60601-2-68 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-68: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF X-RAY-BASED IMAGE-GUIDED RADIOTHERAPY EQUIPMENT FOR USE WITH ELECTRON ACCELERATORS, LIGHT ION BEAM THERAPY EQUIPMENT AND RADIONUCLIDE BEAM THERAPY EQUIPMENT Organization: CENELEC
Date: 2015-05-01
Description: This particular standard, with the inclusion of TYPE TESTS and SITE TESTS, applies respectively to the MANUFACTURER and some installation aspects of X-IGRT EBE SYSTEMS intended to be for NORMAL USE, operated under the authority of appropriately licensed or QUALIFIED PERSONS by OPERATORS having the required skills for a particular medical application, for particular specified clinical purposes, e.g.
CEI - EN 60601-2-8 - MEDICAL ELECTRICAL EQUIPMENT PART 2: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF THERAPEUTIC X-RAY EQUIPMENT OPERATING IN THE RANGE 10 KV TO 1 MV Organization: CEI
Date: 2016-01-01
Description: This international standard applies to the basic safety and essential performance of therapeutic X-RAY EQUIPMENT with NOMINAL X-RAY TUBE VOLTAGES in the range 10 kV to 1 MV when connected to alternating current SUPPLY MAINS, hereafter referred to as ME EQUIPMENT.
SNZ AS/NZS IEC 60601.2.8 - MEDICAL ELECTRICAL EQUIPMENT PART 2.8: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF THERAPEUTIC X-RAY EQUIPMENT OPERATING IN THE RANGE 10 KV TO 1 MV Organization: SNZ
Date: 2015-12-18
Description: This international standard applies to the basic safety and essential performance of therapeutic X-RAY EQUIPMENT with NOMINAL X-RAY TUBE VOLTAGES in the range 10 kV to 1 MV when connected to alternating current SUPPLY MAINS, hereafter referred to as ME EQUIPMENT.
ASTM E2119 - STANDARD PRACTICE FOR QUALITY SYSTEMS FOR CONDUCTING IN SITU MEASUREMENTS OF LEAD CONTENT IN PAINT OR OTHER COATINGS USING FIELD-PORTABLE X-RAY FLUORESCENCE (XRF) DEVICES Organization: ASTM
Date: 2016-03-01
Description: This practice covers the collection and documentation of quality control (QC) measurements for determining acceptable levels of instrumental performance when using field-portable energy-dispersive x-ray fluorescence spectrometry devices (XRFs) for the purposes of generating lead classification results from measurements on paint and other coating films within buildings and related structures.
ASTM PS95 - STANDARD PROVISIONAL PRACTICE FOR QUALITY SYSTEMS FOR CONDUCTING IN SITU MEASUREMENTS OF LEAD CONTENT IN PAINT OR OTHER COATINGS USING FIELD-PORTABLE X-RAY FLUORESCENCE (XRF) DEVICES Organization: ASTM
Date: 1998-08-04
Description: Scope 1.1 This provisional practice covers the collection and documentation of quality control (QC) measurements for determining acceptable levels of instrumental performance when using field-portable energy-dispersive X-ray fluorescence spectrometry devices (XRFs) for the purposes of generating lead classification results from measurements on paint and other coating films within buildings and related structures.
IEC 60601-2-8 - MEDICAL ELECTRICAL EQUIPMENT – PART 2-8: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF THERAPEUTIC X-RAY EQUIPMENT OPERATING IN THE RANGE 10 KV TO 1 MV - EDITION 2.1; CONSOLIDATED REPRINT Organization: IEC
Date: 2015-09-01
Description: This international standard applies to the basic safety and essential performance of therapeutic X-RAY EQUIPMENT with NOMINAL X-RAY TUBE VOLTAGES in the range 10 kV to 1 MV when connected to alternating current SUPPLY MAINS, hereafter referred to as ME EQUIPMENT.
ASTM E1735 - STANDARD TEST METHOD FOR DETERMINING RELATIVE IMAGE QUALITY OF INDUSTRIAL RADIOGRAPHIC FILM EXPOSED TO X-RADIATION FROM 4 TO 25 MEV Organization: ASTM
Date: 2007-02-15
Description: For the purposes of this test method, it is assumed that all components of the X-ray system are operating properly and are capable of producing a given image quality.
TSE - TS EN 13723 - PETROLEUM PRODUCTS - DETERMINATION OF LOW LEAD CONTENTS IN GASOLINES - WAVELENGTH-DISPERSIVE X-RAY FLUORESCENCE SPECTROMETRY (XRF) Organization: TSE
Date: 2002-11-11
Description: The present document applies to constant envelope angle modulation systems for use in the land mobile service, using the available bandwidth, operating on radio frequencies between 30 MHz and 1000 MHz, with channel separations of 12.5 kHz, 20 kHz and 25 kHz intended for data transmissions.
ASTM E1411 - STANDARD PRACTICE FOR QUALIFICATION OF RADIOSCOPIC SYSTEMS Organization: ASTM
Date: 2016-06-01
Description: This practice provides test and measurement details for measuring the performance of X-ray and gamma ray radioscopic systems. Radioscopic examination applications are diverse.
SAE/TP - 2008-01-1999 - THERMAL-VACUUM TEST DATA FOR JEM/MAXI LOOP HEAT PIPE SYSTEM WITH TWO RADIATORS Organization: SAE/TP
Date: 2008-06-29
Description: This paper presents thermal-vacuum test data obtained for the JEM MAXI loop heat pipe (LHP) with two separate radiators operating under transient regimes representative of those to be encountered during the flight. The Monitor of All-sky X-ray Image (MAXI) in the Japanese Experiment Module (JEM), on the International Space Station (ISS), is an X-ray camera with wide fields of view to monitor the universe.
ASTM C1572 - STANDARD GUIDE FOR DRY LEAD GLASS AND OIL-FILLED LEAD GLASS RADIATION SHIELDING WINDOW COMPONENTS FOR REMOTELY OPERATED FACILITIES Organization: ASTM
Date: 2010-11-01
Description: It does not address glovebox, water, x-ray glass or zinc bromide windows. Supplementary information on viewing systems in hot cells may be found in Guides C1533 and C1661.
CENELEC - EN 60601-2-8 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-8: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF THERAPEUTIC XRAY EQUIPMENT OPERATING IN THE RANGE 10 KV TO 1 MV - INCORPORATES AMENDMENT A1: 2016 Organization: CENELEC
Date: 2015-06-01
Description: This international standard applies to the basic safety and essential performance of therapeutic X-RAY EQUIPMENT with NOMINAL X-RAY TUBE VOLTAGES in the range 10 kV to 1 MV when connected to alternating current SUPPLY MAINS, hereafter referred to as ME EQUIPMENT.
ASTM F1532 - STANDARD GUIDE FOR QUALIFICATION, SELECTION, TRAINING, UTILIZATION, AND SUPERVISION OF SECURITY SCREENING PERSONNEL Organization: ASTM
Date: 1994-07-15
Description: Scope 1.1 This guide covers the qualification, selection, training, utilization, and supervision of personnel assigned duties at security check-points equipped with metal detection, X-ray inspection, and explosives detection equipment or systems operated to prevent the introduction of weapons, explosives, or other prohibited articles into secure or restricted areas, or to prevent the egress of valuable or sensitive materials from controlled facilities.
CRC - BIOMEDICAL IMAGING - BIOMEDICAL IMAGING Organization: CRC
Date: 2003-03-26
Description: Consider the following: • Some of the systems, such as ultrasound, are relatively inexpensive, while others, such as positron emission tomography (PET) facilities, cost millions of dollars for the hardware and the employment of Ph.D.-level personnel to operate them. • Systems that make use of x-rays have been designed to image anatomic structures, while others that make use of radioisotopes provide functional information.

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