EN 60627:2015
Current
The latest, up-to-date edition.
Diagnostic X-ray imaging equipment - Characteristics of general purpose and mammographic anti-scatter grids
05-22-2015
FOREWORD
INTRODUCTION
1 Scope
2 Normative references
3 Terms and definitions
4 Structure of ANTI-SCATTER GRIDS
5 Measurement and determination of physical characteristics
6 Requirements for ANTI-SCATTER GRIDS
Annex A (normative) - Calculation of the APPLICATION
LIMITS
Annex B (informative) - Influence of scatter fraction on
the physical characteristics
Bibliography
Index of defined terms used in this standard
Annex ZA (normative) - Normative references to
international publications with their
corresponding European publications
Annex ZZ (informative) - Coverage of Essential
Requirements of EU Directives
IEC 60627:2013 is applicable to anti-scatter grids used in medical diagnostic X-ray imaging equipment. Anti-Scatter Grids are used to reduce the incidence of scattered radiation, produced particularly in the body of the patient, upon the image reception area and thus to improve the contrast of the X-ray pattern. This International Standard specifies the definitions, determination and indication of characteristics of anti-scatter grids. In this standard only linear grids are considered. Since at present only focused grids are used in mammography, this standard is restricted to focused grids where mammographic anti-scatter grids are concerned. This standard is not intended to be applied for acceptance tests. This standard does not cover the homogeneity of performance over the area of a grid. This standard is intended to be applied for the determination of the characteristics of anti-scatter grids under test conditions. These conditions are not usually available at the site of the responsible organization. This third edition cancels and replaces the second edition published in 2001, and constitutes a technical revision. In this revision calcium tungstate phosphor fluorescent screens, which are no longer available, have been replaced by gadolinium oxysulphide (GOS) fluorescent screens. Further, a new quality parameter is introduced: the Image Improvement Factor or Q-factor, which better describes the properties of the anti-scatter grid, especially for digital detector applications. Further differences between this third edition and the previous second edition are: - new instrumentation is prescribed for measurements of the transmission of primary radiation, the transmission of scattered radiation and the transmission of total radiation, because fluorescent screens made of calcium tungstate phosphors are outdated and are no longer available; - the definition of the phantom used for measurements of the transmission of primary radiation, the transmission of scattered radiation and the transmission of total radiation is modified and references to IEC 61267 are omitted; - and the radiation conditions used for the measurements have been adapted and are now the RQR and RQR-M conditions specified in IEC 61267:2005.
Committee |
CLC/TC 62
|
DevelopmentNote |
Supersedes EN 61953. (11/2002)
|
DocumentType |
Standard
|
PublisherName |
European Committee for Standards - Electrical
|
Status |
Current
|
Supersedes |
Standards | Relationship |
NF EN 60627 : 2015 | Identical |
IEC 60627:2013 | Identical |
NBN EN 60627 : 2015 | Identical |
NEN EN IEC 60627 : 2015 | Identical |
I.S. EN 60627:2015 | Identical |
PN EN 60627 : 2015 | Identical |
SN EN 60627:2015 | Identical |
BS EN 60627:2015 | Identical |
CEI EN 60627 : 2016 | Identical |
DIN EN 60627:2016-08 | Identical |
UNE-EN 60627:2002 | Identical |
UNE-EN 60627:2015 | Identical |
BS EN 63080:2017 | Identical |
PNE-FprEN 60627 | Identical |
BS EN 60601-2-54:2009 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-54: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF X-RAY EQUIPMENT FOR RADIOGRAPHY AND RADIOSCOPY |
EN 60601-2-54:2009/A1:2015 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-54: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF X-RAY EQUIPMENT FOR RADIOGRAPHY AND RADIOSCOPY |
EN 60601-1-3 : 2008 AMD 11 2016 | MEDICAL ELECTRICAL EQUIPMENT - PART 1-3: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: RADIATION PROTECTION IN DIAGNOSTIC X-RAY EQUIPMENT (IEC 60601-1-3:2008/A1:2013) |
EN 61267:2006 | Medical diagnostic X-ray equipment - Radiation conditions for use in the determination of characteristics |
IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
IEC TR 60788:2004 | Medical electrical equipment - Glossary of defined terms |
IEC 60601-1-3:2008+AMD1:2013 CSV | Medical electrical equipment - Part 1-3: General requirements forbasic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment |
IEC 61267:2005 | Medical diagnostic X-ray equipment - Radiation conditions for use in the determination of characteristics |
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