IEC 61223-2-11:1999
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
Evaluation and routine testing in medical imaging departments - Part 2-11: Constancy tests - Equipment for general direct radiography
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
31-12-2021
English
16-09-1999
Foreword
1 Scope and object
1.1 Scope
1.2 Object
2 Normative references
3 Terminology
3.1 Degree of requirements
3.2 Use of terms
4 General aspects of CONSTANCY TESTS
4.1 General conditions affecting test procedures
4.2 Establishment of BASELINE VALUES
4.3 Frequency of CONSTANCY TESTS
4.4 Identification of equipment, instrumentation
and test conditions
4.5 Measured functional parameters
5 Performance tests
5.1 RADIATION output from the X-RAY SOURCE ASSEMBLY
5.2 RADIATION input to the IMAGE RECEPTION AREA
5.3 Geometric characteristics
5.4 Resolution of high-contrast detail
5.5 Variation in optical density throughout a
RADIOGRAM
6 Statement of compliance
Figure 1 - Example of a film marker TEST DEVICE
Figure 2 - Example of a TEST DEVICE for perpendicular position
Figure 3 - Example of an alignment TEST DEVICE
Figure 4 - Examples of a high-contrast TEST DEVICE
Figure 5 - Arrangements for testing geometric conditions
Figure 6 - Geometric coincidences
Annex A (normative) Terminology - Index of defined terms
Annex B (informative) Example of a form for the standardized
test report
Annex C (informative) Guidance on action to be taken
Annex D (normative) PHANTOMS and TEST DEVICES
Applies to those components of X-ray equipment which - generate, influence the propagation of, and detect X-radiation; and - process, present and store radiographic information in radiological installations with diagnostic X-ray systems using radiographic films in direct radiography. This standard defines - the essential parameters which describe or affect the performance of the above components of X-ray equipment; - methods of checking that variations in measured quantities related to those parameters are within acceptable limits, in order to maintain adequate standards of imaging whilst reducing unnecessary irradiation of the patient.
DocumentType |
Standard
|
Pages |
39
|
PublisherName |
International Electrotechnical Committee
|
Status |
Withdrawn
|
Standards | Relationship |
AS/NZS 4184.2.11:2002 | Similar to |
GOST R IEC 61223-2-11 : 2001 | Identical |
CEI 62-115 : 2001 | Identical |
NEN IEC 61223-2-11 : 1999 | Identical |
BS IEC 61223-2.11 : 1999 | Identical |
JIS Z 4752-2-11:2005 | Identical |
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 |
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