EN 60601-2-54:2009/A2:2019

SLOVENSKI STANDARD
01-julij-2019
Medicinska električna oprema - 2-54. del: Posebne zahteve za osnovno varnost in
bistvene lastnosti rentgenske opreme za radiografijo in radioskopijo - Dopolnilo
A2 (IEC 60601-2-54:2009/A2:2018)
Medical electrical equipment - Part 2-54: Particular requirements for the basic safety and
essential performance of X-ray equipment for radiography and radioscopy (IEC 60601-2-
54:2009/A2:2018)
Medizinische elektrische Geräte - Teil 2-54: Besondere Festlegungen für die Sicherheit
und die wesentlichen Leistungsmerkmale von Röntgeneinrichtungen für Radiographie
und Radioskopie (IEC 60601-2-54:2009/A2:2018)
Appareils électromédicaux - Partie 2-54: Exigences particulières pour la sécurité de base
et les performances essentielles des appareils à rayonnement X utilisés pour la
radiographie et la radioscopie (IEC 60601-2-54:2009/A2:2018)
Ta slovenski standard je istoveten z: EN 60601-2-54:2009/A2:2019
ICS:
11.040.50 Radiografska oprema Radiographic equipment
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

EUROPEAN STANDARD EN 60601-2-54:2009/A2

NORME EUROPÉENNE
EUROPÄISCHE NORM
May 2019
ICS 11.040.50
English Version
Medical electrical equipment - Part 2-54: Particular requirements
for the basic safety and essential performance of X-ray
equipment for radiography and radioscopy
(IEC 60601-2-54:2009/A2:2018)
Appareils électromédicaux - Partie 2-54: Exigences Medizinische elektrische Geräte - Teil 2-54: Besondere
particulières pour la sécurité de base et les performances Festlegungen für die Sicherheit und die wesentlichen
essentielles des appareils à rayonnement X utilisés pour la Leistungsmerkmale von Röntgeneinrichtungen für
radiographie et la radioscopie Radiographie und Radioskopie
(IEC 60601-2-54:2009/A2:2018) (IEC 60601-2-54:2009/A2:2018)
This amendment A2 modifies the European Standard EN 60601-2-54:2009; it was approved by CENELEC on 2018-08-03. CENELEC
members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this amendment the
status of a national standard without any alteration.
Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN-CENELEC
Management Centre or to any CENELEC member.
This amendment exists in three official versions (English, French, German). A version in any other language made by translation under the
responsibility of a CENELEC member into its own language and notified to the CEN-CENELEC Management Centre has the same status as
the official versions.
CENELEC members are the national electrotechnical committees of Austria, Belgium, Bulgaria, Croatia, Cyprus, the Czech Republic,
Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia,
Lithuania, Luxembourg, Malta, the Netherlands, Norway, Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden,
Switzerland, Turkey and the United Kingdom.

European Committee for Electrotechnical Standardization
Comité Européen de Normalisation Electrotechnique
Europäisches Komitee für Elektrotechnische Normung
CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2019 CENELEC All rights of exploitation in any form and by any means reserved worldwide for CENELEC Members.
Ref. No. EN 60601-2-54:2009/A2:2019 E

European foreword
The text of document 62B/1089/FDIS, future IEC 60601-2-54/A2, prepared by SC 62B "Diagnostic
imaging equipment" of IEC/TC 62 "Electrical equipment in medical practice" was submitted to the
IEC-CENELEC parallel vote and approved by CENELEC as EN 60601-2-54:2009/A2:2019.
The following dates are fixed:
• latest date by which the document has to be implemented at national (dop) 2019-11-24
level by publication of an identical national standard or by endorsement
• latest date by which the national standards conflicting with the (dow) 2022-05-24
document have to be withdrawn
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CENELEC shall not be held responsible for identifying any or all such patent rights.

Endorsement notice
The text of the International Standard IEC 60601-2-54:2009/A2:2018 was approved by CENELEC as
a European Standard without any modification.
In the official version, for Bibliography, the following notes have to be added for the standards
indicated:
IEC 62220-1-3:2008 NOTE Harmonized as EN 62220-1-3:2008 (not modified)
IEC 62563-1:2009 NOTE Harmonized as EN 62563-1:2010 (not modified)
IEC 60601-1-9 NOTE Harmonized as EN 60601-1-9

Annex ZA
(normative)
Normative references to international publications
with their corresponding European publications
The following documents are referred to in the text in such a way that some or all of their content
constitutes requirements of this document. For dated references, only the edition cited applies. For
undated references, the latest edition of the referenced document (including any amendments)
applies.
NOTE 1  Where an International Publication has been modified by common modifications, indicated by (mod), the relevant
EN/HD applies.
NOTE 2  Up-to-date information on the latest versions of the European Standards listed in this annex is available here:
www.cenelec.eu.
Annex ZA of EN 60601-2-54:2009 applies, except as follows:
Publication Year Title EN/HD Year

Replacement
IEC 62220-1-1 2015 Medical electrical equipment - EN 62220-1-1 2015
Characteristics of digital X-ray imaging
devices - Part 1-1: Determination of the
detective quantum efficiency - Detectors
used in radiographic imaging
Addition
IEC 61910-1 2014 Medical electrical equipment - Radiation EN 61910-1 2014
dose documentation - Part 1: Radiation
dose structured reports for radiography
and radioscopy
IEC 62494-1 2008 Medical electrical equipment - Exposure EN 62494-1 2008
index of digital X-ray imaging systems -
Part 1: Definitions and requirements for
general radiography
IEC 60601-2-54 ®
Edition 1.0 2018-06
INTERNATIONAL
STANDARD
NORME
INTERNATIONALE
AM ENDMENT 2
AM ENDEMENT 2
Medical electrical equipment –

Part 2-54: Particular requirements for the basic safety and essential performance

of X-ray equipment for radiography and radioscopy

Appareils électromédicaux –
Partie 2-54: Exigences particulières pour la sécurité de base et les performances

essentielles des appareils à rayonnement X utilisés pour la radiographie et la

radioscopie
INTERNATIONAL
ELECTROTECHNICAL
COMMISSION
COMMISSION
ELECTROTECHNIQUE
INTERNATIONALE
ICS 11.040.50 ISBN 978-2-8322-5758-6

– 2 – IEC 60601-2-54:2009/AMD2:2018
© IEC 2018
FOREWORD
This amendment has been prepared by subcommittee 62B: Diagnostic imaging equipment, of
IEC technical committee 62: Electrical equipment in medical practice.
The text of this amendment is based on the following documents:
FDIS Report on voting
62B/1089/FDIS 62B/1097/RVD
Full information on the voting for the approval of this amendment can be found in the report
on voting indicated in the above table.
The committee has decided that the contents of this amendment and the base publication will
remain unchanged until the stability date indicated on the IEC website under
"http://webstore.iec.ch" in the data related to the specific publication. At this date, the
publication will be
• reconfirmed,
• withdrawn,
• replaced by a revised edition, or
• amended.
_____________
INTRODUCTION TO AMENDMENT 2
The purpose of this second amendment to IEC 60601-2-54:2009 is to introduce changes
which take the current state of the art into account. Therefore, X-RAY EQUIPMENT specified for
DIRECT RADIOSCOPY is no longer in the scope of this document. The normative references were
also updated in this amendment, and editorial clarifications and new terms and definitions
were added. Provisions for QUALITY CONTROL PROCEDURES to be recommended by the
MANUFACTURER are emphasized. Specific attention is paid to EXAMINATION PROTOCOLS in a new
subclause which differentiate between adult and paediatric applications, in particular for
X-RAY EQUIPMENT without an AUTOMATIC CONTROL SYSTEM. In addition, fixed periods for
termination of LOADING after release of the RADIATION control by the OPERATOR are stipulated
for RADIOSCOPY.
A new subclause on electronic documentation of EXAMINATION PROTOCOLS is introduced. It
recommends providing access to electronic documentation containing relevant parameters of
the PRE-PROGRAMMED EXAMINATION PROTOCOL. In another new subclause, the creation of basic
documentation of the RADIATION DOSE STRUCTURED REPORT (RDSR) according to IEC 61910-1 is
recommended. Furthermore, the subclause describing the LAST IMAGE HOLD RADIOGRAM has
been revised and requires that the last image in RADIOSCOPY be displayed rather than provide
just a means to display it.
This amendment recommends providing a graphical DISPLAY of the position of the BEAM
LIMITING DEVICE blades on the IMAGE DISPLAY DEVICE in the subclause "Indication on the X-RAY
EQUIPMENT".
IEC 60601-2-54:2009/AMD2:2018 – 3 –
© IEC 2018
Finally, the requirement for providing means to limit the FOCAL SPOT TO SKIN DISTANCES for
radioscopic X-RAY EQUIPMENT differentiates between MOBILE and FIXED EQUIPMENT and
extends, in the latter case, the minimum distance in possible clinical applications.
201.1.1 Scope
Replace, in the first paragraph, the first existing sentence by the following new sentence:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ME
EQUIPMENT and ME SYSTEMS intended to be used for projection RADIOGRAPHY and INDIRECT
RADIOSCOPY.
Replace the second existing paragraph by the following new paragraph:
ME EQUIPMENT and ME SYSTEMS intended to be used for bone or tissue absorption
densitometry, computed tomography, mammography, dental or radiotherapy applications are
excluded from the scope of this International Standard.
Delete the note.
201.1.3 Collateral standards
Replace the second paragraph, modified by IEC 60601-2-54:2009/AMD1:2015, by the
following new paragraph:
IEC 60601-1-2 and IEC 60601-1-3 apply as modified in Clauses 202 and 203 respectively.
IEC 60601-1-8, IEC 60601-1-9, IEC 60601-1-10, IEC 60601-1-11 and IEC 60601-1-12 do not
apply. All other published collateral standards in the IEC 60601-1 series apply as published.
201.2 Normative references
Replace the existing reference to IEC 62220-1:2003 by the following new reference:
IEC 62220-1-1:2015, Medical electrical equipment – Characteristics of digital X-ray imaging
devices – Part 1-1: Determination of the detective quantum efficiency – Detectors used in
radiographic imaging
Add, to the existing list, the following new references:
IEC 61910-1:2014, Medical electrical equipment – Radiation dose documentation – Part 1:
Radiation dose structured reports for radiography and radioscopy
IEC 62494-1:2008, Medical electrical equipment – Exposure index of digital X-ray imaging
systems – Part 1: Definitions and requirements for general radiography
201.3 Terms and definitions
Add, after the existing definition 201.3.209, the following new terms and definitions:
201.3.210
EXAMINATION PROTOCOL
full set of any programmed technical factors, control functions and settings, including image
processing settings, designed to optimize the image acquisition and DISPLAY

– 4 – IEC 60601-2-54:2009/AMD2:2018
© IEC 2018
201.3.211
EXAMINATION PROTOCOL SELECTION CONTROL
control to select a PRE-PROGRAMMED EXAMINATION PROTOCOL
201.3.212
LAST-IMAGE HOLD RADIOGRAM
LIH RADIOGRAM
single image obtained by sampling or temporal processing of one or more images from the
end of a radioscopic IRRADIATION
Note 1 to entry: This note applies to the French language only.
201.3.213
PRE-PROGRAMMED EXAMINATION PROTOCOL
single hardware or software setting, or both, which is associated with an EXAMINATION
PROTOCOL
201.3.214
RADIOSCOPY REPLAY IMAGE SEQUENCE
series of the most recent images of the most recent RADIOSCOPY IRRADIATION-EVENT
201.7.9.1 General
Replace the first paragraph after "Addition:" by the following new paragraph and note:
The ACCOMPANYING DOCUMENTS shall contain instructions for MANUFACTURER-recommended
QUALITY CONTROL PROCEDURES and tests to be performed on the X-RAY EQUIPMENT by the
RESPONSIBLE ORGANIZATION. These shall include acceptance criteria for each test and
frequency for each test.
NOTE The intention is to perform these QUALITY CONTROL PROCEDURES and tests using only the supplied
information.
Replace the first dash in the second paragraph by the following new dash:
– an identification of adjustable or selectable image processing settings applied to ORIGINAL
DATA including the version number or how to determine it;
Add, before the compliance statement at the end of this subclause, the following new
paragraph:
If the test or PROCEDURE requires a device-specific TOOL that is only available from the
MANUFACTURER, the MANUFACTURER shall make this TOOL available to the RESPONSIBLE
ORGANIZATION.
201.7.9.3.101 X-RAY SOURCE ASSEMBLY
Replace, at the end of the item a), the colon by a semicolon.
201.9.8 HAZARDS associated with support systems
Replace the existing title of this subclause by the following new title:
201.9.8 MECHANICAL HAZAR
...