EN 60601-2-41:2009

SLOVENSKI STANDARD
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Medical electrical equipment - Part 2-41: Particular requirements for basic safety and
essential performance of surgical luminaires and luminaires for diagnosis (IEC 60601-2-
41:2009)
Medizinische elektrische Geräte - Teil 2-41: Besondere Festlegungen für die Sicherheit
einschließlich der wesentlichen Leistungsmerkmale von Operationsleuchten und
Untersuchungsleuchten (IEC 60601-2-41:2009)
Appareils électromédicaux - Partie 2-41: Exigences particulières pour la sécurité de base
et les performances essentielles des éclairages chirurgicaux et des éclairages de
diagnostic (CEI 60601-2-41:2009)
Ta slovenski standard je istoveten z: EN 60601-2-41:2009
ICS:
11.040.30 Operacijski instrumenti in Surgical instruments and
materiali materials
11.040.55 'LDJQRVWLþQDRSUHPD Diagnostic equipment
29.140.40 Svetila Luminaires
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

EUROPEAN STANDARD
EN 60601-2-41
NORME EUROPÉENNE
December 2009
EUROPÄISCHE NORM
ICS 11.040.20; 11.040.55; 11.040.99 Supersedes EN 60601-2-41:2000

English version
Medical electrical equipment -
Part 2-41: Particular requirements for basic safety
and essential performance of surgical luminaires
and luminaires for diagnosis
(IEC 60601-2-41:2009)
Appareils électromédicaux -  Medizinische elektrische Geräte -
Partie 2-41: Exigences particulières Teil 2-41: Besondere Festlegungen
pour la sécurité de base für die Sicherheit einschließlich
et les performances essentielles der wesentlichen Leistungsmerkmale
des éclairages chirurgicaux von Operationsleuchten
et des éclairages de diagnostic und Untersuchungsleuchten
(CEI 60601-2-41:2009) (IEC 60601-2-41:2009)

This European Standard was approved by CENELEC on 2009-11-01. CENELEC members are bound to comply
with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European Standard
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 Central Secretariat or to any CENELEC member.

This European Standard 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 Central Secretariat has the same status as the official versions.

CENELEC members are the national electrotechnical committees of Austria, Belgium, Bulgaria, Cyprus, the
Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia,
Lithuania, Luxembourg, Malta, the Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain,
Sweden, Switzerland and the United Kingdom.

CENELEC
European Committee for Electrotechnical Standardization
Comité Européen de Normalisation Electrotechnique
Europäisches Komitee für Elektrotechnische Normung

Central Secretariat: Avenue Marnix 17, B - 1000 Brussels

© 2009 CENELEC - All rights of exploitation in any form and by any means reserved worldwide for CENELEC members.
Ref. No. EN 60601-2-41:2009 E
Foreword
The text of document 62D/773/FDIS, future edition 2 of IEC 60601-2-41, prepared by SC 62D,
Electromedical equipment, of IEC TC 62, Electrical equipment in medical practice, was submitted to the
IEC-CENELEC parallel vote and was approved by CENELEC as EN 60601-2-41 on 2009-11-01.
This European Standard supersedes EN 60601-2-41:2000.
EN 60601-2-41:2000 was revised to be consistent with EN 60601-1:2006.
The following dates were fixed:
– latest date by which the EN has to be implemented
at national level by publication of an identical
national standard or by endorsement (dop) 2010-08-01
– latest date by which the national standards conflicting
with the EN have to be withdrawn (dow) 2012-11-01
This European Standard has been prepared under a mandate given to CENELEC by the European
Commission and the European Free Trade Association and covers essential requirements of
EC Directive MDD (93/42/EEC). See Annex ZZ.
In this standard, the following print types are used:
– Requirements and definitions: roman type.
– Test specifications: italic type.
– Informative material appearing outside of tables, such as notes, examples and references: in smaller type. Normative text of
tables is also in a smaller type.
– TERMS DEFINED IN CLAUSE 3 OF THE GENERAL STANDARD, IN THIS PARTICULAR STANDARD OR AS NOTED:
SMALL CAPITALS.
In referring to the structure of this standard, the term
– “clause” means one of the seventeen numbered divisions within the table of contents, inclusive of all
subdivisions (e.g. Clause 7 includes subclauses 7.1, 7.2, etc.);
– “subclause” means a numbered subdivision of a clause (e.g. 7.1, 7.2 and 7.2.1 are all subclauses of
Clause 7).
References to clauses within this standard are preceded by the term “Clause” followed by the clause
number. References to subclauses within this particular standard are by number only.
In this standard, the conjunctive “or” is used as an “inclusive or” so a statement is true if any combination
of the conditions is true.
The verbal forms used in this standard conform to usage described in Annex H of the ISO/IEC Directives,
Part 2. For the purposes of this standard, the auxiliary verb:
− “shall” means that compliance with a requirement or a test is mandatory for compliance with this
standard;
− “should” means that compliance with a requirement or a test is recommended but is not mandatory for
compliance with this standard;
− “may” is used to describe a permissible way to achieve compliance with a requirement or test.
An asterisk (*) as the first character of a title or at the beginning of a paragraph or table title indicates that
there is guidance or rationale related to that item in Annex AA.

- 3 - EN 60601-2-41:2009
Annexes ZA and ZZ have been added by CENELEC.
__________
Endorsement notice
The text of the International Standard IEC 60601-2-41:2009 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 60598-1 NOTE  Harmonized as EN 60598-1:2008 (modified).
IEC 60598-2-1 NOTE  Harmonized as EN 60598-2-1:1989 (not modified).
IEC 60598-2-4 NOTE  Harmonized as EN 60598-2-4:1997 (not modified).
IEC 60598-2-22 NOTE  Harmonized as EN 60598-2-22:1998 (modified).
IEC 60598-2-25 NOTE  Harmonized as EN 60598-2-25:1994 (not modified).
ISO 9680 NOTE  Harmonized as EN ISO 9680:2007 (not modified)
__________
Annex ZA
(normative)
Normative references to international publications
with their corresponding European publications

The following referenced documents are indispensable for the application 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  When an international publication has been modified by common modifications, indicated by (mod), the relevant EN/HD
applies.
Annex ZA of EN 60601-1:2006 applies, except as follows:

Publication Year Title EN/HD Year

Addition:
IEC 60417 data- Graphical symbols for use on equipment - -
base
1) 2)
IEC 60598-2-9 - Luminaires - EN 60598-2-9 1989
Part 2: Particular requirements -
Section 9: Photo and film luminaires (non-
professional)
1)
ISO 11664-1 - Colorimetry - - -
Part 1: CIE standard colorimetric observers

1)
CIE 13.3 - Method of measuring and specifying colour - -
rendering of light sources
1)
CIE 15 - Colorimetry - -
1)
CIE 69 - Methods of characterizing illuminance meters - -
and luminance meters: Performance,
characteristics and specifications

1)
Undated reference.
2)
Valid edition at date of issue.

- 5 - EN 60601-2-41:2009
Annex ZZ
(informative)
Coverage of Essential Requirements of EC Directives
This European Standard has been prepared under a mandate given to CENELEC by the European
Commission and the European Free Trade Association and within its scope the standard covers all
relevant essential requirements as given in Annex I of the EC Directive 93/42/EEC.
Compliance with this standard provides one means of conformity with the specified essential
requirements of the Directive concerned.
WARNING: Other requirements and other EC Directives may be applicable to the products falling within
the scope of this standard.
___________
IEC 60601-2-41 ®
Edition 2.0 2009-08
INTERNATIONAL
STANDARD
NORME
INTERNATIONALE
Medical electrical equipment –
Part 2-41: Particular requirements for the basic safety and essential
performance of surgical luminaires and luminaires for diagnosis

Appareils électromédicaux –
Partie 2-41: Exigences particulières pour la sécurité de base et les
performances essentielles des éclairages chirurgicaux et des éclairages de
diagnostic
INTERNATIONAL
ELECTROTECHNICAL
COMMISSION
COMMISSION
ELECTROTECHNIQUE
PRICE CODE
INTERNATIONALE
W
CODE PRIX
ICS 11.040.20; 11.040.55; 11.040.99 ISBN 2-8318-1054-4
– 2 – 60601-2-41 © IEC:2009
CONTENTS
FOREWORD.4
INTRODUCTION.6
201.1 Scope, object and related standards.7
201.2 Normative references .8
201.3 Terms and definitions .9
201.4 General requirements.12
201.5 General requirements for testing of ME EQUIPMENT .13
201.6 Classification of ME EQUIPMENT and ME SYSTEMS .13
201.7 ME EQUIPMENT Identification, marking and documents.14
201.8 Protection against electrical HAZARDS from ME EQUIPMENT .15
201.9 Protection against mechanical hazards of ME EQUIPMENT and ME SYSTEMS .15
201.10 Protection against unwanted and excessive radiation HAZARDS .18
201.11 Protection against excessive temperatures and other HAZARDS .18
201.12 Accuracy of controls and instruments and protection against hazardous
outputs .19
201.13 HAZARDOUS SITUATIONS and fault conditions .33
201.14 PROGRAMMABLE ELECTRICAL MEDICAL SYSTEMS (PEMS).33
201.15 Construction of ME EQUIPMENT .33
201.16 ME SYSTEMS .33
201.17 Electromagnetic compatibility of ME EQUIPMENT and ME SYSTEMS.33
Annex AA (informative) Guidance and rationale for particular clauses and subclauses.35
Bibliography.38
Index of defined terms .39

Figure 201.101 – Example of power supplies for SURGICAL LUMINAIRES .10
Figure 201.102 – DETACHABLE HANDLE attachment and detachment tests.16
Figure 201.103 – Test for ease of motion.17
Figure 201.104 – Light distribution.22
Figure 201.105 – CENTRAL ILLUMINANCE measurement.24
Figure 201.106 – Measurements of LIGHT FIELD DIAMETER and diameter at 50 % of
CENTRAL ILLUMINANCE .24
Figure 201.107 – Illuminance measurement with one mask.25
Figure 201.108 – Illuminance measurement with two masks .25
Figure 201.109 – Illuminance measurement with four different positions of the two
masks.26
Figure 201.110 – Tube for illuminance measurement .27
Figure 201.111 – Detail of the inner surface of the tube (example) .27
Figure 201.112 – Illuminance measurement at the bottom of a cavity, with one mask .28
Figure 201.113 – Illuminance measurement at the bottom of a cavity, with two masks .29
Figure 201.114 – Illuminance measurement at the bottom of a cavity, with four different
positions of the two masks.30
Figure 201.115 – Measurement of DEPTH OF ILLUMINATION .31
Figure AA.1 – Changeover cycle to an emergency backup system .36

60601-2-41 © IEC:2009 – 3 –
Table 201.101 – Classification of SURGICAL LUMINAIRES and LUMINAIRES FOR DIAGNOSIS.12
Table 201.102 – Distributed ESSENTIAL PERFORMANCE requirements .13
Table 201.103 – Allowable maximum temperatures for ME EQUIPMENT parts that are
likely to be touched.19

– 4 – 60601-2-41 © IEC:2009
INTERNATIONAL ELECTROTECHNICAL COMMISSION
____________
MEDICAL ELECTRICAL EQUIPMENT –

Part 2-41: Particular requirements for the basic safety and essential
performance of surgical luminaires and luminaires for diagnosis

FOREWORD
1) The International Electrotechnical Commission (IEC) is a worldwide organization for standardization comprising
all national electrotechnical committees (IEC National Committees). The object of IEC is to promote
international co-operation on all questions concerning standardization in the electrical and electronic fields. To
this end and in addition to other activities, IEC publishes International Standards, Technical Specifications,
Technical Reports, and Guides (hereafter referred to as “IEC Publication(s)”). Their preparation is entrusted to
technical committees; any IEC National Committee interested in the subject dealt with may participate in this
preparatory work. International, governmental and non-governmental organizations liaising with the IEC also
participate in this preparation. IEC collaborates closely with the International Organization for Standardization
(ISO) in accordance with conditions determined by agreement between the two organizations.
2) The formal decisions or agreements of IEC on technical matters express, as nearly as possible, an international
consensus of opinion on the relevant subjects since each technical committee has representation from all
interested IEC National Committees.
3) IEC Publications have the form of recommendations for international use and are accepted by IEC National
Committees in that sense. While all reasonable efforts are made to ensure that the technical content of IEC
Publications is accurate, IEC cannot be held responsible for the way in which they are used or for any
misinterpretation by any end user.
4) In order to promote international uniformity, IEC National Committees undertake to apply IEC Publications
transparently to the maximum extent possible in their national and regional publications. Any divergence
between any IEC Publication and the corresponding national or regional publication shall be clearly indicated in
the latter.
5) IEC provides no marking procedure to indicate its approval and cannot be rendered responsible for any
equipment declared to be in conformity with an IEC Publication.
6) All users should ensure that they have the latest edition of this publication.
7) No liability shall attach to IEC or its directors, employees, servants or agents including individual experts and
members of its technical committees and IEC National Committees for any personal injury, property damage or
other damage of any nature whatsoever, whether direct or indirect, or for costs (including legal fees) and
expenses arising out of the publication, use of, or reliance upon, this IEC Publication or any other IEC
Publications.
8) Attention is drawn to the Normative references cited in this publication. Use of the referenced publications is
indispensable for the correct application of this publication.
9) Attention is drawn to the possibility that some of the elements of this IEC Publication may be the subject of
patent rights. IEC shall not be held responsible for identifying any or all such patent rights.
International standard IEC 60601-2-41 has been prepared by subcommittee 62D:
Electromedical equipment, of IEC technical committee 62: Electrical equipment in medical
practice.
This second edition cancels and replaces the first edition published in 2000. This edition
constitutes a technical revision to be consistent with the third edition of the IEC 60601-1.
The text of this particular standard is based on the following documents:
FDIS Report on voting
62D/773/FDIS 62D/787/RVD
Full information on the voting for the approval of this particular standard can be found in the
report on voting indicated in the above table.
This publication has been drafted in accordance with the ISO/IEC Directives, Part 2.

60601-2-41 © IEC:2009 – 5 –
In this standard, the following print types are used:
– Requirements and definitions: roman type.
– Test specifications: italic type.
– Informative material appearing outside of tables, such as notes, examples and references: in smaller type.
Normative text of tables is also in a smaller type.
– TERMS DEFINED IN CLAUSE 3 OF THE GENERAL STANDARD, IN THIS PARTICULAR STANDARD OR AS
NOTED: SMALL CAPITALS.
In referring to the structure of this standard, the term
– “clause” means one of the seventeen numbered divisions within the table of contents,
inclusive of all subdivisions (e.g. Clause 7 includes subclauses 7.1, 7.2, etc.);
– “subclause” means a numbered subdivision of a clause (e.g. 7.1, 7.2 and 7.2.1 are all
subclauses of Clause 7).
References to clauses within this standard are preceded by the term “Clause” followed by the
clause number. References to subclauses within this particular standard are by number only.
In this standard, the conjunctive “or” is used as an “inclusive or” so a statement is true if any
combination of the conditions is true.
The verbal forms used in this standard conform to usage described in Annex H of the ISO/IEC
Directives, Part 2. For the purposes of this standard, the auxiliary verb:
– “shall” means that compliance with a requirement or a test is mandatory for compliance
with this standard;
– “should” means that compliance with a requirement or a test is recommended but is not
mandatory for compliance with this standard;
– “may” is used to describe a permissible way to achieve compliance with a requirement or
test.
An asterisk (*) as the first character of a title or at the beginning of a paragraph or table title
indicates that there is guidance or rationale related to that item in Annex AA.
A list of all parts of the IEC 60601 series, published under the general title Medical electrical
equipment, can be found on the IEC website.
The committee has decided that the contents of this publication will remain unchanged until
the maintenance result date indicated on the IEC web site 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.
– 6 – 60601-2-41 © IEC:2009
INTRODUCTION
This particular standard concerns the basic safety and essential performance of SURGICAL
LUMINAIRES and LUMINAIRES FOR DIAGNOSIS.
It amends and supplements IEC 60601-1 (third Edition 2005), hereinafter referred to as the
general standard.
The requirements of this particular standard take priority over those of the general standard,
entitled “Medical electrical equipment Part 1: General requirements for basic safety and
essential performance.
60601-2-41 © IEC:2009 – 7 –
MEDICAL ELECTRICAL EQUIPMENT –

Part 2-41: Particular requirements for the basic safety and essential
performance of surgical luminaires and luminaires for diagnosis

201.1 Scope, object and related standards
1)
Clause 1 of the general standard applies, except as follows:
201.1.1 *Scope
Replacement:
This particular standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of SURGICAL
LUMINAIRES AND LUMINAIRES FOR DIAGNOSIS, hereafter referred to as ME EQUIPMENT.
This particular standard does not apply to
– headlights;
– endoscopes, laparoscopes and their light sources, which are covered by IEC 60601-2-18;
– luminaires used in dentistry, which are covered by ISO 9680;
– luminaires for general purposes, which are covered by IEC 60598-2-1 and IEC 60598-2-4;
– luminaires dedicated to therapeutic purposes;
– special purpose lights with different conditions of use such as UV lights for dermatological
diagnosis, slit lamps for ophthalmology, lights for surgical microscopes and lights for
surgical navigation systems;
– lights connected to surgical instruments;
– luminaires of an emergency lighting, which are covered by IEC 60598-2-22.
NOTE See also 4.2 of the general standard.
201.1.2 Object
Replacement:
The object of this particular standard is to establish particular BASIC SAFETY and ESSENTIAL
PERFORMANCE requirements for SURGICAL LUMINAIRES and LUMINAIRES FOR DIAGNOSIS as
defined in 201.3.
201.1.4 Particular standards
Replacement:
In the IEC 60601 series, particular standards may modify, replace or delete requirements
contained in the general standard and collateral standards as appropriate for the particular
ME EQUIPMENT under consideration, and may add other BASIC SAFETY and ESSENTIAL
PERFORMANCE requirements.
A requirement of a particular standard takes priority over the general standard.
—————————
1)
The general standard is IEC 60601-1:2005, Medical electrical equipment – Part 1: General requirements for
basic safety and essential performance.

– 8 – 60601-2-41 © IEC:2009
For brevity, IEC 60601-1 is referred to in this particular standard as the general standard.
Collateral standards are referred to by their document number.
The numbering of clauses and subclauses of this particular standard corresponds to that of
the general standard with the prefix “201” (e.g. 201.1 in this standard addresses the content
of Clause 1 of the general standard) or applicable collateral standard with the prefix “20x”
where x is the final digit(s) of the collateral standard document number (e.g. 202.4 in this
particular standard addresses the content of Clause 4 of the 60601-1-2 collateral standard,
203.4 in this particular standard addresses the content of Clause 4 of the 60601-1-3 collateral
standard, etc.). The changes to the text of the general standard are specified by the use of
the following words:
"Replacement" means that the clause or subclause of the general standard or applicable
collateral standard is replaced completely by the text of this particular standard.
"Addition" means that the text of this particular standard is additional to the requirements of
the general standard or applicable collateral standard.
"Amendment" means that the clause or subclause of the general standard or applicable
collateral standard is amended as indicated by the text of this particular standard.
Subclauses, figures or tables which are additional to those of the general standard are
numbered starting from 201.101. However, due to the fact that definitions in the general
standard are numbered 3.1 through 3.139, additional definitions in this standard are
numbered beginning from 201.3.201. Additional annexes are lettered AA, BB, etc., and
additional items aa), bb), etc.
Subclauses or figures which are additional to those of a collateral standard are numbered
starting from 20x, where “x” is the number of the collateral standard, e.g. 202 for IEC 60601-
1-2, 203 for IEC 60601-1-3, etc.
The term "this standard" is used to make reference to the general standard, any applicable
collateral standards and this particular standard taken together.
Where there is no corresponding clause or subclause in this particular standard, the clause or
subclause of the general standard or applicable collateral standard, although possibly not
relevant, applies without modification; where it is intended that any part of the general
standard or applicable collateral standard, although possibly relevant, is not to be applied, a
statement to that effect is given in this particular standard.
201.2 Normative references
Clause 2 of the general standard applies except as follows:
Addition:
IEC 60417, Graphical symbols for use on equipment
IEC 60598-2-9, Luminaires – Part 2: Particular requirements. Section Nine: Photo and film
luminaires (non-professional)
ISO 11664-1, Colorimetry – Part 1: CIE standard colorimetric observers
CIE 13.3, Method of Measuring and Specifying Colour Rendering Properties of Light Sources
CIE 15, Colorimetry
60601-2-41 © IEC:2009 – 9 –
CIE 69, Methods of characterizing illuminance meters and luminance meters: Performance,
characteristics and specifications
201.3 Terms and definitions
For the purposes of this document, the terms and definitions given in IEC 60601-1:2005,
apply, except as follows:
NOTE An index of defined terms is found beginning on page 39.
201.3.63
MEDICAL ELECTRICAL EQUIPMENT
Addition:
NOTE See Figure 201.101 as an example of possible POWER SUPPLIES for SURGICAL LUMINAIRES.

– 10 – 60601-2-41 © IEC:2009
B
a)
M
G
B DC/AC
b)
M
G
M
c)
G
Key Lamp
B Battery
Transformer
M  Mains
G  Generator
DC/AC  Direct current to alternative
current converter
Switch
IEC  1370/09
Figure 201.101 – Example of power supplies for SURGICAL LUMINAIRES
Addition:
201.3.101
CENTRAL ILLUMINANCE
E
c
illuminance at a 1 000 mm distance (or a measurement distance specified by the
MANUFACTURER if the specified working range does not include 1 000 mm) from the light-
emitting area of the ME EQUIPMENT in the LIGHT FIELD CENTRE without any obstruction of the
light beam
60601-2-41 © IEC:2009 – 11 –
201.3.102
DEPTH OF ILLUMINATION
working distance around the 1 000 mm distance (or a measurement distance specified by the
MANUFACTURER if the specified working range does not include 1 000 mm) below the emitting
surface of the ME EQUIPMENT, in which the illuminance reaches at least 60 % of CENTRAL
ILLUMINANCE (E )
c
201.3.103
*FAIL SAFE
capability of an ME EQUIPMENT to provide a minimum illuminance and to be directed on the
SINGLE FAULT CONDITION
operation area even in
201.3.104
LIGHT FIELD CENTRE
LFC
point of maximum illuminance in the light field (lighted area)
NOTE It is the reference point for light field size and distribution measurements.
201.3.105
LIGHT FIELD DIAMETER
d
diameter of a circle around the LIGHT FIELD CENTRE (point of CENTRAL ILLUMINANCE) where the
illuminance reaches 10 % of E
c
201.3.106
LUMINAIRE FOR DIAGNOSIS
luminaire to illuminate the body of the PATIENT locally in order to support diagnosis or
treatment which could be interrupted without any hazard for the PATIENT in case of failure of
the light
NOTE It is not intended to be used in operating rooms. See Table 201.101.
201.3.107
MAJOR SURGICAL LUMINAIRE
single luminaire in the PATIENT ENVIRONMENT which is intended to support treatment and
diagnosis where interruption of the illumination would be a HAZARDOUS CONDITION and to be
used in operating rooms
NOTE A MAJOR SURGICAL LUMINAIRE needs to provide an adequate CENTRAL ILLUMINANCE to illuminate locally the
body of the PATIENT even in SINGLE FAULT CONDITION. See Table 201.101.
201.3.108
MINOR SURGICAL LUMINAIRE (TREATMENT LUMINAIRE)
single luminaire in the PATIENT ENVIRONMENT which is intended to support treatment and
diagnosis which can be interrupted without any HAZARD for the PATIENT in case of failure of the
light and to be used in operating rooms
NOTE A MINOR SURGICAL LUMINAIRE needs to provide an adequate CENTRAL ILLUMINANCE to illuminate locally the
body of the PATIENT. See Table 201.101.
201.3.109
SHADOW DILUTION
ability of the ME EQUIPMENT to minimise the impact of shadows in the working area due to the
partial obstruction by the OPERATOR of the emitted light
201.3.110
DETACHABLE HANDLE
device that is intended to position and adjust the luminaire which can be removed from the ME
EQUIPMENT
– 12 – 60601-2-41 © IEC:2009
NOTE The DETACHABLE HANDLE may be sterilisable in order to maintain it under aseptic conditions.
201.3.111
SURGICAL LUMINAIRE
a generic term applicable to MINOR SURGICAL LUMINAIREs, MAJOR SURGICAL LUMINAIREs and a SURGICAL
LUMINAIRE SYSTEM
NOTE See Table 201.101.
201.3.112
SURGICAL LUMINAIRE SYSTEM
combination of several SURGICAL LUMINAIRES that is intended to support treatment and
diagnosis and to be used in operating rooms
NOTE 1 A SURGICAL LUMINAIRE SYSTEM needs to be FAIL SAFE and to provide an adequate CENTRAL ILLUMINANCE to
illuminate locally the body of the PATIENT even in SINGLE FAULT CONDITION. See Table 201.101.
EXAMPLE A proven FAIL SAFE combination of two or more MINOR SURGICAL LUMINAIRES is a SURGICAL LUMINAIRE
SYSTEM.
NOTE 2 This SURGICAL LUMINAIRE SYSTEM is not a system in the sense of Clause 16 (ME SYSTEMS).
Table 201.101 – Classification of SURGICAL LUMINAIRES and LUMINAIRES FOR DIAGNOSIS
Type of luminaire
SURGICAL LUMINAIREs
Requirements Clause Luminaires for Minor (treatment) Major and system
diagnosis
ME EQUIPMENT 201.6 No requirement Class I, or Class II Class I, or Class II

a a
classification with connector to PA with connector to PA
FAIL SAFE 201.3.103 No No Yes
Intended location Examination room Operating room Operating room
Ease of motion 201.9.4.2.2.101 Yes Yes Yes
CENTRAL ILLUMINANCE 201.12.1.102.1.1 a) No requirement
40 klx ≤ E ≤ 160 klx 40 klx ≤ E ≤ 160 klx
c c
(E )
c
b b
LIGHT FIELD 201.12.1.102.1.1 b) No requirement Specified Specified
DIAMETER(d )
Light distribution(d ) 201.12.1.102.1.1 b) No requirement d at least 50 % of d at least 50 % of
50 50
the LIGHT FIELD the LIGHT FIELD
c c
DIAMETER d DIAMETER d
10 10
d d
SHADOW DILUTION 201.12.1.102.1.1 c) No requirement Specified  Specified
Colour temperature 201.12.1.102.2.1 3 000 K ≤ T ≤ 6 700 K 3 000 K ≤ T ≤ 6 700 K 3 000 K ≤ T ≤ 6 700 K
c c c
Colour rendering index 201.12.1.102.2.1 85 ≤ R ≤ 100 85 ≤ R ≤ 100 85 ≤ R ≤ 100
a a a
2 2 2
Maximum value for 201.12.1.102.3.1 E < 1 000 W/m  E < 1 000 W/m  E < 1 000 W/m
e e e
total irradiance E
e
a
PA means potential equalization conductor.
b
LIGHT FIELD DIAMETER(d ) where the illuminance reaches 10 % of CENTRAL ILLUMINANCE E .
10 c
c
Diameter d where the illuminance reaches 50 % of CENTRAL ILLUMINANCE E .
50 c
d
Percentage of remaining illuminance when the beam is obstructed by one or two masks, with or without tube.

201.4 General requirements
Clause 4 of the general standard applies, except as follows:

60601-2-41 © IEC:2009 – 13 –
201.4.3 ESSENTIAL PERFORMANCE
Addition:
The ESSENTIAL PERFORMANCE is the delivery of illumination and the limitation of energy to the
operating field.
Table 201.102 – Distributed ESSENTIAL PERFORMANCE requirements
Requirement Subclause
DELIVERY OF A MINIMUM AND ADEQUATE ILLUMINATION ON THE OPERATING FIELD 201.12.1.102.1.1 a)
and 201.12.1.102.4
LIMITATION OF ENERGY IN THE OPERATING FIELD 201.12.1.102.1.1 a)
201.10.7 and
201.12.1.102.3
201.5 General requirements for testing of ME EQUIPMENT
Clause 5 of the general standard applies except as follows:
201.5.4 Other conditions
Addition:
aa) In order to measure stabilised performances, the output values shall be measured after a
pre-ageing period, depending on the light source technology, at RATED VOLTAGE under
NORMAL CONDITIONS. This pre-aging period is:
– 3 h for halogen lamp and LED;
– 50 h for discharge lamp;
– for other light sources, the preaging period after which the performances variation
does not exceed 1% per 100 h.
201.5.8 Sequence of test
Addition:
The photometric tests and the tests for the quality of illuminance of the ME EQUIPMENT are
performed after inspection of the marking.
201.6 Classification of ME EQUIPMENT and ME SYSTEMS
Clause 6 of the general standard applies, except as follows:
201.6.2 Protection against electric shock
Addition:
NOTE Except if intended for such purpose, a SURGICAL LUMINAIRE or LUMINAIRE FOR DIAGNOSIS has no APPLIED
PART on the PATIENT.
201.6.6 Mode of operation
Amendment:
Delete all but CONTINUOUS OPERATION.

– 14 – 60601-2-41 © IEC:2009
201.7 ME EQUIPMENT Identification, marking and documents
Clause 7 of the general standard applies, except as follows:
201.7.2 Marking on the outside of ME EQUIPMENT or ME EQUIPMENT parts
Addition:
201.7.2.101 Connection to the SUPPLY MAINS
MOBILE ME EQUIPMENT with a fixed flexible POWER SUPPLY CORD with no MAINS PLUG attached
for connection to the SUPPLY MAINS shall have a clearly visible label to show the correct
method of connection to a MAINS PLUG.
Rated voltage and power consumption shall be marked on each light head. If these values
differ from power input and voltage at the MAINS TERMINAL DEVICE of each ME EQUIPMENT,
additional marking of voltage and power consumption is required near the MAINS TERMINAL
DEVICE.
201.7.3 Marking on the inside of ME EQUIPMENT or ME EQUIPMENT parts
Addition:
201.7.3.101 Marking of light sources
Identification and characteristics of the light source (power, voltage) shall be marked near the
light source holder and on the light source or its packaging if it is intended to be replaced by
the USER.
201.7.9.2 Instructions for use
201.7.9.2.1 General
Addition:
Instructions for use shall contain information on
– cleaning and disinfection of the ME EQUIPMENT including suitable temperature conditions;
– CENTRAL ILLUMINANCE and the corresponding measurement distance;
– LIGHT FIELD DIAMETER;
– DEPTH OF ILLUMINATION (see 201.12.1.102.1.3. i), not for LUMINAIRES FOR DIAGNOSIS);
– SHADOW DILUTION (see 201.12.1.102.1.3. d) to h), not for LUMINAIRES FOR DIAGNOSIS);
– correlated colour temperature and general colour rendering index Ra and the specific
index R9;
– total irradiance;
– cleaning, disinfection and sterilisation of any DETACHABLE HANDLE;
– handling of the lamps in case of lamp changing;
– the fact that the RESPONSIBLE ORGANIZATION shall follow the national requirements
(standards and directives) for hygiene and disinfection.
201.7.9.2.2 Warning and safety notices
Addition:
If optical filters are used, the instructions for use shall include the safety aspects of these
filters (purpose and warning to prevent their removal).

60601-2-41 © IEC:2009 – 15 –
201.7.9.2.12 Cleaning, disinfection and sterilization
Addition:
This subclause also applies to any DETACHABLE HANDLE.
201.8 Protection against electrical HAZARDS from ME EQUIPMENT
Clause 8 of the general standard applies, except as follows:
201.8.6.7 POTENTIAL EQUALIZATION CONDUCTOR
Addition:
URGICAL LUMINAIRES of CLASS II with a conductive enclosure shall have a terminal for the
S
connection of a POTENTIAL EQUALIZATION CONDUCTOR
NOTE Surgical luminaries are set up in operating theatres in which the equipotential bonding has been placed
between exposed conductive parts.
201.8.11 MAINS PARTS, components and layout
201.8.11.1 Isolation from the SUPPLY MAINS
Addition:
In case of several SUPPLY MAINS, ME EQUIPMENT shall have means to isolate its circuits
electrically from the several SUPPLY MAINS, on all poles simultaneously.
201.9 Protection against mechanical hazards of ME EQUIPMENT and ME SYSTEMS
Clause 9 of the general standard applies, except as follows:
201.9.2 HAZARDS associated with moving parts
Addition:
201.9.2.101 * DETACHABLE HANDLE
Attachment and detachment of any DETACHABLE HANDLE: See rationale (Annex AA).
The force for intentional detachment of the DETACHABLE HANDLE shall not exceed 10 N. The
RISK MANAGEMENT FILE shall identify an appropriate test procedure.

Compliance is checked as specified in the RISK MANAGEMENT FILE.

The attachment of the DETACHABLE HANDLE shall not exceed 10 N. The maximum attachment
and detachment torque shall not exceed 1 Nm.
The force for unintended detachment shall exceed 100 N.
The torque for unintended detachment shall exceed 5 Nm or require 3 or more 360° rotations
of the DETACHABLE HANDLE.
Compliance is checked by tests according to Figure 201.102 (a, b, c, d).

– 16 – 60601-2-41 © IEC:2009
At the end of the tests no damage shall be detected on the shaft (or carrier) of the
DETACHABLE HANDLE or on the DETACHABLE HANDLE itself.
a)
10 N Attachment force
DETACHABLE HANDLE
ME EQUIPMENT
b)
ME EQUIPMENT
DETACHABLE HANDLE
Unintended detachment force
100 N
c)
DETACHABLE HANDLE
100 N
Unintended detachment force
d)
ME EQUIPMENT
DETACHABLE HANDLE
Attachment and detachment torque
1 Nm for voluntary attachment and detachment
5 Nm for unintended detachment
IEC  1371/09
Figure 201.102 – DETACHABLE HANDLE attachment and detachment tests
201.9.4 Instability HAZARDS
Addition:
201.9.4.2.2.101 Ease of motion and stability
The mechanical parts of the ME EQUIPMENT shall be designed to have very easy motions
during handling.
The ME EQUIPMENT shall remain in the intended position after adjustment or positioning.
ME EQUIPMENT
60601-2-41 © IEC:2009 – 17 –
Compliance is checked as follows:
The manipulation of the light head is tested along three perpendicular axes as described in
Figure 201.103 a). The application point of the force shall be in the middle of the gripping
area defined by the MANUFACTURER as described in Figure 201.103 b).
The maximum force for positioning in the vertical plane (z) shall not exceed 55 N.
The maximum force for positioning in the horizontal plane (x and y) shall not exceed 25 N.
Compliance is checked manually along one axis at a time, the other axes of rotation being
locked for the duration of the test.

a)
ME EQUIPMENT
Z
Y
X
DETACHABLE HANDLE
b)
Application point
Detail of DETACHABLE HANDLE
IEC  1372/09
Figure 201.103 – Test for ease of motion
d/2 d/2
Gripping area = d
– 18 – 60601-2-41 © IEC:2009
201.9.5 Expelled parts HAZARD
201.9.5.1 Protective means
Addition:
201.9.5.1.101 The ME EQUIPMENT shall be designed so that, in case of lamp burst, all
fragments and broken parts are kept inside the ME EQUIPMENT in all possible positions of the
light head in the INTENDED USE.
Compliance is checked by a test in accordance with IEC 60598-2-9.
Only the structural integrity of the enclosure shall be checked at the end of the test.
201.10 Protection against unwanted and excessive radiation HAZARDS
Clause 10 of the general standard applies, except as follows:
201.10.7 Ultraviolet radiation
Replacement:
The UV-irradiance for wavelengths below 400 nm shall not exceed 10 W/m .
In the case of SURGICAL LUMINAIRE SYSTEMS, it is possible to exceed this limit by overlapping
the light fields of several luminaires. Therefore, information in this regard shall be given in the
instruction for use.
Compliance is checked by inspection or measurement. Measurement is to be carried out in
conditions in accordance with 201.12.1.102.1.2.
201.11 Protection against excessive temperatures and other HAZARDS
Clause 11 of the general standard applies, except as follows:
201.11.1 Excessive temperatures in ME EQUIPMENT
201.11.1.1 Maximum temperature during NORMAL USE
Replacement of Table 23:
60601-2-41 © IEC:2009 – 19 –
Table 201.103 – Allowable maximum temperatures for ME EQUIPMENT parts
that are likely to be touched
a
Maximum temperature
°C
ME EQUIPMENT and its parts Moulded
material,
Metal Glass, porcelain, plastic, rubber,
wood
and liquids vitreous material
For surfaces of
74 80 86
ENCLOSURES
External surfaces of
ME EQUIPMENT that are
likely to be touched
DETACHABLE
HANDLE and 51 56 60
other rails
a
These temperature limit values are applicable for touching the healthy skin of adults. They are not applicable
when large areas of the skin (10 % of total body surface or more) can be in contact with a hot surface. This also
applies in the case of skin contact with over 10 % of the head surface. Where this is the case, appropriate limits
shall be determined and documented in the RISK MANAGEMENT FILE.
The light-transmitting surface (e.g. lens or cover glass) is excluded from the so-called "likely to be touched"
parts for the following reasons: As a protective surface, it absorbs a part of the energy delivered to the surgical
site. The sterile OPERATOR shall not touch a non-sterile illuminating surface during surgery.

201.11.1.4 GUARDS
Addition:
When
...