Luminaires - Part 2-25: Particular requirements - Luminaires for use in clinical areas of hospitals and health care buildings

Details specific requirements for luminaires for use with tungsten filament, fluorescent and other discharge lamps on supply voltages not exceeding 1 000 V for use in clinical areas in which medical treatment, examination and medical care takes place in hospital and health care buildings.

Leuchten - Teil 2-25: Besondere Anforderungen - Leuchten zur Verwendung in klinischen Bereichen von Krankenhäusern und Gebäuden zur Gesundheitsfürsorge

Luminaires - Partie 2-25: Règles particulières - Luminaires pour les unités de soins des hôpitaux et les maisons de santé

Détaille les prescriptions spécifiques aux luminaires à utiliser avec les lampes à filament de tungstène, les lampes tubulaires à fluorescence et autres lampes à décharge, sous des tensions d'alimentation ne dépassant pas 1 000 V, dans les unités de soins des hôpitaux et les maisons de santé, où sont effectués des examens et des traitements médicaux.

Svetilke - 2-25. del: Posebne zahteve - Svetilke za uporabo v kliničnih območjih bolnišnic in zdravstvenih ustanovah (IEC 60598-2-25:1994 + corrigendum Sep.1994)

General Information

Status
Published
Publication Date
08-Dec-1994
Withdrawal Date
30-Sep-1995
Drafting Committee
IEC/SC 34D - IEC_SC_34D
Parallel Committee
IEC/SC 34D - IEC_SC_34D
Current Stage
6060 - Document made available - Publishing
Start Date
09-Dec-1994
Completion Date
09-Dec-1994

Relations

Effective Date
29-Jan-2023

Overview

EN 60598-2-25:1994 (IEC 598-2-25) specifies particular safety and performance requirements for luminaires used in clinical areas of hospitals and health care buildings. It covers luminaires using tungsten filament, fluorescent and other discharge lamps on supply voltages up to 1 000 V, and complements general luminaire requirements in EN/IEC 60598-1. The section focuses on patient-area types such as bedded-area, bedhead, night-light, general examination and hand-held inspection luminaires and defines construction, testing and marking expectations for safe clinical use.

Key topics and technical requirements

  • Scope & exclusions: Applies to clinical-area luminaires but excludes medical electrical equipment (per IEC 601-1), emergency lighting, non-clinical general illumination, autoclave‑sterilizable luminaires and operating‑table luminaires.
  • Normative references: Integrates EN/IEC 60598-1 (general tests/requirements) and IEC 601-1 (medical electrical equipment safety).
  • Classification & marking: Luminaires must be classified per IEC 60598-1; hand‑held inspection luminaires are Class II or III. Hospital systems and service outlets require clear, indelible marking.
  • Construction & components:
    • Switches must not be in non‑detachable supply cords; hand‑held switches are enclosed and actuated through a flexible cover.
    • Protective covers for lamps must be fixed so they cannot be removed by hand and allow lamp replacement without full removal.
    • Lampholders (hand‑held tungsten) must be locked against rotation by at least two independent means (one tool‑operable).
    • Hospital‑system luminaires require separate compartments for controlgear, cabling and medical gas pipes.
    • Cord storage devices for portable luminaires.
  • Mechanical strength & tests:
    • Guard pull test: protective guard must withstand a 250 N axial pull for 1 minute.
    • Impact swing tests for hand‑held luminaires: repeated impacts from specified heights against a steel bar; no unsafe damage allowed.
    • Portable examination luminaires must not overbalance.
  • Electrical & safety tests: Creepage/clearances, earthing, insulation resistance, thermal/endurance testing and photometric performance (Annex A) where safety depends on light output.

Applications and users

This standard is essential for:

  • Luminaire manufacturers designing clinical lighting (bedhead, examination, hand‑held inspection).
  • Product safety and compliance engineers performing tests and CE/EN conformity assessments.
  • Hospital facilities managers and procurement specifying safe clinical lighting and hospital system integration.
  • Test labs and certification bodies performing mechanical, electrical and photometric verification.

Related standards

  • EN/IEC 60598-1: General requirements and tests for luminaires
  • IEC 601-1 (now IEC 60601-1): Medical electrical equipment - general safety requirements
  • Other sections of EN/IEC 60598-2 for specialized luminaire types

Keywords: luminaires for clinical areas, hospital lighting standards, EN 60598-2-25, IEC 598-2-25, clinical luminaires safety, hand‑held inspection luminaire, bedhead luminaire, photometric performance.

Frequently Asked Questions

EN 60598-2-25:1994 is a standard published by CLC. Its full title is "Luminaires - Part 2-25: Particular requirements - Luminaires for use in clinical areas of hospitals and health care buildings". This standard covers: Details specific requirements for luminaires for use with tungsten filament, fluorescent and other discharge lamps on supply voltages not exceeding 1 000 V for use in clinical areas in which medical treatment, examination and medical care takes place in hospital and health care buildings.

Details specific requirements for luminaires for use with tungsten filament, fluorescent and other discharge lamps on supply voltages not exceeding 1 000 V for use in clinical areas in which medical treatment, examination and medical care takes place in hospital and health care buildings.

EN 60598-2-25:1994 is classified under the following ICS (International Classification for Standards) categories: 29.140.40 - Luminaires. The ICS classification helps identify the subject area and facilitates finding related standards.

EN 60598-2-25:1994 has the following relationships with other standards: It is inter standard links to EN 60598-2-25:1994/A1:2004. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

EN 60598-2-25:1994 is associated with the following European legislation: EU Directives/Regulations: 2006/95/EC, 2014/35/EU, 2014/53/EU, 73/23/EEC. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.

You can purchase EN 60598-2-25:1994 directly from iTeh Standards. The document is available in PDF format and is delivered instantly after payment. Add the standard to your cart and complete the secure checkout process. iTeh Standards is an authorized distributor of CLC standards.

Standards Content (Sample)


SLOVENSKI STANDARD
01-julij-1999
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Luminaires - Part 2-25: Particular requirements - Luminaires for use in clinical areas of
hospitals and health care buildings
Leuchten - Teil 2-25: Besondere Anforderungen - Leuchten zur Verwendung in
klinischen Bereichen von Krankenhäusern und Gebäuden zur Gesundheitsfürsorge
Luminaires - Partie 2-25: Règles particulières - Luminaires pour les unités de soins des
hôpitaux et les maisons de santé
Ta slovenski standard je istoveten z: EN 60598-2-25:1994
ICS:
29.140.40 Svetila Luminaires
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

NORME CEI
INTERNATIONALE IEC
598 -2-25
INTERNATIONAL
Première édition
STANDARD
First edition
1994-08
Luminaires —
Partie 2:
Règles particulières —
Section 25: Luminaires pour
les unités
de soins des
hôpitaux et les maisons de santé
Luminaires —
Part 2:
Particular requirements

Section 25: Luminaires for
use in clinical
areas of hospitals and health care buildings
© IEC 1994 Droits de reproduction
réservés — Copyright - all rights reserved
Aucune partie de cette publication ne peut être reproduite ni No part of this publication may be reproduced or utilized in
utilisée
sous quelque forme que ce soit et par aucun any form or by any means, electronic or mechanical,
procédé, électronique ou mécanique, y compris la photo- including photocopying and microfilm, without permission in
copie et les microfilms, sans l'accord écrit de l'éditeur. writing from the publisher.
International Electrotechnical Commission 3, rue de Varembé Geneva, Switzerland
Telefax: +41 22 919 0300 e-mail: inmail@iec.ch IEC web site http: //www.iec.ch
CODE PRIX
Commission Electrotechnique Internationale
N
PRICE CODE
International Electrotechnical Commission
IEC MerenyHapozmac 3neitTpoTeXHH4eCHaa HOMHCCHA
Pour prix, voir catalogue en vigueur

• For price, see current catalogue

IEC Publication 598-2-25
Publication 598-2-25 de la CEI
(First edition - 1994)
(Première édition - 1994)
Luminaires -
Luminaires -
Part 2: Particular requirements -
Partie 2: Règles particulières -
Section 25: Luminaires for use
Section 25: Luminaires pour les unités de soins
in clinical areas of hospitals and
des hôpitaux et les maisons de santé
health care buildings
C O R R I G E N D U M 1
Couverture, page 1 Cover, page 1
Remplacer Replace the existing title by the following
le titre existant par le nouveau
titre suivant: new title:
Luminaires -
2:
Partie
Règles particulières -
Section 25: Luminaires pour les unités
des hôpitaux et
de soins les maisons de sant
Luminaires -
Part 2:
Particular requirements -
Section 25: Luminaires for use in clinical
areas of hospitals and health care buildings
Page 4 et page 6 Page 5 and page 7
Replace the main title by the following new
Remplacer le titre principal par le nouveau
titre suivant: title:
LUMINAIRES - LUMINAIRES -
2: Part 2:
Partie
Règles particulières - Particular requirements -
Section 25: Luminaires for use in
Section 25: Luminaires pour les
unités de soins des hôpitaux et les clinical areas of hospitals and health
care buildings
maisons de santé
Septembre 1994 September 1994
598-2-25 © IEC:1994 – 3 –
CONTENTS
Page
FOREWORD 5
Clause
25.1 General 7
25.1.1 Scope 7
25.1.2 Normative references 7
25.2 General test requirements 7
25.3 Definitions 9
25.4 Classification
25.5 Marking
25.6 Construction
25.7 Creepage distances and clearances
25.8 Provision for earthing
25.9 Terminals
17 25.10 External and internal wiring
25.11 Protection against electric shock
25.12 Endurance test and thermal tests 19
25.13 Resistance to dust, solid objects and moisture 21
25.14 Insulation resistance and electric strength
25.15 Resistance to heat, fire and tracking
Figures
1 Arrangement for impact test for hand-held inspection luminaires
2 Apparatus for flexing test for hand-held inspection luminaires
3 Crush test apparatus for hand-held inspection luminaires
photometric performance 27
Annex A – Luminaire
598-2-25 © IEC:1994 – 5 –
INTERNATIONAL ELECTROTECHNICAL COMMISSION
LUMINAIRES
Part
2: Particular requirements —
Section 25: Luminaires for use in clinical areas
of hospitals and health care buildings
FOREWORD
The IEC (International Electrotechnical Commission) is a worldwide organization for standardization
1)
comprising all national electrotechnical committees (IEC National Committees). The object of the IEC is to
promote international cooperation on all questions concerning standardization in the electrical and
electronic fields. To this end and in addition to other activities, the IEC publishes International Standards.
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. The 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 the IEC on technical matters, prepared by technical committees on
which all the National Committees having a special interest therein are represented, express, as nearly as
possible, an international consensus of opinion on the subjects dealt with.
3) They have the form of recommendations for international use published in the form of standards, technical
reports or guides and they are accepted by the National Committees in that sense.
4) In order to promote international unification, IEC National Committees undertake to apply IEC International
Standards transparently to the maximum extent possible in their national and regional standards. Any
divergence between the IEC Standard and the corresponding national or regional standard shall be clearly
indicated in the latter.
5) The IEC provides no marking procedure to indicate its approval and cannot be rendered responsible for any
equipment declared to be in conformity with one of its standards.
International Standard IEC 598-2-25 has been prepared by sub-committee 34D:
Luminaires, of IEC technical committee 34: Lamps and related equipment.
The text of this standard is based on the following documents:
DIS Report on voting
34D(CO)254 34D(CO)263
Full information on the voting for the approval of this standard can be found in the report
on voting indicated in the above table.

– 7 –
598-2-25 © IEC:1994
LUMINAIRES
Part 2: Particular requirements —
Section 25: Luminaires for use in clinical areas
of hospitals and health care buildings
25.1 General
25.1.1 Scope
This section of IEC 598-2 details specific requirements for luminaires for use with tungsten
filament, fluorescent and other discharge lamps on supply voltages not exceeding 1 000 V
for use in clinical areas in which medical treatment, examination and medical care takes
place in hospitals and health care buildings.
This standard does not apply to medical electrical equipment, as defined in 2.2.15 of
IEC 601-1, containing a light source.
NOTE 1 — Subclause 2.2.15 of IEC 601-1 states: Electrical equipment, provided with not more than one
connection to a particular supply mains and intended to diagnose, treat, or monitor the patient under
medical supervision and which makes physical or electrical contact with the patient and/or transfers energy
to or from the patient and/or detects such energy transfer to or from the patient.
This standard does not apply to luminaires for emergency lighting and luminaires for
general illumination in non-clinical areas (e.g. offices).
types, reference should be made to other sections of IEC 598-2.
NOTE 2 — For these luminaire
This standard does not apply to luminaires or parts of luminaires which are designed to be
sterilized by the autoclave process and luminaires for operating tables.
25.1.2 Normative references
The following normative documents contain provisions which, through reference in this
text, constitute provisions of this section of IEC 598-2. At the time of publication, the
editions indicated were valid. All normative documents are subject to revision, and pa rties
to agreements based on this section of IEC 598-2 are encouraged to investigate the
of the normative documents indicated
possibility of applying the most recent editions
below. Members of IEC and ISO maintain registers of currently valid International
Standards.
IEC 598-1: 1992, Luminaires – Part 1: General requirements and tests
Medical electrical equipment – Part 1: General requirements for safety
IEC 601-1: 1988,
25.2 General test requirements
The provisions of section 0 of IEC 598-1 apply. The tests detailed in each section of
IEC 598-1 shall be carried out in the order listed in this section of IEC 598-2. Reference to
other sections of IEC 598-1 may be necessary in such instances. In addition to the test
requirements of this section of IEC 598-2, luminaires having features covered by other
sections of IEC 598-2, for example recessed luminaires with built-in transformers, shall
also comply with the relevant provisions of those sections.

598-2-25 © IEC:1994
— 9 —
25.3 Definitions
For the purpose of this section, the definitions given in section 1 of IEC 598-1 apply
together with the following definitions:
25.3.1 bedded area: Area where one or more patients' beds are in use.
NOTE – A ward will incorporate a bedded area or areas together with the associated services such as the
nurses' station, utility rooms and toilets.
25.3.2 enclosed luminaire: Luminaire
with the main-part and translucent cover
constructed to minimize the entry of dust and other bodies.
25.3.3 bedded area luminaire: General purpose luminaire for lighting in the area of
patients.
NOTE – It may be surface mounted (wall or ceiling), pendant or recessed.
25.3.4 bedhead luminaire: Special luminaire which can be operated by the patient.
NOTES
1 It may be surface mounted and it may have an adjustable arm.
2 This luminaire type should not be regarded as a general examination luminaire or as a hand-held
inspection luminaire.
25.3.5 night light luminaire: Luminaire designed to give a low level of light, at night, in
bedded areas and adjacent areas.
25.3.6 hospital system: System for bedded areas with provision for attaching other
services, for example supply voltage outlets, connections for medical gases, telephone
sockets, radio, luminaires or light dimming devices.
25.3.7 general examination luminaire: Totally enclosed adjustable luminaire, for
surface mounting (wall or ceiling) or for fixing to a mobile stand for medical examination
and minor surgical purposes (for example dental or veterinary use).
25.3.8 hand-held inspection luminaire: Totally-enclosed luminaire for medical
inspection purposes but not intended for the internal examination of patients.
25.3.9 rewirable hand-held inspection
luminaire: Hand-held inspection luminaire so
constructed that the flexible cable or cord can be replaced.
25.3.10 non-rewirable hand-held inspection luminaire: Hand-held inspection luminaire
so constructed that the flexible cable or cord cannot be separated from the luminaire
without making it permanently useless.

598-2-25 © IEC:1994 —11 —
25.4 Classification
Luminaires shall be classified in accordance with the provisions of section 2 of IEC 598-1
together with the requirements of 25.4.1.
25.4.1 According to the type of protection against electric shock, hand-held inspection
luminaires shall be classified as class ll or class Ill.
25.5 Marking
The provisions of section 3 of IEC 598-1 apply together with the requirements of 25.5.1.
25.5.1 Hospital system shall have the service outlets clearly and indelibly marked. Any
warning notices shall be positioned so that they are clearly visible. The requirements of
clause 6 of IEC 601-1 also apply.
Compliance is checked by inspection.
25.6 Construction
The provisions of section 4 of IEC 598-1 apply together with the requirements of 25.6.1
to 25.6.4.
25.6.1 Components
25.6.1.1 Switches or supply interruption devices shall not be included in the
non-detachable cable or cord supplied with the luminaires.
In hand-held inspection luminaires switches, including their actuating members, shall be
completely enclosed within the handle or body. The cover of the actuating member shall
be of flexible material, such as rubber or polychloroprene, to enable the switch to be
operated.
Compliance is checked by inspection and by manual test.
25.6.1.2 The lamp(s) in hand-held inspection luminaires, and examination luminaires shall
be protected against accidental damage. Any protective device, such as a translucent
cover, shall be fixed to the body of the luminaire. It shall not be possible to remove the
protective device by hand and it shall be possible to replace the lamp without completely
removing this device from the luminaire.
NOTE — For example the protective device may be attached to the luminaire by means of a hinge so that
it may be moved away from its normal position.
Compliance is checked by inspection and by the manual test of 4.12.4 of section 4 of
IEC 598-1.
25.6.1.3 Lampholders for tungsten filament lamps used in hand-held inspection
luminaires shall be locked against rotation by at least two independ
...

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The article talks about the specific requirements for luminaires used in clinical areas of hospitals and healthcare buildings. It mentions that these luminaires are designed to work with tungsten filament, fluorescent, and other discharge lamps, and should not exceed 1,000 volts in supply voltage. These luminaires are used in areas where medical treatment, examination, and care are provided.

기사 제목: EN 60598-2-25:1994 - 조명장치 - 파트 2-25: 특수 요구사항 - 병원과 의료 건물의 임상 영역에서 사용되는 조명 기사 내용: 이 기사는 병원과 의료 건물의 임상 영역에서 사용되는 조명장치에 대한 특정 요구사항에 대해 설명합니다. 이 조명장치는 텅스텐 필라멘트, 형광등 및 기타 방전등과 함께 사용되도록 설계되었으며, 공급 전압은 1,000V를 초과해서는 안됩니다. 이러한 조명장치는 의료 치료, 검사 및 의료 관리가 이루어지는 임상 영역에서 사용됩니다.

記事のタイトル: EN 60598-2-25:1994 - 照明器具 - パート2-25: 特定の要件 - 病院および医療施設の臨床エリアで使用する照明器具 記事の内容: この記事は、病院や医療施設の臨床エリアで使用される照明器具の特定の要件について詳しく説明しています。これらの照明器具は、タングステンフィラメント、蛍光灯、その他の放電ランプと組み合わせて使用するために設計されており、供給電圧は1,000Vを超えてはなりません。これらの照明器具は、医療治療、検査、および医療ケアが行われる臨床エリアで使用されます。