EN 60601-2-4:2003
(Main)Medical electrical equipment - Part 2-4: Particular requirements for the safety of cardiac defibrillators
Medical electrical equipment - Part 2-4: Particular requirements for the safety of cardiac defibrillators
Specifies requirements for the safety of cardiac defibrillators.
Medizinische elektrische Geräte - Teil 2-4: Besondere Festlegungen für die Sicherheit von Defibrillatoren
Appareils électromédicaux - Partie 2-4: Règles particulières de sécurité pour les défibrillateurs cardiaques
Medicinska električna oprema - 2-4. del: Posebne varnostne zahteve za srčne defibrilatorje (IEC 60601-2-4:2002)
General Information
Relations
Standards Content (Sample)
SLOVENSKI STANDARD
SIST EN 60601-2-4:2003
01-april-2003
1DGRPHãþD
SIST HD 395.2.4 S1:1998
0HGLFLQVNDHOHNWULþQDRSUHPDGHO 3RVHEQHYDUQRVWQH]DKWHYH]DVUþQH
GHILEULODWRUMH ,(&
Medical electrical equipment - Part 2-4: Particular requirements for the safety of cardiac
defibrillators (IEC 60601-2-4:2002)
Medizinische elektrische Geräte - Teil 2-4: Besondere Festlegungen für die Sicherheit
von Defibrillatoren (IEC 60601-2-4:2002)
Appareils électromédicaux - Partie 2-4: Règles particulières de sécurité pour les
défibrillateurs cardiaques (CEI 60601-2-4:2002)
Ta slovenski standard je istoveten z: EN 60601-2-4:2003
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
SIST EN 60601-2-4:2003 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
---------------------- Page: 1 ----------------------
EUROPEAN STANDARD EN 60601-2-4
NORME EUROPÉENNE
EUROPÄISCHE NORM January 2003
ICS 11.040.10 Supersedes HD 395.2.4 S1:1988
English version
Medical electrical equipment
Part 2-4: Particular requirements for the safety of cardiac defibrillators
(IEC 60601-2-4:2002)
Appareils électromédicaux Medizinische elektrische Geräte
Partie 2-4: Règles particulières de Teil 2-4: Besondere Festlegungen für die
sécurité pour les défibrillateurs cardiaques Sicherheit von Defibrillatoren
(CEI 60601-2-4:2002) (IEC 60601-2-4:2002)
This European Standard was approved by CENELEC on 2002-10-01. 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, Czech Republic,
Denmark, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Luxembourg, Malta,
Netherlands, Norway, Portugal, Slovakia, Spain, Sweden, Switzerland and United Kingdom.
CENELEC
European Committee for Electrotechnical Standardization
Comité Européen de Normalisation Electrotechnique
Europäisches Komitee für Elektrotechnische Normung
Central Secretariat: rue de Stassart 35, B - 1050 Brussels
© 2003 CENELEC - All rights of exploitation in any form and by any means reserved worldwide for CENELEC members.
Ref. No. EN 60601-2-4:2003 E
---------------------- Page: 2 ----------------------
EN 60601-2-4:2003 - 2 -
Foreword
The text of document 62D/455/FDIS, future edition 2 of IEC 60601-2-4, prepared by the Technical
Committee CENELEC TC 62, Electrical equipment in medical practice, was submitted to the
IEC-CENELEC parallel vote and was approved by CENELEC as EN 60601-2-4 on 2002-10-01.
This European Standard supersedes HD 395.2.4 S1:1988.
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) 2003-08-01
– latest date by which the national standards conflicting
with the EN have to be withdrawn (dow) 2005-10-01
In this standard, the following print types are used:
– requirements, compliance with which can be tested, and definitions: roman type;
– explanations, advice, notes, general statements and exceptions: smaller roman type;
– test specifications: italic type;
– TERMS DEFINED IN CLAUSE 2 OF THE GENERAL STANDARD OR THIS PARTICULAR STANDARD: SMALL
CAPITALS.
Annexes designated "normative" are part of the body of the standard.
Annexes designated "informative" are given for information only.
In this standard, annex ZA is normative and annexes AA, BB and ZB are informative.
Annexes ZA and ZB have been added by CENELEC.
__________
Endorsement notice
The text of the International Standard IEC 60601-2-4:2002 was approved by CENELEC as a European
Standard without any modification.
__________
---------------------- Page: 3 ----------------------
- 3 - EN 60601-2-4:2003
Annex ZA
(normative)
Normative references to international publications
with their corresponding European publications
This European Standard incorporates by dated or undated reference, provisions from other
publications. These normative references are cited at the appropriate places in the text and the
publications are listed hereafter. For dated references, subsequent amendments to or revisions of any
of these publications a
...
Questions, Comments and Discussion
Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.