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SIST EN 60601-2-20:2010
01-januar-2010
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SIST EN 60601-2-20:1998
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Medical electrical equipment - Part 2-20: Particular requirements for basic safety and
essential performance of transport incubators (IEC 60601-2-20:2009)
Medizinische elektrische Geräte - Teil 2-20: Besondere Festlegungen für die Sicherheit
einschlißlich der wesentlichen Leistungsmerkmale von Transportinkubatoren (IEC 60601
-2-20:2009)
Appareils électromédicaux - Partie 2-20: Règles particulières de sécurité de base et de
performances essentielles des incubateurs de transport (CEI 60601-2-20:2009)
Ta slovenski standard je istoveten z: EN 60601-2-20:2009
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
SIST EN 60601-2-20:2010 en,fr
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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SIST EN 60601-2-20:2010
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SIST EN 60601-2-20:2010
EUROPEAN STANDARD
EN 60601-2-20
NORME EUROPÉENNE
November 2009
EUROPÄISCHE NORM
ICS 11.040.10 Supersedes EN 60601-2-20:1996
English version
Medical electrical equipment -
Part 2-20: Particular requirements for the basic safety
and essential performance of infant transport incubators
(IEC 60601-2-20:2009)
Appareils électromédicaux - Medizinische elektrische Geräte -
Partie 2-20: Exigences particulières Teil 2-20: Besondere Festlegungen
pour la sécurité de base für die Sicherheit einschließlich
et les performances essentielles der wesentlichen Leistungsmerkmale
des incubateurs de transport von Tranportinkubatoren
pour nouveau-nés (IEC 60601-2-20:2009)
(CEI 60601-2-20:2009)
This European Standard was approved by CENELEC on 2009-09-01. 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 60601-2-20:2009 E
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SIST EN 60601-2-20:2010
EN 60601-2-20:2009 - 2 -
Foreword
The text of document 62D/731/FDIS, future edition 2 of IEC 60601-2-20, 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 60601-2-20 on 2009-09-01.
This European Standard supersedes EN 60601-2-20:1996.
EN 60601-2-20:1996 was revised to structurally align 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) 2010-06-01
– latest date by which the national standards conflicting
with the EN have to be withdrawn (dow) 2012-09-01
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
– “claus
...