Medical electrical equipment - Part 2-52: Particular requirements for basic safety and essential performance of medical beds (IEC 60601-2-52:2009)

EC 60601-2-52:2009 applies to the basic safety and essential performance of medical beds intended for adults. This first edition cancels and replaces the first edition of IEC 60601-2-38, published in 1996, and its Amendment 1 (1999). This edition constitutes a technical revision. IEC 60601-2-52:2009 is the realization of much work in alignment, and scope adjustment between IEC 60601-2-38, EN 1970, and the third edition of IEC 60601-1.

Medizinische elektrische Geräte - Teil 2-52: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von medizinischen Betten (IEC 60601-2-52:2009)

Appareils électromédicaux - Partie 2-52: Exigences particulières pour la sécurité de base et les performances essentielles des lits médicaux (CEI 60601-2-52:2009)

La CEI 60601-2-52:2009 s'applique à la sécurité de base et aux performances essentielles des lits medicaux destinés aux adultes. Cette première édition annule et remplace la première édition de la CEI 60601-2-38, parue en 1996, et son Amendement (1999). Elle constitue une révision technique. La CEI 60601-2-52:2009 est la réalisation d'un travail important d'alignement et d'ajustement de domaines d'application entre la CEI 60601-2-38, la EN 1970, et la troisième édition de la CEI 60601-1.

Medicinska električna oprema - 2-52. del: Posebne zahteve za osnovno varnost in bistvene lastnosti medicinskih postelj (IEC 60601-2-52:2009)

Ta mednarodni standard velja za OSNOVNO VARNOST in BISTVENE LASTNOSTI MEDICINSKIH POSTELJ, namenjenih odraslim, v nadaljevanju MEDICINSKA POSTELJA, kot je opredeljena v 201.3.212. Če je klavzula ali podklavzula posebej namenjena temu, da se uporablja le za MEDICINSKO POSTELJO ali le za ME SISTEME, vsebina te klavzule ali podklavzule tako navaja. V nasprotnem primeru tako klavzula ali podklavzula veljata za ustrezno MEDICINSKO POSTELJO in ME SISTEME. NEVARNOSTI, ki so del fiziološkega delovanja MEDECINSKE POSTELJE ali ME SISTEMOV znotraj področja uporabe tega standarda, niso zajete z posebnimi zahtevami tega standarda, razen v točkah 7.2.13 in 8.4.1 splošnega standarda.

General Information

Status
Published
Publication Date
08-Apr-2010
Withdrawal Date
31-Mar-2013
Current Stage
6060 - Document made available - Publishing
Start Date
09-Apr-2010
Completion Date
09-Apr-2010

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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN 60601-2-52:2010
01-junij-2010
0HGLFLQVNDHOHNWULþQDRSUHPDGHO3RVHEQH]DKWHYH]DRVQRYQRYDUQRVWLQ
ELVWYHQHODVWQRVWLPHGLFLQVNLKSRVWHOM ,(&
Medical electrical equipment - Part 2-52: Particular requirements for basic safety and
essential performance of medical beds (IEC 60601-2-52:2009)
Medizinische elektrische Geräte - Teil 2-52: Besondere Festlegungen für die Sicherheit
einschließlich der wesentlichen Leistungsmerkmale von medizinischen Betten (IEC
60601-2-52:2009)
Appareils électromédicaux - Partie 2-52: Exigences particulières de sécurité de base et
de performances essentielles des lits médicaux (CEI 60601-2-52:2009)
Ta slovenski standard je istoveten z: EN 60601-2-52:2010
ICS:
11.140 Oprema bolnišnic Hospital equipment
SIST EN 60601-2-52:2010 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN 60601-2-52:2010

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SIST EN 60601-2-52:2010

EUROPEAN STANDARD
EN 60601-2-52

NORME EUROPÉENNE
April 2010
EUROPÄISCHE NORM

ICS 11.140 Supersedes EN 60601-2-38:1996 + A1:2000, EN 1970:2000


English version


Medical electrical equipment -
Part 2-52: Particular requirements for basic safety and essential
performance of medical beds
(IEC 60601-2-52:2009)


Appareils électromédicaux -  Medizinische elektrische Geräte -
Partie 2-52: Exigences particulières Teil 2-52: Besondere Festlegungen
pour la sécurité de base für die Sicherheit einschließlich
et les performances essentielles der wesentlichen Leistungsmerkmale
des lits médicaux von medizinischen Betten
(CEI 60601-2-52:2009) (IEC 60601-2-52:2009)




This European Standard was approved by CENELEC on 2010-04-01. 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, Croatia, 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.

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

Central Secretariat: Avenue Marnix 17, B - 1000 Brussels


© 2010 CEN-CENELEC - All rights of exploitation in any form and by any means reserved worldwide for CEN-CENELEC members.
Ref. No. EN 60601-2-52:2010 E

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SIST EN 60601-2-52:2010
EN 60601-2-52:2010 - 2 -
Foreword
The text of document 62D/795/FDIS, future edition 1 of IEC 60601-2-52, 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 60601-2-52 on 2010-04-01.
This European Standard supersedes EN 60601-2-38:1996 + A1:2000 and EN 1970:2000.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN and CENELEC shall not be held responsible for identifying any or all such patent
rights.
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) 2011-01-01
– latest date by which the national standards conflicting
with the EN have to be withdrawn (dow) 2013-04-01
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 93/42/EEC. See Annex ZZ.
Annexes ZA and ZZ have been added by CENELEC.
__________
Endorsement notice
The text of the International Standard IEC 60601-2-52:2009 was approved by CENELEC as a European
Standard without any modification.
In the official version, for Bibliography, the following note has to be added for the standards indicated:
IEC 60601-2-38 NOTE  Harmonized as EN 60601-2-38
__________

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SIST EN 6060
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