Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment (IEC 60601-2-50:2009/A1:2016)

Medizinische elektrische Geräte - Teil 2-50: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Säuglings-Phototherapiegeräten

Appareils électromédicaux - Partie 2-50: Exigences particulières pour la sécurité de base et les performances essentielles des appareils de photothérapie pour nouveau-nés

Medicinska električna oprema - 2-50. del: Posebne zahteve za osnovno varnost in bistvene lastnosti za otroško fototerapevtsko opremo - Dopolnilo A1 (IEC 60601-2-50:2009/A1:2016)

General Information

Status
Published
Publication Date
10-Jan-2017
Current Stage
6060 - National Implementation/Publication (Adopted Project)
Start Date
04-Jan-2017
Due Date
11-Mar-2017
Completion Date
11-Jan-2017

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Standards Content (sample)

SLOVENSKI STANDARD
SIST EN 60601-2-50:2009/A1:2017
01-februar-2017
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Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and

essential performance of infant phototherapy equipment (IEC 60601-2-50:2009/A1:2016)

Medizinische elektrische Geräte - Teil 2-50: Besondere Festlegungen für die Sicherheit

einschließlich der wesentlichen Leistungsmerkmale von Säuglings-Phototherapiegeräten

Appareils électromédicaux - Partie 2-50: Exigences particulières pour la sécurité de base

et les performances essentielles des appareils de photothérapie pour nouveau-nés
Ta slovenski standard je istoveten z: EN 60601-2-50:2009/A1:2016
ICS:
11.040.60 Terapevtska oprema Therapy equipment
SIST EN 60601-2-50:2009/A1:2017 en

2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN 60601-2-50:2009/A1:2017
---------------------- Page: 2 ----------------------
SIST EN 60601-2-50:2009/A1:2017
EUROPEAN STANDARD EN 60601-2-50:2009/A1
NORME EUROPÉENNE
EUROPÄISCHE NORM
December 2016
ICS 11.040.60
English Version
Medical electrical equipment - Part 2-50: Particular requirements
for the basic safety and essential performance of infant
phototherapy equipment
(IEC 60601-2-50:2009/A1:2016)

Appareils électromédicaux - Partie 2-50: Exigences particulières Medizinische elektrische Geräte - Teil 2-50: Besondere

pour la sécurité de base et les performances essentielles des Festlegungen für die Sicherheit einschließlich der wesentlichen

appareils de photothérapie pour nouveau-nés Leistungsmerkmale von Säuglings-Phototherapiegeräten

(IEC 60601-2-50:2009/A1:2016) (IEC 60601-2-50:2009/A1:2016)

This amendment A1 modifies the European Standard EN 60601-2-50:2009; it was approved by CENELEC on 2016-06-03. CENELEC

members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this amendment 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 CEN-CENELEC

Management Centre or to any CENELEC member.

This amendment 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 CEN-CENELEC Management Centre 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, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia,

Lithuania, Luxembourg, Malta, the Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland,

Turkey and the United Kingdom.
European Committee for Electrotechnical Standardization
Comité Européen de Normalisation Electrotechnique
Europäisches Komitee für Elektrotechnische Normung
CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels

© 2016 CENELEC All rights of exploitation in any form and by any means reserved worldwide for CENELEC Members.

Ref. No. EN 60601-2-50:2009/A1:2016 E
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SIST EN 60601-2-50:2009/A1:2017
EN 60601-2-50:2009/A1:2016
European foreword

The text of document 62D/1327/FDIS, future IEC 60601-2-50:2009/A1, prepared by SC 62D

"Electromedical equipment", of IEC/TC 62 "Electrical equipment in medical practice" was submitted to

the IEC-CENELEC parallel vote and approved by CENELEC as EN 60601-2-50:2009/A1:2016.

The following dates are fixed:
(dop) 2017-06-16
• latest date by which the document has to be implemented at
national level by publication of an identical national
standard or by endorsement
(dow) 2019-12-16
• latest date by which the national standards conflicting with
the document have to be withdrawn

Attention is drawn to the possibility that some of the elements of this document may be the subject of

patent rights. CENELEC [and/or CEN] shall not be held responsible for identifying any or all such

patent rights.

This document has been prepared under a mandate given to CENELEC by the European Commission

and the European Free Trade Association, and supports essential requirements of EU Directive(s).

For the relationship with EU Directive 93/42/EEC, see informative Annex ZZ, included in

EN 60601-2-50:2009/A11:2011.
Endorsement notice

The text of the International Standard IEC 60601-2-50:2009/A1:2016 was approved by CENELEC as

a European Standard without any modification.

In the Bibliography of EN 60601-2-50:2009, replace the existing reference to ISO 3743-1 by the following:

IEC 61672-1 NOTE Harmonized as EN 61672-1.
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SIST EN 60601-2-50:2009/A1:2017
EN 60601-2-50:2009/A1:2016
Annex ZA
(normative)
Normative references to international publications
with their corresponding European publications

The following documents, in whole or in part, are normatively referenced in this document and are

indispensable for its application. For dated references, only the edition cited applies. For undated

references, the latest edition of the referenced document (including any amendments) applies.

NOTE 1 When an International Publication has been modified by common modifications, indicated by (mod),

the relevant EN/HD applies.
NOTE 2 Up-to-date information on the latest versions of t
...

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