EN 60601-2-50:2009/A1:2016
(Amendment)Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment
Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment
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
- Withdrawn
- Publication Date
- 15-Dec-2016
- Withdrawal Date
- 15-Dec-2019
- Technical Committee
- CLC/TC 62 - Electrical equipment in medical practice
- Drafting Committee
- IEC/SC 62D - IEC_SC_62D
- Current Stage
- 9960 - Withdrawal effective - Withdrawal
- Start Date
- 16-Jul-2024
- Completion Date
- 16-Jul-2024
Relations
- Effective Date
- 20-Jul-2021
- Effective Date
- 07-Jun-2022
- Effective Date
- 10-Mar-2015
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Frequently Asked Questions
EN 60601-2-50:2009/A1:2016 is a amendment published by CLC. Its full title is "Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment". This standard covers: Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment
Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment
EN 60601-2-50:2009/A1:2016 is classified under the following ICS (International Classification for Standards) categories: 11.040.60 - Therapy equipment. The ICS classification helps identify the subject area and facilitates finding related standards.
EN 60601-2-50:2009/A1:2016 has the following relationships with other standards: It is inter standard links to EN IEC 60601-2-50:2021, EN 60601-2-50:2009, EN 60601-2-50:2009/A11:2011. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 60601-2-50:2009/A1:2016 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: M/432. 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.
EN 60601-2-50:2009/A1:2016 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.
Standards Content (Sample)
SLOVENSKI STANDARD
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
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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
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.
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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