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EN IEC 60601-2-50:2021/A1:2023

(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 60601-2-50:2020/AMD1:2023)

General Information

Status
Published
Publication Date
07-Dec-2023
ICS
11.040.60 - Therapy equipment
Technical Committee
CLC/TC 62 - Electrical equipment in medical practice
Drafting Committee
IEC/SC 62D - IEC_SC_62D
Current Stage
6060 - Document made available - Publishing
Start Date
08-Dec-2023
Due Date
30-Jun-2022
Completion Date
08-Dec-2023
Ref Project
SIST EN IEC 60601-2-50:2021/A1:2024 - Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment (IEC 60601-2-50:2020/AMD1:2023)

Relations

Amends
EN IEC 60601-2-50:2021 - Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment
Effective Date
26-Jul-2021

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EN IEC 60601-2-50:2021/A1:2024EN IEC 60601-2-50:2021/A1:2024
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EN IEC 60601-2-50:2021/A1:2024
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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN IEC 60601-2-50:2021/A1:2024
01-februar-2024
Medicinska električna oprema - 2-50. del: Posebne zahteve za osnovno varnost in
bistvene lastnosti za otroško fototerapevtsko opremo - Dopolnilo A1 (IEC 60601-2-
50:2020/AMD1:2023)
Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and
essential performance of infant phototherapy equipment (IEC 60601-2-
50:2020/AMD1:2023)
Medizinische elektrische Geräte - Teil 2-50: Besondere Festlegungen für die Sicherheit
einschließlich der wesentlichen Leistungsmerkmale von Säuglings-Phototherapiegeräten
(IEC 60601-2-50:2020/AMD1:2023)
Appareils électromédicaux - Partie 2-50: Exigences particulières pour la sécurité de base
et les performances essentielles des appareils de photothérapie pour nouveau-nés (IEC
60601-2-50:2020/AMD1:2023)
Ta slovenski standard je istoveten z: EN IEC 60601-2-50:2021/A1:2023
ICS:
11.040.60 Terapevtska oprema Therapy equipment
SIST EN IEC 60601-2-50:2021/A1:2024 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN IEC 60601-2-50:2021/A1:2024

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SIST EN IEC 60601-2-50:2021/A1:2024


EUROPEAN STANDARD EN IEC 60601-2-50:2021/A1

NORME EUROPÉENNE

EUROPÄISCHE NORM December 2023
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 60601-2-50:2020/AMD1:2023)
Appareils électromédicaux - Partie 2-50: Exigences Medizinische elektrische Geräte - Teil 2-50: Besondere
particulières pour la sécurité de base et les performances Festlegungen für die Sicherheit einschließlich der
essentielles des appareils de photothérapie pour nouveau- wesentlichen Leistungsmerkmale von Säuglings-
nés Phototherapiegeräten
(IEC 60601-2-50:2020/AMD1:2023) (IEC 60601-2-50:2020/AMD1:2023)
This amendment A1 modifies the European Standard EN IEC 60601-2-50:2021; it was approved by CENELEC on 2023-11-30. 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, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, the
Netherlands, Norway, Poland, Portugal, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland,
Türkiye and the United Kingdom.


European Committee for Electrotechnical Standardization
Comité Européen de Normalisation Electrotechnique
Europäisches Komitee für Elektrotechnische Normung
CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2023 CENELEC All rights of exploitation in any form and by any means reserved worldwide for CENELEC Members.
 Ref. No. EN IEC 60601-2-50:2021/A1:2023 E

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SIST EN IEC 60601-2-50:2021/A1:2024
EN IEC 60601-2-50:2021/A1:2023 (E)
European foreword
The text of document 62D/2069/FDIS, future IEC 60601-2-50/AMD1, 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 IEC 60601-2-50:2021/A1:2023.
The following dates are fixed:
• latest date by which the document has to be implemented at national (dop) 2024-08-30
level by publication of an identical national standard or by endorsement
• latest date by which the national standards conflicting with the (dow) 2026-11-30
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 shall not be held responsible for identifying any or all such patent rights.
Any feedback and questions on this document should be directed to the users’ national committee. A
complete listing of these bodies can be found on the CENELEC website.
Endorsement notice
The text of the International Standard IEC 60601-2-50:2020/AMD1:2023 was approved by CENELEC
as a European Standard without any modification.
2

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SIST EN IEC 60601-2
...

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