Medical electrical equipment - Medical image display systems - Part 1: Evaluation methods

Medizinische elektrische Geräte - Medizinische Bildwiedergabesysteme - Teil 1: Bewertungsmethoden

Appareils électromédicaux - Systèmes d'imagerie médicale - Partie 1: Méthodes d'évaluation

Medicinska električna oprema - Sistemi za prikazovanje medicinskih slik - 1. del: Metode vrednotenja - Dopolnilo A2 (IEC 62563-1:2009/AMD2:2021)

General Information

Status
Published
Publication Date
26-Aug-2021
Current Stage
6060 - Document made available - Publishing
Start Date
27-Aug-2021
Completion Date
27-Aug-2021

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SLOVENSKI STANDARD
SIST EN 62563-1:2010/A2:2021
01-november-2021
Medicinska električna oprema - Sistemi za prikazovanje medicinskih slik - 1. del:
Metode vrednotenja - Dopolnilo A2 (IEC 62563-1:2009/AMD2:2021)
Medical electrical equipment - Medical image display systems - Part 1: Evaluation
methods (IEC 62563-1:2009/AMD2:2021)
Medizinische elektrische Geräte - Medizinische Bildwiedergabesysteme - Teil 1:
Bewertungsmethoden (IEC 62563-1:2009/AMD2:2021)
Appareils électromédicaux - Systèmes d'imagerie médicale - Partie 1: Méthodes
d'évaluation (IEC 62563-1:2009/AMD2:2021)
Ta slovenski standard je istoveten z: EN 62563-1:2010/A2:2021
ICS:
11.040.55 Diagnostična oprema Diagnostic equipment
SIST EN 62563-1:2010/A2:2021 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN 62563-1:2010/A2:2021

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SIST EN 62563-1:2010/A2:2021


EUROPEAN STANDARD EN 62563-1:2010/A2

NORME EUROPÉENNE

EUROPÄISCHE NORM
August 2021
ICS 11.040.55

English Version
Medical electrical equipment - Medical image display systems -
Part 1: Evaluation methods
(IEC 62563-1:2009/AMD2:2021)
Appareils électromédicaux - Systèmes d'imagerie médicale Medizinische elektrische Geräte - Medizinische
- Partie 1: Méthodes d'évaluation Bildwiedergabesysteme - Teil 1: Bewertungsmethoden
(IEC 62563-1:2009/AMD2:2021) (IEC 62563-1:2009/AMD2:2021)
This amendment A2 modifies the European Standard EN 62563-1:2010; it was approved by CENELEC on 2021-08-23. 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,
Turkey 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
© 2021 CENELEC All rights of exploitation in any form and by any means reserved worldwide for CENELEC Members.
 Ref. No. EN 62563-1:2010/A2:2021 E

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SIST EN 62563-1:2010/A2:2021
EN 62563-1:2010/A2:2021 (E)
European foreword
The text of document 62B/1168/CDV, future IEC 62563-1/AMD2, prepared by SC 62B “Diagnostic
imaging equipment” of IEC/TC 62 “Electrical equipment in medical practice” was submitted to the IEC-
CENELEC parallel vote and approved by CENELEC as EN 62563-1:2010/A2:2021.
The following dates are fixed:
• latest date by which the document has to be implemented at national (dop) 2022–05–23
level by publication of an identical national standard or by endorsement
• latest date by which the national standards conflicting with the (dow) 2024–08–23
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 62563-1:2009/AMD2:2021 was approved by CENELEC as
a European Standard without any modification.


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SIST EN 62563-1:2010/A2:2021



IEC 62563-1

®


Edition 1.0 2021-07




INTERNATIONAL



STANDARD




NORME


INTERNATIONALE





AM ENDMENT 2

AM ENDEMENT 2





Medical electrical equipment – Medical image display systems –

Part 1: Evaluation methods




Appareils electromedicaux – Systemes d'imagerie medicale –

Partie 1: Méthodes d’évaluation

















INTERNATIONAL

ELECTROTECHNICAL

COMMISSION


COMMISSION

ELECTROTECHNIQUE

INTERNATIONALE




ICS 11.040.55 ISB
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