SIST EN IEC 80601-2-59:2019/oprA1:2021
(Amendment)Amendment 1 - Medical electrical equipment - Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening
Amendment 1 - Medical electrical equipment - Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening
20211012-JO-Link to 93/42/EEC and M/295 removed
Medizinische elektrische Geräte - Teil 2-59: Besondere Anforderungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Wärmebildkameras für Reihenuntersuchungen von Menschen auf Fieber
Appareils électromédicaux - Partie 2-59: Exigences particulières pour la sécurité de base et les performances essentielles des imageurs thermiques pour le dépistage des humains fébriles
Dopolnilo A1 - Medicinska električna oprema - 2-59. del: Posebne zahteve za osnovno varnost in bistvene lastnosti presejalnih termografov za spremljanje človekove temperature pri mrzlici
General Information
RELATIONS
Standards Content (sample)
SLOVENSKI STANDARD
SIST EN IEC 80601-2-59:2019/oprA1:2021
01-november-2021
Dopolnilo A1 - Medicinska električna oprema - 2-59. del: Posebne zahteve za
osnovno varnost in bistvene lastnosti presejalnih termografov za spremljanje
človekove temperature pri mrzlici
Amendment 1 - Medical electrical equipment - Part 2-59: Particular requirements for the
basic safety and essential performance of screening thermographs for human febrile
temperature screeningMedizinische elektrische Geräte - Teil 2-59: Besondere Anforderungen für die Sicherheit
einschließlich der wesentlichen Leistungsmerkmale von Wärmebildkameras fürReihenuntersuchungen von Menschen auf Fieber
Appareils électromédicaux - Partie 2-59: Exigences particulières pour la sécurité de base
et les performances essentielles des imageurs thermiques pour le dépistage deshumains fébriles
Ta slovenski standard je istoveten z: EN IEC 80601-2-59:2019/prA1:2021
ICS:
11.040.55 Diagnostična oprema Diagnostic equipment
SIST EN IEC 80601-2- en
59:2019/oprA1:2021
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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SIST EN IEC 80601-2-59:2019/oprA1:2021
62D/1892/CDV
COMMITTEE DRAFT FOR VOTE (CDV)
PROJECT NUMBER:
IEC 80601-2-59/AMD1 ED2
DATE OF CIRCULATION: CLOSING DATE FOR VOTING:
2021-09-10 2021-12-03
SUPERSEDES DOCUMENTS:
62D/1888/RR
IEC SC 62D : ELECTROMEDICAL EQUIPMENT
SECRETARIAT: SECRETARY:
United States of America Ms Ladan Bulookbashi
OF INTEREST TO THE FOLLOWING COMMITTEES: PROPOSED HORIZONTAL STANDARD:
Other TC/SCs are requested to indicate their interest, if
any, in this CDV to the secretary.
FUNCTIONS CONCERNED:
EMC ENVIRONMENT QUALITY ASSURANCE SAFETY
SUBMITTED FOR CENELEC PARALLEL VOTING NOT SUBMITTED FOR CENELEC PARALLEL VOTING
This document is still under study and subject to change. It should not be used for reference purposes.
Recipients of this document are invited to submit, with their comments, notification of any relevant patent rights of
which they are aware and to provide supporting documentation.TITLE:
Amendment 1 - Medical electrical equipment - Part 2-59: Particular requirements for the basic
safety and essential performance of screening thermographs for human febrile temperature
screeningPROPOSED STABILITY DATE: 2027
NOTE FROM TC/SC OFFICERS:
IEC 80601-2-59:2017 ED2 is being amended to align to the Amendment projects of the IEC 60601 -1
series. Refer to IEC 62D/1808/INF and 62D/1828/AC for more information.Copyright © 2021 International Electrotechnical Commission, IEC. All rights reserved. It is permitted to
download this electronic file, to make a copy and to print out the content for the sole purpose of preparing National
Committee positions. You may not copy or "mirror" the file or printed version of the document, or any part of it,
for any other purpose without permission in writing from IEC.---------------------- Page: 3 ----------------------
SIST EN IEC 80601-2-59:2019/oprA1:2021
IEC CDV 80601-2-59:2017 AMD1:2021
© IEC:2021
– 2 –
FOREWORD
This amendment has been prepared by subcommittee 62D: Electromedical equipment, of IEC
technical committee 62: Electrical equipment in medical practice.The text of this amendment is based on the following documents:
Draft Report on voting
62D/XXXX/FDIS 62D/XXXX/RVD
Full information on the voting for its approval can be found in the report on voting indicated in
the above table.The committee has decided that the contents of this document will remain unchanged until the
stability date indicated on the IEC website under "http://webstore.iec.ch" in the data related to
the specific document. At this date, the document will be• reconfirmed,
• withdrawn,
• replaced by a revised edition, or
• amended.
NOTE The attention of users of this document is drawn to the fact that equipment manufacturers and testing
organizations may need a transitional period following publication of a new, amended or revised IEC or
ISO publication in which to make products in accordance with the new requirements and to equip themselves for
conducting new or revised tests. It is the recommendation of the committee that the content of this publication be
adopted for mandatory implementation nationally not earlier than 3 years from the date of publication.
IMPORTANT – The 'colour inside' logo on the cover page of this publication indicates that it
contains colours which are considered to be useful for the correct understanding of its
contents. Users should therefore print this document using a colour printer...
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