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

Status
Not Published
Public Enquiry End Date
30-Nov-2021
Current Stage
4020 - Public enquire (PE) (Adopted Project)
Start Date
17-Sep-2021
Due Date
04-Feb-2022

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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 screening

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
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
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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

screening
PROPOSED 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.
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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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