EN 80601-2-59:2009

Medical electrical equipment - Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening

IEC 80601-2-59:2008 applies to the basic safety and essential performance of screening thermographs intended to be used for the individual non-invasive febrile temperature screening of humans under indoor environmental conditions. IEC 80601-2-59:2008 sets laboratory characterization test limits for the screening thermograph. The contents of the corrigendum of April 2009 have been included in this copy.

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

La CEI 80601-2-59:2008 s'applique à la sécurite de base et aux performances essentielles des imageurs thermiques destinés à être utilisés pour le dépistage non invasif des humains fébriles parmi des individus dans des conditions d'environnement à l'intérieur. La CEI 80601-2-59:2008 fixe des limites d'essais de caractérisation en laboratoire pour les imageurs thermiques. Le contenu du corrigendum d'avril 2009 a été pris en considération dans cet exemplaire.

Medicinska električna oprema - 2-59. del: Posebne zahteve za osnovno varnost in bistvene lastnosti presejalnih termografov za spremljanje človekove temperature pri mrzlici (IEC 80601-2-59:2008 + popravek Apr. 2009)

Ta mednarodni standard velja za OSNOVNO VARNOST in BISTVENE LASTNOSTI PRESEJALNIH TOMOGRAFOV, uporabljenih za posamezno neinvazivno spremljanje človeške temperature pri mrzlici pod pogoji okoliških zaprtih prostorov, v nadaljevanju ME OPREMA. Ta mednarodni standard postavlja meje testov laboratorijskih značilnosti za PRESEJALNI TOMOGRAF.

General Information

• Status: Withdrawn
• Publication Date: 22-Dec-2009
• Withdrawal Date: 30-Nov-2012
• ICS: 11.040.55 - Diagnostic equipment
• Technical Committee: CLC/TC 62 - Electrical equipment in medical practice
• Drafting Committee: IEC/SC 62D - IEC_SC_62D
• Parallel Committee: IEC/SC 62D - IEC_SC_62D
• Current Stage: 9960 - Withdrawal effective - Withdrawal
• Start Date: 11-Oct-2022
• Completion Date: 11-Oct-2022
• Directive: 93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Mandate: M/295 - Standardization mandate to CEN/CENELEC concerning the development of European standards relating to medical devices
• Ref Project: SIST EN 80601-2-59:2010 - Medical electrical equipment - Part 2-59: Particular requirements for basic safety and essential performance of screening thermographs for human febrile temperature screening (IEC 80601-2-59:2008 + corrigendum Apr. 2009)

Relations

• Replaced By: EN IEC 80601-2-59:2019 - Medical electrical equipment - Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening
• Effective Date: 23-Jan-2023

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN 80601-2-59:2010
01-marec-2010
0HGLFLQVNDHOHNWULþQDRSUHPDGHO3RVHEQH]DKWHYH]DRVQRYQRYDUQRVWLQ
ELVWYHQHODVWQRVWLSUHVHMDOQLKWHUPRJUDIRY]DVSUHPOMDQMHþORYHNRYHWHPSHUDWXUH
SULPU]OLFL,(&SRSUDYHN$SU
Medical electrical equipment - Part 2-59: Particular requirements for basic safety and
essential performance of screening thermographs for human febrile temperature
screening (IEC 80601-2-59:2008 + corrigendum Apr. 2009)
Medizinische elektrische Geräte - Teil 2-59: Besondere Anforderungen für die Sicherheit
einschließlich der wesentlichen Leistungsmerkmale von Wärembildkameras für
Reihenuntersuchungen von Menschen auf Fieber (IEC 80601-2-59:2008 + corrigendum
Apr. 2009)
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 (CEI 80601-2-59:2008 + corrigendum Apr. 2009)
Ta slovenski standard je istoveten z: EN 80601-2-59:2009
ICS:
11.040.55 'LDJQRVWLþQDRSUHPD Diagnostic equipment
SIST EN 80601-2-59:2010 en,fr
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN 80601-2-59:2010

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SIST EN 80601-2-59:2010

EUROPEAN STANDARD
EN 80601-2-59

NORME EUROPÉENNE
December 2009
EUROPÄISCHE NORM

ICS 11.040.55


English version


Medical electrical equipment -
Part 2-59: Particular requirements for the basic safety
and essential performance of screening thermographs
for human febrile temperature screening
(IEC 80601-2-59:2008 + corrigendum 2009)


Appareils électromédicaux -  Medizinische elektrische Geräte -
Partie 2-59: Exigences particulières Teil 2-59: Besondere Anforderungen
pour la sécurité de base für die Sicherheit einschließlich
et les performances essentielles der wesentlichen Leistungsmerkmale
des imageurs thermiques von Wärmebildkameras
pour le dépistage des humains fébriles für Reihenuntersuchungen
(CEI 80601-2-59:2008 von Menschen auf Fieber
+ corrigendum 2009) (IEC 80601-2-59:2008
+ Corrigendum 2009)



This European Standard was approved by CENELEC on 2009-11-17. CENELEC members are bound to comply
with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European Standard
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 Central Secretariat or to any CENELEC member.

This European Standard 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 Central Secretariat has the same status as the official versions.

CENELEC members are the national electrotechnical committees of Austria, Belgium, Bulgaria, Cyprus, the
Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia,
Lithuania, Luxembourg, Malta, the Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain,
Sweden, Switzerland and the United Kingdom.

CENELEC
European Committee for Electrotechnical Standardization
Comité Européen de Normalisation Electrotechnique
Europäisches Komitee für Elektrotechnische Normung

Central Secretariat: Avenue Marnix 17, B - 1000 Brussels


© 2009 CENELEC - All rights of exploitation in any form and by any means reserved worldwide for CENELEC members.
Ref. No. EN 80601-2-59:2009 E

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SIST EN 80601-2-59:2010
EN 80601-2-59:2009 - 2 -
Foreword
The text of document 62D/697/FDIS, future edition 1 of IEC 80601-2-59, prepared by SC 62D,
Electromedical equipment, of IEC TC 62, Electrical equipment in medical practice, and SC 3, Lung
ventilators and related equipment, of ISO TC 121, Anaesthetic and respiratory equipment, was submitted
to the IEC-CENELEC parallel vote and was approved by CENELEC as EN 80601-2-59 on 2009-11-17.
The following dates were fixed:
– latest date by which the EN has to be implemented
at national level by publication of an identical
(dop) 2010-09-01
national standard or by endorsement
– latest date by which the national standards conflicting
(dow) 2012-12-01
with the EN have to be withdrawn
This European Standard has been prepared under a mandate given to CENELEC by the European
Commission and the European Free Trade Association and covers essential requirements of
EC Directive MDD (93/42/EEC). See Annex ZZ.
In this standard, the following print types are used:
– Requirements and definitions: roman type.
– Test specifications: italic type.
– Informative material appearing outside of tables,
...