Medical electrical equipment - Part 2-83: Particular requirements for the basic safety and essential performance of home light therapy equipment

IEC 60601-2-83:2019 is applicable to the BASIC SAFETY and ESSENTIAL PERFORMANCE of HOME LIGHT THERAPY EQUIPMENT, intended for use in the HOME HEALTHCARE ENVIRONMENT. HOME LIGHT THERAPY EQUIPMENT is typically used by a LAY OPERATOR. The scope of this document includes all light sources except laser.

Medizinische elektrische Geräte - Teil 2-83: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Heim-Lichttherapiegeräten

Appareils électromédicaux - Partie 2-83: Exigences particulières pour la sécurité de base et les performances essentielles des appareils de luminothérapie à domicile

IEC 60601-2-83:2019 s'applique à la SÉCURITÉ DE BASE et aux PERFORMANCES ESSENTIELLES des APPAREILS DE LUMINOTHÉRAPIE À DOMICILE conçus pour être utilisés dans l'ENVIRONNEMENT DES SOINS A DOMICILE. Les APPAREILS DE LUMINOTHÉRAPIE À DOMICILE sont généralement utilisés par un OPERATEUR NON SPECIALISTE. Le domaine d'application du présent document comprend toutes les sources de lumière à l'exception des lasers.

Medicinska električna oprema - 2-83. del: Posebne zahteve za osnovno varnost in bistvene lastnosti opreme za svetlobno terapijo na domu (IEC 60601-2-83:2019)

General Information

Status
Published
Publication Date
02-Apr-2020
Current Stage
6060 - Document made available - Publishing
Start Date
03-Apr-2020
Completion Date
03-Apr-2020

Relations

Buy Standard

Standard
EN IEC 60601-2-83:2020 - BARVE
English language
34 pages
sale 10% off
Preview
sale 10% off
Preview
e-Library read for
1 day

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN IEC 60601-2-83:2020
01-junij-2020
Medicinska električna oprema - 2-83. del: Posebne zahteve za osnovno varnost in
bistvene lastnosti opreme za svetlobno terapijo na domu (IEC 60601-2-83:2019)
Medical electrical equipment - Part 2-83: Particular requirements for the basic safety and
essential performance of home light therapy equipment (IEC 60601-2-83:2019)
Medizinische elektrische Geräte - Teil 2-83: Besondere Festlegungen für die Sicherheit
einschließlich der wesentlichen Leistungsmerkmale von Heim-Lichttherapiegeräten (IEC
60601-2-83:2019)
Medizinische elektrische Geräte - Teil 2-83: Besondere Festlegungen für die Sicherheit
einschließlich der wesentlichen Leistungsmerkmale von Heim-Lichttherapiegeräten (IEC
60601-2-83:2019)
Ta slovenski standard je istoveten z: EN IEC 60601-2-83:2020
ICS:
11.040.60 Terapevtska oprema Therapy equipment
SIST EN IEC 60601-2-83:2020 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------
SIST EN IEC 60601-2-83:2020

---------------------- Page: 2 ----------------------
SIST EN IEC 60601-2-83:2020


EUROPEAN STANDARD EN IEC 60601-2-83

NORME EUROPÉENNE

EUROPÄISCHE NORM
April 2020
ICS 11.040.60

English Version
Medical electrical equipment - Part 2-83: Particular requirements
for the basic safety and essential performance of home light
therapy equipment
(IEC 60601-2-83:2019)
Appareils électromédicaux - Partie 2-83: Exigences Medizinische elektrische Geräte - Teil 2-83: Besondere
particulières pour la sécurité de base et les performances Festlegungen für die Sicherheit einschließlich der
essentielles des appareils de luminothérapie à domicile wesentlichen Leistungsmerkmale von Heim-
(IEC 60601-2-83:2019) Lichttherapiegeräten
(IEC 60601-2-83:2019)
This European Standard was approved by CENELEC on 2020-01-01. 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 CEN-CENELEC
Management Centre 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 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
© 2020 CENELEC All rights of exploitation in any form and by any means reserved worldwide for CENELEC Members.
 Ref. No. EN IEC 60601-2-83:2020 E

---------------------- Page: 3 ----------------------
SIST EN IEC 60601-2-83:2020
EN IEC 60601-2-83:2020 (E)
European foreword
The text of document 62D/1682/FDIS, future edition 1 of IEC 60601-2-83, 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 60601-2-83:2020.
The following dates are fixed:
• latest date by which the document has to be implemented at national (dop) 2020-10-03
level by publication of an identical national standard or by endorsement
• latest date by which the national standards conflicting with the (dow) 2023-04-03
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.
This document has been prepared under a mandate given to CENELEC by the European
Commission and the European Free Trade Association.
Endorsement notice
The text of the International Standard IEC 60601-2-83:2019 was approved by CENELEC as a
European Standard without any modification.
In the official version, for Bibliography, the following notes have to be added for the standards
indicated:
IEC 60335-2-113 NOTE Harmonized as FprEN 60335-2-113 to be published
IEC 60601-2-57:2011 NOTE Harmonized as EN 60601-2-57:2011 (not modified)
IEC 60601-1-10 NOTE Harmonized as EN 60601-1-10
IEC 60601-1-12 NOTE Harmonized as EN 6
...

Questions, Comments and Discussion

Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.