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SIST EN 60601-2-6:2015/A1:2016

(Amendment)

Medical electrical equipment - Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipment - Proposed Horizontal Standard (IEC 60601-2-6:2012/A1:2016)

Medical electrical equipment - Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipment - Proposed Horizontal Standard (IEC 60601-2-6:2012/A1:2016)

Medizinische elektrische Geräte - Teil 2-6: Besondere Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale von Mikrowellen-Therapiegeräten (IEC 60601-2-6:2012/A1:2016)

Appareils électromédicaux - Partie 2-6: Exigences particulières pour la sécurité de base et les performances essentielles des appareils de thérapie à micro-ondes (IEC 60601-2-6:2012/A1:2016)

Medicinska električna oprema - 2-6. del: Posebne zahteve za osnovno varnost in bistvene lastnosti opreme za mikrovalovno terapijo - Predlagani horizontalni standard - Dopolnilo A1 (IEC 60601-2-6:2012/A1:2016)

General Information

Status
Published
Publication Date
19-Oct-2016
ICS
11.040.60 - Therapy equipment
Technical Committee
IEMO - Electrical equipment in medical practice
Current Stage
6060 - National Implementation/Publication (Adopted Project)
Start Date
05-Oct-2016
Due Date
10-Dec-2016
Completion Date
20-Oct-2016
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
EN 60601-2-6:2015/A1:2016 - Medical electrical equipment - Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipment

Relations

Amends
SIST EN 60601-2-6:2015 - Medical electrical equipment - Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipment
Effective Date
10-Mar-2015

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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN 60601-2-6:2015/A1:2016
01-december-2016
0HGLFLQVNDHOHNWULþQDRSUHPDGHO3RVHEQH]DKWHYH]DRVQRYQRYDUQRVWLQ
ELVWYHQHODVWQRVWLRSUHPH]DPLNURYDORYQRWHUDSLMR3UHGODJDQLKRUL]RQWDOQL
VWDQGDUG'RSROQLOR$ ,(&$
Medical electrical equipment - Part 2-6: Particular requirements for the basic safety and
essential performance of microwave therapy equipment - Proposed Horizontal Standard
(IEC 60601-2-6:2012/A1:2016)
Medizinische elektrische Geräte - Teil 2-6: Besondere Festlegungen für die Sicherheit
einschließlich der wesentlichen Leistungsmerkmale von Mikrowellen-Therapiegeräten
(IEC 60601-2-6:2012/A1:2016)
Appareils électromédicaux - Partie 2-6: Exigences particulières pour la sécurité de base
et les performances essentielles des appareils de thérapie à micro-ondes (IEC 60601-2-
6:2012/A1:2016)
Ta slovenski standard je istoveten z: EN 60601-2-6:2015/A1:2016
ICS:
11.040.60 Terapevtska oprema Therapy equipment
SIST EN 60601-2-6:2015/A1:2016 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------

SIST EN 60601-2-6:2015/A1:2016

---------------------- Page: 2 ----------------------

SIST EN 60601-2-6:2015/A1:2016


EUROPEAN STANDARD EN 60601-2-6:2015/A1

NORME EUROPÉENNE

EUROPÄISCHE NORM
September 2016
ICS 11.040.60

English Version
Medical electrical equipment - Part 2-6: Particular requirements
for the basic safety and essential performance of microwave
therapy equipment
(IEC 60601-2-6:2012/A1:2016)
Appareils électromédicaux - Partie 2-6: Exigences Medizinische elektrische Geräte - Teil 2-6: Besondere
particulières pour la sécurité de base et les performances Festlegungen für die Sicherheit einschließlich der
essentielles des appareils de thérapie à micro-ondes wesentlichen Leistungsmerkmale von Mikrowellen-
(IEC 60601-2-6:2012/A1:2016) Therapiegeräten
(IEC 60601-2-6:2012/A1:2016)
This amendment A1 modifies the European Standard EN 60601-2-6:2015; it was approved by CENELEC on 2016-06-03. 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, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia,
Lithuania, Luxembourg, Malta, the Netherlands, Norway, Poland, Portugal, Romania, 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: Avenue Marnix 17, B-1000 Brussels
© 2016 CENELEC All rights of exploitation in any form and by any means reserved worldwide for CENELEC Members.
 Ref. No. EN 60601-2-6:2015/A1:2016 E

---------------------- Page: 3 ----------------------

SIST EN 60601-2-6:2015/A1:2016
EN 60601-2-6:2015/A1:2016
European foreword
The text of document 62D/1331/FDIS, future IEC 60601-2-6:2012/A1, 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 60601-2-6:2015/A1:2016.
The following dates are fixed:
(dop) 2017-03-30
• latest date by which the document has to be implemented at
national level by publication of an identical national
standard or by endorsement
(dow) 2019-09-30
• latest date by which the national standards conflicting with
the document have to be withdrawn

Attention is drawn to t
...

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