Medical electrical equipment - Part 1-12: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment

2020-10-13:JO-CLC/TC 62 Decision  2019-05-21/22 in Oslo to remove the link to the published standard

Medizinische elektrische Geräte - Teil 1-12: Allgemeine Festlegungen für die Sicherheit einschließlich der wesentlichen Leistungsmerkmale - Ergänzungsnorm: Anforderungen an medizinische elektrische Geräte und medizinische elektrische Systeme in der Umgebung für den Notfalleinsatz

Appareils électromédicaux - Partie 1-12: Exigences générales pour la sécurité de base et les performances essentielles - Norme collatérale: Exigences pour les appareils électromédicaux et les systèmes électromédicaux destinés à être utilisés dans l'environnement des services médicaux d'urgence

Medicinska električna oprema - 1-12. del: Splošne zahteve za osnovno varnost in bistvene lastnosti - Spremljevalni standard: Zahteve za elektromedicinsko opremo in elektromedicinske sisteme, namenjene za uporabo v okolju nujne medicinske pomoči - Dopolnilo A1 (IEC 60601-1-12:2014/A1:2020)

General Information

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

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EN 60601-1-12:2015/A1:2020
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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN 60601-1-12:2015/A1:2020
01-november-2020
Medicinska električna oprema - 1-12. del: Splošne zahteve za osnovno varnost in
bistvene lastnosti - Spremljevalni standard: Zahteve za elektromedicinsko opremo
in elektromedicinske sisteme, namenjene za uporabo v okolju nujne medicinske
pomoči - Dopolnilo A1 (IEC 60601-1-12:2014/A1:2020)
Medical electrical equipment - Part 1-12: General requirements for basic safety and
essential performance - Collateral Standard: Requirements for medical electrical
equipment and medical electrical systems intended for use in the emergency medical
services environment (IEC 60601-1-12:2014/A1:2020)
Medizinische elektrische Geräte - Teil 1-12: Allgemeine Festlegungen für die Sicherheit
einschließlich der wesentlichen Leistungsmerkmale - Ergänzungsnorm: Anforderungen
an medizinische elektrische Geräte und medizinische elektrische Systeme in der
Umgebung für den Notfalleinsatz (IEC 60601-1-12:2014/A1:2020)
Appareils électromédicaux - Partie 1-12: Exigences générales pour la sécurité de base
et les performances essentielles - Norme collatérale: Exigences pour les appareils
électromédicaux et les systèmes électromédicaux destinés à être utilisés dans
l'environnement des services médicaux d'urgence (IEC 60601-1-12:2014/A1:2020)
Ta slovenski standard je istoveten z: EN 60601-1-12:2015/A1:2020
ICS:
11.040.01 Medicinska oprema na Medical equipment in general
splošno
SIST EN 60601-1-12:2015/A1:2020 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN 60601-1-12:2015/A1:2020

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SIST EN 60601-1-12:2015/A1:2020


EUROPEAN STANDARD EN 60601-1-12:2015/A1

NORME EUROPÉENNE

EUROPÄISCHE NORM
September 2020
ICS 11.040

English Version
Medical electrical equipment - Part 1-12: General requirements
for basic safety and essential performance - Collateral Standard:
Requirements for medical electrical equipment and medical
electrical systems intended for use in the emergency medical
services environment
(IEC 60601-1-12:2014/A1:2020)
Appareils électromédicaux - Partie 1-12: Exigences Medizinische elektrische Geräte - Teil 1-12: Allgemeine
générales pour la sécurité de base et les performances Festlegungen für die Sicherheit einschließlich der
essentielles - Norme collatérale: Exigences pour les wesentlichen Leistungsmerkmale - Ergänzungsnorm:
appareils électromédicaux et les systèmes électromédicaux Anforderungen an medizinische elektrische Geräte und
destinés à être utilisés dans l'environnement des services medizinische elektrische Systeme in der Umgebung für den
médicaux d'urgence Notfalleinsatz
(IEC 60601-1-12:2014/A1:2020) (IEC 60601-1-12:2014/A1:2020)
This amendment A1 modifies the European Standard EN 60601-1-12:2015; it was approved by CENELEC on 2020-08-26. 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, 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 60601-1-12:2015/A1:2020 E

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SIST EN 60601-1-12:2015/A1:2020
EN 60601-1-12:2015/A1:2020 (E)
European foreword
The text of document 62A/1396/FDIS, future IEC 60601-1-12/A1, prepared by SC 62A "Common
aspects of electrical equipment used in medical practice" of IEC/TC 62 "Electrical equipment in
medical practice" was submitted to the IEC-CENELEC parallel vote and approved by CENELEC as
EN 60601-1-12:2015/A1:2020.
The following dates are fixed:
• latest date by which the document has to be implemented at na
...

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