International Standards and Conformity Assessment for all electrical, electronic and related technologies

SC 62A

Common aspects of electrical equipment used in medical practice

 
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SC 62A Publications (48)

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IEC TR 60513:1994

Edition 2.0 (1994-01-08)

Fundamental aspects of safety standards for medical electrical equipment

EN-FR
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IEC 60601-1:2005+AMD1:2012 CSV

Edition 3.1 (2012-08-20)

Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

EN
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IEC 60601-1:2005/COR1:2012+AMD1:2012 CSV

Edition 3.1 (2012-11-14)

Corrigendum 1 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

EN
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IEC 60601-1:2005

Edition 3.0 (2005-12-15)

Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

EN-FR, EN, FR, ES
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IEC 60601-1:2005/ISH1:2008

Edition 3.0 (2008-04-25)

Interpretation sheet 1 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

EN-FR
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IEC 60601-1:2005/ISH2:2009

Edition 3.0 (2009-01-28)

Interpretation sheet 2 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

EN-FR
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IEC 60601-1:2005/ISH3:2013

Edition 3.0 (2013-05-22)

Interpretation sheet 3 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

EN-FR
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IEC 60601-1:2005/COR1:2006

Edition 3.0 (2006-12-12)

Corrigendum 1 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

EN-FR
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IEC 60601-1:2005/COR2:2007

Edition 3.0 (2007-12-07)

Corrigendum 2 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

EN-FR
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IEC 60601-1:2005/AMD1:2012

Edition 3.0 (2012-07-13)

Amendment 1 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

EN-FR
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IEC 60601-1:2005/AMD1:2012/COR1:2014

Edition 3.0 (2014-07-22)

Corrigendum 1 - Amendment 1 - Medical electrical equipment - Part 1: General requirements for basic safety and essential performance

EN-FR
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IEC 60601-1:2014 SER

Edition 1.0 (2014-06-19)

Medical electrical equipment - ALL PARTS

EN-FR
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IEC 60601-1-2:2014

Edition 4.0 (2014-02-25)

Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests

EN-FR
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IEC 60601-1-6:2010+AMD1:2013 CSV

Edition 3.1 (2013-10-29)

Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability

EN-FR
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IEC 60601-1-6:2010

Edition 3.0 (2010-01-27)

Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability

EN-FR, ES
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IEC 60601-1-6:2010/AMD1:2013

Edition 3.0 (2013-10-29)

Amendment 1 - Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability

EN-FR
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IEC 60601-1-8:2006+AMD1:2012 CSV

Edition 2.1 (2012-11-28)

Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems

EN-FR
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IEC 60601-1-8:2006

Edition 2.0 (2006-10-25)

Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems

EN-FR, ES
No preview
IEC 60601-1-8:2006/AMD1:2012

Edition 2.0 (2012-11-28)

Amendment 1 - Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems

EN-FR, ES
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IEC 60601-1-9:2007+AMD1:2013 CSV

Edition 1.1 (2013-06-18)

Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design

EN-FR
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IEC 60601-1-9:2007

Edition 1.0 (2007-07-10)

Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design

EN-FR, ES
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IEC 60601-1-9:2007/AMD1:2013

Edition 1.0 (2013-06-18)

Amendment 1 - Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design

EN-FR, ES
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IEC 60601-1-10:2007+AMD1:2013 CSV

Edition 1.1 (2013-11-27)

Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers

EN-FR
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IEC 60601-1-10:2007

Edition 1.0 (2007-11-21)

Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers

EN-FR, ES
No preview
IEC 60601-1-10:2007/AMD1:2013

Edition 1.0 (2013-11-27)

Amendment 1 - Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers

EN-FR
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IEC 60601-1-11:2010

Edition 1.0 (2010-04-28)

Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment

EN-FR
No preview
IEC 60601-1-11:2010/COR1:2011

Edition 1.0 (2011-04-20)

Corrigendum 1 - Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment

EN-FR
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IEC 60601-1-12:2014

Edition 1.0 (2014-06-19)

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

EN-FR
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IEC TR 60878:2003

Edition 2.0 (2003-07-07)

Graphical symbols for electrical equipment in medical practice

EN-FR
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IEC TR 60930:2008

Edition 2.0 (2008-09-19)

Guidelines for administrative, medical and nursing staff concerned with the safe use of medical electrical equipment and medical electrical systems

EN
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IEC TR 61258:2008

Edition 2.0 (2008-08-28)

Guidelines for the development and use of medical electrical equipment educational materials

EN
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IEC TR 62296:2009

Edition 2.0 (2009-01-22)

Considerations of unaddressed safety aspects in the second edition of IEC 60601-1 and proposals for new requirements

EN
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IEC 62304:2006

Edition 1.0 (2006-05-09)

Medical device software - Software life cycle processes

EN-FR, EN, FR, ES
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IEC TR 62348:2012

Edition 2.0 (2012-12-12)

Assessment of the impact of the most significant changes in Amendment 1 to IEC 60601-1:2005 and mapping of the clauses of IEC 60601-1:2005 to the previous edition

EN
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IEC 62353:2014

Edition 2.0 (2014-09-04)

Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment

EN-FR
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IEC TR 62354:2014

Edition 3.0 (2014-09-25)

General testing procedures for medical electrical equipment

EN
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IEC 62366:2007+AMD1:2014 CSV

Edition 1.1 (2014-01-28)

Medical devices - Application of usability engineering to medical devices

EN-FR
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IEC 62366:2007

Edition 1.0 (2007-10-18)

Medical devices - Application of usability engineering to medical devices

EN-FR, ES
No preview
IEC 62366:2007/AMD1:2014

Edition 1.0 (2014-01-28)

Amendment 1 - Medical devices - Application of usability engineering to medical devices

EN-FR
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IEC 80001-1:2010

Edition 1.0 (2010-10-27)

Application of risk management for IT-networks incorporating medical devices - Part 1: Roles, responsibilities and activities

EN-FR, ES
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IEC TR 80001-2-1:2012

Edition 1.0 (2012-07-10)

Application of risk management for IT-networks incorporating medical devices - Part 2-1: Step by step risk management of medical IT-networks - Pratical applications and examples

EN
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IEC TR 80001-2-2:2012

Edition 1.0 (2012-07-10)

Application of risk management for IT-networks incorporating medical devices - Part 2-2: Guidance for the disclosure and communication of medical device security needs, risks and controls

EN
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IEC TR 80001-2-3:2012

Edition 1.0 (2012-07-10)

Application of risk management for IT-networks incorporating medical devices - Part 2-3: Guidance for wireless networks

EN
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IEC TR 80001-2-4:2012

Edition 1.0 (2012-11-29)

Application of risk management for IT-networks incorporating medical devices - Part 2-4: Application guidance - General implementation guidance for healthcare delivery organizations

EN
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IEC TR 80002-1:2009

Edition 1.0 (2009-09-23)

Medical device software - Part 1: Guidance on the application of ISO 14971 to medical device software

EN
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IEC TR 80002-3:2014

Edition 1.0 (2014-06-04)

Medical device software - Part 3: Process reference model of medical device software life cycle processes (IEC 62304)

EN
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ISO TR 17791/COR1:2013

Edition .0 (2013-12-05)

Health informatics -- Guidance on standards for enabling safety in health software

EN
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ISO TR 24971:2013

Edition 1.0 (2013-06-19)

Medical devices -- Guidance on the application of ISO 14971

EN