IEC 80601-2-30:2009
Medical electrical equipment - Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometers

Standard No.

IEC 80601-2-30:2009

Release Date

2009

Published By

International Electrotechnical Commission (IEC)

Status

Be replaced 2013-09

Replace By

IEC 80601-2-30:2009/COR1:2010

Latest

IEC 80601-2-30:2018 RLV

Replace

IEC 62D/721/FDIS:2008 IEC 60601-2-30:1999 IEC/FDIS 80601-2-30:2008

Scope

Inhaltsverzeichnis

IEC 80601-2-30:2009 Referenced Document

• IEC 60068-2-27:2008 Environmental testing - Part 2-27: Tests - Test Ea and guidance: Shock
• IEC 60068-2-31:2008 Environmental testing - Part 2-31: Tests - Test Ec: Rough handling shocks, primarily for equipment-type specimens
• IEC 60068-2-64:2008 Environmental testing - Part 2-64: Tests - Test Fh: Vibration, broad-band random and guidance
• IEC 60601-1-11:2010 Medical electrical equipmentPart 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*， 2013-12-02 Update
• IEC 60601-1-2:2007 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests
• IEC 60601-1-6:2010 Medical electrical equipment - General requirements for basic safety and essential performance - Collateral Standard: Usability*， 2010-01-01 Update
• IEC 60601-1-8:2006 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
• IEC 60601-2-2:2009 Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories*， 2009-02-01 Update
• IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
• ISO 594-1:1986 Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment; Part 1 : General requirements
• ISO 594-2:1991 Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment; part 2: lock fittings
• ISO 81060-2:2013 Non-invasive sphgmomanometers-Part 2:Clinical investigation of automated measurement type*， 2024-04-19 Update

IEC 80601-2-30:2009 history

• 0000 IEC 80601-2-30:2018 RLV
• 2013 IEC 80601-2-30:2009/AMD1:2013 Amendment 1 - Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated type non-invasive sphygmomanometers
• 2013 IEC 80601-2-30:2013 Medical electrical equipment - Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygnomanometers
• 2010 IEC 80601-2-30:2009/COR1:2010 Appareils électromédicaux – Partie 2-30: Exigences particulières pour la sécurité de base et les performances essentielles des sphygmomanomètres non invasifs automatiques CORRIGENDUM 1 (Edition 1.0)
• 2009 IEC 80601-2-30:2009 Medical electrical equipment - Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometers

IEC 80601-2-30:2009 Medical electrical equipment - Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometers has been changed from IEC 60601-2-30:1999 Medical electrical equipment - Part 2-30: Particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment.