SIST EN 60601-2-30:2002

Medical electrical equipment - Part 2-30: Particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment (IEC 60601-2-30:1999)

Specifies particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment, with special attention being paid to the avoidance of hazards due to the inflation process.

Medizinische elektrische Geräte - Teil 2-30: Besondere Festlegungen für die Sicherheit, einschließlich der wesentlichen Leistungsfähigkeit von automatischen, zyklischen, nicht-invasiven Blutdrucküberwachungsgeräten (IEC 60601-2-30:1999)

Appareils électromédicaux - Partie 2-30: Règles particulières de sécurité et performances essentielles des appareils de surveillance de la pression sanguine prélevée indirectement, automatiquement et périodiquement (CEI 60601-2-30:1999)

Medicinska električna oprema - 2-30. del: Posebne varnostne zahteve za opremo, vključno z njenimi osnovnimi lastnostmi, za posredno nadzorovanje krvnega tlaka z avtomatičnim cikliranjem (IEC 60601-2-30:1999)

General Information

• Status: Withdrawn
• Publication Date: 31-Jan-2002
• Withdrawal Date: 19-Apr-2016
• ICS: 11.040.55 - Diagnostic equipment
• Technical Committee: IEMO - Electrical equipment in medical practice
• Current Stage: 9900 - Withdrawal (Adopted Project)
• Start Date: 19-Apr-2016
• Due Date: 12-May-2016
• Completion Date: 20-Apr-2016
• Directive: 93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Mandate: M/023 - Standardization mandate to CEN/CENELEC concerning the development of European standards relating to medical devices
• Ref Project: EN 60601-2-30:2000 - Medical electrical equipment - Part 2-30: Particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment

Relations

• Revised: SIST EN 80601-2-30:2010 - Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers (IEC 80601-2-30:2009 + corrigendum Jan. 2010)
• Effective Date: 03-Sep-2013
• Replaced By: SIST EN 80601-2-30:2010 - Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers (IEC 80601-2-30:2009 + corrigendum Jan. 2010)
• Effective Date: 28-Jan-2023
• Replaced By: SIST EN 80601-2-30:2010 - Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers (IEC 80601-2-30:2009 + corrigendum Jan. 2010)
• Effective Date: 07-Jun-2022
• Official Journal Project Relation: SIST EN 60601-2-30:1998 - Medical electrical equipment -- Part 2: Particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment
• Effective Date: 18-May-2009
• Replaces: SIST EN 60601-2-30:1998 - Medical electrical equipment -- Part 2: Particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment
• Effective Date: 29-Jan-2023
• Replaces: SIST EN 60601-2-30:1998 - Medical electrical equipment -- Part 2: Particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment
• Effective Date: 07-Jun-2022

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN 60601-2-30:2002
01-februar-2002
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SIST EN 60601-2-30:1998
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Medical electrical equipment - Part 2-30: Particular requirements for the safety, including
essential performance, of automatic cycling non-invasive blood pressure monitoring
equipment (IEC 60601-2-30:1999)
Medizinische elektrische Geräte - Teil 2-30: Besondere Festlegungen für die Sicherheit,
einschließlich der wesentlichen Leistungsfähig
...