EN 1060-3:1997/A1:2005

Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems

Few changes in the text, deletion of Annex A and changes in Annex ZA.1.

Nichtinvasive Blutdruckmessgeräte - Teil 3: Ergänzende Anforderungen für elektromechanische Blutdruckmesssysteme

Tensiomètres non invasifs - Partie 3: Exigences complémentaires concernant les systèmes électromécaniques de measure de la pression sanguine

Neinvazivni sfigmomanometri - 3. del: Dodatne zahteve za elektromehanske sisteme za merjenje krvnega tlaka

General Information

• Status: Withdrawn
• Publication Date: 20-Dec-2005
• Withdrawal Date: 17-Nov-2009
• ICS: 11.040.50 - Radiographic equipment
• Technical Committee: CEN/SS S99 - Health, environment and medical equipment - Undetermined
• Drafting Committee: CEN/SS S99 - Health, environment and medical equipment - Undetermined
• Current Stage: 9960 - Withdrawal effective - Withdrawal
• Start Date: 18-Nov-2009
• Completion Date: 18-Nov-2009
• 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: SIST EN 1060-3:2000/A1:2006 - Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems

Relations

• Merged Into: EN 1060-3:1997+A2:2009 - Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems
• Effective Date: 26-Sep-2009
• Amends: EN 1060-3:1997 - Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems
• Effective Date: 22-Dec-2008

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN 1060-3:2000/A1:2006
01-februar-2006
Neinvazivni sfigmomanometri - 3. del: Dodatne zahteve za elektromehanske
sisteme za merjenje krvnega tlaka
Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-
mechanical blood pressure measuring systems
Nichtinvasive Blutdruckmessgeräte - Teil 3: Ergänzende Anforderungen für
elektromechanische Blutdruckmesssysteme
Tensiometres non invasifs - Partie 3: Exigences complémentaires concernant les
systemes électromécaniques de measure de la pression sanguine
Ta slovenski standard je istoveten z: EN 1060-3:1997/A1:2005
ICS:
11.040.55 'LDJQRVWLþQDRSUHPD Diagnostic equipment
SIST EN 1060-3:2000/A1:2006 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN 1060-3:2000/A1:2006

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SIST EN 1060-3:2000/A1:2006
EUROPEAN STANDARD
EN 1060-3:1997/A1
NORME EUROPÉENNE
EUROPÄISCHE NORM
December 2005
ICS 11.040.50

English Version
Non-invasive sphygmomanometers - Part 3: Supplementary
requirements for electro-mechanical blood pressure measuring
systems
Tensiomètres non invasifs - Partie 3: Exigences Nichtinvasive Blutdruckmessgeräte - Teil 3: Ergänzende
complémentaires concernant les systèmes Anforderungen für elektromechanische
électromécaniques de measure de la pression sanguine Blutdruckmesssysteme
This amendment A1 modifies the European Standard EN 1060-3:1997; it was approved by CEN on 24 November 2005.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for inclusion of this
amendment into the relevant national standard without any alteration. Up-to-date lists and bibliographical references concerning such
national standards may be obtained on application to the Central Secretariat or to any CEN 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 CEN member into its own language and notified to the Central Secretariat has the same status as the official versions.
CEN members are the national standards bodies of Austria, Belgium, Cyprus, Czech Republic, Denmark, Estonia, Finland, France,
Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Slovakia,
Slovenia, Spain, Sweden, Switzerland and United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre: rue de Stassart, 36  B-1050 Brussels
© 2005 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN 1060-3:1997/A1:2005: E
worldwide for CEN national Members.

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SIST EN 1060-3:2000/A1:2006
EN 1060-3:1997/A1:2005 (E)
Contents Page
Foreword .3
Revised text.4
2 Normative references.4
3 Terms and definitions.4
7.3.1 Internal electrical power source .5
7.3.2 External electrical power source .5
7.9 Overall system accuracy .5

Annex A .5
Annex ZA.1:.5

2

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SIST EN 1060-3:2000/A1:2006
EN 1060-3:1997/A1:2005 (E)
Foreword
This European Standard (EN 1060-3:1997/A1:2005) has been prepared by Technical Committee CEN/TC 205
“Non-active medical devices”, the secretariat of which is held by DIN.
This Amendment to the European Standard EN 1060-3:1997 shall be given the status of a national standard,
either by publication of an identical text or by endorsement, at the latest by June 2006, and conflicting national
standards shall be withdrawn at the latest by June 2006.
This document has been prepared unde
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