EN 1060-1:1995/FprA2
(Amendment)Non-invasive sphygmomanometers - Part 1: General requirements
Non-invasive sphygmomanometers - Part 1: General requirements
Nichtinvasive Blutdruckmeßgeräte - Teil 1: Allgemeine Anforderungen
Tensiomètres non invasifs - Partie 1: Exigences générales
Neinvazivni sfigmomanometri - 1. del: Splošne zahteve
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Standards Content (Sample)
SLOVENSKI STANDARD
01-september-2009
Neinvazivni sfigmomanometri - 1. del: Splošne zahteve
Non-invasive sphygmomanometers - Part 1: General requirements
Nichtinvasive Blutdruckmeßgeräte - Teil 1: Allgemeine Anforderungen
Tensiomètres non invasifs - Partie 1: Exigences générales
Ta slovenski standard je istoveten z: EN 1060-1:1995/FprA2
ICS:
11.040.55 'LDJQRVWLþQDRSUHPD Diagnostic equipment
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
EUROPEAN STANDARD
FINAL DRAFT
EN 1060-1:1995
NORME EUROPÉENNE
EUROPÄISCHE NORM
FprA2
May 2009
ICS 11.040.55
English Version
Non-invasive sphygmomanometers - Part 1: General
requirements
Tensiomètres non invasifs - Partie 1: Exigences générales Nichtinvasive Blutdruckmeßgeräte - Teil 1: Allgemeine
Anforderungen
This draft amendment is submitted to CEN members for unique acceptance procedure. It has been drawn up by the Technical Committee
CEN/TC 205.
This draft amendment A2, if approved, will modify the European Standard EN 1060-1:1995. If this draft becomes an amendment, 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.
This draft amendment was established by CEN 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 CEN Management Centre has the same
status as the official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland,
France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal,
Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
Warning : This document is not a European Standard. It is distributed for review and comments. It is subject to change without notice and
shall not be referred to as a European Standard.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2009 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN 1060-1:1995/FprA2:2009: E
worldwide for CEN national Members.
Contents Page
Foreword .3
1 Modifications to Clause 2 .4
2 Modification to 9.1 .4
3 Modification to 9.2 .4
4 Modification to 9.3 .4
5 Modifications to Annex ZA .4
Foreword
This document (EN 1060-1:1995/FprA2:2009) has been prepared by Technical Committee CEN/TC 205 “Non-
active medical devices”, the secretariat of which is held by DIN.
This document is currently submitted to the Unique Acceptance Procedure.
This document has been prepared under a mandate given to CEN by the European Commission and the
European Free Trade Association, and supports essential requiremen
...
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