NF EN 1060-1+A2
NF EN 1060-1+A2

NF EN 1060-1+A2

March 2010
Standard Cancelled

Non-invasive sphygmomanometers - Part 1 : general requirements

Le présent document spécifie les exigences applicables aux tensiomètres non invasifs et à leurs accessoires, utilisés pour la mesure de la pression artérielle, ainsi que les méthodes d'essai correspondantes.Le présent document est une norme harmonisée rentrant dans le cadre des directives 98/42/CE et 2007/47/CE.

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Main informations

Collections

National standards and national normative documents

Publication date

March 2010

Number of pages

13 p.

Reference

NF EN 1060-1+A2

ICS Codes

11.040.55   Diagnostic equipment

Classification index

S97-101

Print number

1 - février 2010

European kinship

EN 1060-1+A2:2009
Sumary
Non-invasive sphygmomanometers - Part 1 : general requirements

Le présent document spécifie les exigences applicables aux tensiomètres non invasifs et à leurs accessoires, utilisés pour la mesure de la pression artérielle, ainsi que les méthodes d'essai correspondantes. Le présent document est une norme harmonisée rentrant dans le cadre des directives 98/42/CE et 2007/47/CE.
Replaced standards (2)
NF EN 1060-1
NF EN 1060-1
January 1996
Standard Cancelled
Non-invasive sphygmomanometers. Part 1 : general requirements.

Le présent document spécifie les exigences applicables aux tensiomètres non invasifs et à leurs accessoires, utilisés pour la mesure de la pression artérielle, ainsi que les méthodes d'essai correspondantes.

NF EN 1060-1/A1
NF EN 1060-1/A1
September 2002
Standard Cancelled
Non-invasive sphygmomanometers - Part 1 : general requirements

Le présent document modifie l'item a) du paragraphe 9.3.

Standard replaced by (1)
NF EN ISO 81060-1
NF EN ISO 81060-1
August 2012
Standard Current
Non-invasive sphygmomanometers — Part 1: Requirements and test methods for non-automated measurement type

Table of contents
  • Avant-propos
    3
  • 1 Domaine d'application
    4
  • 2 Références normatives
    4
  • 3 Définitions
    4
  • 4 Brassard
    5
  • 5 Affichage
    5
  • 6 Unités
    5
  • 7 Exigences
    5
  • 8 Méthodes d'essai
    6
  • 9 Informations fournies par le fabricant
    8
  • Annexe ZA (informative) PD Relation entre la présente Norme européenne et les exigences essentielles de la Directive européenne 93/42/CEE relative aux dispositifs médicaux
    10
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