NF EN ISO 10555-1

NF EN ISO 10555-1

August 2009
Standard Cancelled

Sterile, single-use intravascular catheters - Part 1 : general requirements

Le présent document fixe des prescriptions générales relatives aux cathéters intravasculaires stériles non réutilisables. Il ne s'applique pas aux accessoires.

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Main informations

Collections

National standards and national normative documents

Publication date

August 2009

Number of pages

27 p.

Reference

NF EN ISO 10555-1

ICS Codes

11.040.25   Syringes, needles and catheters

Classification index

S93-031-1

Print number

1 - 20/07/2009

International kinship

ISO 10555-1:1995

European kinship

EN ISO 10555-1:2009
Sumary
Sterile, single-use intravascular catheters - Part 1 : general requirements

Le présent document fixe des prescriptions générales relatives aux cathéters intravasculaires stériles non réutilisables. Il ne s'applique pas aux accessoires.
Replaced standards (3)
NF EN ISO 10555-1
January 1997
Standard Cancelled
Sterile, single-use intravascular catheters - Part 1 : general requirements

NF EN ISO 10555-1/A1
February 2000
Standard Cancelled
Sterile, single-use intravascular catheters - Part 1 : general requirements

Le présent document introduit dans la NF EN ISO 10555-1 des prescriptions générales relatives aux cathéters hydratables.

NF EN ISO 10555-1/A2
November 2004
Standard Cancelled
Sterile, single-use intravascular catheters - Part 1 : general requirements

Le présent document ajoute les informations relatives au revêtement, en vue de modifier les propriétés antithrombiques et/ou antimicrobiennes des cathéters.

Standard replaced by (1)
NF EN ISO 10555-1
August 2013
Standard Cancelled
Intravascular catheters - Sterile and single-use catheters - Part 1 : general requirements

ISO 10555-1:2013 specifies general requirements for intravascular catheters, supplied in the sterile condition and intended for single use, for any application.

Table of contents
  • 1 Domaine d'application
    1
  • 2 Références normatives
    1
  • 3 Définitions
    1
  • 4 Prescriptions
    3
  • 5 Désignation de la dimension nominale
    3
  • 6 Informations à fournir par le fabricant
    4 Annexe A Méthode d'essai de résistance à la corrosion 5
  • Annexe B Méthode de détermination de la force de rupture
    6
  • Annexe C Méthode d'essai de fuite de liquide sous pression
    7
  • Annexe D Méthode d'essai de fuite d'air au niveau de l'assemblage de l'embase pendant l'aspiration
    8
  • Annexe E Bibliographie
    9
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