NF EN ISO 11608-2

NF EN ISO 11608-2

July 2012
Standard Cancelled

Needle-based injection systems for medical use - Requirements and test methods - Part 2 : needles

ISO 11608-2:2012 specifies requirements and test methods for single-use, double-ended, sterile needles for needle-based injection systems (NISs) that fulfil the specifications of ISO 11608-1.

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Main informations

Collections

National standards and national normative documents

Publication date

July 2012

Number of pages

25 p.

Reference

NF EN ISO 11608-2

ICS Codes

11.040.20   Transfusion, infusion and injection equipment
11.040.25   Syringes, needles and catheters

Classification index

S93-020-2

Print number

1 - 09/07/2012

International kinship

European kinship

EN ISO 11608-2:2012
Sumary
Needle-based injection systems for medical use - Requirements and test methods - Part 2 : needles

ISO 11608-2:2012 specifies requirements and test methods for single-use, double-ended, sterile needles for needle-based injection systems (NISs) that fulfil the specifications of ISO 11608-1.

Replaced standards (1)
NF EN ISO 11608-2
July 2001
Standard Cancelled
Pen-injectors for medical use - Part 2 : needles - Requirements and test methods

La présente partie de l'ISO 11608 spécifie les exigences et les méthodes d'essai des aiguilles non réutilisables stériles à deux pointes, destinées aux stylos-injecteurs conformes aux spécifications de l'ISO 11608-1. Elle ne s'applique pas aux aiguilles pour usage dentaire.

Standard replaced by (1)
Standard Current
Needle-based injection systems for medical use - Requirements and test methods - Part 2 : double-ended pen needles

This document specifies requirements and test methods for single-use, double-ended, sterile needles intended to be used with some needle-based injection systems (NISs) that use a non-integrated double-ended needle according to ISO 11608-1. This document is not applicable to the following: —    needles for dental use; —    pre-attached syringe needles; —    hypodermic needles; —    needles intended for different routes of administration (e.g. intravenous, intrathecal, intraocular); —    materials that form the medicinal product contact surfaces of the primary container closure. However, while this document is not intended to directly apply to these needle products, it does contain requirements and tests methods that can be used to help design and evaluate them. NOTE       Needles provided by the manufacturer integrated into the fluid path or container are covered in ISO 11608‑3, and hypodermic needles provided separately are covered in ISO 7864.

Table of contents
  • Avant-propos
    iv
  • Introduction
    v
  • 1 Domaine d'application
    1
  • 2 Références normatives
    1
  • 3 Termes et définitions
    1
  • 4 Exigences
    3
  • 4.1 Matériaux
    3
  • 4.2 Dimensions
    3
  • 4.3 Détermination du débit à travers l'aiguille
    3
  • 4.4 Liaison du tube de l'aiguille avec l'embase
    4
  • 4.5 Biseau de l'aiguille
    4
  • 4.6 Absence de défauts
    4
  • 4.7 Lubrification
    4
  • 4.8 Décalage du point de mesure à l'extrémité patient
    4
  • 4.9 Détermination de la compatibilité fonctionnelle avec les systèmes d'injection à aiguille
    4
  • 4.10 Facilité d'assemblage/de désassemblage
    4
  • 4.11 Stérilité
    4
  • 5 Échantillonnage
    5
  • 6 Préconditionnement des aiguilles
    5
  • 6.1 Préconditionnement en atmosphère de chaleur sèche
    5
  • 6.2 Préconditionnement en atmosphère de stockage froide
    5
  • 6.3 Préconditionnement en atmosphère cyclique
    5
  • 7 Atmosphère normale et appareillage d'essai
    6
  • 7.1 Généralités
    6
  • 7.2 Atmosphère normale d'essai
    6
  • 7.3 Gabarit d'essai
    7
  • 8 Détermination du décalage du point de mesure à l'extrémité patient
    7
  • 9 Liaison du tube de l'aiguille avec l'embase
    8
  • 10 Emballage
    8
  • 11 Méthode d'essai pour la validation de la compatibilité aiguille/systèmes d'injection
    8
  • 11.1 Principe
    8
  • 11.2 Appareillage/équipement
    9
  • 11.3 Exigences de quantité d'aiguilles pour un échantillon
    9
  • 11.4 Mode opératoire
    9
  • 11.5 Critères d'acceptation
    11
  • 11.6 Rapport d'essai
    12
  • 12 Informations fournies par le fabricant
    12
  • 12.1 Généralités
    12
  • 12.2 Marquage
    13
  • 12.3 Mode d'emploi
    14
  • Annexe A (normative) Détermination du débit à travers l'aiguille
    15
  • Bibliographie
    17
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