Injection containers and accessories - Part 6: Caps made of aluminium-plastics combinations for injection vials (ISO 8362-6:2010)

ISO 8362‑6:2010 specifies caps made of aluminium-plastics combinations for injection vials as specified in ISO 8362‑1 and ISO 8362‑4.

Injektionsbehältnisse und Zubehör - Teil 6: Bördelkappen aus Aluminium-Kunststoffkombinationen für Injektionsflaschen (ISO 8362-6:2010)

Dieser Teil von ISO 8362 legt Bördelkappen aus Aluminium-Kunststoffkombinationen für Injektionsflaschen nach ISO 8362-1 und ISO 8362-4 fest.

Récipients et accessoires pour produits injectables - Partie 6: Capsules pour flacons d'injection fabriquées en un mélange aluminium-plastique (ISO 8362-6:2010)

L'ISO 8362-6:2010 spécifie des capsules en combinaison aluminium‑plastique pour flacons d'injection tels que spécifiés dans l'ISO 8362‑1 et l'ISO 8362‑4.

Vsebniki za parenteralne farmacevtske oblike in dodatna oprema - 6. del: Pokrovček vsebnika, izdelan iz kombinacije aluminija in plastike, za viale (ISO 8362-6:2010)

Ta del ISO 8362 določa pokrovčke vsebnika, izdelane iz kombinacije aluminija in plastike, za viale, kot je določeno v ISO 8362-1 in ISO 8362-4.

General Information

Status
Published
Publication Date
26-Apr-2011
Withdrawal Date
30-Oct-2011
Current Stage
6060 - Definitive text made available (DAV) - Publishing
Start Date
27-Apr-2011
Due Date
21-Jun-2012
Completion Date
27-Apr-2011

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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 8362-6:2011
01-julij-2011
9VHEQLNL]DSDUHQWHUDOQHIDUPDFHYWVNHREOLNHLQGRGDWQDRSUHPDGHO
3RNURYþHNYVHEQLNDL]GHODQL]NRPELQDFLMHDOXPLQLMDLQSODVWLNH]DYLDOH ,62

Injection containers and accessories - Part 6: Caps made of aluminium-plastics
combinations for injection vials (ISO 8362-6:2010)
Injektionsbehältnisse und Zubehör - Teil 6: Bördelkappen aus Aluminium-
Kunststoffkombinationen für Injektionsflaschen (ISO 8362-6:2010)
Récipients et accessoires pour produits injectables - Partie 6: Capsules pour flacons
d'injection fabriquées en un mélange aluminium-plastique (ISO 8362-6:2010)
Ta slovenski standard je istoveten z: EN ISO 8362-6:2011
ICS:
11.040.20 Transfuzijska, infuzijska in Transfusion, infusion and
injekcijska oprema injection equipment
SIST EN ISO 8362-6:2011 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 8362-6:2011

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SIST EN ISO 8362-6:2011


EUROPEAN STANDARD
EN ISO 8362-6

NORME EUROPÉENNE

EUROPÄISCHE NORM
April 2011
ICS 11.040.20
English Version
Injection containers and accessories - Part 6: Caps made of
aluminium-plastics combinations for injection vials (ISO 8362-
6:2010)
Récipients et accessoires pour produits injectables - Partie Injektionsbehältnisse und Zubehör - Teil 6: Bördelkappen
6: Capsules pour flacons d'injection fabriquées en un aus Aluminium-Kunststoffkombinationen für
mélange aluminium-plastique (ISO 8362-6:2010) Injektionsflaschen (ISO 8362-6:2010)
This European Standard was approved by CEN on 24 March 2011.

CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European
Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national
standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN member.

This European Standard 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 CEN-CENELEC Management Centre has the same
status as the official versions.

CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, 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.





EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2011 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 8362-6:2011: E
worldwide for CEN national Members.

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SIST EN ISO 8362-6:2011
EN ISO 8362-6:2011 (E)
Contents Page
Foreword .3

2

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SIST EN ISO 8362-6:2011
EN ISO 8362-6:2011 (E)
Foreword
The text of ISO 8362-6:2010 has been prepared by Technical Committee ISO/TC 76 “Transfusion, infusion
and injection, and blood processing equipment for medical and pharmaceutical use” of the International
Organization for Standardization (ISO) and has been taken over as EN ISO 8362-6:2011 by Technical
Committee CEN/TC 205 “Non-active medical devices” the secretariat of which is held by DIN.
This European Standard shall be given the status of a national standard, either by publication of an identical
text or by endorsement, at the latest by October 2011, and conflicting national standards shall be withdrawn at
the latest by October 2011.
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent
rights. CEN [and/or CENELEC] shall not be held responsible for identifying any or all such patent rights.
According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following
countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, 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 the United Kingdom.
Endorsement notice
The text of ISO 8362-6:2010 has been approved by CEN as a EN ISO 8362-6:2011 without any modification.

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