SIST EN ISO 8362-7:2011

SLOVENSKI STANDARD
SIST EN ISO 8362-7:2011
01-marec-2011
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Injection containers and accessories - Part 7: Injection caps made of aluminium-plastics
combinations without overlapping plastics part (ISO 8362-7:2006)
Injektionsbehältnisse und Zubehör - Teil 7: Bördelkappen aus Aluminium-
Kunststoffkombinationen für Injektionsflaschen ohne überstehendes Kunststoffteil (ISO
8362-7:2006)
Récipients et accessoires pour produits injectables - Partie 7: Capsules d'injection en
combinaison aluminium-plastique avec élément plastique non débordant (ISO 8362-
7:2006)
Ta slovenski standard je istoveten z: EN ISO 8362-7:2010
ICS:
11.040.20 Transfuzijska, infuzijska in Transfusion, infusion and
injekcijska oprema injection equipment
SIST EN ISO 8362-7:2011 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 8362-7:2011

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SIST EN ISO 8362-7:2011


EUROPEAN STANDARD
EN ISO 8362-7

NORME EUROPÉENNE

EUROPÄISCHE NORM
December 2010
ICS 11.040.20
English Version
Injection containers and accessories - Part 7: Injection caps
made of aluminium-plastics combinations without overlapping
plastics part (ISO 8362-7:2006)
Récipients et accessoires pour produits injectables - Partie Injektionsbehältnisse und Zubehör - Teil 7: Bördelkappen
7: Capsules d'injection en combinaison aluminium- aus Aluminium-Kunststoffkombinationen für
plastique avec élément plastique non débordant (ISO 8362- Injektionsflaschen ohne überstehendes Kunststoffteil (ISO
7:2006) 8362-7:2006)
This European Standard was approved by CEN on 21 November 2010.

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
© 2010 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 8362-7:2010: E
worldwide for CEN national Members.

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SIST EN ISO 8362-7:2011
EN ISO 8362-7:2010 (E)
Contents Page
Foreword .3

2

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SIST EN ISO 8362-7:2011
EN ISO 8362-7:2010 (E)
Foreword
The text of ISO 8362-7:2006 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 8362-7:2010 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 June 2011, and conflicting national standards shall be withdrawn at
the latest by June 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 8362-7:2006 has been approved by CEN as a EN ISO 8362-7:2010 without any modification.

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SIST EN ISO 8362-7:2011

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SIST EN ISO 8362-7:2011

INTERNATIONAL ISO
STANDARD 8362-7
Second edition
2006-04-15


Injection containers and accessories —
Part 7:
Injection caps made of aluminium-
plastics combinations without
overlapping plastics part
Récipients et accessoires pour produits injectables —
Partie 7: Capsules d'injection en combinaison aluminium-plastique avec
élément plastique non débordant





Reference number
ISO 8362-7:2006(E)
©
ISO 2006

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SIST EN ISO 8362-7:2011
ISO 8362-7:2006(E)
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ii © ISO 2006 – All rights reserved

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SIST EN ISO 8362-7:2011
ISO 8362-7:2006(E)
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies
(ISO member bodies). The work of preparing International Standards is normally carried out through ISO
technical committees. Each member body interested in a subject for which a technical committee has been
established has the right to be represented on that committee. International organizations, governmental and
non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the
International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.
International Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 2.
The main task of technical committees is to prepare International Standards. Draft International Standards
adopted by the technical committees are circulated to the member bodies for voting. Publication as an
International Standard requires approval by at least 75 % of the member bodies casting a vote.
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent
rights. ISO shall not be held responsible
...