EN ISO 18777:2005

SLOVENSKI STANDARD
SIST EN ISO 18777:2005
01-junij-2005
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Transportable liquid oxygen systems for medical use - Particular requirements (ISO
18777:2005)
Flüssigsauerstoffsysteme für medizinische Anwendungen - Besondere Anforderungen
(ISO 18777:2005)
Systemes transportables d'oxygene liquide a usage médical - Exigences particulieres
(ISO 18777:2005)
Ta slovenski standard je istoveten z: EN ISO 18777:2005
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
SIST EN ISO 18777:2005 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 18777:2005

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SIST EN ISO 18777:2005
EUROPEAN STANDARD
EN ISO 18777
NORME EUROPÉENNE
EUROPÄISCHE NORM
February 2005
ICS 11.040.99
English version
Transportable liquid oxygen systems for medical use - Particular
requirements (ISO 18777:2005)
Systèmes transportables d'oxygène liquide à usage Flüssigsauerstoffsysteme für medizinische Anwendungen -
médical - Exigences particulières (ISO 18777:2005) Besondere Anforderungen (ISO 18777:2005)
This European Standard was approved by CEN on 28 January 2005.
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 Central Secretariat 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 Central Secretariat has the same status as the official
versions.
CEN members are the national standards bodies of Austria, Belgium, Cyprus, Czech Republic, Denmark, Estonia, Finland, France,
Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Slovakia,
Slovenia, Spain, Sweden, Switzerland and United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre: rue de Stassart, 36  B-1050 Brussels
© 2005 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 18777:2005: E
worldwide for CEN national Members.

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SIST EN ISO 18777:2005
EN ISO 18777:2005 (E)




Foreword



This document (EN ISO 18777:2005) has been prepared by Technical Committee CEN/TC 215 "Respiratory
and anaesthetic equipment", the secretariat of which is held by BSI, in collaboration with Technical
Committee ISO/TC 121 "Anaesthetic and respiratory equipment”.

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 August 2005, and conflicting national standards shall be withdrawn
at the latest by August 2005.

This document has been prepared under a mandate given to CEN by the European Commission and the
European Free Trade Association, and supports essential requirements of EU Directive(s).

For relationship with EU Directive(s), see informative Annex ZA, which is an integral part of this document.

According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following
countries are bound to implement this European Standard: Austria, Belgium, Cyprus, Czech Republic,
Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania,
Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Slovakia, Slovenia, Spain, Sweden, Switzerland
and United Kingdom.



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SIST EN ISO 18777:2005
EN ISO 18777:2005 (E)


ANNEX ZA
(informative)

Relationship between this International Standard and the Essential
Requirements of EU Directive 93/42 EEC Medical devices




This International Standard has been prepared under a mandate given to CEN by the European Commission
and the European Free Trade Association to provide one means of conforming to Essential Requirements of
the New Approach Directive 93/42 EEC Medical devices.

Once this standard is cited in the Official Journal of the European Communities under that Directive and has
been implemented as a national standard in at least one Member State, compliance with the normative
clauses of this standard given in Table ZA.1 confers, within the limits of the scope of this standard, a
presumption of conformity with the corresponding Essential Requirements of that Directive and a
...