EN ISO 5360:2009

Anaesthetic vaporizers - Agent-specific filling systems (ISO 5360:2006)

ISO 5360:2006 specifies the dimensions of agent-specific filling systems for agent-specific anaesthetic vaporizers.
This International Standard does not specify construction materials.
Because of the unique properties of desflurane, dimensions for this agent have not been specified in ISO 5360:2006.

Anästhesiemittelverdampfer - Substanzspezifische Füllsysteme (ISO 5360:2006)

Diese Internationale Norm legt Maße für substanzspezifische Füllsysteme zur Verwendung mit substanzspezifischen
Anästhesiemittelverdampfern fest.
Diese Internationale Norm legt keine Werkstoffe für die Konstruktion fest. Werkstoffe für diejenigen Teile des
substanzspezifischen Füllsystems, die mit flüssigem Anästhesiemittel in Berührung kommen, sollten
ausgewählt werden im Hinblick auf:
a) Toxizität;
b) Verträglichkeit mit Anästhesiemitteln;
c) Herabsetzung von Gesundheitsrisiken infolge von Substanzen, die aus dem Werkstoff herausgelöst
werden.
Aufgrund der besonderen Eigenschaften von Desfluran wurden die Maße für dieses Anästhesiemittel nicht in
dieser Internationalen Norm festgelegt.
ANMERKUNG Ausführungen von Anschlusssystemen werden unterstützt, die das Eingreifen der substanzspezifischen
Flaschenadapter in die Flasche nur dann zulassen, wenn der Flaschenkragen am richtigen Platz ist.

Évaporateurs d'anesthésie - Systèmes de remplissage spécifiques à l'agent (ISO 5360:2006)

L'ISO 5360:2006 spécifie les dimensions des systèmes de remplissage spécifiques à l'agent utilisés avec des évaporateurs d'anesthésie spécifiques à l'agent.
L'ISO 5360:2006 ne spécifie pas les matériaux utilisés.
En raison des propriétés uniques du desflurane, les dimensions pour cet agent n'ont pas été spécifiées dans l'ISO 5360:2006.

Anestezijski hlapilniki (vaporizatorji) - Sistemi za nalivanje posebnih hlapnih anestetikov (ISO 5360:2006)

General Information

• Status: Withdrawn
• Publication Date: 14-Apr-2009
• Withdrawal Date: 17-Jan-2012
• ICS: 11.040.10 - Anaesthetic, respiratory and reanimation equipment
• Technical Committee: CEN/TC 215 - Respiratory and anaesthetic equipment
• Drafting Committee: CEN/TC 215/WG 1 - Anaesthetic machines, medical breathing systems and anaesthetic gas scavenging systems
• Current Stage: 9960 - Withdrawal effective - Withdrawal
• Start Date: 18-Jan-2012
• Completion Date: 18-Jan-2012
• Directive: 2007/47/EC - Directive 2007/47/EC of the European Parliament and of the council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market
• Directive: 93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Mandate: M/023 - Standardization mandate to CEN/CENELEC concerning the development of European standards relating to medical devices
• Ref Project: SIST EN ISO 5360:2009 - Anaesthetic vaporizers - Agent-specific filling systems (ISO 5360:2006)

Relations

• Replaces: EN ISO 5360:2007 - Anaesthetic vaporizers - Agent-specific filling systems (ISO 5360:2006)
• Effective Date: 08-Jun-2022
• Replaced By: EN ISO 5360:2012 - Anaesthetic vaporizers - Agent-specific filling systems (ISO 5360:2012)
• Effective Date: 13-Nov-2010

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 5360:2009
01-junij-2009
1DGRPHãþD
SIST EN ISO 5360:2008
Anestezijski hlapilniki (vaporizatorji) - Sistemi za nalivanje posebnih hlapnih
anestetikov (ISO 5360:2006)
Anaesthetic vaporizers - Agent-specific filling systems (ISO 5360:2006)
Anästhesiemittelverdampfer - Substanzspezifische Füllsysteme (ISO 5360:2006)
Evaporateurs d'anesthésie - Systèmes de remplissage spécifiques à l'agent (ISO
5360:2006)
Ta slovenski standard je istoveten z: EN ISO 5360:2009
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
SIST EN ISO 5360:2009 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 5360:2009

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SIST EN ISO 5360:2009
EUROPEAN STANDARD
EN ISO 5360
NORME EUROPÉENNE
EUROPÄISCHE NORM
April 2009
ICS 11.040.10 Supersedes EN ISO 5360:2007
English Version
Anaesthetic vaporizers - Agent-specific filling systems (ISO
5360:2006)
Évaporateurs d'anesthésie - Systèmes de remplissage Anästhesiemittelverdampfer - Substanzspezifische
spécifiques à l'agent (ISO 5360:2006) Füllsysteme (ISO 5360:2006)
This European Standard was approved by CEN on 21 March 2009.
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 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 Management Centre has the same status as the
official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, 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
© 2009 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 5360:2009: E
worldwide for CEN national Members.

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SIST EN ISO 5360:2009
EN ISO 5360:2009 (E)
Contents Page
Foreword .3
Annex ZA (Informative) Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC .4

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SIST EN ISO 5360:2009
EN ISO 5360:2009 (E)
Foreword
The text of ISO 5360:2006 has been prepared by Technical Committee ISO/TC 121 “Anaesthetic and
respiratory equipment” of the International Organization for Standardization (ISO) and has been taken over as
EN ISO 5360:2009 by Technical Committee CEN/TC 215 “Respiratory and anaesthetic equipment” the
secretariat of which is held by BSI.
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 2009, and conflicting national standards shall be withdrawn at
the latest by March 2010.
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.
This document supersedes EN ISO 5360:2007.
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 EC Directive.
For relationship with EC Directive, 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, Bulgaria, 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 5360:2006 has been approved by CEN as a EN ISO 5360:2009 without any modification.
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