Anaesthetic and respiratory equipment - Oropharyngeal airways (ISO 5364:2008)

ISO 5364:2008 specifies requirements for oropharyngeal airways of plastics materials and/or rubber, including those with a reinforcement insert made of plastics materials and/or metal. Flammability of oropharyngeal airways, for example if flammable anaesthetics, electrosurgical units or lasers are used, is a well-recognized hazard. It is addressed by appropriate clinical management, which is outside the scope of this International Standard.

Anästhesie- und Beatmungsgeräte - Oropharyngealtuben (ISO 5364:2008)

Diese Internationale Norm legt Anforderungen an Oropharyngealtuben aus Kunststoff und/oder Gummi, mit oder ohne Verstärkungseinsatz aus Kunststoff und/oder Metall, fest.
Diese Internationale Norm gilt nicht für Oropharyngealtuben aus Metall und enthält keine Anforderungen an die Entflammbarkeit von Oropharyngealtuben.
Die Entflammbarkeit von Oropharyngealtuben, z. B. bei Anwendung von entflammbaren Anästhesiemitteln, elektrochirurgischen Geräten oder Laser, stellt eine bekannte Gefährdung dar. Sie wird durch entsprechendes klinisches Management berücksichtigt, das jedoch nicht Gegenstand dieser Internationalen Norm ist.
Diese Internationale Norm gilt nicht für supralaryngeale Atemwege ohne einen internen, integrierten Abdichtmechanismus.

Matériel d'anesthésie et de réanimation respiratoire - Canules oropharyngées (ISO 5364:2008)

L'ISO 5364:2008 spécifie les exigences relatives aux canules oropharyngées en matière plastique et/ou en caoutchouc, notamment celles qui comportent un renfort inséré en matière plastique et/ou en métal. L'inflammabilité des canules oropharyngées, par exemple en cas d'utilisation de produits anesthésiques, d'appareils d'électrochirurgie ou de lasers, représente un danger bien connu. Ce problème est pris en compte par une gestion clinique appropriée, qui ne relève pas du domaine d'application de la présente Norme internationale.

Anestezijska in dihalna oprema - Ustno-žrelne (orofaringealne) dihalne cevke (ISO 5364:2008)

Ta mednarodni standard določa zahteve za ustno-žrelne (orofaringalne) dihalne cevke iz plastičnih materialov in/ali gume, vključno s tistimi, katerih vložek za ojačanje je izdelan iz plastičnih materialov in/ali kovine. Ta mednarodni standard ne velja za kovinske ustno-žrelne (orofaringealne) dihalne cevke niti za zahteve, ki zadevajo gorljivost ustno-žrelnih (orofaringealnih) dihalnih cevk. Gorljivost ustno-žrelnih (orofaringealnih) dihalnih cevk, če se na primer uporabijo gorljivi anestetiki, elektrokirurške enote ali laserji, je dobro znana nevarnost. Je predmet kliničnega nadzorovanja, ki je zunaj področja uporabe tega mednarodnega standarda. Ta mednarodni standard ne velja za supralaringealne dihalne cevke brez notranjih vgrajenih tesnilnih mehanizmov.

General Information

Status
Withdrawn
Publication Date
26-Apr-2011
Withdrawal Date
27-Sep-2016
Current Stage
9960 - Withdrawal effective - Withdrawal
Completion Date
28-Sep-2016

Relations

Effective Date
07-May-2011

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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 5364:2011
01-julij-2011
1DGRPHãþD
SIST EN 12181:2000
Anestezijska in dihalna oprema - Ustno-žrelne (orofaringealne) dihalne cevke (ISO
5364:2008)
Anaesthetic and respiratory equipment - Oropharyngeal airways (ISO 5364:2008)
Anästhesie- und Beatmungsgeräte - Oropharyngealtuben (ISO 5364:2008)
Matériel d'anesthésie et de réanimation respiratoire - Canules oropharyngées (ISO
5364:2008)
Ta slovenski standard je istoveten z: EN ISO 5364:2011
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
SIST EN ISO 5364:2011 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 5364:2011

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SIST EN ISO 5364:2011


EUROPEAN STANDARD
EN ISO 5364

NORME EUROPÉENNE

EUROPÄISCHE NORM
April 2011
ICS 11.040.10
English Version
Anaesthetic and respiratory equipment - Oropharyngeal airways
(ISO 5364:2008)
Matériel d'anesthésie et de réanimation respiratoire - Anästhesie- und Beatmungsgeräte - Oropharyngealtuben
Canules oropharyngées (ISO 5364:2008) (ISO 5364:2008)
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 5364:2011: E
worldwide for CEN national Members.

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SIST EN ISO 5364:2011
EN ISO 5364:2011 (E)
Contents Page
Foreword .3

2

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SIST EN ISO 5364:2011
EN ISO 5364:2011 (E)
Foreword
The text of ISO 5364:2008 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 5364:2011 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 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 5364:2008 has been approved by CEN as a EN ISO 5364:2011 without any modification.

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SIST EN ISO 5364:2011

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SIST EN ISO 5364:2011
INTERNATIONAL ISO
STANDARD 5364
Fourth edition
2008-07-15
Corrected version
2009-01-15
Anaesthetic and respiratory equipment —
Oropharyngeal airways
Matériel d'anesthésie et de réanimation respiratoire — Canules
oropharyngées

Reference number
ISO 5364:2008(E)
©
ISO 2008

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