EN ISO 8836:2014
(Main)Suction catheters for use in the respiratory tract (ISO 8836:2014)
Suction catheters for use in the respiratory tract (ISO 8836:2014)
ISO 8836:2014 specifies requirements for suction catheters, including closed suction catheters, made of flexible materials and intended for use in suctioning of the respiratory tract.
Angled-tip suction catheters (e.g. Coudé catheters) and suction catheters with aspirator collectors are not considered to be specialized and are therefore included in the scope of ISO 8836:2014.
Absaugkatheter zur Verwendung im Atemtrakt (ISO 8836:2014)
Diese Internationale Norm legt Anforderungen an Absaugkatheter aus flexiblen Materialien, einschließlich
geschlossene Absaugkatheter, zur Verwendung bei der Absaugung im Atemtrakt fest.
Absaugkatheter mit abgewinkelter Spitze (z. B. Coudé-Katheter) und Absaugkatheter mit Aspirator-
Sammlern werden nicht als Spezial-Absaugkatheter betrachtet und gehören deshalb zum
Anwendungsbereich dieser Internationalen Norm.
Absaugkatheter zur Verwendung mit brennbaren Anästhesiegasen oder Anästhesiemitteln, mit Lasern oder
elektrochirurgischen Geräten sind nicht Gegenstand dieser Internationalen Norm.
ANMERKUNG ISO/TR 11991 enthält einen Leitfaden zur Sicherung der Luftwege bei Laseranwendung in den oberen
Atemwegen.[6]
Sondes d'aspiration pour les voies respiratoires (ISO 8836:2014)
L'ISO 8836:2014 spécifie les exigences applicables aux sondes d'aspiration, notamment les sondes d'aspiration fermées, constituées de matériaux souples et destinées à une utilisation dans l'aspiration des voies respiratoires.
Les sondes d'aspiration à extrémité coudée (par exemple les sondes Coudé) et les sondes d'aspiration avec des collecteurs ne sont pas considérées comme étant spécialisées et elles sont donc incluses dans le domaine d'application de l'ISO 8836:2014.
Aspiracijski katetri za čiščenje dihalnih poti (ISO 8836:2014)
Ta mednarodni standard določa zahteve za aspiracijske katetre, vključno z zaprtimi aspiracijskimi katetri, izdelane iz prožnih materialov in namenjene čiščenju dihalnih poti. Aspiracijski katetri s poševno konico (npr. ukrivljeni katetri) in aspiracijski katetri z zbiralniki aspiratorjev se ne štejejo za specializirane, zato so vključeni v področje uporabe tega mednarodnega standarda. Aspiracijski katetri, namenjeni uporabi z vnetljivimi anestezijskimi plini ali sredstvi, laserji ali elektrokirurško
opremo, niso obravnavani v tem mednarodnem standardu.
OPOMBA: Glej standard ISO/TR 11991 za navodila za oskrbo dihal med lasersko operacijo zgornjih dihal.[6]
General Information
Relations
Standards Content (Sample)
SLOVENSKI STANDARD
SIST EN ISO 8836:2015
01-januar-2015
1DGRPHãþD
SIST EN ISO 8836:2009
$VSLUDFLMVNLNDWHWUL]DþLãþHQMHGLKDOQLKSRWL ,62
Suction catheters for use in the respiratory tract (ISO 8836:2014)
Absaugkatheter zur Verwendung im Atemtrakt (ISO 8836:2014)
Sondes d'aspiration pour les voies respiratoires (ISO 8836:2014)
Ta slovenski standard je istoveten z: EN ISO 8836:2014
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
11.040.25 Injekcijske brizge, igle in Syringes, needles an
katetri catheters
SIST EN ISO 8836:2015 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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SIST EN ISO 8836:2015
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SIST EN ISO 8836:2015
EUROPEAN STANDARD
EN ISO 8836
NORME EUROPÉENNE
EUROPÄISCHE NORM
October 2014
ICS 11.040.25; 11.040.10 Supersedes EN ISO 8836:2009
English Version
Suction catheters for use in the respiratory tract (ISO 8836:2014)
Sondes d'aspiration pour les voies respiratoires (ISO Absaugkatheter zur Verwendung im Atemtrakt (ISO
8836:2014) 8836:2014)
This European Standard was approved by CEN on 25 July 2014.
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, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania,
Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and United
Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2014 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 8836:2014 E
worldwide for CEN national Members.
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SIST EN ISO 8836:2015
EN ISO 8836:2014 (E)
Contents Page
Foreword .3
Annex ZA (informative) Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC .4
2
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SIST EN ISO 8836:2015
EN ISO 8836:2014 (E)
Foreword
This document (EN ISO 8836:2014) has been prepared by Technical Committee ISO/TC 121 "Anaesthetic
and respiratory equipment" in collaboration with 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 April 2015, and conflicting national standards shall be withdrawn at the
latest by April 2015.
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 8836:2009.
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, Bulgaria, Croatia, Cyprus, Czech
Republic, Denmark, Estonia, Finland, Former Yugoslav Republic of Macedonia, France, Germany, Greece,
Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal,
Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the United Kingdom.
Endorsement notice
The text of ISO 8836:2014 has been approved b
...
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