Medical suction equipment - Part 3: Suction equipment powered from a vacuum or positive pressure gas source (ISO 10079-3:2014)

ISO 10079-3:2014 specifies safety and performance requirements for medical suction equipment powered from a vacuum or positive pressure gas source generating venturi suction. It applies to equipment connected to medical gas pipeline systems or cylinders and venturi attachments.
The equipment can be stand-alone or part of an integrated system.

Medizinische Absauggeräte - Teil 3: Vakuum- oder druckquellenbetriebene Absauggeräte (ISO 10079-3:2014)

Dieser Teil von ISO 10079 legt Anforderungen für die Sicherheit und für die Leistung von vakuum- oder druckquellenbetriebenen medizinischen Absauggeräten fest. Er gilt für Geräte, die an Rohrleitungssysteme für medizinische Gase oder Gasflaschen und Saugdüsen-Zubehör angeschlossen sind. Anhang D stellt die drei Teile von ISO 10079 dar, in dem eine schematische Darstellung der typischen Systeme angegeben wird.
Die Geräte können eigenständige Geräte oder Teil eines integrierten Systems sein.
Zusätzliche Anforderungen an Absauggeräte zur Verwendung im Freien und/oder beim Transport sind in diesem Teil von ISO 10079 enthalten.
Dieser Teil von ISO 10079 gilt nicht für Folgendes:
a) zentrale Leistungsversorgung (durch Erzeugung von Vakuum/Druckluft), Rohrleitungssysteme von Fahrzeugen und Gebäuden sowie Wandanschlüsse;
b) Endstücke wie Absaugkatheter, Yankauer-Sauger und Absaugtüllen;
c) Spritzen;
d) zahnmedizinische Absauggeräte;
e) Anästhesiegas-Fortleitungssysteme;
f) Laborabsaugung;
g) Autotransfusionssysteme;
h) geschlossene Systeme für Wunddrainage;
i) mundbetriebene Schleimabsauger, einschließlich Schleimabsauger für Neugeborene;
j) Geräte für Geburtshilfe;
k) Milchpumpen;
l) Fettabsaugung;
m) Absaugung aus dem Uterus;
n) Rauchgasabsaugsysteme.

Appareils d'aspiration médicale - Partie 3: Appareils d'aspiration alimentés par une source de vide ou de pression (ISO 10079-3:2014)

L'ISO 10079-3:2013 spécifie les exigences de sécurité et de performance relatives aux appareils d'aspiration médicale alimentés par une source de vide ou de gaz à pression positive générant une aspiration Venturi. Elle est applicable aux appareils raccordés à des bouteilles ou des systèmes de distribution de gaz médicaux et aux systèmes venturi.
L'appareil peut être autonome ou faire partie d'un système intégré.

Medicinska sukcijska (aspiracijska) oprema - 3. del: Podtlačna ali tlačna sukcijska (aspiracijska) oprema (ISO 10079-3:2014)

EN ISO 10079-3 določa zahteve glede varnosti in učinkovitosti za medicinsko podtlačno ali tlačno sukcijsko (aspiracijsko) opremo. Velja za opremo, ki je povezana s sistemi napeljav za medicinske pline ali jeklenkami in priključki venturijeve cevi. Priloga D s shematskim prikazom tipičnih sistemov prikazuje tri dele ISO 10079. Oprema je lahko samostojen sistem ali del integriranega sistema. Dodatne zahteve za sukcijsko (aspiracijsko) opremo, ki je namenjena uporabi na prostem in/ali med prevozom, so vključene v ta del standarda ISO 10079. Ta del standarda ISO 10079 ne velja za naslednje: a) centralno oskrbo z električno energijo (ustvarjeno z vakuumom ali stisnjenim zrakom), cevne sisteme vozil in stavb ter stenske priključke; b) zaključke, kot so aspiracijski katetri, aspiracijske cevke Yankauer in konice za sukcijo; c) injekcijske brizge; d) opremo za zobno sukcijo; e) sisteme za odstranjevanje anestezijskih plinov in hlapov; f) laboratorijsko sukcijo; g) sisteme za avtotransfuzijo; h) zaprte sisteme za drenažo rane; i) ekstrakcijske aparate za sluz, vključno z ekstrakcijskimi aparati za sluz za novorojenčke; j) opremo za vakuumsko ekstrakcijo (porodna oprema); k) prsne črpalke; l) liposukcijo; m) endometrijsko aspiracijo; n) sisteme za odvod dima.

General Information

Status
Withdrawn
Publication Date
06-May-2014
Withdrawal Date
24-May-2022
Current Stage
9960 - Withdrawal effective - Withdrawal
Completion Date
25-May-2022

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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 10079-3:2014
01-julij-2014
1DGRPHãþD
SIST EN ISO 10079-2:2009
SIST EN ISO 10079-3:2009
0HGLFLQVNDVXNFLMVND DVSLUDFLMVND RSUHPDGHO3RGWODþQDDOLWODþQDVXNFLMVND
DVSLUDFLMVND RSUHPD ,62
Medical suction equipment - Part 3: Suction equipment powered from a vacuum or
positive pressure gas source (ISO 10079-3:2014)
Medizinische Absauggeräte - Teil 3: Vakuum- oder druckquellenbetriebene
Absauggeräte (ISO 10079-3:2014)
Appareils d'aspiration médicale - Partie 3: Appareils d'aspiration alimentés par une
source de vide ou de pression (ISO 10079-3:2014)
Ta slovenski standard je istoveten z: EN ISO 10079-3:2014
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
SIST EN ISO 10079-3:2014 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 10079-3:2014

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SIST EN ISO 10079-3:2014

EUROPEAN STANDARD
EN ISO 10079-3

NORME EUROPÉENNE

EUROPÄISCHE NORM
May 2014
ICS 11.040.10 Supersedes EN ISO 10079-3:2009
English Version
Medical suction equipment - Part 3: Suction equipment powered
from a vacuum or positive pressure gas source (ISO 10079-
3:2014)
Appareils d'aspiration médicale - Partie 3: Appareils Medizinische Absauggeräte - Teil 3: Vakuum- oder
d'aspiration alimentés par une source de vide ou de druckquellenbetriebene Absauggeräte (ISO 10079-3:2014)
pression (ISO 10079-3:2014)
This European Standard was approved by CEN on 15 February 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 10079-3:2014 E
worldwide for CEN national Members.

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SIST EN ISO 10079-3:2014
EN ISO 10079-3:2014 (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 10079-3:2014
EN ISO 10079-3:2014 (E)
Foreword
This document (EN ISO 10079-3:2014) 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 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 November 2014, and conflicting national standards shall be withdrawn
at the latest by May 2017.
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 10079-3:2009.
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.
For relationship with EU 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
...

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