Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment - Test method to determine the resistance to wet bacterial penetration (ISO 22610:2006)

ISO 22610:2006 specifies a test method, with associated test apparatus, which is used to determine the resistance of a material to the penetration of bacteria, carried by a liquid, when subjected to mechanical rubbing.

Operationsabdecktücher, -mäntel und Rein-Luft-Kleidung zur Verwendung als Medizinprodukte für Patienten, Klinikpersonal und Geräte - Prüfverfahren für die Widerstandsfähigkeit gegen Keimdurchtritt im feuchten Zustand (ISO 22610:2006)

Diese Internationale Norm legt ein Prüfverfahren mit der dazugehörigen Ausrüstung fest (siehe Anhang A), das für die Bestimmung der Widerstandsfähigkeit eines Materials gegen den Durchtritt von durch Flüssigkeit übertragende Bakterien verwendet wird, während das Material mechanischem Reiben oder mechanischer Belastung ausgesetzt wird.

Champs chirurgicaux, casaques et tenues de bloc, utilisés en tant que dispositifs médicaux, pour les patients, le personnel et les équipements - Méthode d'essai de résistance à la pénétration de la barrière bactérienne à l'état humide (ISO 22610:2006)

L'ISO 22610:2006 spécifie une méthode d'essai ainsi que l'équipement associé susceptibles d'être utilisés pour déterminer la résistance d'un matériau à la pénétration de bactéries dans un liquide lorsque ce matériau est soumis à un frottement mécanique.

Kirurške zastirke, ogrinjala in garniture za čisti zrak, ki se uporabljajo kot medicinski pripomočki za paciente, zdravstveno osebje in opremo – Preskusne metode za določanje odpornosti proti prodiranju vlažnih bakterij (ISO 22610:2006)

General Information

Status
Published
Publication Date
30-Jun-2006
Withdrawal Date
30-Jan-2007
Current Stage
9092 - Decision on results of review/2YR ENQ - revise - Review Enquiry
Start Date
07-Aug-2008
Completion Date
07-Aug-2008

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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 22610:2006
01-oktober-2006
.LUXUãNH]DVWLUNHRJULQMDODLQJDUQLWXUH]DþLVWL]UDNNLVHXSRUDEOMDMRNRW
PHGLFLQVNLSULSRPRþNL]DSDFLHQWH]GUDYVWYHQRRVHEMHLQRSUHPR±3UHVNXVQH
PHWRGH]DGRORþDQMHRGSRUQRVWLSURWLSURGLUDQMXYODåQLKEDNWHULM ,62
Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical
staff and equipment - Test method to determine the resistance to wet bacterial
penetration (ISO 22610:2006)
Operationsabdecktücher, -mäntel und Rein-Luft-Kleidung zur Verwendung als
Medizinprodukte für Patienten, Klinikpersonal und Geräte - Prüfverfahren für die
Widerstandsfähigkeit gegen Keimdurchtritt im feuchten Zustand (ISO 22610:2006)
Champs chirurgicaux, casaques et tenues de bloc, utilisés en tant que dispositifs
médicaux, pour les patients, le personnel et les équipements - Méthode d'essai de
résistance a la pénétration de la barriere bactérienne a l'état humide (ISO 22610:2006)
Ta slovenski standard je istoveten z: EN ISO 22610:2006
ICS:
11.140 Oprema bolnišnic Hospital equipment
13.340.10 Varovalna obleka Protective clothing
SIST EN ISO 22610:2006 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 22610:2006

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SIST EN ISO 22610:2006
EUROPEAN STANDARD
EN ISO 22610
NORME EUROPÉENNE
EUROPÄISCHE NORM
July 2006
ICS 13.340.10

English Version
Surgical drapes, gowns and clean air suits, used as medical
devices, for patients, clinical staff and equipment - Test method
to determine the resistance to wet bacterial penetration (ISO
22610:2006)
Champs chirurgicaux, casaques et tenues de bloc, utilisés Operationsabdecktücher, -mäntel und Rein-Luft-Kleidung,
en tant que dispositifs médicaux, pour les patients, le zur Verwendung als Medizinprodukte, für Patienten,
personnel et les équipements - Méthode d'essai de Klinikpersonal und Geräte - Prüfverfahren für die
résistance à la pénétration de la barrière bactérienne à Widerstandsfähigkeit gegen Keimdurchtritt im feuchten
l'état humide (ISO 22610:2006) Zustand (ISO 22610:2006)
This European Standard was approved by CEN on 24 May 2006.
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, Romania,
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
© 2006 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 22610:2006: E
worldwide for CEN national Members.

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SIST EN ISO 22610:2006

EN ISO 22610:2006 (E)





Foreword


This document (EN ISO 22610:2006) has been prepared by Technical Committee CEN/TC 205
"Non-active medical devices", the secretariat of which is held by DIN, in collaboration with
Technical Committee ISO/TC 94 "Personal safety - Protective clothing and 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 January 2007, and conflicting national standards
shall be withdrawn at the latest by January 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 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, Romania,
Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.

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