EN ISO 24072:2023

Aerosol bacterial retention test method for air-inlet on administration devices (ISO 24072:2023)

This document specifies a test method to assess bacterial retention ability of finished stand-alone and integrated air-inlet filters on administration devices for infusion and transfusion applications.

Prüfverfahren für die Aerosol-Bakterienrückhaltung beim Lufteinlass an Verabreichungsgeräten (ISO 24072:2023)

Dieses Dokument legt ein Prüfverfahren fest, um die Bakterienrückhaltefähigkeit von fertigen eigenständigen und integrierten Belüftungsfiltern auf Verabreichungsgeräten für medizinische Infusions- und Transfusionsvorrichtungen zu beurteilen.

Méthode d’essai de rétention bactérienne dans les aérosols pour les filtres d'admission d’air utilisés sur les dispositifs d’administration (ISO 24072:2023)

Le présent document spécifie une méthode d’essai pour évaluer la capacité de rétention bactérienne des filtres d’admission d’air finis, indépendants et intégrés, utilisés sur les dispositifs d’administration employés dans le cadre d’applications de perfusion et de transfusion.

Preskusna metoda za zadrževanje bakterij v aerosolu pri napravah za vnos zraka (ISO 24072:2023)

Ta dokument določa preskusno metodo, ki se uporablja za ocenjevanje sposobnosti zadrževanja bakterij končnih filtrov naprav za vnos zraka pri kompletih za infuzijo in transfuzijo ter pripomočkih za prenos.
Ocena sposobnosti zadrževanja bakterij membranskih materialov za filtriranje zraka pri kompletih za infuzijo in transfuzijo ter pripomočkih za prenos se lahko nanaša na ta dokument.

General Information

• Status: Published
• Publication Date: 04-Jul-2023
• ICS: 11.040.20 - Transfusion, infusion and injection equipment
• Technical Committee: CEN/TC 205 - Non-active medical devices
• Drafting Committee: CEN/TC 205 - Non-active medical devices
• Current Stage: 6060 - Definitive text made available (DAV) - Publishing
• Start Date: 05-Jul-2023
• Due Date: 30-Jun-2024
• Completion Date: 05-Jul-2023
• Ref Project: SIST EN ISO 24072:2023 - Aerosol bacterial retention test method for air-inlet on administration devices (ISO 24072:2023)

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 24072:2023
01-oktober-2023
Preskusna metoda za zadrževanje bakterij v aerosolu pri napravah za vnos zraka
(ISO 24072:2023)
Aerosol bacterial retention test method for air-inlet on administration devices (ISO
24072:2023)
Prüfverfahren für die Aerosol-Bakterienrückhaltung beim Lufteinlass an
Verabreichungsgeräten (ISO 24072:2023)
Méthode d’essai de rétention bactérienne dans les aérosols pour les filtres d'admission
d’air utilisés sur les dispositifs d’administration (ISO 24072:2023)
Ta slovenski standard je istoveten z: EN ISO 24072:2023
ICS:
11.040.20 Transfuzijska, infuzijska in Transfusion, infusion and
injekcijska oprema injection equipment
SIST EN ISO 24072:2023 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------
SIST EN ISO 24072:2023

---------------------- Page: 2 ----------------------
SIST EN ISO 24072:2023


EN ISO 24072
EUROPEAN STANDARD

NORME EUROPÉENNE

July 2023
EUROPÄISCHE NORM
ICS 11.040.20
English Version

Aerosol bacterial retention test method for air-inlet on
administration devices (ISO 24072:2023)
Méthode d'essai de rétention bactérienne dans les Prüfverfahren für die Aerosol-Bakterienrückhaltung
aérosols pour les filtres d'admission d'air utilisés sur beim Lufteinlass an Verabreichungsgeräten (ISO
les dispositifs d'administration (ISO 24072:2023) 24072:2023)
This European Standard was approved by CEN on 4 April 2023.

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, Republic of North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Türkiye and
United Kingdom.





EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

CEN-CENELEC Management Centre: Rue de la Science 23, B-1040 Brussels
© 2023 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 24072:2023 E
worldwide for CEN national Members.

---------------------- Page: 3 ----------------------
SIST EN ISO 24072:2023
EN ISO 24072:2023 (E)
Contents Page
European foreword . 3

2

---------------------- Page: 4 ----------------------
SIST EN ISO 24072:2023
EN ISO 24072:2023 (E)
European foreword
This document (EN ISO 24072:2023) has been prepared by Technical Committee ISO/TC 76
"Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical
use" in collaboration with Technical Committee CEN/TC 205 “Non-active medical devices” 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 January 2024, and conflicting national standards shall
be withdrawn at the latest by January 2024.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN shall not be held responsible for identifying any or all such patent rights.
Any feedback and questions on this document should be directed to the users’ national standards
body/national committee. A complete listing of these bodies can be found on the CEN website.
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, Republic of
North Macedonia, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland, Türkiye and the
United Kingdom.
Endorsement notice
The text of ISO 24072:2023 has been approved by CEN as EN ISO 24072:2023 without any modification.


3

----
...