EN 143:2021
(Main)Respiratory protective devices - Particle filters - Requirements, testing, marking
Respiratory protective devices - Particle filters - Requirements, testing, marking
This document specifies particle filters for use as replaceable components in unassisted respiratory protective devices (RPD) with the exception of escape devices and filtering face pieces.
Laboratory tests are included for the assessment of compliance with the requirements.
Some filters complying with this document can also be suitable for use with other types of respiratory protective devices and/or escape devices. If so, they need to be tested and marked according to the appropriate European Standard.
This document does not cover requirements concerning respiratory hygiene. Requirements for decrease of the microbiological hazards caused by the growth of bacteria and viruses on the filtration material are not determined.
Atemschutzgeräte - Partikelfilter - Anforderungen, Prüfung, Kennzeichnung
Dieses Dokument spezifiziert Partikelfilter zur Verwendung als austauschbare Bestandteile von Atemschutz¬geräten (ASG) ohne Luftversorgung mit der Ausnahme von Fluchtgeräten und filtrierenden Atemanschlüssen.
Laborprüfungen sind enthalten, um die Übereinstimmung mit den Anforderungen feststellen zu können.
Einige Filter, die diesem Dokument entsprechen, können auch für die Verwendung mit anderen Typen von Atemschutzgeräten und/oder Fluchtgeräten geeignet sein. Falls dies zutrifft, müssen sie gemäß der ent-sprechenden Europäischen Norm geprüft und gekennzeichnet werden.
Dieses Dokument enthält keine Anforderungen an die Atemhygiene. Die Anforderungen zur Verringerung der mikrobiologischen Gefahren, die durch das Wachstum von Bakterien und Viren auf dem Filtrationsmaterial verursacht werden, werden nicht bestimmt.
Appareils de protection respiratoire - Filtres à particules - Exigences, essais, marquage
Le présent document spécifie les filtres à particules destinés à être utilisés comme composants de remplacement pour les appareils de protection respiratoire (APR) non assistés, à l’exception des appareils destinés à l’évacuation et des pièces faciales filtrantes.
Le présent document comporte des essais en laboratoire destinés à l’évaluation de la conformité aux exigences.
Certains filtres conformes au présent document peuvent aussi convenir à d’autres types d’appareils de protection respiratoire et/ou d’appareils destinés à l’évacuation. Dans ce cas, ils doivent être soumis à essai et marqués conformément à la Norme européenne appropriée.
Le présent document ne couvre pas les exigences concernant l’hygiène respiratoire. Les exigences relatives à la diminution des risques microbiologiques engendrés par le développement de bactéries et de virus sur le matériel de filtration ne sont pas déterminées.
Oprema za varovanje dihal - Filtri za zaščito pred delci - Zahteve, preskušanje, označevanje
General Information
Relations
Standards Content (Sample)
SLOVENSKI STANDARD
01-julij-2021
Nadomešča:
SIST EN 143:2001
SIST EN 143:2001/A1:2006
SIST EN 143:2001/AC:2002
SIST EN 143:2001/AC:2005
Oprema za varovanje dihal - Filtri za zaščito pred delci - Zahteve, preskušanje,
označevanje
Respiratory protective devices - Particle filters - Requirements, testing, marking
Atemschutzgeräte - Partikelfilter - Anforderungen, Prüfung, Kennzeichnung
Appareils de protection respiratoire - Filtres à particules - Exigences, essais, marquage
Ta slovenski standard je istoveten z: EN 143:2021
ICS:
13.340.30 Varovalne dihalne naprave Respiratory protective
devices
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
EN 143
EUROPEAN STANDARD
NORME EUROPÉENNE
February 2021
EUROPÄISCHE NORM
ICS 13.340.30 Supersedes EN 143:2000
English Version
Respiratory protective devices - Particle filters -
Requirements, testing, marking
Appareils de protection respiratoire - Filtres à Atemschutzgeräte - Partikelfilter - Anforderungen,
particules - Exigences, essais, marquage Prüfung, Kennzeichnung
This European Standard was approved by CEN on 4 January 2021.
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, Turkey 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
© 2021 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN 143:2021 E
worldwide for CEN national Members.
Contents Page
European foreword . 3
1 Scope . 4
2 Normative references . 4
3 Terms, definitions and symbols . 4
3.1 Terms and definitions . 4
3.2 Symbols . 5
4 Classification . 6
5 Designation. 6
6 Requirements . 7
6.1 General . 7
6.2 Values and tolerances . 7
6.3 Connection . 7
6.4 Ergonomics . 7
6.5 Mass . 7
6.6 Twin or multiple filter devices . 7
6.7 Design . 8
6.8 Materials . 8
6.9 Packaging . 8
6.10 Conditioning . 8
6.10.1 Temperature . 8
6.10.2 Mechanical strength . 8
6.11 Inhalation resistance . 8
6.12 Filter penetration . 9
7 Testing . 9
7.1 Test performance . 9
7.1.1 General . 9
7.1.2 Test flow conditions . 9
7.2 Test schedule . 10
7.3 Inspection . 11
7.4 Conditioning . 11
7.4.1 Temperature . 11
7.4.2 Mechanical strength . 11
7.5 Inhalation resistance . 12
8 Marking . 13
8.1 General . 13
8.2 Filters . 13
8.3 Filter package . 13
9 Information supplied by the manufacturer . 14
Annex ZA (informative) Relationship between this European Standard and the essential
health and safety requirements of Regulation 2016/425/EU [2016 OJ L81] aimed to
be covered . 15
Bibliography . 17
European foreword
This document (EN 143:2021) has been prepared by Technical Committee CEN/TC 79 “Respiratory
protective 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 August 2021, and conflicting national standards shall
be withdrawn at the latest by August 2021.
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.
This document supersedes EN 143:2000, EN 143:2000/A1:2006 and EN 143:2000/AC:2005.
The following main technical changes have been made compared to EN 143:2000:
a) definitions and symbols added;
b) description deleted;
c) nominal values and tolerances changed;
d) use of a risk assessment, e.g. a Failure Modes and Effect Analysis (FMEA) added;
e) twin filters added;
f) clogging deleted;
g) visual inspection changed to inspection and detailed list inserted;
h) filter penetration test changed to refer to EN 13274-7;
i) marking changed to filters in general;
j) all figures adapted to the changes made in the test procedures, where appropriate.
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 organisations 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, Turkey and the
United Kingdom.
1 Scope
This document specifies particle filters for use as replaceable components in unassisted respiratory
protective devices (RPD) with the exception of escape devices and filtering face pieces.
Laboratory tests are included for the assessment of compliance with the requirements.
Some filters complying with this document can also be suitable for use with other types of respiratory
protective devices and/or escape devices. If so, they need to be tested and marked according to the
appropriate European Standard.
This document does not cover requirements concerning respiratory hygiene. Requirements for
decrease of the microbiological hazards caused by the growth of bacteria and viruses on the filtration
material are not determined.
2 Normative references
The following documents are referred to in the text in such a way that some or all of their content
constitutes requirements of this document. For dated references, only the edition cited applies. For
undated references, the latest edition of the referenced document (including any amendments) applies.
EN ISO 16972:2020, Respiratory protective devices - Vocabulary and graphical symbols (ISO 16972:2020)
EN 134:1998, Respiratory protective devices - Nomenclature of components
EN 148-1:2018, Respiratory protective devices - Threads for facepieces - Part 1: Standard thread
connection
EN 13274-3:2001, Respiratory protective devices - Methods of test - Part 3: Determination of breathing
resistance
EN 13274-7:2019, Respiratory protective devices - Methods of test - Part 7: Determination of particle filter
penetration
3 Terms, definitions and symbols
3.1 Terms and definitions
For the purposes of this document, the terms and definitions given in EN ISO 16972:2020 and
EN 134:1998 and the following apply.
ISO and IEC maintain terminological databases for use in standardization at the following addresses:
— ISO Online browsing platform: available at https://www.iso.org/obp
— IEC Electropedia: available at http://www.electropedia.org/
3.1.1
as received
not pre-conditioned or modified to carry out a test
[SOURCE: EN ISO 16972:2020, definition 3.16]
3.1.2
ready for assembly state
component with seals, plugs or other environmental protective means, if applicable, still in place
[SOURCE: EN ISO 16972:2020, definition 3.195]
3.1.3
ready for use state
respiratory protective device (RPD) ready to be donned as described by the manufacturer
Note 1 to entry: In line with the information supplied by the manufacturer for donning the RPD, further actions
can be necessary.
[SOURCE: EN ISO 16972:2020, definition 3.198]
3.2 Symbols
For the purposes of this document, the following symbols apply.
3.2.1
See information supplied by the manufacturer
3.2.2
Crossed out 2: Symbol “for single shift use only”
NOTE: Dur
...
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