Respiratory protective devices - Powered filtering devices incorporating a loose fitting respiratory interface - Requirements, testing, marking

This document specifies minimum requirements for powered filtering Respiratory Protective Devices (RPD) incorporating a loose fitting respiratory interface (RI). It does not cover devices designed for use in circumstances where there is or might be an oxygen deficiency.
Escape RPD and filters for use against CO are not covered by this document.
Laboratory and practical performance tests are included for the assessment of compliance with the requirements.

Atemschutzgeräte - Gebläsefiltergeräte mit einem Atemanschluss ohne Dichtsitz (Haube) - Anforderungen, Prüfung, Kennzeichnung

Dieses Dokument legt Mindestanforderungen für Atemschutzgeräte (ASG) mit Gebläsefiltergerät und Atemanschluss ohne Dichtsitz fest. Es ist nicht anwendbar für Geräte, die für die Verwendung bei möglichem Sauerstoff Mangel vorgesehen sind.
Fluchtgeräte (ASG zu Fluchtzwecken) und Filter zur Verwendung gegen CO werden von diesem Dokument nicht abgedeckt.
Laborprüfungen und praktische Leistungsprüfungen sind enthalten, um die Übereinstimmung mit den Anforderungen feststellen zu können.

Appareils de protection respiratoire - Appareils filtrants à ventilation assistée avec interface respiratoire à ajustement lâche - Exigences, essais, marquage

Le présent document spécifie les caractéristiques minimales exigées des appareils de protection respiratoire (APR) filtrants à assistance motorisée avec interface respiratoire (IR) à ajustement lâche. Il ne s'applique pas aux appareils destinés à être utilisés dans des circonstances présentant ou pouvant présenter un défaut d'oxygène.
Les APR d'évacuation et les filtres pour utilisation contre le CO ne sont pas couverts par le présent document.
Il comporte des essais en laboratoire et des essais pratiques de performance pour évaluer la conformité aux exigences.

Oprema za varovanje dihal - Napajana oprema za filtriranje z vgrajenim ohlapno prilegajočim dihalnim vmesnikom - Zahteve, preskušanje, označevanje

Dokument določa minimalne zahteve za napajano opremo za filtriranje z vgrajenim ohlapno prilegajočim dihalnim vmesnikom. Ne zajema naprav, ki so zasnovane za uporabo v okoliščinah, kjer obstaja ali se lahko pojavi pomanjkanje kisika (koncentracija kisika, manjša od deleža prostornine 17 %).
Ta dokument ne zajema opreme za varovanje dihal za izhod v sili.
Vključeni so tudi laboratorijski in praktični preskusi za ocenjevanje skladnosti z zahtevami.

General Information

Status
Published
Publication Date
19-Dec-2023
Withdrawal Date
10-Apr-2022
Current Stage
6060 - Definitive text made available (DAV) - Publishing
Start Date
20-Dec-2023
Due Date
13-Jan-2019
Completion Date
20-Dec-2023

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SLOVENSKI STANDARD
01-april-2024
Nadomešča:
SIST EN 12941:1999
SIST EN 12941:1999/A1:2004
SIST EN 12941:1999/A2:2009
Oprema za varovanje dihal - Napajana oprema za filtriranje z vgrajenim ohlapno
prilegajočim dihalnim vmesnikom - Zahteve, preskušanje, označevanje
Respiratory protective devices - Powered filtering devices incorporating a loose fitting
respiratory interface - Requirements, testing, marking
Atemschutzgeräte - Gebläsefiltergeräte mit einem Atemanschluss ohne Dichtsitz
(Haube) - Anforderungen, Prüfung, Kennzeichnung
Appareils de protection respiratoire - Appareils filtrants à ventilation assistée avec
interface respiratoire à ajustement lâche - Exigences, essais, marquage
Ta slovenski standard je istoveten z: EN 12941:2023
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 12941
EUROPEAN STANDARD
NORME EUROPÉENNE
December 2023
EUROPÄISCHE NORM
ICS 13.340.30 Supersedes EN 12941:1998
English Version
Respiratory protective devices - Powered filtering devices
incorporating a loose fitting respiratory interface -
Requirements, testing, marking
Appareils de protection respiratoire - Appareils Atemschutzgeräte - Gebläsefiltergeräte mit einem
filtrants à ventilation assistée avec interface Atemanschluss ohne Dichtsitz (Haube) -
respiratoire à ajustement lâche - Exigences, essais, Anforderungen, Prüfung, Kennzeichnung
marquage
This European Standard was approved by CEN on 9 August 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, 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 12941:2023 E
worldwide for CEN national Members.

Contents Page
European foreword . 4
1 Scope . 5
2 Normative references . 5
3 Terms and definitions, description and symbols . 5
3.1 Terms and definitions . 5
3.2 Description . 6
3.3 Symbols . 7
4 Classification . 7
5 Requirements . 8
5.1 General . 8
5.2 Values and tolerances . 10
5.3 Ergonomics . 10
5.4 Design . 10
5.5 Materials . 10
5.6 Mechanical strength (optional) . 10
5.7 Resistance to temperature . 10
5.8 Respiratory Interface (RI) . 11
5.9 Inward leakage . 11
5.10 Breathing resistance . 12
5.11 Air supply . 12
5.12 Warning facilities . 12
5.13 Electrical components . 13
5.14 Breathing hose, if applicable, and couplings . 13
5.15 Filters . 14
5.16 Noise level . 19
5.17 Carbon dioxide content of the inhalation air . 20
5.18 Flammability . 20
5.19 Exhalation means, if applicable . 20
5.20 Mass of RPD . 21
5.21 Practical performance . 21
6 Testing . 22
6.1 Test schedule . 22
6.2 Conditioning . 24
6.3 Inspection . 24
6.4 Inward leakage . 25
6.5 Visor robustness . 26
6.6 Breathing resistance . 26
6.7 Air supply flow rate . 26
6.8 Resistance to collapse of breathing hose . 29
6.9 Strength of hose and couplings . 30
6.10 Mechanical strength . 30
6.11 Filter performance testing . 31
6.12 Mass carried by the head . 34
7 Marking . 35
7.1 General . 35
7.2 RI . 35
7.3 Blower-unit and battery casing (if separate from the blower-unit) . 35
7.4 Filters . 35
7.5 Filter package . 37
7.6 RPD packages . 37
8 Information supplied by the manufacturer . 37
8.1 Complete RPD . 37
8.2 Filters . 38
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 . 39
Bibliography . 41

European foreword
This document (EN 12941:2023) 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 June 2024 and conflicting national standards shall be
withdrawn at the latest by June 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.
This document supersedes EN 12941:1998.
This document has been prepared under a standardization request addressed to CEN by the European
Commission. The Standing Committee of the EFTA States subsequently approves these requests for its
Member States.
For the relationship with EU Legislation, see informative Annex ZA, which is an integral part of this
document.
The following main technical changes have been made compared to EN 12941:1998:
a) Clause 4 Designation was deleted;
b) number of test samples was added to the requirements, where necessary;
c) classification table was amended to cover Hg and NO filter for all classes (TH1, TH2 and TH3);
d) nominal values and tolerances were added;
e) clogging was deleted;
f) warning facilities were amended to cover low energy and low flow warning;
g) visual inspection was changed to inspection and detailed list inserted;
h) test substances and number of test subjects for inward leakage test was changed;
i) requirement for field of vision integrated into the requirements for visor (5.8.3);
j) test for noise level was adapted to the test procedure specified in ISO 16900-14:2020;
k) Annex A was deleted;
l) Annex B was deleted;
m) figures were adapted to the changes made in the test procedures, where appropriate.
Any feedback and questions on this document should be directed to the users’ national standards body.
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, F
...

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