ISO/TS 16974:2011
(Main)Respiratory protective devices — Marking and information supplied by the manufacturer
Respiratory protective devices — Marking and information supplied by the manufacturer
ISO/TS 16974:2011 gives guidance on the marking to be used on respiratory protective devices (RPD) and the information to be supplied by the manufacturer/supplier.
Dispositifs de protection respiratoire — Marquage et informations fournies par le fabricant
General Information
Standards Content (Sample)
TECHNICAL ISO/TS
SPECIFICATION 16974
First edition
2011-06-01
Respiratory protective devices —
Marking and information supplied by the
manufacturer
Dispositifs de protection respiratoire — Marquage et informations
fournies par le fabricant
Reference number
ISO/TS 16974:2011(E)
©
ISO 2011
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ISO/TS 16974:2011(E)
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ISO/TS 16974:2011(E)
Foreword
ISO (the International Organization for Standardization) is a worldwide federation of national standards bodies
(ISO member bodies). The work of preparing International Standards is normally carried out through ISO
technical committees. Each member body interested in a subject for which a technical committee has been
established has the right to be represented on that committee. International organizations, governmental and
non-governmental, in liaison with ISO, also take part in the work. ISO collaborates closely with the
International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization.
International Standards are drafted in accordance with the rules given in the ISO/IEC Directives, Part 2.
The main task of technical committees is to prepare International Standards. Draft International Standards
adopted by the technical committees are circulated to the member bodies for voting. Publication as an
International Standard requires approval by at least 75 % of the member bodies casting a vote.
In other circumstances, particularly when there is an urgent market requirement for such documents, a
technical committee may decide to publish other types of normative document:
⎯ an ISO Publicly Available Specification (ISO/PAS) represents an agreement between technical experts in
an ISO working group and is accepted for publication if it is approved by more than 50 % of the members
of the parent committee casting a vote;
⎯ an ISO Technical Specification (ISO/TS) represents an agreement between the members of a technical
committee and is accepted for publication if it is approved by 2/3 of the members of the committee casting
a vote.
An ISO/PAS or ISO/TS is reviewed after three years in order to decide whether it will be confirmed for a
further three years, revised to become an International Standard, or withdrawn. If the ISO/PAS or ISO/TS is
confirmed, it is reviewed again after a further three years, at which time it must either be transformed into an
International Standard or be withdrawn.
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent
rights. ISO shall not be held responsible for identifying any or all such patent rights.
ISO/TS 16974 was prepared by Technical Committee ISO/TC 94, Personal safety — Protective clothing and
equipment, Subcommittee SC 15, Respiratory protective devices.
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TECHNICAL SPECIFICATION ISO/TS 16974:2011(E)
Respiratory protective devices — Marking and information
supplied by the manufacturer
1 Scope
This Technical Specification gives guidance on the marking to be used on respiratory protective devices
(RPD) and the information to be supplied by the manufacturer/supplier.
2 Normative references
The following referenced documents are indispensable for the application 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.
ISO 7000, Graphical symbols for use on equipment — Index and synopsis
ISO 16972, Respiratory protective devices — Terms, definitions, graphical symbols and units of measurement
3 Terms and definitions
For the purposes of this document, the terms and definitions given in ISO 7000 and ISO 16972 apply.
4 General
4.1 Levels of marking and information system used for RPD
The marking and information system required for RPD shall have the following two levels.
Level 1: RPD system
For Level 1 the manufacturer shall provide minimum marking and information, as described in Clause 5,
on or with the respiratory protective device as worn by the individual.
Level 2: RPD components and replacement parts
For Level 2 the manufacturer shall provide minimum marking and information, as described in Clause 6,
on some components and replacement parts. This is only applicable to the listed components and
replaceable parts which are designated by the manufacturer as replaceable. Whenever feasible, this
marking shall be included on each individual part. If this is not feasible, the marking shall be on the
smallest commercially available package of parts.
4.2 Written information and marking
4.2.1 Written information should be at least in the official language(s) of the country of destination, or
nationally recognized language(s), as accepted.
4.2.2 Written information should explain the meaning of any graphical symbols.
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ISO/TS 16974:2011(E)
4.2.3 All marking and information should be readable, permanent and clearly visible.
NOTE Permanent marking is marking that cannot be removed without evidence of its removal.
4.2.4 When applicable, marking and information should be added in order to comply with national or local
regulations.
4.2.5 If additional marking is required in parts of the ISO 17420 series, the system or component shall be
marked accordingly.
5 Level 1: RPD system
5.1 Marking of RPD
The RPD should include at least the following marking:
a) manufacturer name, logo or identifying mark;
b) RPD model number, name or any other type identifying mark;
c) reference to ISO 17420-1 or ISO 17420-2, as applicable;
d) RPD classification;
NOTE This classification requirement will be updated in the next revision after a classification scheme has been
created.
e) means of traceability;
NOTE Format to be chosen by the manufacturer.
f) instructions to read the information supplied by the manufacturer (which may be done using ISO graphical
symbols);
g) size designation, if applicable.
5.2 Accompanying information
In addition to 5.1, information supplied by the manufacturer should include all the information, if applicable,
necessary for trained and qualified personnel on:
a) application(s) and limitations of the RPD and warnings and cautions associated with its use;
b) RPD model number, name or any other type identifying mark;
c) RPD classification;
d) assembly and operational instructions (description of pre-use checks and the mounting and orientation of
RPD components and parts);
e) meaning of graphical symbols;
f) warning devices, such as alarms, signals, etc., related to the use of the product;
g) storage conditions prior to use and between each use;
h) pre-use checks (e.g. wearer seal checks, adequate airflow) and post-use checks for damage during use;
i) compatibility with other personal protective equipment (PPE);
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ISO/TS 16974:2011(E)
j) correct donning and doffing;
k) shelf life, which may include a shelf life indicator attached to the packaging, RPD, component or expiry
date (if shelf life is associated with time, then an ISO 16972 graphical symbol which includes the year and
month should be used);
l) user maintenance, repair and inspection;
m) correct components and replacement parts of the RPD;
n) cleaning, disinfection and decontamination;
o) reusability of the RPD;
p) service life of the RPD, which may include components;
q) contact information of the manufacturer or supplier;
r) disposal.
This information may be contained on packaging or in the information supplied by the manufacturer (i.e. user
instructions). If the RPD is reusable, instructions shall be given that the information is to be retained for the life
of the RPD. In certain cases, national regulations may require certain information to be on the shipping
container.
6 Level 2: RPD components and replacement parts
6.1 General information
In addition to the requirements of Clause 5, all components, as mentioned in 6.2 to 6.7, and replacement
parts, as specified by the manufacturer, should contain the manufacturer name, logo or identifying mark and
part number or type identifying mark.
Whenever feasible, this marking should be included on replacement parts.
If this is not feasible, the marking should be on the smallest commercially available package of replacement
parts. Contact information of the manufacturer should be included.
6.2 Particle, gas/vapour or combination filters
6.2.1 Filter marking
The filter shall be marked with the following information:
a) filter type and class (colour, mark, number, etc.);
b) reference to ISO 17420-1, ISO 17420-2 or 17420-3, as applicable;
c) shelf life indication, e.g. end of shelf life ISO graphical symbol in accordance with ISO 16942;
d) means of traceability;
NOTE Format to be chosen by the manufacturer.
e) specific requirements (e.g. single use, maximum service life, etc.);
f) instructions to read the information supplied by the manufacturer (which may be done using ISO graphical
symbols).
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ISO/TS 16974:2011(E)
6.2.2 Accompanying information
In addition to 6.2.1, information supplied by the manufacturer should include all the information, if applicable,
necessary for trained and qualified personnel on:
a) application(s) and limitations of the filter, and warnings and cautions associated with its use;
b) explanation of filtration code (colour, mark, number, etc.) and its relation to the RPD classification;
c) assembly and operational instructions (description of pre-use checks and the mounting and orientation of
the filters in the RPD for which they are designed to be used);
d) meaning of graphical symbols;
e) warning devices, such as alarms, signals, etc., related to the use of the filter and RPD;
f) correct components and replacement parts of the RPD;
g) storage conditions prior to use and between each use;
h) explanation of the shelf life indication;
NOTE Indication may be related to time or the use of an indicator.
i) how to estimate or determine service life of the filter(s);
j) cleaning, disinfection and decontamination;
k) disposal.
This information may be contained on packaging or in the information supplied by the manufacturer (i.e. user
instructions). If the RPD is reusable, instructions shall be given that the information is to be retained for the lif
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