prEN ISO 11199-2
(Main)Assistive products for walking, manipulated by both arms - Requirements and test methods - Part 2: Rollators (ISO/DIS 11199-1:2020)
Assistive products for walking, manipulated by both arms - Requirements and test methods - Part 2: Rollators (ISO/DIS 11199-1:2020)
Mit beiden Armen gehandhabte Gehhilfen - Anforderungen und Prüfverfahren - Teil 2: Rollatoren (ISO/DIS 11199-1:2020)
Dieser Teil von ISO 11199 legt Anforderungen und Prüfverfahren für Rollatoren, die als Gehhilfen mit Rädern genutzt und mit beiden Armen gehandhabt werden, ohne Zubehör fest, sofern es in dem bestimmten Prüfverfahren nicht anders festgelegt ist. Dieser Teil von ISO 11199 enthält außerdem Anforderungen bezüglich der Sicherheit, Ergonomie und Leistungsfähigkeit und der vom Hersteller bereitzustellenden Informationen, einschließlich Kennzeichnung und Aufschriften.
Die Anforderungen und Prüfungen beruhen auf dem alltäglichen Gebrauch von Rollatoren als Gehhilfen für Personen mit einem vom Hersteller festgelegtem Höchstgewicht. Dieser Teil von ISO 11199 schließt Rollatoren ein, die für Personen mit einem Körpergewicht von mindestens 35 kg bestimmt sind.
Dieser Teil von ISO 11199 gilt nicht für Rollatoren mit waagerechten Unterarmstützen, die als Gehwagen eingeteilt sind und für die ISO 11199-3 gilt.
Aides à la marche manipulées avec les deux bras - Exigences et méthodes d'essai - Partie 2: Déambulateurs (ISO/DIS 11199-1:2020)
Pripomočki za hojo, ki se upravljajo z obema rokama - Zahteve in preskusne metode - 2. del: Rolatorji (ISO/DIS 11199-2:2020)
General Information
RELATIONS
Standards Content (sample)
SLOVENSKI STANDARD
oSIST prEN ISO 11199-2:2020
01-september-2020
Pripomočki za hojo, ki se upravljajo z obema rokama - Zahteve in preskusne
metode - 2. del: Rolatorji (ISO/DIS 11199-2:2020)
Assistive products for walking, manipulated by both arms - Requirements and test
methods - Part 2: Rollators (ISO/DIS 11199-2:2020)
Mit beiden Armen gehandhabte Gehhilfen - Anforderungen und Prüfverfahren - Teil 2:
Rollatoren (ISO/DIS 11199-2:2020)Aides à la marche manipulées avec les deux bras - Exigences et méthodes d'essai -
Partie 2: Déambulateurs (ISO/DIS 11199-2:2020)Ta slovenski standard je istoveten z: prEN ISO 11199-2
ICS:
11.180.10 Pripomočki in prilagoditve za Aids and adaptation for
gibanje moving
oSIST prEN ISO 11199-2:2020 en,fr,de
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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oSIST prEN ISO 11199-2:2020
DRAFT INTERNATIONAL STANDARD
ISO/DIS 11199-2
ISO/TC 173 Secretariat: SIS
Voting begins on: Voting terminates on:
2020-06-11 2020-09-03
Assistive products for walking, manipulated by both
arms — Requirements and test methods —
Part 2:
Rollators
Aides à la marche manipulées avec les deux bras — Exigences et méthodes d'essai —
Partie 2: DéambulateursICS: 11.180.10
THIS DOCUMENT IS A DRAFT CIRCULATED
This document is circulated as received from the committee secretariat.
FOR COMMENT AND APPROVAL. IT IS
THEREFORE SUBJECT TO CHANGE AND MAY
NOT BE REFERRED TO AS AN INTERNATIONAL
STANDARD UNTIL PUBLISHED AS SUCH.
IN ADDITION TO THEIR EVALUATION AS
ISO/CEN PARALLEL PROCESSING
BEING ACCEPTABLE FOR INDUSTRIAL,
TECHNOLOGICAL, COMMERCIAL AND
USER PURPOSES, DRAFT INTERNATIONAL
STANDARDS MAY ON OCCASION HAVE TO
BE CONSIDERED IN THE LIGHT OF THEIR
POTENTIAL TO BECOME STANDARDS TO
WHICH REFERENCE MAY BE MADE IN
Reference number
NATIONAL REGULATIONS.
ISO/DIS 11199-2:2020(E)
RECIPIENTS OF THIS DRAFT ARE INVITED
TO SUBMIT, WITH THEIR COMMENTS,
NOTIFICATION OF ANY RELEVANT PATENT
RIGHTS OF WHICH THEY ARE AWARE AND TO
PROVIDE SUPPORTING DOCUMENTATION. ISO 2020
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oSIST prEN ISO 11199-2:2020
ISO/DIS 11199-2:2020(E)
COPYRIGHT PROTECTED DOCUMENT
© ISO 2020
All rights reserved. Unless otherwise specified, or required in the context of its implementation, no part of this publication may
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ii © ISO 2020 – All rights reserved
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oSIST prEN ISO 11199-2:2020
ISO/DIS 11199-2:2020(E)
Contents Page
Foreword ..........................................................................................................................................................................................................................................v
Introduction ................................................................................................................................................................................................................................vi
1 Scope ................................................................................................................................................................................................................................. 1
2 Normative references ...................................................................................................................................................................................... 1
3 Terms and definitions ..................................................................................................................................................................................... 1
4 Apparatus ..................................................................................................................................................................................................................... 6
5 Test conditions ....................................................................................................................................................................................................... 7
6 General requirements and test methods .................................................................................................................................... 8
6.1 Risk analysis .............................................................................................................................................................................................. 8
6.2 Rollators that can be dismantled ......... .................................................................................................................................... 8
6.3 Fasteners ...................................................................................................................................................................................................... 8
6.4 User mass/Load limits ..................................................................................................................................................................... 8
6.5 Structure requirements ................................................................................................................................................................... 8
6.6 Brakes ............................................................................................................................................................................................................. 9
6.6.1 General requirements .................................................................................................................................................. 9
6.6.2 Brake test ...................................................................... .......................................................................................................... 9
6.7 Handgrip ....................................................................................................................................................................................................10
7 Materials ....................................................................................................................................................................................................................10
7.1 General ........................................................................................................................................................................................................10
7.2 Flammability ..........................................................................................................................................................................................10
7.2.1 Upholstered parts ........................................................................................................................................................10
7.3 Biocompatibility and toxicity ..................................................................................................................................................10
7.4 Infection and microbiological contamination ...........................................................................................................11
7.4.1 General...................................................................................................................................................................................11
7.4.2 Cleaning and disinfection ......................................................................................................................................11
7.5 Resistance to corrosion ................................................................................................................................................................11
8 Ingress of liquids ...............................................................................................................................................................................................11
9 Temperatures of parts that come in contact with human skin .........................................................................11
10 Safety of moving parts .................................................................................................................................................................................12
10.1 Squeezing ..................................................................................................................................................................................................12
10.2 Mechanical wear .................................................................................................................................................................................12
11 Prevention of traps for parts of the human body ............................................................................................................13
11.1 Holes and clearances ......................................................................................................................................................................13
12 Folding, adjusting and locking mechanisms .........................................................................................................................13
12.1 General ........................................................................................................................................................................................................13
12.2 Folding mechanisms ........................................................................................................................................................................14
12.3 Locking mechanisms .......................................................................................................................................................................14
13 Carrying handles ...............................................................................................................................................................................................14
13.1 General ........................................................................................................................................................................................................14
13.2 Requirement ..........................................................................................................................................................................................14
13.3 Test method ............................................................................................................................................................................................14
14 Surfaces, corners and edges ..................................................................................................................................................................15
15 Stability .......................................................................................................................................................................................................................15
15.1 Requirements for static stability ..........................................................................................................................................15
15.2 Test method for static stability ..............................................................................................................................................15
15.2.1 Forward-direction stability test .......................................................................................................................15
15.2.2 Rearward-direction stability test ...................................................................................................................16
15.2.3 Sideway-direction stability test .......................................................................................................................17
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15.2.4 Accessory equipment stability test ...............................................................................................................18
16 Static strength ......................................................................................................................................................................................................18
16.1 Static strength of resting seat ..................................................................................................................................................18
16.1.1 Requirements for static strength of resting seat ...............................................................................18
16.1.2 Test method for static strength of resting seat ...................................................................................18
16.2 Static strength of the rollator ..................................................................................................................................................19
16.2.1 Requirements for static strength of the rollator................................................................................19
16.2.2 Test method for static strength of the rollator ....................................................................................19
16.3 Strength of Backrest ........................................................................................................................................................................19
16.3.1 Requirement for strength of backrest ........................................................................................................19
16.3.2 Test method for strength of backrest ..........................................................................................................20
17 Durability test .......................................................................................................................................................................................................20
17.1 Requirement for durability .......................................................................................................................................................20
17.2 Test method for durability .........................................................................................................................................................20
18 Ergonomic principles ...................................................................................................................................................................................21
19 Packaging ..................................................................................................................................................................................................................22
20 Information supplied by the manufacturer ..........................................................................................................................22
20.1 General ........................................................................................................................................................................................................22
20.2 Information marked on the product .................................................................................................................................23
20.3 Instruction manual ...........................................................................................................................................................................23
20.4 Test report ................................................................................................................................................................................................24
Annex A (informative) Consideration items for hazards when designing the products ..............................25
Annex B (informative) General recommendations .............................................................................................................................27
Annex C (informative) Environmental and consumer-related requirements ........................................................30
Annex D (informative) Cognitive impairment ..........................................................................................................................................35
Bibliography .............................................................................................................................................................................................................................36
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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.The procedures used to develop this document and those intended for its further maintenance are
described in the ISO/IEC Directives, Part 1. In particular, the different approval criteria needed for the
different types of ISO documents should be noted. This document was drafted in accordance with the
editorial rules of the ISO/IEC Directives, Part 2 (see www .iso .org/ directives).
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. Details of
any patent rights identified during the development of the document will be in the Introduction and/or
on the ISO list of patent declarations received (see www .iso .org/ patents).Any trade name used in this document is information given for the convenience of users and does not
constitute an endorsement.For an explanation of the voluntary nature of standards, the meaning of ISO specific terms and
expressions related to conformity assessment, as well as information about ISO's adherence to the
World Trade Organization (WTO) principles in the Technical Barriers to Trade (TBT), see www .iso .org/
iso/ foreword .html.This document was prepared by Technical Committee 173, Assistive products for persons with
disability.This third edition cancels and replaces the second edition (ISO 11199-2:2005), which has been
technically revised.The main changes compared to the previous edition are as follows:
— corrected the definition of Rollator to conform to the definition described in ISO 9999:2016
(classification no.: 12 06 06)— added the clause for requirements and test methods for backrest
— added the clauses for relevant general requirements for assistive products for walking based upon
ISO/DIS 21856, ISO 17966, and EN12182Assistive products for walking manipulated by both arms are covered by the following International
Standards:— Part 1: Walking frames
— Part 2: Rollators
— Part 3: Walking tables
— ISO 19894: Walking trolleys
These Standards can be found on the ISO website.
Any feedback or questions on this document should be directed to the user’s national standards body. A
complete listing of these bodies can be found at www .iso .org/ members .html.© ISO 2020 – All rights reserved v
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Introduction
A rollator, as defined in ISO 11199-2 can be used when a person needs assistance when walking. The
rollator can provide stability when walking and standing and reduce the risk of falling. Rollators are
designed to support the user inside a frame to carry the user’s weight. Rollators may be equipped with
a resting seat, backrest and/or shopping bag. Rollators are not intended to be moved with the user on
the seat like a wheelchair. The seat is provided as a resting seat with brakes engaged. In addition to the
requirements in this international standard, Annex B gives general recommendations.
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oSIST prEN ISO 11199-2:2020
DRAFT INTERNATIONAL STANDARD ISO/DIS 11199-2:2020(E)
Assistive products for walking, manipulated by both
arms — Requirements and test methods —
Part 2:
Rollators
1 Scope
This part of ISO 11199 specifies requirements and test methods of rollators being used as assistive
products for walking with wheels, manipulated by both arms, without accessories, unless specified
in the particular test procedure. This part of ISO 11199 also gives requirements relating to safety,
ergonomics, performance and information supplied by the manufacturer including marking and
labelling.The requirements and tests are based on every-day use of rollators as assistive products for walking
for a maximum user mass as specified by the manufacturer. This part of ISO 11199 includes rollators
specified for a user mass of no less than 35 kg.This part of ISO 11199 is not applicable to rollators with horizontal forearm supports, classified as
walking tables, for which ISO 11199-3 is applicable.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.
ISO 8191-2, Furniture — Assessment of ignitability of upholstered furniture — Part 2: Ignition source:
match-flame equivalentISO 9227, Corrosion tests in artificial atmospheres — Salt spray tests
ISO 10993-1, Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk
management processISO 14971, Medical devices — Application of risk management to medical devices
ISO 15223-1, Medical device – Symbols to be used with medical device labels, labelling and information to
be supplied – Part 1: Genera; requirementsISO 20417, Information to be provided by the manufacturer
ISO 7000, Graphical symbols for use on equipment — Registered symbols
ISO/IEC Guide 71, Guide for addressing accessibility in standards
EN 12182, Assistive products for persons with disability. General requirements and test methods
EN 614-1, Safety of machinery - Ergonomic design principles - Part 1: Terminology and general principles
3 Terms and definitionsFor the purposes of this document, the terms and definitions provided with the following sites apply in
addition to the ones described in this clause.© ISO 2020 – All rights reserved 1
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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
rollator
Frames which can be moved by pushing or pulling, that enable a person to support full body weight
and to maintain stability and balance while walking and standing with hand grips and three or more
castors/wheels without forearm supports. (See Figure 1)Note 1 to entry: Double or more castors/wheels used for one pivot position shall be counted as one castor/wheel.
Included are e.g., rollators with a seat for resting, reverse rollators that are pulled with the opening in the front.
Note 2 to entry: ISO 9999 2016, Classification No. 12 06 06Key
1 rear 6 resting seat
2 brake handle 7 front
3 height adjustment mechanism 8 bracing member
4 folding mechanism 9 wheels
5 handle/handgrip
Figure 1 — Example of Rollator
3.2
maximum user mass
greatest permissible weight of the person using the product declared by the manufacture
3.3maximum length
maximum outside dimension of a rollator when the adjustments are at their maximum, measured
parallel to the direction of straight forward movement when the rollator is in normal use
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ISO/DIS 11199-2:2020(E)
See Figure 2.
3.4
maximum width
maximum outside dimension of a rollator when the width is adjusted at its maximum, measured
horizontally at right angles to the direction of movementSee Figure 2.
3.5
rollator height
vertical distance from the highest point of the handle to the ground surface
See Figure 2.
3.6
turning width
minimum distance between two parallel limiting walls in between which a rollator can be turned 180°
See Figure 2.Note 1: The adjustments are to be at their maximum.
Key
1 turning width 4 width
2 Width between handles 5 height
3 length
Figure 2 — Dimensions of a rollator
3.7
folded dimensions
height, width and length of the rollator measured with the rollator folded together without the use of tools
3.8handgrip
that part of the rollator which is intended by the manufacturer to be held by the hand when the rollator
is in useSee Figure 3.
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3.9
handle
that part of the rollator to which the handgrip is attached
3.10
front handgrip reference point
that point on the upper surface of the handgrip located 30 mm from the front end of the handgrip length
See Figure 3.3.11
rear handgrip reference point
that point on the upper surface of the handgrip located 30 mm from the rear end of the handgrip length
See Figure 3.3.12
handgrip length
dimension of the handgrip measured where the hand rests
See Figure 3.
Note 1 to entry: Where the front end or the rear end of the handgrip is not clear, the full length of the handgrip
that may comfortably support the mass of the user is defined as the handgrip length.
3.13handgrip width
outside dimension of the handgrip measured at the thickest point where the hand rests
See Figure 3.3.14
brake grip distance
the distance measured, with the brake handle in the neutral position, at the midpoint of the handgrip
length and normal to the centerline of the handle tubing, from the upper surface of the handgrip to the
lower surface of the brake handleSEE: Figure 4.
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Key
1 rear handgrip reference point 4 handgrip width
2 front handgrip reference point 5 front
3 handgrip length
Figure 3 — Detailed drawing of a handgrip
Key
1 brake grip distance 3 front handgrip reference point
2 rear handgrip reference point 4 front
Figure 4 — Brake grip distance
3.15
parking brake
a brake that stays engaged after being activated
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3.16
running brake
a brake that is operated by the user during walking and where the braking effect depends proportionally
on the activation force applied3.17
wheel width
maximum dimension of the tyre of the wheel measured within 5 mm up from the walking surface when
the rollator is unloadedSEE: Figure 5.
Key
1 tyre 3 wheel width
2 0 to 5 mm up from the walking surface
Figure 5 — Wheel width measurement
3.18
resting seat
seat for the user to take a rest
3.19
shopping bag
bag attached on the rollator to carry goods
4 Apparatus
4.1 Means to apply a force with an accuracy of ± 5 % and with a rate of application less than 1 N/s.
4.2 Means to measure force with an accuracy of ± 5 % in increments of 1 N.4.3 Means to measure distance in the range of 0 m to 3 m with an accuracy of ± 5 mm or ± 2 %
whichever is the greater4.4 Means to measure angles to an accuracy of ± 0,5°.
4.5 Means to measure torque with an accuracy of ± 5 % in increments of 1 Nm in the range of 0,5 Nm
to 10 Nm6 © ISO 2020 – All rights reserved
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4.6 A test plane of sufficient size and stiffness to support the rollator during testing, such that the
whole surface is contained between two imaginary parallel planes 5 mm a part. The test plane may be
adjustable, or fixed.Note 1 A wooden or steel frame with a plywood surface can be used.
Note 2 A test surface of 1.5 m x 2 m is usually of sufficient size.
4.7 Stoppers devices of sufficient height to prevent the rollator from moving during testing, without
interfering with the test or the rollator4.8 Equipment for measuring pressure of air with an accuracy of ± 5 %
4.9 Seat loading pad shall be of a rectangular construction 340 mm ± 3 mm width, minimu
...
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