Amendment 1 - Medical electrical equipment - Part 2-52: Particular requirements for the basic safety and essential performance of medical beds

Amendement 1 - Appareils électromédicaux - Partie 2-52: Exigences particulières de sécurité de base et de performances essentielles des lits médicaux

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Published
Publication Date
17-Mar-2015
Current Stage
PPUB - Publication issued
Start Date
31-Mar-2015
Completion Date
18-Mar-2015
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IEC 60601-2-52:2009/AMD1:2015 - Amendment 1 - Medical electrical equipment - Part 2-52: Particular requirements for the basic safety and essential performance of medical beds
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IEC 60601-2-52
Edition 1.0 2015-03
INTERNATIONAL
STANDARD
NORME
INTERNATIONALE
A MENDMENT 1
AM ENDEMENT 1
Medical electrical equipment –
Part 2-52: Particular requirements for the basic safety and essential performance
of medical beds
Appareils électromédicaux –
Partie 2-52: Exigences particulières de sécurité de base et de performances
essentielles des lits médicaux

IEC 60601-2-52:2009-12/AMD1:2015-03(en-fr)

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IEC 60601-2-52
Edition 1.0 2015-03
INTERNATIONAL
STANDARD
NORME
INTERNATIONALE
A MENDMENT 1
AM ENDEMENT 1
Medical electrical equipment –

Part 2-52: Particular requirements for the basic safety and essential performance

of medical beds
Appareils électromédicaux –
Partie 2-52: Exigences particulières de sécurité de base et de performances

essentielles des lits médicaux

INTERNATIONAL
ELECTROTECHNICAL
COMMISSION
COMMISSION
ELECTROTECHNIQUE
INTERNATIONALE
ICS 11.140 ISBN 978-2-8322-2390-1

– 2 – IEC 60601-2-52:2009/AMD1:2015
© IEC 2015
FOREWORD
This amendment has been prepared by subcommittee 62D: Electromedical equipment, of IEC
technical committee 62: Electrical equipment in medical practice.
The text of this amendment is based on the following documents:
FDIS Report on voting
62D/1186/FDIS 62D/1232/RVD
Full information on the voting for the approval of this amendment can be found in the report
on voting indicated in the above table.
The committee has decided that the contents of this amendment and the base publication will
remain unchanged until the stability date indicated on the IEC web site under
"http://webstore.iec.ch" in the data related to the specific publication. At this date, the
publication will be
• reconfirmed,
• withdrawn,
• replaced by a revised edition, or
• amended.
_____________
201.1.1 * Scope
Replace the existing text of the first paragraph with the following:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of
MEDICAL BEDS as defined in 201.3.212, intended for ADULTS as defined in 201.3.219.
201.1.2 Object
Replace the existing text of the replacement with the following:
The object of this particular standard is to establish particular BASIC SAFETY and ESSENTIAL
PERFORMANCE requirements for MEDICAL BEDS as defined in 201.3.212 intended for ADULTS as
defined in 201.3.219.
201.3 Terms and definitions
Add the following new term and definition:
201.3.219
* ADULT
PATIENT having a physical size equal to or more than 146 cm, a mass equal to or more than
40 kg and a body mass index (BMI) equal to or more than 17

201.4 General requirements
Replace the existing text of the clause by the following:

© IEC 2015
Clause 4 of the general standard applies, except as follows:
201.4.2.2 * General requirement for RISK MANAGEMENT
Addition:
The MANUFACTURER shall include, in the RISK MANAGEMENT PROCESS, HAZARDS related to
PATIENTS taller than 185 cm.
Compliance is checked by inspection of the RISK MANAGEMENT FILE.

Figure 201.103 – Entrapment test tools
Replace the existing figure by the following new figure:
Dimensions in millimetres
Ø120 -0,5
228 ±1
115 ±1
IEC
Key
1 Total weight 5,1 kg ±0,05 kg
2 Marked centre line
3 Surface roughness 1,6
4 Drilling hole for weight adjustment
Figure 201.103a) – Cone tool schematic
Ø60 -0,5
– 4 – IEC 60601-2-52:2009/AMD1:2015
© IEC 2015
Dimensions in millimetres
+1
318 0
1 3
IEC
Key
1 Total weight 3,34 kg ±0,05 kg
2 Marked centre line
3 Surface roughness 1,6
4 Drilling hole for weight adjustment
Figure 201.103b) – Cylinder tool schematic
Figure 201.103 – Entrapment test tools
201.7 ME EQUIPMENT identification, marking and documents
201.7.2.2 Identification
Add, after 201.7.2.2.106, the following new subclause:
201.7.2.2.107 Marking on the MEDICAL BED for ADULTS
The MEDICAL BEDS shall be marked on a prominent place with the symbol indicated in Figure
201.106.
IEC
Figure 201.120 – Physical description of an ADULT
Ø60 -0,5
Ø43,9 ±0,2
© IEC 2015
201.7.9.2 Instructions for use
201.7.9.2.1 General
Add the following new item:
e) a description of the intended PATIENT group(s).

201.7.9.2.2 Warning and safety notices
Add the following new items:
e) The instructions for use shall provide a warning if a MEDICAL BED is limited to a specific
group of PATIENTS.
f) The instructions for use shall provide a warning that incompatible SIDE RAILS and
mattresses can cause an entrapment hazard

201.9 Protection against MECHANICAL HAZARDS of ME EQUIPMENT and ME SYSTEMS
Figure 201.107 – Example of MEDICAL BED with segmented or split SIDE RAIL
Replace the existing figure with the following:
IEC
Only applies when the area C above is < 60 mm.
A represents the different areas A , A , A , A , A and A
x
1 2 3 4 5 6
Key
1 Area of TOOL representing neck diameter (60 mm).
2 Area of TOOL representing chest breadth (318 mm).
3 Area of TOOL representing head breadth (120 mm).

– 6 – IEC 60601-2-52:2009/AMD1:2015
© IEC 2015
4 MATTRESS SUPPORT PLATFORM
5 HEAD BOARD
6 FOOT BOARD
7 Mattress
8 SIDE RAIL
Figure 201.107 – Example of MEDICAL BED with segmented or split SIDE RAIL
Figure 201.108 – Example of MEDICAL BED with single piece SIDE RAIL
Replace the existing figure with the following:
IEC
Only applies when the area C is < 60 mm.
Key
1 Area of TOOL representing neck diameter (60 mm).
2 Area of TOOL representing chest breadth (318 mm).
3 Area of TOOL representing head breadth (120 mm).
4 MATTRESS SUPPORT PLATFORM
5 HEAD BOARD
6 FOOT BOARD
7 Mattress
8 SIDE RAIL
Figure 201.108 – Example of MEDICAL BED with single piece SIDE RAIL

© IEC 2015
201.9.8.3.2 *Static forces due to loading from persons
Add, after the existing second paragraph the following note:
NOTE It might be necessary to support assemblies that are connected to the assembly under test but do not
require such a high safety factor, e.g. an assembly under test requires a TENSILE SAFETY FACTOR of 4 and the
assembly supporting it is designed with a lower TENSILE SAFETY FACTOR. Use of additional support should be
explained in the test report.
Annex AA – Particular guidance and rationale
AA.2 Rationale for particular clauses and subclauses
Subclause 201.1.1 – Scope
Add, at the end of the existing third sentence, the phrase: ", a weight of equal to or more than
40 kg and a body mass index (BMI) equal to or more than 17."

Add the following new rationales:
Definition 201.3.201 – ADULT
The body mass index is calculated by the following formula:
m
BMI=
l
Where:
m in kg
l in m
The body mass index (BMI) as an additional measure for the shape of the human body was
included in IEC 60601-2-52, since the physical size of some patients is indeed inside the
limits of the first version of IEC 60601-2 52 (exceeding 146 cm and 40 kg) but nevertheless
due to their particular atypical anatomy there might be a risk of being entrapped in the side
rails.
The body mass index (BMI) is a measure for the human body shape based on an individual's
mass and height. BMI provides a simple numeric measure of a person's thickness or thinness,
allowing health professionals to discuss overweight and underweight problems more
objectively with their PATIENTS.
For an explanation see also 201.1.1.
Subclause 201.4.2 – RISK MANAGEMENT PROCESS for ME EQUIPMENT or ME SYSTEMS
Possible HAZARDS may be: rolling over the SIDE RAIL, entrapment in MEDICAL BED extension and
HAZARDS related to the TRAPPING ZONES described in 201.9.2.2.

– 8 – IEC 60601-2-52:2009/AMD1:2015
© IEC 2015
Subclause 201.9.101 – Protection against inadvertent PATIENT falls
Delete the existing fourth paragraph of this rationale.

_____________
– 10 – IEC 60601-2-52:2009/AMD1:2015
© IEC 2015
AVANT-PROPOS
Le présent amendement a été établi par le sous-comité 62D: Appareils électromédicaux, du
comité d'études 62 de l'IEC: Equipements électriques dans la pratique médicale.
Le texte de cet amendement est issu des documents suivants:
FDIS Rapport de vote
62D/1186/FDIS 62D/1232/RVD
Le rapport de vote indiqué dans le tableau ci-dessus donne toute information sur le vote ayant
abouti à l'approbation de cet amendement.
Le comité a décidé que le contenu de cet amendement et de la publication de base ne sera
pas modifié avant la date de stabilité indiquée sur le site web de l’IEC sous
"http://webstore.iec.ch" dans les données relatives à la publication recherchée. A cette date,
la publication sera
• reconduite,
• supprimée,
• remplacée
...

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