Philips C240P4QPYEW-27 - Manual (Page 3)

1
1. Important
1. Important
The monitor is intended for use with Medical
Equipment to display alpha, numerical and
graphical data. The subject equipment Philips
monitor is powered by an external recognized
AC/DC adaptor. (IEC/EN60601-1).
1.1 Power adapter safety Information
Power adapter
This adapter (Manufacture: Philips, Model:
PMP60-13-1-HJ-S) is a forming part of the
medical device.
The connection of external equipments
External equipment intended for connection to
signal input/output or other connectors, shall
comply with relevant UL / IEC standard (e.g.
UL 60950 for IT equipment, UL 60601-1-1 and
ANSI/AAMI ES60601-1 / IEC 60601 series for
systems – shall comply with the standard IEC
60601-1-1, Safety requirements for medical
electrical systems. Equipment not complying
with MOPP of ANSI/AAMI ES60601-1 shall be
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in the standard.
Disconnecting Device
The mains plug or appliance coupler is used as
the disconnect device, the disconnect device
shall remain readily operable. Always completely
disconnect the power cord set from your
product whenever you are working or cleaning
on it. Do not make connections while the
power is on, because a sudden rush of power
can damage sensitive electronic components.
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‡ Degree of protection against the ingress of
water: IPX0
‡ Equipment not suitable for use in the
presence of a flammable anesthetic mixture
with air or with oxygen or nitrous oxide.
(Non AP or APG Category)
‡ Mode of operation: Continuous
‡ Type of protection against electric shock:
Class I ME Equipment
‡ No Applied part.
Shutdown Procedure
We strongly recommended that you should
shut down the system before you start to clean
any single components.
Please follow the steps below.
‡ Close all application programs
‡ Close operating software
‡ Turn off power switch
‡ Disconnect power cord set
‡ Remove all devices
Safety Symbol Description
The following safety symbols are the further
explanations for your reference.
Medical component
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mechanical hazards only in accordance with
ANSI/AAMI ES60601-1, and CAN/CSA C22.2
NO. 60601-1
Attention, consult ACCOMPANYING
DOCUMENTS.
Type of Current- AC
Dircet Current
European Community Approval,
The monitor complies with the 93/42/EEC and
2007/47/EC and conforms to the applicable
following standards: EN60601-1, EN 60601-1-2,
EN 61000-3-2 and EN 61000-3-3.
TUV Type Testing Approval,
The monitor complies with the EN60601-1
and IEC60601-1 of European Standards.
Power "ON"
Power "OFF"
Medical Equipment With respect to electric
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accordance with ANSI/AAMI ES 60601-1:2005,
and CAN/CSA C22.2 NO.60601-1:2008
Note
‡ Caution: Use suitable mounting apparatus
to avoid risk of injury.
‡ Use a power cord that matches the voltage
of the power outlet, which has been
approved and complies with the safety
standards of your particular country.
‡ Make sure user does not contact SIP/SOPs
and the patient at the same time.