Philips C240P4QPYEW/00 Lcd Monitor With Clinical Dimage

User Manual - Page 3

For C240P4QPYEW/00.

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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 monitor.
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.
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.
Classification
• 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.
With respect to electric shock, fire and
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 shock,, fire and mechanical
hazards only in accordance with ANSI/
AAMI ES 60601-1:2005, and CAN/CSA
C22.2 NO.60601-1:2008
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