Philips C240P4QPYEW C240P4QPYEW/27 Data Sheet

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.

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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.

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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.