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Out-of-hospital Transport - Standards Compliance - Philips IntelliVue MP5 Instructions For Use Manual

Patient monitor.
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31 Installation and Specifications
High power radars are allocated as primary users (meaning they have priority) of 5250-5350 MHz and
CAUTION
5650-5850 MHz and these radars could cause interference and /or damage to LE-LAN devices.
IntelliVue 802.11 Bedside Adapter CE compliances:
The MP5 including the short range radio interface - FCC and Industry Canada Radio Compliance:
This device complies with Part 15 of the FCC Rules and RSS-210 of Industry Canada. Operation is
subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this
device must accept any interference received, including interference that may cause undesired
operation. Any changes or modifications to this equipment not expressly approved by Philips Medical
Systems may cause harmful radio frequency interference and void your authority to operate this
equipment.
In addition the product complies with: ETSI EN 300 328; AS/NZS 4771+A1; ARIB STD-T66.

Out-Of-Hospital Transport - Standards Compliance

The MP5 patient monitor with measurements and interfaces other than those listed below, and the
MP5T, cannot be used for patient transport outside of the hospital environment.
The MP5 patient monitor with the following measurements and interfaces:
– ECG/Respiration, NBP, SpO
and Microstream CO
– LAN, Video Out, Battery, Nurse Call, RS232, and recorder interfaces
can be used in a transport environment such as a road ambulance, airplane or helicopter. For this
purpose the monitor fulfils the following additional mechanical, EMC and environmental
requirements:
• Shock Tests according to IEC TR 60721-4-7, Class 7M3. Test procedure according to IEC/EN
60068-2-27 (peak acceleration up to 100g).
• Random Vibration according to IEC TR 60721-4-7, Class 7M3. Test procedure according to IEC/
EN 60068-2-64 (RMS acceleration 5g).
• Sinusoidal Vibration according to IEC TR 60721-4-7, Class 7M3. Test procedure according to
IEC/EN 60068-2-6 (acceleration up to amplitude 2g).
• Bump Test according to IEC/EN60068-2-29 (peak acceleration 15 g, 1000 bumps).
• Free Fall Test according to EN1789 (covers also IEC TR 60721-4-7 and Class 7M3). Test
procedure according to EN 60068-2-32 (height 0.75 m).
302
This device is compliant to Council Directive 73/23/EEC (Low voltage directive) & 89/
336/EEC (EMC directive) & 1999/5/EC (Radio Equipment and Telecommunications
Terminal Equipment Directive)
The radio component contained in this device is compliant to Council Directive 1999/5/
EC (Radio Equipment and Telecommunications Terminal Equipment Directive)
The radio device used in this product is in compliance with the essential requirements and
other relevant provisions of Directive 1999/5/EC (Radio Equipment and
Telecommunications Terminal Equipment Directive). Class 1 radio equipment.
2
)
2
Out-Of-Hospital Transport - Standards Compliance
, Pressure, Temperature, CO
(only Mainstream Sensor M2501A
2

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