Out-Of-Hospital Transport - Standards Compliance - Philips IntelliVue X2 Instructions For Use Manual

Out-Of-Hospital Transport - Standards Compliance

The X2 including the Wireless IntelliVue Adapter - CC 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.
The maximum antenna gain permitted (for devices in the 5250-5350 MHz and 5470-5725 MHz
bands) complies with the e.i.r.p. limits as stated in RSS-210.
The maximum antenna gain permitted (for devices in the 5725-5825 MHz band) complies with the
e.i.r.p. limits specified for point-to-point operation, as stated in RSS-210.
The device for the band 5150-5250 MHz is only for indoor usage to reduce potential for harmful
interference to co-channel mobile satellite systems.
CAUTION High power radars are allocated as primary users (meaning they have priority) of 5250-5350 MHz and
5650-5850 MHz and these radars could cause interference and /or damage to LE-LAN devices.
The radio device used in this product is in compliance with the essential requirements and other
relevant provisions of Directive 1999/5/EC. This product is intended to be connected to the Publicly
Available Interfaces (PAI) and used throughout the EEA.
In addition the product complies with: ETSI EN 300 328; ETSI EN 301 893; AS/NZS 4771+A1;
ARIB STD-T66.
The X2 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 X2 Multi-Measurement Module/patient monitor with measurements and interfaces other than
those listed below cannot be used for patient transport outside of the hospital environment.
The X2 Multi-Measurement Module/patient monitor, with the following measurements and
interfaces:
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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.
– ECG/Respiration, NBP, SpO
or call 1-800-674-3655
, Pressure, Temperature, CO
2
24 Specifications
(only Mainstream Sensor M2501A)
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