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34 Installation and Specifications Altitude Setting
336
Altitude Setting
Altitude affects tcGas and CO
2
measurements. The monitor must be configured at installation to the
correct altitude.
Monitor Safety Specifications
The monitors, together with the Multi-Measurement Server (M3001A), and the Flexible Module
Server (M8048A), all modules and measurement server extensions, comply with the Medical Device
Directive 93/42/EEC.
In addition, the product complies with:
IEC 60601-1:1988 + A1:1991 + A2:1995; EN60601-1:1990 + A1:1993 + A2:1995; UL 60601-
1:2003; UL 2601.1:1994; CAN/CSA C22.2#601.1-M90; JIS T 1001-1992; IEC 60601-1-1:2000;
EN 60601-1-1:2001; IEC 60601-1-2:2001; EN 60601-1-2:2001.
Classification (according to IEC 60601-1): Class 1, Type CF, Continuous Operation. The BIS
measurement uses a Type BF applied part.
The possibility of hazards arising from software errors was minimized in compliance with ISO
14971:2000, EN60601-1-4:1996 + A1:1999 and IEC 60601-1-4:1996 + A1:1999.
This ISM device complies with Canadian ICES-001. Cet appareil ISM est conforme a la norme NMB-
001 du Canada.
185-0145-PH Aspect BISx, 185-0111 Aspect BIS Engine and 185-0124 Aspect DSC comply with the
requirements of the Council Directive 93/42/EEC of 14 June 1993 (Medical Device Directive).
The MP20/30 including IntelliVue Instrument Telemetry and the MP40/50 with the IntelliVue
Instrument Telemetry adapter
comply with part 15 of the FCC Rules. Operation is subject to the
condition that these devices do not cause harmful interference
. Operation of this equipment requires
the prior coordination with a frequency coordinator designated by the FCC for the Wireless Medical
Telemetry Service.
IntelliVue 802.11 Bedside Adapter (Option J35 Wireless Network Adapter) - 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.
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 5150-5350 MHz is only for indoor usage to reduce potential for harmful
interference to co-channel mobile satellite systems.
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