Download  Print this page

Emc And Radio Regulatory Compliance - Philips IntelliVue MP5 Instructions For Use Manual

Patient monitor.
Hide thumbs

Advertisement

Table of Contents

EMC And Radio Regulatory Compliance

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; CAN/CSA C22.2#601.1-M90; JIS T 0601-1:1999; IEC 60601-1-1:2001; 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 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.
EMC And Radio Regulatory Compliance
This ISM device complies with Canadian ICES-001. Cet appareil ISM est conforme a la norme NMB-
001 du Canada.
The MP5 including IntelliVue Instrument Telemetry WMTS (US only)
FCC Rules. Operation is subject to the condition that this device does 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.
The MP5 including IntelliVue Instrument Telemetry ISM (2.4 GHz) - 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.
This product is intended to be connected to the Publicly Available Interfaces (PAI) and used
throughout the EEA.
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 5150-5250 MHz is only for indoor usage to reduce potential for harmful
interference to co-channel mobile satellite systems.
The OEM 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.
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 2 radio equipment. Member
states may apply restrictions on putting this device into service or placing it on the market.
31 Installation and Specifications
complies with part 15 of the
.
301

Advertisement

Table of Contents

Comments to this Manuals

Symbols: 0
Latest comments: