Product Specifications
96
Operator’s Manual
11.8
Product Compliance
11.9
Manufacturer’s Declaration
11.9.1
Electromagnetic Compatibility (EMC)
WARNING:
The use of accessories, pulse oximetry sensors, and cables other than those
specified may result in inaccurate readings of the monitoring system and
increased emission of the monitoring system.
Caution:
For best product performance and measurement accuracy, use only
accessories supplied or recommended by Covidien. Use accessories according
to the
Directions for Use
. Use only accessories that have passed the
recommended biocompatibility testing in compliance with ISO10993-1.
The use of accessories, sensors, and cables other than those specified may
result in inaccurate readings of the monitoring system and increased emission
and/or decreased electromagnetic immunity of the monitoring system.
Standards Compliance
EN ISO 9919:2009, EN ISO 80601-2-61:2011
EN IEC 60601-1:2005
EN IEC 60601-1-2:2nd edition
EN IEC 60601-1:1998 + A1:1991 + A2:1995
EN 60601-1:1990 + A11:1993 + A12:1993 + A13:1996
CAN/CSA C22.2 No. 601.1 M90
UL 60601-1: 1st edition
Equipment Classifications
Type of Protection against electric shock
Class I (internally powered)
Degree of Protection against electric shock
Type BF - Applied part
Mode of Operation
Continuous
Electromagnetic Compatibility
IEC 60601-1-2:2007
Liquid Ingress
IPX2
Degree of Safety
Not suitable for use in the presence of flammable anesthetics
Содержание Nellcor
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