Notice
iii
As with all electronic equipment, Electromagnetic Interference (EMI)
between the defibrillator and any existing EMI transmitting or receiving
equipment at the installation site, including electrosurgical equipment,
should be evaluated carefully and any limitations noted before the
equipment is placed in service.
Do not attempt to perform pacing during surgery. Monitoring during
quiescent periods of electrosurgery is possible but electromagnetic
interference generated by electrosurgical tools during operation is
sufficient to mask cardiac signals. A momentary recovery period is required
for the monitor to return to normal operation and will be longer if the
diagnostic monitoring mode is used. Defib or monitoring electrodes should
be placed as far from the surgical area as reasonable while still performing
normal functions to minimize the possibility of burns. EMI frequency
generation from electrosurgical equipment and close proximity
transmitters may seriously degrade performance of the HP CodeMaster
100 .
Hewlett-Packard assumes no liability for failures resulting from EMI
between HP medical electronics and any radio frequency generating
equipment at levels exceeding those established by applicable standards.
Federal law (USA) restricts this device to sale by or on the order of a
physician.
THIS PRODUCT IS NOT INTENDED FOR HOME USE.
This product complies with the requirements of the Medical Device Directive
93/42/EEC and carries the CE
0123
marking accordingly. Authorized EU-
representative: Hewlett-Packard GmbH, Department MPG-E Regulations,
Herrenberger Str. 110-140, 71034 Boblingen (FAX: +49-7031-14-2346)
This product complies with the telecom regulatory standards for internal
modems set by the Federal Communications Commission (FCC) in the
United States, Industry Canada, and the Department of Trade and Industry in
the United Kingdom.
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