Introduction
2067634-077 Revision B
SEER™ 1000
17
Category
Classification
Degree of safety of application in
the presence of a flammable anes-
thetic mixture with air or with oxy-
gen or with nitrous oxide
Equipment is not suitable for use in the
presence of a flammable anesthetic
mixture with air or with oxygen or with
nitrous oxide.
Method(s) of sterilization recom-
mended by the manufacturer
Not applicable
Mode of operation
Continuous operation.
Certification
Medical Equipment
With respect to electric shock, fire, and mechanical and
other specified hazards only in accordance with
IEC 60601-1, CAN/USA C22.2 NO. 601.1, IEC 60601-1-2,
and IEC 60601-2-47
Input Signal Reproduction Accuracy
The frequency response meets the following IEC 60601-2-47 Part 51.5.9
requirements:
The response of the recorder to a 5 mV 100 ms rectangular pulse
does not show a baseline amplitude displacement after the pulse of
more than 0.1 mV referred to the baseline before the pulse. The slope
outside the pulse is less than 0.3 mV/s. The leading edge overshoot is
less than 10%.
The responses to all pulses of a 1.5 mV, 40 ms triangular pulse train,
which simulates a series of narrow R-waves, is within 80% to 110% of
the response to a train of 1.5 mV, 200 ms triangular pulses.
EMI/EMC/RF Caution
This system is designed and tested to comply with applicable regulations
regarding EMC. Changes or modifications to this system not expressly ap-
proved by manufacturer could cause EMC issues with this or other equip-
ment.
