User's Manual Part 1

1-14
should not be required, but if the specified operation does not occur, have a qualified service
person recheck the calibration. Proper re-calibration can only be performed during factory
service.
Gas sampling patient tubing and associated components are intended for single-patient use
only. Avoid cleaning or disinfecting these items for reuse. Inaccurate gas measurements or
cross contamination could result.
To prevent inaccurate or missed readings, keep the CO
2
patient tubing clear of any moving
mechanisms which may kink, cut or dislodge the patient tubing.
Avoid connecting the CO
2
calibration gas canister to the monitor by any method other than with
the designated calibration tubing. Connecting by any other method could invalidate the
calibration, and/or damage the monitor.
The gas measurements are displayed within 1 second of when the gas was sampled internally
to the associated analyzer.
1.3.7.5. Other
When positioned upon an IV pole or mobile cart, always secure the wheel locks when placed
within the MRI Magnet Room (Zone IV).
This product, or any of its parts, should not be repaired other than in accordance with written
instructions provided by
IRadimed Corporation, or altered without prior written approval of
IRadimed Corporation.
No parts of the 3880 Patient Monitoring System shall be serviced while they are in use with a
patient.
The user of this product shall have the sole responsibility for any malfunction which results from
improper use, faulty maintenance, improper repair, damage, or alteration by anyone other than
IRadimed Corporation, or its authorized service personnel.
This monitor is equipped with a demonstration mode which displays simulated electronic patient
data for training or demonstration purposes. Do not attach a patient to the monitor whenever
this simulation is present on the monitor display (“SIMULATION” can also be seen in the screen
center).
All monitor alarms are categorized as medium priority, unless otherwise specified.
The patient connector inputs for all parameters are protected against the use of a defibrillator by
internal circuitry, and when the recommended patient cables or accessories are used. Though
not intended for use with High Frequency Surgical Equipment, the use of this circuitry and the
recommended cables and accessories provided in section 9 protect against the hazards
resulting from use of high frequency surgical equipment.
This monitor should not be synchronized with a defibrillator.
There are no known electromagnetic or other hazardous interference between the monitor and
other devices. However, care should be taken to avoid the use of cellular phones or other
unintended radio-frequency transmitters in the proximity of the monitoring system.
This monitor is not intended to be used with exposure to Linear Accelerator beam.