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SPILLAGE
Liquid spilled onto the monitor may cause damage to the monitor and may present a
safety hazard to the user/patient.
Should this monitor become wet, wipe off all moisture and allow sufficient
time for drying before operating.
INCORRECT AC POWER RATINGS CAN DAMAGE MONITOR
Incorrect AC power ratings could damage the Genesis DM monitor.
Verify that the AC ratings noted on the power supply label match the AC
ratings at your installation site. If the site ratings do not match the power
supply, do not use the monitor. Contact Honeywell HomMed Customer
Service.
USE ONLY HOMMED AUTHORIZED MEDICAL EQUIPMENT
Attaching unauthorized equipment to the Honeywell HomMed Genesis DM monitor
may cause damage or equipment failure, including increased emissions or decreased
immunity of the Genesis DM.
Vital sign measurements may be inaccurate if unauthorized equipment is used with the
Genesis DM monitor.
DO NOT attach unauthorized medical equipment to the Genesis DM
monitor. When connecting this device to any instrument, verify proper
operation before clinical use. Refer to the equipment's user manual for full
instructions.
Any peripheral medical devices connected to the data interface must be certified
according to the respective IEC standards: IEC 60950 for data-processing equipment or
IEC 60601-1 for electromedical equipment.
All combinations of equipment must comply with IEC 60601-1-1 systems requirements.
IEC 60950 approved equipment must be placed outside of the "patient environment."
The patient environment is defined as an area 1.5 meters (4.92 feet) from the patient.
For a list of Honeywell HomMed equipment and compatible peripheral medical devices,
refer to Appendix E.
•
Operation of this device may be adversely affected in the presence of strong EMI or RF sources,
such as electrosurgery equipment.
•
Operation of this device may be adversely affected in the presence of computed tomograph (CT)
equipment.
•
Ability to obtain blood pressure measurement may be impacted by patients with tremors.
•
Blood pressure measurements may not be representative for patients experiencing moderate to
severe arrhythmias.
P.4510EN.01
GENESIS DM CLINICIAN GUIDE
CAUTION
CAUTION
CAUTION
NOTES
12/5/2007
Getting Started
7
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