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IMPORTANT & SAFETY INSTRUCTIONS
1. SAVE THESE INSTRUCTIONS — This manual contains important safety and operating
instructions for inverter.
2. Do not expose inverter to rain or snow.
3. Use of an attachment not recommended or sold by the inverter manufacturer may result
in a risk of re, electric shock, or injury to persons.
4. Do not disassemble inverter; take it to a qualied serviceman when service or repair is
required. Incorrect reassembly may result in a risk of electric shock or re.
5. To reduce risk of electric shock, unplug inverter from outlet before attempting any mainte-
nance or cleaning. Turning off controls will not reduce this risk.
6. Never place inverter directly above battery; gases from battery will corrode and damage
marine inverter.
7. Never allow battery acid to drip on inverter when reading gravity or lling battery.
GROUNDING AND AC POWER CORD CONNECTION INSTRUCTIONS
Inverters should be grounded to reduce risk of electric shock. Inverter is equipped with electric
receptacles capable of accepting an equipment-grounding conductor and a grounding plug.
DANGER — Never alter AC cord or plug provided — if it will not t outlet, have proper
cord installed by a qualied electrician. Improper connection can result in a risk of an electric
shock.
Analytic Systems does not recommend the use of the IPS2000 Series Inverters in life support
applications where failure or malfunction of this product can be reasonably expected to cause
failure of the life support device or to signicantly affect its safety or effectiveness.
Analytic Systems does not recommend the use of any of its products in direct patient care.
Examples of devices considered to be life support devices are neonatal oxygen analyzers,
nerve stimulators (whether used for anesthesia, pain relief, or other purposes), autotransfu-
sion devices, blood pumps, debrillators, arrhythmia detectors and alarms, pacemakers,
hemodialysis systems, peritoneal dialysis systems, neonatal ventilator incubators, ventilators
for both adults and infants, anesthesia ventilators, and infusion pumps as well as any other
devices designated as “critical” by the U.S. FDA.
