USER SAFETY INFORMATION
ix
Note(s)
Proper patient preparation is important to proper application of ECG electrodes and operation of the device.
If electrode is not properly connected to the patient, or one or more of the patient cable lead wires is damaged,
display will indicate a lead fault for the lead(s) where the condition is present.
For additional instructions and warnings, refer to the user manual of the receiving monitoring device.
As defined by IEC 60601-1 and IEC 60601-2-25, the device is classified as follows:
- Class I equipment or internally powered
- Type CF defibrillation-proof applied parts
- Ordinary equipment
- Equipment not suitable for use in the presence of a flammable anesthetic mixture
- Continuous operation
The device will automatically turn off (blank screen) if the batteries have been severely discharged.
The device is UL classified:
Medical Equipment
WITH RESPECT TO ELECTRIC SHOCK, FIRE, AND MECHANICAL HAZARDS
ONLY, IN ACCORDANCE WITH UL 60601-1, CAN/CSA C22.2 No. 601.1,
IEC60601-1 AND IEC60601-2-25.
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