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Note(s)
·
Proper patient preparation is important to proper application of ECG electrodes and operation of the device.
·
If an 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 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 (ECG) defibrillation-proof applied parts
- IPX1 with regards to the harmful ingress of water
- Equipment not suitable for use in the presence of a flammable anesthetic mixture
- Continuous operation
·
The device will automatically start flashing LED’s if the batteries have been discharged below 1.0 volts.
·
The device will automatically turn off (LED’s off) if the battery has 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.
