Initial Inspection; Installation; Function Checks; Setting Up The Unit - Bovie Aaron 1250 User Manual

INITIAL INSPECTION

When you first unpack your Aaron 1250™, inspect it visually:
• Look for any signs of damage.
• Verify that the shipping package contains all items listed on the packing list.
If the unit or any accessories are damaged, notify Bovie Medical Corporation's Customer Service immediately.
Do not use any damaged equipment.

INSTALLATION

Place the Aaron 1250™ on any flat surface with a tilt angle not more than 10˚. The unit relies on natural convection
cooling. Do not block its bottom or rear vents. Ensure that air flows freely on all sides of the unit.
WARNING:
Connect the power cord to a properly polarized and grounded power source with the frequency
and voltage characteristics that match those listed on the back of the unit.

FUNCTION CHECKS

Upon initial installation of the unit, perform the tests listed below. Refer to the figures in the previous chapter for the
location of connectors and controls.
WARNING:
At no time should you touch the active electrode or bipolar forceps. A burn could result.
Active cord removal during activation could result in a shock to the operator at the generator
connector plug interface should activation occur by footswitch.

Setting Up the Unit

1. Verify that the Power Switch is in the Off position and that no accessories are connected to the unit.
2. Connect a hospital grade power cable to the AC power cable receptacle on the back of the unit, then to a properly
grounded wall outlet.
3. Connect a two-pedal footswitch to the appropriate receptacle on the back of the unit. Use only Bovie® Medical
footswitches. Although other types of footswitches may fit, they may not be compatible
4. Do not connect a patient return electrode at this time.
5. Turn the unit on by switching the power switch to the On position.

Checking the Return Electrode Alarm

1. Adjust the power settings for each mode (Cut, Blend, Coagulation, Fulguration, and Bipolar) to one watt.
2. Press the Cut pedal of the footswitch. Verify that an alarm sounds for three seconds and the Patient Return
Electrode Sensing Alarm Indicator light illuminates, indicating that no return electrode is connected to the unit.
3. Verify that adjusting the volume control on the back of the unit while the alarm is sounding does not change the
alarm volume.
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