Baylis RFP-100A - CONNECT THE DISPERSIVE (RETURN) ELECTRODE

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Refer to the Connector Cable Instructions for Use for further details.

To connect the BMC RF Device to the BMC Connector Cable, please refer to the individual

Instructions for Use of each BMC RF Device.

Note: Position the Generator near the table where the procedure is to be performed. The

Generator may only be connected to recording systems providing patient electrical

isolation in accordance with IEC 60601.

7.5. CONNECT THE DISPERSIVE (RETURN) ELECTRODE

Only use dispersive electrodes that meet or exceed IEC 60601-2-2:2017 requirements.

Connect the dispersive (return) electrode (also referred to as a grounding pad) connector to

the Return Electrode Connection found on the Generator front panel. Line up the pins in

the Generator receptacle with the sockets of the electrode connector and gently push the

dispersive electrode connector until it sits firmly in place. To unplug, grasp the dispersive

electrode connector and gently pull it out from the receptacle.

Before use, it is important to check the dispersive electrode’s sealed foil packaging for

damage. Exposure to air, due to a damaged package, could cause the dispersive electrode

to become dry and limit its capability to provide an appropriate return path for RF energy.

Be sure the pad is moist and sticky to the touch before placing it on the patient. Do not

attempt to relocate the patient dispersive electrode after its initial application. Electrode

gel that is separate from and additional to any gel that is an integral part of the dispersive

electrode is not required and should not be used.

The dispersive electrode should be placed on a well-vascularized, convex skin surface.

Dispersive electrode placement on the thigh may be associated with higher impedance.

Avoid scar tissue, bony prominence, adipose tissue, or any areas where fluid may pool.

Shave, clean, and dry the application site as needed. Check for wrinkles or folds when

applying the dispersive electrode, as they can inhibit adequate contact and decrease

conductivity.

The Generator is equipped with a Return Electrode Fault Monitor that measures the

impedance between the two conductors of the dispersive electrode. For a single foil

electrode, the monitor will indicate a fault (the Return Electrode Fault Indicator will

illuminate red) if either one or both of the conductors are faulty. For a dual foil electrode,

the monitor will indicate a fault if the impedance between the conductors is greater than

150 ohms, which may indicate poor patient contact.

WARNING: Unless a compatible dual foil dispersive electrode is used that meets or

exceeds IEC 60601-2-2:2017 requirements (such as ConMed

MacroLyte

Dual

Dispersive Electrode), loss of safe contact between the dispersive electrode and the patient

may not result in an auditory alarm.