Symbols And Controls - Philips HeartStart FR3 Guía De Configuración, Funcionamiento Y Mantenimiento

maintenance The FR3 was designed to be sturdy and reliable for many different field use conditions.
However, excessively rough handling can result in damage to the FR3 or its accessories.
Inspect the unit and accessories periodically according to instructions.
Improper maintenance may damage the FR3 or cause it to function improperly. Maintain the
FR3 according to directions.
Electrical shock hazard. Dangerous high voltages and currents are present. Do not open the
FR3, remove its covers, or attempt repair. There are no user-serviceable components in the
FR3. The FR3 should be returned to Philips for repair.
batteries Follow all instructions supplied with the FR3 batteries. For non-rechargeable FR3 batteries,
install the battery before the "Install before" labeled date.
Do not use the 861394 battery charger on aircraft.
advanced use The FR3 advanced use mode's manual charge feature is intended for use only by authorized
operators who have been specifically trained in cardiac rhythm recognition and in defibrillation
therapy using manual charge and shock delivery.
monitoring The LCD screen on the FR3 model 861389 is intended only for basic ECG rhythm
identification. The frequency response of the FR3 display is not intended to provide the
resolution needed for diagnostic and ST segment interpretation.
pads Follow all instructions supplied with the HeartStart defibrillator pads. Use the defibrillator
pads before the expiration date shown on the package. Do not reuse the defibrillator pads.
Discard them after use.
Aggressive handling of the defibrillator pads in storage or prior to use can damage the pads.
Discard the defibrillator pads if they become damaged.
Do not place the pads directly over an implanted pacemaker or defibrillator. A noticeable
lump with a surgical scar should indicate its position.

SYMBOLS AND CONTROLS

The following table explains the symbols and controls used on the FR3, its accessories, and their
packaging.
Meets the requirements of the
European medical device
directives 93/42/EEC.
This product has passed relevant
U.S. and Canadian safety tests by
CSA, a Nationally Recognized
Test Laboratory.
CAUTIONS
REGULATORY MARKS AND GENERAL
N11695
V00341
Meets the requirements of the
applicable European directive.
This product has been certified by
the Australian Communication
Authority.
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