Philips HeartStart FR2+, Instructions For Use Manual

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C l i n i c a l a n d S a f e t y C o n s i d e r a t i o n s
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safety level possible improper device performance
WARNING Prolonged or aggressive CPR to a patient with defibrillator pads
attached can damage the pads. Replace the defibrillator pads if they
are damaged during use or handling.
WARNING Using damaged or expired equipment or accessories may cause the
HeartStart FR2+ to perform improperly, and/or injure the patient or
the user.
WARNING CPR rates significantly above 100 compressions per minute can
cause incorrect or delayed analysis by the HeartStart FR2+.
WARNING Poor electrode pad-to-patient contact may result in a related
defibrillator prompt or other indication. Check all electrical and
patient connections.
CAUTION The HeartStart FR2+ is designed to be used only with Philips-approved
accessories. The HeartStart FR2+ may perform improperly if
non-approved accessories are used.
CAUTION 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.
CAUTION Aggressive handling of the defibrillator pads in storage or prior to use can
damage the pads. Discard the defibrillator pads if they become damaged.
CAUTION Follow all instructions supplied with the M3863A FR2 standard battery.
Install the battery before the expiration date shown on the battery.
CAUTION Follow all instructions supplied with the M3848A FR2+ rechargeable
battery. Recharge using the M3849A charger only.
CAUTION Do not use the M3849A charger on aircraft.
CAUTION The HeartStart FR2+ was designed to be sturdy and reliable for many
different field use conditions. However, excessively rough handling can
result in damage to the HeartStart FR2+ or its accessories. Inspect the
unit and accessories periodically according to instructions.
CAUTION Alteration of the factory default setup of the FR2+ can affect its
performance and should be performed under the authorization of your
Medical Director. Modifications to device operation resulting from
changes to the default settings should be specifically covered in user
training.