ZOLL M Series Defibrillator Rev G Base PowerCharger 4x4 - Manual (Page 6)

ZOLL Base PowerCharger
4x4
Operator’s Manual
2
because it does not test the battery capacity with each
recharge. The ZOLL Base PowerCharger
4x4 with
QuickCharge relies on the user to manually initiate the
battery test cycle at recommended intervals (see
“Manual Battery Testing Procedure” on page 9) in order
to confirm adequate battery capacity.
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This manual provides information necessary for the use
and care of the ZOLL Base PowerCharger
4x4 , PD 4410/
Smart/Smart Ready Battery and all XL Battery packs. A
thorough understanding of this information is required for
proper charging and maintenance of ZOLL batteries.
Reliable operation of ZOLL Medical Corporation
resuscitation devices requires proper battery care.
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This manual is divided into five sections. The operator
should read each section carefully.
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Provides Cautions, Warnings and a general product
overview of the ZOLL Base PowerCharger
4x4 . Includes
detailed product specifications, important ZOLL service
information, and ZOLL’s warranty statement.
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Describes the function of all controls and indicator lights
of the ZOLL Base PowerCharger
4x4 with QuickCharge.
Discusses proper setup of the ZOLL Base
PowerCharger
4x4 and provides charging and testing
instructions.
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Describes the function of all controls and indicator lights
of the ZOLL Base PowerCharger
4x4 with AutoTest.
Discusses proper setup of the ZOLL Base
PowerCharger
4x4 and provides charging and testing
instructions.
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This section describes several routine checks to assure
proper unit operation. It includes cleaning and
maintenance instructions and troubleshooting guides
intended for use by non-technical personnel.
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Provides information for determining your particular
battery requirements and program implementation steps
to set up a comprehensive, effective and safe battery
management program.
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If you purchased your product more than three years
ago, contact ZOLL to determine whether updates to your
documentation are available. For information relating to
recent manual updates, contact ZOLL Medical
Corporation's Technical Service Department at
1-978-421-9655.
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Carefully inspect each container for damage. If the
shipping container or cushion material is damaged, it
should be kept until the contents have been checked for
mechanical and electrical integrity. If the contents are
incomplete, if there is mechanical damage, or if the
instrument does not pass its electrical self-test, U.S.A.
customers should call ZOLL Technical Service
(1-800-348-9011). International customers should
contact the nearest ZOLL authorized representative. If
the shipping container is damaged, also notify the
carrier.
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As a health care provider, you may have responsibilities
under the Safe Medical Devices Act (SMDA), for
reporting to ZOLL and possibly to the FDA the
occurrence of certain events. These events, described in
21 CFR Part 803, include device-related death and
serious injury or illness.
In any event, as part of our Quality Assurance Program,
ZOLL Medical Corporation should be notified of any
device failures or malfunctions. This information is
required to assure that ZOLL provides only the highest
quality products.