3-1
3
Basic Operations and Settings
3.1
Installation
WARNING
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The equipment shall be installed by personnel authorized by the manufacturer.
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The software copyright of the equipment is solely owned by the the manufacturer. No organization or
individual shall resort to juggling, copying, or exchanging it or to any other infringement on it in any form
or by any means without due permission.
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Devices connected to the equipment must meet the requirements of the applicable IEC standards (e.g. IEC
60950 safety standards for information technology equipment and IEC 60601-1 safety standards for medical
electrical equipment). The system configuration must meet the requirements of the IEC 60601-1-1 medical
electrical systems standard. Any personnel who connect devices to the equipment’s signal input/output
port is responsible for providing evidence that the safety certification of the devices has been performed in
accordance to the IEC 60601-1-1. If you have any question, please contact the the manufacturer.
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If it is not evident from the equipment specifications whether a particular combination is hazardous, for
example, due to summation of leakage currents, consult the manufacturers or else an expert in the field, to
ensure the necessary safety of all devices concerned will not be impaired by the proposed combination.
3.1.1
Unpacking
and
Checking
Before unpacking, examine the packing case carefully for signs of damage. If any damage is detected, contact the carrier
or the manufacturer. If the packing case is intact, open the package and remove the equipment and accessories carefully.
Check all materials against the packing list and check for any mechanical damage. If you have any question, please
contact us.
WARNING
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Package material may contaminate the environment. Properly dispose of the package material according to
applicable waste control regulations and keep it out of children’s reach.
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The equipment might be contaminated during storage and transport. Before use, please verify whether the
packages are intact, especially the packages of single use accessories. In case of any damage, do not apply it
to patients.
NOTE
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Save the packing case and packaging material as they can be used if the equipment must be reshipped.
Summary of Contents for BeneHeart D3
Page 1: ...BeneHeart D3 Defibrillator Monitor Operator s Manual...
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Page 8: ...VI FOR YOUR NOTES...
Page 16: ...8 FOR YOUR NOTES...
Page 22: ...1 6 FOR YOUR NOTES...
Page 40: ...4 2 FOR YOUR NOTES...
Page 62: ...6 12 FOR YOUR NOTES...
Page 78: ...8 10 FOR YOUR NOTES...
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Page 102: ...14 2 FOR YOUR NOTES...
Page 170: ...D 6 FOR YOUR NOTES...
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