6
Aeroneb
®
Professional Nebulizer System Instruction Manual
To avoid mechanical or electrical damage, do not drop the
nebulizer unit or the control module.
Do not use in the presence of devices generating high
electromagnetic fields such as magnetic resonance imaging
(MRI) equipment.
The Aeroneb Pro control module contains a nickel metal
hydride (NiMH) rechargeable battery, which should be
disposed of in accordance with local governing restrictions at
the end of its useful life.
Electromagnetic susceptibility
This device meets the requirements of the Electromagnetic
Compatibility (EMC), pursuant to the Collateral Standard,
IEC/EN 60601-1-2 which addresses EMC in North America,
Europe and other global communities. This includes immunity
to radio frequency electric fields and electrostatic discharge, in
addition to the other applicable requirements of the standard.
Compliance with EMC standards does not mean a device has
total immunity; certain devices (cellular phones, pagers, etc.)
can interrupt operation if they are used near medical
equipment. Follow institutional protocol regarding the use and
location of devices that could interfere with medical equipment
operation.
Note
: This device is classified as Class II Type BF medical
electrical equipment and the device complies with specified
safety levels for electrical isolation and leakage current. The
Aeroneb
Pro AC/DC adapter has no connection to earth
ground because the necessary level of protection is achieved
through the use of double insulation.
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