Aeroneb
®
Solo System Instruction Manual
7
Do not use in the presence of devices generating high
electromagnetic fields such as magnetic resonance imaging
(MRI) equipment.
The Aeroneb
®
Pro-X 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.
Follow local laws and recycling plans regarding disposal or
recycling of components, batteries and packaging.
The Aeroneb
®
Solo nebulizer is designed for use in continuous
mode only when used with the Aeroneb
®
Pro –X controller.
Do Not
use the Aeroneb
®
Pro Nebulizer in continuous mode.
Caution:
Federal law restricts this device to sale by or on the
order of a physician
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
®
Solo AC/DC adapter (AG-AP1040-XX) has no
connection to earth ground because the necessary level of
protection is achieved through the use of double insulation.
Warnings
Содержание Solo System
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