Dräger Babylog 8000 plus Operating Instructions Manual page 18

Intended Use
Intended Medical Applications
Restrictions of Use
Intended Medical Application
WARNING !
Babylog 8000 plus is solely intended for use by
physicians or by allied health care profession-
als on the order of a physician. All users must
be properly trained and completely familiar with
these Operating Instructions.
Babylog 8000 plus is a long term ventilator to be used in
the intensive care of premature and newborn babies and
of infants up to 10 kg (22 lbs).
Available Ventilation Modes
CMV Continuous Mandatory Ventilation,
Time-controlled, time-cycled, pressure-
limited continuous flow ventilation.
A/C Assist Control Ventilation
Time-controlled, volume triggered, time-
cycled, pressure-limited continuous flow venti-
lation that is synchronized with each spontane-
ous patient breath.
SIMV Synchronized Intermittent Mandatory
Ventilation,
Time-controlled, volume triggered, time-
cycled, pressure-limited continuous flow venti-
lation, synchronized with patient's spontane-
ous breathing at the set ventilation rate.
PSV Pressure Support Ventilation
(available option),
Time-controlled, volume-triggered, flow
cycled, pressure-limited ventilation synchron-
ized with each spontaneous patient breath.
CPAP Continuous Positive Airway Pressure,
Spontaneous breathing with positive
airway pressure.
Ventilation Mode Extensions
VG Volume Guarantee (available option)
Volume controlled ventilation. The ventilator
controls inspiratory pressure in order to
deliver the preset tidal volume. May be com-
bined with A/C, SIMV, and PSV.
VIVE Variable Inspiratory, Variable Expiratory Flow
Separate continuous flow during expiration in
mandatory ventilation modes.
18
Restrictions of Use
CAUTION !
Restriction of Distribution
Federal Law and Regulations in the United States
and Canada restrict this device to sale by or on the
order of a physician.
WARNING !
This device is to be used only in rooms with
line power installations complying with
national safety standards for hospital patient
rooms. (e.g., IEC 601.1, "Safety of Medical
Equipment).
To maintain grounding integrity, connect only
to a"hospital grade" receptacle.
Always disconnect supply before servicing.
WARNING !
DANGER, risk of explosion if used in the
presence of flammable anesthetics.
This device is neither approved nor certified
for use in areas where combustible or explo-
sive gas mixtures with air or with nitrous oxide
are likely.
WARNING !
Mobile telephones must not be used within 10
meters (33 feet) of the equipment. Mobile
telephones can interfere with the function of
electromedical equipment and therefore
endanger the patient*!
WARNING !
Do not use ventilator in conjunction with
nuclear spin tomography (MRT, NMR, or NMI)!
Equipment malfunction may result.
____________
*
Dräger medical equipment conforms to the interference immunity
requirements laid down in product-specific standards or in
EN 60601-1-2 (IEC 601-1-2). However, depending on the design
of a mobile phone and the use situation, field strengths exceeding
the values laid down in the specified standards may be generated
in the immediate vicinity of mobile phones, thereby causing
interference and malfunctions.