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Dräger Polaris 50 User Manual

Dräger Polaris 50
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ENG
26
2. SAFETY INSTRUCTIONS
2.1 Intended use
The Polaris 50 luminaire is a treatment lamp (small surgical
lamp). It is an individual lamp for use in treatment rooms. It is
used near the patient to assist in diagnosis or treatment. It poses
no risk to the patient if a light failure causes interruption. It is
intended for continuous operation and should not be combined
with other medical devices.
2.2 User profiles
Health Professional
All individuals who have completed medical training and work
in the professional field for which they are trained.
Cleaning specialist
Trained in national and workplace hygiene regulations.
Qualified electrician
Trained in electronics and electrical technology and knows
the relevant standards and regulations.
Qualified specialist
Qualified to perform assembly/dismantling as a result of his
technical training, knowledge and experience and knowledge
of the rules.
2.3 Safety instructions
Operation by health professionals
This manual is part of the product and must be stored
and made available to all future users.
All work on the luminaire (including repairs) may only be
performed by a qualified electrician. Assembly may only
be carried out by a qualified specialist.
The luminaire may not be altered or tampered with. Only
approved original parts may be used. Any use other than
that intended, with the use of original parts, can change
technical parameters and pose a danger to life.
Do not exceed the maximum weight and do not hang,
lean or climb on the arm, because this may cause the
device to tip over, which could result in serious injury.
Operation in potentially explosive areas is prohibited.
The luminaire’s current supply is a potential ignition
source.
The luminaire must only be used in dry, dust-free rooms.
The luminaire should not be left on without supervision.
Only connect the luminaire to the supply network with a
protective earth conductor (PE), to prevent electric shock.
In the case of luminaires of protection class I, the
protective earth conductor (PE) must be connected to
housing of the luminaire.
Do not use a damaged luminaire. Defective cables and
a defective hand grip also pose a potential hazard. Do
not place a cable near heat sources or sharp edges.
Do not place extra loads on the luminaire head and arm
system.
The luminaire must not be covered with a cloth or similar
item during operation.
The ventilation openings (if present) must always be kept
clear during operation!
The luminaire must not be operated near external heat
sources which exceed the maximum ambient temperature
for the luminaire.
The luminaire must not be used outside the specified
ambient conditions.
Do not use with medical devices which may have
sensitivity reactions to a light spectrum within the visible
range (such as pulsating light and/or light with high
luminous intensity).
The luminaire may only be used for the intended use
described here.
The manufacturer cannot be held responsible for any
damage resulting from use other than the intended use,
or failure to observe the safety instructions and warnings.
When using more than one luminaire at the same time,
the total luminous intensity must not exceed Ee 1000W/m².
Before connecting to the power grid, it is essential to
check that the grid data matches the device data.
Polaris 50 Mobile
The luminaire must be secured during transport within
the clinic.
2.4 Warning levels
WARNING
Warning of hazards which may result in injury if the
instructions are not followed.
CAUTION
Warning of hazards which may cause material damage if
the instructions are not followed.
DANGER
Warning of hazards which may result in death or serious
injury if the instructions are not followed.

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Dräger Polaris 50 Specifications

General IconGeneral
BrandDräger
ModelPolaris 50
CategoryMedical Equipment
LanguageEnglish

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