Safety Instructions; Intended Use; User Profiles; Warning Levels - Dräger Polaris 50 Installation And Operating Instructions Manual

Luminaire for diagnosis
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  • ENGLISH, page 137
EN
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
that 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 is not to 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 they trained for.
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 due to his technical training, knowledge and expe-
rience and knowledge of the rules, to perform assembly/
dismantling.
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 done 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, using original parts, can
change technical parameters and pose a death hazard.
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 be used only in dry, dust-free
rooms.
The light must not be left switched on unattended.
Only connect the luminaire to the supply network with a
protective ground conductor (PE), to prevent electrical
shock.
In the case of luminaires of protection class I, the
protective ground conductor (PE) must be connected to
luminaires housing.
Do not use a damaged luminaire. Defective cables and
a defective hand grip also pose a potential hazard. Do
not place a cord near heat sources or sharp edges.
140
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 that exceed the luminaire's maximum ambient
temperature.
The luminaire must not be used outside the specified
ambient conditions.
Do not use with medical devices that may react
sensitively to a light spectrum within the visible range
(such as pulsating light and/or light with high
illumination intensity).
The luminaire may only be used for the intended use
described here.
The manufacturer cannot be held responsible for any
damages resulting from use deviating from the intended
use, or failure to observe the safety instructions and
warnings.
When using more than one luminaire at the same time,
the total illumination intensity must not exceed Ee
1000W/m².
Before connecting to the power grid, it is essential to
check that the grid data match the device data.
Polaris 50 Mobile
The luminaire must be secured during transport within
the clinic.
2.4

Warning levels

DANGER
Warning of hazards that can result in death or serious
injury if instructions are not followed.
WARNING
Warning of hazards that can result in injury if instructions
are not followed.
CAUTION
Warning of hazards that can cause material damage if
instructions are not followed.

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