arjo Enterprise 9600X Notice D'utilisation page 6

WARNING
It is recommended to use the Function Lockout facility on the Attendant
Control Panel to prevent unintended movement in situations where
objects may press against the patient's controls.
When the bed is operated, make sure that obstacles such as feet, oxygen
bottles, bedside furniture or any other objects do not restrict its
movement.
To avoid potential damage or injury, do not leave oxygen bottle or any
other obstacles under the bed frame while operated.
The bed can only be moved on firm surfaces. Gradients must not exceed
an angle of 10 degrees.
When moving or operating the bed, take care that any accessories
attached to it (e.g. lifting pole) do not strike doors, ceilings, etc.
Hold the head board or foot board when pushing or pulling the bed;
do not hold the side rails or any attached accessories.
Before operating the bed, make sure the patient is positioned correctly
to avoid entrapment or imbalance.
Take care when using equipment that needs to be positioned under the
base frame to ensure there is no contact with any part of the bed frame
or components.
Take care not to squeeze or trap trailing cables from other equipment
between moving parts of the bed.
Take care not to allow clothing or bed linen to become snagged on
moving parts of the bed.
When operating moving parts of the bed, ensure the bed does not come
into contact with adjacent equipment which could be damaged by the
beds operation.
This product complies with the requirements of applicable standards
for electromagnetic compatibility (EMC). However, medical electrical
equipment requires special precautions regarding EMC and should be
installed and used in accordance with the EMC information in the
product service manual.
Medical electrical equipment can be affected by portable and mobile
radio frequency communications equipment, e.g. cellular telephones.
If a serious incident occurs in relation to this medical device, affecting
the user, or the patient then the user or patient should report the serious
incident to the medical device manufacturer or the distributor. In the
European Union, the user should also report the serious incident to the
Competent Authority in the member state where they are located.
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