arjo Enterprise 5000X E5X Notice D'utilisation page 5

WARNING
Always apply the brakes when the bed is stationary.
To reduce the risk of injury due to falls, lower the bed to minimum height when the
patient is unattended.
Patients should not be left in the Trendelenburg position when unattended.
To reduce the risk of overbalancing, do not allow the patient to get on or off the bed
when the mattress platform is in a tilted (head down or foot down) position.
Where risk assessment indicates that a patient is at high risk of entrapment owing to
their medical condition or other circumstances, and where there is no medical benefit
from their being left in a contoured position, place the mattress platform in the flat
position and disable the controls (Function lockout)when the patient is unattended.
When the bed is operated, make sure that obstacles such as bedside furniture do not
restrict its movement.
When moving or operating the bed, take care that any attached accessories (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 not to squeeze or trap trailing cables from the handset/ACP and 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.
Do not place the bed on an incline greater than 7 as this may, in extreme
circumstances, cause the bed to overbalance.
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.
5