Page 6 213960EN(1) - P290 Mattress Instructions for Use
Avoid mechanical impacts.
Notice to Users and/or Patients:
Any serious incident that has occurred in relation to the device, should be reported to
the manufacturer and the competent authority of the Member State in which the user
and/or patient is established.
Complying with Electrical Safety Standards
The mains power supply must comply with following standards:
• NF C15-100 and NF C15-211 (France);
• International Electrotechnical Commission (IEC) 60364 for other countries.
Check that the supply voltage of the device shown on the identification label matches
the voltage of the establishment’s mains power system (See “Locating the Labels on
the Device” on page 16).
The device should be connected to a power system equipped with a
maximum 30 mA earth leakage circuit breaker, in compliance with
IEC 60364-5-53.
Connect the device to the nearest wall plug in order to
leave the shortest possible length of cable on the floor.
In compliance with standards relating to electromagnetic
interference for medical devices, this device does not interfere
with other medical devices nor is it susceptible to interference when combined with
other medical devices that also comply with the electromagnetic standards in place.
However, some devices, particularly older ones that do not comply with the
electromagnetic compatibility standards, may undergo interference or may themselves
interfere with the functionality of this product.
The users of such devices are responsible for ensuring that any malfunctions will not
endanger the patient or any other person.
When intravascular or intracardiac connections are in use, the electric potentials of all
the unprotected metal parts of the appliance and the bed need to be equalized.
This label indicates that
oxygen tents must never be used
and that only
the use of nasal tubes and oxygen masks is authorized. For reasons of safety,
masks and tubes should always be kept at a higher level than the mattress
support platform
.
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