Medel ELITE Gebrauchsanweisung Seite 74

• Do not use solvents to clean this device. Switch off the de-
vice and disconnect it from the power supply. The device
can be cleaned with a damp cloth. Use lukewarm water
and a non-abrasive liquid household cleaner (no abrasive,
no alcohol content solution).
• During using, the patient will contact with the cuff. The
materials of the cuff have been tested and found to comply
with requirements of ISO 10993-5:2009 and ISO 10993-
10:2010. It will not cause any potential sensization or ir-
ritation reaction.
• Warning: No servicing/maintenance while the ME equip-
ment is in use.
• The patient is an intended operator. The patient can mea-
sure data and change battery under normal circumstances
and maintain the device and its accessories according to
the user manual.
• Adaptor is specified as a part of ME equipment.
• The plug/adapter plug pins insulates the device from the
main supply. Do not position the device in a position where
it is difficult to disconnect from the supply mains to safely
terminate operation of ME equipment.
• If the pressure of the cuff reaches 40kPa (300mmHg), the
unit will automatically deflate. If the cuff don't deflate when
its pressure reaches 40kPa (300mmHg), detach the cuff
from the arm and press the O/I button to stop inflation.
• Before every use, check the device, do not use the device if
it is damaged in any way. The continuous use of a damaged
unit may cause injury, improper results, or serious danger.
• It is recommended that the performance should be che-
cked every 2 years and after maintenance and repair, by
retesting at least the requirements in limits of the error of
the cuff pressure indication and air leakage (testing at least
at 50mmHg and 200mmHg).
• Warning: No modification of this equipment is allowed.
• Manufacturer will make available on request circuit dia-
grams, component parts list etc.,.
• The operator shall not touch output of batteries/adapter
and the patient simultaneously.
• The user must check that the equipment does not have
visible evidence of damage that may affect patient safety
or monitoring capability before use.
• It is intended for adult indoor use only. It is not intended
for use with neonatal, pregnant or pre-eclamptic patients.
• Warning: Be careful to regarding the effect of blood flow
interference and resulting harmful injury to the patient cau-
sed by continuous cuff pressure due to connection tubing
kinking; During measurement, please avoid compression
or restriction of the connection tubing.
• When using this device, please pay attention to the follo-
wing situation which may interrupt blood flow and influen-
ce blood circulation of the patient, thus cause harmful in-
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