The (I.H.B.) symbol
You move your arm
EN
"
" is displayed,
or arm muscles during
but my heart beat rate
measurement.
should be normal.
The light on the display
The batteries are flat or
is dim or not lit
inserted incorrectly
6. MAINTENANCE AND REPAIRS
For any repair operations, only refer to a technical assistance centre authorized
by the Medel International Srl and request original spare parts. Never open
the device. There are no user-serviceable parts within. The device requires no
lubrication or maintenance. Failure to comply with what expressed above may
compromise the safety of MEDEL CHECK.
7. CARE, MAINTENANCE AND STORAGE
1. For cleaning only use a soft, lightly moistened cloth.
2. Do not use petroleum spirits, thinners or similar solvents.
3. Do not wash the cuff.
4. Take care to ensure the cuff is not damaged by sharp or pointed objects such
as scissors, knives, etc.
5. Take the batteries out if the device is not used for a long period.
6. In case the device becomes malfunction due to the influence of strong electro-
magnetic fields, power off the device and repeat the procedure again.
7. Disposal of the device (and used batteries) should be carried out according to
the national regulations for the disposal of electronic products.
8. REFERENCE TO STANDARDS
Device standard: Device corresponds to the requirements of the European stand-
ard for non-invasive blood-pressure monitor.
• EN1060-3 Non-invasive sphygmomanometers - Supplementary
requirements for electro-mechanical blood pressure measuring
systems.
• EN 60601-1Safety requirements
• EN 60601-1-2 Electromagnetical compatibility
• IEC 80601- 2- 30 Particular requirements for the basic safety and essential
performance of automated non-invasive sphygmomanometers.
30
100042_MEDEL CHECK USER MANUAL_ ALL LANGUAGES.indd 30-31
Remain still and do
not move /contract the
muscles during measure-
ment.
Replace the flat batteries
with new ones. Insert the
batteries correctly.
9. SYMBOLS
!
WARNING!
REFER TO THE INSTRUCTIONS
TYPE BF APPLIED PART
DIRECT CURRENT
MANUFACTURER
TEMPERATURE LIMITATION FOR TRANSPORT AND STORAGE
KEEP DRY
Comply with the Medical Device Directive 93/42/EEC
Separate collection for waste electrical and electronic equipment.
Applicable to European Union countries and countries with separate col-
lection systems) This symbol on the product or its literature indicates that
the product complies with the Electrical and electronic equipment and should not
be disposed of as household waste. The user is responsible for the transfer of
the equipment at end of life with the appropriate collection facilities, subject to
the penalties provided for by current legislation on waste. For more detailed in-
formation collection systems available contact your local waste disposal service.
MANUFACTURER'S CATALOGUE DEVICE NUMBER
SERIAL NUMBER
EN
31
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