Riester ri-champion N Manual Del Usario página 29

carefully with a damp cloth and soapsuds. The cuff must not
be washed!
d) Remove the batteries if the device is not used for a longer peri-
od.
e) Do not drop the instrument or treat it roughly in any way. Avoid
strong vibrations.
f) Never open the device! Otherwise the manufacturer calibra-
tion becomes invalid!
EMC-Notes
The device corresponds to the EMC requirements according to IEC
60601-1-2. Portable and mobile HF-equipments (e.g. mobile phones)
can influence medical devices. Medical-electronic devices need spe-
cial requirements concerning EMC.
You may find a detailed description of the manufacturers EMC decla-
ration at the end of this user manual.
Instructions for technical inspection
EU countries except Germany:
Legal regulations for monitoring instruments apply to all EU
countries except Germany.
Countries outside the EU:
For any countries where no legal regulations exist for monitoring
instruments, it is recommended to examine the accuracy of
measuring instruments in 2-year intervals.
The test is conducted according to the following procedure:
1. Procedure for checking and meeting the margin of
error of the measurement display for cuff pressures
1.1. Test Equipment
a) A sturdy metal vessel with a volume of 500 ml +/- 5%.
b) A calibrated inspection manometer with a maximum
permissible margin of error of 1.0 mmHg (0.1 kPa)
c) A means of generating pressure, e.g., a bulb with release
valve
d) "T" connectors and tubes.
e) Special connector for calibration approval of ri-champion® N
No. 12752.
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