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REFLEXOTHERAPY DEVICE
REFLEXOTHERAPY DEVICE
MAINTENANCE
Technical specifications
• Please disconnect the cable from the plug after use.
• Check the device is disconnected prior to cleaning.
• Any oil stains should be cleaned using a cloth and
cleaning material.
• Do not clean the switch and the remote control with a damp cloth,
as this may result in irreversible mechanical failure.
• Do not clean the device with brushes or hard materials which might
TIPS
• To ensure the device operates correctly the user should pace both
bare feet, with no socks, on the base of the device; otherwise it will
not work.
• If your device does not work after being turned on, check it is
properly connected, check the cable connecting the device to the
plug and turn the device on and off once again.
• If it stops suddenly, check the time has not elapsed and restart the
reflexotherapy device.
• Do not use the reflexotherapy device for more than 25 minutes a
day.
• The use of electrodes is intended to activate the muscles of the
arms, legs, back and abdomen. Do not use them on any other areas
of the body not specified in this manual. Specific programmes exist
for the treatment of the rest of the body using reflexotherapy (placing
the bare feet on the device).
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(Symbol for "BATCH CODE". This symbol should be with
Production Batch No, and next to graph, batch code and lot
number and batch number and so on) Examples: ABC123
(Symbol for "DATE OF MANUFACTURE". This symbol should be
next to number)
Production date of medical equipment (use mark in front of
theoroduction date)
After the adoption of the CE certification, CE mark is, as followed,
drawn. Its vertical height shall not be less than 5mm, clearly visible,
clear, durable, the CE conformity assessment procedures are
made by a Notified Body, the Notified Body registration number
should be the side of CE mark (Usually in the bottom right). The
diameter of the CE marking should be not less than the 5MM
semicircle of the two makes up, the XXXX at the lower right corner
is the Notified Body identification number, such as the ITS-0413.
All medical products sold in the EU market must have the 'ICE".
Affix the CE mark indicates that:
A. The equipment to meet the basic requirements of the MDD;
B. The equipment within the EU can be legally sold in the market
C. The device has passed the conformity assessment procedures.
The CE marks affixed to the medical devices have two types. That
is, CE mark without Notified Body identification number and CE
Mark with Notified Body identification number.
Symbol for "ATTENTION, CONSULT ACCOMPANYING
DOCUMENTS"
The Symbol for the Manufacturer (the “manufacturer" tag), the tag
should contain the company name and address of the
manufacturer.
Product manufacturers, CE represents the name and address of
importers and/or distributors.
Explantion of figures, symbols, warning stanents and abbreviations on the
equipmen
Legs Symptoms (Legmuscular pain and so on) Cutline
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