English
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English
tor must be made before a further stimulation. A lightweight, non-persistent erythema
after the stimulation in the area of the electrode is normal, because the blood circulation
is improved by the stimulation.
Precautionary Measures
Patients with an implanted electronic device (e.g. heart pacemaker) should not be treated
with a stimulating current therapy with the
MiniFG
device without consulting a doctor
beforehand. The
MiniFG
device must only be connected to one patient for stimulation.
Warning!
The connection of the patient to a high frequency surgical device at the same time can result
in burning in the stimulating current elements.
Operation near (e.g. 1m) to a short or medium wave device can cause fluctuations in the
output levels of the stimulating current device.
Description of the Signs
Attention: Read accompanying documents, especially user manual!
By labelling with CE mark, the manufacturer asserts that the product fulfills all
relevant requirements of the respective EC Directives. A conformation assessment
process has been successfully completed.
Type BF applied part
Serial number
Catalogue number
Date of manufacture
Manufacturer
Environment
Do not dispose of the appliance with the normal household waste at the end of its
life, but hand it in at an official collection point for recycling. By doing this you will
help to protect the environment.
Follow instructions for use
