Classification
The MIO-IONOTENS has the following classification:
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class IIa (Directive 93/42/CEE, Annex IX, rule 9 and further
amendments);
class II with BF type applied part (classif. EN 60601-1);
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equipment protection level IP22 against liquid and dust penetration;
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•
equipment and accessories not subject to sterilization;
equipment unsuitable for use in presence of a flammable anesthetic
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mixture containing air, oxygen and nitrous oxide;
equipment suitable for continuous operation;
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equipment unsuitable for outdoors use.
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Purpose and scope
Clinical intended use:
Environmental intended use:
MIO-IONOTENS is indicated for the treatment and the functional rehabilitation
of the following pathologies and anatomical zones:
wrist articulation;
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hand articulation;
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shoulder articulation;
foot articulation;
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ankle articulation;
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knee articulation;
skeletal motor apparatus;
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arthrosis;
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atrophies and muscular dystrophy;
bruises;
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sprains;
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neuralgias;
benign lesions and muscular tears;
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tendinitis.
The MIO-IONOTENS electronic stimulator is a medical device specifically
intended for domestic use. It is also intended to be used by therapist, by
personal trainer in a center or private clinic.
MIO-IONOTENS is used to apply electrical micro impulses which create energy.
This energy, modulated with different parameters specific for different
impulses, can give the patient many benefits from pain relief to muscles cool
IACER Srl
Therapeutic
Ambulatory and home
49
MNPG151-07