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Twin-Up t7 is classified as a Class IIA Medical Device and conforms with the requirements of the European Directive on medical devices 93/42/EEC. The appliance bears the CE0197 mark authorised by the Notified Institute TÜV Product Safety GmbH.
Twin-Up T7 has been designed and manufactured in compliance with the requirements of the company Quality System certified in accordance with EN ISO 9001: 2004 and EN ISO 13485: 2000 standard.
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• During the menstrual period, skin conduction changes; stimulation could prove less comfortable.
• Stimulation causes reddening of the skin where the electrodes are placed, especially in the case of persons with sensitive skin. Such reddening is perfectly normal and usually disappears quickly.
• In case of allergy to the electrode gel, suspend treatment and see a doctor.
• Do not apply the electrodes to areas with hyperpigmentation (moles) or varicose veins.
• Do not apply the electrodes directly to the breasts, but to the muscles which support them.
• Do not use in intimate areas, under the armpits, in the groin or behind the knees.
• Do not use on the abdomen of expectant mothers.
• Do not use Twin-Up T7 on children, people with pace-makers or those in poor psychophysical conditions or with physiological or organic disorders.
• The appliance is not suited for wearers of metal prostheses or aortoabdominal bypasses.
• Do not apply in transthoracic mode to prevent interference with heart frequency and, in general, only use on facial muscles.
IN CASE OF DOUBT, SEE A DOCTOR.
If adhesive gel electrodes of other makes are used, keep strictly to the following instructions:
electrode dimensions: 3.5x4.5 cm. or 9x4 cm.
Minimum electrode surface: 15 sq cm |
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© Copyright 2003 Vupiesse Italia S.r.l.
- All rights reserved - Disclaimer |
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