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Elettroterapia Antalgica

Apparecchi che utilizzano queste applicazioni:

New Age No Limits, New Pocket Global, New Pocket Family, New Pocket Fit4, New Tens Terapix, New Onecare, New T-Sonic, New Beauty Fit, Pocket Physio Pro, Rheab, Ionotens, Uro, New Pocket Tenvit, New Pocket Ionovit, Card Sport, Card Physio, Card Aesthetic, Onecare 200 Plus, Well 2000, Biophysio.

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Elettroterapia Estetica

Apparecchi che utilizzano queste applicazioni:

New Age No Limits, New Pocket Global, New Pocket Family, New Pocket Fit4, New Tens Terapix, New Onecare, New T-Sonic, New Beauty Fit, New Pocket Physio Pro, Rheab, Ionotens, Uro, New Pocket Tenvit, New Pocket Ionovit, Card Sport, Card Physio, Card Aesthetic, Onecare 200 Plus, Well 2000, Biophysio.

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Elettroterapia Ionoforesi

Apparecchi che utilizzano queste applicazioni:

New Age No Limits, New Onecare, Onecare 200 Plus, New Pocket Ionovit, New Pocket Physio Pro, New Pocket Physio Ionotens, Card Physio, Biophysio, New Poket Fit4.

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Elettroterapia Muscolari

Apparecchi che utilizzano queste applicazioni:

New Age No Limits, New Pocket Global, New Pocket Family, New Pocket Fit4, New Tens Terapix, New T-Sonic, New Beauty Fit, New Pocket Physio Pro, Rheab, Card Sport, Card Physio, Card Aesthetic, Well 2000, Biophysio.

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Magnetoterapia

Apparecchi che utilizzano queste applicazioni:

New Dolpass, New Pocket Emavit, Magneter Card, New Pocket Magneter, Magneton Cmp200, New Magneter Cmp50.

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Ultrasuonoterapia

Apparecchi che utilizzano queste applicazioni:

New T-Sonic, New Pocket Sonovit, Farmasonyc Card, Biosonyc.

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    Italian Legislative Decree No. 46 of 24th February 1997, Article 21
    1. It is prohibited to advertise to the general public devices that, according to regulations adopted by Ministry of Health decree, may only be sold on prescription or be employed under the supervision of a doctor or other healthcare professional.
    2. Advertising to the general public of devices other than those referred to in paragraph 1 are subject to authorization by the Ministry of Health. Opinions on applications for authorization are expressed by the Commission of Experts provided for in Article 6, paragraph 3, of Legislative Decree No. 541 of 30th December 1992, and comprising a representative of the Department of the Ministry of Health responsible for medical devices and a representative of the Ministry of Industry, Trade and Commerce.

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