Magneter PRO

CODE PF0701012



Magneter Pro is a professional device for magnetotherapy, characterized by the simplicity of use and by the emission of low-frequency magnetic fields. Thanks to the solenoids in endowment it is possible to make applications on the whole body without problems. Magneter PRO includes 72 preset programs with parameters for the most common applications and works by power mains and the possibility to add 20 free protocols. Applications: fractures, arthrosis, osteoporosis. Technical features:
Power supply: 230V – 50/60 Hz
Output channels: two independent Programs: 72 preset programs + 20 free programs
Display: 4,3” LCD touch screen.
Frequency: 1-100 Hz.
Output: continuous
Power: max 200 Gauss (4×50 Gauss).

  • cavo alimentazione
  • Manuale d’uso e applicazioni
  • Applicazione lunga 4 ore
  • Applicazione notturna lunga 8 ore
  • Artrite/artrosi
  • Cicatrici /dermatiti/dermatosi
  • Distorsioni
  • Dolori protesi articolari
  • Ematomi
  • Ernia discale
  • Flebiti
  • Fratture
  • Insufficienza microcircolatoria
  • Lussazioni
  • Mialgie
  • Osteoporosi
  • Pseudoartrosi
  • Reumatismi
  • Sciatalgia
  • Tendinite
  • Traumi/contusioni
  • Vene varicose/varici/circolazione perif
Technical features not available.
Terapy: Line: Pro Line

Optional Accessories …

Are you a sector professional?

Access to the full site and the presentation of products and all relevant information is reserved for sector professionals in accordance with current legislation.

NewAge Italia Srl therefore requires you to identify yourself as a sector professional in order to continue to use the site.

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.

Information request (Fisiotek)

    First name

    Last name



    I authorise the use of my personal data in compliance with Italian legislative decree 196/2003. Privacy Policy | Cookie Policy

    Log in with your credentials


    Forgot your details?

    Create Account