£450.00
The ItechMedical UK 'Magneto' is aimed at home users who want a super-effective PEMF device but are on a tighter budget.
Not quite as powerful as our 'Magneto Pro' devices, the Magneto is our mid-range, home-PEMF device for localised and targeted assistance.

It certainly still packs a punch at a maximum intensity 300 GAUSS. (30,000 microtesla). Still far more powerful than any other similarly priced professional systems.

Specified for targeting specific areas of the body where its 2 belt type applicators deliver powerful healing and pain-relieving forces. For example in sports injuries, knee disorders and localised pain to name a few.
All named (condition-specific) programs operate up to 200 gauss when using both applicators simultaneously. The AUTOSCAN program operates at up to 300 gauss. Again when both applicators are used together.

The current state of clinical knowledge, achieved by unifying 2400 independent global studies over the past 20 years (Research Sources: Here), is that a PEMF field intensity of 10-100 gauss (1-10 MilliTesla), provides the most effective intensity for effective assistance.
All our devices operate across this range (and higher if required), and are individually programmable too. So you can choose your own intensity. You can do that yourself or we can help you. All included and all part of the service!
For the most intensive support a maximum 300 gauss intensity is achieved through simultaneous use of both small applicators at a single site.
ItechMedical UK Magneto device in shockproof case
Applicator Belt: 1 x belt with 3 solenoids
Applicator Belt: 1 x belt with 3 solenoids
Additional applicators can be purchased at any time - see our Accessories page HERE.
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USER MANUAL
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PRODUCT LEAFLET
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CE DECLARATION
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NOTE: ALL OUR DEVICES ARE UK REGISTERED AS CLASS 2 MEDICAL DEVICES WITH THE MHRA (MEDICINES AND HEALTH REGULATORY AUTHORITY) ALL MEDICAL DEVICES SOLD IN THE UK ARE REQUIRED BY LAW TO MEET THE REGISTRATION REQUIREMENTS. YOU CAN SEE OUR REGISTRATIONS HERE…
THEY ALSO MEET THE EU MEDICAL DEVICE REGULATION REQUIREMENTS (MDR). THE EU CE DECLARATION IS REQUIRED FOR ALL DEVICES SOLD IN THE EU.