No 1 MANUFACTURER OF MEDICAL EQUIPMENT
IN RUSSIA RECOGNIZED WORLDWIDE

ALMAG®-01

  • Hospital use
  • Home use
  • PEMF therapy

Almag®-01 is a unique tPEMF device that acts on damaged organs by the Travelling Pulsed Electromagnetic Field (tPEMF) and contributes to the disappearance of pain and relief of inflammation symptoms.

It has helped its numerous users to restore vitality while reducing the drug intake.

Curative effect of magnetic field is associated with its ability to control the flow of charged particles and to act on magnetised objects regardless of their motion state. This results in a positive effect on natural biological processes as the intracellular and intercellular metabolism intensifies. The unique design of ALMAG’s induction coils (i.e. emitters) ensures tPEMF penetration of up to 8 cm deep into the patient’s tissues, which is the key to treatment of internal organs diseases. The regular rhythmical travelling tPEMF emitted by the device produces a healing effect on the cells of diseased organs and stimulates recovery.

Indications

Musculoskeletal system diseases:

  • osteochondrosis;
  • deforming osteoarthritis;
  • humeroscapular periarthrosis;
  • arthritis;
  • epicondylitis;
  • gout;
  • bursitis;
  • myositis;
  • tenosynovitis.

Injuries and their after-effects:

  • bone fractures;
  • internal joint injuries;
  • posttraumatic joint contracture;
  • wounds;
  • soft tissue bruises;
  • hematoma;
  • posttraumatic edema;
  • ligament and muscle injuries;
  • postoperative woundss;
  • keloid scar;
  • sluggish purulent wounds, phlegmons, burns.

Diseases of peripheral nervous system

Neuritis:

  • facial nerve neuritis;
  • radial nerve neuritis;
  • ulnar nerve neuritis;
  • median nerve neuritis;
  • sciatic nerve (ischias) neuritis;
  • peroneal nerve neuritis.
  • plexitis;

Neuralgia:

  • trigeminal neuralgia;
  • occipital neuralgia;
  • intercostal neuralgia.

Traumas of central nervous system:

  • vertebral column and spinal cord traumas;
  • disorders of the spinal blood circulation.

Pancreatic diabetes complications:

  • diabetic angiopathy;
  • diabetic polyneuropathy.

Diseases of venous system:

  • deep vein thrombosis of the lower leg;
  • chronic thrombophlebitis;
  • varicose veins.

Contraindications

  • inflammatory diseases in the acute phase;
  • haemorrhage and predisposition to it;
  • high-grade hypotension;
  • purulent processes before surgical treatment;
  • severe cardiac ischemia;
  • early post infarction period;
  • acute phase of cerebral blood circulation disturbance (stroke);
  • pregnancy;
  • systemic blood diseases;
  • oncological diseases;
  • thyrotoxicosis;
  • diencephalic syndrome;
  • presence of an implanted pacemaker in the treated area.

Inclusions of metal elements in bone tissues are not a contraindication for therapeutic usage of the device.

Specifications

  1. AC power supply:
    • o~230V (-10%; +6%), frequency 50Hz;
    • o~120V (-10V; +6V), frequency 60Hz.
  2. Power consumption: ≤ 35 VA.
  3. Weight: max. 0.62 kg.
  4. Overall dimensions:
    • Power supply unit - 137x60x44 mm;
    • Emitter (single piece) - 15x90 mm.
    • Note: max deviations: ±3%.
  5. The number of emitters - 4.
  6. Amplitude value of magnetic induction on an emitter’s surface (both flat sides) - (20±6) mT.
  7. Pulse duration: 1.5-2.5 ms.
  8. Magnetic field frequency: 6 Hz.
  9. The device has LED indicators that light up when it is connected to the power line and PEMF is generated.
  10. The device operates in the following mode within 6 hours: operation period of 22 min for 50Hz versions of the device (or 18 min for 60Hz versions) followed by a 10 min break.
  11. The device automatically shuts down:
    • after (22±1) min of operation for 50Hz versions of the device;
    • or after (18±1) min of operation for 60Hz versions of the device.
  12. The surfaces of the device can be safely disinfected with any solution approved for disinfection of plastic objects in medical institutions.
  13. Mean lifetime – 8 (eight) years.
  14. The device is made of hypoallergenic materials and may be used by hyper-sensitive patients.
  15. Maximum temperature after one operation cycle:
    • Control unit, max: +45°C;
    • Emitter, max: +41°C.
  16. Class of the device according to MDD 93/42/EEC – Class IIa.
  • inflammatory diseases in the acute phase;
  • haemorrhage and predisposition to it;
  • high-grade hypotension;
  • purulent processes before surgical treatment;
  • severe cardiac ischemia;
  • early post infarction period;
  • acute phase of cerebral blood circulation disturbance (stroke);
  • pregnancy;
  • systemic blood diseases;
  • oncological diseases;
  • thyrotoxicosis;
  • diencephalic syndrome;
  • presence of an implanted pacemaker in the treated area.

Inclusions of metal elements in bone tissues are not a contraindication for therapeutic usage of the device.

10/31/2016   /   16:41   /   Annie, Illinoise, USA
I've been struggling with knee problems for over a decade now. It all started when I dislocated my left knee while ice skating. Unfortunately this accident wasn't the last one... So, pain and discomfort in the knee joing area have been my companions for the most part of my life, and I've been looking for a remedy obviosly. Some things helped, some didn't. Anyways, the biggest and the happiest surprise has been this amazing little device called Almag-01. I'm so so happy someone told me about it and my interest was greater than skepticism - so I ended up trying it out. Thank you so much for inventing Almag and making it affordable for ordinary people and home use.
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ATTENTION! Prior to first usage of the device, please study this Operating Manual carefully, and follow its instructions during further use to ensure proper treatment procedure and effectiveness.    0.89 MB Download

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© Yelatma Instrument Making Enterprise, JSC, 2009—2016
The production is certified: EN ISO 13485:2012, MDD 93/42EEC (TUV NORD CERT GmbH, Germany)
BIN 1026200861620 from 20.11.02 serial 62 N 000337033