ALMAG ACTIVE™ PEMF Therapy Device (Made in Russia)

ALMAG ACTIVE™ CAN RELIEVE PAIN AND RETURN YOU TO AN ACTIVE LIFE

ALMAG ACTIVE is a portable high intensity PEMF device for relief of acute back and joint pain.

Design to relieve acute pain, including that caused by injures (fractures, ligament sprain, dislocations); rheumatoid arthritis; osteoarthritis; osteochondrosis, including that complicated by prolapse; rehabilitation after orthopedic traumas and injuries.

ALMAG ACTIVE is intended to provide physiotherapeutic treatment of pain as well as recovery and rehabilitation measures using a low-frequency pulsed magnetic field, either in medical facilities or at home, upon the recommendation of a doctor. Suitable for all family members or for use in medical centers and hospitals.

ALMAG ACTIVE™ THE MOST EFFECTIVE PEMF THERAPY

ALMAG ACTIVE offers the most effective PEMF treatment for Arthritis and Osteoarthritis, help to relieve inflammation, constricting pain and swelling, due to a special medical technology — by a particular combination of several exposure modes according to a mode scheme allows you to use ALMAG ACTIVE immediately after the injury!

INDICATIONS FOR USE OF ALMAG ACTIVE

• Arthritides, arthroses, osteochondropathy, or bone spur;
• Dorsopathy including osteochondrosis vertebralis, herniated nucleus pulposus, or scoliosis;
• Osteoporosis; - Hypertensive disease of the I and II degree;
• Dystonia (vegetovascular dystonia);
• Complications of diabetes mellitus Type I and II;
• Atherosclerosis;
• Vein and lymph vascular disease including varicosity and its complications as well as lymphostasis;
• Asthma;
• Bronchitis;
• Nerve root and plexus disorders in extremities including post-traumatic as well as poststroke disorders;
• Injuries (fractures).

ALMAG ACTIVE ENABLES TO:

• Reduce inflammation of joints and pain syndrome, increase blood flow & circulation and improve cell metabolism.
• Relieve exacerbation of pain associated with musculoskeletal system disorders and muscle cramps.
• Relieve joint stiffness caused by rheumatoid arthritis.
• Increase joint mobility and improved join function.
• Promote restore of bones and joints, acceleration of the healing process.
• Keep the disease from turning chronic.

CERTIFIED TO MEET INTERNATIONAL QUALITY STANDARDS

ALMAG ACTIVE comply with the Medical Devices Directive 93/42/ EEC of the European Union (EU). Our enterprise’s quality assurance system meets the requirements of the International standard EN ISO 13485:2016, also confirmed by the German experts of TUV NORD CERT GmbH. U.S. FDA-approved.

INSTRUCTIONS FOR USE

For effective treatment device is sufficient to apply from 3 to 20 minutes, once a day - depending on the rate and disease and age. 7 days per treatment cycle. An instructional user manual attached to the product guide you through using the device.

ALMAG ACTIVE™ CAN OPERATE USING THREE DIFFERENT MODES

- Analgesic mode

Enables to stop an attack of a very first disease, ALMAG ACTIVE can be used in the acute phase of a disease, that is rare for physiotherapy.

- Basic mode

Uses a running pulsed magnetic field in the prevention of joint diseases and their treatment during the subacute period, rehabilitation after injuries (including fractures).

- Pediatric mode

Sets special parameters on a running pulsed magnetic field, suitable for the treatment of children one month of age and older.

TECHNICAL INFORMATION

• Maximum Intensity (Gauss): 200 (+-60)
• Number of programs: 3
• Coil excitation frequencies: 6.25/7.5 for basic mode; 6.25/7.5 for pediatric mode; 100/120 for analgesic mode.
• Dimensions: 142*75*35mm for a control unit; 890*88*18mm for an emitter.
• Weight: < 0.8 kg
• Maximum operating temperature: +41°C for coils; +45°C for a pulse generator.
• Operation time: 20 minutes per working cycle
• Power supply: AC mains ~230V 50Hz
• Warranty: 1 Year

Contraindications

• Acute pyoinflammatory conditions;
• Aortic aneurysm;
• Pregnancy;
• Systemic blood diseases;
• Malignancies;
• Thyrotoxicosis;
• Alcoholic intoxication;
• Atrial fibrillation;
• Implanted cardiostimulator present in the exposure area.

Metal inclusions, if present in bone tissue, is not a contraindication to administration of the device in therapeutic doses. Metal dental crowns, if present in mouth cavity, is not a contraindication to administration of the device in therapeutic doses.