BIOPTRON MEDALL

BIOPTRON MEDALL: LIGHT THAT HEALS

PAG-960-NZM

DELIVERY UPON PAYMENT FROM AUCKLAND

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Our breakthrough medical light therapy device is based on Nobel Prize winning technology, and is fully certified for non-invasive, accelerated healing and medical prevention of a remarkable range of conditions, including: acne, skin wounds, sports injuries, anti-aging, arthritic and low back pain. 5 to 10 minutes exposure to BIOPTRON Medical light, twice a day, is all that is needed for accelerated healing.
BIOPTRON: BEAUTY & HEALTH REBORN  
 
30 years of intensive research, hundreds of clinical trials, and significant investment make BIOPTRON the world’s leading Light Therapy Device for health and beauty. Small yet powerful, the Swiss-made BIOPTRON MedAll light system is clinically proven and certified across the world, for faster healing and pain relief of medical conditions. Easy to use and absolutely safe, the deeply penetrating hyper-polarized medical device is designed for use at home, but can also be used by healthcare professionals in hospitals, clinics, and wellness/sports centers. Importantly, the 100% safe spectrum of BIOPTRON polychromatic light does not contain any UV radiation.

 
Put the power of BIOPTRON MedAll in the palm of your hand and effectively treat a wide range of medical conditions, including:
 
  • Chronic Pain              
  • Neck & Back Pain    
  • Wounds/Scars           
  • Acne & Psoriasis       
  • Sports Injuries   
  • Anti-Aging
  • Inflammation
  • Arthritis
  • Immune System Defense
  • Seasonal Affective Disorder      

BIOPTRON'S Wide Spectrum Of Therapeutic Indications:
 
  • Improved microcirculation;
  • Reduced Inflammation;
  • Harmonized Metabolic Processes;
  • Reinforced human defense system; 
  • Stimulated regenerative and reparative processes of the entire organism;
  • Wound healing is promoted;
  • Pain is relieved or its intensity decreased.
Professionals choose BIOPTRON – 3 Devices, 1 Technology

In addition to BIOPTRON MedAll, there are two more models in the BIOPTRON medical light therapy range: BIOPTRON Pro 1 and BIOPTRON 2. Differing only in treatment surface area size and design, BIOPTRON devices all have the same physical light characteristics and the same beneficial medical effects on the human body. Professionals therefore can also use BIOPTRON MedAll in their medical, sports medicine, physiotherapy or wellness practice. Our light therapy system has been tested and recommended by renowned doctors and scientists all over the world.
ITEM CODE
PAG-960-NZM
PRODUCT NAME
BIOPTRON MEDALL
GROSS WEIGHT [KG]
1.48
NET WEIGHT [KG]
1
WEIGHT WITHOUT STAND
0.5 kg
APPLICATION
Professional medical device for the treatment with polarized light
PRODUCER
BIOPTRON AG - Sihleggstrasse 23, CH-8832 Wollerau - Switzerland
MADE IN
Switzerland
FILTER/GLASS DIAMETER
ap. 5 cm
COLOR
White & Gray (dark)
VOLTAGE
Power supply 100-230 V~, 50/60 Hz
POWER CONSUMPTION
0.29 - 0.12 A
RATED POWER OF HALOGEN
20 W
POWER CORD
detachable
LIGHT ENERGY PER MINUTE
an av. of 2.4 J/cm²
PROTECTION AGAINST OVERHEATING
YES
POWER DENSITY
on av. of 40 mW/cm²
SAFETY CLASS
IIa IP20
WORKING TEMPERATURE
when used: from+10°C to + 30°C; for storage: from 0°C to + 40°C
SETTING THERAPY TIME
YES
WAVELENGTH
480 - 3400 nm
DEGREE OF POLARIZATION
>95% (590 - 1550 nm)
COMPOSITION
* MedAll with basic filter * suitcase for a device * power cord (detachable) * protective band on babies eyes * Oxy Sterile Spray * User manual * Warranty
DISPLAY
YES - digital
WARRANTY
5 years
CERTIFICATIONS/DECLARATION
* Declaration of Conformity with the medical Directive 93/42 / EEC issued by the producer. *Confirmation of application a medical device in the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products * CE conformity for electrical equipment. * Certificate for Quality Assurance (EN ISO 13485) * Certificate for the Quality Assurance System (Directive 93/42 / EEC) issued by the FDA * DEKRA Certificate for quality control EN ISO 13485:2012 + AC:2012 * DEKRA Certificate for medical devices complying with Annex II, Section 3 of Directive 93/42 / EEC - (Notified Body ID 0124) * Declaration of conformity from DEKRA (European notified body) for all products issued in 2013 (07.21.2013)
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