Our medical light technology is based on Nobel Prize winning technology, and is fully certified for non-invasive, accelerated healing and medical prevention of a wide range of conditions including: acne, skin wounds, sports injuries, anti-aging, arthritic and low back pain. Just 5 to 10 minutes of treatment with BIOPTRON twice a day is all that is needed for accelerated healing. BIOPTRON Pro 1 has a filter diameter of 11cm and is designed for use at home, in hospitals and in therapeutic centers.
BIOPTRON PRO 1 - SPOT THE DIFFERENCE
Introducing the medium-sized Light Therapy device in the BIOPTRON product range. The only difference between the BIOPTRON family of devices is the size of the light spot and thus the treated areas surface. All BIOPTRON medical light therapy devices ensure optimal penetration through the tissues to bio-stimulate the immune system for faster and more effective healing and pain relief. Equally, all BIOPTRON devices promote safe cell activation, accelerate local blood circulation and systemic stimulation of the whole body's regenerative and reparative healing and preventive processes.
The Main Benefits Of BIOPTRON Pro 1:
Please Note: All BIOPTRON medical light therapy devices are 100% safe and use a spectrum of polychromatic light which does not contain UV radiation.
PAG-991-SAA
Bioptron Pro 1 with Floor Stand
10.45
9
Professional medical device for the treatment with polarized light
BIOPTRON AG - Sihleggstrasse 23, CH-8832 Wollerau - Switzerland
Switzerland/p>
ap. 11 cm
white
Power supply 100-240 V~, 50/60 Hz
75 W
50 W
detachable
an av. of 2.4 J/cm2
YES
on av. of 40 mW/cm²
IIa IP20
YES
when used 10°C to + 30°C; for storage 0°C to + 40°C
480 - 3400 nm
>95% (590 - 1550 nm)
BIOPTRON PRO1 device with basic filter * Floor stand * Power cord (detachable) * Protective band on babies eyes * Protective cover * Protective bag * Oxy Sterile Spray * User manual * Warranty
YES - digital
5 Years (2 Years Bulb and Fan, 5 Years on All Other Parts, Does Not Cover Material Damage)
* 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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