Featuring state-of-the-art electronics, this medical light therapy device is ergonomic, easy to handle and portable. It can be carried anywhere and programmed anytime thanks to its integrated timer and advanced display.
The BIOPTRON Pro 1 is the medium-sized light therapy device in the BIOPTRON model range. It has a filter diameter of 11cm and a light-coverage area (spot size) of about 154cm2. It is designed for use at home, in hospitals and in therapeutic centers.
BIOPTRON DEVICES: BIOPTRON devices are medical devices used in hospitals, specialist institutions, wellness and sports centers and as well as at home.
BIOPTRON LIGHT THERAPY SYSTEM: Suitable for everybody. It can be used to treat a wide range of medical conditions. Easy to use, painless and time-effective, it has no known side effects.
INNOVATIVE TECHNOLOGY: BIOPTRON devices have an innovative technology and are designed to be user-friendly.
FLOOR STANDS: Each device has floor stands that allow optimal positioning and a convenient treatment of the whole body to meet everyone’s needs.
In this way, each part of the body can be easily treated so that the user can just relax and enjoy the treatment. Differing only in size and design, all three devices have the same physical light characteristics and thus have the same beneficial effect on the human body.
SWISS-MADE: All BIOPTRON Light Therapy devices are made in Switzerland by BIOPTRON AG.
BIOPTRON AG: A Swiss company, founded in 1988, that became part of the Zepter Group in the mid-1990s. Distinguished results in the field of light therapy stem from the scientific research, experience and expertise potential of the Zepter Group. These findings have been continuously implemented in the production of the BIOPTRON Light Therapy System.
BIOPTRON devices can be used to treat:
BIOPTRON LIGHT THERAPY: A FAST, EASY, SAFE AND EFFECTIVE TREATMENT
(EN ISO 13485)
Certificate for the
BIOPTRON AG in-house laboratories are constantly engaged in the testing and optimisation of BIOPTRON devices in line with the latest scientific studies carried out by independent institutions. Simultaneously, BIOPTRON devices are further certified by accredited, independent testing institutions. Our business processes, including R&D, supplier evaluation, the supply of components to production, ongoing inspections and the product itself, comply with the European Community medical directive 93/427EEC, as well as with specific local market regulations.
510 (k) clearance for pain
For further information visit "510(k) Premarket Notification Database" Our 510(k) No: K032216