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BIOPTRON 2 with floor stand PAG-880-SET
BIOPTRON 2 with floor stand PAG-880-SET
Regular price
Dhs. 50,500.00 AED
Regular price
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Dhs. 50,500.00 AED
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Our light technology is based on Nobel Prize winning technology, and is fully certified for non-invasive, accelerated healing and prevention of a wide range of conditions, including: acne, skin wounds, sports injuries, anti-aging, arthritic and low back pain. 5 to 10 minutes of treatment with BIOPTRON, twice a day, is all one needs for accelerated healing. Health professionals choose BIOPTRON 2 because of its larger 15cm filter diameter, angled shape and choice of three stands.
Tech Data
ITEM CODE: PAG-880-SET
PRODUCT NAME: BIOPTRON 2 with floor stand
GROSS WEIGHT [KG]: 15.56
NET WEIGHT [KG]: 13.27
STAND WEIGHT: 8.80 kg gross/8.20 kg net
APPLICATION: Professional device for the treatment with polarized light
DIMENSIONS IN BOX: Dimensions of the device in package 54,5 x 40 x 25 cm
DIMENSIONS IN BOX - STAND: 85 x 94 x 26,5 cm
FILTER/GLASS DIAMETER: ap. 15 cm
PRODUCER: BIOPTRON AG - Sihleggstrasse 23, CH-8832 Wollerau - Switzerland
MADE IN: Switzerland
COLOR: White
VOLTAGE: Power supply 100-240 V~, 50/60 Hz
POWER CONSUMPTION: 1.4 -1.0 A
POWER DENSITY: on av. of 40 mW/cm²
LIGHT ENERGY PER MINUTE: an av. of 2.4 J/cm²
RATED POWER OF HALOGEN: 90 W
POWER CORD: Detachable
FUSE: T2A/250 V
PROTECTION AGAINST OVERHEATING: YES
SAFETY CLASS: I
WORKING TEMPERATURE: when using 10°C to + 30°C; for storing 0°C to + 40°C
WAVELENGTH: 480 - 3400 nm
DEGREE OF POLARIZATION: >95% (590 - 1550 nm)
COMPOSITION: BIOPTRON 2 device * Floor stand * Power cord (detechable) * Protective band on babies eyes * User manual * Warranty
DISPLAY: YES - digital
WARRANTY: 5 years
CERTIFICATIONS/DECLARATION:
* Declaration of Conformity with the Directive 93/42 / EEC issued by the producer. *Confirmation of application device in the Office for Registration of Products, 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 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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