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BIOPTRON MedAll with hyperlight optic PAG-960

BIOPTRON MedAll with hyperlight optic PAG-960

Regular price Dhs. 5,650.00 AED
Regular price Sale price Dhs. 5,650.00 AED
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Our breakthrough light therapy device is based on Nobel Prize winning technology, and is fully certified for non-invasive, accelerated healing and 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 light, twice a day, is all that is needed for accelerated healing.

Tech Data


Item code: PAG-960
Product name: BIOPTRON MEDALL with hyperlight optics
Gross weight [KG]: 1.48
Net weight [KG]: 1
Weight without stand: 0.5 kg
Application: Professional 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 100-240 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: 350 - 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 * 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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