Item code
PAG-960
Product name
BIOPTRON MEDALL with hyperlight optics
Warranty
5 years
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 100-240 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
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Safety class
IIa IP20
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Vestibulum nec consequat erat. Quisque id neque consequat, ullamcorper orci eget, accumsan mi. Ut lobortis eros a erat vestibulum, sed sollicitudin erat vehicula. Morbi facilisis ante in quam luctus pellentesque. Aenean accumsan nibh mi, vel vulputate mauris dignissim ac. Sed eu justo efficitur, feugiat ligula at, aliquam elit. Duis aliquet sem a neque porttitor, sit amet dignissim lectus cursus. Suspendisse posuere facilisis lectus id tincidunt. In hac habitasse platea dictumst. Maecenas urna urna, fringilla id pharetra quis, maximus ut orci. Vestibulum molestie tempor venenatis.
Proin sapien tellus, congue sit amet sem pulvinar, laoreet gravida magna. Sed placerat molestie sapien, mollis pretium velit congue ac. Curabitur sed placerat libero. Vivamus posuere porttitor ipsum, ac volutpat justo elementum in. Curabitur eget rutrum arcu, vel blandit ante. Interdum et malesuada fames ac ante ipsum primis in faucibus. Etiam dignissim diam vitae diam malesuada vestibulum.
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 * Oxy Sterile Spray * User manual * Warranty
Display
YES - digital
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)