Methacrylate podoscope with green light. System to highly reflect the footprint. It allows for studying defects in the feet, identifies the different loads on the sole with different shades of green.

Ultralight podoscope has been designed and made for the obtention of footprints through an inclined mirror and is specially thought for professional podiatrists, orthopaedists, physiotherapists, etc. and for the analysis and research of the feet’s sole. It offers the possibilityof having a real view of the foot and emphasises the areas with more and less load.

 Do not exceed the working conditions indicated in the section ‘Technical features’.
 Do not remove the tags on the device with the CE marking. If they are damaged or replaced, the current guarantee will not be covered.

USE RECOMMENDATIONS:
The equipment must be used in situations of good stability.
Do not expose the mirror and the glass to impacts.
Make sure the patient does not stumble on the front plate.

COMPONENTS OF THE PODOSCOPE
Footprinting area in PCO.
Handle for transport.
Mirror with ABS base.
Identification CE marking.
ON/OFF switch.
Power cord.

TECHNICAL FEATURES:
Voltage: 230 V.c.a. monophase / 50 Hz
Absorpton of the machine: 0.15 A
Lighting: 2 Fluorescents 8 W
Maximum load: 180 Kg
Footprint capturing: Green light
Mirror of footprint capturing: Polycarbonate base (no glass)
Weight of the machine: 8 Kg
Dimensions of work: 380 × 400 mm
Dimensions of the equipment: 520 mm × 450 mm × 180 mm H.

CLEANING
To clean the external surfaces of the podoscope (plastic, polycarbonate, painted, etc.) use your frequent cleaning products taking into consideration that the active substances are present in the maximum concentration indicated:

 Aldéhyde glutérique 2 %: 10 %
 Ethanol 96 %: 40 %
 Formaldéhyde: 0.01 %
 Glyoxal: 0.15 %
 Propanol: 35 %

GENERAL INSTRUCTIONS
Keep the surface of the polycarbonate and the mirror constantly neat, avoid the accumulation of dust on the footprinting area and on the mirror.

 Avoid pouring liquids on the work area; in case of accident, dry as soon as possible.
 In accordance with the 93/42/CEE directive of 14 June 1993 and later amendment 2007/47/CE Type 1 concerning medical devices, offering maximum safety to the user, the patient and the environment.