Classification And Reference Norms - Gima 27363 Notice D'utilisation

17
43,5 cm
17,12 in

1.4 Classification and reference norms

The Podoscope 27363 allows to evaluate the foot print, supplying secondary
indirect information on the heel alignment and on the toes situation. It allows
to evaluate the signs and the symptoms of a particular condition of the foot,
in order to formulate a judgement on the health conditons and establish
a therapy or a chiropody treatment.
The device is designed and realized according to the law prescriptions
concerning electromedical equipment, and it's therefore indicated for medical
purposes and used in clinics, consultation rooms and sports centres
by operators with knowledge of biomechanics, like doctors in sport medicine,
orthopedic specialists and physiotherapists.
Reference harmonized norms:
- CEI EN 60601-1 "Safety of electromedical devices"
- CEI EN 60601-1-2 "Collateral harmonized norm for electromedical devices –
Electromagnetic compatibility."
Classification according to safety norm EN 60601-1:
- Portable device
- Class II
- Type B
- Ordinary protection against humidity
- Do never use with inflammable anaesthetics
- Voltage: 220-240 V ~ 50/60 Hz.
The device highlights areas of the foot plant with heavest pressure thanks to
different intensity of light. In order to visualize them the patient just needs to
step on the podoscope barefoot. The particular features of this device grant
adequate protection and isolation against direct or indirect electric shocks
22 cm
8,67 in
Height
Total weight
(with package)
42,5 cm
16,75 in
Maximum load Kg 135 (297 lb)
ENGLISH
22 cm (8.67 in)
Kg 9,0 (19.84 lb)