Technical Specifications - NOVAFON Pro User Manual

· Skin irritation
· Reflex / involuntary muscle contractions
Please stop the treatment immediately, should any of these side effects occur.
Please note that slight reddening and warming of the skin is not a cause for
concern. This is a desired effect of local vibration therapy, which is caused by
the increased blood flow.

6. TECHNICAL SPECIFICATIONS

6.1. SYMBOLS USED
Alternating current
Device of protection class II according to DIN EN 61140
IP44 (splash-proof)
Hertz
Short-time duty
Milliampere
Volt
Disposal according to the EU Directive on Waste Electrical and Electronic
Equipment (WEEE)
Displays the manufacturer of the medical device according to the EU Direc-
tives 93/42/EEC.
Displays the serial number of the manufacturer so that a specific medical
SN
device is identified
Type BF: A type BF (Body Floating, conductive contact with the body) applied
part/device is connected to the patient's body to transmit electrical energy or
an electrophysiological signal to or from the body
Temperature limit: refers to the temperature limits to which the medical
device can be safely exposed.
Humidity limitation
%
Atmospheric pressure limitation
Refer to instruction manual/booklet
General warning sign
6.2. TECHNICAL SPECIFICATIONS
· Operating conditions: 5 °C to 30 °C; 15% to 93% relative humidity, not con-
densing; 700 hPa to 1060 hPa atmospheric pressure
· Storage/transport: -25 °C to 70 °C; up to 93% relative humidity, not condens-
ing; 700 hPa to 1060 hPa atmospheric pressure
· Nominal voltage: Primary 230V~, 50 Hz, 65mA; Secondary 17V~, 100Hz,
450mA
· Nominal frequency: 50 Hz
· Operating mode: KB 20/15 min
· Nominal consumption: 9.5W